3e74:D (GLY54) to (ILE62) CRYSTAL STRUCTURE OF E. COLI ALLANTOINASE WITH IRON IONS AT THE METAL CENTER | (BETA/ALPHA)8-BARREL DOMAIN, SMALL BETA-SHEET DOMAIN, HYDROLASE, METAL-BINDING, PURINE METABOLISM, ZINC
3e7g:C (THR109) to (GLY117) STRUCTURE OF HUMAN INOSOX WITH INHIBITOR AR-C95791 | NITRIC OXIDE, NOS, HEME, TETRAHYDROBIOPTERIN, OXIDOREDUCTASE, ALTERNATIVE SPLICING, CALCIUM, CALMODULIN- BINDING, FAD, FMN, IRON, METAL-BINDING, NADP, PHOSPHOPROTEIN, POLYMORPHISM, ZINC
3e7s:A (PRO92) to (GLY100) STRUCTURE OF BOVINE ENOS OXYGENASE DOMAIN WITH INHIBITOR AR- C95791 | NITRIC OXIDE SYNTHASE, NOS, HEME, TETRAHYDROBIOPTERIN, OXIDOREDUCTASE CALMODULIN-BINDING, FAD, FMN, IRON, METAL- BINDING, NADP, OXIDOREDUCTASE, POLYMORPHISM, ZINC
4wd5:A (GLU711) to (ALA722) CRYSTAL STRUCTURE OF EGFR 696-1022 T790M IN COMPLEX WITH QL-X138 | EGFR, T790M, GATEKEEPER MUTATION, INHIBITOR, TRANSFERASE-INHIBITOR COMPLEX
3rma:C (PRO35) to (ASP51) CRYSTAL STRUCTURE OF A REPLICATIVE DNA POLYMERASE BOUND TO DNA CONTAINING THYMINE GLYCOL | DNA LESION, THYMINE GLYCOL, PROTEIN-DNA COMPLEX, TRANSFERASE-DNA COMPLEX
3rmb:C (PRO35) to (ASP51) CRYSTAL STRUCTURE OF A REPLICATIVE DNA POLYMERASE BOUND TO DNA CONTAINING THYMINE GLYCOL | DNA LESION, THYMINE GLYCOL, PROTEIN-DNA COMPLEX, TRANSFERASE-DNA COMPLEX
3rmb:D (PRO35) to (ASP51) CRYSTAL STRUCTURE OF A REPLICATIVE DNA POLYMERASE BOUND TO DNA CONTAINING THYMINE GLYCOL | DNA LESION, THYMINE GLYCOL, PROTEIN-DNA COMPLEX, TRANSFERASE-DNA COMPLEX
4wdy:B (LEU27) to (PRO45) JC POLYOMAVIRUS VP1 FIVE-FOLD PORE MUTANT N221Q | BETA-SANDWICH, JELLY-ROLL, VIRAL MAJOR CAPSID PROTEIN, FIVE-FOLD PORE, VIRAL PROTEIN
4wdz:A (LEU27) to (GLU46) JC POLYOMAVIRUS VP1 FIVE-FOLD PORE MUTANT N221W | BETA-SANDWICH, JELLY-ROLL, VIRAL MAJOR CAPSID PROTEIN, FIVE-FOLD PORE, VIRAL PROTEIN
4wdz:B (LEU27) to (GLU46) JC POLYOMAVIRUS VP1 FIVE-FOLD PORE MUTANT N221W | BETA-SANDWICH, JELLY-ROLL, VIRAL MAJOR CAPSID PROTEIN, FIVE-FOLD PORE, VIRAL PROTEIN
4wdz:C (LEU27) to (GLU46) JC POLYOMAVIRUS VP1 FIVE-FOLD PORE MUTANT N221W | BETA-SANDWICH, JELLY-ROLL, VIRAL MAJOR CAPSID PROTEIN, FIVE-FOLD PORE, VIRAL PROTEIN
4wdz:E (LEU27) to (PRO45) JC POLYOMAVIRUS VP1 FIVE-FOLD PORE MUTANT N221W | BETA-SANDWICH, JELLY-ROLL, VIRAL MAJOR CAPSID PROTEIN, FIVE-FOLD PORE, VIRAL PROTEIN
1na7:A (ASP38) to (LYS49) CRYSTAL STRUCTURE OF THE CATALYTIC SUBUNIT OF HUMAN PROTEIN KINASE CK2 | CK2, PROTEIN KINASE, MICROCRYSTALS, THIN-FILM NANOTECHNOLOGY, MICROFOCUS ESRF, TRANSFERASE
1nae:A (TYR56) to (LYS66) STRUCTURE OF CSCBM6-3 FROM CLOSTRIDIUM STERCORARIUM IN COMPLEX WITH XYLOTRIOSE | CARBOHYDRATE-BINDING MODULE, BETA-SANDWICH, XYLAN, XYLOOLIGOSACCHARIDE, HYDROLASE
3rmc:C (PRO35) to (ASP51) CRYSTAL STRUCTURE OF A REPLICATIVE DNA POLYMERASE BOUND TO DNA CONTAINING THYMINE GLYCOL | DNA LESION, THYMINE GLYCOL, PROTEIN-DNA COMPLEX, TRANSFERASE-DNA COMPLEX
3rmc:D (PRO35) to (ASP51) CRYSTAL STRUCTURE OF A REPLICATIVE DNA POLYMERASE BOUND TO DNA CONTAINING THYMINE GLYCOL | DNA LESION, THYMINE GLYCOL, PROTEIN-DNA COMPLEX, TRANSFERASE-DNA COMPLEX
1a4s:C (ILE324) to (GLY338) BETAINE ALDEHYDE DEHYDROGENASE FROM COD LIVER | OXIDOREDUCTASE, ALDEHYDE OXIDATION
1a5h:A (ALA31) to (LEU53) CATALYTIC DOMAIN OF HUMAN TWO-CHAIN TISSUE PLASMINOGEN ACTIVATOR COMPLEX OF A BIS-BENZAMIDINE | TRYPSIN LIKE SERINE PROTEASE, FIBRINOLYTIC ENZYME, HYDROLASE
2akm:A (TRP364) to (GLU376) FLUORIDE INHIBITION OF ENOLASE: CRYSTAL STRUCTURE OF THE INHIBITORY COMPLEX | ENOLASE; FLUORIDE INHIBITION; NEGATIVE COOPERATIVITY; GLYCOLYSIS; CRYSTAL STRUCTURE; ISOTHERMAL TITRATION CALORIMETRY, LYASE
3ebe:C (VAL359) to (GLY373) CRYSTAL STRUCTURE OF XENOPUS LAEVIS REPLICATION INITIATION FACTOR MCM10 INTERNAL DOMAIN | OB-FOLD, ZINC FINGER, CCCH, DNA REPLICATION, METAL-BINDING, NUCLEUS, ZINC-FINGER, REPLICATION
1a9m:B (ASP30) to (GLY49) G48H MUTANT OF HIV-1 PROTEASE IN COMPLEX WITH A PEPTIDIC INHIBITOR U-89360E | ASPARTYL PROTEASE, DRUG RESISTANT, MUTATION
3rqj:A (GLY325) to (GLY333) STRUCTURE OF THE NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-((1S,2R)-2-(3-FLUOROPHENYL)CYCLOPROPYLAMINO) ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, ENZYME-INHIBITOR COMPLEX, OXIDOREDUCTASE-INHIBITOR COMPLEX
3rqj:B (GLY325) to (GLY333) STRUCTURE OF THE NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-((1S,2R)-2-(3-FLUOROPHENYL)CYCLOPROPYLAMINO) ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, ENZYME-INHIBITOR COMPLEX, OXIDOREDUCTASE-INHIBITOR COMPLEX
1a9x:D (PRO3558) to (ASP3567) CARBAMOYL PHOSPHATE SYNTHETASE: CAUGHT IN THE ACT OF GLUTAMINE HYDROLYSIS | AMIDOTRANSFERASE, THIOESTER
3rqk:A (GLY325) to (GLY333) STRUCTURE OF THE NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-{[(3R,4R)-4-(2-{[(1R,2S)-2-(3-METHYLPHENYL) CYCLOPROPYL]AMINO}ETHOXY)PYRROLIDIN-3-YL]METHYL}PYRIDIN-2-AMINE AND ITS ISOMER | OXIDOREDUCTASE, ENZYME-INHIBITOR COMPLEX, OXIDOREDUCTASE-INHIBITOR COMPLEX
3rqk:B (GLY325) to (GLY333) STRUCTURE OF THE NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-{[(3R,4R)-4-(2-{[(1R,2S)-2-(3-METHYLPHENYL) CYCLOPROPYL]AMINO}ETHOXY)PYRROLIDIN-3-YL]METHYL}PYRIDIN-2-AMINE AND ITS ISOMER | OXIDOREDUCTASE, ENZYME-INHIBITOR COMPLEX, OXIDOREDUCTASE-INHIBITOR COMPLEX
3rqm:A (GLY325) to (GLY333) STRUCTURE OF THE NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-{[(3R,4R)-4-(2-{[(2R/2S)-1-(3-FLUOROPHENYL)PROPAN-2- YL]AMINO}ETHOXY)PYRROLIDIN-3-YL]METHYL}-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, ENZYME-INHIBITOR COMPLEX, OXIDOREDUCTASE-INHIBITOR COMPLEX
3rqm:B (GLY325) to (GLY333) STRUCTURE OF THE NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-{[(3R,4R)-4-(2-{[(2R/2S)-1-(3-FLUOROPHENYL)PROPAN-2- YL]AMINO}ETHOXY)PYRROLIDIN-3-YL]METHYL}-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, ENZYME-INHIBITOR COMPLEX, OXIDOREDUCTASE-INHIBITOR COMPLEX
3rql:A (GLY325) to (GLY333) STRUCTURE OF THE NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-((1S,2R/1R,2S)-2-(3-CLOROPHENYL) CYCLOPROPYLAMINO)ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2- AMINE | OXIDOREDUCTASE, ENZYME-INHIBITOR COMPLEX, OXIDOREDUCTASE-INHIBITOR COMPLEX
3rql:B (GLY325) to (GLY333) STRUCTURE OF THE NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-((1S,2R/1R,2S)-2-(3-CLOROPHENYL) CYCLOPROPYLAMINO)ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2- AMINE | OXIDOREDUCTASE, ENZYME-INHIBITOR COMPLEX, OXIDOREDUCTASE-INHIBITOR COMPLEX
3rqn:A (GLY325) to (GLY333) STRUCTURE OF THE NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3*R*,4*R*)-4-(2-(((*S* )-1-(3-FLUOROPHENYL)PROPAN-2-YL) AMINO)ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, ENZYME-INHIBITOR COMPLEX, OXIDOREDUCTASE-INHIBITOR COMPLEX
3rqn:B (GLY325) to (GLY333) STRUCTURE OF THE NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3*R*,4*R*)-4-(2-(((*S* )-1-(3-FLUOROPHENYL)PROPAN-2-YL) AMINO)ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, ENZYME-INHIBITOR COMPLEX, OXIDOREDUCTASE-INHIBITOR COMPLEX
2arb:B (ASN41) to (PHE52) PTEROCARPUS ANGOLENSIS LECTIN (PAL) IN COMPLEX WITH THE GLCNAC(BETA1- 2)MAN DISACCHARIDE | LECTIN, CARBOHYDRATE RECOGNITION, SUGAR BINDING PROTEIN
2arx:B (ASN41) to (PHE52) PTEROCARPUS ANGOLENSIS SEED LECTIN IN COMPLEX WITH THE DECASACCHARIDE NA2F | LECTIN, CARBOHYDRATE, LEGUME LECTIN, SUGAR BINDING PROTEIN
3ed4:B (GLY369) to (GLY378) CRYSTAL STRUCTURE OF PUTATIVE ARYLSULFATASE FROM ESCHERICHIA COLI | STRUCTURAL GENOMICS, SULFATASE, PSI-2, PROTEIN STRUCTURE INITIATIVE, NEW YORK STRUCTURAL GENOMIX RESEARCH CONSORTIUM, NYSGXRC, TRANSFERASE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS
2atq:A (PRO35) to (ASP51) RB69 SINGLE-STRANDED DNA BINDING PROTEIN-DNA POLYMERASE FUSION | DNA POLYMERASE, PALM DOMAIN, FINGERS DOMAIN, THUMB DOMAIN, SINGLE-STRANDED DNA BINDING PROTEIN, OB-FOLD, TRANSFERASE/DNA BINDING PROTEIN COMPLEX
2auy:A (ASN41) to (PHE52) PTEROCARPUS ANGOLENSIS LECTIN IN COMPLEX WITH THE TRISACCHARIDE GLCNAC(B1-2)MAN(A1-3)MAN | LECTIN, CARBOHYDRATE, SUGAR, LEGUME LECTIN, SUGAR BINDING PROTEIN
4gz7:A (GLY5) to (GLU17) THE CRYSTAL STRUCTURE OF APO-DIHYDROPYRIMIDINASE FROM TETRAODON NIGROVIRIDIS | CARBOXYLATION, ZINC BINDING, ALPHA-BETA BARREL, HYDROLASE
2avm:B (ASP30) to (GLY49) KINETICS, STABILITY, AND STRUCTURAL CHANGES IN HIGH RESOLUTION CRYSTAL STRUCTURES OF HIV-1 PROTEASE WITH DRUG RESISTANT MUTATIONS L24I, I50V, AND G73S | HIV-1 PROTEASE, DRUG RESISTANCE, SUBSTRATE ANALOG, NON-ACTIVE SITE MUTANTS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2avo:A (ASP30) to (ILE50) KINETICS, STABILITY, AND STRUCTURAL CHANGES IN HIGH RESOLUTION CRYSTAL STRUCTURES OF HIV-1 PROTEASE WITH DRUG RESISTANT MUTATIONS L24I, I50V, AND G73S | DRUG RESISTANCE; HIV-1 PROTEASE,INDINAVIR, SUBSTRATE ANALOG,NON- ACTIVE SITE MUTANTS., HYDROLASE
2omn:B (ARG107) to (PRO118) BENCE JONES KWR PROTEIN- IMMUNOGLOBULIN LIGHT CHAIN DIMER, P4(3)2(1)2 CRYSTAL FORM | IMMUNOGLOBULIN LIGHT CHAIN, IMMUNE SYSTEM
2axc:A (ILE243) to (PRO253) CRYSTAL STRUCTURE OF COLE7 TRANSLOCATION DOMAIN | COLICIN, TRANSLOCATION DOMAIN, HYDROLASE
3egx:A (CYS444) to (PRO453) CRYSTAL STRUCTURE OF THE MAMMALIAN COPII-COAT PROTEIN SEC23A/24A COMPLEXED WITH THE SNARE PROTEIN SEC22B AND BOUND TO THE TRANSPORT SIGNAL SEQUENCE OF THE SNARE PROTEIN BET1 | COPII COAT PROTEIN, VESICLE TRANSPORT, TRANSPORT SIGNAL SEQUENCE, DISEASE MUTATION, ENDOPLASMIC RETICULUM, ER-GOLGI TRANSPORT, GOLGI APPARATUS, MEMBRANE, PROTEIN TRANSPORT, TRANSPORT, PHOSPHOPROTEIN, TRANSMEMBRANE
2onn:A (ARG329) to (PRO343) ARG475GLN MUTANT OF HUMAN MITOCHONDRIAL ALDEHYDE DEHYDROGENASE, APO FORM | OXIDOREDUCTASE, ALDH, NAD, ROSSMANN FOLD
4h00:A (GLY5) to (GLU17) THE CRYSTAL STRUCTURE OF MON-ZN DIHYDROPYRIMIDINASE FROM TETRAODON NIGROVIRIDIS | HYDROLASE, CARBOXYLATION, ZINC BINDING, ALPHA-BETA BARREL
1amh:A (GLN30) to (VAL53) UNCOMPLEXED RAT TRYPSIN MUTANT WITH ASP 189 REPLACED WITH SER (D189S) | SERINE PROTEASE, ACTIVATION DOMAIN, SUBSTRATE SPECIFICITY HYDROLASE
4h1s:A (PRO138) to (GLY148) CRYSTAL STRUCTURE OF A TRUNCATED SOLUBLE FORM OF HUMAN CD73 WITH ECTO- 5'-NUCLEOTIDASE ACTIVITY | 5'-NUCLEOTIDASE, HYDROLASE
4h1s:B (PRO138) to (GLY148) CRYSTAL STRUCTURE OF A TRUNCATED SOLUBLE FORM OF HUMAN CD73 WITH ECTO- 5'-NUCLEOTIDASE ACTIVITY | 5'-NUCLEOTIDASE, HYDROLASE
3rwu:A (PRO35) to (ASP51) RB69 DNA POLYMERASE (Y567A) TERNARY COMPLEX WITH DATP OPPOSITE DIFLUOROTOLUENE NUCLEOSIDE | DIFLUOROTOLUENE, DATP, Y567A, Y567A MUTANT, TRANSFERASE-DNA COMPLEX
4h1y:P (PRO138) to (GLY148) HUMAN ECTO-5'-NUCLEOTIDASE (CD73): CRYSTAL FORM II (OPEN) IN COMPLEX WITH PSB11552 | DIMERIC, NUCLEOTIDASE, HYDROLASE, AMP BINDING, ZINC BINDING, EXTRACELLULAR
3rxt:A (GLN33) to (SER55) CRYSTAL STRUCTURE OF TRYPSIN COMPLEXED WITH (3-METHOXYPHENYL) METHANAMIN (F04 AND F03, COCKTAIL EXPERIMENT) | TRYPSIN-LIKE SERINE PROTEASES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4h2b:A (PRO138) to (GLY148) HUMAN ECTO-5'-NUCLEOTIDASE (CD73): CRYSTAL FORM II (OPEN) IN COMPLEX WITH BAICALIN | DIMER, HYDROLASE PHOSPHATASE NUCLEOTIDASE, EXTRACELLULAR, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3eid:C (ASN3) to (THR14) CDK2/CYCLINA COMPLEXED WITH A PYRAZOLOPYRIDAZINE INHIBITOR | CDK2, CYCLIN, ATP-BINDING, CELL CYCLE, CELL DIVISION, KINASE, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE- PROTEIN KINASE, TRANSFERASE, NUCLEUS, TRANSFERASE-CELL CYCLE COMPLEX
1nqk:A (ASN4) to (HIS16) STRUCTURAL GENOMICS, CRYSTAL STRUCTURE OF ALKANESULFONATE MONOOXYGENASE | STRUCTURAL GENOMICS, BETA BARREL, PSI, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, OXIDOREDUCTASE
1aq7:A (GLN30) to (SER54) TRYPSIN WITH INHIBITOR AERUGINOSIN 98-B | HYDROLASE, SERINE PROTEASE, INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1aqb:A (GLY22) to (GLU33) RETINOL-BINDING PROTEIN (RBP) FROM PIG PLASMA | RETINOL TRANSPORT, RETINOIDS, VITAMIN A, CADMIUM ION
1nsi:D (THR109) to (GLY117) HUMAN INDUCIBLE NITRIC OXIDE SYNTHASE, ZN-BOUND, L-ARG COMPLEX | NITRIC OXIDE SYNTHASE, HEME PROTEIN, TETRAHYDROBIOPTERIN, OXIDOREDUCTASE
3ek1:C (LEU317) to (PRO331) CRYSTAL STRUCTURE OF ALDEHYDE DEHYDROGENASE FROM BRUCELLA MELITENSIS BIOVAR ABORTUS 2308 | SSGCID, ALDEHYDE DEHYDROGENASE,, OXIDOREDUCTASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE
3ek1:D (LEU317) to (PRO331) CRYSTAL STRUCTURE OF ALDEHYDE DEHYDROGENASE FROM BRUCELLA MELITENSIS BIOVAR ABORTUS 2308 | SSGCID, ALDEHYDE DEHYDROGENASE,, OXIDOREDUCTASE, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE
2ova:A (GLY29) to (SER38) X-RAY STRUCTURE OF HUMAN COMPLEMENT PROTEIN C8GAMMA Y83W MUTANT | LIPOCALIN; BETA BARREL, TRANSPORT PROTEIN,LIGAND BINDING PROTEIN
2ovd:A (GLY29) to (SER38) CRYSTAL STRUCTURE OF HUMAN COMPLEMENT PROTEIN C8GAMMA WITH LAURATE | LIPOCALIN; BETA BARREL, TRANSPORT PROTEIN,LIGAND BINDING PROTEIN
2ove:A (GLY29) to (SER38) CRYSTAL STRUCTURE OF RECOMBINANT HUMAN COMPLEMENT PROTEIN C8GAMMA | LIPOCALIN; BETA BARREL, TRANSPORT PROTEIN,LIGAND BINDING PROTEIN
2oxy:B (ASP38) to (LYS49) PROTEIN KINASE CK2 IN COMPLEX WITH TETRABROMOBENZOIMIDAZOLE DERIVATIVES K17, K22 AND K32 | PROTEIN KINASE CK2, INHIBITORS, TETRABROMOBENZOIMIDAZOLE DERIVATIVES, TRANSFERASE
4h97:A (THR147) to (PRO160) CANDIDA ALBICANS DIHYDROFOLATE REDUCTASE COMPLEXED WITH NADPH AND 5- {3-[3-METHOXY-5-(4-METHYLPHENYL)PHENYL]BUT-1-YN-1-YL}-6- METHYLPYRIMIDINE-2,4-DIAMINE (UCP111D4M) | ANTIFUNGAL AGENTS, CANDIDA ALBICANS, DRUG DESIGN, ENZYME INHIBITORS, FUNGAL PROTEINS, TETRAHYDROFOLATE DEHYDROGENASE, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
2ozk:A (SER287) to (ASP296) STRUCTURE OF AN N-TERMINAL TRUNCATED FORM OF NENDOU (NSP15) FROM SARS-CORONAVIRUS | ENDONUCLEASE NENDOU, RIBONUCLEASE, HOMOLOG OF XENOPUS XENDOU, SARS NSP15, N-TERMINAL TRUNCATED CONSTRUCT, VIRAL PROTEIN
2b8o:H (GLN30) to (VAL53) CRYSTAL STRUCTURE OF GLU-GLY-ARG-CHLOROMETHYL KETONE-FACTOR VIIA/SOLUBLE TISSUE FACTOR COMPLEX | SERINE PROTEASE, TISSUE FACTOR, EGR, BLOOD COAGUALTION, CLOTTING, CLOTTING FACTOR, COAGULATION FACTOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1b0e:A (GLN30) to (MET53) CRYSTAL STRUCTURE OF PORCINE PANCREATIC ELASTASE WITH MDL 101,146 | SERINE PROTEASE, FLUOROETHYL KETONES, HYDROLASE
2b9j:A (ASP12) to (ALA23) CRYSTAL STRUCTURE OF FUS3 WITH A DOCKING MOTIF FROM FAR1 | TRANSFERASE
3eqr:A (LEU117) to (GLU130) CRYSTAL STRUCTURE OF ACK1 WITH COMPOUND T74 | ACK1, ALTERNATIVE SPLICING, ATP-BINDING, CELL MEMBRANE, KINASE, MAGNESIUM, MEMBRANE, METAL-BINDING, NUCLEOTIDE- BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SH3 DOMAIN, TRANSFERASE, TYROSINE-PROTEIN KINASE
4ww8:A (PRO100) to (SER108) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH 4- PROPYLTHIOBENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLE, LYASE
4ww8:C (PRO100) to (SER108) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH 4- PROPYLTHIOBENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLE, LYASE
4hcr:B (LYS116) to (LEU129) CRYSTAL STRUCTURE OF HUMAN MADCAM-1 D1D2 COMPLEXED WITH FAB PF-547659 | IMMUNOGLOBULIN SUPERFAMILY, ROLLING AND FIRM ADHESION, INTEGRIN ALPHA4BETA7, IMMUNE SYSTEM
4hd9:A (LYS116) to (LEU129) CRYSTAL STRUCTURE OF NATIVE HUMAN MADCAM-1 D1D2 DOMAIN | IMMUNOGLOBULIN SUPERFAMILY, ROLLING AND FIRM ADHESION, INTEGRIN ALPHA4BETA7, IMMUNE SYSTEM
2p4s:C (GLY212) to (LEU223) STRUCTURE OF PURINE NUCLEOSIDE PHOSPHORYLASE FROM ANOPHELES GAMBIAE IN COMPLEX WITH DADME-IMMH | PURINE NUCLEOSIDE PHOSPHORYLASE, TRANSFERASE
2p5g:D (PRO35) to (ASP51) CRYSTAL STRUCTURE OF RB69 GP43 IN COMPLEX WITH DNA WITH DAMP OPPOSITE AN ABASIC SITE ANALOG IN A 21MER TEMPLATE | DNA POLYMERASE, ABASIC SITE, DNA LESION, DAMP, TRANSFERASE/DNA COMPLEX
1b6j:B (ASP130) to (GLY149) HIV-1 PROTEASE COMPLEXED WITH MACROCYCLIC PEPTIDOMIMETIC INHIBITOR 1 | COMPLEX (ACID PROTEINASE-PEPTIDE), HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4hfl:A (ASP97) to (GLY113) CRYSTAL STRUCTURE OF THE TYPE VI EFFECTOR TAE4 FROM ENTEROBACTER CLOACAE | AMIDASE, HYDROLASE
2bgo:A (ALA16) to (VAL25) MANNAN BINDING MODULE FROM MAN5C | CARBOHYDRATE BINDING PROTEIN, MANNAN, CARBOHYDRATE BINDING MODULE
3s2k:B (VAL1051) to (ARG1060) STRUCTURAL BASIS OF WNT SIGNALING INHIBITION BY DICKKOPF BINDING TO LRP5/6. | WNT CO-RECEPTOR, BETA-PROPELLER, EGF DOMAIN, WNT SIGNALING, WNT INHIBITOR, GLYCOSYLATION, SIGNALING PROTEIN
2bhv:A (LYS176) to (SER188) STRUCTURE OF COMB10 OF THE COM TYPE IV SECRETION SYSTEM OF HELICOBACTER PYLORI | BACTERIAL PROTEIN, BACTERIAL TYPE IV SECRETION
2bhv:B (LYS176) to (SER188) STRUCTURE OF COMB10 OF THE COM TYPE IV SECRETION SYSTEM OF HELICOBACTER PYLORI | BACTERIAL PROTEIN, BACTERIAL TYPE IV SECRETION
2bhv:D (LYS176) to (SER188) STRUCTURE OF COMB10 OF THE COM TYPE IV SECRETION SYSTEM OF HELICOBACTER PYLORI | BACTERIAL PROTEIN, BACTERIAL TYPE IV SECRETION
2bhv:E (LYS176) to (SER188) STRUCTURE OF COMB10 OF THE COM TYPE IV SECRETION SYSTEM OF HELICOBACTER PYLORI | BACTERIAL PROTEIN, BACTERIAL TYPE IV SECRETION
4x12:D (LEU27) to (GLU46) JC POLYOMAVIRUS GENOTYPE 3 VP1 IN COMPLEX WITH GD1B OLIGOSACCHARIDE | BETA-SANDWICH, JELLY-ROLL, VIRAL MAJOR CAPSID PROTEIN, GLYCAN, VIRAL PROTEIN
4x0y:B (LEU27) to (GLU46) JC POLYOMAVIRUS VP1 FROM A GENOTYPE 3 STRAIN | BETA-SANDWICH, JELLY-ROLL, VIRAL CAPSID PROTEIN, VIRAL PROTEIN
4x0y:C (LEU27) to (GLU46) JC POLYOMAVIRUS VP1 FROM A GENOTYPE 3 STRAIN | BETA-SANDWICH, JELLY-ROLL, VIRAL CAPSID PROTEIN, VIRAL PROTEIN
4x0y:E (LEU27) to (GLU46) JC POLYOMAVIRUS VP1 FROM A GENOTYPE 3 STRAIN | BETA-SANDWICH, JELLY-ROLL, VIRAL CAPSID PROTEIN, VIRAL PROTEIN
4x0z:B (LEU27) to (GLU46) JC POLYOMAVIRUS GENOTYPE 3 VP1 IN COMPLEX WITH GM1 OLIGOSACCHARIDE | BETA-SANDWICH, JELLY-ROLL, VIRAL CAPSID PROTEIN, GLYCAN, VIRAL PROTEIN
4hj1:B (ALA1009) to (GLY1024) CRYSTAL STRUCTURE OF GLYCOPROTEIN C FROM RIFT VALLEY FEVER VIRUS (GLYCOSYLATED) | CLASS II FUSION PROTEIN, MEMBRANE FUSION, VIRAL ENVELOPE, VIRAL PROTEIN
4x10:B (LEU27) to (GLU46) JC POLYOMAVIRUS GENOTYPE 3 VP1 IN COMPLEX WITH GM2 OLIGOSACCHARIDE | BETA-SANDWICH, JELLY-ROLL, VIRAL CAPSID PROTEIN, GLYCAN, VIRAL PROTEIN
4hj9:A (ARG16) to (LYS25) CRYSTAL STRUCTURE OF SCHIZOSACCHAROMYCES POMBE POT1PC BOUND TO SSDNA (CGGTTACGGT) | SPECIFICITY, PLASTICITY, PROMISCUITY, OB-FOLD, SSDNA-BINDING, SINGLE- STRANDED TELOMERIC DNA, DNA BINDING PROTEIN
4x13:B (GLU28) to (GLU46) JC POLYOMAVIRUS GENOTYPE 3 VP1 IN COMPLEX WITH LSTC PENTASACCHARIDE | BETA-SANDWICH, JELLY-ROLL, VIRAL MAJOR CAPSID PROTEIN, GLYCAN, VIRAL PROTEIN
4x13:E (LEU27) to (GLU46) JC POLYOMAVIRUS GENOTYPE 3 VP1 IN COMPLEX WITH LSTC PENTASACCHARIDE | BETA-SANDWICH, JELLY-ROLL, VIRAL MAJOR CAPSID PROTEIN, GLYCAN, VIRAL PROTEIN
4x16:A (LEU27) to (GLU46) JC MAD-1 POLYOMAVIRUS VP1 IN COMPLEX WITH GD1A OLIGOSACCHARIDE | BETA-SANDWICH, JELLY-ROLL, VIRAL MAJOR CAPSID PROTEIN, GLYCAN, VIRAL PROTEIN
4x16:B (LEU27) to (GLU46) JC MAD-1 POLYOMAVIRUS VP1 IN COMPLEX WITH GD1A OLIGOSACCHARIDE | BETA-SANDWICH, JELLY-ROLL, VIRAL MAJOR CAPSID PROTEIN, GLYCAN, VIRAL PROTEIN
1bk2:A (GLY51) to (ASP62) A-SPECTRIN SH3 DOMAIN D48G MUTANT | SH3-DOMAIN, CYTOSKELETON, CALMODULIN-BINDING, ACTIN-BINDING
1o2h:A (GLN30) to (VAL53) ELABORATE MANIFOLD OF SHORT HYDROGEN BOND ARRAYS MEDIATING BINDING OF ACTIVE SITE-DIRECTED SERINE PROTEASE INHIBITORS | SERINE PROTEASE, SHORT HYDROGEN BOND, INHIBITION MECHANISM, SHIFT OF PKA, TRYPSIN, THROMBIN, UROKINASE, FACTOR XA, HYDROLASE
2bm5:B (ASP141) to (GLY161) THE STRUCTURE OF MFPA (RV3361C, P21 CRYSTAL FORM). THE PENTAPEPTIDE REPEAT PROTEIN FROM MYCOBACTERIUM TUBERCULOSIS FOLDS AS A RIGHT-HANDED QUADRILATERAL BETA- HELIX. | PENTAPEPTIDE REPEAT PROTEIN, FLUROQUINOLONE RESISTANCE, DNA GYRASE, DNA MIMICRY, RIGHT-HANDED QUADRILATERAL BETA-HELIX
2pfe:A (GLY179) to (GLY192) CRYSTAL STRUCTURE OF THERMOBIFIDA FUSCA PROTEASE A (TFPA) | BETA-BARRELS; SERINE PROTEASE; THERMOPHILE; KINETIC STABILITY; THERMOSTABILITY; PROTEIN FOLDING; ALPHA-LYTIC PROTEASE; FOLDING TRANSITION STATE STRUCTURE, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2pfe:B (GLY179) to (GLY192) CRYSTAL STRUCTURE OF THERMOBIFIDA FUSCA PROTEASE A (TFPA) | BETA-BARRELS; SERINE PROTEASE; THERMOPHILE; KINETIC STABILITY; THERMOSTABILITY; PROTEIN FOLDING; ALPHA-LYTIC PROTEASE; FOLDING TRANSITION STATE STRUCTURE, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1bou:B (ASP116) to (HIS127) THREE-DIMENSIONAL STRUCTURE OF LIGAB | EXTRADIOL TYPE DIOXYGENASE, OXIDOREDUCTASE
1bou:D (ASP116) to (HIS127) THREE-DIMENSIONAL STRUCTURE OF LIGAB | EXTRADIOL TYPE DIOXYGENASE, OXIDOREDUCTASE
1bpw:A (ILE324) to (GLY338) BETAINE ALDEHYDE DEHYDROGENASE FROM COD LIVER | OXIDOREDUCTASE, ALDEHYDE OXIDATION, NAD COMPLEX
1bpw:B (ILE324) to (GLY338) BETAINE ALDEHYDE DEHYDROGENASE FROM COD LIVER | OXIDOREDUCTASE, ALDEHYDE OXIDATION, NAD COMPLEX
1bpw:C (ILE324) to (GLY338) BETAINE ALDEHYDE DEHYDROGENASE FROM COD LIVER | OXIDOREDUCTASE, ALDEHYDE OXIDATION, NAD COMPLEX
1bpw:D (ILE324) to (GLY338) BETAINE ALDEHYDE DEHYDROGENASE FROM COD LIVER | OXIDOREDUCTASE, ALDEHYDE OXIDATION, NAD COMPLEX
1o7a:A (SER62) to (ALA73) HUMAN BETA-HEXOSAMINIDASE B | HYDROLASE, GLYCOSYL HYDROLASE, HEXOSAMINIDASE, LYSOSOMAL, SPHINGOLIPID DEGRADATION, SANDHOFF DISEASE, BA8-BARREL, GLYCOSIDASE
1o7a:C (LEU61) to (ALA73) HUMAN BETA-HEXOSAMINIDASE B | HYDROLASE, GLYCOSYL HYDROLASE, HEXOSAMINIDASE, LYSOSOMAL, SPHINGOLIPID DEGRADATION, SANDHOFF DISEASE, BA8-BARREL, GLYCOSIDASE
1o7a:D (LEU61) to (ALA73) HUMAN BETA-HEXOSAMINIDASE B | HYDROLASE, GLYCOSYL HYDROLASE, HEXOSAMINIDASE, LYSOSOMAL, SPHINGOLIPID DEGRADATION, SANDHOFF DISEASE, BA8-BARREL, GLYCOSIDASE
1bqo:A (GLY138) to (SER145) DISCOVERY OF POTENT, ACHIRAL MATRIX METALLOPROTEINASE INHIBITORS | STROMELYSIN, MATRIX METALLOPROTEASE, OSTEOARTHRITIS, STRUCTURE-BASED DRUG DESIGN, METALLOPROTEASE
4hoe:A (THR147) to (PRO160) CANDIDA ALBICANS DIHYDROFOLATE REDUCTASE COMPLEXED WITH NADPH AND 5- [3-(2,5-DIMETHOXY-4-PHENYLPHENYL)BUT-1-YN-1-YL]-6-METHYLPYRIMIDINE-2, 4-DIAMINE (UCP111E) | ANTIFUNGAL AGENTS, CANDIDA ALBICANS, DRUG DESIGN, ENZYME INHIBITORS, FUNGAL PROTEINS, STRUCTURE-ACTIVITY RELATIONSHIP, TETRAHYDROFOLATE DEHYDROGENASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3s85:C (ASP30) to (GLY49) DISCOVERY OF NEW HIV PROTEASE INHIBITORS WITH POTENTIAL FOR CONVENIENT DOSING AND REDUCED SIDE EFFECTS: A-790742 AND A-792611. | BETA BARREL, ACID PROTEASE, ASPARTIC-TYPE ENDOPEPIDASE ACTIVITY, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1bru:P (GLN30) to (THR54) STRUCTURE OF PORCINE PANCREATIC ELASTASE COMPLEXED WITH THE ELASTASE INHIBITOR GR143783 | SERINE PROTEASE, HYDROLASE
2bs2:A (SER174) to (ALA183) QUINOL:FUMARATE REDUCTASE FROM WOLINELLA SUCCINOGENES | OXIDOREDUCTASE, RESPIRATORY CHAIN,, CITRIC ACID CYCLE, IRON-SULPHUR PROTEIN
3s8v:B (VAL1051) to (ARG1060) CRYSTAL STRUCTURE OF LRP6-DKK1 COMPLEX | WNT, RECEPTOR, LRP5, LRP6, LDL RECEPTOR-LIKE PROTEIN, DICKKOPF (DKK), YWTD B-PROPELLER, SIGNALING PROTEIN
3s8z:A (VAL1051) to (ARG1060) CRYSTAL STRUCTURE OF LRP6-E3E4 | WNT, RECEPTOR, LRP5, LRP6, LDL RECEPTOR-LIKE PROTEIN, DICKKOPF (DKK), YWTD B-PROPELLER, SIGNALING PROTEIN
2bsd:A (GLY192) to (LYS199) STRUCTURE OF LACTOCOCCAL BACTERIOPHAGE P2 RECEPTOR BINDING PROTEIN | LACTOCOCCUS LACTIS, PHAGE, LLAMA VHH, RECEPTOR BINDING PROTEIN, RECEPTOR
2bsd:B (GLY192) to (LYS199) STRUCTURE OF LACTOCOCCAL BACTERIOPHAGE P2 RECEPTOR BINDING PROTEIN | LACTOCOCCUS LACTIS, PHAGE, LLAMA VHH, RECEPTOR BINDING PROTEIN, RECEPTOR
2bsd:C (GLY192) to (LYS199) STRUCTURE OF LACTOCOCCAL BACTERIOPHAGE P2 RECEPTOR BINDING PROTEIN | LACTOCOCCUS LACTIS, PHAGE, LLAMA VHH, RECEPTOR BINDING PROTEIN, RECEPTOR
2bse:A (GLY192) to (LYS199) STRUCTURE OF LACTOCOCCAL BACTERIOPHAGE P2 RECEPTOR BINDING PROTEIN IN COMPLEX WITH A LLAMA VHH DOMAIN | LACTOCOCCUS LACTIS, PHAGE, RECEPTOR BINDING PROTEIN, LLAMA ANTIBODY, VHH, RECEPTOR
4x8v:H (GLN30) to (VAL53) FACTOR VIIA IN COMPLEX WITH THE INHIBITOR (METHYL {3-[(2R)-1-{(2R)-2- (3,4-DIMETHOXYPHENYL)-2-[(1-OXO-1,2,3,4-TETRAHYDROISOQUINOLIN-7-YL) AMINO]ACETYL}PYRROLIDIN-2-YL]-4-(PROPAN-2-YLSULFONYL) PHENYL}CARBAMATE) | GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM- BINDING
4x8s:H (GLN30) to (VAL53) FACTOR VIIA IN COMPLEX WITH THE INHIBITOR 4-BROMO-2-METHOXYPHENOL | GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM- BINDING
4x8u:H (GLN30) to (VAL53) FACTOR VIIA IN COMPLEX WITH THE INHIBITOR 5-CHLORO-1H-INDOLE-2- CARBOXYLIC ACID | GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM- BINDING, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3faa:E (THR204) to (ARG215) CRYSTAL STRUCTURE OF TGFBRI COMPLEXED WITH A 2- AMINOIMIDAZOLE INHIBITOR | KINASE, TGFBETA, STRUCTURE-BASED DRUG DESIGN, PROTEIN- INHIBITOR COMPLEX, ATP-BINDING, CRANIOSYNOSTOSIS, DISEASE MUTATION, GLYCOPROTEIN, MAGNESIUM, MANGANESE, MEMBRANE, METAL-BINDING, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, RECEPTOR, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, TRANSMEMBRANE
4hrx:A (VAL125) to (GLY133) CRYSTAL STRUCTURE OF KAI2 | ALPHA/BETA HYDROLASE, SIGNALING PROTEIN, HYDROLASE
4ht2:A (PRO100) to (SER108) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH THE INHIBITOR. | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX, CATALYTIC ACTIVITY, CARBON-OXYGEN LYASE ACTIVITY, CARBONATE DEHYDRATASE ACTIVITY, MEMBRANE
4ht2:B (PRO100) to (SER108) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH THE INHIBITOR. | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX, CATALYTIC ACTIVITY, CARBON-OXYGEN LYASE ACTIVITY, CARBONATE DEHYDRATASE ACTIVITY, MEMBRANE
4ht2:C (PRO100) to (SER108) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH THE INHIBITOR. | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX, CATALYTIC ACTIVITY, CARBON-OXYGEN LYASE ACTIVITY, CARBONATE DEHYDRATASE ACTIVITY, MEMBRANE
4ht2:D (PRO100) to (SER108) CRYSTAL STRUCTURE OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH THE INHIBITOR. | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX, CATALYTIC ACTIVITY, CARBON-OXYGEN LYASE ACTIVITY, CARBONATE DEHYDRATASE ACTIVITY, MEMBRANE
4xau:B (SER-1) to (VAL9) CRYSTAL STRUCTURE OF ATS13 FROM ACTINOMADURA MELLIAURA | SUGAR AMINOTRANSFERASE, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, ENZYME DISCOVERY FOR NATURAL PRODUCT BIOSYNTHESIS, NATPRO, TRANSFERASE
4xau:D (SER-1) to (VAL9) CRYSTAL STRUCTURE OF ATS13 FROM ACTINOMADURA MELLIAURA | SUGAR AMINOTRANSFERASE, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, ENZYME DISCOVERY FOR NATURAL PRODUCT BIOSYNTHESIS, NATPRO, TRANSFERASE
3fc5:A (GLY325) to (GLY333) G586S MUTANT NNOSOXY | NNOS, OXYGENASE, G586S, ARGININE, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3fc5:B (GLY325) to (GLY333) G586S MUTANT NNOSOXY | NNOS, OXYGENASE, G586S, ARGININE, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
1ocx:A (GLY55) to (GLU63) E. COLI MALTOSE-O-ACETYLTRANSFERASE | TRANSFERASE, ACETYL TRANSFERASE, LEFT-HANDED PARALLEL BETA-HELIX
1ocx:C (GLY55) to (GLU63) E. COLI MALTOSE-O-ACETYLTRANSFERASE | TRANSFERASE, ACETYL TRANSFERASE, LEFT-HANDED PARALLEL BETA-HELIX
3feo:A (TYR404) to (PRO417) THE CRYSTAL STRUCTURE OF MBTD1 | MBTL1, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, METAL-BINDING, NUCLEUS, ZINC-FINGER, METAL BINDING PROTEIN
3feo:B (TYR404) to (PRO417) THE CRYSTAL STRUCTURE OF MBTD1 | MBTL1, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, METAL-BINDING, NUCLEUS, ZINC-FINGER, METAL BINDING PROTEIN
3fez:A (ALA51) to (GLY60) CRYSTAL STRUCTURE OF UNCHARACTERIZED FERREDOXIN FOLD PROTEIN RELATED TO ANTIBIOTIC BIOSYNTHESIS MONOOXYGENASES (YP_014836.1) FROM LISTERIA MONOCYTOGENES 4B F2365 AT 2.10 A RESOLUTION | YP_014836.1, UNCHARACTERIZED FERREDOXIN FOLD PROTEIN RELATED TO ANTIBIOTIC BIOSYNTHESIS MONOOXYGENASES, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, UNKNOWN FUNCTION
2bz6:H (GLN30) to (VAL53) ORALLY AVAILABLE FACTOR7A INHIBITOR | SERINE PROTEASE, COAGULATION, ENZYME COMPLEX, HYDROLASE
2bz8:A (GLY46) to (LYS57) N-TERMINAL SH3 DOMAIN OF CIN85 BOUND TO CBL-B PEPTIDE | SH3 DOMAIN, CIN85 ADAPTOR PROTEIN, CBL UBIQUITIN LIGASE, ENDOCYTOSIS
2bzd:C (GLY432) to (ALA444) GALACTOSE RECOGNITION BY THE CARBOHYDRATE-BINDING MODULE OF A BACTERIAL SIALIDASE. | SIALIDASE, HYDROLASE, CARBOHYDRATE BINDING MODULE, GLYCOSIDASE
4i0e:A (PHE435) to (ASP442) DESIGN AND SYNTHESIS OF THIOPHENE DIHYDROISOQUINOLINS AS NOVEL BACE-1 INHIBITORS | BACE, ASPARTIC PROTEASE, HYDROLYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1ogs:A (LEU383) to (PRO401) HUMAN ACID-BETA-GLUCOSIDASE | HYDROLASE, GAUCHER DISEASE, GLUCOSIDASE, GLUCOCEREBROSIDASE, CEREZYME HYDROLASE, GLYCOSIDASE, SPHINGOLIPID METABOLISM, GLYCOPROTE LYSOSOME, MEMBRANE, SIGNAL, DISEASE MUTATI POLYMORPHISM, ALTERNATIVE INITIATION, PHARMACEUTICAL, ISRAEL STRUCTURAL PROTEOMICS CENTER, ISPC, STRUCTURAL GENOMICS
1ogs:B (LEU383) to (PRO401) HUMAN ACID-BETA-GLUCOSIDASE | HYDROLASE, GAUCHER DISEASE, GLUCOSIDASE, GLUCOCEREBROSIDASE, CEREZYME HYDROLASE, GLYCOSIDASE, SPHINGOLIPID METABOLISM, GLYCOPROTE LYSOSOME, MEMBRANE, SIGNAL, DISEASE MUTATI POLYMORPHISM, ALTERNATIVE INITIATION, PHARMACEUTICAL, ISRAEL STRUCTURAL PROTEOMICS CENTER, ISPC, STRUCTURAL GENOMICS
4i0z:A (ALA429) to (ASP442) STRUCTURE-BASED DESIGN OF NOVEL DIHYDROISOQUINOLINE BACE-1 INHIBITORS THAT DO NOT ENGAGE THE CATALYTIC ASPARTATES | ASPARTIC PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4i24:A (LEU703) to (LYS716) STRUCTURE OF T790M EGFR KINASE DOMAIN CO-CRYSTALLIZED WITH DACOMITINIB | KINASE DOMAIN, PHOSPHOTRASFER, ATP BINDING, TRANSFERASE
4i24:B (LEU703) to (LYS716) STRUCTURE OF T790M EGFR KINASE DOMAIN CO-CRYSTALLIZED WITH DACOMITINIB | KINASE DOMAIN, PHOSPHOTRASFER, ATP BINDING, TRANSFERASE
4i30:A (GLY163) to (PHE175) CRYSTAL STRUCTURE OF CANAVALIA MARITIMA SEEDS LECTIN (CONM) CO- CRYSTALIZED WITH GAMMA-AMINOBUTYRIC ACID (GABA) AND SOAKED WITH ADENINE | BETA-SANDWICH; JELLY-ROLL, SUGAR-BINDING PROTEIN, SUGAR BINDING PROTEIN
3fj2:A (LYS51) to (GLY60) CRYSTAL STRUCTURE OF A MONOOXYGENASE-LIKE PROTEIN (LIN2316) FROM LISTERIA INNOCUA AT 1.85 A RESOLUTION | MONOOXYGENASE-LIKE PROTEIN, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, UNKNOWN FUNCTION
1cb0:A (GLY105) to (MET119) STRUCTURE OF HUMAN 5'-DEOXY-5'-METHYLTHIOADENOSINE PHOSPHORYLASE AT 1.7 A RESOLUTION | METHYLTHIOADENOSINE PHOSPHORYLASE, PURINE NUCLEOSIDE PHOSPHORYLASE, PURINE SALVAGE, ADENINE, TRANSFERASE
4i3u:A (LEU318) to (THR332) STRUCTURE OF PHOSPHONOACETALDEHYDE DEHYDROGENASE IN COMPLEX WITH PHOSPHONOACETALDEHYDE | ALDEHYDE DEHYDROGENASE, PHOSPHONATE CATABOLISM, OXIDOREDUCTASE
4i3u:F (LEU318) to (THR332) STRUCTURE OF PHOSPHONOACETALDEHYDE DEHYDROGENASE IN COMPLEX WITH PHOSPHONOACETALDEHYDE | ALDEHYDE DEHYDROGENASE, PHOSPHONATE CATABOLISM, OXIDOREDUCTASE
4i3u:G (LEU318) to (THR332) STRUCTURE OF PHOSPHONOACETALDEHYDE DEHYDROGENASE IN COMPLEX WITH PHOSPHONOACETALDEHYDE | ALDEHYDE DEHYDROGENASE, PHOSPHONATE CATABOLISM, OXIDOREDUCTASE
3sjj:A (PRO35) to (ASP51) RB69 DNA POLYMERASE TRIPLE MUTANT (L561A/S565G/Y567A) TERNARY COMPLEX WITH DUPNPP AND A DEOXY-TERMINATED PRIMER IN THE PRESENCE OF MN2+ | DNA BINDING, TRANSFERASE-DNA COMPLEX
1okx:A (GLN30) to (MET56) BINDING STRUCTURE OF ELASTASE INHIBITOR SCYPTOLIN A | PROTEASE, ELASTASE, INHIBITOR, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1okx:B (GLN30) to (MET56) BINDING STRUCTURE OF ELASTASE INHIBITOR SCYPTOLIN A | PROTEASE, ELASTASE, INHIBITOR, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2pu1:A (GLY364) to (GLU377) CRYSTAL STRUCTURE OF THE T. BRUCEI ENOLASE COMPLEXED WITH FLUORO-PHOSPHONOACETOHYDROXAMATE (FPAH) | LYASE, GLYCOLYSIS,HIS-TAG
1om5:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NOS HEME DOMAIN WITH 3-BROMO-7- NITROINDAZOLE BOUND | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME
1om5:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NOS HEME DOMAIN WITH 3-BROMO-7- NITROINDAZOLE BOUND | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME
3fmo:A (PRO10) to (PHE28) CRYSTAL STRUCTURE OF THE NUCLEOPORIN NUP214 IN COMPLEX WITH THE DEAD- BOX HELICASE DDX19 | NUCLEAR PORIN, NUCLEAR PORE COMPLEX, NUCLEOCYTOPLASMIC TRANSPORT, MRNA EXPORT, PROTEIN INTERACTION, HELICASE, BETA-PROPELLER, DEAD BOX, GLYCOPROTEIN, MRNA TRANSPORT, NUCLEUS, PHOSPHOPROTEIN, PROTEIN TRANSPORT, PROTO-ONCOGENE, TRANSLOCATION, TRANSPORT, ATP-BINDING, HYDROLASE, MEMBRANE, NUCLEOTIDE-BINDING, RNA-BINDING, PROTEIN TRANSPORT-HYDROLASE COMPLEX, ONCOPROTEIN-HYDROLASE COMPLEX
4i5c:B (LEU875) to (HIS885) THE JAK1 KINASE DOMAIN IN COMPLEX WITH INHIBITOR | KINASE, TRANSFERASE
2c4f:H (GLN30) to (VAL53) CRYSTAL STRUCTURE OF FACTOR VII.STF COMPLEXED WITH PD0297121 | BLOOD COAGULATION, SERINE PROTEASE, EGF, EGF-LIKE DOMAIN, GLA, RECEPTOR ENZYME, GLYCOPROTEIN, HYDROLASE, PROTEASE, HYDROXYLATION, LIPOPROTEIN, PALMITATE, TRANSMEMBRANE
2pyg:A (GLY197) to (ASP206) AZOTOBACTER VINELANDII MANNURONAN C-5 EPIMERASE ALGE4 A-MODULE | BETA-HELIX, EPIMERASE, ISOMERASE
2pyg:B (GLY197) to (ASP206) AZOTOBACTER VINELANDII MANNURONAN C-5 EPIMERASE ALGE4 A-MODULE | BETA-HELIX, EPIMERASE, ISOMERASE
2c4y:C (THR5) to (GLY13) MS2-RNA HAIRPIN (2THIOURACIL-5) COMPLEX | VIRUS/RNA, CAPSID, COMPLEX (CAPSID PROTEIN-RNA HAIRPIN), HAIRPIN, LEVIVIRUS, VIRUS/VIRAL PROTEIN/RNA, VIRUS COAT PROTEIN, RNA- BINDING, ICOSAHEDRAL VIRUS
3sq4:A (PRO35) to (ASP51) RB69 DNA POLYMERASE TERNARY COMPLEX WITH DTTP OPPOSITE 2AP (GC RICH SEQUENCE) | 2-AMINOPURINE, GC RICH, TRANSFERASE-DNA COMPLEX
3fvf:B (GLN30) to (LEU53) THE CRYSTAL STRUCTURE OF PROSTASIN COMPLEXED WITH CAMOSTAT AT 1.6 ANGSTROMS RESOLUTION | PROSTASIN, HCAP-1, CHANNEL ACTIVATING PROTEASE, INHIBITOR, SERINE PROTEASE, ENAC, CELL MEMBRANE, GLYCOPROTEIN, HYDROLASE, MEMBRANE, PROTEASE, SECRETED, TRANSMEMBRANE, ZYMOGEN
1cvs:C (MET149) to (SER157) CRYSTAL STRUCTURE OF A DIMERIC FGF2-FGFR1 COMPLEX | FGF, FGFR, IMMUNOGLOBULIN-LIKE, SIGNAL TRANSDUCTION, DIMERIZATION, GROWTH FACTOR/GROWTH FACTOR RECEPTOR COMPLEX
1cvs:D (MET149) to (SER157) CRYSTAL STRUCTURE OF A DIMERIC FGF2-FGFR1 COMPLEX | FGF, FGFR, IMMUNOGLOBULIN-LIKE, SIGNAL TRANSDUCTION, DIMERIZATION, GROWTH FACTOR/GROWTH FACTOR RECEPTOR COMPLEX
3fw5:A (GLY29) to (GLY38) CRYSTAL STRUCTURE OF SIDEROCALIN (NGAL, LIPOCALIN 2) COMPLEXED WITH FERRIC 4-METHYL-CATECHOL | 8-STRANDED ANTI-PARALLEL BETA BARREL, 310-HELIX, GLYCOPROTEIN, PYRROLIDONE CARBOXYLIC ACID, SECRETED, TRANSPORT PROTEIN
1cvw:H (GLN30) to (VAL53) CRYSTAL STRUCTURE OF ACTIVE SITE-INHIBITED HUMAN COAGULATION FACTOR VIIA (DES-GLA) | BLOOD COAGULATION, FACTOR VIIA, SERINE PROTEASE, EGF, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
2c9a:A (GLY25) to (SER41) CRYSTAL STRUCTURE OF THE MAM-IG MODULE OF RECEPTOR PROTEIN TYROSINE PHOSPHATASE MU | GLYCOPROTEIN, HYDROLASE, IMMUNOGLOBULIN DOMAIN, RECEPTOR
3fww:A (GLY424) to (GLU433) THE CRYSTAL STRUCTURE OF THE BIFUNCTIONAL N-ACETYLGLUCOSAMINE-1- PHOSPHATE URIDYLTRANSFERASE/GLUCOSAMINE-1-PHOSPHATE ACETYLTRANSFERASE FROM YERSINIA PESTIS CO92 | N-ACETYLGLUCOSAMINE-1-PHOSPHATE URIDYLTRANSFERASE/GLUCOSAMINE-1- PHOSPHATE ACETYLTRANSFERASE, STRUCTURAL GENOMICS, CSGID, ACYLTRANSFERASE, CELL SHAPE, CELL WALL BIOGENESIS/DEGRADATION, MAGNESIUM, METAL-BINDING, MULTIFUNCTIONAL ENZYME, NUCLEOTIDYLTRANSFERASE, PEPTIDOGLYCAN SYNTHESIS, TRANSFERASE, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES
3fx5:B (ASP130) to (GLY149) STRUCTURE OF HIV-1 PROTEASE IN COMPLEX WITH POTENT INHIBITOR KNI-272 DETERMINED BY HIGH RESOLUTION X-RAY CRYSTALLOGRAPHY | ACID PROTEASE, HOMODIMER, PROTEASE, HYDROLASE, NUCLEOTIDYLTRANSFERASE, TRANSFERASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3sti:A (GLY188) to (ILE219) CRYSTAL STRUCTURE OF THE PROTEASE DOMAIN OF DEGQ FROM ESCHERICHIA COLI | SERINE PROTEASE, PDZ DOMAIN, PROTEASE, CHAPERONE, HYDROLASE
1cx8:A (ALA226) to (ASN236) CRYTAL STRUCTURE OF THE ECTODOMAIN OF HUMAN TRANSFERRIN RECEPTOR | HUMAN TRANSFERRIN RECEPTOR, METAL TRANSPORT
1cx8:B (ALA226) to (ASN236) CRYTAL STRUCTURE OF THE ECTODOMAIN OF HUMAN TRANSFERRIN RECEPTOR | HUMAN TRANSFERRIN RECEPTOR, METAL TRANSPORT
1cx8:C (ALA226) to (ASN236) CRYTAL STRUCTURE OF THE ECTODOMAIN OF HUMAN TRANSFERRIN RECEPTOR | HUMAN TRANSFERRIN RECEPTOR, METAL TRANSPORT
1cx8:D (ALA226) to (ASN236) CRYTAL STRUCTURE OF THE ECTODOMAIN OF HUMAN TRANSFERRIN RECEPTOR | HUMAN TRANSFERRIN RECEPTOR, METAL TRANSPORT
1cx8:E (ALA226) to (ASN236) CRYTAL STRUCTURE OF THE ECTODOMAIN OF HUMAN TRANSFERRIN RECEPTOR | HUMAN TRANSFERRIN RECEPTOR, METAL TRANSPORT
1cx8:F (ALA226) to (ASN236) CRYTAL STRUCTURE OF THE ECTODOMAIN OF HUMAN TRANSFERRIN RECEPTOR | HUMAN TRANSFERRIN RECEPTOR, METAL TRANSPORT
1cx8:G (ALA226) to (ASN236) CRYTAL STRUCTURE OF THE ECTODOMAIN OF HUMAN TRANSFERRIN RECEPTOR | HUMAN TRANSFERRIN RECEPTOR, METAL TRANSPORT
1cx8:H (ALA226) to (ASN236) CRYTAL STRUCTURE OF THE ECTODOMAIN OF HUMAN TRANSFERRIN RECEPTOR | HUMAN TRANSFERRIN RECEPTOR, METAL TRANSPORT
2q7d:B (GLY221) to (ASN231) CRYSTAL STRUCTURE OF HUMAN INOSITOL 1,3,4-TRISPHOSPHATE 5/6-KINASE (ITPK1) IN COMPLEX WITH AMPPNP AND MN2+ | INOSITOL, INOSITOL KINASE, KINASE, ITPK1, INOSITOL 1,3,4-5/6-KINASE, PHOSPHATE, INOSITOL PHOSPHATE, INOSITOLPHOSPHATE, POLYPHOSPHATE, TRANSFERASE
3sue:A (GLY1023) to (GLY1031) CRYSTAL STRUCTURE OF NS3/4A PROTEASE VARIANT R155K IN COMPLEX WITH MK- 5172 | DRUG RESISTANCE, DRUG DESIGN, PROTEASE INHIBITORS, HCV, SERINE PROTEASE, VIRAL PROTEIN, HYDROLASE-INHIBITOR COMPLEX
3suf:C (GLY1023) to (GLY1031) CRYSTAL STRUCTURE OF NS3/4A PROTEASE VARIANT D168A IN COMPLEX WITH MK- 5172 | DRUG RESISTANCE, DRUG DESIGN, PROTEASE INHIBITORS, HCV, SERINE PROTEASE, VIRAL PROTEIN, HYDROLASE-INHIBITOR COMPLEX
3sun:A (PRO35) to (ASP51) RB69 DNA POLYMERASE (Y567A) TERNARY COMPLEX WITH DTTP OPPOSITE 2AP (AT RICH SEQUENCE) | 2-AMINOPURINE, AT RICH, RB69POL, TRANSFERASE-DNA COMPLEX
3sup:A (PRO35) to (ASP51) RB69 DNA POLYMERASE (Y567A) TERNARY COMPLEX WITH DCTP OPPOSITE 2AP (GC RICH SEQUENCE) | 2-AMINOPURINE, GC RICH, RB69POL, TRANSFERASE-DNA COMPLEX
3suq:A (PRO35) to (ASP51) RB69 DNA POLYMERASE (Y567A) TERNARY COMPLEX WITH DCTP OPPOSITE 2AP (AT RICH SEQUENCE) | 2-AMINOPURINE, AT RICH, DCTP, RB69POL, Y567A, TRANSFERASE-DNA COMPLEX
1cz5:A (PRO161) to (ARG173) NMR STRUCTURE OF VAT-N: THE N-TERMINAL DOMAIN OF VAT (VCP- LIKE ATPASE OF THERMOPLASMA) | DOUBLE-PSI BETA-BARREL, BETA-CLAM, SUBSTRATE RECOGNITION DOMAIN, FUSION PROTEIN, HYDROLASE
3sv0:A (LYS8) to (SER19) CRYSTAL STRUCTURE OF CASEIN KINASE-1 LIKE PROTEIN IN PLANT | KINASE, TYPICAL KINASE DOMAIN FOLD, CYTOSOL, TRANSFERASE
3svq:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-((2,2-DIFLUORO-2-(2,3-DIFLUOROPHENYL)ETHYL) AMINO)ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3svq:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-((2,2-DIFLUORO-2-(2,3-DIFLUOROPHENYL)ETHYL) AMINO)ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
1d1x:B (PRO95) to (GLY103) BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 1, 4-PBITU (H4B BOUND) | AHPHA-BETA FOLD, OXIDOREDUCTASE
2qb5:B (GLY221) to (ASN231) CRYSTAL STRUCTURE OF HUMAN INOSITOL 1,3,4-TRISPHOSPHATE 5/6-KINASE (ITPK1) IN COMPLEX WITH ADP AND MN2+ | INOSITOL, INOSITOL KINASE, KINASE, ITPK1, INOSITOL 1,3,4-5/6-KINASE, PHOSPHATE, INOSITOL PHOSPHATE, INOSITOLPHOSPHATE, POLYPHOSPHATE, TRANSFERASE
4xob:E (GLN32) to (SER39) CRYSTAL STRUCTURE OF A FIMH*DSF COMPLEX FROM E.COLI K12 WITH BOUND HEPTYL ALPHA-D-MANNOPYRANNOSIDE | FOLDASE, PROLYL ISOMERASE, PROTEIN SECRETION, GRAM-POSITIVE, ISOMERASE, CELL ADHESION
1p5q:B (GLY149) to (GLY160) CRYSTAL STRUCTURE OF FKBP52 C-TERMINAL DOMAIN | ISOMERASE
1p5q:C (GLY149) to (GLY160) CRYSTAL STRUCTURE OF FKBP52 C-TERMINAL DOMAIN | ISOMERASE
1d4h:A (ASP30) to (GLY49) HIV-1 PROTEASE IN COMPLEX WITH THE INHIBITOR BEA435 | DIMER, HYDROLASE
1d4i:A (ASP30) to (GLY49) HIV-1 PROTEASE IN COMPLEX WITH THE INHIBITOR BEA425 | DIMER, HYDROLASE
1d4l:B (ASP30) to (GLY49) HIV-1 PROTEASE COMPLEXED WITH A MACROCYCLIC PEPTIDOMIMETIC INHIBITOR | HIV, PROTEASE, INHIBITOR, ANTIVIRAL, STRUCTURE, HYDROLASE
1p6h:A (GLY325) to (GLY333) RAT NEURONAL NOS HEME DOMAIN WITH L-N(OMEGA)-NITROARGININE- 2,4-L-DIAMINOBUTYRIC AMIDE BOUND | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME
1p6h:B (GLY325) to (GLY333) RAT NEURONAL NOS HEME DOMAIN WITH L-N(OMEGA)-NITROARGININE- 2,4-L-DIAMINOBUTYRIC AMIDE BOUND | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME
1p6k:A (GLY325) to (GLY333) RAT NEURONAL NOS D597N MUTANT HEME DOMAIN WITH L-N(OMEGA)- NITROARGININE-2,4-L-DIAMINOBUTYRIC AMIDE BOUND | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME
1p6k:B (GLY325) to (GLY333) RAT NEURONAL NOS D597N MUTANT HEME DOMAIN WITH L-N(OMEGA)- NITROARGININE-2,4-L-DIAMINOBUTYRIC AMIDE BOUND | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME
1p6i:A (GLY325) to (GLY333) RAT NEURONAL NOS HEME DOMAIN WITH (4S)-N-(4-AMINO-5- [AMINOETHYL]AMINOPENTYL)-N'-NITROGUANIDINE BOUND | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME
1p6i:B (GLY325) to (GLY333) RAT NEURONAL NOS HEME DOMAIN WITH (4S)-N-(4-AMINO-5- [AMINOETHYL]AMINOPENTYL)-N'-NITROGUANIDINE BOUND | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME
1p6j:A (GLY325) to (GLY333) RAT NEURONAL NOS HEME DOMAIN WITH L-N(OMEGA)-NITROARGININE- (4R)-AMINO-L-PROLINE AMIDE BOUND | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME
1p6j:B (GLY325) to (GLY333) RAT NEURONAL NOS HEME DOMAIN WITH L-N(OMEGA)-NITROARGININE- (4R)-AMINO-L-PROLINE AMIDE BOUND | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME
1p6n:A (PRO95) to (GLY103) BOVINE ENDOTHELIAL NOS HEME DOMAIN WITH L-N(OMEGA)-NITROARGININE-(4R)- AMINO-L-PROLINE AMIDE BOUND | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME
4xpj:B (ASP16) to (THR27) CRYSTAL STRUCTURE OF NERVE GROWTH FACTOR IN COMPLEX WITH LYSOPHOSPHATIDYLINOSITOL | NERVE GROWTH FACTOR, LYSOPI, HORMONE
3sz9:H (ARG329) to (PRO343) CRYSTAL STRUCTURE OF HUMAN ALDH2 MODIFIED WITH THE BETA-ELIMINATION PRODUCT OF ALDI-3; 1-(4-ETHYLBENZENE)PROP-2-EN-1-ONE | ALDH, ALDI-3, INHIBITOR, ROSSMANN FOLD, OXIDOREDUCTASE, COVALENT ADDUCT, MITOCHONDRIA, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
2cgw:A (ASP8) to (ALA19) IDENTIFICATION OF CHEMICALLY DIVERSE CHK1 INHIBITORS BY RECEPTOR-BASED VIRTUAL SCREENING | TRANSFERASE, DOCKING, DRUG DESIGN, ONCOLOGY, VIRTUAL SCREENING, ATP- BINDING, CELL CYCLE, DNA DAMAGE, DNA REPAIR, KINASE, NUCLEAR PROTEIN, NUCLEOTIDE-BINDING, PHOSPHORYLATION, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, UBL CONJUGATION
2qeq:B (ILE591) to (ALA599) CRYSTAL STRUCTURE OF KUNJIN VIRUS NS3 HELICASE | HELICASE; FLAVIVIRUS, HYDROLASE
2qf3:B (ASN188) to (HIS198) STRUCTURE OF THE DELTA PDZ TRUNCATION OF THE DEGS PROTEASE | DEGS, PROTEASE, PERIPLASMIC STRESS SENSOR, HTRA, ALLOSTERIC ACTIVATION, HYDROLASE
2qf4:B (SER163) to (ALA175) HIGH RESOLUTION STRUCTURE OF THE MAJOR PERIPLASMIC DOMAIN FROM THE CELL SHAPE-DETERMINING FILAMENT MREC (ORTHORHOMBIC FORM) | FILAMENT A-LYTIC PROTEASE FOLD, STRUCTURAL PROTEIN
1p9m:C (LYS185) to (ASP198) CRYSTAL STRUCTURE OF THE HEXAMERIC HUMAN IL-6/IL-6 ALPHA RECEPTOR/GP130 COMPLEX | IG DOMAIN, FOUR HELIX BUNDLE, CYTOKINE, INTERLEUKIN-6, GP130, SIGNALING PROTEIN-CYTOKINE COMPLEX
1pb8:A (LEU6) to (PRO21) CRYSTAL STRUCTURE OF THE NR1 LIGAND BINDING CORE IN COMPLEX WITH D-SERINE AT 1.45 ANGSTROMS RESOLUTION | LIGAND BINDING RECEPTOR; RAT; NR1, LIGAND BINDING PROTEIN
4ima:C (VAL214) to (PRO224) THE STRUCTURE OF C436M-HLPYK IN COMPLEX WITH CITRATE/MN/ATP/FRU-1,6-BP | HUMAN LIVER PYRUVATE KINASE, OXIDIZABLE CYSTEINE, PHOSPHORYLATION, PHOSPHOENOLPYRUVATE, PEP, TRANSFERASE
4imt:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE IN COMPLEX WITH 6,6'- ((4-(3-AMINOPROPYL)-1,3-PHENYLENE)BIS(ETHANE-2,1-DIYL))BIS(4- METHYLPYRIDIN-2-AMINE) | OXIDOREDUCTASE NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4imt:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE IN COMPLEX WITH 6,6'- ((4-(3-AMINOPROPYL)-1,3-PHENYLENE)BIS(ETHANE-2,1-DIYL))BIS(4- METHYLPYRIDIN-2-AMINE) | OXIDOREDUCTASE NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4imw:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE IN COMPLEX WITH 3,5- BIS(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL)BENZONITRILE | OXIDOREDUCTASE NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4imw:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE IN COMPLEX WITH 3,5- BIS(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL)BENZONITRILE | OXIDOREDUCTASE NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
2cmy:A (GLN30) to (SER54) CRYSTAL COMPLEX BETWEEN BOVINE TRYPSIN AND VERONICA HEDERIFOLIA TRYPSIN INHIBITOR | ACYL-ENZYME INTERMEDIATE, SERINE PROTEASE INHIBITOR, ZYMOGEN, PROTEASE, DIGESTION, HYDROLASE, METAL-BINDING, SERINE PROTEASE
3t1d:B (GLY29) to (GLY38) THE MUTANT STRUCTURE OF HUMAN SIDEROCALIN W79A, R81A, Y106F BOUND TO ENTEROBACTIN | SSGCID, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, BETA-BARREL, SIDEROCALIN, W79A, R81A, Y106F, ANTIMICROBIAL PROTEIN
2qmh:E (GLU135) to (ASP145) STRUCTURE OF V267F MUTANT HPRK/P | V267F MUTATION, ATP-BINDING, CARBOHYDRATE METABOLISM, KINASE, MAGNESIUM, METAL-BINDING, MULTIFUNCTIONAL ENZYME, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, METAL BINDING PROTEIN
2qmh:I (GLU135) to (ASP145) STRUCTURE OF V267F MUTANT HPRK/P | V267F MUTATION, ATP-BINDING, CARBOHYDRATE METABOLISM, KINASE, MAGNESIUM, METAL-BINDING, MULTIFUNCTIONAL ENZYME, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, METAL BINDING PROTEIN
1dm6:A (PRO95) to (GLY103) BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N- (4-CHLOROPHENYL)-N'-HYDROXYGUANIDINE (H4B FREE) | ALPHA-BETA FOLD, OXIDOREDUCTASE
1pjk:A (ASP38) to (LYS49) CRYSTAL STRUCTURE OF A C-TERMINAL DELETION MUTANT OF HUMAN PROTEIN KINASE CK2 CATALYTIC SUBUNIT | EUKARYOTIC PROTEIN KINASE FOLD, TRANSFERASE
2qo3:B (GLY397) to (LEU422) CRYSTAL STRUCTURE OF [KS3][AT3] DIDOMAIN FROM MODULE 3 OF 6- DEOXYERTHRONOLIDE B SYNTHASE | KETOSYNTHASE, ACYLTRANSFERASE, PHOSPHOPANTETHEINE, TRANSFERASE
4isi:H (GLN30) to (VAL53) STRUCTURE OF FACTOR VIIA IN COMPLEX WITH THE INHIBITOR (6S)-N-(4- CARBAMIMIDOYLBENZYL)-1-CHLORO-3-(CYCLOBUTYLAMINO)-8,8-DIETHYL-4-OXO- 4,6,7,8-TETRAHYDROPYRROLO[1,2-A]PYRAZINE-6-CARBOXAMIDE | GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM-BINDING, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
1dpo:A (GLN30) to (SER54) STRUCTURE OF RAT TRYPSIN | HYDROLASE, SERINE PROTEASE, DIGESTION, PANCREAS, ZYMOGEN, SIGNAL, MULTIGENE FAMILY
1dq3:A (TRP42) to (LYS54) CRYSTAL STRUCTURE OF AN ARCHAEAL INTEIN-ENCODED HOMING ENDONUCLEASE PI-PFUI | ENDONUCLEASE, PI-PFUI, INTEIN-ENCODED, HYDROLASE
3ggv:G (ASP30) to (GLY49) HIV PROTEASE, PSEUDO-SYMMETRIC INHIBITORS | HIV PROTEASE, PSEUDO-SYMMETRIC INHIBITORS, HYDROLASE, PROTEASE
2cwm:D (GLY163) to (PHE175) NATIVE CRYSTAL STRUCTURE OF NO RELEASING INDUCTIVE LECTIN FROM SEEDS OF THE CANAVALIA MARITIMA (CONM) | LECTIN, CANAVALIA MARITIMA, METAL BINDING PROTEIN
3gi0:B (ASP30) to (ILE50) CRYSTAL STRUCTURE OF A CHEMICALLY SYNTHESIZED 203 AMINO ACID 'COVALENT DIMER' [L-ALA51,D-ALA51'] HIV-1 PROTEASE MOLECULE COMPLEXED WITH JG- 365 INHIBITOR | BETA-BARREL, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ix3:B (LEU352) to (PRO360) CRYSTAL STRUCTURE OF A STT7 HOMOLOG FROM MICROMONAS ALGAE | PROTEIN KINASE, CANONICAL PROTEIN KINASE FOLD, ATP BINDING, TRANSFERASE
4ix5:B (LEU352) to (PRO360) CRYSTAL STRUCTURE OF A STT7 HOMOLOG FROM MICROMONAS ALGAE IN COMPLEX WITH AMP-PNP | PROTEIN KINASE, CANONICAL PROTEIN KINASE FOLD, ATP BINDING, TRANSFERASE
2cxv:A (GLN159) to (PRO169) DUAL MODES OF MODIFICATION OF HEPATITIS A VIRUS 3C PROTEASE BY A SERINE-DERIVED BETALACTONE: SELECTIVE CRYSTALLIZATION AND HIGH-RESOLUTION STRUCTURE OF THE HIS-102 ADDUCT | HEPATITIS A, PICORNAVIRUS, 3C, CYSTEINE PROTEASE, INHIBITOR, BETA-LACTONE, HYDROLASE
2cy6:A (SER164) to (PHE175) CRYSTAL STRUCTURE OF CONM IN COMPLEX WITH TREHALOSE AND MALTOSE | LECTIN, CANAVALIA MARITIMA, TREHALOSE, METAL BINDING PROTEIN
2cyf:C (SER164) to (PHE175) THE CRYSTAL STRUCTURE OF CANAVALIA MARITIMA LECTIN (CONM) IN COMPLEX WITH TREHALOSE AND MALTOSE | CANACALIA MARITIMA, LECTIN, MALTOSE, CRYSTAL STRUCTURE, METAL BINDING PROTEIN
2d04:F (ASN2) to (HIS11) CRYSTAL STRUCTURE OF NEOCULIN, A SWEET PROTEIN WITH TASTE-MODIFYING ACTIVITY. | ALL BETA, PLANT PROTEIN
4iyk:A (GLY108) to (SER124) CRYSTAL STRUCTURE OF A PUTATIVE CARBOHYDRATE BINDING PROTEIN (BACUNI_04699) FROM BACTEROIDES UNIFORMIS ATCC 8492 AT 2.00 A RESOLUTION | PF12866 FAMILY PROTEIN, DUF3823, PUTATIVE CARBOHYDRATE BINDING PROTEIN, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-BIOLOGY, UNKNOWN FUNCTION
4xzy:A (ASP572) to (GLY582) CRYSTAL STRUCTURE OF DIPEPTIDYL PEPTIDASE 11 (DPP11) FROM PORPHYROMONAS GINGIVALIS | WILD TYPE, HYDROLASE
4iym:F (GLY365) to (PRO373) CRYSTAL STRUCTURE OF PUTATIVE METHYLMALONATE-SEMIALDEHYDE DEHYDROGENASE FROM SINORHIZOBIUM MELILOTI 1021 COMPLEXED WITH NAD, TARGET 011934 | STRUCTURAL GENOMICS, PSI-BIOLOGY, NEW YORK STRUCTURAL GENOMICS RESEARCH CONSORTIUM, NYSGRC, OXIDOREDUCTASE
4iym:J (GLY365) to (PRO373) CRYSTAL STRUCTURE OF PUTATIVE METHYLMALONATE-SEMIALDEHYDE DEHYDROGENASE FROM SINORHIZOBIUM MELILOTI 1021 COMPLEXED WITH NAD, TARGET 011934 | STRUCTURAL GENOMICS, PSI-BIOLOGY, NEW YORK STRUCTURAL GENOMICS RESEARCH CONSORTIUM, NYSGRC, OXIDOREDUCTASE
1prt:D (TYR4) to (SER15) THE CRYSTAL STRUCTURE OF PERTUSSIS TOXIN | TOXIN
1e0o:B (ASN150) to (ASN158) CRYSTAL STRUCTURE OF A TERNARY FGF1-FGFR2-HEPARIN COMPLEX | GROWTH FACTOR, RECEPTOR TYROSINE KINASE, HEPARIN, TERNARY COMPLEX, SIGNAL TRANSDUCTION
1pwt:A (GLY50) to (ASP61) THERMODYNAMIC ANALYSIS OF ALPHA-SPECTRIN SH3 AND TWO OF ITS CIRCULAR PERMUTANTS WITH DIFFERENT LOOP LENGTHS: DISCERNING THE REASONS FOR RAPID FOLDING IN PROTEINS | CIRCULAR PERMUTANT, SH3 DOMAIN, CYTOSKELETON
3tag:B (PRO35) to (ASP51) 5-FLUOROCYTOSINE PAIRED WITH DAMP IN RB69 GP43 | TRANSFERASE-DNA COMPLEX
3tag:D (PRO35) to (ASP51) 5-FLUOROCYTOSINE PAIRED WITH DAMP IN RB69 GP43 | TRANSFERASE-DNA COMPLEX
2qzw:B (LYS62) to (GLY77) SECRETED ASPARTIC PROTEINASE (SAP) 1 FROM CANDIDA ALBICANS | ASPARTIC PROTEINASE, CANDIDA ALBICANS, ASPARTYL PROTEASE, CLEAVAGE ON PAIR OF BASIC RESIDUES, GLYCOPROTEIN, HYDROLASE, PROTEASE, SECRETED, ZYMOGEN
2r0t:A (ASN3) to (TRP11) CRYSTAL SRUCTURE OF GDP-4-KETO-6-DEOXYMANNOSE-3-DEHYDRATASE WITH A TRAPPED PLP-GLUTAMATE GEMINAL DIAMINE | COLITOSE, X-RAY STRUCUTRE, ASPARTATE AMINOTRANSFERASE, GEMINAL DIAMINE, PYRIDOXAL PHOSPHATE
2r1d:A (ARG59) to (THR73) CRYSTAL STRUCTURE OF RAT NEUREXIN 1BETA IN THE CA2+ CONTAINING FORM | BETA-SANDWICH, CELL ADHESION, SPLICING
2r1d:B (ARG59) to (VAL74) CRYSTAL STRUCTURE OF RAT NEUREXIN 1BETA IN THE CA2+ CONTAINING FORM | BETA-SANDWICH, CELL ADHESION, SPLICING
2r1d:C (ARG59) to (THR73) CRYSTAL STRUCTURE OF RAT NEUREXIN 1BETA IN THE CA2+ CONTAINING FORM | BETA-SANDWICH, CELL ADHESION, SPLICING
2r1d:C (ASN202) to (GLU214) CRYSTAL STRUCTURE OF RAT NEUREXIN 1BETA IN THE CA2+ CONTAINING FORM | BETA-SANDWICH, CELL ADHESION, SPLICING
2r1d:D (ARG59) to (THR73) CRYSTAL STRUCTURE OF RAT NEUREXIN 1BETA IN THE CA2+ CONTAINING FORM | BETA-SANDWICH, CELL ADHESION, SPLICING
2r1d:E (ARG59) to (THR73) CRYSTAL STRUCTURE OF RAT NEUREXIN 1BETA IN THE CA2+ CONTAINING FORM | BETA-SANDWICH, CELL ADHESION, SPLICING
2r1d:F (ARG59) to (THR73) CRYSTAL STRUCTURE OF RAT NEUREXIN 1BETA IN THE CA2+ CONTAINING FORM | BETA-SANDWICH, CELL ADHESION, SPLICING
2r1d:G (ARG59) to (THR73) CRYSTAL STRUCTURE OF RAT NEUREXIN 1BETA IN THE CA2+ CONTAINING FORM | BETA-SANDWICH, CELL ADHESION, SPLICING
2r1d:G (ASN202) to (GLU214) CRYSTAL STRUCTURE OF RAT NEUREXIN 1BETA IN THE CA2+ CONTAINING FORM | BETA-SANDWICH, CELL ADHESION, SPLICING
2r1d:H (ARG59) to (THR73) CRYSTAL STRUCTURE OF RAT NEUREXIN 1BETA IN THE CA2+ CONTAINING FORM | BETA-SANDWICH, CELL ADHESION, SPLICING
3gr9:C (ASN3) to (TRP11) CRYSTAL STRUCTURE OF COLD H188K S187N | COLITOSE, PEROSAMINE, PLP, AMINOTRANSFERASE, O-ANTIGEN, LIPOPOLYSACCHARIDE, TRANSFERASE
3gr9:F (ASN3) to (TRP11) CRYSTAL STRUCTURE OF COLD H188K S187N | COLITOSE, PEROSAMINE, PLP, AMINOTRANSFERASE, O-ANTIGEN, LIPOPOLYSACCHARIDE, TRANSFERASE
3gt8:A (LEU679) to (LYS692) CRYSTAL STRUCTURE OF THE INACTIVE EGFR KINASE DOMAIN IN COMPLEX WITH AMP-PNP | INACTIVE KINASE, DIMER, ALTERNATIVE SPLICING, ANTI-ONCOGENE, ATP-BINDING, CELL CYCLE, CELL MEMBRANE, DISEASE MUTATION, DISULFIDE BOND, GLYCOPROTEIN, ISOPEPTIDE BOND, KINASE, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, RECEPTOR, SECRETED, TRANSFERASE, TRANSMEMBRANE, TYROSINE- PROTEIN KINASE, UBL CONJUGATION
2r5h:L (TYR27) to (THR39) PENTAMER STRUCTURE OF MAJOR CAPSID PROTEIN L1 OF HUMAN PAPILLOMA VIRUS TYPE 16 | CAPSID, PENTAMER, PROTEIN, STRUCTURE, TYPE SPECIFIC EPITOPE, CAPSID PROTEIN, VIRION, VIRAL PROTEIN
2r5i:C (TYR27) to (SER39) PENTAMER STRUCTURE OF MAJOR CAPSID PROTEIN L1 OF HUMAN PAPILLOMA VIRUS TYPE 18 | HPV18, PENTAMER, STRUCTURE, TYPE SPECIFIC EPITOPE, CAPSID, CAPSID PROTEIN, VIRION, VIRAL PROTEIN
2r5i:F (TYR27) to (SER39) PENTAMER STRUCTURE OF MAJOR CAPSID PROTEIN L1 OF HUMAN PAPILLOMA VIRUS TYPE 18 | HPV18, PENTAMER, STRUCTURE, TYPE SPECIFIC EPITOPE, CAPSID, CAPSID PROTEIN, VIRION, VIRAL PROTEIN
2r5i:I (TYR27) to (SER39) PENTAMER STRUCTURE OF MAJOR CAPSID PROTEIN L1 OF HUMAN PAPILLOMA VIRUS TYPE 18 | HPV18, PENTAMER, STRUCTURE, TYPE SPECIFIC EPITOPE, CAPSID, CAPSID PROTEIN, VIRION, VIRAL PROTEIN
2r5i:M (TYR27) to (SER39) PENTAMER STRUCTURE OF MAJOR CAPSID PROTEIN L1 OF HUMAN PAPILLOMA VIRUS TYPE 18 | HPV18, PENTAMER, STRUCTURE, TYPE SPECIFIC EPITOPE, CAPSID, CAPSID PROTEIN, VIRION, VIRAL PROTEIN
2r5k:B (TYR26) to (SER38) PENTAMER STRUCTURE OF MAJOR CAPSID PROTEIN L1 OF HUMAN PAPILLOMA VIRUS TYPE 11 | HPV11, CAPSID, PENTAMER, STRUCTURE, TYPE SPECIFIC EPITOPE, CAPSID PROTEIN, LATE PROTEIN, VIRION, VIRAL PROTEIN
2r5k:D (TYR26) to (SER38) PENTAMER STRUCTURE OF MAJOR CAPSID PROTEIN L1 OF HUMAN PAPILLOMA VIRUS TYPE 11 | HPV11, CAPSID, PENTAMER, STRUCTURE, TYPE SPECIFIC EPITOPE, CAPSID PROTEIN, LATE PROTEIN, VIRION, VIRAL PROTEIN
3tf6:A (GLY29) to (GLY38) CRYSTAL STRUCTURE OF NEUTROPHIL GELATINASE-ASSOCIATED LIPOCALIN (C87S MUTANT) IN COMPLEX WITH EUROPIUM AND THE SIDEROPHORE ANALOG TREN(CAM)(1,2-HOPO)2 | SSGCID, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, ANTIMICROBIAL PROTEIN
3tf6:C (GLY29) to (GLY38) CRYSTAL STRUCTURE OF NEUTROPHIL GELATINASE-ASSOCIATED LIPOCALIN (C87S MUTANT) IN COMPLEX WITH EUROPIUM AND THE SIDEROPHORE ANALOG TREN(CAM)(1,2-HOPO)2 | SSGCID, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, ANTIMICROBIAL PROTEIN
4j7f:A (VAL234) to (GLY247) SET7/9Y335PAF IN COMPLEX WITH TAF10 PEPTIDE AND ADOHCY | SET DOMAIN, LYSINE METHYLTRANSFERASE, Y335PAF MUTATION, TRANSFERASE- PEPTIDE COMPLEX
4j8o:A (VAL234) to (GLY247) SET7/9 IN COMPLEX WITH TAF10K189A PEPTIDE AND ADOHCY | SET DOMAIN, LYSINE METHYLTRANSFERASE, TRANSFERASE-PEPTIDE COMPLEX
3tgx:O (GLY91) to (PRO103) IL-21:IL21R COMPLEX | CLASS I CYTOKINE, CLASS I CYTOKINE RECEPTOR, SUGARBRIDGE, FIBRONECTIN DOMAIN, SIGNALING, CYTOKINE-CYTOKINE RECEPTOR COMPLEX
4j95:C (LEU481) to (ALA491) CRYSTAL STRUCURE OF FGF RECEPTOR 2 (FGFR2) KINASE DOMAIN HARBORING THE PATHOGENIC K659N MUTATION RESPONSIBLE FOR AN UNCLASSIFIED CRANIOSYNOSTOSIS SYNDROME IN SPACE GROUP C2. | KINASE DOMAIN FOLD CONSISTING OF N- AND C-LOBES, RECEPTOR TYROSINE KINASE, ATP BINDING, TRANSFERASE
4j96:A (LEU481) to (ALA491) CRYSTAL STRUCURE OF FGF RECEPTOR 2 (FGFR2) KINASE DOMAIN HARBORING THE PATHOGENIC GAIN-OF-FUNCTION K659M MUTATION IDENTIFIED IN CERVICAL CANCER. | KINASE DOMAIN FOLD CONSISTING OF N- AND C-LOBES, RECEPTOR TYROSINE KINASE, ATP BINDING, TRANSFERASE
1e9i:A (TYR363) to (GLU375) ENOLASE FROM E.COLI | DEGRADOSOME, LYASE
1e9i:C (TYR363) to (GLU375) ENOLASE FROM E.COLI | DEGRADOSOME, LYASE
1e9i:D (GLY362) to (GLU375) ENOLASE FROM E.COLI | DEGRADOSOME, LYASE
4jbi:M (GLU28) to (ASN39) 2.35A RESOLUTION STRUCTURE OF NADPH BOUND THERMOSTABLE ALCOHOL DEHYDROGENASE FROM PYROBACULUM AEROPHILUM | ALCOHOL DEHYDROGENASE, THERMOSTABILITY, ZINC BINDING, NADPH, OXIDOREDUCTASE
4jbj:A (GLY11) to (MET22) STRUCTURAL MIMICRY FOR FUNCTIONAL ANTAGONISM | OB FOLD, DS DNA, DNA BINDING PROTEIN
4jbj:B (GLY11) to (VAL21) STRUCTURAL MIMICRY FOR FUNCTIONAL ANTAGONISM | OB FOLD, DS DNA, DNA BINDING PROTEIN
4jbk:A (ALA12) to (MET22) MOLECULAR BASIS FOR ABROGATION OF ACTIVATION OF PRO-INFLAMMATORY CYTOKINES | OB FOLD, DNA, DNA BINDING PROTEIN-DNA COMPLEX
4jbk:B (ALA12) to (MET22) MOLECULAR BASIS FOR ABROGATION OF ACTIVATION OF PRO-INFLAMMATORY CYTOKINES | OB FOLD, DNA, DNA BINDING PROTEIN-DNA COMPLEX
4jbk:C (VAL13) to (MET22) MOLECULAR BASIS FOR ABROGATION OF ACTIVATION OF PRO-INFLAMMATORY CYTOKINES | OB FOLD, DNA, DNA BINDING PROTEIN-DNA COMPLEX
4jbk:D (ALA12) to (MET22) MOLECULAR BASIS FOR ABROGATION OF ACTIVATION OF PRO-INFLAMMATORY CYTOKINES | OB FOLD, DNA, DNA BINDING PROTEIN-DNA COMPLEX
1eas:A (GLN30) to (MET53) NONPEPTIDIC INHIBITORS OF HUMAN LEUKOCYTE ELASTASE. 3. DESIGN, SYNTHESIS, X-RAY CRYSTALLOGRAPHIC ANALYSIS, AND STRUCTURE-ACTIVITY RELATIONSHIPS FOR A SERIES OF ORALLY ACTIVE 3-AMINO-6-PHENYLPYRIDIN- 2-ONE TRIFLUOROMETHYL KETONES | HYDROLASE (SERINE PROTEASE)
4jc0:A (GLY410) to (GLU422) CRYSTAL STRUCTURE OF THERMOTOGA MARITIMA HOLO RIMO IN COMPLEX WITH PENTASULFIDE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET VR77 | STRUCTURAL GENOMICS, PSI-BIOLOGY, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, THREE-DOMAINED ENZYME, ALPHA-BETA N-TERMINAL DOMAIN, SEMI-TIM BARREL RADICAL-SAM DOMAIN, BETA BARREL C-TERMINAL TRAM DOMAIN, RIBOSOMAL PROTEIN S12, TRANSFERASE
4jc0:B (GLY410) to (GLU422) CRYSTAL STRUCTURE OF THERMOTOGA MARITIMA HOLO RIMO IN COMPLEX WITH PENTASULFIDE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET VR77 | STRUCTURAL GENOMICS, PSI-BIOLOGY, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, THREE-DOMAINED ENZYME, ALPHA-BETA N-TERMINAL DOMAIN, SEMI-TIM BARREL RADICAL-SAM DOMAIN, BETA BARREL C-TERMINAL TRAM DOMAIN, RIBOSOMAL PROTEIN S12, TRANSFERASE
1ebw:A (ASP30) to (GLY49) HIV-1 PROTEASE IN COMPLEX WITH THE INHIBITOR BEA322 | DIMER, PROTEIN-INHIBITOR COMPLEX, HYDROLASE/HYDROLASE INHIBITOR COMPLEX
1ec0:A (ASP30) to (GLY49) HIV-1 PROTEASE IN COMPLEX WITH THE INHIBITOR BEA403 | DIMER, PROTEIN-INHIBITOR COMPLEX, HYDROLASE/HYDROLASE INHIBITOR COMPLEX
1ec1:A (ASP30) to (GLY49) HIV-1 PROTEASE IN COMPLEX WITH THE INHIBITOR BEA409 | DIMER, PROTEIN-INHIBITOR COMPLEX, HYDROLASE/HYDROLASE INHIBITOR COMPLEX
4jcf:B (LEU27) to (GLU46) S268F VARIANT OF JC POLYOMAVIRUS MAJOR CAPSID PROTEIN VP1 IN COMPLEX WITH LSTC | BETA-SANDWICH, JELLY ROLL TOPOLOGY, VIRAL PROTEIN, MAJOR CAPSID PROTEIN, PML-ASSOCIATED VP1 MUTATION, LSTC RECEPTOR MOTIF
4jcf:E (LEU27) to (GLU46) S268F VARIANT OF JC POLYOMAVIRUS MAJOR CAPSID PROTEIN VP1 IN COMPLEX WITH LSTC | BETA-SANDWICH, JELLY ROLL TOPOLOGY, VIRAL PROTEIN, MAJOR CAPSID PROTEIN, PML-ASSOCIATED VP1 MUTATION, LSTC RECEPTOR MOTIF
1ed4:A (PRO95) to (GLY103) BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH IPITU (H4B FREE) | NITRIC OXIDE SYNTHASE, HEME PROTEIN, ALPHA-BETA FOLD, OXIDOREDUCTASE
1ed5:B (PRO95) to (GLY103) BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH NNA(H4B FREE) | NITRIC OXIDE SYNTHASE, HEME PROTEIN, ALPHA-BETA FOLD, OXIDOREDUCTASE
3gvd:E (GLY141) to (CYS152) CRYSTAL STRUCTURE OF SERINE ACETYLTRANSFERASE CYSE FROM YERSINIA PESTIS | LEFT-HANDED BETA-HELIX, STRUCTURAL GENOMICS OF NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES, ACYLTRANSFERASE, TRANSFERASE, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID
1q8p:A (ASN41) to (PHE52) PTEROCARPUS ANGOLENSIS LECTIN PAL IN COMPLEX WITH THE DIMANNOSIDE MAN(ALPHA1-3)MAN | LECTIN, CARBOHYDRATE, MANNOSE, SUGAR BINDING PROTEIN
1q8p:B (ASN41) to (PHE52) PTEROCARPUS ANGOLENSIS LECTIN PAL IN COMPLEX WITH THE DIMANNOSIDE MAN(ALPHA1-3)MAN | LECTIN, CARBOHYDRATE, MANNOSE, SUGAR BINDING PROTEIN
1q8q:B (ASN41) to (PHE52) PTEROCARPUS ANGOLENSIS LECTIN (PAL) IN COMPLEX WITH THE DIMANNOSIDE MAN(ALPHA1-4)MAN | LECTIN, CARBOHYDRATE, MANNOSE, SUGAR BINDING PROTEIN
2drv:A (ASN47) to (SER55) STRUCTURE OF PH1069 PROTEIN FROM PYROCOCCUS HORIKOSHII OT3 | HYPOTHETICAL PROTEIN, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, STRUCTURAL GENOMICS, UNKNOWN FUNCTION
3gxf:B (LEU383) to (PRO401) CRYSTAL STRUCTURE OF ACID-BETA-GLUCOSIDASE WITH ISOFAGOMINE AT NEUTRAL PH | HYDROLASE, ALTERNATIVE INITIATION, DISEASE MUTATION, DISULFIDE BOND, GAUCHER DISEASE, GLYCOPROTEIN, GLYCOSIDASE, ICHTHYOSIS, LIPID METABOLISM, LYSOSOME, MEMBRANE, SPHINGOLIPID METABOLISM
3gxf:D (LEU383) to (PRO401) CRYSTAL STRUCTURE OF ACID-BETA-GLUCOSIDASE WITH ISOFAGOMINE AT NEUTRAL PH | HYDROLASE, ALTERNATIVE INITIATION, DISEASE MUTATION, DISULFIDE BOND, GAUCHER DISEASE, GLYCOPROTEIN, GLYCOSIDASE, ICHTHYOSIS, LIPID METABOLISM, LYSOSOME, MEMBRANE, SPHINGOLIPID METABOLISM
1qa7:A (GLN159) to (LEU168) CRYSTAL COMPLEX OF THE 3C PROTEINASE FROM HEPATITIS A VIRUS WITH ITS INHIBITOR AND IMPLICATIONS FOR THE POLYPROTEIN PROCESSING IN HAV | CHYMOTRYPSIN-LIKE CYSTEINE PROTEINASE VIRAL PROTEASE P'-SITE INHIBITOR, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3gxi:B (LEU383) to (PRO401) CRYSTAL STRUCTURE OF ACID-BETA-GLUCOSIDASE AT PH 5.5 | HYDROLASE, ALTERNATIVE INITIATION, DISEASE MUTATION, DISULFIDE BOND, GAUCHER DISEASE, GLYCOPROTEIN, GLYCOSIDASE, ICHTHYOSIS, LIPID METABOLISM, LYSOSOME, MEMBRANE, SPHINGOLIPID METABOLISM
3gxi:C (LEU383) to (PRO401) CRYSTAL STRUCTURE OF ACID-BETA-GLUCOSIDASE AT PH 5.5 | HYDROLASE, ALTERNATIVE INITIATION, DISEASE MUTATION, DISULFIDE BOND, GAUCHER DISEASE, GLYCOPROTEIN, GLYCOSIDASE, ICHTHYOSIS, LIPID METABOLISM, LYSOSOME, MEMBRANE, SPHINGOLIPID METABOLISM
3gxi:D (LEU383) to (PRO401) CRYSTAL STRUCTURE OF ACID-BETA-GLUCOSIDASE AT PH 5.5 | HYDROLASE, ALTERNATIVE INITIATION, DISEASE MUTATION, DISULFIDE BOND, GAUCHER DISEASE, GLYCOPROTEIN, GLYCOSIDASE, ICHTHYOSIS, LIPID METABOLISM, LYSOSOME, MEMBRANE, SPHINGOLIPID METABOLISM
4jg8:A (GLY421) to (SER432) STRUCTURE OF RSK2 T493M CTD MUTANT BOUND TO 2-CYANO-N-(1-HYDROXY-2- METHYLPROPAN-2-YL)-3-(3-(3,4,5-TRIMETHOXYPHENYL)-1H-INDAZOL-5-YL) ACRYLAMIDE | PROTEIN KINASE, PHOSPHORYLATION, COVALENT INHIBITOR, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX
3tog:D (ASP30) to (GLY49) HIV-1 PROTEASE - EPOXYDIC INHIBITOR COMPLEX (PH 9 - MONOCLINIC CRYSTAL FORM P21) | HIV PR, EPOXIDE, IN-CRYSTAL REACTION, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3gyl:B (GLN30) to (LEU53) STRUCTURE OF PROSTASIN AT 1.3 ANGSTROMS RESOLUTION IN COMPLEX WITH A CALCIUM ION. | PROSTASIN, ENAC, ZYMOGEN, DIVALENT CATION, CHANNEL ACTIVATING, CELL MEMBRANE, DISULFIDE BOND, GLYCOPROTEIN, HYDROLASE, MEMBRANE, PROTEASE, SECRETED, SERINE PROTEASE, TRANSMEMBRANE
4yb5:A (ASN181) to (ALA193) ADENOSINE TRIPHOSPHATE PHOSPHORIBOSYLTRANSFERASE FROM CAMPYLOBACTER JEJUNI IN COMPLEX WITH THE ALLOSTERIC INHIBITOR HISTIDINE | PHOSPHORIBOSYLTRANSFERASE, HEXAMER, HISTIDINE COMPLEX, TRANSFERASE
4yb5:B (ASN181) to (ALA193) ADENOSINE TRIPHOSPHATE PHOSPHORIBOSYLTRANSFERASE FROM CAMPYLOBACTER JEJUNI IN COMPLEX WITH THE ALLOSTERIC INHIBITOR HISTIDINE | PHOSPHORIBOSYLTRANSFERASE, HEXAMER, HISTIDINE COMPLEX, TRANSFERASE
4yb5:C (ASN181) to (ALA193) ADENOSINE TRIPHOSPHATE PHOSPHORIBOSYLTRANSFERASE FROM CAMPYLOBACTER JEJUNI IN COMPLEX WITH THE ALLOSTERIC INHIBITOR HISTIDINE | PHOSPHORIBOSYLTRANSFERASE, HEXAMER, HISTIDINE COMPLEX, TRANSFERASE
4yb5:F (ASN181) to (ALA193) ADENOSINE TRIPHOSPHATE PHOSPHORIBOSYLTRANSFERASE FROM CAMPYLOBACTER JEJUNI IN COMPLEX WITH THE ALLOSTERIC INHIBITOR HISTIDINE | PHOSPHORIBOSYLTRANSFERASE, HEXAMER, HISTIDINE COMPLEX, TRANSFERASE
2rce:C (ASN188) to (HIS198) DFP MODIFIED DEGS DELTA PDZ | DFP MODIFIED ACTIVE SITE SERINE, HYDROLASE, PROTEASE, SERINE PROTEASE
2rce:H (ASN188) to (HIS198) DFP MODIFIED DEGS DELTA PDZ | DFP MODIFIED ACTIVE SITE SERINE, HYDROLASE, PROTEASE, SERINE PROTEASE
2dty:A (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN COMPLEXED WITH N-ACETYL- D-GALACTOSAMINE | LEGUME LECTIN, GLYCOSYLATED PROTEIN, AGGLUTININ, SUGAR BINDING PROTEIN
2dty:C (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN COMPLEXED WITH N-ACETYL- D-GALACTOSAMINE | LEGUME LECTIN, GLYCOSYLATED PROTEIN, AGGLUTININ, SUGAR BINDING PROTEIN
2dty:D (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN COMPLEXED WITH N-ACETYL- D-GALACTOSAMINE | LEGUME LECTIN, GLYCOSYLATED PROTEIN, AGGLUTININ, SUGAR BINDING PROTEIN
2du0:B (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH ALPHA-D- GALACTOSE | LEGUME LECTIN, GLYCOSYLATED PROTEIN, AGGLUTININ, SUGAR BINDING PROTEIN
2du0:C (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH ALPHA-D- GALACTOSE | LEGUME LECTIN, GLYCOSYLATED PROTEIN, AGGLUTININ, SUGAR BINDING PROTEIN
2du1:A (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH METHYL- ALPHA-N-ACETYL-D GALACTOSAMINE | LEGUME LECTIN, GLYCOSYLATED PROTEIN, AGGLUTININ, SUGAR BINDING PROTEIN
2du1:B (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH METHYL- ALPHA-N-ACETYL-D GALACTOSAMINE | LEGUME LECTIN, GLYCOSYLATED PROTEIN, AGGLUTININ, SUGAR BINDING PROTEIN
2du1:C (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH METHYL- ALPHA-N-ACETYL-D GALACTOSAMINE | LEGUME LECTIN, GLYCOSYLATED PROTEIN, AGGLUTININ, SUGAR BINDING PROTEIN
1ei6:B (GLY243) to (LEU259) CRYSTAL STRUCTURE OF PHOSPHONOACETATE HYDROLASE COMPLEXED WITH PHOSPHONOFORMATE | PHOSPHONOACETATE, HYDROLASE, ZINC, CRYSTAL STRUCTURE
1ei6:D (GLY243) to (LEU259) CRYSTAL STRUCTURE OF PHOSPHONOACETATE HYDROLASE COMPLEXED WITH PHOSPHONOFORMATE | PHOSPHONOACETATE, HYDROLASE, ZINC, CRYSTAL STRUCTURE
1qcn:A (ALA106) to (LEU117) CRYSTAL STRUCTURE OF FUMARYLACETOACETATE HYDROLASE | MIXED BETA SANDWICH ROLL, HYDROLASE
3tqf:B (LYS15) to (VAL24) STRUCTURE OF THE HPR(SER) KINASE/PHOSPHATASE FROM COXIELLA BURNETII | TRANSFERASE, HYDROLASE
4ycq:A (THR209) to (ASP218) BETA1 SYNTHETIC SOLENOID PROTEIN | SOLENOID, SCAFFOLD, STRUCTURAL PROTEIN
1qe5:B (GLY146) to (LEU157) PURINE NUCLEOSIDE PHOSPHORYLASE FROM CELLULOMONAS SP. IN COMPLEX WITH PHOSPHATE | ENZYME, PURINE NUCLEOSIDE PHOSPHORYLASE, TRANSFERASE
1qe5:C (GLY146) to (LEU157) PURINE NUCLEOSIDE PHOSPHORYLASE FROM CELLULOMONAS SP. IN COMPLEX WITH PHOSPHATE | ENZYME, PURINE NUCLEOSIDE PHOSPHORYLASE, TRANSFERASE
2rfy:B (ARG2) to (HIS11) CRYSTAL STRUCTURE OF CELLOBIOHYDROLASE FROM MELANOCARPUS ALBOMYCES COMPLEXED WITH CELLOBIOSE | HYDROLASE, GLYCOSIDASE
1qia:D (GLY138) to (SER145) CRYSTAL STRUCTURE OF STROMELYSIN CATALYTIC DOMAIN | INHIBITOR, MATRIXIN, MATRIX METALLOPROTEINASE-3 (MMP-3), STROMELYSIN- 1, METZINCIN, HYDROLASE
1est:A (GLN30) to (MET53) THE ATOMIC STRUCTURE OF CRYSTALLINE PORCINE PANCREATIC ELASTASE AT 2.5 ANGSTROMS RESOLUTION. COMPARISONS WITH THE STRUCTURE OF ALPHA- CHYMOTRYPSIN | HYDROLASE (SERINE PROTEINASE), HYDROLASE
1evt:C (MET149) to (SER157) CRYSTAL STRUCTURE OF FGF1 IN COMPLEX WITH THE EXTRACELLULAR LIGAND BINDING DOMAIN OF FGF RECEPTOR 1 (FGFR1) | IMMUNOGLOBULIN (IG) LIKE DOMAINS BELONGING TO THE I-SET SUBGROUP WITHIN IG-LIKE DOMAINS, B-TREFOIL FOLD, GROWTH FACTOR/GROWTH FACTOR RECEPTOR COMPLEX
1evt:D (MET149) to (SER157) CRYSTAL STRUCTURE OF FGF1 IN COMPLEX WITH THE EXTRACELLULAR LIGAND BINDING DOMAIN OF FGF RECEPTOR 1 (FGFR1) | IMMUNOGLOBULIN (IG) LIKE DOMAINS BELONGING TO THE I-SET SUBGROUP WITHIN IG-LIKE DOMAINS, B-TREFOIL FOLD, GROWTH FACTOR/GROWTH FACTOR RECEPTOR COMPLEX
1qlv:B (LEU21) to (ALA37) PYRONE SYNTHASE (PYS) FROM GERBERA HYBRIDA | POLYKETIDE SYNTHASE, POLYKETIDE, PYRONE BIOSYNTHESIS, CHALCONE
2rmn:A (THR130) to (PHE142) THE SOLUTION STRUCTURE OF THE P63 DNA-BINDING DOMAIN | PROTEIN, BETA SANDWICH, DNA BINDING, P53 FAMILY, ACTIVATOR, ALTERNATIVE PROMOTER USAGE, APOPTOSIS, DEVELOPMENTAL PROTEIN, DISEASE MUTATION, DNA-BINDING, ECTODERMAL DYSPLASIA, METAL-BINDING, NOTCH SIGNALING PATHWAY, NUCLEUS, PHOSPHORYLATION, TRANSCRIPTION, TRANSCRIPTION REGULATION, CELL CYCLE, ANTITUMOR PROTEIN
3tvv:A (ILE73) to (SER83) STRUCTURE OF THE TANDEM PH DOMAINS OF RTT106 (RESIDUES 68-315) | TANDEM PLECKSTRIN-HOMOLOGY DOMAINS, CHROMOSOMAL PROTEIN, NUCLEUS, PHOSPHOPROTEIN, TRANSCRIPTION, TRANSCRIPTION REGULATION, CHAPERONE
2rst:A (ALA112) to (SER131) NMR STRUCTURE OF THE C-TERMINAL DOMAIN OF EW29 | R-TYPE LECTIN, SUGAR BINDING PROTEIN
4jou:A (HIS50) to (GLY59) STRUCTURAL STUDY OF BACILLUS SUBTILIS HMOB IN COMPLEX WITH HEME | ABM DOMAIN, HEME MONOOXYGENASE, HEME, ANTIBIOTIC
3h3v:H (VAL86) to (GLN96) YEAST RNAP II CONTAINING POLY(A)-SIGNAL SEQUENCE IN THE ACTIVE SITE | TRANSFERASE/DNA/RNA, DNA-BINDING, PHOSPHORYLATION, RNA POLYMERASE II, METAL-BINDING, NUCLEAR PROTEIN, TRANSCRIPTION BUBBLE, ELONGATION COMPLEX, TRANSFERASE, TRANSCRIPTION, POLYADENYLATION, TERMINATION, DNA-DIRECTED RNA POLYMERASE, ISOPEPTIDE BOND, MAGNESIUM, NUCLEOTIDYLTRANSFERASE, NUCLEUS, PHOSPHOPROTEIN, ZINC-FINGER, DNA DAMAGE, DNA REPAIR, MRNA PROCESSING, TRANSFERASE-DNA-RNA COMPLEX
4jra:D (ASP554) to (HIS564) CRYSTAL STRUCTURE OF THE BOTULINUM NEUROTOXIN A RECEPTOR-BINDING DOMAIN IN COMPLEX WITH THE LUMINAL DOMAIN OF SV2C | BETA-HELIX, VESICLES, LUMEN, TOXIN, HYDROLASE
1f1b:B (GLU101) to (ASN111) CRYSTAL STRUCTURE OF E. COLI ASPARTATE TRANSCARBAMOYLASE P268A MUTANT IN THE R-STATE IN THE PRESENCE OF N-PHOSPHONACETYL-L-ASPARTATE | ASPARTATE TRANSCARBAMOYLASE, ASPARTATE CARBAMOYLTRANSFERASE, CIS- PROLINE, CIS-AMINO ACID, TRANSFERASE
4yir:A (ASN558) to (GLU575) CRYSTAL STRUCTURE OF RAD4-RAD23 CROSSLINKED TO AN UNDAMAGED DNA | DNA DAMAGE REPAIR, NUCLEOTIDE EXCISION REPAIR, PROTEIN-DNA INTERACTIONS, PROTEIN-DNA CROSSLINKING, PROTEIN-DNA COMPLEX, XERODERMA PIGMENTOSUM, BETA-HAIRPIN, TRANSGLUTAMINASE DOMAIN, DISULFIDE CROSSLINKING, DNA BINDING PROTEIN-DNA COMPLEX
3tyl:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3S,4S)-4-(2-((2-FLUOROBENZYL)AMINO)ETHOXY)PYRROLIDIN-3-YL) METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
3tyl:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3S,4S)-4-(2-((2-FLUOROBENZYL)AMINO)ETHOXY)PYRROLIDIN-3-YL) METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4jse:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6,6'-(PENTANE-1,5-DIYL)BIS(4-METHYLPYRIDIN-2-AMINE) | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4jse:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6,6'-(PENTANE-1,5-DIYL)BIS(4-METHYLPYRIDIN-2-AMINE) | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3tym:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3S,4S)-4-(2-((2-METHOXYBENZYL)AMINO)ETHOXY)PYRROLIDIN-3- YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
3tym:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3S,4S)-4-(2-((2-METHOXYBENZYL)AMINO)ETHOXY)PYRROLIDIN-3- YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4jsf:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6,6'-(HEPTANE-1,7-DIYL)BIS(4-METHYLPYRIDIN-2-AMINE) | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4jsf:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6,6'-(HEPTANE-1,7-DIYL)BIS(4-METHYLPYRIDIN-2-AMINE) | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
2e51:A (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH A BLOOD GROUP DISACCHARIDE | LECTIN, SUGAR BINDING PROTEIN, JELLY ROLL
2e51:C (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH A BLOOD GROUP DISACCHARIDE | LECTIN, SUGAR BINDING PROTEIN, JELLY ROLL
2e51:D (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH A BLOOD GROUP DISACCHARIDE | LECTIN, SUGAR BINDING PROTEIN, JELLY ROLL
3tyn:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 2-(((2-(((3S,4S)-4-((6-AMINO-4-METHYLPYRIDIN-2-YL)METHYL) PYRROLIDIN-3-YL)OXY)ETHYL)AMINO)METHYL)PHENOL | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3tyn:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 2-(((2-(((3S,4S)-4-((6-AMINO-4-METHYLPYRIDIN-2-YL)METHYL) PYRROLIDIN-3-YL)OXY)ETHYL)AMINO)METHYL)PHENOL | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4jsg:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-((3-(3-AMINOPROPOXY)PHENOXY)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4jsg:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-((3-(3-AMINOPROPOXY)PHENOXY)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
2e53:A (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH B BLOOD GROUP DISACCHARIDE | WINGED BEAN, JELLY ROLL, SUGAR BINDING PROTEIN
2e53:C (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH B BLOOD GROUP DISACCHARIDE | WINGED BEAN, JELLY ROLL, SUGAR BINDING PROTEIN
2e53:D (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH B BLOOD GROUP DISACCHARIDE | WINGED BEAN, JELLY ROLL, SUGAR BINDING PROTEIN
4jsi:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-((3-(((3-FLUOROPHENETHYL)AMINO)METHYL)PHENOXY)METHYL)-4- METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4jsi:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-((3-(((3-FLUOROPHENETHYL)AMINO)METHYL)PHENOXY)METHYL)-4- METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4jsl:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6,6'-(HEPTANE-1,7-DIYL)BIS(4-METHYLPYRIDIN-2-AMINE) | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4jsm:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((5-(((3-FLUOROPHENETHYL)AMINO)METHYL)PYRIDIN-3-YL) OXY)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3tzs:C (GLY29) to (GLY38) CRYSTAL STRUCTURE OF NEUTROPHIL GELATINASE-ASSOCIATED LIPOCALIN NGAL (C87S MUTANT) IN COMPLEX WITH FRAGMENT 1026, PHENYLUREA | STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, SSGCID, IRON TRAFFICKING, LIPOCALIN, SIDEROCALIN, FRAGMENT BASED DRUG DESIGN, FBDD, FRAGMENTS OF LIFE, EBSI-01644, APOPTOSIS
2e7q:D (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH B BLOOD GROUP TRISACCHARIDE | WINGED BEAN, JELLY ROLL, SUGAR BINDING PROTEIN
3h8a:D (TYR363) to (GLU375) CRYSTAL STRUCTURE OF E. COLI ENOLASE BOUND TO ITS COGNATE RNASE E RECOGNITION DOMAIN | GLYCOLYTIC ENZYME, PROTEIN-PROTEIN INTERACTION, LYASE, METAL-BINDING, LYASE-PROTEIN BINDING COMPLEX
1qw6:A (GLY325) to (GLY333) RAT NEURONAL NITRIC OXIDE SYNTHASE OXYGENASE DOMAIN IN COMPLEX WITH N- OMEGA-PROPYL-L-ARG. | RAT NNOSOXY COMPLEX WITH N-OMEGA-PROPYL-L-ARG, OXIDOREDUCTASE
1qwc:A (GLY325) to (GLY333) RAT NEURONAL NITRIC OXIDE SYNTHASE OXYGENASE DOMAIN IN COMPLEX WITH W1400 INHIBITOR. | RAT NNOSOXY W1400 INHIBITOR COMPLEX, OXIDOREDUCTASE
1r0b:G (GLU101) to (ASN111) ASPARTATE TRANSCARBAMYLASE (ATCASE) OF ESCHERICHIA COLI: A NEW CRYSTALLINE R STATE BOUND TO PALA, OR TO PRODUCT ANALOGUES PHOSPHATE AND CITRATE | ASPARTATE TRANSCARBAMYLASE, ASPARTATE CARBAMOYLTRANSFERASE, PRODUCT ANALOGUE, CITRATE, PHOSPHATE, ATCASE-CITRATE- PHOSPHATE COMPLEX, R STATE
4jwx:A (SER10) to (ASP24) GLUN2A LIGAND-BINDING CORE IN COMPLEX WITH PROPYL-NHP5G | BILOBED STRUCTURE, UNKNOWN FUNCTION
1fak:H (GLN30) to (VAL53) HUMAN TISSUE FACTOR COMPLEXED WITH COAGULATION FACTOR VIIA INHIBITED WITH A BPTI-MUTANT | COMPLEX(SERINE PROTEASE/COFACTOR/LIGAND), BLOOD COAGULATION, SERINE PROTEASE, COMPLEX, CO-FACTOR, RECEPTOR ENZYME, INHIBITOR, GLA, EGF, COMPLEX (SERINE PROTEASE/COFACTOR/LIGAND), BLOOD CLOTTING
1fc5:A (GLY391) to (PHE404) CRYSTAL STRUCTURE OF MOLYBDOPTERIN BIOSYNTHESIS MOEA PROTEIN | MOLYBDOPTERIN, FOUR MODULES, WITH MAGNESIUM, MONTREAL- KINGSTON BACTERIAL STRUCTURAL GENOMICS INITIATIVE, BSGI, STRUCTURAL GENOMICS, BIOSYNTHETIC PROTEIN
3u7s:A (VAL12) to (GLU34) HIV PR DRUG RESISTANT PATIENT'S VARIANT IN COMPLEX WITH DARUNAVIR | DARUNVIR, RESISTANCE, MUTATION SCORE, HIV PROTEASE, TMC-114, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4jym:B (VAL125) to (GLY133) CRYSTAL STRUCTURE OF KAI2 IN COMPLEX WITH 3-METHYL-2H-FURO[2,3- C]PYRAN-2-ONE | ALPHA/BETA-HYDROLASE, HYDROLASE
4jyp:A (VAL125) to (GLY133) CRYSTAL STRUCTURE OF KAI2 APO FORM | ALPHA/BETA HYDROLASE, HYDROLASE
4jyv:H (GLN30) to (VAL53) STRUCTURE OF FACTOR VIIA IN COMPLEX WITH THE INHIBITOR (2R)-2-[3- ETHOXY-4-(PROPAN-2-YLOXY)PHENYL]-2-(ISOQUINOLIN-6-YLAMINO)-N-[(3- SULFAMOYLPHENYL)SULFONYL]ETHANAMIDE | GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM-BINDING, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3u87:B (TYR39) to (LYS49) STRUCTURE OF A CHIMERIC CONSTRUCT OF HUMAN CK2ALPHA AND HUMAN CK2ALPHA' IN COMPLEX WITH A NON-HYDROLYSABLE ATP-ANALOGUE | PROTEIN KINASE CK2 CASEIN KINASE 2, PROTEIN KINASE FOLD, EUKARYOTIC PROTEIN KINASE, TRANSFERASE
2eic:A (LYS112) to (PRO120) CRYSTAL STRUCTURE OF GALACTOSE OXIDASE MUTANT W290F | GALACTOSE OXIDASE W290F MUTANT, OXIDOREDUCTASE
4jzd:H (GLN30) to (VAL53) STRUCTURE OF FACTOR VIIA IN COMPLEX WITH THE INHIBITOR 2-{2-[(4- CARBAMIMIDOYLPHENYL)CARBAMOYL]-6-METHOXYPYRIDIN-3-YL}-5-{[(2S)-1- HYDROXY-3,3-DIMETHYLBUTAN-2-YL]CARBAMOYL}BENZOIC ACID | GLYCOPROTEIN, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM BINDING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4jze:H (GLN30) to (VAL53) STRUCTURE OF FACTOR VIIA IN COMPLEX WITH THE INHIBITOR 2-{2-[(1- AMINOISOQUINOLIN-6-YL)CARBAMOYL]-6-METHOXYPYRIDIN-3-YL}-5-{[(2S)-1- HYDROXY-3,3-DIMETHYLBUTAN-2-YL]CARBAMOYL}BENZOIC ACID | GLYCOPROTEIN, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM BINDING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ylq:H (GLN30) to (VAL53) CRYSTAL STRUCTURE OF A FVIIA-TRYPSIN CHIMERA (FT) IN COMPLEX WITH SOLUBLE TISSUE FACTOR | TRYPSIN-FOLD, PROTEIN-PROTEIN COMPLEX, HYDROLASE
2uzb:A (ASN3) to (THR14) CRYSTAL STRUCTURE OF HUMAN CDK2 COMPLEXED WITH A THIAZOLIDINONE INHIBITOR | TRANSFERASE, ATP-BINDING, PHOSPHORYLATION, CDK2, KINASE, CYCLIN, MITOSIS, CELL CYCLE, CELL DIVISION, NUCLEOTIDE- BINDING, SERINE/THREONINE-PROTEIN KINASE, THIAZOLIDINONE LIGAND
1fh0:A (GLY61) to (PHE69) CRYSTAL STRUCTURE OF HUMAN CATHEPSIN V COMPLEXED WITH AN IRREVERSIBLE VINYL SULFONE INHIBITOR | CATHEPSIN, PAPAIN, PROTEASE, CANCER, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4k19:C (GLY29) to (GLY38) THE STRUCTURE OF HUMAN SIDEROCALIN BOUND TO THE BACTERIAL SIDEROPHORE FLUVIBACTIN | BETA BARREL, ANTIBACTERIAL, SIDEROPHORE, METAL BINDING PROTEIN- INHIBITOR COMPLEX
1fi1:A (GLN619) to (PHE633) FHUA IN COMPLEX WITH LIPOPOLYSACCHARIDE AND RIFAMYCIN CGP4832 | OUTER MEMBRANE PROTEIN; TONB-DEPENDENT RECEPTOR; FHUA; SIDEROPHORE RECEPTOR; INTEGRAL MEMBRANE PROTEIN; LIPOPOLYSACCHARIDE; RIFAMYCIN CGP 4832; BETA-BARREL; ANTIBIOTIC, METAL TRANSPORT
3ucb:A (THR12) to (ASP35) CRYSTAL STRUCTURE OF MULTIDRUG RESISTANT HIV-1 PROTEASE CLINICAL ISOLATE PR20 IN COMPLEX WITH DARUNAVIR | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2v3d:A (LEU383) to (PRO401) ACID-BETA-GLUCOSIDASE WITH N-BUTYL-DEOXYNOJIRIMYCIN | ACID-BETA-GLUCOSIDASE, N-BUTYL-DEOXYNOJIRIMYCINALTERNATIVE INITIATION, SPHINGOLIPID METABOLISM, GAUCHER DISEASE, DISEASE MUTATION, LIPID METABOLISM, POLYMORPHISM, GLYCOPROTEIN, PHARMACEUTICAL, N-BUTYL-DEOXYNOJIRIMYCIN, ALTERNATIVE SPLICING, MEMBRANE, LYSOSOME, HYDROLASE, GLYCOSIDASE
2v3d:B (LEU383) to (PRO401) ACID-BETA-GLUCOSIDASE WITH N-BUTYL-DEOXYNOJIRIMYCIN | ACID-BETA-GLUCOSIDASE, N-BUTYL-DEOXYNOJIRIMYCINALTERNATIVE INITIATION, SPHINGOLIPID METABOLISM, GAUCHER DISEASE, DISEASE MUTATION, LIPID METABOLISM, POLYMORPHISM, GLYCOPROTEIN, PHARMACEUTICAL, N-BUTYL-DEOXYNOJIRIMYCIN, ALTERNATIVE SPLICING, MEMBRANE, LYSOSOME, HYDROLASE, GLYCOSIDASE
2v3e:A (LEU383) to (PRO401) ACID-BETA-GLUCOSIDASE WITH N-NONYL-DEOXYNOJIRIMYCIN | ACID-BETA-GLUCOSIDASE, N-NONYL-DEOXYNOJIRIMYCINALTERNATIVE INITIATION, SPHINGOLIPID METABOLISM, N-NONYL-DEOXYNOJIRIMYCIN, GAUCHER DISEASE, DISEASE MUTATION, LIPID METABOLISM, POLYMORPHISM, GLYCOPROTEIN, PHARMACEUTICAL, ALTERNATIVE SPLICING, MEMBRANE, LYSOSOME, HYDROLASE, GLYCOSIDASE
2v3e:B (LEU383) to (PRO401) ACID-BETA-GLUCOSIDASE WITH N-NONYL-DEOXYNOJIRIMYCIN | ACID-BETA-GLUCOSIDASE, N-NONYL-DEOXYNOJIRIMYCINALTERNATIVE INITIATION, SPHINGOLIPID METABOLISM, N-NONYL-DEOXYNOJIRIMYCIN, GAUCHER DISEASE, DISEASE MUTATION, LIPID METABOLISM, POLYMORPHISM, GLYCOPROTEIN, PHARMACEUTICAL, ALTERNATIVE SPLICING, MEMBRANE, LYSOSOME, HYDROLASE, GLYCOSIDASE
2v3f:A (LEU383) to (PRO401) ACID-BETA-GLUCOSIDASE PRODUCED IN CARROT | ALTERNATIVE INITIATION, SPHINGOLIPID METABOLISM, GAUCHER DISEASE, DISEASE MUTATION, LIPID METABOLISM, POLYMORPHISM, GLYCOPROTEIN, PHARMACEUTICAL, N-BUTYL-DEOXYNOJIRIMYCIN, ALTERNATIVE SPLICING, ACID-BETA-GLUCOSIDASE, MEMBRANE, LYSOSOME, HYDROLASE, GLYCOSIDASE
2v3f:B (LEU383) to (PRO401) ACID-BETA-GLUCOSIDASE PRODUCED IN CARROT | ALTERNATIVE INITIATION, SPHINGOLIPID METABOLISM, GAUCHER DISEASE, DISEASE MUTATION, LIPID METABOLISM, POLYMORPHISM, GLYCOPROTEIN, PHARMACEUTICAL, N-BUTYL-DEOXYNOJIRIMYCIN, ALTERNATIVE SPLICING, ACID-BETA-GLUCOSIDASE, MEMBRANE, LYSOSOME, HYDROLASE, GLYCOSIDASE
3udc:A (MET171) to (PRO189) CRYSTAL STRUCTURE OF A MEMBRANE PROTEIN | MEMBRANE PROTEIN, CHANNEL, MECHANOSENSITIVE
3udc:B (MET171) to (PRO189) CRYSTAL STRUCTURE OF A MEMBRANE PROTEIN | MEMBRANE PROTEIN, CHANNEL, MECHANOSENSITIVE
3udc:C (MET171) to (PRO189) CRYSTAL STRUCTURE OF A MEMBRANE PROTEIN | MEMBRANE PROTEIN, CHANNEL, MECHANOSENSITIVE
3udc:D (MET171) to (PRO189) CRYSTAL STRUCTURE OF A MEMBRANE PROTEIN | MEMBRANE PROTEIN, CHANNEL, MECHANOSENSITIVE
3udc:E (MET171) to (PRO189) CRYSTAL STRUCTURE OF A MEMBRANE PROTEIN | MEMBRANE PROTEIN, CHANNEL, MECHANOSENSITIVE
1fl7:D (TYR39) to (CYS51) HUMAN FOLLICLE STIMULATING HORMONE | CYSTEINE KNOT, HETERODIMER, HORMONE-GROWTH FACTOR COMPLEX
1fle:E (GLN30) to (MET53) CRYSTAL STRUCTURE OF ELAFIN COMPLEXED WITH PORCINE PANCREATIC ELASTASE | HYDROLASE, SERINE PROTEASE, 3D-STRUCTURE, ZYMOGEN, PANCREAS, SIGNAL, COMPLEX (SERINE PROTEASE/INHIBITOR)
4k3b:A (HIS340) to (GLY356) THE CRYSTAL STRUCTURE OF BAMA FROM NEISSERIA GONORRHOEAE | BETA-BARREL MEMBRANE PROTEIN, INSERTASE, MEMBRANE PROTEIN
1fm8:A (PHE89) to (SER102) CHALCONE ISOMERASE COMPLEXED WITH 5,4'-DIDEOXYFLAVANONE | NATURAL PRODUCT BIOSYNTHESIS, CHALCONE, ISOMERASE
1fm8:B (PHE89) to (SER102) CHALCONE ISOMERASE COMPLEXED WITH 5,4'-DIDEOXYFLAVANONE | NATURAL PRODUCT BIOSYNTHESIS, CHALCONE, ISOMERASE
3uf9:A (ASP256) to (ASP262) CRYSTAL STRUCTURE OF SSOPOX IN COMPLEX WITH THE PHOSPHOTRIESTER FENSULFOTHION | (BETA/ALPHA)8-HYDROLASE, LACTONASE, HYDROLASE
3ufq:A (GLY325) to (GLY333) STRUCTURE OF RAT NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6- (((3S,4S)-4-(((E)-5-(3-FLUOROPHENYL)PENT-4-EN-1-YL)OXY)PYRROLIDIN-3- YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3ufq:B (GLY325) to (GLY333) STRUCTURE OF RAT NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6- (((3S,4S)-4-(((E)-5-(3-FLUOROPHENYL)PENT-4-EN-1-YL)OXY)PYRROLIDIN-3- YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3ufo:A (GLY325) to (GLY333) STRUCTURE OF RAT NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6- (((3S,4S)-4-((5-(3-FLUOROPHENYL)PENTYL)OXY)PYRROLIDIN-3-YL)METHYL)-4- METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
3ufo:B (GLY325) to (GLY333) STRUCTURE OF RAT NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6- (((3S,4S)-4-((5-(3-FLUOROPHENYL)PENTYL)OXY)PYRROLIDIN-3-YL)METHYL)-4- METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
3ufp:A (GLY325) to (GLY333) STRUCTURE OF RAT NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6- (((3R,4R)-4-((5-(3-FLUOROPHENYL)PENTYL)OXY)PYRROLIDIN-3-YL)METHYL)-4- METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3ufp:B (GLY325) to (GLY333) STRUCTURE OF RAT NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6- (((3R,4R)-4-((5-(3-FLUOROPHENYL)PENTYL)OXY)PYRROLIDIN-3-YL)METHYL)-4- METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3ufr:A (GLY325) to (GLY333) STRUCTURE OF RAT NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6- (((3R,4R)-4-(((E)-5-(3-FLUOROPHENYL)PENT-4-EN-1-YL)OXY)PYRROLIDIN-3- YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
3ufr:B (GLY325) to (GLY333) STRUCTURE OF RAT NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6- (((3R,4R)-4-(((E)-5-(3-FLUOROPHENYL)PENT-4-EN-1-YL)OXY)PYRROLIDIN-3- YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
3ufs:A (GLY325) to (GLY333) STRUCTURE OF RAT NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6- (((3R,4R)-4-((5-(3-CHLORO-5-FLUOROPHENYL)PENTYL)OXY)PYRROLIDIN-3-YL) METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
3ufs:B (GLY325) to (GLY333) STRUCTURE OF RAT NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6- (((3R,4R)-4-((5-(3-CHLORO-5-FLUOROPHENYL)PENTYL)OXY)PYRROLIDIN-3-YL) METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
3uft:A (GLY325) to (GLY333) STRUCTURE OF RAT NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6- (((3R,4R)-4-(4-(3-CHLORO-5-FLUOROPHENOXY)BUTOXY)PYRROLIDIN-3-YL) METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
3uft:B (GLY325) to (GLY333) STRUCTURE OF RAT NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6- (((3R,4R)-4-(4-(3-CHLORO-5-FLUOROPHENOXY)BUTOXY)PYRROLIDIN-3-YL) METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
3ufu:A (GLY325) to (GLY333) STRUCTURE OF RAT NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4- METHYL-6-(((3R,4R)-4-((5-(PYRIDIN-2-YL)PENTYL)OXY)PYRROLIDIN-3-YL) METHYL)PYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
3ufu:B (GLY325) to (GLY333) STRUCTURE OF RAT NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4- METHYL-6-(((3R,4R)-4-((5-(PYRIDIN-2-YL)PENTYL)OXY)PYRROLIDIN-3-YL) METHYL)PYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
3ufv:A (GLY325) to (GLY333) STRUCTURE OF RAT NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4- METHYL-6-(((3R,4R)-4-((5-(4-METHYLPYRIDIN-2-YL)PENTYL)OXY)PYRROLIDIN- 3-YL)METHYL)PYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
3ufv:B (GLY325) to (GLY333) STRUCTURE OF RAT NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4- METHYL-6-(((3R,4R)-4-((5-(4-METHYLPYRIDIN-2-YL)PENTYL)OXY)PYRROLIDIN- 3-YL)METHYL)PYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
3ufw:A (GLY325) to (GLY333) STRUCTURE OF RAT NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6- (((3R,4R)-4-((5-(6-AMINOPYRIDIN-2-YL)PENTYL)OXY)PYRROLIDIN-3-YL) METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
3ufw:B (GLY325) to (GLY333) STRUCTURE OF RAT NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6- (((3R,4R)-4-((5-(6-AMINOPYRIDIN-2-YL)PENTYL)OXY)PYRROLIDIN-3-YL) METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4k5d:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-1,2-BIS((2-AMINO-4-METHYLPYRIDIN-6-YL)-METHOXY)-PROPAN-3- AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4k5d:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-1,2-BIS((2-AMINO-4-METHYLPYRIDIN-6-YL)-METHOXY)-PROPAN-3- AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4k5f:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-1,3-BIS((2-AMINO-4-METHYLPYRIDIN-6-YL)-METHOXY)-BUTAN-4- AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4k5f:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-1,3-BIS((2-AMINO-4-METHYLPYRIDIN-6-YL)-METHOXY)-BUTAN-4- AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4k5g:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH ((2S, 3S)-1,3-BIS((6-(2,5-DIMETHYL-1H-PYRROL-1-YL)-4- METHYLPYRIDIN-2-YL)METHOXY)-2-AMINOBUTANE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4k5g:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH ((2S, 3S)-1,3-BIS((6-(2,5-DIMETHYL-1H-PYRROL-1-YL)-4- METHYLPYRIDIN-2-YL)METHOXY)-2-AMINOBUTANE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4k5h:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-1,2-BIS((2-AMINO-4-METHYLPYRIDIN-6-YL)-METHOXY)- PROPAN-3-AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4k5h:B (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-1,2-BIS((2-AMINO-4-METHYLPYRIDIN-6-YL)-METHOXY)- PROPAN-3-AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4k5i:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (R)-1,2-BIS((2-AMINO-4-METHYLPYRIDIN-6-YL)-METHOXY)- PROPAN-3-AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4k5j:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-1,3-BIS((2-AMINO-4-METHYLPYRIDIN-6-YL)-METHOXY)- BUTAN-4-AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4k5k:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH ((2S, 3S)-1,3-BIS((6-(2,5-DIMETHYL-1H-PYRROL-1-YL)-4- METHYLPYRIDIN-2-YL)METHOXY)-2-AMINOBUTANE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4k5k:B (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH ((2S, 3S)-1,3-BIS((6-(2,5-DIMETHYL-1H-PYRROL-1-YL)-4- METHYLPYRIDIN-2-YL)METHOXY)-2-AMINOBUTANE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
1foj:B (PRO95) to (GLY103) BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 7- NITROINDAZOLE-2-CARBOXAMIDINE (H4B PRESENT) | ALPHA-BETA FOLD, NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE
1fol:A (PRO95) to (GLY103) REDUCED BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH L-ARG(H4B-FREE) | ALPHA-BETA FOLD, NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE
4yt6:H (GLN30) to (VAL53) FACTOR VIIA IN COMPLEX WITH THE INHIBITOR 4-{[(R)-[5-ETHOXY-2-FLUORO- 3-(PROPAN-2-YLOXY)PHENYL](4-PHENYL-1H-IMIDAZOL-2-YL) METHYL]AMINO}BENZENECARBOXIMIDAMIDE | GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM-BINDING, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3ugv:A (LYS9) to (ALA25) CRYSTAL STRUCTURE OF AN ENOLASE FROM ALPHA PRETOBACTERIUM BAL199 (EFI TARGET EFI-501650) WITH BOUND MG | ENOLASE, ENZYME FUNCTION INITIATIVE, EFI, LYASE
3ugv:B (LYS9) to (ALA25) CRYSTAL STRUCTURE OF AN ENOLASE FROM ALPHA PRETOBACTERIUM BAL199 (EFI TARGET EFI-501650) WITH BOUND MG | ENOLASE, ENZYME FUNCTION INITIATIVE, EFI, LYASE
3ugv:D (LYS9) to (ALA25) CRYSTAL STRUCTURE OF AN ENOLASE FROM ALPHA PRETOBACTERIUM BAL199 (EFI TARGET EFI-501650) WITH BOUND MG | ENOLASE, ENZYME FUNCTION INITIATIVE, EFI, LYASE
3ugv:F (LYS9) to (ALA25) CRYSTAL STRUCTURE OF AN ENOLASE FROM ALPHA PRETOBACTERIUM BAL199 (EFI TARGET EFI-501650) WITH BOUND MG | ENOLASE, ENZYME FUNCTION INITIATIVE, EFI, LYASE
3ugv:G (LYS9) to (ALA25) CRYSTAL STRUCTURE OF AN ENOLASE FROM ALPHA PRETOBACTERIUM BAL199 (EFI TARGET EFI-501650) WITH BOUND MG | ENOLASE, ENZYME FUNCTION INITIATIVE, EFI, LYASE
3uhl:D (THR12) to (GLU34) CRYSTAL STRUCTURE OF MULTIDRUG RESISTANT HIV-1 PROTEASE CLINICAL ISOLATE PR20 IN COMPLEX WITH P2-NC SUBSTRATE ANALOG | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1fq1:B (ASN3) to (THR14) CRYSTAL STRUCTURE OF KINASE ASSOCIATED PHOSPHATASE (KAP) IN COMPLEX WITH PHOSPHO-CDK2 | PHOSPHO-PROTEIN/PROTEIN COMPLEX, HYDROLASE/TRANSFERASE COMPLEX
1fq9:C (MET149) to (SER157) CRYSTAL STRUCTURE OF A TERNARY FGF2-FGFR1-HEPARIN COMPLEX | I-SET SUBGROUP WITHIN THE IMMUNOGLOBULIN SUPERFAMILY, B-TREFOIL FOLD, GROWTH FACTOR-GROWTH FACTOR RECEPTOR COMPLEX
1fq9:D (MET149) to (SER157) CRYSTAL STRUCTURE OF A TERNARY FGF2-FGFR1-HEPARIN COMPLEX | I-SET SUBGROUP WITHIN THE IMMUNOGLOBULIN SUPERFAMILY, B-TREFOIL FOLD, GROWTH FACTOR-GROWTH FACTOR RECEPTOR COMPLEX
1fqv:K (SER191) to (ASN202) INSIGHTS INTO SCF UBIQUITIN LIGASES FROM THE STRUCTURE OF THE SKP1-SKP2 COMPLEX | SKP1, SKP2, F-BOX, LRR, LEUCINE-RICH REPEAT, SCF, UBIQUITIN, E3, UBIQUITIN PROTEIN LIGASE
1rev:A (GLY285) to (PRO294) HIV-1 REVERSE TRANSCRIPTASE | AIDS, POLYPROTEIN, HYDROLASE, ASPARTYL PROTEASE, ENDONUCLEASE, NUCLEOTIDYLTRANSFERASE, HIV-1 REVERSE TRANSCRIPTASE
3ujo:A (ASN25) to (GLN42) GALACTOSE-SPECIFIC SEED LECTIN FROM DOLICHOS LABLAB IN COMPLEX WITH ADENINE AND GALACTOSE | LEGUME LECTIN FOLD, CARBOHYDRATE-BINDING, GALACTOSE, ADENINE, SUGAR BINDING PROTEIN
3ujq:B (LEU26) to (GLN42) GALACTOSE-SPECIFIC LECTIN FROM DOLICHOS LABLAB IN COMPLEX WITH GALACTOSE | LEGUME LECTIN FOLD, CARBOHYDRATE/SUGAR-BINDING, GALACTOSE, ADENINE, SEED, SUGAR BINDING PROTEIN
1ft9:B (ARG24) to (GLY37) STRUCTURE OF THE REDUCED (FEII) CO-SENSING PROTEIN FROM R. RUBRUM | CARBON MONOXIDE, HEME SENSOR, CATABOLITE GENE ACTIVATOR PROTEIN, TRANSCRIPTION
3ujr:B (TRP364) to (GLU376) ASYMMETRIC COMPLEX OF HUMAN NEURON SPECIFIC ENOLASE-5-PGA/PEP | LYASE
1rir:A (ALA98) to (LEU106) CRYSTAL STRUCTURE OF MESO-TETRASULPHONATOPHENYLPORPHYRIN IN COMPLEX WITH PEANUT LECTIN. | SUGAR BINDING PROTEIN
1rir:D (ALA98) to (LEU106) CRYSTAL STRUCTURE OF MESO-TETRASULPHONATOPHENYLPORPHYRIN IN COMPLEX WITH PEANUT LECTIN. | SUGAR BINDING PROTEIN
2f3k:A (ASP30) to (GLY49) SUBSTRATE ENVELOPE AND DRUG RESISTANCE: CRYSTAL STRUCTURE OF R01 IN COMPLEX WITH WILD-TYPE HIV-1 PROTEASE | SUBSTRATE ENVELOPE, DRUG RESISTANCE, HIV PROTEASE, RO1, HYDROLASE
3ulu:A (GLN483) to (ASN494) STRUCTURE OF QUATERNARY COMPLEX OF HUMAN TLR3ECD WITH THREE FABS (FORM1) | TOLL-LIKE RECEPTOR-3, TLR3,INNATE IMMUNITY, LEUCINE RICH REPEAT, LRR, IMMUNOGLOBULIN, IMMUNE SYSTEM
2f5t:X (ASP327) to (MET337) CRYSTAL STRUCTURE OF THE SUGAR BINDING DOMAIN OF THE ARCHAEAL TRANSCRIPTIONAL REGULATOR TRMB | SUGAR-BINDING, TRANSCRIPTION
2vc5:C (ASP256) to (ASP262) STRUCTURAL BASIS FOR NATURAL LACTONASE AND PROMISCUOUS PHOSPHOTRIESTERASE ACTIVITIES | PHOSPHOTRIESTERASE, PROMISCUOUS ACTIVITIES, ENZYME EVOLUTION, HYPERTHERMOPHILIC, LACTONASE, HYDROLASE, BIOTECHNOLOGY, QUORUM SENSING
4yz0:A (SER166) to (ASN177) C. BESCII FAMILY 3 PECTATE LYASE DOUBLE MUTANT K108A/E39Q IN COMPLEX WITH TRIGALACTURONIC ACID | PL3, PARALLEL BETA-HELIX, LYASE
4yza:A (VAL165) to (ASN177) C. BESCII FAMILY 3 PECTATE LYASE DOUBLE MUTANT K108A/Q111A IN COMPLEX WITH TRIGALACTURONIC ACID | PL3, PARALLEL BETA-HELIX, LYASE
4kci:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N,N'-(ETHANE-1,2-DIYLBIS(3,1-PHENYLENE))BIS(THIOPHENE-2- CARBOXIMIDAMIDE) | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4kci:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N,N'-(ETHANE-1,2-DIYLBIS(3,1-PHENYLENE))BIS(THIOPHENE-2- CARBOXIMIDAMIDE) | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4kcj:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N,N'-((ETHANE-1,2-DIYLBIS(OXY))BIS(3,1-PHENYLENE))BIS(THIOPHENE- 2-CARBOXIMIDAMIDE) | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4kcj:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N,N'-((ETHANE-1,2-DIYLBIS(OXY))BIS(3,1-PHENYLENE))BIS(THIOPHENE- 2-CARBOXIMIDAMIDE) | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4kck:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(3-(2-((3-(THIOPHENE-2-CARBOXIMIDAMIDO)BENZYL)AMINO)ETHYL) PHENYL)THIOPHENE-2-CARBOXIMIDAMIDE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4kck:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(3-(2-((3-(THIOPHENE-2-CARBOXIMIDAMIDO)BENZYL)AMINO)ETHYL) PHENYL)THIOPHENE-2-CARBOXIMIDAMIDE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4kcl:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(4-(2-((3-(THIOPHENE-2-CARBOXIMIDAMIDO)BENZYL)AMINO)ETHYL) PHENYL)THIOPHENE-2-CARBOXIMIDAMIDE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4kcl:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(4-(2-((3-(THIOPHENE-2-CARBOXIMIDAMIDO)BENZYL)AMINO)ETHYL) PHENYL)THIOPHENE-2-CARBOXIMIDAMIDE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4kcm:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(4-(2-(ETHYL(3-(THIOPHENE-2-CARBOXIMIDAMIDO)BENZYL)AMINO) ETHYL)PHENYL)THIOPHENE-2-CARBOXIMIDAMIDE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4kcm:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(4-(2-(ETHYL(3-(THIOPHENE-2-CARBOXIMIDAMIDO)BENZYL)AMINO) ETHYL)PHENYL)THIOPHENE-2-CARBOXIMIDAMIDE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4kcn:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(3-(((3-FLUOROPHENETHYL)AMINO)METHYL)PHENYL)THIOPHENE-2- CARBOXIMIDAMIDE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4kcn:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(3-(((3-FLUOROPHENETHYL)AMINO)METHYL)PHENYL)THIOPHENE-2- CARBOXIMIDAMIDE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4kco:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(3-((ETHYL(3-FLUOROPHENETHYL)AMINO)METHYL)PHENYL)THIOPHENE-2- CARBOXIMIDAMIDE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4kco:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(3-((ETHYL(3-FLUOROPHENETHYL)AMINO)METHYL)PHENYL)THIOPHENE-2- CARBOXIMIDAMIDE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4yzq:A (VAL165) to (ASN177) C. BESCII FAMILY 3 PECTATE LYASE DOUBLE MUTANT K108A/Q111N IN COMPLEX WITH TRIGALACTURONIC ACID | PL3, PARALLEL BETA-HELIX, LYASE
4kcp:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHEIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(4-(2-((3-(THIOPHENE-2-CARBOXIMIDAMIDO)BENZYL)AMINO) ETHYL)PHENYL)THIOPHENE-2-CARBOXIMIDAMIDE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4yzx:A (SER166) to (ASN177) C. BESCII FAMILY 3 PECTATE LYASE DOUBLE MUTANT K108A/D107N IN COMPLEX WITH TRIGALACTURONIC ACID | PL3, PARALLEL BETA-HELIX, LYASE
4z07:A (TYR135) to (GLU148) CO-CRYSTAL STRUCTURE OF THE TANDEM CNB (CNB-A/B) DOMAINS OF HUMAN PKG I BETA WITH CGMP | CGMP-BINDING DOMAINS, CGMP MEDIATED DIMERIC INTERFACE, ALLOSTERIC REGULATORY DOMAIN, SERINE-THREONINE KINASE, TRANSFERASE
1rs6:A (GLY325) to (GLY333) RAT NEURONAL NOS HEME DOMAIN WITH D-LYSINE-D-NITROARGININE AMIDE BOUND | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME
1rs6:B (GLY325) to (GLY333) RAT NEURONAL NOS HEME DOMAIN WITH D-LYSINE-D-NITROARGININE AMIDE BOUND | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME
1rs7:A (GLY325) to (GLY333) RAT NEURONAL NOS HEME DOMAIN WITH D-PHENYLALANINE-D-NITROARGININE AMIDE BOUND | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME
1rs7:B (GLY325) to (GLY333) RAT NEURONAL NOS HEME DOMAIN WITH D-PHENYLALANINE-D-NITROARGININE AMIDE BOUND | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME
2fa2:B (ASP12) to (ALA23) CRYSTAL STRUCTURE OF FUS3 WITHOUT A PEPTIDE FROM STE5 | MAP KINASE, TRANSFERASE
1g2k:A (ASP30) to (GLY49) HIV-1 PROTEASE WITH CYCLIC SULFAMIDE INHIBITOR, AHA047 | HIV, PROTEASE INHIBITORS, HYDROLASE
1g2o:A (GLN132) to (LEU142) CRYSTAL STRUCTURE OF PURINE NUCLEOSIDE PHOSPHORYLASE FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH A TRANSITION- STATE INHIBITOR | TRIMER, TRANSITION-STATE COMPLEX, TRANSFERASE
1g2o:C (GLN132) to (LEU142) CRYSTAL STRUCTURE OF PURINE NUCLEOSIDE PHOSPHORYLASE FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH A TRANSITION- STATE INHIBITOR | TRIMER, TRANSITION-STATE COMPLEX, TRANSFERASE
1g35:A (ASP30) to (GLY49) CRYSTAL STRUCTURE OF HIV-1 PROTEASE IN COMPLEX WITH INHIBITOR, AHA024 | PROTEIN-INHIBITOR COMPLEX, HYDROLASE
1rwr:A (GLN142) to (GLY156) CRYSTAL STRUCTURE OF FILAMENTOUS HEMAGGLUTININ SECRETION DOMAIN | TYPE V SECRETION, BETA-HELIX, ADHESINS, FILAMENTOUS HEMAGGLUTININ, TPS DOMAIN, CELL ADHESION
4khq:A (PRO35) to (ASP51) TERNARY COMPLEX OF RB69 MUTANT L415F WIT DUMPNPP | NUCLEOTIDE, TRANSFERASE-DNA COMPLEX
1g7y:C (ALA1) to (GLN19) THE CRYSTAL STRUCTURE OF THE 58KD VEGETATIVE LECTIN FROM THE TROPICAL LEGUME DOLICHOS BIFLORUS | JELLY ROLL FOLD, LECTIN, SUGAR BINDING PROTEIN
1g7y:D (ASP2) to (GLN19) THE CRYSTAL STRUCTURE OF THE 58KD VEGETATIVE LECTIN FROM THE TROPICAL LEGUME DOLICHOS BIFLORUS | JELLY ROLL FOLD, LECTIN, SUGAR BINDING PROTEIN
4khs:A (PRO35) to (ASP51) TERNARY COMPLEX OF RB69 MUTANT L415F WITH A RIBONUCLEOTIDE AT 0 POSITION | RIBONUCLEOTIDE, TRANSFERASE-DNA COMPLEX
4khu:A (PRO35) to (ASP51) TERNARY COMPLEX OF RB69 MUTANT L415F WITH A RIBONUCLEOTIDE AT -1 POSITION | RIBONUCLEOTIDE, TRANSFERASE-DNA COMPLEX
4ki4:A (PRO35) to (ASP51) TERNARY COMPLEX OF RB69 MUTANT L415F WITH RIBONUCLEOTIDES AT 0 AND -1 POSITION | RIBONUCLEOTIDE, TRANSFERASE-DNA COMPLEX
4ki6:A (PRO35) to (ASP51) TERNARY COMPLEX OF RB69 MUTANT L415F WITH RIBONUCLEOTIDES AT -1 AND -2 POSITION | RIBONUCLEOTIDE, TRANSFERASE-DNA COMPLEX
2vgg:C (GLU241) to (SER248) HUMAN ERYTHROCYTE PYRUVATE KINASE: R479H MUTANT | METAL-BINDING, PHOSPHORYLATION, PYRUVATE KINASE IN THE ACTIVE R-STATE, KINASE, PYRUVATE, MAGNESIUM, GLYCOLYSIS, TRANSFERASE, DISEASE MUTATION
1rzo:B (LEU2048) to (ASP2094) AGGLUTININ FROM RICINUS COMMUNIS WITH GALACTOAZA | RIBOSOME-INACTIVATING PROTEIN, IMMUNOTOXIN, AGGLUTININ RICIN, HYDROLASE
2vhe:A (SER82) to (GLU92) PGLD-COA COMPLEX: AN ACETYL TRANSFERASE FROM CAMPYLOBACTER JEJUNI | COENZYME A, TRANSFERASE, N-ACETYL TRANSFERASE
3ut0:C (ILE800) to (LEU809) CRYSTAL STRUCTURE OF EXO-1,3/1,4-BETA-GLUCANASE (EXOP) FROM PSEUDOALTEROMONAS SP. BB1 | (ALPHA/BETA)8 BARREL, (ALPHA/BETA)6 SHEET, BETA-SANDWICH, HYDROLASE
4z6a:H (GLN30) to (VAL53) CRYSTAL STRUCTURE OF A FVIIA-TRYPSIN CHIMERA (YT) IN COMPLEX WITH SOLUBLE TISSUE FACTOR | TRYPSIN-FOLD, PROTEIN-PROTEIN COMPLEX, HYDROLASE
4z7k:A (ASP110) to (LEU124) CRYSTAL STRUCTURE OF CRISPR RNA PROCESSING ENDORIBONUCLEASE CAS6B | CAS6, ENDORIBONUCLEASE, CRISPR RNA, HYDROLASE-RNA-DNA COMPLEX
2flb:H (GLN30) to (VAL53) DISCOVERY OF A NOVEL HYDROXY PYRAZOLE BASED FACTOR IXA INHIBITOR | ACTIVE SITE-DIRECTED, SHORT HYDROGEN BOND-MEDIATED, PYRAZOLE-BASED INHIBITOR, HYDROLASE/BLOOD CLOTTING COMPLEX
2fnt:B (ASP30) to (GLY48) CRYSTAL STRUCTURE OF A DRUG-RESISTANT (V82A) INACTIVE (D25N) HIV-1 PROTEASE COMPLEXED WITH AP2V VARIANT OF HIV-1 NC-P1 SUBSTRATE. | STRUCTURAL INTERMEDIATE, SUBSTRATE RECOGNITION, HIV-1 PROTEASE, NC-P1 SUBSTRATE, DRUG RESISTANCE, FLAP CONFORMATION, HYDROLASE
4za0:B (TRP365) to (GLU377) STRUCTURE OF HUMAN ENOLASE 2 IN COMPLEX WITH PHOSPHONOACETOHYDROXAMATE | ENOLASE GAMMA, GLYCOLYSIS, NEURON SPECIFIC ENOLASE, CARBOHYDRATE METABOLISM, LYASE-LYASE INHIBITOR COMPLEX
3hso:A (GLY325) to (GLY333) TERNARY STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE WITH NHA AND NO BOUND(1) | NITRIC OXIDE SYNTHASE HEME ENZYME DIATOMIC LIGAND, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL- BINDING, NADP, OXIDOREDUCTASE
3hso:B (GLY325) to (GLY333) TERNARY STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE WITH NHA AND NO BOUND(1) | NITRIC OXIDE SYNTHASE HEME ENZYME DIATOMIC LIGAND, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL- BINDING, NADP, OXIDOREDUCTASE
3hsn:A (GLY325) to (GLY333) TERNARY STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE WITH NHA AND CO BOUND | NITRIC OXIDE SYNTHASE,HEME ENZYME, DIATOMIC LIGAND, CALMODULIN- BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3hsn:B (GLY325) to (GLY333) TERNARY STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE WITH NHA AND CO BOUND | NITRIC OXIDE SYNTHASE,HEME ENZYME, DIATOMIC LIGAND, CALMODULIN- BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
2fsd:A (ASN96) to (ALA110) A COMMON FOLD FOR THE RECEPTOR BINDING DOMAINS OF LACTOCOCCAL PHAGES? THE CRYSTAL STRUCTURE OF THE HEAD DOMAIN OF PHAGE BIL170 | PHAGE, LACTOCOCCUS LACTIS, RECEPTOR BINDING PROTEIN, HEAD DOMAIN, VIRAL PROTEIN
2fsd:B (ASN96) to (ALA110) A COMMON FOLD FOR THE RECEPTOR BINDING DOMAINS OF LACTOCOCCAL PHAGES? THE CRYSTAL STRUCTURE OF THE HEAD DOMAIN OF PHAGE BIL170 | PHAGE, LACTOCOCCUS LACTIS, RECEPTOR BINDING PROTEIN, HEAD DOMAIN, VIRAL PROTEIN
3hwf:C (GLY29) to (GLY38) CRYSTAL STRUCTURE OF SIDEROCALIN (NGAL, LIPOCALIN 2) COMPLEXED WITH FE-TRENCAM2-HOPO | LIPOCALIN, SIDEROPHORE, BETA-BARREL, DISULFIDE BOND, GLYCOPROTEIN, PYRROLIDONE CARBOXYLIC ACID, SECRETED, TRANSPORT PROTEIN
3hwg:B (GLY29) to (GLY38) CRYSTAL STRUCTURE OF SIDEROCALIN (NGAL, LIPOCALIN 2) COMPLEXED WITH FE-TRENCAM-HOPO2 | LIPOCALIN, SIDEROPHORE, BETA-BARREL, DISULFIDE BOND, GLYCOPROTEIN, PYRROLIDONE CARBOXYLIC ACID, SECRETED, TRANSPORT PROTEIN
3hwg:C (GLY29) to (GLY38) CRYSTAL STRUCTURE OF SIDEROCALIN (NGAL, LIPOCALIN 2) COMPLEXED WITH FE-TRENCAM-HOPO2 | LIPOCALIN, SIDEROPHORE, BETA-BARREL, DISULFIDE BOND, GLYCOPROTEIN, PYRROLIDONE CARBOXYLIC ACID, SECRETED, TRANSPORT PROTEIN
3v44:A (THR200) to (THR232) CRYSTAL STRUCTURE OF THE N-TERMINAL FRAGMENT OF ZEBRAFISH TLR5 | FLAGELLIN, INNATE IMMUNITY, LEUCINE-RICH REPEAT, INNATE IMMUNE RECEPTOR, IMMUNE SYSTEM
3v47:A (THR200) to (THR232) CRYSTAL STRUCTURE OF THE N-TETMINAL FRAGMENT OF ZEBRAFISH TLR5 IN COMPLEX WITH SALMONELLA FLAGELLIN | INNATE IMMUNITY, LEUCINE-RICH REPEAT, INNATE IMMUNE RECEPTOR, IMMUNE SYSTEM
3v47:B (THR200) to (THR232) CRYSTAL STRUCTURE OF THE N-TETMINAL FRAGMENT OF ZEBRAFISH TLR5 IN COMPLEX WITH SALMONELLA FLAGELLIN | INNATE IMMUNITY, LEUCINE-RICH REPEAT, INNATE IMMUNE RECEPTOR, IMMUNE SYSTEM
1sd1:A (GLY105) to (MET119) STRUCTURE OF HUMAN 5'-DEOXY-5'-METHYLTHIOADENOSINE PHOSPHORYLASE COMPLEXED WITH FORMYCIN A | METHYLTHIOADENOSINE PHOSPHORYLASE, PURINE NUCLEOSIDE PHOSPHORYLASE, PURINE SALVAGE,FORMYCIN A, TRANSFERASE
3v4p:B (GLN83) to (PRO91) CRYSTAL STRUCTURE OF A4B7 HEADPIECE COMPLEXED WITH FAB ACT-1 | CELL ADHESION, MADCAM-1, MEMBRANE
3v4p:D (GLN83) to (PRO91) CRYSTAL STRUCTURE OF A4B7 HEADPIECE COMPLEXED WITH FAB ACT-1 | CELL ADHESION, MADCAM-1, MEMBRANE
2vle:A (ARG329) to (PRO343) THE STRUCTURE OF DAIDZIN, A NATURALLY OCCURRING ANTI ALCOHOL-ADDICTION AGENT, IN COMPLEX WITH HUMAN MITOCHONDRIAL ALDEHYDE DEHYDROGENASE | TRANSIT PEPTIDE, ALDEHYDE DEHYDROGENASE, NAD, DAIDZIN, ACETYLATION, POLYMORPHISM, MITOCHONDRION, ALCOHOL ABUSE, OXIDOREDUCTASE
2vle:B (ARG329) to (PRO343) THE STRUCTURE OF DAIDZIN, A NATURALLY OCCURRING ANTI ALCOHOL-ADDICTION AGENT, IN COMPLEX WITH HUMAN MITOCHONDRIAL ALDEHYDE DEHYDROGENASE | TRANSIT PEPTIDE, ALDEHYDE DEHYDROGENASE, NAD, DAIDZIN, ACETYLATION, POLYMORPHISM, MITOCHONDRION, ALCOHOL ABUSE, OXIDOREDUCTASE
2vle:C (ARG329) to (PRO343) THE STRUCTURE OF DAIDZIN, A NATURALLY OCCURRING ANTI ALCOHOL-ADDICTION AGENT, IN COMPLEX WITH HUMAN MITOCHONDRIAL ALDEHYDE DEHYDROGENASE | TRANSIT PEPTIDE, ALDEHYDE DEHYDROGENASE, NAD, DAIDZIN, ACETYLATION, POLYMORPHISM, MITOCHONDRION, ALCOHOL ABUSE, OXIDOREDUCTASE
2vle:E (ARG329) to (PRO343) THE STRUCTURE OF DAIDZIN, A NATURALLY OCCURRING ANTI ALCOHOL-ADDICTION AGENT, IN COMPLEX WITH HUMAN MITOCHONDRIAL ALDEHYDE DEHYDROGENASE | TRANSIT PEPTIDE, ALDEHYDE DEHYDROGENASE, NAD, DAIDZIN, ACETYLATION, POLYMORPHISM, MITOCHONDRION, ALCOHOL ABUSE, OXIDOREDUCTASE
2vle:F (ARG329) to (PRO343) THE STRUCTURE OF DAIDZIN, A NATURALLY OCCURRING ANTI ALCOHOL-ADDICTION AGENT, IN COMPLEX WITH HUMAN MITOCHONDRIAL ALDEHYDE DEHYDROGENASE | TRANSIT PEPTIDE, ALDEHYDE DEHYDROGENASE, NAD, DAIDZIN, ACETYLATION, POLYMORPHISM, MITOCHONDRION, ALCOHOL ABUSE, OXIDOREDUCTASE
2vle:G (ARG329) to (PRO343) THE STRUCTURE OF DAIDZIN, A NATURALLY OCCURRING ANTI ALCOHOL-ADDICTION AGENT, IN COMPLEX WITH HUMAN MITOCHONDRIAL ALDEHYDE DEHYDROGENASE | TRANSIT PEPTIDE, ALDEHYDE DEHYDROGENASE, NAD, DAIDZIN, ACETYLATION, POLYMORPHISM, MITOCHONDRION, ALCOHOL ABUSE, OXIDOREDUCTASE
2vle:H (ARG329) to (PRO343) THE STRUCTURE OF DAIDZIN, A NATURALLY OCCURRING ANTI ALCOHOL-ADDICTION AGENT, IN COMPLEX WITH HUMAN MITOCHONDRIAL ALDEHYDE DEHYDROGENASE | TRANSIT PEPTIDE, ALDEHYDE DEHYDROGENASE, NAD, DAIDZIN, ACETYLATION, POLYMORPHISM, MITOCHONDRION, ALCOHOL ABUSE, OXIDOREDUCTASE
4kp8:A (PRO100) to (SER108) CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH 3-[(PYRIMIDIN-2-YLSULFANYL)ACETYL]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4kp8:B (PRO100) to (SER108) CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH 3-[(PYRIMIDIN-2-YLSULFANYL)ACETYL]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4kp8:C (PRO100) to (SER108) CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH 3-[(PYRIMIDIN-2-YLSULFANYL)ACETYL]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4kp8:D (PRO100) to (SER108) CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH 3-[(PYRIMIDIN-2-YLSULFANYL)ACETYL]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4zfx:B (GLY29) to (GLY38) SIDEROCALIN-MEDIATED RECOGNITION AND CELLULAR UPTAKE OF ACTINIDES | METAL BINDING PROTEIN-INHIBITOR COMPLEX
2fxd:A (ASP30) to (ILE50) X-RAY CRYSTAL STRUCTURE OF HIV-1 PROTEASE IRM MUTANT COMPLEXED WITH ATAZANAVIR (BMS-232632) | HUMAN IMMUNODEFICIENCY VIRUS (HIV), HIV-1 PROTEASE, REYATAZ, ATAZANAVIR, BMS-232632, HYDROLASE
2fym:A (TYR363) to (GLU375) CRYSTAL STRUCTURE OF E. COLI ENOLASE COMPLEXED WITH THE MINIMAL BINDING SEGMENT OF RNASE E. | RNA DEGRADOSOME, ENOLASE, RNASE E, LYASE
2fym:D (TYR363) to (GLU375) CRYSTAL STRUCTURE OF E. COLI ENOLASE COMPLEXED WITH THE MINIMAL BINDING SEGMENT OF RNASE E. | RNA DEGRADOSOME, ENOLASE, RNASE E, LYASE
2vn9:A (GLU13) to (ALA24) CRYSTAL STRUCTURE OF HUMAN CALCIUM CALMODULIN DEPENDENT PROTEIN KINASE II DELTA ISOFORM 1, CAMKD | SERINE/THREONINE-PROTEIN KINASE, SERINE-THREONINE KINASE, CELLULAR DIFFERENTIATION, VASCULAR SMOOTH MUSCLE, KINASE, TRANSFERASE, ATP-BINDING, PHOSPHOPROTEIN, CALMODULIN-BINDING, NUCLEOTIDE-BINDING
2vn9:B (GLU13) to (ALA24) CRYSTAL STRUCTURE OF HUMAN CALCIUM CALMODULIN DEPENDENT PROTEIN KINASE II DELTA ISOFORM 1, CAMKD | SERINE/THREONINE-PROTEIN KINASE, SERINE-THREONINE KINASE, CELLULAR DIFFERENTIATION, VASCULAR SMOOTH MUSCLE, KINASE, TRANSFERASE, ATP-BINDING, PHOSPHOPROTEIN, CALMODULIN-BINDING, NUCLEOTIDE-BINDING
3i0a:B (GLY29) to (GLY38) CRYSTAL STRUCTURE OF SIDEROCALIN (NGAL, LIPOCALIN 2) K134A MUTANT COMPLEXED WITH FERRIC ENTEROBACTIN | NGAL, P25, 25 KDA ALPHA-2-MICROGLOBULIN-RELATED SUBUNIT OF MMP-9, LIPOCALIN-2, ONCOGENE 24P3, DISULFIDE BOND, GLYCOPROTEIN, PYRROLIDONE CARBOXYLIC ACID, SECRETED, ANTIMICROBIAL PROTEIN
3i0a:C (GLY29) to (GLY38) CRYSTAL STRUCTURE OF SIDEROCALIN (NGAL, LIPOCALIN 2) K134A MUTANT COMPLEXED WITH FERRIC ENTEROBACTIN | NGAL, P25, 25 KDA ALPHA-2-MICROGLOBULIN-RELATED SUBUNIT OF MMP-9, LIPOCALIN-2, ONCOGENE 24P3, DISULFIDE BOND, GLYCOPROTEIN, PYRROLIDONE CARBOXYLIC ACID, SECRETED, ANTIMICROBIAL PROTEIN
4kr5:A (PHE337) to (LEU348) CRYSTAL STRUCTURE OF LACTOCOCCUS LACTIS GLNP SUBSTRATE BINDING DOMAIN 2 (SBD2) IN OPEN CONFORMATION | GLUTAMINE/GLUTAMIC ACID BINDING, AMINO ACID TRANSPORT, TRANSPORT PROTEIN, EXTRACELLULAR
4krc:A (GLN6) to (THR17) CRYSTAL STRUCTURE OF PHO85-PCL10-ATP-GAMMA-S COMPLEX | GLYCOGEN SYNTHESIS, GLYCOGEN SYNTHESIS REGULATION, TRANSFERASE- SIGNALING PROTEIN COMPLEX
3i29:A (GLN30) to (VAL53) CRYSTAL STRUCTURE OF A BINARY COMPLEX BETWEEN AN MUTANT TRYPSIN INHIBITOR WITH BOVINE TRYPSIN | P1 AND P2 MUTANT, TRYPSIN INHIBITOR, BOVINE TRYPSIN, COMPLEX, DIGESTION, HYDROLASE, METAL-BINDING, PROTEASE, SECRETED, SERINE PROTEASE, ZYMOGEN, PROTEASE INHIBITOR, SERINE PROTEASE INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, DISULFIDE BOND
2vr3:A (ASP481) to (ASN498) STRUCTURAL AND BIOCHEMICAL CHARACTERIZATION OF FIBRINOGEN BINDING TO CLFA FROM STAPHYLOCCCUS AUREUS | PLATELET AGGREGATION, PEPTIDOGLYCAN-ANCHOR, CELL ADHESION, STAPHYLOCOCCUS AUREUS, FIBRINOGEN GAMMA-CHAIN, SECRETED, CELL WALL, VIRULENCE, CLUMPING FACTOR
2vr3:B (ASP481) to (ASN498) STRUCTURAL AND BIOCHEMICAL CHARACTERIZATION OF FIBRINOGEN BINDING TO CLFA FROM STAPHYLOCCCUS AUREUS | PLATELET AGGREGATION, PEPTIDOGLYCAN-ANCHOR, CELL ADHESION, STAPHYLOCOCCUS AUREUS, FIBRINOGEN GAMMA-CHAIN, SECRETED, CELL WALL, VIRULENCE, CLUMPING FACTOR
4zhc:B (GLY29) to (GLY38) SIDEROCALIN-MEDIATED RECOGNITION AND CELLULAR UPTAKE OF ACTINIDES | METAL BINDING PROTEIN-INHIBITOR COMPLEX
4zhc:C (GLY29) to (GLY38) SIDEROCALIN-MEDIATED RECOGNITION AND CELLULAR UPTAKE OF ACTINIDES | METAL BINDING PROTEIN-INHIBITOR COMPLEX
4zhd:A (GLY29) to (GLY38) SIDEROCALIN-MEDIATED RECOGNITION AND CELLULAR UPTAKE OF ACTINIDES | METAL BINDING PROTEIN-INHIBITOR COMPLEX
4zhd:B (GLY29) to (GLY38) SIDEROCALIN-MEDIATED RECOGNITION AND CELLULAR UPTAKE OF ACTINIDES | METAL BINDING PROTEIN-INHIBITOR COMPLEX
4zhd:C (GLY29) to (GLY38) SIDEROCALIN-MEDIATED RECOGNITION AND CELLULAR UPTAKE OF ACTINIDES | METAL BINDING PROTEIN-INHIBITOR COMPLEX
4zhf:B (GLY29) to (GLY38) SIDEROCALIN-MEDIATED RECOGNITION AND CELLULAR UPTAKE OF ACTINIDES | METAL BINDING PROTEIN-INHIBITOR COMPLEX
4zhf:C (GLY29) to (GLY38) SIDEROCALIN-MEDIATED RECOGNITION AND CELLULAR UPTAKE OF ACTINIDES | METAL BINDING PROTEIN-INHIBITOR COMPLEX
4zhg:A (GLY29) to (GLY38) SIDEROCALIN-MEDIATED RECOGNITION AND CELLULAR UPTAKE OF ACTINIDES | METAL BINDING PROTEIN-INHIBITOR COMPLEX
4zhg:B (GLY29) to (GLY38) SIDEROCALIN-MEDIATED RECOGNITION AND CELLULAR UPTAKE OF ACTINIDES | METAL BINDING PROTEIN-INHIBITOR COMPLEX
4zhg:C (GLY29) to (GLY38) SIDEROCALIN-MEDIATED RECOGNITION AND CELLULAR UPTAKE OF ACTINIDES | METAL BINDING PROTEIN-INHIBITOR COMPLEX
4zhg:D (GLY29) to (GLY38) SIDEROCALIN-MEDIATED RECOGNITION AND CELLULAR UPTAKE OF ACTINIDES | METAL BINDING PROTEIN-INHIBITOR COMPLEX
1gsl:A (ASN2) to (LEU25) LECTIN (FOURTH ISOLATED FROM (GRIFFONIA SIMPLICIFOLIA)) COMPLEX WITH Y HUMAN BLOOD GROUP DETERMINANT | GLYCOPROTEIN, LECTIN, MANGANESE
2vt0:A (LEU383) to (PRO401) X-RAY STRUCTURE OF A CONJUGATE WITH CONDURITOL-BETA-EPOXIDE OF ACID-BETA-GLUCOSIDASE OVEREXPRESSED IN CULTURED PLANT CELLS | HYDROLASE, ALTERNATIVE INITIATION, SPHINGOLIPID METABOLISM, ISRAEL STRUCTURAL PROTEOMICS CENTER, DISEASE MUTATION, GLUCOCEREBROSIDASE, PHARMACEUTICAL, GAUCHER DISEASE, LIPID METABOLISM, GLUCOSIDASE, GLYCOSIDASE, POLYMORPHISM, GLYCOPROTEIN, ISPC, MEMBRANE, CEREZYME, LYSOSOME, STRUCTURAL GENOMICS, ALTERNATIVE SPLICING
2vt0:B (LEU383) to (PRO401) X-RAY STRUCTURE OF A CONJUGATE WITH CONDURITOL-BETA-EPOXIDE OF ACID-BETA-GLUCOSIDASE OVEREXPRESSED IN CULTURED PLANT CELLS | HYDROLASE, ALTERNATIVE INITIATION, SPHINGOLIPID METABOLISM, ISRAEL STRUCTURAL PROTEOMICS CENTER, DISEASE MUTATION, GLUCOCEREBROSIDASE, PHARMACEUTICAL, GAUCHER DISEASE, LIPID METABOLISM, GLUCOSIDASE, GLYCOSIDASE, POLYMORPHISM, GLYCOPROTEIN, ISPC, MEMBRANE, CEREZYME, LYSOSOME, STRUCTURAL GENOMICS, ALTERNATIVE SPLICING
3vd2:A (THR119) to (PHE131) STRUCTURE OF P73 DNA BINDING DOMAIN TETRAMER MODULATES P73 TRANSACTIVATION | PROTEIN DNA COMPLEX, BETA-IMMUNOGLOBULIN-LIKE FOLD, TUMOUR SUPPRESSOR, DNA, ANTITUMOR PROTEIN-DNA COMPLEX
2g6h:A (GLY325) to (GLY333) STRUCTURE OF RAT NNOS HEME DOMAIN (BH4 BOUND) IN THE REDUCED FORM | NITRIC OXIDE SYNTHASE, HEME PROTEIN, DIATOMIC LIGAND, OXIDOREDUCTASE
2g6h:B (GLY325) to (GLY333) STRUCTURE OF RAT NNOS HEME DOMAIN (BH4 BOUND) IN THE REDUCED FORM | NITRIC OXIDE SYNTHASE, HEME PROTEIN, DIATOMIC LIGAND, OXIDOREDUCTASE
2g6i:B (GLY325) to (GLY333) STRUCTURE OF RAT NNOS HEME DOMAIN (BH2-BOUND) IN THE REDUCED FORM | NITRIC OXIDE SYNTHASE, HEME PROTEIN, DIATOMIC LIGAND, OXIDOREDUCTASE
2g6j:A (GLY325) to (GLY333) STRUCTURE OF RAT NNOS (L337N) HEME DOMAIN (4-AMINOBIOPTERIN BOUND) COMPLEXED WITH NO | NITRIC OXIDE SYNTHASE, HEME PROTEIN, DIATOMIC LIGAND, OXIDOREDUCTASE
2g6j:B (GLY325) to (GLY333) STRUCTURE OF RAT NNOS (L337N) HEME DOMAIN (4-AMINOBIOPTERIN BOUND) COMPLEXED WITH NO | NITRIC OXIDE SYNTHASE, HEME PROTEIN, DIATOMIC LIGAND, OXIDOREDUCTASE
2g6k:A (GLY325) to (GLY333) STRUCTURE OF RAT NNOS HEME DOMAIN (BH4 BOUND) COMPLEXED WITH NO | NITRIC OXIDE SYNTHASE, HEME PROTEIN, DIATOMIC LIGAND, OXIDOREDUCTASE
2g6k:B (GLY325) to (GLY333) STRUCTURE OF RAT NNOS HEME DOMAIN (BH4 BOUND) COMPLEXED WITH NO | NITRIC OXIDE SYNTHASE, HEME PROTEIN, DIATOMIC LIGAND, OXIDOREDUCTASE
2g6l:B (GLY325) to (GLY333) STRUCTURE OF RAT NNOS HEME DOMAIN (BH2 BOUND) COMPLEXED WITH NO | NITRIC OXIDE SYNTHASE, HEME PROTEIN, DIATOMIC LIGAND, OXIDOREDUCTASE
4zim:A (HIS848) to (ASN859) CRYSTAL STRUCTURE OF JANUS KINASE 2 IN COMPLEX WITH A 9H-CARBAZOLE-1- CARBOXAMIDE INHIBITOR | KINASE, TRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
2g6m:A (GLY325) to (GLY333) STRUCTURE OF RAT NNOS HEME DOMAIN (BH4 BOUND) COMPLEXED WITH CO | NITRIC OXIDE SYNTHASE, HEME PROTEIN, DIATOMIC LIGAND, OXIDOREDUCTASE
2g6m:B (GLY325) to (GLY333) STRUCTURE OF RAT NNOS HEME DOMAIN (BH4 BOUND) COMPLEXED WITH CO | NITRIC OXIDE SYNTHASE, HEME PROTEIN, DIATOMIC LIGAND, OXIDOREDUCTASE
2g6n:B (GLY325) to (GLY333) STRCTURE OF RAT NNOS HEME DOMAIN (BH2 BOUND) COMPLEXED WITH CO | NITRIC OXIDE SYNTHASE, HEME PROTEIN, DIATOMIC LIGAND, OXIDOREDUCTASE
2g6o:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENOS HEME DOMAIN (BH4-FREE) COMPLEXED WITH CO | NITRIC OXIDE SYNTHASE, HEME PROTEIN, DIATOMIC LIGAND, OXIDOREDUCTASE
4kwf:F (ARG329) to (PRO343) CRYSTAL STRUCTURE ANALYSIS OF ALDH2+ALDIB33 | ALDH2+ALDIB33, KETONE BINDING, OXIDOREDUCTASE-INHIBITOR COMPLEX
4kwg:C (ARG329) to (PRO343) CRYSTAL STRUCTURE ANALYSIS OF ALDH2+ALDIB13 | ALDH2+B13, KETONE BINDING, OXIDOREDUCTASE-INHIBITOR COMPLEX
1suv:A (ALA226) to (ASN236) STRUCTURE OF HUMAN TRANSFERRIN RECEPTOR-TRANSFERRIN COMPLEX | PROTEIN COMPLEX, METAL TRANSPORT
1suv:B (ALA226) to (ASN236) STRUCTURE OF HUMAN TRANSFERRIN RECEPTOR-TRANSFERRIN COMPLEX | PROTEIN COMPLEX, METAL TRANSPORT
1sxi:D (PRO141) to (SER150) STRUCTURE OF APO TRANSCRIPTION REGULATOR B. MEGATERIUM | ALLOSTERISM; PHOSPHOPROTEIN; TRANSCRIPTION REGULATION; GRAM POSITIVE BACTERIA; CCR
2vz8:A (THR1052) to (ASP1060) CRYSTAL STRUCTURE OF MAMMALIAN FATTY ACID SYNTHASE | TRANSFERASE, PHOSPHOPANTETHEINE, FATTY ACID SYNTHASE, MULTIENZYME, MEGASYNTHASE, FATTY ACID SYNTHESIS
2vz8:B (THR1052) to (ASP1060) CRYSTAL STRUCTURE OF MAMMALIAN FATTY ACID SYNTHASE | TRANSFERASE, PHOSPHOPANTETHEINE, FATTY ACID SYNTHASE, MULTIENZYME, MEGASYNTHASE, FATTY ACID SYNTHESIS
2gjx:A (ASN29) to (TYR40) CRYSTALLOGRAPHIC STRUCTURE OF HUMAN BETA-HEXOSAMINIDASE A | BETA-HEXOSAMINIDASE A, GLYCOSIDASE, TAY-SACHS DISEASE, GM2 GANGLISODE, TIM BARREL, HYDROLASE
2gjx:B (LEU61) to (ALA73) CRYSTALLOGRAPHIC STRUCTURE OF HUMAN BETA-HEXOSAMINIDASE A | BETA-HEXOSAMINIDASE A, GLYCOSIDASE, TAY-SACHS DISEASE, GM2 GANGLISODE, TIM BARREL, HYDROLASE
2gk1:A (ASN29) to (TYR40) X-RAY CRYSTAL STRUCTURE OF NGT-BOUND HEXA | BETA-HEXOASAMINIDASE A, GLYCOSIDASE, TAY-SACHS DISEASE, SANDHOFF DISEASE, NAG-THAZOLINE, GM2 GANGLIODOSIS, HYDROLASE
2gk1:C (ASN29) to (TYR40) X-RAY CRYSTAL STRUCTURE OF NGT-BOUND HEXA | BETA-HEXOASAMINIDASE A, GLYCOSIDASE, TAY-SACHS DISEASE, SANDHOFF DISEASE, NAG-THAZOLINE, GM2 GANGLIODOSIS, HYDROLASE
2gk1:D (SER62) to (ALA73) X-RAY CRYSTAL STRUCTURE OF NGT-BOUND HEXA | BETA-HEXOASAMINIDASE A, GLYCOSIDASE, TAY-SACHS DISEASE, SANDHOFF DISEASE, NAG-THAZOLINE, GM2 GANGLIODOSIS, HYDROLASE
2gk1:F (SER62) to (ALA73) X-RAY CRYSTAL STRUCTURE OF NGT-BOUND HEXA | BETA-HEXOASAMINIDASE A, GLYCOSIDASE, TAY-SACHS DISEASE, SANDHOFF DISEASE, NAG-THAZOLINE, GM2 GANGLIODOSIS, HYDROLASE
4l5c:A (GLY99) to (GLY113) METHYLTHIOADENOSINE PHOSPHORYLASE FROM SCHISTOSOMA MANSONI IN COMPLEX WITH ADENINE IN SPACE GROUP P212121 | TRANSFERASE, PHSOPHORYLASE, NUCLEOSIDE PHOSPHORYLASE, ENZYME
4l5t:C (GLY254) to (VAL262) CRYSTAL STRUCTURE OF THE TETRAMERIC P202 HIN2 | HIN200; OB-FOLD, TETRAMERIZATION, DNA BINDING PROTEIN, IMMUNE SYSTEM
4l5t:D (GLY254) to (VAL262) CRYSTAL STRUCTURE OF THE TETRAMERIC P202 HIN2 | HIN200; OB-FOLD, TETRAMERIZATION, DNA BINDING PROTEIN, IMMUNE SYSTEM
2gmu:A (ASN3) to (TRP11) CRYSTAL STRUCTURE OF E COLI GDP-4-KETO-6-DEOXY-D-MANNOSE-3- DEHYDRATASE COMPLEXED WITH PLP-GLUTAMATE KETIMINE INTERMEDIATE | COLITOSE, DEOXYSUGAR, ASPARTATE AMINOTRANSFERASE, PLP, O- ANTIGEN
1h4w:A (GLN30) to (VAL53) STRUCTURE OF HUMAN TRYPSIN IV (BRAIN TRYPSIN) | SERINE PROTEASE, SIGNAL TRANSDUCTION, INHIBITOR RESISTANCE, ALZHEIMER DISEASE, HYDROLASE
2w3r:B (ARG222) to (GLY229) CRYSTAL STRUCTURE OF XANTHINE DEHYDROGENASE (DESULFO FORM) FROM RHODOBACTER CAPSULATUS IN COMPLEX WITH HYPOXANTHINE | XDH, GOUT, IRON, XANTHINE, IRON-SULFUR, MOLYBDENUM COFACTOR, HYPOXANTHINE, METAL-BINDING, OXIDOREDUCTASE
2w3r:D (ARG222) to (GLY229) CRYSTAL STRUCTURE OF XANTHINE DEHYDROGENASE (DESULFO FORM) FROM RHODOBACTER CAPSULATUS IN COMPLEX WITH HYPOXANTHINE | XDH, GOUT, IRON, XANTHINE, IRON-SULFUR, MOLYBDENUM COFACTOR, HYPOXANTHINE, METAL-BINDING, OXIDOREDUCTASE
1t90:A (TYR362) to (THR374) CRYSTAL STRUCTURE OF METHYLMALONATE SEMIALDEHYDE DEHYDROGENASE FROM BACILLUS SUBTILIS | OXIDOREDUCTASE, NAD
2gs7:A (LEU679) to (LYS692) CRYSTAL STRUCTURE OF THE INACTIVE EGFR KINASE DOMAIN IN COMPLEX WITH AMP-PNP | EGFR, KINASE, INACTIVE, AMP-PNP, TRANSFERASE
4lc3:A (PRO7) to (ILE16) X-RAY CRYSTAL STRUCTURE OF A PUTATIVE UDP-4-AMINO-4-DEOXY-L-ARABINOSE- -OXOGLUTARATE AMINOTRANSFERASE FROM BURKHOLDERIA CENOCEPACIA | STRUCTURAL GENOMICS, NIAID, NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, SSGCID, TRANSFERASE
4lc3:B (PRO7) to (ILE16) X-RAY CRYSTAL STRUCTURE OF A PUTATIVE UDP-4-AMINO-4-DEOXY-L-ARABINOSE- -OXOGLUTARATE AMINOTRANSFERASE FROM BURKHOLDERIA CENOCEPACIA | STRUCTURAL GENOMICS, NIAID, NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, SSGCID, TRANSFERASE
1tab:E (GLN30) to (SER54) STRUCTURE OF THE TRYPSIN-BINDING DOMAIN OF BOWMAN-BIRK TYPE PROTEASE INHIBITOR AND ITS INTERACTION WITH TRYPSIN | HYDROLASE (SERINE PROTEINASE)
4zse:A (LEU703) to (LYS716) CRYSTAL STRUCTURE OF EGFR 696-1022 T790M/V948R, CRYSTAL FORM II | EGFR, T790M, V948R, TRANSFERASE
4lcq:A (GLY5) to (GLU17) THE CRYSTAL STRUCTURE OF DI-ZN DIHYDROPYRIMIDINASE IN COMPLEX WITH NCBI | HYDROLASE, ZINC BINDING, CARBOXYLATION, ALPHA-BETA BARREL, HYDROLASE ACTIVATOR
2w55:H (ARG222) to (GLY229) CRYSTAL STRUCTURE OF XANTHINE DEHYDROGENASE (E232Q VARIANT) FROM RHODOBACTER CAPSULATUS IN COMPLEX WITH HYPOXANTHINE | XDH, GOUT, IRON, XANTHINE, IRON-SULFUR, MOLYBDENUM COFACTOR, HYPOXANTHINE, METAL-BINDING, OXIDOREDUCTASE
4ldb:C (GLN170) to (PRO185) CRYSTAL STRUCTURE OF EBOLA VIRUS VP40 DIMER | VIRAL MATRIX PROTEIN, VIRAL BUDDING, ASSEMBLY, VIRAL TRANSCRIPTION REGULATION, VIRAL PROTEIN
4ldb:D (GLN170) to (PRO185) CRYSTAL STRUCTURE OF EBOLA VIRUS VP40 DIMER | VIRAL MATRIX PROTEIN, VIRAL BUDDING, ASSEMBLY, VIRAL TRANSCRIPTION REGULATION, VIRAL PROTEIN
1tei:A (SER164) to (PHE175) STRUCTURE OF CONCANAVALIN A COMPLEXED TO BETA-D-GLCNAC (1,2)ALPHA-D- MAN-(1,6)[BETA-D-GLCNAC(1,2)ALPHA-D-MAN (1,6)]ALPHA-D-MAN | LECTIN, CONCANAVALIN A, PENTASACCHARIDE BINDING, RECOGNITION COMPLEX
1tei:F (SER164) to (PHE175) STRUCTURE OF CONCANAVALIN A COMPLEXED TO BETA-D-GLCNAC (1,2)ALPHA-D- MAN-(1,6)[BETA-D-GLCNAC(1,2)ALPHA-D-MAN (1,6)]ALPHA-D-MAN | LECTIN, CONCANAVALIN A, PENTASACCHARIDE BINDING, RECOGNITION COMPLEX
3inj:A (ARG329) to (PRO343) HUMAN MITOCHONDRIAL ALDEHYDE DEHYDROGENASE COMPLEXED WITH AGONIST ALDA-1 | OXIDOREDUCTASE, ALDH, E487K, ROSSMANN FOLD, ALDA-1, ACTIVATOR, MITOCHONDRION, NAD, TRANSIT PEPTIDE
4zuk:E (ILE329) to (PRO343) STRUCTURE ALDH7A1 COMPLEXED WITH NAD+ | ALDEHYDE DEHYDROGENASE, NAD, OXIDOREDUCTASE, LYSINE CATABOLISM
4zvw:E (ILE329) to (PRO343) STRUCTURE OF APO HUMAN ALDH7A1 IN SPACE GROUP C2 | ALDEHYDE DEHYDROGENASE, NAD, OXIDOREDUCTASE, LYSINE CATABOLISM
4zvw:H (ILE329) to (PRO343) STRUCTURE OF APO HUMAN ALDH7A1 IN SPACE GROUP C2 | ALDEHYDE DEHYDROGENASE, NAD, OXIDOREDUCTASE, LYSINE CATABOLISM
4zvx:A (ILE329) to (PRO343) STRUCTURE OF APO HUMAN ALDH7A1 IN SPACE GROUP P4212 | ALDEHYDE DEHYDROGENASE, NAD, OXIDOREDUCTASE, LYSINE CATABOLISM
2h6c:A (ILE33) to (PRO46) CRYSTAL STRUCTURE OF REDUCED CPRK IN ABSENCE OF ANY LIGAND | DNA BINDING, HELIX-TURN-HELIX, CHLOROPHENOL, HALORESPIRATION, CPRK, DNA BINDING PROTEIN
4zwv:B (ALA0) to (VAL9) CRYSTAL STRUCTURE OF AMINOTRANSFERASE ATMS13 FROM ACTINOMADURA MELLIAURA | AMINOTRANSFERASE, STRUCTURAL GENOMICS, PSI-BIOLOGY, PROTEIN STRUCTURE INITIATIVE, ENZYME DISCOVERY FOR NATURAL PRODUCT BIOSYNTHESIS, NATPRO, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, TRANSFERASE
1hm9:B (GLY423) to (ALA432) CRYSTAL STRUCTURE OF S.PNEUMONIAE N-ACETYLGLUCOSAMINE-1-PHOSPHATE URIDYLTRANSFERASE, GLMU, BOUND TO ACETYL COENZYME A AND UDP-N- ACETYLGLUCOSAMINE | ACETYLTRANSFERASE, BIFUNCTIONAL, DRUG DESIGN, PYROPHOSPHORYLASE, ROSSMANN-LIKE FOLD, LEFT-HANDED-BETA-HELIX, TRIMER, DOMAIN- INTERCHANGE, TRANSFERASE
1tol:A (THR51) to (GLY61) FUSION OF N-TERMINAL DOMAIN OF THE MINOR COAT PROTEIN FROM GENE III IN PHAGE M13, AND C-TERMINAL DOMAIN OF E. COLI PROTEIN-TOLA | CRYSTAL STRUCTURE, BACTERIOPHAGE M13, PHAGE INFECTION, TOL PATHWAY, FUSION PROTEIN, VIRAL PROTEIN
3vmh:C (ALA199) to (GLY207) OXYGEN-BOUND COMPLEX BETWEEN OXYGENASE AND FERREDOXIN IN CARBAZOLE 1, 9A-DIOXYGENASE | CATALYTIC MECHANISM, ELECTRON TRANSFER COMPLEX, RIESKE NONHEME IRON OXYGENASE SYSTEM, TERMINAL OXYGENASE, RIESKE-TYPE FERREDOXIN, CARBAZOLE 1,9A-DIOXYGENASE, OXIDOREDUCTASE
2wcg:A (LEU383) to (PRO401) X-RAY STRUCTURE OF ACID-BETA-GLUCOSIDASE WITH N-OCTYL( CYCLIC GUANIDINE)-NOJIRIMYCIN IN THE ACTIVE SITE | LIPID METABOLISM, GLUCOCEREBROSIDASE, MEMBRANE, LYSOSOME, HYDROLASE, GLUCOSIDASE, GLYCOPROTEIN, GAUCHER DISEASE, SPHINGOLIPID METABOLISM
2wcg:B (LEU383) to (PRO401) X-RAY STRUCTURE OF ACID-BETA-GLUCOSIDASE WITH N-OCTYL( CYCLIC GUANIDINE)-NOJIRIMYCIN IN THE ACTIVE SITE | LIPID METABOLISM, GLUCOCEREBROSIDASE, MEMBRANE, LYSOSOME, HYDROLASE, GLUCOSIDASE, GLYCOPROTEIN, GAUCHER DISEASE, SPHINGOLIPID METABOLISM
4zxv:C (CYS233) to (GLY244) STREPTOMYCES PEUCETIUS NITROSOSYNTHASE DNMZ IN LIGAND-FREE STATE | NITROSOSYNTHASE, FLAVIN MONOOXYGENASE, AMINOSUGAR, CIS-PEPTIDE, ACYL- COA DEHYDROGENASE, FLAVIN, OXIDOREDUCTASE
4zxv:D (CYS233) to (GLY244) STREPTOMYCES PEUCETIUS NITROSOSYNTHASE DNMZ IN LIGAND-FREE STATE | NITROSOSYNTHASE, FLAVIN MONOOXYGENASE, AMINOSUGAR, CIS-PEPTIDE, ACYL- COA DEHYDROGENASE, FLAVIN, OXIDOREDUCTASE
3iwk:L (PRO377) to (THR385) CRYSTAL STRUCTURE OF AMINOALDEHYDE DEHYDROGENASE 1 FROM PISUM SATIVUM (PSAMADH1) | ROSSMANN FOLD, DIMER, AMINOALDEHYDE DEHYDROGENASE, BETAINE ALDEHYDE DEHYDROGENASE, NAD, OXIDOREDUCTASE
4zyj:B (CYS233) to (GLY244) STREPTOMYCES PEUCETIUS NITROSOSYNTHASE DNMZ IN TDP-BOUND STATE | NITROSOSYNTHASE, FLAVIN MONOOXYGENASE, AMINOSUGAR, CIS-PEPTIDE, ACYL- COA DEHYDROGENASE, FLAVIN, OXIDOREDUCTASE
1tsq:A (ASP30) to (GLY49) CRYSTAL STRUCTURE OF AP2V SUBSTRATE VARIANT OF NC-P1 DECAMER PEPTIDE IN COMPLEX WITH V82A/D25N HIV-1 PROTEASE MUTANT | CO-EVOLUTION, NUCLEOCAPDIS, SUBSTRATE RECOGNITION, HIV-1 PROTEASE, HYDROLASE/VIRAL PROTEIN COMPLEX
1tsq:B (ASP30) to (GLY48) CRYSTAL STRUCTURE OF AP2V SUBSTRATE VARIANT OF NC-P1 DECAMER PEPTIDE IN COMPLEX WITH V82A/D25N HIV-1 PROTEASE MUTANT | CO-EVOLUTION, NUCLEOCAPDIS, SUBSTRATE RECOGNITION, HIV-1 PROTEASE, HYDROLASE/VIRAL PROTEIN COMPLEX
1tsu:B (ASP30) to (ILE50) CRYSTAL STRUCTURE OF DECAMER NCP1 SUBSTRATE PEPTIDE IN COMPLEX WITH WILD-TYPE D25N HIV-1 PROTEASE VARIANT | CO-EVOLUTION, NUCLEOCAPDIS, SUBSTRATE RECOGNITION, HIV-1 PROTEASE, VIRAL PROTEIN/HYDROLASE COMPLEX
4llf:A (VAL206) to (PHE214) CRYSTAL STRUCTURE OF CUCUMBER NECROSIS VIRUS | BETA BARREL, VIRUS, TOMBUSVIRUS, VIRAL BETA BARREL, VIRUS CAPSID, EXTRACELLULAR
4llf:H (VAL206) to (PHE214) CRYSTAL STRUCTURE OF CUCUMBER NECROSIS VIRUS | BETA BARREL, VIRUS, TOMBUSVIRUS, VIRAL BETA BARREL, VIRUS CAPSID, EXTRACELLULAR
1tth:B (ARG102) to (ASN111) ASPARTATE TRANSCARBAMOYLASE CATALYTIC CHAIN MUTANT GLU50ALA COMPLEXED WITH N-(PHOSPHONACETYL-L-ASPARTATE) (PALA) | SITE-SPECIFIC MUTAGENESIS, DOMAIN CLOSURE, ALLOSTERIC TRANSITION, HYDROLASE/HYDROLASE REGULATOR COMPLEX
4llo:A (GLN598) to (ALA611) STRUCTURE OF THE EAG DOMAIN-CNBHD COMPLEX OF THE MOUSE EAG1 CHANNEL | VOLTAGE-GATED POTASSIUM CHANNEL, TRANSPORT PROTEIN
2hle:A (LEU20) to (PRO36) STRUCTURAL AND BIOPHYSICAL CHARACTERIZATION OF THE EPHB4-EPHRINB2 PROTEIN PROTEIN INTERACTION AND RECEPTOR SPECIFICITY. | PROTEIN-PROTEIN INTERACTION, RECEPTOR TRYOSINE KINASE, BI-DIRECTIONAL CELL SIGNALING, TRANSFERASE-TRANSFERASE RECEPTOR COMPLEX, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, ACCELERATED TECHNOLOGIES CENTER FOR GENE TO 3D STRUCTURE, ATCG3D
1hvi:B (ASP30) to (GLY49) INFLUENCE OF STEREOCHEMISTRY ON ACTIVITY AND BINDING MODES FOR C2 SYMMETRY-BASED DIOL INHIBITORS OF HIV-1 PROTEASE | HYDROLASE(ACID PROTEASE)
5a1u:C (LYS4) to (LYS13) THE STRUCTURE OF THE COPI COAT TRIAD | TRANSPORT PROTEIN, STRUCTURAL PROTEIN, COPI, COATOMER, COATED VESICLES
2hoe:A (GLY134) to (ASP149) CRYSTAL STRUCTURE OF N-ACETYLGLUCOSAMINE KINASE (TM1224) FROM THERMOTOGA MARITIMA AT 2.46 A RESOLUTION | TM1224, N-ACETYLGLUCOSAMINE KINASE (EC 2.7.1.59), STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, TRANSFERASE
5a1v:C (LYS4) to (LYS13) THE STRUCTURE OF THE COPI COAT LINKAGE I | TRANSPORT PROTEIN, COPI, COATOMER, COATED VESICLES
5a1v:K (LYS4) to (LYS13) THE STRUCTURE OF THE COPI COAT LINKAGE I | TRANSPORT PROTEIN, COPI, COATOMER, COATED VESICLES
5a1v:T (LYS4) to (LYS13) THE STRUCTURE OF THE COPI COAT LINKAGE I | TRANSPORT PROTEIN, COPI, COATOMER, COATED VESICLES
2wkl:A (LEU383) to (PRO401) VELAGLUCERASE ALFA | ALTERNATIVE INITIATION, SPHINGOLIPID METABOLISM, MEMBRANE, LYSOSOME, HYDROLASE, ICHTHYOSIS, N-NONYL-DEOXYNOJIRIMYCIN, N-NONYL-DEOXYNOJIRIMYCIN ALTERNATIVE INITIATION, DISULFIDE BOND, PHARMACEUTICAL, GAUCHER DISEASE, GLYCOSIDASE, POLYMORPHISM, GLYCOPROTEIN, ALTERNATIVE SPLICING, ACID-BETA-GLUCOSIDASE, LIPID METABOLISM, DISEASE MUTATION, VELAGLUCERASE ALFA
5a1w:C (LYS4) to (LYS13) THE STRUCTURE OF THE COPI COAT LINKAGE II | TRANSPORT PROTEIN, COPI, COATOMER, COATED VESICLES
2wl0:B (ASP130) to (GLY149) HIV-1 PROTEASE INHIBITORS CONTAINING A TERTIARY ALCOHOL IN THE TRANSITION-STATE MIMIC WITH IMPROVED CELL-BASED ANTIVIRAL ACTIVITY | TRANSITION-STATE MIMIC, INHIBITOR, HYDROLASE
5a1x:C (LYS4) to (LYS13) THE STRUCTURE OF THE COPI COAT LINKAGE III | TRANSPORT PROTEIN, COPI, COATOMER, COATED VESICLES
5a1x:K (LYS4) to (LYS13) THE STRUCTURE OF THE COPI COAT LINKAGE III | TRANSPORT PROTEIN, COPI, COATOMER, COATED VESICLES
3vwj:C (SER196) to (SER206) TERNARY CRYSTAL STRUCTURE OF THE HUMAN NKT TCR-CD1D-C20:2 COMPLEX | CD1D, NKT T CELL RECEPTOR, ALPHA-GALACTOSYLCERAMIDE, PROTEIN RECEPTOR COMPLEX, CELL MEMBRANE, DISULFIDE BOND, ENDOSOME, GLYCOPROTEIN, HOST-VIRUS INTERACTION, IMMUNE RESPONSE, IMMUNOGLOBULIN DOMAIN, INNATE IMMUNITY, LYSOSOME, MEMBRANE, TRANSMEMBRANE, DISEASE MUTATION, GLYCATION, MHC I, PYRROLIDONE CARBOXYLIC ACID, SECRETED, IMMUNE SYSTEM
5a1y:C (LYS4) to (LYS13) THE STRUCTURE OF THE COPI COAT LINKAGE IV | TRANSPORT PROTEIN, COPI, COATOMER, COATED VESICLES
5a1y:K (LYS4) to (LYS13) THE STRUCTURE OF THE COPI COAT LINKAGE IV | TRANSPORT PROTEIN, COPI, COATOMER, COATED VESICLES
2hro:A (GLY13) to (VAL23) STRUCTURE OF THE FULL-LENGHT ENZYME I OF THE PTS SYSTEM FROM STAPHYLOCOCCUS CARNOSUS | PTS, PROTEIN PHOSPHORYLATION, SUGAR TRANSPORT, HISTIDINE PHOSPHORYLATION, TRANSFERASE
3vz2:A (LEU289) to (PRO303) STRUCTURAL INSIGHTS INTO SUBSTRATE AND COFACTOR SELECTION BY SP2771 | SUBSTRATE SELECTION, COFACTOR PREFERENCE, OXIDOREDUCTASE
2hs1:B (ASP130) to (GLY149) ULTRA-HIGH RESOLUTION X-RAY CRYSTAL STRUCTURE OF HIV-1 PROTEASE V32I MUTANT WITH TMC114 (DARUNAVIR) INHIBITOR | ULTRA-HIGH RESOLUTION ACTIVE SITE SURFACE BINDING SITE, HYDROLASE
3w0w:D (VAL108) to (PRO117) THE COMPLEX BETWEEN T36-5 TCR AND HLA-A24 BOUND TO HIV-1 NEF134-10(2F) PEPTIDE IN SPACE GROUP P212121 | HIV-1, NEF, HLA-A24, T CELL RECEPTOR, MHC CLASS I, TCR, MHC, IMMUNOGLOBURIN DOMAIN, IMMUNE SYSTEM, IMMUNE RESPONSE
4luw:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-((((3R,5S)-5-(((6-AMINO-4-METHYLPYRIDIN-2-YL)METHOXY) METHYL)PYRROLIDIN-3-YL)OXY)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4lux:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-((((3R,5S)-5-(((6-AMINO-4-METHYLPYRIDIN-2-YL)METHOXY)METHYL) PYRROLIDIN-3-YL)OXY)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4lux:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-((((3R,5S)-5-(((6-AMINO-4-METHYLPYRIDIN-2-YL)METHOXY)METHYL) PYRROLIDIN-3-YL)OXY)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
2wq8:A (LYS223) to (MET233) GLYCAN LABELLING USING ENGINEERED VARIANTS OF GALACTOSE OXIDASE OBTAINED BY DIRECTED EVOLUTION | OXIDOREDUCTASE, KELCH REPEAT, METAL-BINDING, GLYCOENGINEERING, DIRECTED EVOLUTION
2wqz:C (ARG105) to (THR119) CRYSTAL STRUCTURE OF SYNAPTIC PROTEIN NEUROLIGIN-4 IN COMPLEX WITH NEUREXIN-BETA 1: ALTERNATIVE REFINEMENT | TRANSMEMBRANE, DISULFIDE BOND, ALPHA/BETA-HYDROLASE CHOLINESTERASE AUTISM BRAIN, ALTERNATIVE PROMOTER USAGE, MEMBRANE, GLYCOPROTEIN, CELL ADHESION
2hx2:B (PRO95) to (GLY103) BOVINE ENOS HEME DOMAIN COMPLEXED WITH (4S)-N-{4-AMINO-5-[(2- AMINOETHYL)-HYDROXYAMINO]-PENTYL}-N'-NITROGUANIDINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, INHIBITOR, OXIDOREDUCTASE
2hx4:A (GLY325) to (GLY333) RAT NNOS HEME DOMAIN COMPLEXED WITH 4-N-(NW-NITRO-L-ARGININYL)-TRANS- 4-HYDROXYAMINO-L-PROLINE AMIDE | NITRIC OXIDE SYNTHASE, HEME ENZYME, INHIBITOR, OXIDOREDUCTASE
2hx4:B (GLY325) to (GLY333) RAT NNOS HEME DOMAIN COMPLEXED WITH 4-N-(NW-NITRO-L-ARGININYL)-TRANS- 4-HYDROXYAMINO-L-PROLINE AMIDE | NITRIC OXIDE SYNTHASE, HEME ENZYME, INHIBITOR, OXIDOREDUCTASE
1i80:A (GLY131) to (LEU142) CRYSTAL STRUCTURE OF M. TUBERCULOSIS PNP IN COMPLEX WITH IMINORIBITOL, 9-DEAZAHYPOXANTHINE AND PHOSPHATE ION | TRIMER, TRANSITION-STATE COMPLEX, TRANSFERASE
1i80:B (GLN132) to (LEU142) CRYSTAL STRUCTURE OF M. TUBERCULOSIS PNP IN COMPLEX WITH IMINORIBITOL, 9-DEAZAHYPOXANTHINE AND PHOSPHATE ION | TRIMER, TRANSITION-STATE COMPLEX, TRANSFERASE
1i80:C (GLN132) to (LEU142) CRYSTAL STRUCTURE OF M. TUBERCULOSIS PNP IN COMPLEX WITH IMINORIBITOL, 9-DEAZAHYPOXANTHINE AND PHOSPHATE ION | TRIMER, TRANSITION-STATE COMPLEX, TRANSFERASE
1i83:B (PRO95) to (GLY103) BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N1,N14-BIS((S-METHYL)ISOTHIOUREIDO)TETRADECANE (H4B FREE) | ALPHA-BETA FOLD, OXIDOREDUCTASE
5a46:B (LEU478) to (CYS488) FGFR1 IN COMPLEX WITH DOVITINIB | TRANSFERASE, KINASE
3izq:0 (ILE34) to (PHE43) STRUCTURE OF THE DOM34-HBS1-GDPNP COMPLEX BOUND TO A TRANSLATING RIBOSOME | NO-GO MRNA DECAY, RIBOSOMAL PROTEIN,HYDROLASE
4m1e:A (SER125) to (LEU136) CRYSTAL STRUCTURE OF PURINE NUCLEOSIDE PHOSPHORYLASE I FROM PLANCTOMYCES LIMNOPHILUS DSM 3776, NYSGRC TARGET 029364. | STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NYSGRC, PURINE NUCLEOSIDE PHOSPHORYLASE, PSI-BIOLOGY, NEW YORK STRUCTURAL GENOMICS RESEARCH CONSORTIUM, TRANSFERASE
4m1e:E (SER125) to (LEU136) CRYSTAL STRUCTURE OF PURINE NUCLEOSIDE PHOSPHORYLASE I FROM PLANCTOMYCES LIMNOPHILUS DSM 3776, NYSGRC TARGET 029364. | STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NYSGRC, PURINE NUCLEOSIDE PHOSPHORYLASE, PSI-BIOLOGY, NEW YORK STRUCTURAL GENOMICS RESEARCH CONSORTIUM, TRANSFERASE
4m1e:F (ASP126) to (LEU136) CRYSTAL STRUCTURE OF PURINE NUCLEOSIDE PHOSPHORYLASE I FROM PLANCTOMYCES LIMNOPHILUS DSM 3776, NYSGRC TARGET 029364. | STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NYSGRC, PURINE NUCLEOSIDE PHOSPHORYLASE, PSI-BIOLOGY, NEW YORK STRUCTURAL GENOMICS RESEARCH CONSORTIUM, TRANSFERASE
2wvz:A (GLN33) to (GLY41) STRUCTURE OF THE FAMILY GH92 INVERTING MANNOSIDASE BT3990 FROM BACTEROIDES THETAIOTAOMICRON VPI-5482 | HYDROLASE, GH92, BT3990, GLYCOSIDE HYDROLASE FAMILY 92
4m3r:A (PRO35) to (ASP51) RB69 DNA POLYMERASE TERNARY COMPLEX WITH DT/DG AT POSITION N-1 OF PRIMER/TEMPLATE DUPLEX | RB69 POL, QUADRUPLE, DT/DG, N-1, RB69, HYDROLASE-DNA COMPLEX
4m3u:A (PRO35) to (ASP51) RB69 DNA POLYMERASE TERNARY COMPLEX WITH DT/DG AT POSITION N-3 OF PRIMER/TEMPLATE DUPLEX | RB69 POL, QUADRUPLE, DT/DG, N-3, RB69, HYDROLASE-DNA COMPLEX
4m3w:A (PRO35) to (ASP51) RB69 DNA POLYMERASE TERNARY COMPLEX WITH DT/DG AT POSITION N-4 OF PRIMER/TEMPLATE DUPLEX | RB69 POL, QUADRUPLE, DT/DG, N-4, RB69, HYDROLASE-DNA COMPLEX
1ulb:A (GLY127) to (LEU138) APPLICATION OF CRYSTALLOGRAPHIC AND MODELING METHODS IN THE DESIGN OF PURINE NUCLEOSIDE PHOSPHORYLASE INHIBITORS | PENTOSYLTRANSFERASE
4m41:A (PRO35) to (ASP51) RB69 DNA POLYMERASE TERNARY COMPLEX WITH DG/DT AT POSITION N-3 OF PRIMER/TEMPLATE DUPLEX | RB69 POL, QUADRUPLE, DG/DT, N-3, RB69, HYDROLASE-DNA COMPLEX
4m42:A (PRO35) to (ASP51) RB69 DNA POLYMERASE TERNARY COMPLEX WITH DG/DT AT POSITION N-4 OF PRIMER/TEMPLATE DUPLEX | RB69 POL, QUADRUPLE, DG/DT, N-4, RB69, HYDROLASE-DNA COMPLEX
2idr:A (ASN44) to (TRP62) CRYSTAL STRUCTURE OF TRANSLATION INITIATION FACTOR EIF4E FROM WHEAT | EUKARYOTIC INITIATION FACTOR 4E, EIF4E, TRANSLATION REGULATOR
2idr:B (ASN44) to (TRP62) CRYSTAL STRUCTURE OF TRANSLATION INITIATION FACTOR EIF4E FROM WHEAT | EUKARYOTIC INITIATION FACTOR 4E, EIF4E, TRANSLATION REGULATOR
4m9c:C (THR98) to (GLY107) WEEI FROM ACINETOBACTER BAUMANNII AYE | LEFT-HANDED BETA-HELIX, ROSSMANN FOLD, ACETYLTRANSFERASE, TRANSFERASE
4m9c:E (THR98) to (GLY107) WEEI FROM ACINETOBACTER BAUMANNII AYE | LEFT-HANDED BETA-HELIX, ROSSMANN FOLD, ACETYLTRANSFERASE, TRANSFERASE
4m9c:F (THR98) to (GLY107) WEEI FROM ACINETOBACTER BAUMANNII AYE | LEFT-HANDED BETA-HELIX, ROSSMANN FOLD, ACETYLTRANSFERASE, TRANSFERASE
2wz1:B (LYS415) to (ILE427) STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN SOLUBLE GUANYLATE CYCLASE 1 BETA 3. | LYASE, GUCY1, METAL-BINDING, CGMP BIOSYNTHESIS, NUCLEOTIDE-BINDING, CYCLASE, GUCY1B3, GTP-BINDING
2wzi:A (GLN10) to (ASP20) BTGH84 D243N IN COMPLEX WITH 5F-OXAZOLINE | GLYCOSIDE HYDROLASE, HYDROLASE, INHIBITOR, GLYCOSIDASE
5abf:A (GLN11) to (ASP20) STRUCTURE OF GH84 WITH LIGAND | HYDROLASE, TIM-BARREL, INHIBITOR
2wzp:A (GLY192) to (LYS199) STRUCTURES OF LACTOCOCCAL PHAGE P2 BASEPLATE SHED LIGHT ON A NOVEL MECHANISM OF HOST ATTACHMENT AND ACTIVATION IN SIPHOVIRIDAE | BASEPLATE, VIRAL PROTEIN
2wzp:B (GLY192) to (LYS199) STRUCTURES OF LACTOCOCCAL PHAGE P2 BASEPLATE SHED LIGHT ON A NOVEL MECHANISM OF HOST ATTACHMENT AND ACTIVATION IN SIPHOVIRIDAE | BASEPLATE, VIRAL PROTEIN
2wzp:C (GLY192) to (LYS199) STRUCTURES OF LACTOCOCCAL PHAGE P2 BASEPLATE SHED LIGHT ON A NOVEL MECHANISM OF HOST ATTACHMENT AND ACTIVATION IN SIPHOVIRIDAE | BASEPLATE, VIRAL PROTEIN
2wzp:G (GLY192) to (LYS199) STRUCTURES OF LACTOCOCCAL PHAGE P2 BASEPLATE SHED LIGHT ON A NOVEL MECHANISM OF HOST ATTACHMENT AND ACTIVATION IN SIPHOVIRIDAE | BASEPLATE, VIRAL PROTEIN
2wzp:H (GLY192) to (LYS199) STRUCTURES OF LACTOCOCCAL PHAGE P2 BASEPLATE SHED LIGHT ON A NOVEL MECHANISM OF HOST ATTACHMENT AND ACTIVATION IN SIPHOVIRIDAE | BASEPLATE, VIRAL PROTEIN
2wzp:I (GLY192) to (LYS199) STRUCTURES OF LACTOCOCCAL PHAGE P2 BASEPLATE SHED LIGHT ON A NOVEL MECHANISM OF HOST ATTACHMENT AND ACTIVATION IN SIPHOVIRIDAE | BASEPLATE, VIRAL PROTEIN
5abg:A (GLN11) to (ASP20) STRUCTURE OF GH84 WITH LIGAND | HYDROLASE, GH84 GLYCOSIDE HYDROLASE, TIM-BARREL, INHIBITOR
4mb8:C (VAL125) to (HIS133) EVOLUTIONARY HISTORY AND METABOLIC INSIGHTS OF ANCIENT MAMMALIAN URICASES | URIC ACID OXIDASE, LYSOZOME, OXIDOREDUCTASE
5ad4:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-(2-(DIMETHYLAMINO)ETHYL)PHENOXY) METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5ad4:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-(2-(DIMETHYLAMINO)ETHYL)PHENOXY) METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5ad5:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-(2-(METHYLAMINO)ETHYL)PHENOXY) METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5ad5:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-(2-(METHYLAMINO)ETHYL)PHENOXY) METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5ad6:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-(DIMETHYLAMINO)METHYL)PHENOXY) METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5ad6:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-(DIMETHYLAMINO)METHYL)PHENOXY) METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5ad7:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-(METHYLAMINO)METHYL)PHENOXY)METHYL) QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5ad7:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-(METHYLAMINO)METHYL)PHENOXY)METHYL) QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
1uus:A (VAL697) to (PRO704) STRUCTURE OF AN ACTIVATED DICTYOSTELIUM STAT IN ITS DNA-UNBOUND FORM | DICTYOSTELIUM, STAT, SH2, SIGNAL TRANSDUCTION, TRANSDUCER, TRANSCRIPTION FACTOR
5ad8:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-AMINOMETHYL)PHENOXY)METHYL) QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5ad8:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-AMINOMETHYL)PHENOXY)METHYL) QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5adb:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((4-CHLORO-3-((METHYLAMINO)METHYL) PHENOXY)METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5adb:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((4-CHLORO-3-((METHYLAMINO)METHYL) PHENOXY)METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5ad9:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((4-(DIMETHYLAMINO)METHYL)PHENOXY) METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5ad9:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((4-(DIMETHYLAMINO)METHYL)PHENOXY) METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5ada:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-(((3-((DIMETHYLAMINO)METHYL)PHENYL) AMINO)METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5ada:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-(((3-((DIMETHYLAMINO)METHYL)PHENYL) AMINO)METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5adc:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-(((5-((METHYLAMINO)METHYL)PYRIDIN-3- YL)OXY)METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5adc:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-(((5-((METHYLAMINO)METHYL)PYRIDIN-3- YL)OXY)METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5add:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE D597N M336V MUTANT HEME DOMAIN IN COMPLEX WITH 7-((3-(METHYLAMINO)METHYL) PHENOXY)METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5add:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE D597N M336V MUTANT HEME DOMAIN IN COMPLEX WITH 7-((3-(METHYLAMINO)METHYL) PHENOXY)METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5ade:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE M336V D597N MUTANT HEME DOMAIN IN COMPLEX WITH 7-((4-CHLORO-3-(( METHYLAMINO)METHYL)PHENOXY)METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5ade:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE M336V D597N MUTANT HEME DOMAIN IN COMPLEX WITH 7-((4-CHLORO-3-(( METHYLAMINO)METHYL)PHENOXY)METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5adf:A (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH 7-(((3-((DIMETHYLAMINO)METHYL)PHENYL)AMINO) METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE
5adf:B (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH 7-(((3-((DIMETHYLAMINO)METHYL)PHENYL)AMINO) METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE
5adg:A (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH 7-((4-CHLORO-3-((METHYLAMINO)METHYL)PHENOXY) METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE
5adg:B (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH 7-((4-CHLORO-3-((METHYLAMINO)METHYL)PHENOXY) METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE
5adi:A (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH 7-(((5-((METHYLAMINO)METHYL)PYRIDIN-3-YL)OXY) METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE
5adi:B (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH 7-(((5-((METHYLAMINO)METHYL)PYRIDIN-3-YL)OXY) METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE
5adl:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-(METHYLAMINO)METHYL)PHENOXY) METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5adm:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-AMINOMETHYL)PHENOXY)METHYL) QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
3j2w:B (PHE1118) to (ALA1131) ELECTRON CRYO-MICROSCOPY OF CHIKUNGUNYA VIRUS | E1-E2 GLYCOPROTEIN, NUCLEOCAPSID PROTEIN, TRANSMEMBRANE HELIX, VIRUS
3j2w:C (PHE2118) to (ALA2131) ELECTRON CRYO-MICROSCOPY OF CHIKUNGUNYA VIRUS | E1-E2 GLYCOPROTEIN, NUCLEOCAPSID PROTEIN, TRANSMEMBRANE HELIX, VIRUS
3j2w:D (PHE3118) to (ALA3131) ELECTRON CRYO-MICROSCOPY OF CHIKUNGUNYA VIRUS | E1-E2 GLYCOPROTEIN, NUCLEOCAPSID PROTEIN, TRANSMEMBRANE HELIX, VIRUS
5adn:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-(((3-((DIMETHYLAMINO)METHYL) PHENYL)AMINO)METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5agk:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (2S)-2-AMINO-5-(2-(METHYLSULFINYL) ACETIMIDAMIDO)PENTANOIC ACID | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5agk:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (2S)-2-AMINO-5-(2-(METHYLSULFINYL) ACETIMIDAMIDO)PENTANOIC ACID | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5agl:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-2-AMINO-5-(2-(METHYLSULFONYL) ACETIMIDAMIDO)PENTANOIC ACID | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5agl:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-2-AMINO-5-(2-(METHYLSULFONYL) ACETIMIDAMIDO)PENTANOIC ACID | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5agm:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-2-AMINO-5-(2-OXOACETIMIDAMIDO)PENTANOIC ACID | OXIDOREDUCTASE, INHIBITOR COMPLEX
5agm:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-2-AMINO-5-(2-OXOACETIMIDAMIDO)PENTANOIC ACID | OXIDOREDUCTASE, INHIBITOR COMPLEX
5agn:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-2-AMINO-5-(2-HYDROXYACETIMIDAMIDO)PENTANOIC ACID | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5agn:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-2-AMINO-5-(2-HYDROXYACETIMIDAMIDO)PENTANOIC ACID | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5ago:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-2-AMINO-5-(2-MERCAPTOACETIMIDAMIDO) PENTANOIC ACID | OXIDOREDUCTASE, INHIBITOR COMPLEX
5ago:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-2-AMINO-5-(2-MERCAPTOACETIMIDAMIDO) PENTANOIC ACID | OXIDOREDUCTASE, INHIBITOR COMPLEX
5agp:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-2-AMINO-5-(2-MERCAPTOACETIMIDAMIDO) PENTANOIC ACID | OXIDOREDUCTASE, INHIBITOR COMPLEX
5agp:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-2-AMINO-5-(2-MERCAPTOACETIMIDAMIDO) PENTANOIC ACID | OXIDOREDUCTASE, INHIBITOR COMPLEX
5agv:A (THR267) to (MET275) THE SLIDING CLAMP OF MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH A NATURAL PRODUCT. | TRANSFERASE-ANTIBIOTIC COMPLEX, TRANSFERASE, DNAN, NATURAL PRODUCT, SLIDING CLAMP
2iou:D (LEU306) to (GLY315) MAJOR TROPISM DETERMINANT P1 (MTD-P1) VARIANT COMPLEXED WITH BORDETELLA BROCHISEPTICA VIRULENCE FACTOR PERTACTIN EXTRACELLULAR DOMAIN (PRN-E). | MTD; PRN; PERTACTIN, VIRAL PROTEIN-MEMBRANE PROTEIN COMPLEX
2iou:E (LEU306) to (GLY315) MAJOR TROPISM DETERMINANT P1 (MTD-P1) VARIANT COMPLEXED WITH BORDETELLA BROCHISEPTICA VIRULENCE FACTOR PERTACTIN EXTRACELLULAR DOMAIN (PRN-E). | MTD; PRN; PERTACTIN, VIRAL PROTEIN-MEMBRANE PROTEIN COMPLEX
1j16:A (GLN30) to (SER54) BENZAMIDINE IN COMPLEX WITH RAT TRYPSIN MUTANT X99/175/190RT | SERINE PROTEASE, HYDROLASE, SERINE PROTEINASE
5ahs:E (GLY207) to (HIS221) 3-SULFINOPROPIONYL-COENZYME A (3SP-COA) DESULFINASE FROM ADVENELLA MIMGARDEFORDENSIS DPN7T: HOLO CRYSTAL STRUCTURE WITH THE SUBSTRATE ANALOG SUCCINYL-COA | OXIDOREDUCTASE
3wio:A (LEU177) to (GLY185) CRYSTAL STRUCTURE OF OSD14 IN COMPLEX WITH HYDROXY D-RING | ALPHA/BETA-HYDROLASE FOLD, HYDROLASE
1v10:A (SER414) to (ASP425) STRUCTURE OF RIGIDOPORUS LIGNOSUS LACCASE FROM HEMIHEDRALLY TWINNED CRYSTALS | MULTICOPPER BLUE OXIDASE, OXIDASE
2x53:A (GLY192) to (LYS199) STRUCTURE OF THE PHAGE P2 BASEPLATE IN ITS ACTIVATED CONFORMATION WITH SR | BASEPLATE, VIRAL PROTEIN
2x53:C (GLY192) to (LYS199) STRUCTURE OF THE PHAGE P2 BASEPLATE IN ITS ACTIVATED CONFORMATION WITH SR | BASEPLATE, VIRAL PROTEIN
2x53:D (GLY192) to (LYS199) STRUCTURE OF THE PHAGE P2 BASEPLATE IN ITS ACTIVATED CONFORMATION WITH SR | BASEPLATE, VIRAL PROTEIN
2x53:F (GLY192) to (LYS199) STRUCTURE OF THE PHAGE P2 BASEPLATE IN ITS ACTIVATED CONFORMATION WITH SR | BASEPLATE, VIRAL PROTEIN
2x53:G (GLY192) to (LYS199) STRUCTURE OF THE PHAGE P2 BASEPLATE IN ITS ACTIVATED CONFORMATION WITH SR | BASEPLATE, VIRAL PROTEIN
2x53:I (GLY192) to (LYS199) STRUCTURE OF THE PHAGE P2 BASEPLATE IN ITS ACTIVATED CONFORMATION WITH SR | BASEPLATE, VIRAL PROTEIN
2x53:J (GLY192) to (LYS199) STRUCTURE OF THE PHAGE P2 BASEPLATE IN ITS ACTIVATED CONFORMATION WITH SR | BASEPLATE, VIRAL PROTEIN
2x53:L (GLY192) to (LYS199) STRUCTURE OF THE PHAGE P2 BASEPLATE IN ITS ACTIVATED CONFORMATION WITH SR | BASEPLATE, VIRAL PROTEIN
2x53:M (GLY192) to (LYS199) STRUCTURE OF THE PHAGE P2 BASEPLATE IN ITS ACTIVATED CONFORMATION WITH SR | BASEPLATE, VIRAL PROTEIN
2x53:O (GLY192) to (LYS199) STRUCTURE OF THE PHAGE P2 BASEPLATE IN ITS ACTIVATED CONFORMATION WITH SR | BASEPLATE, VIRAL PROTEIN
2x53:P (GLY192) to (LYS199) STRUCTURE OF THE PHAGE P2 BASEPLATE IN ITS ACTIVATED CONFORMATION WITH SR | BASEPLATE, VIRAL PROTEIN
2x53:R (GLY192) to (LYS199) STRUCTURE OF THE PHAGE P2 BASEPLATE IN ITS ACTIVATED CONFORMATION WITH SR | BASEPLATE, VIRAL PROTEIN
5ajq:B (HIS25) to (ASN33) HUMAN LOK (STK10) IN COMPLEX WITH BOSUTINIB | TRANSFERASE
2it1:A (VAL337) to (ASP350) STRUCTURE OF PH0203 PROTEIN FROM PYROCOCCUS HORIKOSHII | ATP BINDING PROTEIN, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, TRANSPORT PROTEIN
1v4n:A (GLU7) to (GLY15) STRUCTURE OF 5'-DEOXY-5'-METHYLTHIOADENOSINE PHOSPHORYLASE HOMOLOGUE FROM SULFOLOBUS TOKODAII | TRANSFERASE, STRUCTURAL GENOMICS
1v4n:C (GLU7) to (GLY15) STRUCTURE OF 5'-DEOXY-5'-METHYLTHIOADENOSINE PHOSPHORYLASE HOMOLOGUE FROM SULFOLOBUS TOKODAII | TRANSFERASE, STRUCTURAL GENOMICS
1j91:B (ASP38) to (LYS49) CRYSTAL STRUCTURE OF Z. MAYS CK2 KINASE ALPHA SUBUNIT IN COMPLEX WITH THE ATP-COMPETITIVE INHIBITOR 4,5,6,7- TETRABROMOBENZOTRIAZOLE | CK2, CASEIN KINASE 2, INHIBITORS, TETRABROMO-BENZOTRIAZOLE, TRANSFERASE
1jcz:A (PRO102) to (SER110) CRYSTAL STRUCTURE OF THE EXTRACELLULAR DOMAIN OF HUMAN CARBONIC ANHYDRASE XII | EXTRACELLULAR DOMAIN, HUMAN CARBONIC ANHYDRASE XII, BITOPIC MEMBRANE PROTEIN, TYPE I MEMBRANE PROTEIN, LYASE
5amj:A (GLN108) to (PRO122) CEREBLON ISOFORM 4 FROM MAGNETOSPIRILLUM GRYPHISWALDENSE IN COMPLEX WITH THALIDOMIDE, WASH II STRUCTURE | SIGNALING PROTEIN, TERATOGENICITY, AROMATIC CAGE
5amj:C (SER20) to (SER62) CEREBLON ISOFORM 4 FROM MAGNETOSPIRILLUM GRYPHISWALDENSE IN COMPLEX WITH THALIDOMIDE, WASH II STRUCTURE | SIGNALING PROTEIN, TERATOGENICITY, AROMATIC CAGE
1vag:A (GLY325) to (GLY333) NEURONAL NITRIC OXIDE SYNTHASE OXYGENASE DOMAIN COMPLEXED WITH THE INHIBITOR AR-R17477 | RAT NNOSOXY COMPLEX WITH AR-R17477, OXIDOREDUCTASE
1jep:A (PHE89) to (SER102) CHALCONE ISOMERASE COMPLEXED WITH 4'-HYDROXYFLAVANONE | OPEN-FACED BETA SANDWICH, ISOMERASE
1jep:B (PHE89) to (SER102) CHALCONE ISOMERASE COMPLEXED WITH 4'-HYDROXYFLAVANONE | OPEN-FACED BETA SANDWICH, ISOMERASE
2izn:C (THR5) to (GLY13) MS2-RNA HAIRPIN (G-10) COMPLEX | VIRUS/RNA, 3D-STRUCTURE, CAPSID, CAPSID PROTEIN, COMPLEX (CAPSID PROTEIN/RNA HAIRPIN), HAIRPIN, LEVIVIRUS, RNA-BINDING, STRUCTURAL PROTEIN, VIRUS/VIRAL PROTEIN/RNA, VIRUS
5apb:A (ALA320) to (ILE348) STRUCTURE OF THE ADENYLATION DOMAIN THR1 INVOLVED IN THE BIOSYNTHESIS OF 4-CHLOROTHREONINE IN STREPTOMYCES SP. OH- 5093, LIGAND BOUND STRUCTURE | TRANSFERASE, ADENYLATION, ADENYLATION ENZYME
2j25:B (LEU383) to (PRO401) PARTIALLY DEGLYCOSYLATED GLUCOCERAMIDASE | PHARMACEUTICAL, GAUCHER DISEASE, DISEASE MUTATION, GLYCOSIDASE, SPHINGOLIPID, POLYMORPHISM, GLYCOPROTEIN, MEMBRANE, LYSOSOME, HYDROLASE, GLUCOSIDASE, GLUCOCEREBROSIDASE, ALTERNATIVE INITIATION, LIPID METABOLISM, CEREZYME HYDROLASE, SPHINGOLIPID METABOLISM
2j3l:A (LEU384) to (LYS404) PROLYL-TRNA SYNTHETASE FROM ENTEROCOCCUS FAECALIS COMPLEXED WITH A PROLYL-ADENYLATE ANALOGUE ('5'-O-(N-(L-PROLYL)- SULFAMOYL)ADENOSINE) | BACTERIAL-TYPE PROLYL-TRNA SYNTHETASE, CLASS II AMINOACYL- TRNA SYNTHETASE, EDITING, TRANSLATION, ATP + L-PROLINE + TRNA (PRO) GIVES AMP + PPI + L-PROLYL-TRNA(PRO), LIGASE
2j6k:C (GLY47) to (LYS58) N-TERMINAL SH3 DOMAIN OF CMS (CD2AP HUMAN HOMOLOG) | PHOSPHORYLATION, ADAPTOR PROTEIN, EGFR DOWNREGULATION, SH3, SH3 DOMAIN, SH3-BINDING, CD2 ASSOCIATED PROTEIN, CYTOSKELETAL REARRANGEMENTS, SURFACE ACTIVE PROTEIN, SIGNALING PROTEIN, PROTEIN BINDING
2j6k:D (GLY47) to (LYS58) N-TERMINAL SH3 DOMAIN OF CMS (CD2AP HUMAN HOMOLOG) | PHOSPHORYLATION, ADAPTOR PROTEIN, EGFR DOWNREGULATION, SH3, SH3 DOMAIN, SH3-BINDING, CD2 ASSOCIATED PROTEIN, CYTOSKELETAL REARRANGEMENTS, SURFACE ACTIVE PROTEIN, SIGNALING PROTEIN, PROTEIN BINDING
2j6k:I (GLY47) to (LYS58) N-TERMINAL SH3 DOMAIN OF CMS (CD2AP HUMAN HOMOLOG) | PHOSPHORYLATION, ADAPTOR PROTEIN, EGFR DOWNREGULATION, SH3, SH3 DOMAIN, SH3-BINDING, CD2 ASSOCIATED PROTEIN, CYTOSKELETAL REARRANGEMENTS, SURFACE ACTIVE PROTEIN, SIGNALING PROTEIN, PROTEIN BINDING
1vmk:A (GLU123) to (ASN132) CRYSTAL STRUCTURE OF PURINE NUCLEOSIDE PHOSPHORYLASE (TM1596) FROM THERMOTOGA MARITIMA AT 2.01 A RESOLUTION | TM1596, PURINE NUCLEOSIDE PHOSPHORYLASE, STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI, JOINT CENTER FOR STRUCTURAL GENOMICS, TRANSFERASE
1vmk:B (GLU123) to (ASN132) CRYSTAL STRUCTURE OF PURINE NUCLEOSIDE PHOSPHORYLASE (TM1596) FROM THERMOTOGA MARITIMA AT 2.01 A RESOLUTION | TM1596, PURINE NUCLEOSIDE PHOSPHORYLASE, STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI, JOINT CENTER FOR STRUCTURAL GENOMICS, TRANSFERASE
1vmk:C (GLU123) to (ASN132) CRYSTAL STRUCTURE OF PURINE NUCLEOSIDE PHOSPHORYLASE (TM1596) FROM THERMOTOGA MARITIMA AT 2.01 A RESOLUTION | TM1596, PURINE NUCLEOSIDE PHOSPHORYLASE, STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI, JOINT CENTER FOR STRUCTURAL GENOMICS, TRANSFERASE
4muv:B (ARG252) to (ILE265) M. LOTI CYCLIC-NUCLEOTIDE BINDING DOMAIN MUTANT DISPLAYING INVERTED LIGAND SELECTIVITY, CYCLIC-GMP BOUND | MLOTIK1 CNBD MUTANT, CGMP-COMPLEX, CYCLIC-NUCLEOTIDE BINDING, MEMBRANE PROTEIN DOMAIN, METAL TRANSPORT, NUCLEOTIDE BINDING PROTEIN
4mvl:B (GLY29) to (GLY38) CRYSTAL STRUCTURE OF AN ENGINEERED LIPOCALIN (ANTICALIN H1GA) IN COMPLEX WITH THE ALZHEIMER AMYLOID PEPTIDE ABETA1-40 | BETA-BARREL, ENGINEERED LIPOCALIN, BINDING PROTEIN, PROTEIN BINDING- PROTEIN FIBRIL COMPLEX
4mwh:A (ASP39) to (LYS50) CRYSTAL STRUCTURE OF SCCK2 ALPHA IN COMPLEX WITH ATP | PROTEIN KINASE, PROTEIN PHOSPHORYLATION, TRANSFERASE
3j7g:A (TYR27) to (THR39) ELECTRON CRYO-MICROSCOPY OF HUMAN PAPILLOMAVIRUS 16 AND H16.V5 FAB FRAGMENTS | PENTAMER OF HUMAN PAPILLOMAVIRUS, QV16-V5 COMPLEX, VIRUS-FAB COMPLEX, NEUTRALIZATION ANTIBODY, MATURATION, VIRUS
3j7g:C (TYR27) to (THR39) ELECTRON CRYO-MICROSCOPY OF HUMAN PAPILLOMAVIRUS 16 AND H16.V5 FAB FRAGMENTS | PENTAMER OF HUMAN PAPILLOMAVIRUS, QV16-V5 COMPLEX, VIRUS-FAB COMPLEX, NEUTRALIZATION ANTIBODY, MATURATION, VIRUS
3j7g:D (TYR27) to (THR39) ELECTRON CRYO-MICROSCOPY OF HUMAN PAPILLOMAVIRUS 16 AND H16.V5 FAB FRAGMENTS | PENTAMER OF HUMAN PAPILLOMAVIRUS, QV16-V5 COMPLEX, VIRUS-FAB COMPLEX, NEUTRALIZATION ANTIBODY, MATURATION, VIRUS
3j7g:E (TYR27) to (THR39) ELECTRON CRYO-MICROSCOPY OF HUMAN PAPILLOMAVIRUS 16 AND H16.V5 FAB FRAGMENTS | PENTAMER OF HUMAN PAPILLOMAVIRUS, QV16-V5 COMPLEX, VIRUS-FAB COMPLEX, NEUTRALIZATION ANTIBODY, MATURATION, VIRUS
4mx3:B (PHE152) to (GLN165) CRYSTAL STRUCTURE OF PKA RIALPHA HOMODIMER | PKA, RIALPHA HOMODIMER, COOPERATIVE CAMP BINDING, CARNEY COMPLEX DISEASE, SIGNALING PROTEIN
2j9j:B (ASP30) to (GLY49) ATOMIC-RESOLUTION CRYSTAL STRUCTURE OF CHEMICALLY-SYNTHESIZED HIV-1 PROTEASE COMPLEXED WITH INHIBITOR JG-365 | HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASE, HYDROLASE, HIGH RESOLUTION, RNA-DIRECTED DNA POLYMERASE, ASPARTYL PROTEASE, HUMAN IMMUNODEFICIENCY VIRUS 1, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3wx2:B (GLU361) to (ASN370) MOUSE CEREBLON THALIDOMIDE BINDING DOMAIN, NATIVE | ZINC FINGER, E3 UBIQUITIN LIGASE, METAL BINDING PROTEIN
1jui:D (SER164) to (PHE175) CONCANAVALIN A-CARBOHYDRATE MIMICKING 10-MER PEPTIDE COMPLEX | LECTIN, SUGAR BINDING PROTEIN
4mzo:D (GLY185) to (TYR193) MOUSE CATHEPSIN S WITH COVALENT LIGAND (3S,4S)-N-[(2E)-2-IMINOETHYL]- 4-(MORPHOLIN-4-YLCARBONYL)-1-(PHENYLSULFONYL)PYRROLIDINE-3- CARBOXAMIDE | HYDROLASE, CYSTEINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4mzo:F (GLY185) to (TYR193) MOUSE CATHEPSIN S WITH COVALENT LIGAND (3S,4S)-N-[(2E)-2-IMINOETHYL]- 4-(MORPHOLIN-4-YLCARBONYL)-1-(PHENYLSULFONYL)PYRROLIDINE-3- CARBOXAMIDE | HYDROLASE, CYSTEINE PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3j8v:A (TYR27) to (THR39) CRYO-EM RECONSTRUCTION OF QUASI-HPV16 COMPLEX WITH H16.14J FAB | L1 PENTAMER, QUASI-HPV16, L1 CAPSOMER, ROSIE ONLINE, VIRUS-IMMUNE SYSTEM COMPLEX
3j8v:C (TYR27) to (THR39) CRYO-EM RECONSTRUCTION OF QUASI-HPV16 COMPLEX WITH H16.14J FAB | L1 PENTAMER, QUASI-HPV16, L1 CAPSOMER, ROSIE ONLINE, VIRUS-IMMUNE SYSTEM COMPLEX
3j8v:D (TYR27) to (THR39) CRYO-EM RECONSTRUCTION OF QUASI-HPV16 COMPLEX WITH H16.14J FAB | L1 PENTAMER, QUASI-HPV16, L1 CAPSOMER, ROSIE ONLINE, VIRUS-IMMUNE SYSTEM COMPLEX
3j8v:E (TYR27) to (THR39) CRYO-EM RECONSTRUCTION OF QUASI-HPV16 COMPLEX WITH H16.14J FAB | L1 PENTAMER, QUASI-HPV16, L1 CAPSOMER, ROSIE ONLINE, VIRUS-IMMUNE SYSTEM COMPLEX
4mzt:B (GLU77) to (GLU89) MAZF FROM S. AUREUS CRYSTAL FORM II, C2221, 2.3 A | CCDB/MAZF FOLD, RIBONUCLEASE, MAZE, HYDROLASE
3j8w:A (TYR27) to (THR39) CRYO-EM RECONSTRUCTION OF QUASI-HPV16 COMPLEX WITH H263.A2 FAB | L1 PENTAMER, QUASI-HPV16, L1 CAPSOMER, ROSIE ONLINE, VIRUS-IMMUNE SYSTEM COMPLEX
3j8w:C (TYR27) to (THR39) CRYO-EM RECONSTRUCTION OF QUASI-HPV16 COMPLEX WITH H263.A2 FAB | L1 PENTAMER, QUASI-HPV16, L1 CAPSOMER, ROSIE ONLINE, VIRUS-IMMUNE SYSTEM COMPLEX
3j8w:D (TYR27) to (THR39) CRYO-EM RECONSTRUCTION OF QUASI-HPV16 COMPLEX WITH H263.A2 FAB | L1 PENTAMER, QUASI-HPV16, L1 CAPSOMER, ROSIE ONLINE, VIRUS-IMMUNE SYSTEM COMPLEX
3j8w:E (TYR27) to (THR39) CRYO-EM RECONSTRUCTION OF QUASI-HPV16 COMPLEX WITH H263.A2 FAB | L1 PENTAMER, QUASI-HPV16, L1 CAPSOMER, ROSIE ONLINE, VIRUS-IMMUNE SYSTEM COMPLEX
3j8z:A (TYR27) to (THR39) CRYO-EM RECONSTRUCTION OF QUASI-HPV16 COMPLEX WITH H16.1A FAB | L1 PENTAMER, QUASI-HPV16, L1 CAPSOMER, ROSIE ONLINE, VIRUS-IMMUNE SYSTEM COMPLEX
3j8z:C (TYR27) to (THR39) CRYO-EM RECONSTRUCTION OF QUASI-HPV16 COMPLEX WITH H16.1A FAB | L1 PENTAMER, QUASI-HPV16, L1 CAPSOMER, ROSIE ONLINE, VIRUS-IMMUNE SYSTEM COMPLEX
3j8z:D (TYR27) to (THR39) CRYO-EM RECONSTRUCTION OF QUASI-HPV16 COMPLEX WITH H16.1A FAB | L1 PENTAMER, QUASI-HPV16, L1 CAPSOMER, ROSIE ONLINE, VIRUS-IMMUNE SYSTEM COMPLEX
3j8z:E (TYR27) to (THR39) CRYO-EM RECONSTRUCTION OF QUASI-HPV16 COMPLEX WITH H16.1A FAB | L1 PENTAMER, QUASI-HPV16, L1 CAPSOMER, ROSIE ONLINE, VIRUS-IMMUNE SYSTEM COMPLEX
1jx0:B (PHE89) to (SER102) CHALCONE ISOMERASE--Y106F MUTANT | MONOMER, UNIQUE FOLD, ISOMERASE
1jx1:B (PHE89) to (SER102) CHALCONE ISOMERASE--T48A MUTANT | OPEN-FACED BETA SANDWICH, UNIQUE FOLD, ISOMERASE
3x0y:C (GLY157) to (GLY164) CRYSTAL STRUCTURE OF FMN-BOUND DSZC FROM RHODOCOCCUS ERYTHROPOLIS D-1 | DBT MONOOXYGENASE, DESULFURIZATION, ACYL-COA DEHYDROGENASE DOMAIN, FMN-DEPENDENT, OXIDOREDUCTASE
1jyi:B (SER164) to (PHE175) CONCANAVALIN A/12-MER PEPTIDE COMPLEX | LECTIN, SUGAR BINDING PROTEIN
3zbd:A (GLY40) to (ILE62) STRUCTURE OF TGEV NSP1 | VIRAL PROTEIN, CORONAVIRUS, ALPHACORONAVIRUS, NSP1
2je4:B (ASP30) to (GLY49) ATOMIC-RESOLUTION CRYSTAL STRUCTURE OF CHEMICALLY-SYNTHESIZED HIV-1 PROTEASE IN COMPLEX WITH JG-365 | PROTEASE, HYDROLASE, HIGH RESOLUTION, ASPARTYL PROTEASE, HUMAN IMMUNODEFICIENCY VIRUS 1, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1w5w:A (ASP30) to (GLY49) HIV-1 PROTEASE IN COMPLEX WITH FLUORO SUBSTITUTED DIOL- BASED C2-SYMMETRIC INHIBITOR | HYDROLASE/HYDROLASE INHIBITOR, HYDROLASE, DIMER, PROTEIN-INHIBITOR COMPLEX
1w5x:A (ASP30) to (GLY49) HIV-1 PROTEASE IN COMPLEX WITH FLUORO SUBSTITUTED DIOL- BASED C2-SYMMETRIC INHIBITOR | HYDROLASE/HYDROLASE INHIBITOR, HYDROLASE, DIMER, PROTEIN-INHIBITOR COMPLEX
1w5y:A (ASP30) to (GLY49) HIV-1 PROTEASE IN COMPLEX WITH FLUORO SUBSTITUTED DIOL- BASED C2-SYMMETRIC INHIBITOR | HYDROLASE/HYDROLASE INHIBITOR, HYDROLASE, DIMER, PROTEIN-INHIBITOR COMPLEX
5bn4:A (GLU155) to (ILE164) STRUCTURE OF A UNIQUE ATP SYNTHASE NEQA-NEQB IN COMPLEX WITH ANP FROM NANOARCHEAUM EQUITANS | ATP SYNTHASE, NANOARCHEAUM EQUITANS, CATALYTIC CORE, HYDROLASE
2xtw:A (ALA2) to (ARG12) STRUCTURE OF QNRB1 (FULL LENGTH), A PLASMID-MEDIATED FLUOROQUINOLONE RESISTANCE PROTEIN | CELL CYCLE, PENTAPEPTIDE REPEAT, PRP, ANTIBIOTIC RESISTANCE, RIGHT HANDED QUADRILATERAL BETA-HELIX
2xtw:B (HIS173) to (GLY193) STRUCTURE OF QNRB1 (FULL LENGTH), A PLASMID-MEDIATED FLUOROQUINOLONE RESISTANCE PROTEIN | CELL CYCLE, PENTAPEPTIDE REPEAT, PRP, ANTIBIOTIC RESISTANCE, RIGHT HANDED QUADRILATERAL BETA-HELIX
2xtx:A (ALA2) to (ASN22) STRUCTURE OF QNRB1 (M102R-TRYPSIN TREATED), A PLASMID- MEDIATED FLUOROQUINOLONE RESISTANCE PROTEIN | CELL CYCLE, PENTAPEPTIDE REPEAT, PRP, ANTIBIOTIC RESISTANCE, RIGHT HANDED QUADRILATERAL BETA-HELIX
2xtx:A (ASN22) to (GLY32) STRUCTURE OF QNRB1 (M102R-TRYPSIN TREATED), A PLASMID- MEDIATED FLUOROQUINOLONE RESISTANCE PROTEIN | CELL CYCLE, PENTAPEPTIDE REPEAT, PRP, ANTIBIOTIC RESISTANCE, RIGHT HANDED QUADRILATERAL BETA-HELIX
2xtx:B (ALA2) to (ASN22) STRUCTURE OF QNRB1 (M102R-TRYPSIN TREATED), A PLASMID- MEDIATED FLUOROQUINOLONE RESISTANCE PROTEIN | CELL CYCLE, PENTAPEPTIDE REPEAT, PRP, ANTIBIOTIC RESISTANCE, RIGHT HANDED QUADRILATERAL BETA-HELIX
2xtx:B (ASN22) to (GLY32) STRUCTURE OF QNRB1 (M102R-TRYPSIN TREATED), A PLASMID- MEDIATED FLUOROQUINOLONE RESISTANCE PROTEIN | CELL CYCLE, PENTAPEPTIDE REPEAT, PRP, ANTIBIOTIC RESISTANCE, RIGHT HANDED QUADRILATERAL BETA-HELIX
2jiv:A (LEU703) to (LYS716) CRYSTAL STRUCTURE OF EGFR KINASE DOMAIN T790M MUTATION IN COMPEX WITH HKI-272 | HKI272, HKI-272, RECEPTOR, CELL CYCLE, ATP-BINDING, TRANSFERASE, TYROSINE-PROTEIN KINASE, TRANSMEMBRANE, PHOSPHORYLATION, DISEASE MUTATION, NUCLEOTIDE-BINDING, ANTI-ONCOGENE, EPIDERMAL GROWTH FACTOR
4na9:H (GLN30) to (VAL53) FACTOR VIIA IN COMPLEX WITH THE INHIBITOR 3'-AMINO-5'-[(2S,4R)-6- CARBAMIMIDOYL-4-PHENYL-1,2,3,4-TETRAHYDROQUINOLIN-2-YL]BIPHENYL-2- CARBOXYLIC ACID | SERINE PROTEASE, HYDROLASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM-BINDING, GLYCOPROTEIN, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
2xwd:A (LEU383) to (PRO401) X-RAY STRUCTURE OF ACID-BETA-GLUCOSIDASE WITH 5N,6O-(N'-(N- OCTYL)IMINO)NOJIRIMYCIN IN THE ACTIVE SITE | GLUCOCEREBROSIDASE, HYDROLASE, GAUCHER DISEASE, SPHINGOLIPID METABOLISM
2xwd:B (LEU383) to (PRO401) X-RAY STRUCTURE OF ACID-BETA-GLUCOSIDASE WITH 5N,6O-(N'-(N- OCTYL)IMINO)NOJIRIMYCIN IN THE ACTIVE SITE | GLUCOCEREBROSIDASE, HYDROLASE, GAUCHER DISEASE, SPHINGOLIPID METABOLISM
2xwe:A (LEU383) to (PRO401) X-RAY STRUCTURE OF ACID-BETA-GLUCOSIDASE WITH 5N,6S-(N'-(N- OCTYL)IMINO)-6-THIONOJIRIMYCIN IN THE ACTIVE SITE | GLUCOCEREBROSIDASE, HYDROLASE, GAUCHER DISEASE, SPHINGOLIPID METABOLISM
2xwe:B (LEU383) to (PRO401) X-RAY STRUCTURE OF ACID-BETA-GLUCOSIDASE WITH 5N,6S-(N'-(N- OCTYL)IMINO)-6-THIONOJIRIMYCIN IN THE ACTIVE SITE | GLUCOCEREBROSIDASE, HYDROLASE, GAUCHER DISEASE, SPHINGOLIPID METABOLISM
1k27:A (ASP106) to (MET119) CRYSTAL STRUCTURE OF 5'-DEOXY-5'-METHYLTHIOADENOSINE PHOSPHORYLASE IN COMPLEX WITH A TRANSITION STATE ANALOGUE | MTAP, METHYLTHIOADENOSINE PHOSPHORYLASE, TRANSITION STATE ANALOGUE, PHOSPHATE, TRANSFERASE
1k2r:A (GLY325) to (GLY333) STRUCTURE OF RAT BRAIN NNOS HEME DOMAIN COMPLEXED WITH NG- NITRO-L-ARGININE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE PROTEIN, OXIDOREDUCTASE
1k2r:B (GLY325) to (GLY333) STRUCTURE OF RAT BRAIN NNOS HEME DOMAIN COMPLEXED WITH NG- NITRO-L-ARGININE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE PROTEIN, OXIDOREDUCTASE
4nb8:C (ALA199) to (GLY207) OXYGENASE WITH ILE262 REPLACED BY LEU AND FERREDOXIN COMPLEX OF CARBAZOLE 1,9A-DIOXYGENASE | RIESKE NON-HEME IRON OXYGENASE, CARBAZOLE 1,9A-DIOXYGENASE, OXIDOREDUCTASE
1k2s:A (GLY325) to (GLY333) STRUCTURE OF RAT BRAIN NNOS HEME DOMAIN COMPLEXED WITH NG- ALLYL-L-ARGININE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE PROTEIN, OXIDOREDUCTASE
1k2s:B (GLY325) to (GLY333) STRUCTURE OF RAT BRAIN NNOS HEME DOMAIN COMPLEXED WITH NG- ALLYL-L-ARGININE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE PROTEIN, OXIDOREDUCTASE
1k2s:B (GLN464) to (ASN476) STRUCTURE OF RAT BRAIN NNOS HEME DOMAIN COMPLEXED WITH NG- ALLYL-L-ARGININE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE PROTEIN, OXIDOREDUCTASE
1k2t:A (GLY325) to (GLY333) STRUCTURE OF RAT BRAIN NNOS HEME DOMAIN COMPLEXED WITH S- ETHYL-N-PHENYL-ISOTHIOUREA | NITRIC OXIDE SYNTHASE, HEME-THIOLATE PROTEIN, OXIDOREDUCTASE
1k2t:B (GLY325) to (GLY333) STRUCTURE OF RAT BRAIN NNOS HEME DOMAIN COMPLEXED WITH S- ETHYL-N-PHENYL-ISOTHIOUREA | NITRIC OXIDE SYNTHASE, HEME-THIOLATE PROTEIN, OXIDOREDUCTASE
1k2u:A (GLY325) to (GLY333) STRUCTURE OF RAT BRAIN NNOS HEME DOMAIN COMPLEXED WITH S- ETHYL-N-[4-(TRIFLUOROMETHYL)PHENYL] ISOTHIOUREA | NITRIC OXIDE SYNTHASE, HEME-THIOLATE PROTEIN, OXIDOREDUCTASE
1k2u:B (GLY325) to (GLY333) STRUCTURE OF RAT BRAIN NNOS HEME DOMAIN COMPLEXED WITH S- ETHYL-N-[4-(TRIFLUOROMETHYL)PHENYL] ISOTHIOUREA | NITRIC OXIDE SYNTHASE, HEME-THIOLATE PROTEIN, OXIDOREDUCTASE
4nbg:C (ALA199) to (GLY207) OXYGENASE WITH GLN282 REPLACED BY TYR AND FERREDOXIN COMPLEX OF CARBAZOLE 1,9A-DIOXYGENASE | RIESKE NON-HEME IRON OXYGENASE, CARBAZOLE 1,9A-DIOXYGENASE, OXIDOREDUCTASE
1waj:A (PRO35) to (ASP51) DNA POLYMERASE FROM BACTERIOPHAGE RB69 | NUCLEOTIDYLTRANSFERASE, RB69 DNA POLYMERASE (GP43)
1k32:F (GLY79) to (PHE86) CRYSTAL STRUCTURE OF THE TRICORN PROTEASE | PROTEIN DEGRADATION, SUBSTRATE GATING, SERINE PROTEASE, BETA PROPELLER, PROTEASOME, HYDROLASE
1wbk:A (ASP30) to (GLY49) HIV-1 PROTEASE IN COMPLEX WITH ASYMMETRIC INHIBITOR, BEA568 | HYDROLASE/INHIBITOR, HYDROLASE/INHIBITOR COMPLEX, AIDS, ASPARTYL PROTEASE, DIMER, HYDROLASE, HYDROLASE/HYDROLASE INHIBITOR, PROTEIN-INHIBITOR COMPLEX
1wbm:A (ASP30) to (GLY49) HIV-1 PROTEASE IN COMPLEX WITH SYMMETRIC INHIBITOR, BEA450 | HYDROLASE/INHIBITOR, HYDROLASE/INHIBITOR COMPLEX, AIDS, ASPARTYL PROTEASE, DIMER, HYDROLASE, HYDROLASE/HYDROLASE INHIBITOR, PROTEIN-INHIBITOR COMPLEX
1wbl:A (ILE109) to (PRO117) WINGED BEAN LECTIN COMPLEXED WITH METHYL-ALPHA-D-GALACTOSE | LEGUME LECTIN, GLYCOSYLATED PROTEIN, BLOOD GROUP SPECIFICITY, QUATERNARY ASSOCIATION, AGGLUTININ, LECTIN
1wbl:D (ILE109) to (PRO117) WINGED BEAN LECTIN COMPLEXED WITH METHYL-ALPHA-D-GALACTOSE | LEGUME LECTIN, GLYCOSYLATED PROTEIN, BLOOD GROUP SPECIFICITY, QUATERNARY ASSOCIATION, AGGLUTININ, LECTIN
2xyf:B (ASP130) to (ILE150) HIV-1 INHIBITORS WITH A TERTIARY-ALCOHOL-CONTAINING TRANSITION-STATE MIMIC AND VARIOUS P2 AND P1 PRIME SUBSTITUENTS | HYDROLASE, AIDS
2jkx:A (LYS223) to (MET233) GALACTOSE OXIDASE. MATGO. COPPER FREE, EXPRESSED IN PICHIA PASTORIS. | METAL-BINDING, THIOETHER BOND, OXIDOREDUCTASE, COPPER, SECRETED, OXIDASES, KELCH REPEAT, COPPER ENZYMES, ENZYME CATALYSIS, PROTEIN ENGINEERING
1wcq:A (LEU503) to (ILE511) MUTAGENESIS OF THE NUCLEOPHILIC TYROSINE IN A BACTERIAL SIALIDASE TO PHENYLALANINE. | HYDROLASE, SIALIDASE, MICROMONOSPORA VIRIDIFACIENS, HYDROLASE NEURAMINIDASE, GLYCOSIDASE
2jmc:A (GLU53) to (SER64) CHIMER BETWEEN SPC-SH3 AND P41 | CHIMER, SPC-SH3, P41, SIGNALING PROTEIN
2joa:A (GLY427) to (ILE435) HTRA1 BOUND TO AN OPTIMIZED PEPTIDE: NMR ASSIGNMENT OF PDZ DOMAIN AND LIGAND RESONANCES | PDZ, BETA-SANDWICH, CYCLICALLY-PERMUTED, PROTEIN BINDING
4nf4:A (LEU6) to (PRO21) CRYSTAL STRUCTURE OF GLUN1/GLUN2A LIGAND-BINDING DOMAIN IN COMPLEX WITH DCKA AND GLUTAMATE | RECEPTOR, DCKA AND GLUTAMATE, TRANSPORT PROTEIN
4nf6:A (LEU6) to (PRO21) CRYSTAL STRUCTURE OF GLUN1/GLUN2A LIGAND-BINDING DOMAIN IN COMPLEX WITH GLYCINE AND PPDA | RECEPTOR, GLYCINE AND PPDA, TRANSPORT PROTEIN
4nf6:B (SER10) to (ASP24) CRYSTAL STRUCTURE OF GLUN1/GLUN2A LIGAND-BINDING DOMAIN IN COMPLEX WITH GLYCINE AND PPDA | RECEPTOR, GLYCINE AND PPDA, TRANSPORT PROTEIN
4nfe:A (GLN30) to (THR54) HUMAN KALLIKREIN-RELATED PEPTIDASE 2 IN COMPLEX WITH BENZAMIDINE | CHYMOTRYPSIN-LIKE PROTEASE, ZINC BINDING, EXTRACELLULAR, HYDROLASE
4nga:H (GLN30) to (VAL53) FACTOR VIIA IN COMPLEX WITH THE INHIBITOR (2R)-2-[(1-AMINOISOQUINOLIN- 6-YL)AMINO]-2-[3-ETHOXY-4-(PROPAN-2-YLOXY)PHENYL]-N-[2-(PROPAN-2- YLSULFONYL)BENZYL]ETHANAMIDE | GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM-BINDING, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
1k9o:E (GLN30) to (SER54) CRYSTAL STRUCTURE OF MICHAELIS SERPIN-TRYPSIN COMPLEX | MICHAELIS SERPIN-PROTEASE COMPLEX INHIBITORY TRIAD, HYDROLASE/HYDROLASE INHIBITOR COMPLEX
4niw:A (GLN30) to (SER54) CRYSTAL STRUCTURE OF TRYPSILIGASE (K60E/N143H/Y151H/D189K TRYPSIN) ORTHORHOMBIC FORM | TRYPSIN, SERINE PROTEINASE, ENZYME DESIGN, ACTIVATION DOMAIN, ZYMOGEN, PEPTIDE LIGATION, REVERSE PROTEOLYSIS, HYDROLASE
4nix:A (GLN30) to (SER54) CRYSTAL STRUCTURE OF TRYPSILIGASE (K60E/N143H/Y151H/D189K TRYPSIN) ORTHORHOMBIC FORM, ZINC-BOUND | TRYPSIN, SERINE PROTEINASE, ENZYME DESIGN, ACTIVATION DOMAIN, ZYMOGEN, PEPTIDE LIGATION, REVERSE PROTEOLYSIS, HYDROLASE
1wnd:A (LEU307) to (PRO321) ESCHERICHIA COLI YDCW GENE PRODUCT IS A MEDIUM-CHAIN ALDEHYDE DEHYDROGENASE AS DETERMINED BY KINETICS AND CRYSTAL STUCTURE | ALDEHYDE DEHYDROGENASE, NADH, FLUORESCENCE, KINETICS, OXIDOREDUCTASE
1wnd:C (LEU307) to (PRO321) ESCHERICHIA COLI YDCW GENE PRODUCT IS A MEDIUM-CHAIN ALDEHYDE DEHYDROGENASE AS DETERMINED BY KINETICS AND CRYSTAL STUCTURE | ALDEHYDE DEHYDROGENASE, NADH, FLUORESCENCE, KINETICS, OXIDOREDUCTASE
1wnd:D (LEU307) to (PRO321) ESCHERICHIA COLI YDCW GENE PRODUCT IS A MEDIUM-CHAIN ALDEHYDE DEHYDROGENASE AS DETERMINED BY KINETICS AND CRYSTAL STUCTURE | ALDEHYDE DEHYDROGENASE, NADH, FLUORESCENCE, KINETICS, OXIDOREDUCTASE
2y5b:A (ARG454) to (LEU463) STRUCTURE OF USP21 IN COMPLEX WITH LINEAR DIUBIQUITIN-ALDEHYDE | PROTEIN BINDING-HYDROLASE COMPLEX, UBIQUITIN, UBIQUITIN SPECIFIC PROTEASE, USP, NEDD8, ISG15, CELL SIGNALING
1ken:A (GLY256) to (MET268) INFLUENZA VIRUS HEMAGGLUTININ COMPLEXED WITH AN ANTIBODY THAT PREVENTS THE HEMAGGLUTININ LOW PH FUSOGENIC TRANSITION | HEMAGGLUTININ, ENVELOPE PROTEIN, GLYCOPROTEIN, VIRAL PROTEIN-IMMUNE SYSTEM COMPLEX
1ken:C (GLY256) to (MET268) INFLUENZA VIRUS HEMAGGLUTININ COMPLEXED WITH AN ANTIBODY THAT PREVENTS THE HEMAGGLUTININ LOW PH FUSOGENIC TRANSITION | HEMAGGLUTININ, ENVELOPE PROTEIN, GLYCOPROTEIN, VIRAL PROTEIN-IMMUNE SYSTEM COMPLEX
3zos:B (ARG609) to (GLN620) STRUCTURE OF THE DDR1 KINASE DOMAIN IN COMPLEX WITH PONATINIB | TRANSFERASE, RTK, COLLAGEN, DISCOIDIN DOMAIN
1wtg:H (GLN30) to (VAL53) HUMAN FACTOR VIIA-TISSUE FACTOR COMPLEXED WITH ETHYLSULFONAMIDE-D-BIPHENYLALANINE-GLN-P-AMINOBENZAMIDINE | SERINE PROTEASE, HYDROLASE/BLOOD CLOTTING COMPLEX
4nmj:D (LEU314) to (PRO329) THERMOSTABLE ALDEHYDE DEHYDROGENASE FROM PYROBACULUM SP. COMPLEXED WITH NADP+ AT 2 A RESOLUTION | ALDEHYDE OXIDATION, NADP REDUCTION, INTRACELLULAR, OXIDOREDUCTASE
5c1x:A (LYS130) to (ASN139) CRYSTAL STRUCTURE OF EV71 3C PROTEINASE IN COMPLEX WITH COMPOUND VIII | HYDROLASE, CYSTEINE PROTEINASE, INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5c1x:B (LYS130) to (ASN139) CRYSTAL STRUCTURE OF EV71 3C PROTEINASE IN COMPLEX WITH COMPOUND VIII | HYDROLASE, CYSTEINE PROTEINASE, INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3zqa:D (ILE313) to (PRO327) CRYSTALLOGRAPHIC STRUCTURE OF BETAINE ALDEHYDE DEHYDROGENASE MUTANT C286A FROM PSEUDOMONAS AERUGINOSA IN COMPLEX WITH NADPH | ALDEHYDE OXIDATION, NADPH COMPLEX, OXIDOREDUCTASE
5c2v:D (GLY150) to (ALA159) KUENENIA STUTTGARTIENSIS HYDRAZINE SYNTHASE | BETA PROPELLER, HEME C, REDOX ENZYME, ANAMMOX, OXIDOREDUCTASE
1kkm:B (GLU135) to (ASP145) L.CASEI HPRK/P IN COMPLEX WITH B.SUBTILIS P-SER-HPR | PHOSPHORYLATION, PROTEIN KINASE, BACTERIA, PROTEIN/PROTEIN INTERACTION, PHOSPHOSERINE, TRANSFERASE, HYDROLASE/TRANSPORT PROTEIN COMPLEX, TRANSFERASE, HYDROLASE/TRANSPORT PROTEIN COMPLEX
3zsc:A (ALA141) to (TYR150) CATALYTIC FUNCTION AND SUBSTRATE RECOGNITION OF THE PECTATE LYASE FROM THERMOTOGA MARITIMA | LYASE, HYDROLASE
1kli:H (GLN30) to (VAL53) COFACTOR-AND SUBSTRATE-ASSISTED ACTIVATION OF FACTOR VIIA | EXTRINSIC COAGULATION PATHWAY, SERINE PROTEASE ACTIVATION, RATIONAL DRUG DESIGN, SUBSTRATE-ASSISTED CATALYSIS, HYDROLASE
1wzo:D (GLU28) to (LEU39) CRYSTAL STRUCTURE OF THE HPCE FROM THERMUS THERMOPHILUS HB8 | STRUCTURAL GENOMICS, HPCE, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, NPPSFA, ISOMERASE
1kob:B (PRO41) to (GLU57) TWITCHIN KINASE FRAGMENT (APLYSIA), AUTOREGULATED PROTEIN KINASE DOMAIN | KINASE, TWITCHIN, INTRASTERIC REGULATION
1ko7:A (THR133) to (ASP141) X-RAY STRUCTURE OF THE HPR KINASE/PHOSPHATASE FROM STAPHYLOCOCCUS XYLOSUS AT 1.95 A RESOLUTION | PROTEIN KINASE, PHOSPHOTRANSFER, PROTEIN PHOSPHATASE, DUAL ACTIVITY, PRODUCT, SUBSTRATE, TRANSFERASE, HYDROLASE, TRANSFERASE,HYDROLASE
5c4a:G (VAL86) to (SER95) CRYSTAL STRUCTURE OF A TRANSCRIBING RNA POLYMERASE II COMPLEX REVEALS A COMPLETE TRANSCRIPTION BUBBLE | PROTEIN-DNA COMPLEX, RNA POLYMERASE II, TRANSCRIBING COMPLEX, TRANSCRIPTION BUBBLE, TRANSFERASE-RNA-DNA COMPLEX
1x71:C (GLY29) to (GLY38) CRYSTAL STRUCTURE OF SIDEROCALIN (NGAL, LIPOCALIN 2) COMPLEXED WITH TRENCAM-3,2-HOPO, A CEPABACTIN ANALOGUE | LIPOCALIN, SIDEROPHORE, ANTIMICROBIAL PROTEIN
1x89:B (GLY29) to (GLY38) CRYSTAL STRUCTURE OF SIDEROCALIN (NGAL, LIPOCALIN 2) COMPLEXED WITH CARBOXYMYCOBACTIN S | LIPOCALIN, SIDEROPHORE, ANTIMICROBIAL PROTEIN
1x89:C (GLY29) to (GLY38) CRYSTAL STRUCTURE OF SIDEROCALIN (NGAL, LIPOCALIN 2) COMPLEXED WITH CARBOXYMYCOBACTIN S | LIPOCALIN, SIDEROPHORE, ANTIMICROBIAL PROTEIN
1xa0:B (ASP32) to (ASN43) CRYSTAL STRUCTURE OF MCSG TARGET APC35536 FROM BACILLUS STEAROTHERMOPHILUS | STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, MCSG, PSI, MIDWEST CENTER FOR STRUCTURAL GENOMICS, UNKNOWN FUNCTION
3zyt:A (MET1) to (PRO8) STRUCTURE DETERMINATION OF ESTA FROM ARTHROBACTER NITROGUAJACOLICUS RUE61A | HYDROLASE, ENZYMATIC PROMISCUITY, BETA-LACTAMASE
5c8n:A (GLU711) to (ALA722) EGFR KINASE DOMAIN MUTANT "TMLR" WITH COMPOUND 23 | PROTEIN KINASE INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
1kxz:G (ILE8) to (THR17) MT0146, THE PRECORRIN-6Y METHYLTRANSFERASE (CBIT) HOMOLOG FROM M. THERMOAUTOTROPHICUM, P1 SPACEGROUP | STRUCTURAL GENOMICS, BETA BARREL, ROSSMANN FOLD, TETRAMER, METHYLTRANSFERASE, DECARBOXYLASE, TRANSFERASE, LYASE
1l1d:A (PRO417) to (THR446) CRYSTAL STRUCTURE OF THE C-TERMINAL METHIONINE SULFOXIDE REDUCTASE DOMAIN (MSRB) OF N. GONORRHOEAE PILB | CACODYLATE COMPLEX, CYS-ARG-ASP CATALYTIC TRIAD, MET-R(O) REDUCTASE, OXIDOREDUCTASE, MSRB
2nqr:B (GLY391) to (ASN405) MOEA D142N | MOLYBDOPTERIN, MPT, MOCO, MOLYBDENUM, MOEA, MOGA, GEPHYRIN, CNX1, CINNAMON, BIOSYNTHETIC PROTEIN
4a0b:C (ILE394) to (ASP403) STRUCTURE OF HSDDB1-DRDDB2 BOUND TO A 16 BP CPD-DUPLEX ( PYRIMIDINE AT D-1 POSITION) AT 3.8 A RESOLUTION (CPD 4) | DNA BINDING PROTEIN-DNA COMPLEX, DNA DAMAGE REPAIR
2nsu:A (ALA226) to (ASN236) CRYSTAL STRUCTURE OF THE ECTODOMAIN OF HUMAN TRANSFERRIN RECEPTOR FITTED INTO A CRYO-EM RECONSTRUCTION OF CANINE PARVOVIRUS AND FELINE TRANSFERRIN RECEPTOR COMPLEX | TRANSFERRIN RECEPTOR, VIRUS-RECEPTOR COMPLEX, METAL TRANSPORT
2nsu:B (ALA226) to (ASN236) CRYSTAL STRUCTURE OF THE ECTODOMAIN OF HUMAN TRANSFERRIN RECEPTOR FITTED INTO A CRYO-EM RECONSTRUCTION OF CANINE PARVOVIRUS AND FELINE TRANSFERRIN RECEPTOR COMPLEX | TRANSFERRIN RECEPTOR, VIRUS-RECEPTOR COMPLEX, METAL TRANSPORT
2nsx:B (LEU383) to (PRO401) STRUCTURE OF ACID-BETA-GLUCOSIDASE WITH PHARMACOLOGICAL CHAPERONE PROVIDES INSIGHT INTO GAUCHER DISEASE | TIM-BARREL GLYCOSIDASE CEREZYME HYDROLYSIS, HYDROLASE
2nsx:D (LEU383) to (PRO401) STRUCTURE OF ACID-BETA-GLUCOSIDASE WITH PHARMACOLOGICAL CHAPERONE PROVIDES INSIGHT INTO GAUCHER DISEASE | TIM-BARREL GLYCOSIDASE CEREZYME HYDROLYSIS, HYDROLASE
2nt0:A (LEU383) to (PRO401) ACID-BETA-GLUCOSIDASE LOW PH, GLYCEROL BOUND | CEREZYME, GLUCOCEREBROSIDASE, GLUCOSYLCERAMIDE, HYDROLYSIS, GAUCHER DISEASE, HYDROLASE
2nt0:B (LEU383) to (PRO401) ACID-BETA-GLUCOSIDASE LOW PH, GLYCEROL BOUND | CEREZYME, GLUCOCEREBROSIDASE, GLUCOSYLCERAMIDE, HYDROLYSIS, GAUCHER DISEASE, HYDROLASE
2nt0:C (LEU383) to (PRO401) ACID-BETA-GLUCOSIDASE LOW PH, GLYCEROL BOUND | CEREZYME, GLUCOCEREBROSIDASE, GLUCOSYLCERAMIDE, HYDROLYSIS, GAUCHER DISEASE, HYDROLASE
2nt0:D (LEU383) to (PRO401) ACID-BETA-GLUCOSIDASE LOW PH, GLYCEROL BOUND | CEREZYME, GLUCOCEREBROSIDASE, GLUCOSYLCERAMIDE, HYDROLYSIS, GAUCHER DISEASE, HYDROLASE
2nt9:A (THR206) to (ALA220) CRYSTAL STRUCTURE OF PECTIN METHYLESTERASE D178A MUTANT IN COMPLEX WITH HEXASACCHARIDE IV | MICHAELIS COMPLEX, HYDROLASE
2nt9:B (THR206) to (ALA220) CRYSTAL STRUCTURE OF PECTIN METHYLESTERASE D178A MUTANT IN COMPLEX WITH HEXASACCHARIDE IV | MICHAELIS COMPLEX, HYDROLASE
2ntb:A (GLY287) to (ASN298) CRYSTAL STRUCTURE OF PECTIN METHYLESTERASE IN COMPLEX WITH HEXASACCHARIDE V | PRODUCT COMPLEX, HYDROLASE
2ntb:B (GLY287) to (ASN298) CRYSTAL STRUCTURE OF PECTIN METHYLESTERASE IN COMPLEX WITH HEXASACCHARIDE V | PRODUCT COMPLEX, HYDROLASE
3jt3:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N~5~-[2-(METHYLSULFANYL)ETHANIMIDOYL]-L- ORNITHINE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE ENZYME, SUBSTRATE- ANALOGUE INHIBITOR, THIOETHER HEME LIGAND, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3jt3:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N~5~-[2-(METHYLSULFANYL)ETHANIMIDOYL]-L- ORNITHINE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE ENZYME, SUBSTRATE- ANALOGUE INHIBITOR, THIOETHER HEME LIGAND, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3jt4:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N~5~-[(3-(ETHYLSULFANYL)PROPANIMIDOYL]-L- ORNITHINE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE ENZYME, SUBSTRATE- ANALOGUE INHIBITOR, THIOETHER HEME LIGAND, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3jt4:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N~5~-[(3-(ETHYLSULFANYL)PROPANIMIDOYL]-L- ORNITHINE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE ENZYME, SUBSTRATE- ANALOGUE INHIBITOR, THIOETHER HEME LIGAND, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3jt5:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N~5~-[2-(ETHYLSULFANYL)ETHANIMIDOYL]-L- ORNITHINE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE ENZYME, SUBSTRATE- ANALOGUE INHIBITOR, THIOETHER HEME LIGAND, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3jt5:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N~5~-[2-(ETHYLSULFANYL)ETHANIMIDOYL]-L- ORNITHINE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE ENZYME, SUBSTRATE- ANALOGUE INHIBITOR, THIOETHER HEME LIGAND, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
2ymz:B (SER40) to (PRO48) CRYSTAL STRUCTURE OF CHICKEN GALECTIN 2 | SUGAR BINDING PROTEIN, CARBOHYDRATE RECOGNITION
3jt6:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N~5~-[4-(METHYLSULFANYL)BUTANIMIDOYL]-L- ORNITHINE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE ENZYME, SUBSTRATE- ANALOGUE INHIBITOR, THIOETHER HEME LIGAND, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3jt6:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N~5~-[4-(METHYLSULFANYL)BUTANIMIDOYL]-L- ORNITHINE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE ENZYME, SUBSTRATE- ANALOGUE INHIBITOR, THIOETHER HEME LIGAND, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3jt7:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N~5~-[2-(PROPYLSULFANYL)ETHANIMIDOYL]-L- ORNITHINE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE ENZYME, SUBSTRATE- ANALOGUE INHIBITOR, THIOETHER HEME LIGAND, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3jt7:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N~5~-[2-(PROPYLSULFANYL)ETHANIMIDOYL]-L- ORNITHINE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE ENZYME, SUBSTRATE- ANALOGUE INHIBITOR, THIOETHER HEME LIGAND, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3jt8:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N~5~-{3-[(1-METHYLETHYL) SULFANYL]PROPANIMIDOYL}-L-ORNITHINE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE ENZYME, SUBSTRATE- ANALOGUE INHIBITOR, THIOETHER HEME LIGAND, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3jt8:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N~5~-{3-[(1-METHYLETHYL) SULFANYL]PROPANIMIDOYL}-L-ORNITHINE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE ENZYME, SUBSTRATE- ANALOGUE INHIBITOR, THIOETHER HEME LIGAND, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3jt9:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN THE FERROUS STATE COMPLEXED WITH N~5~-[2-(ETHYLSULFANYL) ETHANIMIDOYL]-L-ORNITHINE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE ENZYME, SUBSTRATE- ANALOGUE INHIBITOR, THIOETHER HEME LIGAND, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3jt9:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN THE FERROUS STATE COMPLEXED WITH N~5~-[2-(ETHYLSULFANYL) ETHANIMIDOYL]-L-ORNITHINE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE ENZYME, SUBSTRATE- ANALOGUE INHIBITOR, THIOETHER HEME LIGAND, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3juh:B (ASP38) to (LYS49) CRYSTAL STRUCTURE OF A MUTANT OF HUMAN PROTEIN KINASE CK2ALPHA WITH ALTERED COSUBSTRATE SPECIFICITY | EUKARYOTIC PROTEIN KINASE, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, WNT SIGNALING PATHWAY
4a0p:A (VAL1051) to (ARG1060) CRYSTAL STRUCTURE OF LRP6P3E3P4E4 | SIGNALING, LRP6, WNT SIGNALLING, WNT3A, DKK1, MESD
1l8p:A (GLY366) to (GLU379) MG-PHOSPHONOACETOHYDROXAMATE COMPLEX OF S39A YEAST ENOLASE 1 | BETA BARREL, LYASE
3jws:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE R349A MUTANT HEME DOMAIN COMPLEXED WITH N1-[(3' S,4'S)-4'-((6"-AMINO-4"-METHYLPYRIDIN-2"-YL) METHYL)PYRROLIDIN-3'-YL]-N2-(3'-FLUOROPHENETHYL)ETHANE-1,2-DIAMINE TETRAHYDROCHLORIDE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jws:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE R349A MUTANT HEME DOMAIN COMPLEXED WITH N1-[(3' S,4'S)-4'-((6"-AMINO-4"-METHYLPYRIDIN-2"-YL) METHYL)PYRROLIDIN-3'-YL]-N2-(3'-FLUOROPHENETHYL)ETHANE-1,2-DIAMINE TETRAHYDROCHLORIDE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jwt:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE R349A MUTANT HEME DOMAIN IN COMPLEX WITH N1-{(3'R,4'R)-4'-[(6"-AMINO-4"-METHYLPYRIDIN- 2"-YL)METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL)ETHANE-1,2- DIAMINE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jwt:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE R349A MUTANT HEME DOMAIN IN COMPLEX WITH N1-{(3'R,4'R)-4'-[(6"-AMINO-4"-METHYLPYRIDIN- 2"-YL)METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL)ETHANE-1,2- DIAMINE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jwu:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE R349A MUTANT HEME DOMAIN IN COMPLEX WITH N1-{(3'R,4'S)-4'-[(6"-AMINO-4"-METHYLPYRIDIN- 2"-YL)METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL)ETHANE-1,2- DIAMINE TETRAHYDROCHLORIDE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jwu:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE R349A MUTANT HEME DOMAIN IN COMPLEX WITH N1-{(3'R,4'S)-4'-[(6"-AMINO-4"-METHYLPYRIDIN- 2"-YL)METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL)ETHANE-1,2- DIAMINE TETRAHYDROCHLORIDE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jwz:A (PRO95) to (GLY103) STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH N1-[(3' S,4' R)-4'-((6"-AMINO-4"-METHYLPYRIDIN-2"-YL)METHYL) PYRROLIDIN-3'-YL]-N2-(3'-FLUOROPHENETHYL)ETHANE-1,2-DIAMINE TETRAHYDROCHLORIDE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jx1:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE D597N MUTANT HEME DOMAIN IN COMPLEX WITH N1-{(3'R,4'R)-4'-[(6"-AMINO-4"-METHYLPYRIDIN- 2"-YL)METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL)ETHANE-1,2- DIAMINE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jx1:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE D597N MUTANT HEME DOMAIN IN COMPLEX WITH N1-{(3'R,4'R)-4'-[(6"-AMINO-4"-METHYLPYRIDIN- 2"-YL)METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL)ETHANE-1,2- DIAMINE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jx2:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH N1-{(3'S,4'S)-4'-[(6"-AMINO-4"- METHYLPYRIDIN-2"-YL)METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL) ETHANE-1,2-DIAMINE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jx2:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH N1-{(3'S,4'S)-4'-[(6"-AMINO-4"- METHYLPYRIDIN-2"-YL)METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL) ETHANE-1,2-DIAMINE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jx3:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH N1-{(3'R,4'R)-4'-[(6"-AMINO-4"- METHYLPYRIDIN-2"-YL)METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL) ETHANE-1,2-DIAMINE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jx3:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH N1-{(3'R,4'R)-4'-[(6"-AMINO-4"- METHYLPYRIDIN-2"-YL)METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL) ETHANE-1,2-DIAMINE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jx5:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH N1-{(3'S,4'R)-4'-[(6"-AMINO-4"- METHYLPYRIDIN-2"-YL)METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL) ETHANE-1,2-DIAMINE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jx5:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH N1-{(3'S,4'R)-4'-[(6"-AMINO-4"- METHYLPYRIDIN-2"-YL)METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL) ETHANE-1,2-DIAMINE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jx6:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V/Y706A MUTANT HEME DOMAIN COMPLEXED WITH N1-[(3' R,4' R)-4'-((6"-AMINO-4"- METHYLPYRIDIN-2"-YL)METHYL)PYRROLIDIN-3'-YL]-N2-(3'-FLUOROPHENETHYL) ETHANE-1,2-DIAMINE TETRAHYDROCHLORIDE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jx6:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V/Y706A MUTANT HEME DOMAIN COMPLEXED WITH N1-[(3' R,4' R)-4'-((6"-AMINO-4"- METHYLPYRIDIN-2"-YL)METHYL)PYRROLIDIN-3'-YL]-N2-(3'-FLUOROPHENETHYL) ETHANE-1,2-DIAMINE TETRAHYDROCHLORIDE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
4obh:C (ASP30) to (GLY49) CRYSTAL STRUCTURE OF INACTIVE HIV-1 PROTEASE IN COMPLEX WITH THE P1-P6 SUBSTRATE VARIANT (L449F) | CO-EVOLUTION, RESISTANCE, HYDROLASE
2yvk:B (PHE268) to (LYS280) CRYSTAL STRUCTURE OF 5-METHYLTHIORIBOSE 1-PHOSPHATE ISOMERASE PRODUCT COMPLEX FROM BACILLUS SUBTILIS | ISOMERASE, METHIONINE SALVAGE PATHWAY, CRYSTAL STRUCTURE
4oca:A (ASP9) to (MET18) CRYATAL STRUCTURE OF ARNB K188A COMPLEXTED WITH PLP AND UDP-ARA4N | AMINOTRANSFERASE, TRANSFERASE
1led:A (ASN2) to (LEU25) STRUCTURES OF THE LECTIN IV OF GRIFFONIA SIMPLICIFOLIA AND ITS COMPLEX WITH THE LEWIS B HUMAN BLOOD GROUP DETERMINANT AT 2.0 ANGSTROMS RESOLUTION | LECTIN
2yxd:B (ILE11) to (THR19) CRYSTAL STRUCTURE OF COBALAMIN BIOSYNTHESIS PRECORRIN 8W DECARBOXYLASE (CBIT) | ALPHA AND BETA PROTEIN (A/B) CLASS, METHYLTRANSFERASE SUPERFAMILY, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, TRANSFERASE
2yxe:A (ARG149) to (PRO157) CRYSTAL STRUCTURE OF L-ISOASPARTYL PROTEIN CARBOXYL METHYLTRANFERASE | ROSSMAN-TYPE FOLD, ALPHA/BETA/ALPHA SANDWICH STRUCTURE, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, TRANSFERASE
2nxl:A (ASP30) to (GLY49) STRUCTURE OF HIV-1 PROTEASE D25N COMPLEXED WITH THE RT-RH ANALOGUE PEPTIDE GLY-ALA-GLU-VAL-PHE*TYR-VAL-ASP-GLY-ALA | PEPTIDE DESIGN; MOLECULAR DYNAMICS; HIV PROTEASE; SUBSTRATE RECOGNITION; CALORIMETRY, HYDROLASE/HYDROLASE SUBSTRATE COMPLEX
2yyz:A (VAL276) to (ARG289) CRYSTAL STRUCTURE OF SUGAR ABC TRANSPORTER, ATP-BINDING PROTEIN | SUGAR TRANSPORT, ATP BINDING, ALPHA AND BETA PROTEINS (A/B) CLASS, TM0421, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, TRANSPORT PROTEIN
4of1:B (GLU77) to (GLU89) CRYSTAL STRUCTURE OF TOXIN FROM STAPHYLOCOCCUS AUREUS MU50 | TOXIN, RNASE
4of4:A (ILE220) to (ILE228) X-RAY STRUCTURE OF UNLIGANDED URIDINE PHOSPHORYLASE FROM YERSINIA PSEUDOTUBERCULOSIS AT 1.4 A RESOLUTION | ROSSMANN FOLD, TRANSFERASE, PYRIMIDINE BASE, PHOSPHATE ION
2z2w:A (GLU298) to (GLY308) HUMAND WEE1 KINASE COMPLEXED WITH INHIBITOR PF0335770 | WEE1 KINASE, INHIBITOR COMPLEX, TRANSFERASE
3k3s:G (ALA67) to (LEU84) CRYSTAL STRUCTURE OF ALTRONATE HYDROLASE (FRAGMENT 1-84) FROM SHIGELLA FLEXNERI. | ALTRONATE HYDROLASE, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, HYDROLASE
5clp:B (TYR39) to (LYS49) CRYSTAL STRUCTURE OF CK2ALPHA WITH 3,4-DICHLOROPHENETHYLAMINE BOUND | TRANSFERASE, CK2ALPHA, CK2A, FRAGMENT BASED DRUG DISCOVERY, HIGH CONCENTRATION SCREENING, SELECTIVE ATP COMPETITIVE INHIBITORS, SURFACE ENTROPHY REDUCTION
4oi7:A (CYS144) to (PRO151) RAGE RECOGNIZES NUCLEIC ACIDS AND PROMOTES INFLAMMATORY RESPONSES TO DNA | PROTEIN-DNA COMPLEX, IG FOLD, DNA BINDING, EXTRACELLULAR RECEPTOR, TRANSPORT PROTEIN,SIGNALING PROTEIN-DNA COMPLEX
4oi7:B (CYS144) to (PRO151) RAGE RECOGNIZES NUCLEIC ACIDS AND PROMOTES INFLAMMATORY RESPONSES TO DNA | PROTEIN-DNA COMPLEX, IG FOLD, DNA BINDING, EXTRACELLULAR RECEPTOR, TRANSPORT PROTEIN,SIGNALING PROTEIN-DNA COMPLEX
4oi8:A (CYS144) to (PRO151) RAGE IS A NUCLEIC ACID RECEPTOR THAT PROMOTES INFLAMMATORY RESPONSES TO DNA. | IG FOLD, DNA BINDING, TRANSPORT PROTEIN,SIGNALING PROTEIN-DNA COMPLEX
4oi8:B (CYS144) to (PRO151) RAGE IS A NUCLEIC ACID RECEPTOR THAT PROMOTES INFLAMMATORY RESPONSES TO DNA. | IG FOLD, DNA BINDING, TRANSPORT PROTEIN,SIGNALING PROTEIN-DNA COMPLEX
5cno:B (LEU679) to (LYS692) CRYSTAL STRUCTURE OF THE EGFR KINASE DOMAIN MUTANT V924R | KINASE EGFR, TRANSFERASE
2o2p:A (MET734) to (PRO748) CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF RAT 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE | ALDEHYDE DEHYDROGENASE, FDH, OXIDOREDUCTASE
2o2p:B (MET734) to (PRO748) CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF RAT 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE | ALDEHYDE DEHYDROGENASE, FDH, OXIDOREDUCTASE
2o2p:D (MET734) to (PRO748) CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF RAT 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE | ALDEHYDE DEHYDROGENASE, FDH, OXIDOREDUCTASE
2o2r:A (MET734) to (PRO748) CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF RAT 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH NADPH | ALDEHYDE DEHYDROGENASE, FDH, OXIDOREDUCTASE
2o2r:B (MET734) to (PRO748) CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF RAT 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH NADPH | ALDEHYDE DEHYDROGENASE, FDH, OXIDOREDUCTASE
1lpu:A (ASP38) to (LYS49) LOW TEMPERATURE CRYSTAL STRUCTURE OF THE APO-FORM OF THE CATALYTIC SUBUNIT OF PROTEIN KINASE CK2 FROM ZEA MAYS | PROTEIN KINASE, CK2, CASEIN KINASE 2, DUAL-COSUBSTRATE SPECIFICITY, TRANSFERASE
4a3q:A (LYS124) to (ASP143) THE 2.15 ANGSTROM RESOLUTION CRYSTAL STRUCTURE OF STAPHYLOCOCCUS AUREUS ALANINE RACEMASE | ISOMERASE, PLP-DEPENDENT ENZYMES
2o4s:A (ASP30) to (GLY49) CRYSTAL STRUCTURE OF HIV-1 PROTEASE (Q7K) IN COMPLEX WITH LOPINAVIR | PROTEASE, VIRAL PROTEIN
1lu1:A (ASN2) to (GLN19) THE STRUCTURE OF THE DOLICHOS BIFLORUS SEED LECTIN IN COMPLEX WITH THE FORSSMAN DISACCHARIDE | LEGUME LECTINS, FORSSMAN DISACCHARIDE, DOLICHOS BIFLORUS SEED LECTIN
1xkk:A (LEU703) to (LYS716) EGFR KINASE DOMAIN COMPLEXED WITH A QUINAZOLINE INHIBITOR- GW572016 | EGFR, EPIDERMAL GROWTH FACTOR RECEPTOR, KINASE, TRANSFERASE
4oj5:C (GLY395) to (GLY404) CRYSTAL STRUCTURE OF A PUTATIVE TAILSPIKE PROTEIN (TSP1, ORF210) FROM ESCHERICHIA COLI O157:H7 BACTERIOHAGE CBA120 | PARALLEL BETA HELIX, PUTATIVE ENDO-GLYCOSIDASE, BACTERIAL POLYSACCHARIDE, PHAGE BASEPLATE, PHAGE TAIL, VIRAL PROTEIN
1lvy:A (GLN30) to (MET53) PORCINE ELASTASE | SERINE PROTEASE, HYDROLASE, ZYMOGEN, PANCREAS
4ojc:A (LEU110) to (ILE124) CRYSTAL STRUCTURE OF THE WILD-TYPE FULL-LENGTH TRIMERIC ECTODOMAIN OF THE C. ELEGANS FUSION PROTEIN EFF-1 | CLASS II FUSION PROTEIN, MEMBRANE FUSION PROTEIN, CELL SURFACE, MEMBRANE PROTEIN
4ojl:B (GLY395) to (GLY404) CRYSTAL STRUCTURE OF PUTATIVE TAILSPIKE PROTEIN (TSP1, ORF210) FROM ESCHERICHIA COLI O157:H7 BACTERIOHAGE CBA120 IN COMPLEX WITH GLUCOSE | PARALLEL BETA HELIX, PUTATIVE ENDO-GLYCOSIDASE, BACTERIAL POLYSACCHARIDE, PHAGE BASEPLATE, PHAGE TAIL, VIRAL PROTEIN
4a6b:B (ASP130) to (ILE150) STEREOSELECTIVE SYNTHESIS, X-RAY ANALYSIS, AND BIOLOGICAL EVALUATION OF A NEW CLASS OF LACTAM BASED HIV-1 PROTEASE INHIBITORS | HYDROLASE, GAMMA-BUTYROL-LACTAM
4ojo:B (GLY395) to (GLY404) CRYSTAL STRUCTURE OF PUTATIVE TAILSPIKE PROTEIN (TSP1, ORF210) FROM ESCHERICHIA COLI O157:H7 BACTERIOHAGE CBA120 IN COMPLEX WITH LACTOSE | PARALLEL BETA HELIX, PUTATIVE ENDO-GLYCOSIDASE, BACTERIAL POLYSACCHARIDE, PHAGE BASEPLATE, PHAGE TAIL, VIRAL PROTEIN
4ojo:C (GLY395) to (GLY404) CRYSTAL STRUCTURE OF PUTATIVE TAILSPIKE PROTEIN (TSP1, ORF210) FROM ESCHERICHIA COLI O157:H7 BACTERIOHAGE CBA120 IN COMPLEX WITH LACTOSE | PARALLEL BETA HELIX, PUTATIVE ENDO-GLYCOSIDASE, BACTERIAL POLYSACCHARIDE, PHAGE BASEPLATE, PHAGE TAIL, VIRAL PROTEIN
4ojp:B (GLY395) to (GLY404) CRYSTAL STRUCTURE OF PUTATIVE TAILSPIKE PROTEIN (TSP1, ORF210) FROM ESCHERICHIA COLI O157:H7 BACTERIOHAGE CBA120 IN COMPLEX WITH MALTOSE | PARALLEL BETA HELIX, PUTATIVE ENDO-GLYCOSIDASE, BACTERIAL POLYSACCHARIDE, PHAGE BASEPLATE, PHAGE TAIL, VIRAL PROTEIN
1lzx:A (GLY325) to (GLY333) RAT NEURONAL NOS HEME DOMAIN WITH NG-HYDROXY-L-ARGININE BOUND | NITRIC OXIDE SYNTHASE, OXYDOREDUCTASE, HEME-ENZYME, OXIDOREDUCTASE
1lzx:B (GLY325) to (GLY333) RAT NEURONAL NOS HEME DOMAIN WITH NG-HYDROXY-L-ARGININE BOUND | NITRIC OXIDE SYNTHASE, OXYDOREDUCTASE, HEME-ENZYME, OXIDOREDUCTASE
1lzz:A (GLY325) to (GLY333) RAT NEURONAL NOS HEME DOMAIN WITH N-ISOPROPYL-N'-HYDROXYGUANIDINE BOUND | NITRIC OXIDE SYNTHASE, OXYDOREDUCTASE, HEME-ENZYME, OXIDOREDUCTASE
1lzz:B (GLY325) to (GLY333) RAT NEURONAL NOS HEME DOMAIN WITH N-ISOPROPYL-N'-HYDROXYGUANIDINE BOUND | NITRIC OXIDE SYNTHASE, OXYDOREDUCTASE, HEME-ENZYME, OXIDOREDUCTASE
1m00:A (GLY325) to (GLY333) RAT NEURONAL NOS HEME DOMAIN WITH N-BUTYL-N'-HYDROXYGUANIDINE BOUND | NITRIC OXIDE SYNTHASE, OXYDOREDUCTASE, HEME-ENZYME, OXIDOREDUCTASE
1m00:B (GLY325) to (GLY333) RAT NEURONAL NOS HEME DOMAIN WITH N-BUTYL-N'-HYDROXYGUANIDINE BOUND | NITRIC OXIDE SYNTHASE, OXYDOREDUCTASE, HEME-ENZYME, OXIDOREDUCTASE
3k81:C (LYS20) to (ASP33) STRUCTURE OF THE CENTRAL INTERACTION PROTEIN FROM THE TRYPANOSOMA BRUCEI EDITOSOME IN COMPLEX WITH SINGLE DOMAIN ANTIBODIES | KREPA6, VHH, SINGLE DOMAIN ANTIBODY, IMMUNE SYSTEM, RNA BINDING PROTEIN
2zcw:A (GLU5) to (PRO18) CRYSTAL STRUCTURE OF TTHA1359, A TRANSCRIPTIONAL REGULATOR, CRP/FNR FAMILY FROM THERMUS THERMOPHILUS HB8 | FNR/CRP FAMILY, TRANSCRIPTIONAL REGULATOR, THERMUS THERMOPHILUS, STATIONARY PHASE, DNA-BINDING, TRANSCRIPTION REGULATION, WINGED HELIX DNA-BINDING DOMAIN, CAMP-BINDING DOMAIN, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI
1xo2:B (GLN12) to (ALA23) CRYSTAL STRUCTURE OF A HUMAN CYCLIN-DEPENDENT KINASE 6 COMPLEX WITH A FLAVONOL INHIBITOR, FISETIN | CRYSTAL STRUCTURE,HUMAN CYCLIN-DEPENDENT KINASE 6, FISETIN, CELL CYCLE-TRANSFERASE COMPLEX
1m2v:A (SER443) to (PRO452) CRYSTAL STRUCTURE OF THE YEAST SEC23/24 HETERODIMER | ZINC-FINGER, BETA BARREL, VWA DOMAIN, GELSOLIN DOMAIN,, PROTEIN TRANSPORT
2zjc:B (PRO12) to (LEU37) TNFR1 SELECTVE TNF MUTANT; R1-6 | PHAGE DISPLAY SYSTEM, TNFR1 SELECTIVITY, TNF, AGONIST, MUTANT, CYTOKINE, LIPOPROTEIN, MEMBRANE, MYRISTATE, PHOSPHOPROTEIN, SECRETED, SIGNAL-ANCHOR, TRANSMEMBRANE
3ke0:A (LEU383) to (PRO401) CRYSTAL STRUCTURE OF N370S GLUCOCEREBROSIDASE AT ACIDIC PH. | TIM BARREL, ALTERNATIVE INITIATION, DISEASE MUTATION, DISULFIDE BOND, GAUCHER DISEASE, GLYCOPROTEIN, GLYCOSIDASE, HYDROLASE, ICHTHYOSIS, LIPID METABOLISM, LYSOSOME, MEMBRANE, SPHINGOLIPID METABOLISM
3ke0:B (LEU383) to (PRO401) CRYSTAL STRUCTURE OF N370S GLUCOCEREBROSIDASE AT ACIDIC PH. | TIM BARREL, ALTERNATIVE INITIATION, DISEASE MUTATION, DISULFIDE BOND, GAUCHER DISEASE, GLYCOPROTEIN, GLYCOSIDASE, HYDROLASE, ICHTHYOSIS, LIPID METABOLISM, LYSOSOME, MEMBRANE, SPHINGOLIPID METABOLISM
2zml:A (ILE109) to (PRO117) CRYSTAL STUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH GAL-ALPHA 1,4 GAL | LEGUME LECTIN, SUGAR SPECIFICITY, WINGED BEAN LECTIN, SUGAR BINDING PROTEIN
2zml:B (ILE109) to (PRO117) CRYSTAL STUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH GAL-ALPHA 1,4 GAL | LEGUME LECTIN, SUGAR SPECIFICITY, WINGED BEAN LECTIN, SUGAR BINDING PROTEIN
2zml:C (ILE109) to (PRO117) CRYSTAL STUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH GAL-ALPHA 1,4 GAL | LEGUME LECTIN, SUGAR SPECIFICITY, WINGED BEAN LECTIN, SUGAR BINDING PROTEIN
2zml:D (ILE109) to (PRO117) CRYSTAL STUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH GAL-ALPHA 1,4 GAL | LEGUME LECTIN, SUGAR SPECIFICITY, WINGED BEAN LECTIN, SUGAR BINDING PROTEIN
5cya:B (PHE183) to (ASN192) CRYSTAL STRUCTURE OF ARL2 GTPASE-ACTIVATING PROTEIN TUBULIN COFACTOR C (TBCC) | TUBULIN COFACTORS, MIROTUBULE DYNAMICS, TUBULIN CHAPERONES, ARL2 GTPASE-ACTIVATING PROTEIN TBCC, GAP ACTIVITY, BETA HELIX, BETA- SHEETS, CHAPERONE
2zpx:C (ALA35) to (ARG44) TNF RECEPTOR SUBTYPE ONE-SELECTIVE TNF MUTANT WITH ANTAGONISTIC ACTIVITY; R1ANTTNF-T8 | TUMOR NECROSIS FACTOR, TRIMER, ANTAGONISTIC ACTIVITY, TNFR1 SPECIFIC, PHAGE DISPLAY SYSTEM, CYTOKINE, CELL MEMBRANE, LIPOPROTEIN, MEMBRANE, MYRISTATE, PHOSPHOPROTEIN, POLYMORPHISM, SECRETED, SIGNAL-ANCHOR, TRANSMEMBRANE
1xx9:A (GLN30) to (THR54) CRYSTAL STRUCTURE OF THE FXIA CATALYTIC DOMAIN IN COMPLEX WITH ECOTINM84R | FXIA; CATALYTIC DOMAIN; SERINE PROTEIN; ECOTIN, BLOOD CLOTTING- HYDROLASE INHIBITOR COMPLEX
4oul:D (VAL998) to (THR1012) CRYSTAL STRUCTURE OF HUMAN CAPRIN-2 C1Q DOMAIN | C1Q DOMAIN, WNT SIGNALING, SIGNALING PROTEIN
4ova:A (THR102) to (SER114) STRUCTURE OF THE TWO TANDEM TUDOR DOMAINS AND A NEW IDENTIFIED KH0 DOMAIN FROM HUMAN FRAGILE X MENTAL RETARDATION PROTEIN | KH DOMAIN, FRAGILE X MENTAL RETARDATION PROTEIN, FMRP, TANDEM TUDOR DOMAINS, EUKARYOTIC KH DOMAINS, KH0 DOMAIN, RNA BINDING PROTEIN, PROTEIN INTERACTION
3kk8:A (ASN12) to (ALA23) CAMKII SUBSTRATE COMPLEX A | PROTEIN KINASE, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE
1mfz:B (THR426) to (ILE434) PARTIALLY REFINED 2.8 A CRYSTAL STRUCTURE OF GDP-MANNOSE DEHYDROGENASE FROM P. AERUGINOSA | ROSSMANN FOLD, DOMAIN-SWAPPED DIMER, ENZYME COMPLEX WITH COFACTOR AND PRODUCT, OXIDOREDUCTASE
1mfz:C (THR426) to (ILE434) PARTIALLY REFINED 2.8 A CRYSTAL STRUCTURE OF GDP-MANNOSE DEHYDROGENASE FROM P. AERUGINOSA | ROSSMANN FOLD, DOMAIN-SWAPPED DIMER, ENZYME COMPLEX WITH COFACTOR AND PRODUCT, OXIDOREDUCTASE
4oz5:A (HIS50) to (GLY59) BACILLUS SUBTILIS HMOB | HEME MONOOXYGENASE
1y1z:A (LEU6) to (PRO21) CRYSTAL STRUCTURE OF THE NR1 LIGAND BINDING CORE IN COMPLEX WITH ACBC | PROTEIN-LIGAND COMPLEX; LIGAND-BINDING COMPLEX, LIGAND BINDING PROTEIN
4ae5:B (SER51) to (GLY60) STRUCTURE OF A MAJOR REGULATOR OF STAPHYLOCOCCAL PATHOGENESIS | SIGNALING PROTEIN, PHOSPHORYLATION, RNAIII, RAP, QUORUM SENSING, BIOFILM, TOXIN PRODUCTION
4ae5:D (SER51) to (GLY60) STRUCTURE OF A MAJOR REGULATOR OF STAPHYLOCOCCAL PATHOGENESIS | SIGNALING PROTEIN, PHOSPHORYLATION, RNAIII, RAP, QUORUM SENSING, BIOFILM, TOXIN PRODUCTION
1mmw:A (GLY325) to (GLY333) RAT NEURONAL NOS HEME DOMAIN WITH VINYL-L-NIO BOUND | NITRIC OXIDE SYNTHASE, OXYDOREDUCTASE, HEME-ENZYME, OXIDOREDUCTASE
1mmw:B (GLY325) to (GLY333) RAT NEURONAL NOS HEME DOMAIN WITH VINYL-L-NIO BOUND | NITRIC OXIDE SYNTHASE, OXYDOREDUCTASE, HEME-ENZYME, OXIDOREDUCTASE
2zye:A (ASP30) to (GLY49) STRUCTURE OF HIV-1 PROTEASE IN COMPLEX WITH POTENT INHIBITOR KNI-272 DETERMINED BY NEUTRON CRYSTALLOGRAPHY | HIV-1 PROTEASE, ACID PROTEASE, HOMODIMER, HYDROLASE, MULTIFUNCTIONAL ENZYME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4p56:B (ARG224) to (ILE242) CRYSTAL STRUCTURE OF A TRAP PERIPLASMIC SOLUTE BINDING PROTEIN FROM BORDETELLA BRONCHISEPTICA, TARGET EFI-510038 (BB2442), WITH BOUND (R)-MANDELATE AND (S)-MANDELATE | TRAP PERIPLASMIC SOLUTE BINDING FAMILY, ENZYME FUNCTION INITIATIVE, EFI, STRUCTURAL GENOMICS
1y7v:A (LEU383) to (PRO401) X-RAY STRUCTURE OF HUMAN ACID-BETA-GLUCOSIDASE COVALENTLY BOUND TO CONDURITOL B EPOXIDE | GAUCHER DISEASE, GLUCOSIDASE, GLUCOCEREBROSIDASE, CEREZYME, HYDROLASE, GLYCOSIDASE, SPHINGOLIPID METABOLISM, GLYCOPROTEIN, LYSOSOME, MEMBRANE, DISEASE MUTATION, ALTERNATIVE INITIATION, ISRAEL STRUCTURAL PROTEOMICS CENTER, ISPC, STRUCTURAL GENOMICS
1y7v:B (LEU383) to (PRO401) X-RAY STRUCTURE OF HUMAN ACID-BETA-GLUCOSIDASE COVALENTLY BOUND TO CONDURITOL B EPOXIDE | GAUCHER DISEASE, GLUCOSIDASE, GLUCOCEREBROSIDASE, CEREZYME, HYDROLASE, GLYCOSIDASE, SPHINGOLIPID METABOLISM, GLYCOPROTEIN, LYSOSOME, MEMBRANE, DISEASE MUTATION, ALTERNATIVE INITIATION, ISRAEL STRUCTURAL PROTEOMICS CENTER, ISPC, STRUCTURAL GENOMICS
1y7w:B (GLY54) to (LEU75) CRYSTAL STRUCTURE OF A HALOTOLERANT CARBONIC ANHYDRASE FROM DUNALIELLA SALINA | ALPHA-TYPE CARBONIC ANHYDRASE, HALTOLERANT PROTEIN, ALGAL CARBONIC ANHYDRASE, SALT TOLERANT PROTEIN, ZINC ENZYME, ANION TOLERANCE, DUNALIELLA SALINA CARBONIC ANHYDRASE, DCA II, ISRAEL STRUCTURAL PROTEOMICS CENTER, ISPC, STRUCTURAL GENOMICS, LYASE
3a0i:X (PHE195) to (ASN204) HUMAN GLUCOKINASE IN COMPLEX WITH A SYNTHETIC ACTIVATOR | GLUCOKINASE, DIABETES, ACTIVATOR, ALTERNATIVE SPLICING, ATP- BINDING, DIABETES MELLITUS, DISEASE MUTATION, GLYCOLYSIS, KINASE, NUCLEOTIDE-BINDING, POLYMORPHISM, TRANSFERASE
4p7e:A (LEU849) to (ASN859) TRIAZOLOPYRIDINE COMPOUNDS AS SELECTIVE JAK1 INHIBITORS: FROM HIT IDENTIFICATION TO GLPG0634 | TRANSFERASE, JAK1 INHIBITOR, TRIAZOLOPYRIDINE
4p8b:A (LYS232) to (LEU244) CRYSTAL STRUCTURE OF A TRAP PERIPLASMIC SOLUTE BINDING PROTEIN FROM RALSTONIA EUTROPHA H16 (H16_A1328), TARGET EFI-510189, WITH BOUND (S)-2-HYDROXY-2-METHYL-3-OXOBUTANOATE ((S)-2-ACETOLACTATE) | TRAP PERIPLASMIC SOLUTE BINDING FAMILY, ENZYME FUNCTION INITIATIVE, EFI, STRUCTURAL GENOMICS
4p93:A (GLU199) to (ALA214) STRUCTURE OF DIENELACTONE HYDROLASE AT 1.85 A RESOLUTION CRYSTALLISED IN THE C2 SPACE GROUP | HYDROLASE, A/B HYDROLASE FOLD
1mt7:B (ASP30) to (GLY49) VIABILITY OF A DRUG-RESISTANT HIV-1 PROTEASE MUTANT: STRUCTURAL INSIGHTS FOR BETTER ANTIVIRAL THERAPY | MATRIX, CAPSID, GAG CLEAVAGE, DRUG RESISTANCE, SUBSTRATE RECOGNITION, HYDROLASE/HYDROLASE INHIBITOR COMPLEX
1muu:C (THR426) to (ILE434) 2.0 A CRYSTAL STRUCTURE OF GDP-MANNOSE DEHYDROGENASE | ROSSMANN FOLD; DOMAIN-SWAPPED DIMER; ENZYME COMPLEX WITH COFACTOR AND PRODUCT, OXIDOREDUCTASE
1muu:D (THR426) to (ILE434) 2.0 A CRYSTAL STRUCTURE OF GDP-MANNOSE DEHYDROGENASE | ROSSMANN FOLD; DOMAIN-SWAPPED DIMER; ENZYME COMPLEX WITH COFACTOR AND PRODUCT, OXIDOREDUCTASE
1muz:A (ARG470) to (PRO482) NMR STRUCTURE OF THE TUMOR SUPPRESSOR BIN1: ALTERNATIVE SPLICING IN MELANOMA AND INTERACTION WITH C-MYC | TUMOR SUPPRESSOR, ENDOCYTOSIS/EXOCYTOSIS COMPLEX
1ygc:H (GLN30) to (VAL53) SHORT FACTOR VIIA WITH A SMALL MOLECULE INHIBITOR | INVERTED OXY-ANION HOLE, HYDROLASE
3kt2:A (ASP1030) to (GLY1049) CRYSTAL STRUCTURE OF N88D MUTANT HIV-1 PROTEASE | DRUG RESISTANT MUTATION, N88D, NELFINAVIR, HIV-1 PROTEASE, HYDROLASE, PROTEASE
5d9z:B (LEU8) to (GLY17) STRUCTURE OF COLOCASIA ESCULENTA AGGLUTININ WITH MANNOSE BOUND | LECTIN, PROTEIN-CARBOHYDRATE INTERACTIONS, DIETARY PROTEIN, BETA PRISM II FOLD, 18-AUG, SUGAR BINDING PROTEIN
3kwc:D (GLU19) to (HIS29) OXIDIZED, ACTIVE STRUCTURE OF THE BETA-CARBOXYSOMAL GAMMA-CARBONIC ANHYDRASE, CCMM | LEFT-HANDED BETA HELIX, GAMMA CARBONIC ANHYDRASE, DISULFIDE BOND DEPENDENT ACTIVITY, CARBOXYSOME, LYASE, PROTEIN BINDING, PHOTOSYNTHESIS
5dc2:A (GLY290) to (LYS299) X-RAY CRYSTAL STRUCTURE OF A ENZYMATICALLY DEGRADED BIAPENEM-ADDUCT OF L,D-TRANSPEPTIDASE 2 FROM MYCOBACTERIUM TUBERCULOSIS | L, D-TRANSPEPTIDASE, CARBAPENEMS BIAPENEM-ADDUCT, LDTMT2, MYCOBACTERIUM TUBERCULOSIS, TRANSFERASE
1n0v:C (GLY67) to (SER82) CRYSTAL STRUCTURE OF ELONGATION FACTOR 2 | G-PROTEIN CIS-PROLINE, TRANSLATION
4pgo:A (MET51) to (PRO61) CRYSTAL STRUCTURE OF HYPOTHETICAL PROTEIN PF0907 FROM PYROCOCCUS FURIOSUS SOLVED BY SULFUR SAD USING SWISS LIGHT SOURCE DATA | SULFUR SAD, SOUTHEAST COLLABORATORY FOR STRUCTURAL GENOMICS, SECSG, STRUCTURAL GENOMICS, UNKNOWN FUNCTION
1n3i:B (GLN132) to (LEU142) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PNP WITH TRANSITION STATE ANALOG DADME-IMMH | TRANSITION STATE COMPLEX, TRIMER, PNP, TRANSFERASE
1n3i:C (GLN132) to (LEU142) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS PNP WITH TRANSITION STATE ANALOG DADME-IMMH | TRANSITION STATE COMPLEX, TRIMER, PNP, TRANSFERASE
1n3q:A (ASN41) to (PHE52) PTEROCARPUS ANGOLENSIS LECTIN COMPLEXED WITH TURANOSE | LECTIN, CARBOHYDRATE RECOGNITION, TURANOSE, SUGAR BINDING PROTEIN
1n3q:B (ASN41) to (PHE52) PTEROCARPUS ANGOLENSIS LECTIN COMPLEXED WITH TURANOSE | LECTIN, CARBOHYDRATE RECOGNITION, TURANOSE, SUGAR BINDING PROTEIN
5di5:A (THR217) to (ASP226) BETA1 T801 LOOP VARIANT IN P3221 | SYNTHETIC PROTEIN, PROTEIN DESIGN, DE NOVO PROTEIN
1ytj:A (ASP30) to (ILE50) SIV PROTEASE CRYSTALLIZED WITH PEPTIDE PRODUCT | AIDS, POLYPROTEIN, HYDROLASE, ASPARTYL PROTEASE, ENDONUCLEASE, RNA- DIRECTED DNA POLYMERASE, HYDROLASE-PEPTIDE COMPLEX
1n67:A (ASP481) to (ASN498) CLUMPING FACTOR A FROM STAPHYLOCOCCUS AUREUS | DEV-IGG, IGG, IMMUNOGLOBULIN, IGSF, CLUMPING FACTOR, STAPHYLOCOCCUS AUREUS, FIBRINONGEN-BINDING, CELL ADHESION
5djr:F (THR177) to (LEU185) CRYSTAL STRUCTURE OF HUMAN FPPS IN COMPLEX WITH BIARYL COMPOUND 6 | TRANSFERASE, ISOPRENE BIOSYNTHESIS, CHOLESTEROL BIOSYNTHESIS
1yw4:B (LYS143) to (VAL156) CRYSTAL STRUCTURE OF THE SUCCINYLGLUTAMATE DESUCCINYLASE FROM CHROMOBACTERIUM VIOLACEUM, NORTHEAST STRUCTURAL GENOMICS TARGET CVR22. | ALPHA-BETA PROTEIN, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, HYDROLASE
4por:D (GLU37) to (PRO54) STRUCTURE OF HUMAN POLYOMAVIRUS 9 VP1 PENTAMER IN COMPLEX WITH 3'- SIALYLLACTOSE | JELLY ROLL FOLD, CAPSID FORMATION, RECEPTOR INTERACTION, CARBOHYDRATE, SIALYLOLIGOSACCHARIDE, VIRAL COAT PROTEIN, VIRAL PROTEIN
4pos:E (GLU37) to (PRO54) STRUCTURE OF HUMAN POLYOMAVIRUS 9 VP1 PENTAMER IN COMPLEX WITH 3'- SIALYLLACTOSAMINE | JELLY ROLL FOLD, CAPSID FORMATION, RECEPTOR INTERACTION, CARBOHYDRATE, SIALYLOLIGOSACCHARIDE, VIRAL COAT PROTEIN, VIRAL PROTEIN
5dns:A (ALA163) to (ASN172) T1428 LOOP VARIANT IN P3221 | SYNTHETIC PROTEIN, PROTEIN DESIGN, DE NOVO PROTEIN
5dns:B (THR217) to (ASP226) T1428 LOOP VARIANT IN P3221 | SYNTHETIC PROTEIN, PROTEIN DESIGN, DE NOVO PROTEIN
3la8:A (GLY122) to (LEU133) THE CRYSTAL STRUCTURE OF SMU.1229 FROM STREPTOCOCCUS MUTANS UA159 | PUNA, GLYCOSYLTRANSFERASE, TRANSFERASE
1z5h:A (MET1) to (ASP13) CRYSTAL STRUCTURES OF THE TRICORN INTERACTING FACTOR F3 FROM THERMOPLASMA ACIDOPHILUM | ZINC AMINOPEPTIDASE, GLUZICINS, TRICORN PROTEASE, SUPERHELIX, HYDROLASE
1z5h:B (MET1) to (ASP13) CRYSTAL STRUCTURES OF THE TRICORN INTERACTING FACTOR F3 FROM THERMOPLASMA ACIDOPHILUM | ZINC AMINOPEPTIDASE, GLUZICINS, TRICORN PROTEASE, SUPERHELIX, HYDROLASE
1z6j:H (GLN30) to (VAL53) CRYSTAL STRUCTURE OF A TERNARY COMPLEX OF FACTOR VIIA/TISSUE FACTOR/PYRAZINONE INHIBITOR | BLOOD COAGULATION, SERINE PROTEASE, THROMBOSIS, GLA, PYRAZINONE, BENZAMIDINE, TISSUE FACTOR, COFACTOR, ENZYME INHIBITOR COMPLEX, HYDROLASE
4pt6:A (ILE21) to (ARG29) THE DISCOBODY: AN ENGINEERED DISCOIDIN DOMAIN FROM FACTOR VIII THAT BINDS V 3 INTEGRIN WITH ANTIBODY-LIKE AFFINITIES | INTEGRIN BINDING, INTEGRIN, CELL ADHESION
5dp1:A (ASN32) to (PHE45) CRYSTAL STRUCTURE OF CURK ENOYL REDUCTASE | POLYKETIDE SYNTHASE, ENOYL REDUCTASE, OXIDOREDUCTASE
5dp9:A (LYS130) to (ASN139) CRYSTAL STRUCTURE OF EV71 3C PROTEINASE IN COMPLEX WITH COMPOUND 9 | HAND, FOOT AND MOUTH DISEASE, 3C PROTEINASE, PEPTIDOMIMETICS, DRUG DESIGN, RUPINTRIVIR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5dqa:A (THR217) to (ASP226) T3284 LOOP VARIANT OF BETA1 | SYNTHETIC PROTEIN, LOOP DESIGN, DE NOVO PROTEIN
5dqa:B (ILE40) to (ASN49) T3284 LOOP VARIANT OF BETA1 | SYNTHETIC PROTEIN, LOOP DESIGN, DE NOVO PROTEIN
5dqa:C (ILE40) to (ASN49) T3284 LOOP VARIANT OF BETA1 | SYNTHETIC PROTEIN, LOOP DESIGN, DE NOVO PROTEIN
1z8y:A (ASP117) to (VAL131) MAPPING THE E2 GLYCOPROTEIN OF ALPHAVIRUSES | ICOSAHEDRAL ENVELOPED VIRUS, CRYO-ELECTRON MICROSCOPY, ICOSAHEDRAL VIRUS
1z8y:C (ASP117) to (VAL131) MAPPING THE E2 GLYCOPROTEIN OF ALPHAVIRUSES | ICOSAHEDRAL ENVELOPED VIRUS, CRYO-ELECTRON MICROSCOPY, ICOSAHEDRAL VIRUS
1z8y:E (ASP117) to (VAL131) MAPPING THE E2 GLYCOPROTEIN OF ALPHAVIRUSES | ICOSAHEDRAL ENVELOPED VIRUS, CRYO-ELECTRON MICROSCOPY, ICOSAHEDRAL VIRUS
1z8y:G (ASP117) to (VAL131) MAPPING THE E2 GLYCOPROTEIN OF ALPHAVIRUSES | ICOSAHEDRAL ENVELOPED VIRUS, CRYO-ELECTRON MICROSCOPY, ICOSAHEDRAL VIRUS
3alq:A (ASN34) to (ASP45) CRYSTAL STRUCTURE OF TNF-TNFR2 COMPLEX | LIGAND-RECEPTOR COMPLEX, CYTOKINE, CYTOKINE-CYTOKINE RECEPTOR COMPLEX
3alq:E (ASN34) to (ASP45) CRYSTAL STRUCTURE OF TNF-TNFR2 COMPLEX | LIGAND-RECEPTOR COMPLEX, CYTOKINE, CYTOKINE-CYTOKINE RECEPTOR COMPLEX
4anm:A (ASP38) to (LYS49) COMPLEX OF CK2 WITH A CDC7 INHIBITOR | TRANSFERASE
3lgt:A (GLY202) to (ILE236) Y162A/H198P DOUBLE MUTANT OF DEGS-DELTAPDZ PROTEASE | PROTEASE, STRESS-SENSOR, HTRA, PDZ OMP, HYDROLASE, SERINE PROTEASE
3lgu:A (GLY202) to (ILE236) Y162A MUTANT OF THE DEGS-DELTAPDZ PROTEASE | PROTEASE, STRESS-SENSOR, HTRA, PDZ OMP, HYDROLASE, SERINE PROTEASE
3lha:B (GLY81) to (ALA94) CRYSTAL STRUCTURE OF MOUSE VPS26B(R240S/G241A/E242S) IN SPACEGROUP P41 21 2 | ARRESTIN, FIBRONECTIN, MEMBRANE, PROTEIN TRANSPORT, TRANSPORT
4pxl:A (SER330) to (PRO344) STRUCTURE OF ZM ALDH2-3 (RF2C) IN COMPLEX WITH NAD | OXIDOREDUCTASE
4pxl:B (SER330) to (PRO344) STRUCTURE OF ZM ALDH2-3 (RF2C) IN COMPLEX WITH NAD | OXIDOREDUCTASE
4aq2:L (ASN308) to (GLU322) RESTING STATE OF HOMOGENTISATE 1,2-DIOXYGENASE | OXIDOREDUCTASE
4aq6:H (ASN308) to (GLU322) SUBSTRATE BOUND HOMOGENTISATE 1,2-DIOXYGENASE | OXIDOREDUCTASE, EXTRADIOL-TYPE, EXTRADIOL-TYPE DIOXYGENASE
5dyi:D (TYR173) to (GLU185) STRUCTURE OF P97 N-D1 WILD-TYPE IN COMPLEX WITH ADP | VCP, AAA ATPASE, HYDROLASE
5dyv:B (ASP27) to (VAL35) ABYU - WILDTYPE | ABYU, DIELS-ALDERASE, DIELS-ALDER, CYCLASE, [4+2] CYCLOADDITION, TETRONATE, SPIROTETRONATE, POLYKETIDE, ABYSSOMICIN, LIGASE
5dyv:D (ASP27) to (VAL35) ABYU - WILDTYPE | ABYU, DIELS-ALDERASE, DIELS-ALDER, CYCLASE, [4+2] CYCLOADDITION, TETRONATE, SPIROTETRONATE, POLYKETIDE, ABYSSOMICIN, LIGASE
5dyv:H (ASP27) to (VAL35) ABYU - WILDTYPE | ABYU, DIELS-ALDERASE, DIELS-ALDER, CYCLASE, [4+2] CYCLOADDITION, TETRONATE, SPIROTETRONATE, POLYKETIDE, ABYSSOMICIN, LIGASE
5dzb:A (ASP214) to (GLY234) 6BETA1 | SYNTHETIC PROTEIN, LOOP DESIGN, DE NOVO PROTEIN
5dzb:D (THR229) to (ASP238) 6BETA1 | SYNTHETIC PROTEIN, LOOP DESIGN, DE NOVO PROTEIN
5dzb:E (THR229) to (ASP238) 6BETA1 | SYNTHETIC PROTEIN, LOOP DESIGN, DE NOVO PROTEIN
5dzb:F (GLY33) to (GLU44) 6BETA1 | SYNTHETIC PROTEIN, LOOP DESIGN, DE NOVO PROTEIN
5dzb:F (ALA85) to (GLU94) 6BETA1 | SYNTHETIC PROTEIN, LOOP DESIGN, DE NOVO PROTEIN
5dzb:F (ALA100) to (GLU109) 6BETA1 | SYNTHETIC PROTEIN, LOOP DESIGN, DE NOVO PROTEIN
5dzb:F (THR229) to (ASP238) 6BETA1 | SYNTHETIC PROTEIN, LOOP DESIGN, DE NOVO PROTEIN
5dzp:A (GLY290) to (LYS299) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS L,D-TRANSPEPTIDASE 2 WITH CARBAPENEM DRUG T206 IN CONFORMATION B | PEPTIDOGLYCAN SYNTHESIS ENZYME, CELL WALL ENZYME, TRANSFERASE
1zoe:A (ASP38) to (LYS49) CRYSTAL STRUCTURE OF PROTEIN KINASE CK2 IN COMPLEX WITH TBB- DERIVATIVES INHIBITORS | PROTEIN KINASE, INHIBITOR, COMPLEX, TRANSFERASE
1zqz:A (THR225) to (GLU232) DNA POLYMERASE BETA (POL B) (E.C.2.7.7.7), 31-KD DOMAIN; SOAKED IN THE PRESENCE OF MNCL2 (50 MILLIMOLAR) | DNA-DIRECTED DNA POLYMERASE, DNA REPLICATION, DNA REPAIR, NUCLEOTIDYLTRANSFERASE
1zsf:A (ASP30) to (ILE50) CRYSTAL STRUCTURE OF COMPLEX OF A HYDROXYETHYLAMINE INHIBITOR WITH HIV-1 PROTEASE AT 2.0A RESOLUTION | HIV, PROTEASE, PEPTIDOMIMETIC INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3ltf:C (GLY35) to (GLY60) CRYSTAL STRUCTURE OF THE DROSOPHILA EPIDERMAL GROWTH FACTOR RECEPTOR ECTODOMAIN IN COMPLEX WITH SPITZ | RECEPTOR-LIGAND COMPLEX ECTODOMAIN CYSTEINE RICH DOMAIN EGF DOMAIN, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, RECEPTOR, TRANSFERASE, TYROSINE-PROTEIN KINASE, CELL MEMBRANE, DEVELOPMENTAL PROTEIN, DIFFERENTIATION, DISULFIDE BOND, EGF-LIKE DOMAIN, ENDOPLASMIC RETICULUM, GLYCOPROTEIN, GOLGI APPARATUS, MEMBRANE, NEUROGENESIS, TRANSMEMBRANE, TRANSFERASE-TRANSFERASE REGULATOR COMPLEX
1zvi:A (GLY325) to (GLY333) RAT NEURONAL NITRIC OXIDE SYNTHASE OXYGENASE DOMAIN | RAT NNOSOXY, TARGETING TETRAHYDROBIOPTERIN BINDING SITE, OXIDOREDUCTASE
1zvl:B (GLY325) to (GLY333) RAT NEURONAL NITRIC OXIDE SYNTHASE OXYGENASE DOMAIN COMPLEXED WITH NATURAL SUBSTRATE L-ARG. | RAT NNOSOXY, TARGETING TETRAHYDROBIOPTERIN BINDING SITE., OXIDOREDUCTASE
3luc:C (MET483) to (GLY497) CRYSTAL STRUCTURE OF MID DOMAIN FROM HAGO2 | MID DOMAIN, RIBONUCLEOPROTEIN, RNA-BINDING, RNA-MEDIATED GENE SILENCING, TRANSLATION REGULATION, RNA BINDING PROTEIN
1zzq:A (GLY325) to (GLY333) RAT NNOS D597N MUTANT WITH L-N(OMEGA)-NITROARGININE-(4R)- AMINO-L-PROLINE AMIDE BOUND | OXYDOREDUCTASE ENZYME-INHIBITOR COMPLEX, OXIDOREDUCTASE
1zzq:B (GLY325) to (GLY333) RAT NNOS D597N MUTANT WITH L-N(OMEGA)-NITROARGININE-(4R)- AMINO-L-PROLINE AMIDE BOUND | OXYDOREDUCTASE ENZYME-INHIBITOR COMPLEX, OXIDOREDUCTASE
1zzr:A (GLY325) to (GLY333) RAT NNOS D597N/M336V DOUBLE MUTANT WITH L-N(OMEGA)-NITROARGININE-(4R)- AMINO-L-PROLINE AMIDE BOUND | OXYDOREDUCTASE ENZYME-INHIBTOR COMPLEX, OXIDOREDUCTASE
1zzr:B (GLY325) to (GLY333) RAT NNOS D597N/M336V DOUBLE MUTANT WITH L-N(OMEGA)-NITROARGININE-(4R)- AMINO-L-PROLINE AMIDE BOUND | OXYDOREDUCTASE ENZYME-INHIBTOR COMPLEX, OXIDOREDUCTASE
1zzu:A (GLY325) to (GLY333) RAT NNOS D597N/M336V DOUBLE MUTANT WITH L-N(OMEGA)-NITROARGININE-2,4- L-DIAMINOBUTYRIC AMIDE BOUND | OXYDOREDUCTASE, ENZYME-INHIBTOR COMPLEX, OXIDOREDUCTASE
1zzu:B (GLY325) to (GLY333) RAT NNOS D597N/M336V DOUBLE MUTANT WITH L-N(OMEGA)-NITROARGININE-2,4- L-DIAMINOBUTYRIC AMIDE BOUND | OXYDOREDUCTASE, ENZYME-INHIBTOR COMPLEX, OXIDOREDUCTASE
5e8v:A (PRO243) to (ARG254) TGF-BETA RECEPTOR TYPE 2 KINASE DOMAIN (E431A,R433A,E485A,K488A,R493A, R495A) | KINASE DOMAIN, TRANSFERASE
3lzi:A (PRO35) to (ASP51) RB69 DNA POLYMERASE (Y567A) TERNARY COMPLEX WITH DATP OPPOSITE 7,8- DIHYDRO-8-OXOGUANINE | DNA POLYMERASE, REPLICATION FIDELITY, 7,8-DIHYDRO-8-OXOGUANINE, POLYMERASE-DNA-DNTP TERNARY COMPLEX, TRANSFERASE-DNA COMPLEX
5e92:A (PRO243) to (ARG254) TGF-BETA RECEPTOR TYPE 2 KINASE DOMAIN (E431A,R433A,E485A,K488A,R493A, R495A) IN COMPLEX WITH AMPPNP | KINASE DOMAIN, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4b20:A (ASP105) to (LEU114) STRUCTURAL BASIS OF DNA LOOP RECOGNITION BY ENDONUCLEASE V | HYDROLASE
4b2a:C (GLN30) to (VAL53) STRUCTURE OF THE FACTOR XA-LIKE TRYPSIN VARIANT TRIPLE-ALA (TGA) IN COMPLEX WITH EGLIN C | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2a38:C (THR2) to (GLN10) CRYSTAL STRUCTURE OF THE N-TERMINUS OF TITIN | TITIN, Z1Z2, STRUCTURAL PROTEIN
4qae:A (GLY29) to (GLY38) CRYSTAL STRUCTURE OF AN ENGINEERED LIPOCALIN (ANTICALIN) IN COMPLEX WITH HUMAN HEPCIDIN | BETA-BARREL, ENGINEERED LIPOCALIN, BINDING PROTEIN, PROTEIN-PEPTIDE COMPLEX, TRANSPORT PROTEIN-SIGNALING PROTEIN COMPLEX
4qae:B (GLY29) to (GLY38) CRYSTAL STRUCTURE OF AN ENGINEERED LIPOCALIN (ANTICALIN) IN COMPLEX WITH HUMAN HEPCIDIN | BETA-BARREL, ENGINEERED LIPOCALIN, BINDING PROTEIN, PROTEIN-PEPTIDE COMPLEX, TRANSPORT PROTEIN-SIGNALING PROTEIN COMPLEX
4qae:C (GLY29) to (GLY38) CRYSTAL STRUCTURE OF AN ENGINEERED LIPOCALIN (ANTICALIN) IN COMPLEX WITH HUMAN HEPCIDIN | BETA-BARREL, ENGINEERED LIPOCALIN, BINDING PROTEIN, PROTEIN-PEPTIDE COMPLEX, TRANSPORT PROTEIN-SIGNALING PROTEIN COMPLEX
4qae:D (GLY29) to (GLY38) CRYSTAL STRUCTURE OF AN ENGINEERED LIPOCALIN (ANTICALIN) IN COMPLEX WITH HUMAN HEPCIDIN | BETA-BARREL, ENGINEERED LIPOCALIN, BINDING PROTEIN, PROTEIN-PEPTIDE COMPLEX, TRANSPORT PROTEIN-SIGNALING PROTEIN COMPLEX
4qae:E (GLY29) to (GLY38) CRYSTAL STRUCTURE OF AN ENGINEERED LIPOCALIN (ANTICALIN) IN COMPLEX WITH HUMAN HEPCIDIN | BETA-BARREL, ENGINEERED LIPOCALIN, BINDING PROTEIN, PROTEIN-PEPTIDE COMPLEX, TRANSPORT PROTEIN-SIGNALING PROTEIN COMPLEX
4qae:F (GLY29) to (GLY38) CRYSTAL STRUCTURE OF AN ENGINEERED LIPOCALIN (ANTICALIN) IN COMPLEX WITH HUMAN HEPCIDIN | BETA-BARREL, ENGINEERED LIPOCALIN, BINDING PROTEIN, PROTEIN-PEPTIDE COMPLEX, TRANSPORT PROTEIN-SIGNALING PROTEIN COMPLEX
2a45:E (GLN30) to (LEU53) CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN THROMBIN AND THE CENTRAL "E" REGION OF FIBRIN | THROMBIN, FIBRIN, FRAGMENT E, THROMBIN-FIBRIN COMPLEX, COILED COILS, DISULFIDE RINGS, BLOOD CLOTTING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3m0r:A (GLY51) to (ASP62) CRYSTAL STRUCTURE OF THE R21D MUTANT OF ALPHA-SPECTRIN SH3 DOMAIN. CRYSTAL OBTAINED IN AMMONIUM SULPHATE AT PH 6. | SH3-LIKE BARREL, ACTIN CAPPING, ACTIN-BINDING, CALMODULIN-BINDING, CYTOSKELETON, PHOSPHOPROTEIN, SH3 DOMAIN, SIGNALING PROTEIN
3m0u:A (GLY51) to (ASP62) CRYSTAL STRUCTURE OF THE R21D MUTANT OF ALPHA-SPECTRIN SH3 DOMAIN. HEXAGONAL CRYSTAL OBTAINED IN SODIUM FORMATE AT PH 6.5. | SH3-LIKE BARREL, ACTIN CAPPING, ACTIN-BINDING, CALMODULIN-BINDING, CYTOSKELETON, PHOSPHOPROTEIN, SH3 DOMAIN, SIGNALING PROTEIN
4b2r:A (LEU620) to (CYS630) SOLUTION STRUCTURE OF CCP MODULES 10-11 OF COMPLEMENT FACTOR H | IMMUNE SYSTEM, SHORT CONSENSUS REPEAT
3awj:A (PRO26) to (GLU42) CRYSTAL STRUCTURE OF THE HUPERZIA SERRATA POLYKETIDE SYNTHASE 1 COMPLEXED WITH COA-SH | TYPE III POLYKETIDE SYNTHASE, CHALCONE SYNTHASE, TRANSFERASE
3axw:A (ASP38) to (LYS49) CRYSTAL STRUCTURE OF HUMAN CK2ALPHA COMPLEXED WITH A POTENT INHIBITOR | KINASE DOMAIN, SERINE/THREONINE KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
3m46:A (LYS397) to (ILE408) THE CRYSTAL STRUCTURE OF THE D73A MUTANT OF GLYCOSIDE HYDROLASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174 | GLYCOSIDE HYDROLASE (FAMILY 31), STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MCSG, MIDWEST CENTER FOR STRUCTURAL GENOMICS, HYDROLASE
3m53:A (VAL234) to (GLY247) SET7/9 IN COMPLEX WITH TAF10 PEPTIDE AND ADOHCY | TERNARY COMPLEX, SET DOMAIN, METHYLTRANSFERASE, S-ADENOSYL-L- HOMOCYSTEINE, TAF10 PEPTIDE, CHROMATIN REGULATOR, CHROMOSOMAL PROTEIN, NUCLEUS, S-ADENOSYL-L-METHIONINE, TRANSCRIPTION, TRANSCRIPTION REGULATION, TRANSFERASE
3m55:A (VAL234) to (GLY247) SET7/9 Y305F IN COMPLEX WITH TAF10-K189ME1 PEPTIDE AND ADOHCY | TERNARY COMPLEX, SET DOMAIN, METHYLTRANSFERASE, S-ADENOSYL-L- HOMOCYSTEINE, TAF10 PEPTIDE, N-MONOMETHYLLYSINE, CHROMATIN REGULATOR, CHROMOSOMAL PROTEIN, NUCLEUS, S-ADENOSYL-L-METHIONINE, TRANSCRIPTION, TRANSCRIPTION REGULATION, TRANSFERASE
3m5m:B (GLY1023) to (GLY1031) AVOIDING DRUG RESISTANCE AGAINST HCV NS3/4A PROTEASE INHIBITORS | HCV, HEPATITIS C VIRUS, NS3, PROTEASE, DRUG RESISTANCE, SERINE PROTEASE, CHIMERA PROTEIN, FUSION PROTEIN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3m5n:B (GLY1023) to (GLY1031) CRYSTAL STRUCTURE OF HCV NS3/4A PROTEASE IN COMPLEX WITH N-TERMINAL PRODUCT 4B5A | HCV, HEPATITIS C VIRUS, NS3, PROTEASE, DRUG RESISTANCE, SERINE PROTEASE, CHIMERA PROTEIN, FUSION PROTEIN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3m65:A (GLU4) to (ARG15) CRYSTAL STRUCTURE OF BACILLUS SUBTILIS LON N-TERMINAL DOMAIN | COILED-COIL, ATP-BINDING, HYDROLASE, NUCLEOTIDE-BINDING, PROTEASE, SERINE PROTEASE, STRESS RESPONSE
3b3n:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NOS HEME DOMAIN IN COMPLEX WITH A INHIBITOR (+-)-N1-{CIS-4'-[(6"-AMINOPYRIDIN-2"-YL) METHYL]PYRROLIDIN-3'-YL}ETHANE-1,2-DIAMINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, INHIBITOR, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL PROJECTION, FAD, FMN, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3b3n:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NOS HEME DOMAIN IN COMPLEX WITH A INHIBITOR (+-)-N1-{CIS-4'-[(6"-AMINOPYRIDIN-2"-YL) METHYL]PYRROLIDIN-3'-YL}ETHANE-1,2-DIAMINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, INHIBITOR, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL PROJECTION, FAD, FMN, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3b3m:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NOS HEME DOMAIN IN COMPLEX WITH A INHIBITOR (+-)-3-{CIS-4'-[(6"-AMINOPYRIDIN-2"-YL) METHYL]PYRROLIDIN-3'-YLAMINO}PROPAN-1-OL | NITRIC OXIDE SYNTHASE, HEME ENZYME, INHIBITOR, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL PROJECTION, FAD, FMN, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3b3m:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NOS HEME DOMAIN IN COMPLEX WITH A INHIBITOR (+-)-3-{CIS-4'-[(6"-AMINOPYRIDIN-2"-YL) METHYL]PYRROLIDIN-3'-YLAMINO}PROPAN-1-OL | NITRIC OXIDE SYNTHASE, HEME ENZYME, INHIBITOR, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL PROJECTION, FAD, FMN, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3b3o:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NOS HEME DOMAIN IN COMPLEX WITH A INHIBITOR (+-)-N1-{CIS-4'-[(6"-AMINO-4"-METHYLPYRIDIN-2"- YL)METHYL]PYRROLIDIN-3'-YL}-N2-(4'-CHLOROBENZYL)ETHANE-1,2- DIAMINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, INHIBITOR, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL PROJECTION, FAD, FMN, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3b3o:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NOS HEME DOMAIN IN COMPLEX WITH A INHIBITOR (+-)-N1-{CIS-4'-[(6"-AMINO-4"-METHYLPYRIDIN-2"- YL)METHYL]PYRROLIDIN-3'-YL}-N2-(4'-CHLOROBENZYL)ETHANE-1,2- DIAMINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, INHIBITOR, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL PROJECTION, FAD, FMN, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3b3p:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NOS HEME DOMAIN IN COMPLEX WITH A INHIBITOR (+-)-N1-{CIS-4'-[(6"-AMINO-4"-METHYLPYRIDIN-2"- YL)METHYL]PYRROLIDIN-3'-YL}-N2-(4'-CHLOROBENZYL)ETHANE-1,2- DIAMINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, INHIBITOR, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL PROJECTION, FAD, FMN, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3b3p:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NOS HEME DOMAIN IN COMPLEX WITH A INHIBITOR (+-)-N1-{CIS-4'-[(6"-AMINO-4"-METHYLPYRIDIN-2"- YL)METHYL]PYRROLIDIN-3'-YL}-N2-(4'-CHLOROBENZYL)ETHANE-1,2- DIAMINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, INHIBITOR, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL PROJECTION, FAD, FMN, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3mao:A (PRO18) to (THR47) CRYSTAL STRUCTURE OF HUMAN METHIONINE-R-SULFOXIDE REDUCTASE B1 (MSRB1) | OXIDOREDUCTASE, STRUCTURAL GENOMICS CONSORTIUM, SGC, CYTOPLASM, METAL-BINDING, NUCLEUS, SELENOCYSTEINE, ZINC
4qj0:A (PRO100) to (SER108) CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4qj0:C (PRO100) to (SER108) CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
2ach:A (MET221) to (PRO228) CRYSTAL STRUCTURE OF CLEAVED HUMAN ALPHA1-ANTICHYMOTRYPSIN AT 2.7 ANGSTROMS RESOLUTION AND ITS COMPARISON WITH OTHER SERPINS | PROTEINASE INHIBITOR
4qjw:A (PRO100) to (SER108) CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4qjw:B (PRO100) to (SER108) CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4qjw:C (PRO100) to (SER108) CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4qjw:D (PRO100) to (SER108) CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4qmg:C (PRO45) to (GLY57) THE STRUCTURE OF MTDH-SND1 COMPLEX REVEALS NOVEL CANCER-PROMOTING INTERACTIONS | SN DOMAINS, OLIGONUCLEOTIDE/OLIGOSACCHARIDE BINDING-FOLD (OB-FOLD), DNA/RNA-BINDING, MIRNA-MEDIATED SILENCING, NUCLEASE, BREAST CANCER, TUMORIGENESIS, SND1, MTDH, TRANSCRIPTION
2agm:A (TYR61) to (ASP74) SOLUTION STRUCTURE OF THE R-MODULE FROM ALGE4 | PARALLEL BETA-ROLL, ISOMERASE
3b8x:A (ASN3) to (ASP13) CRYSTAL STRUCTURE OF GDP-4-KETO-6-DEOXYMANNOSE-3-DEHYDRATASE (COLD) H188N MUTANT WITH BOUND GDP-PEROSAMINE | ASPARTATE AMINOTRANSFERASE, COLITOSE, PEROSAMINE, O-ANTIGEN, PLP, PYRIDOXAL PHOSPHATE,, TRANSFERASE
5ek6:E (LEU314) to (PRO329) THERMOSTABLE ALDEHYDE DEHYDROGENASE FROM PYROBACULUM SP. 1860 COMPLEXED WITH NADP AND ISOBUTYRALDEHYDE | THERMOSTABLE ALDEHYDE DEHYDROGENASE, OXIDOREDUCTASE
4be9:A (GLY61) to (CYS72) OPEN CONFORMATION OF O. PICEAE STEROL ESTERASE | HYDROLASE, OPHIOSTOMA
4qpy:A (PRO7) to (TYR22) CRYSTAL STRUCTURE OF C1QL2 | JELLY ROLL FOLD, BRAIN-SPECIFIC ANGIOGENESIS INHIBITOR ADHESION G- PROTEIN COUPLED RECEPTOR 3, EXTRACELLULAR, PROTEIN BINDING
4qpy:B (PRO7) to (TYR22) CRYSTAL STRUCTURE OF C1QL2 | JELLY ROLL FOLD, BRAIN-SPECIFIC ANGIOGENESIS INHIBITOR ADHESION G- PROTEIN COUPLED RECEPTOR 3, EXTRACELLULAR, PROTEIN BINDING
3mji:A (SER67) to (ASN75) ACTIVATION OF CATALYTIC CYSTEINE WITHOUT A BASE IN A MUTANT PENICILLIN ACYLASE PRECURSOR | ZYMOGEN, HYDROLASE, PENICILLIN, AUTOPROTEOLYSIS, ANTIBIOTIC RESISTANCE, CATALYSIS, PENICILLIN V ACYLASE, AMIDASE
5eqx:A (ARG315) to (PHE334) CRYSTAL STRUCTURE OF HUMAN DESMOGLEIN-3 ECTODOMAIN | EXTRACELLULAR CADHERIN DOMAIN, CELL ADHESION, CELL SURFACE, DESMOSOME
3mqh:F (THR7) to (GLY17) CRYSTAL STRUCTURE OF THE 3-N-ACETYL TRANSFERASE WLBB FROM BORDETELLA PETRII IN COMPLEX WITH COA AND UDP-3-AMINO-2-ACETAMIDO-2,3-DIDEOXY GLUCURONIC ACID | BETA HELIX, ACETYLTRANSFERASE, TRANSFERASE
3biw:E (ARG105) to (VAL120) CRYSTAL STRUCTURE OF THE NEUROLIGIN-1/NEUREXIN-1BETA SYNAPTIC ADHESION COMPLEX | PROTEIN-PROTEIN COMPLEX, ESTERASE DOMAIN, LNS DOMAIN, ALPHA-BETA HYDROLASE, CELL ADHESION, CELL JUNCTION, GLYCOPROTEIN, MEMBRANE, POSTSYNAPTIC CELL MEMBRANE, SYNAPSE, TRANSMEMBRANE, ALTERNATIVE PROMOTER USAGE, CELL ADHESION-CELL ADHESION COMPLEX
3biw:F (ARG105) to (VAL120) CRYSTAL STRUCTURE OF THE NEUROLIGIN-1/NEUREXIN-1BETA SYNAPTIC ADHESION COMPLEX | PROTEIN-PROTEIN COMPLEX, ESTERASE DOMAIN, LNS DOMAIN, ALPHA-BETA HYDROLASE, CELL ADHESION, CELL JUNCTION, GLYCOPROTEIN, MEMBRANE, POSTSYNAPTIC CELL MEMBRANE, SYNAPSE, TRANSMEMBRANE, ALTERNATIVE PROMOTER USAGE, CELL ADHESION-CELL ADHESION COMPLEX
3biw:G (ARG105) to (VAL120) CRYSTAL STRUCTURE OF THE NEUROLIGIN-1/NEUREXIN-1BETA SYNAPTIC ADHESION COMPLEX | PROTEIN-PROTEIN COMPLEX, ESTERASE DOMAIN, LNS DOMAIN, ALPHA-BETA HYDROLASE, CELL ADHESION, CELL JUNCTION, GLYCOPROTEIN, MEMBRANE, POSTSYNAPTIC CELL MEMBRANE, SYNAPSE, TRANSMEMBRANE, ALTERNATIVE PROMOTER USAGE, CELL ADHESION-CELL ADHESION COMPLEX
3biw:H (ARG105) to (VAL120) CRYSTAL STRUCTURE OF THE NEUROLIGIN-1/NEUREXIN-1BETA SYNAPTIC ADHESION COMPLEX | PROTEIN-PROTEIN COMPLEX, ESTERASE DOMAIN, LNS DOMAIN, ALPHA-BETA HYDROLASE, CELL ADHESION, CELL JUNCTION, GLYCOPROTEIN, MEMBRANE, POSTSYNAPTIC CELL MEMBRANE, SYNAPSE, TRANSMEMBRANE, ALTERNATIVE PROMOTER USAGE, CELL ADHESION-CELL ADHESION COMPLEX
5eyy:A (THR42) to (TYR53) TETRAGONAL FORM OF CENTROLOBIUM TOMENTOSUM SEED LECTIN (CTL) COMPLEXED WITH MAN1-3MAN-OME. | LECTIN, CENTROLOBIUM TOMENTOSUM, DALBERGIEAE, CTL, METHYL DIMANNOSIDE., SUGAR BINDING PROTEIN
3bn1:A (LEU4) to (LEU14) CRYSTAL STRUCTURE OF GDP-PEROSAMINE SYNTHASE | PEROSAMINE, ASPARTATE AMINOTRANSFERASE, DEOXYSUGAR, O-ANTIGEN, TRANSFERASE
3mw4:A (ARG103) to (THR117) CRYSTAL STRUCTURE OF BETA-NEUREXIN 3 WITHOUT THE SPLICE INSERT 4 | NEUREXIN, LNS DOMAIN, CALCIUM-BINDING, CELL ADHESION, GLYCOPROTEIN
3mw4:C (ARG103) to (THR117) CRYSTAL STRUCTURE OF BETA-NEUREXIN 3 WITHOUT THE SPLICE INSERT 4 | NEUREXIN, LNS DOMAIN, CALCIUM-BINDING, CELL ADHESION, GLYCOPROTEIN
4qyg:A (ASP8) to (ALA19) CHK1 KINASE DOMAIN IN COMPLEX WITH DIAZACARBAZOLE COMPOUND 14 | PROTEIN KINASE, PHOSPHOTRANSFER CATALYST, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4qyg:B (GLU7) to (ALA19) CHK1 KINASE DOMAIN IN COMPLEX WITH DIAZACARBAZOLE COMPOUND 14 | PROTEIN KINASE, PHOSPHOTRANSFER CATALYST, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4qyh:B (GLU7) to (ALA19) CHK1 KINASE DOMAIN IN COMPLEX WITH DIAZACARBAZOLE GNE-783 | PROTEIN KINASE, PHOSPHOTRANSFER CATALYST, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
3mxl:A (ARG220) to (GLY232) CRYSTAL STRUCTURE OF NITROSOSYNTHASE FROM MICROMONOSPORA CARBONACEA VAR. AFRICANA | FLAVIN MONOOXYGENASE, NITROSOSYNTHASE, ACYL-COA DEHYDROGENASE, OXIDOREDUCTASE
3bx8:A (GLY29) to (GLY38) ENGINEERED HUMAN LIPOCALIN 2 (LCN2), APO-FORM | PROTEIN DESIGN, LIGAND BINDING PROTEIN, DE NOVO PROTEIN, PROTEIN BINDING
3bx8:C (GLY29) to (GLY38) ENGINEERED HUMAN LIPOCALIN 2 (LCN2), APO-FORM | PROTEIN DESIGN, LIGAND BINDING PROTEIN, DE NOVO PROTEIN, PROTEIN BINDING
3bx8:D (GLY29) to (GLY38) ENGINEERED HUMAN LIPOCALIN 2 (LCN2), APO-FORM | PROTEIN DESIGN, LIGAND BINDING PROTEIN, DE NOVO PROTEIN, PROTEIN BINDING
3bxr:B (ASP130) to (ILE150) CRYSTAL STRUCTURES OF HIGHLY CONSTRAINED SUBSTRATE AND HYDROLYSIS PRODUCTS BOUND TO HIV-1 PROTEASE. IMPLICATIONS FOR CATALYTIC MECHANISM | HIV PROTEASE, HIVPR, SUBSTRATE, PRODUCT, MECHANISM, AIDS, ASPARTYL PROTEASE, CAPSID MATURATION, CORE PROTEIN, CYTOPLASM, DNA INTEGRATION, DNA RECOMBINATION, DNA-DIRECTED DNA POLYMERASE, ENDONUCLEASE, HYDROLASE, LIPOPROTEIN, MAGNESIUM, MEMBRANE, METAL-BINDING, MULTIFUNCTIONAL ENZYME, MYRISTATE, NUCLEASE, NUCLEOTIDYLTRANSFERASE, NUCLEUS, PHOSPHOPROTEIN, RNA-BINDING, RNA-DIRECTED DNA POLYMERASE, TRANSFERASE, VIRAL NUCLEOPROTEIN, VIRION, ZINC, ZINC-FINGER
3bxs:B (ASP130) to (GLY149) CRYSTAL STRUCTURES OF HIGHLY CONSTRAINED SUBSTRATE AND HYDROLYSIS PRODUCTS BOUND TO HIV-1 PROTEASE. IMPLICATIONS FOR CATALYTIC MECHANISM | HIV PROTEASE, HIVPR, SUBSTRATE, PRODUCT, MECHANISM, AIDS, ASPARTYL PROTEASE, CAPSID MATURATION, CORE PROTEIN, CYTOPLASM, DNA INTEGRATION, DNA RECOMBINATION, DNA-DIRECTED DNA POLYMERASE, ENDONUCLEASE, HYDROLASE, LIPOPROTEIN, MAGNESIUM, MEMBRANE, METAL-BINDING, MULTIFUNCTIONAL ENZYME, MYRISTATE, NUCLEASE, NUCLEOTIDYLTRANSFERASE, NUCLEUS, PHOSPHOPROTEIN, RNA-BINDING, RNA-DIRECTED DNA POLYMERASE, TRANSFERASE, VIRAL NUCLEOPROTEIN, VIRION, ZINC, ZINC-FINGER
3by0:C (GLY29) to (GLY38) CRYSTAL STRUCTURE OF SIDEROCALIN (NGAL, LIPOCALIN 2) W79A-R81A COMPLEXED WITH FERRIC ENTEROBACTIN | BETA BARREL, LIGAND BINDING PROTEIN
3n2r:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R/3S,4S)-4-(3-PHENOXYPHENOXY)PYRROLIDIN-3-YL)METHYL) PYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE INHIBITOR, OXIDOREDUCTASE
3n2r:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R/3S,4S)-4-(3-PHENOXYPHENOXY)PYRROLIDIN-3-YL)METHYL) PYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE INHIBITOR, OXIDOREDUCTASE
4bvq:A (PRO92) to (ARG121) CYANURIC ACID HYDROLASE: EVOLUTIONARY INNOVATION BY STRUCTURAL CONCATENATION. | HYDROLASE, AMIDASE, CYANURIC ACID
4bvq:B (PRO92) to (ARG121) CYANURIC ACID HYDROLASE: EVOLUTIONARY INNOVATION BY STRUCTURAL CONCATENATION. | HYDROLASE, AMIDASE, CYANURIC ACID
4bvs:A (PRO92) to (ARG121) CYANURIC ACID HYDROLASE: EVOLUTIONARY INNOVATION BY STRUCTURAL CONCATENATION. | HYDROLASE, AMIDASE
5fdp:A (ARG609) to (GLN620) STRUCTURE OF DDR1 RECEPTOR TYROSINE KINASE IN COMPLEX WITH D2099 INHIBITOR AT 2.25 ANGSTROMS RESOLUTION. | TRANSFERASE, DDR1 KINASE, INHIBITORS, STRUCTURAL GENOMICS, PSI- BIOLOGY, STRUCTURAL GENOMICS CONSORTIUM, SGC
3n5w:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6,6'-(2,2'-(PYRIDINE-3,5-DIYL)BIS(ETHANE-2,1-DIYL))BIS(4- METHYLPYRIDIN-2-AMINE) | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n5w:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6,6'-(2,2'-(PYRIDINE-3,5-DIYL)BIS(ETHANE-2,1-DIYL))BIS(4- METHYLPYRIDIN-2-AMINE) | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n5z:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-(2-(6-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL)PYRIDIN-2-YL) ETHYL)-6-METHYLPYRIDIN-2-AMINE | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n5z:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-(2-(6-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL)PYRIDIN-2-YL) ETHYL)-6-METHYLPYRIDIN-2-AMINE | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n60:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6,6'-(2,2'-(5-AMINO-1,3-PHENYLENE)BIS(ETHANE-2,1-DIYL))BIS(4- METHYLPYRIDIN-2-AMINE) | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n60:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6,6'-(2,2'-(5-AMINO-1,3-PHENYLENE)BIS(ETHANE-2,1-DIYL))BIS(4- METHYLPYRIDIN-2-AMINE) | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n62:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE D597N MUTANT HEME DOMAIN IN COMPLEX WITH 6,6'-(2,2'-(PYRIDINE-3,5-DIYL)BIS(ETHANE-2,1-DIYL)) BIS(4-METHYLPYRIDIN-2-AMINE) | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n62:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE D597N MUTANT HEME DOMAIN IN COMPLEX WITH 6,6'-(2,2'-(PYRIDINE-3,5-DIYL)BIS(ETHANE-2,1-DIYL)) BIS(4-METHYLPYRIDIN-2-AMINE) | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n63:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH 6,6'-(2,2'-(5-AMINO-1,3-PHENYLENE)BIS(ETHANE- 2,1-DIYL))BIS(4-METHYLPYRIDIN-2-AMINE) | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n63:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH 6,6'-(2,2'-(5-AMINO-1,3-PHENYLENE)BIS(ETHANE- 2,1-DIYL))BIS(4-METHYLPYRIDIN-2-AMINE) | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n65:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE S602H MUTANT HEME DOMAIN IN COMPLEX WITH 6,6'-(2,2'-(PYRIDINE-3,5-DIYL)BIS(ETHANE-2,1-DIYL)) BIS(4-METHYLPYRIDIN-2-AMINE) | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n65:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE S602H MUTANT HEME DOMAIN IN COMPLEX WITH 6,6'-(2,2'-(PYRIDINE-3,5-DIYL)BIS(ETHANE-2,1-DIYL)) BIS(4-METHYLPYRIDIN-2-AMINE) | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n66:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE S602H MUTANT HEME DOMAIN IN COMPLEX WITH 6,6'-(2,2'-(5-AMINO-1,3-PHENYLENE)BIS(ETHANE-2,1- DIYL))BIS(4-METHYLPYRIDIN-2-AMINE) | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n66:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE S602H MUTANT HEME DOMAIN IN COMPLEX WITH 6,6'-(2,2'-(5-AMINO-1,3-PHENYLENE)BIS(ETHANE-2,1- DIYL))BIS(4-METHYLPYRIDIN-2-AMINE) | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n6g:B (PRO95) to (GLY103) STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE N368D SINGLE MUTANT HEME DOMAIN COMPLEXED WITH 4-(2-(5-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL) ETHYL)PYRIDIN-3-YL)ETHYL)-6-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4r5s:A (GLU711) to (ALA722) CRYSTAL STRUCTURE OF EGFR 696-1022 L858R IN COMPLEX WITH FIIN-3 | EGFR, L858R, KINASE, FIIN-3, TRANSFERASE
4r5y:B (GLN456) to (SER467) THE COMPLEX STRUCTURE OF BRAF V600E KINASE DOMAIN WITH A NOVEL BRAF INHIBITOR | KINASE, SIGNAL TRANSDUCTION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
3n81:G (ARG329) to (PRO343) T244A MUTANT OF HUMAN MITOCHONDRIAL ALDEHYDE DEHYDROGENASE, APO FORM | OXIDOREDUCTASE, ALDH, ROSSMANN FOLD
3c8w:A (PRO33) to (GLU47) CRYSTAL STRUCTURE OF ACETOACETATE DECARBOXYLASE (ADC) (YP_094708.1) FROM LEGIONELLA PNEUMOPHILA SUBSP. PNEUMOPHILA STR. PHILADELPHIA 1 AT 1.60 A RESOLUTION | YP_094708.1, ACETOACETATE DECARBOXYLASE (ADC), STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, LYASE
3c8w:D (PRO33) to (GLU47) CRYSTAL STRUCTURE OF ACETOACETATE DECARBOXYLASE (ADC) (YP_094708.1) FROM LEGIONELLA PNEUMOPHILA SUBSP. PNEUMOPHILA STR. PHILADELPHIA 1 AT 1.60 A RESOLUTION | YP_094708.1, ACETOACETATE DECARBOXYLASE (ADC), STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, LYASE
4bzi:A (SER443) to (PRO452) THE STRUCTURE OF THE COPII COAT ASSEMBLED ON MEMBRANES | TRANSPORT PROTEIN, SECRETION, TRAFFICKING, SEC23, SEC24, SAR1
4bzi:D (SER443) to (PRO452) THE STRUCTURE OF THE COPII COAT ASSEMBLED ON MEMBRANES | TRANSPORT PROTEIN, SECRETION, TRAFFICKING, SEC23, SEC24, SAR1
4bzi:G (SER443) to (PRO452) THE STRUCTURE OF THE COPII COAT ASSEMBLED ON MEMBRANES | TRANSPORT PROTEIN, SECRETION, TRAFFICKING, SEC23, SEC24, SAR1
5fj3:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((4-CHLORO-3-((METHYLAMINO)METHYL) PHENOXY)METHYL)QUINOLIN-2-AMINE IN THE ABSENCE OF ACETATE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
3nae:A (PRO35) to (ASP51) RB69 DNA POLYMERASE (Y567A) TERNARY COMPLEX WITH DATP OPPOSITE GUANIDINOHYDANTOIN | RB69 DNA POLYMERASE, FIDELITY, GUANIDINOHYDANTOIN, TRANSFERASE-DNA COMPLEX
3cbc:C (GLY29) to (GLY38) CRYSTAL STRUCTURE OF SIDEROCALIN (NGAL, LIPOCALIN 2) Y106F COMPLEXED WITH FERRIC ENTEROBACTIN | SIDEROCALIN, NGAL, 24P3, ENTEROBACTIN, GLYCOPROTEIN, PYRROLIDONE CARBOXYLIC ACID, SECRETED, ANTIMICROBIAL PROTEIN
4c0s:B (LYS392) to (LYS408) MAMMALIAN TRANSLATION ELONGATION FACTOR EEF1A2 | TRANSLATION
4c2m:G (VAL132) to (ALA142) STRUCTURE OF RNA POLYMERASE I AT 2.8 A RESOLUTION | TRANSCRIPTION, RIBOSOME BIOGENESIS
3cf1:C (TYR173) to (GLU185) STRUCTURE OF P97/VCP IN COMPLEX WITH ADP/ADP.ALFX | AAA, CDC48, ERAD, ATPASE, TRANSPORT PROTEIN
4c39:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-((((3S, 5R)-5-(((6-AMINO-4-METHYLPYRIDIN- 2-YL)METHOXY)METHYL)PYRROLIDIN-3-YL)OXY)METHYL)-4- METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4c39:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-((((3S, 5R)-5-(((6-AMINO-4-METHYLPYRIDIN- 2-YL)METHOXY)METHYL)PYRROLIDIN-3-YL)OXY)METHYL)-4- METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4c3a:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-((((3S, 5R)-5-(((6-AMINO-4- METHYLPYRIDIN-2-YL)METHOXY)METHYL)PYRROLIDIN-3-YL)OXY) METHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
3ndx:A (ASP30) to (GLY49) HIV-1 PROTEASE SAQUINAVIR:RITONAVIR 1:50 COMPLEX STRUCTURE | HIV-1 PROTEASE, HYDROLASE, AIDS, ASPARTYL PROTEASE, SAQUINAVIR, CARBAMYLATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3cfo:A (PRO35) to (ASP51) TRIPLE MUTANT APO STRUCTURE | APO, HALF-CLOSED, OPEN, CLOSED, BASE SELECTIVITY, DNA REPLICATION, DNA-BINDING, DNA-DIRECTED DNA POLYMERASE, EXONUCLEASE, HYDROLASE, NUCLEASE, NUCLEOTIDYLTRANSFERASE, TRANSFERASE
3cfp:A (PRO35) to (ASP51) STRUCTURE OF THE REPLICATING COMPLEX OF A POL ALPHA FAMILY DNA POLYMERASE, TERNARY COMPLEX 1 | DNA POLYMERASE, CATALYTIC COMPLEX, FIDELITY, TWO METAL ION MECHANISM, DNA REPLICATION, DNA-BINDING, DNA-DIRECTED DNA POLYMERASE, EXONUCLEASE, HYDROLASE, NUCLEASE, NUCLEOTIDYLTRANSFERASE, TRANSFERASE, TRANSFERASE-DNA COMPLEX
3cjj:A (CYS144) to (PRO151) CRYSTAL STRUCTURE OF HUMAN RAGE LIGAND-BINDING DOMAIN | MEMBRANE PROTEIN, SIGNALING PROTEIN, IMMUNOGLOBULIN DOMAIN, GLYCOPROTEIN, MEMBRANE, SECRETED, TRANSMEMBRANE
3nlh:A (PRO95) to (GLY103) STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN N368D MUTANT COMPLEXED WITH 6-{{(3'S,4'S)-3'-[2"-(3'''- FLUOROPHENETHYLAMINO)ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN- 2-AMINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3nlj:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V/Y706A TRIPLE MUTANT HEME DOMAIN COMPLEXED WITH 6-{{(3'R,4'R)-3'-[2"-(3'''- FLUOROPHENETHYLAMINO)ETHOXY] PYRROLIDIN-4'-YL}METHYL}-4- METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3nlj:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V/Y706A TRIPLE MUTANT HEME DOMAIN COMPLEXED WITH 6-{{(3'R,4'R)-3'-[2"-(3'''- FLUOROPHENETHYLAMINO)ETHOXY] PYRROLIDIN-4'-YL}METHYL}-4- METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3nli:B (PRO95) to (GLY103) STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE N368D MUTANT HEME DOMAIN COMPLEXED WITH 6-{{(3'R,4'R)-3'-[2"-(3'''- FLUOROPHENETHYLAMINO)ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN- 2-AMINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3nlk:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE R349A MUTANT HEME DOMAIN IN COMPLEX WITH 6-{{(3'S,4'S)-3'-[2"-(3'''-FLUOROPHENETHYLAMINO) ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR, HEME ENZYME, OXIDOREDUCTASE
3nlk:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE R349A MUTANT HEME DOMAIN IN COMPLEX WITH 6-{{(3'S,4'S)-3'-[2"-(3'''-FLUOROPHENETHYLAMINO) ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR, HEME ENZYME, OXIDOREDUCTASE
3nlm:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-{{(3'R,4'R)-3'-[2"-(3'''-FLUOROPHENETHYLAMINO) ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR, HEME ENZYME, OXIDOREDUCTASE
3nlm:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-{{(3'R,4'R)-3'-[2"-(3'''-FLUOROPHENETHYLAMINO) ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR, HEME ENZYME, OXIDOREDUCTASE
3nlp:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH 6-{{(3'S,4'S)-3'-[2"-(3'''- FLUOROPHENETHYLAMINO)ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN- 2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR, HEME ENZYME, OXIDOREDUCTASE
3nlp:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH 6-{{(3'S,4'S)-3'-[2"-(3'''- FLUOROPHENETHYLAMINO)ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN- 2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR, HEME ENZYME, OXIDOREDUCTASE
3nlq:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH 6-{{(3'R,4'R)-3'-[2"-(3'''- FLUOROPHENETHYLAMINO)ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN- 2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR, HEME ENZYME, OXIDOREDUCTASE
3nlq:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH 6-{{(3'R,4'R)-3'-[2"-(3'''- FLUOROPHENETHYLAMINO)ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN- 2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR, HEME ENZYME, OXIDOREDUCTASE
3nlv:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3S,4S)-4-(2-(2,2-DIFLUORO-2-(3-FLUOROPHENYL)ETHYLAMINO) ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME THIOLATE ENZYME, INHIBITOR, OXIDOREDUCTASE
3nlv:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3S,4S)-4-(2-(2,2-DIFLUORO-2-(3-FLUOROPHENYL)ETHYLAMINO) ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME THIOLATE ENZYME, INHIBITOR, OXIDOREDUCTASE
3nlw:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3S,4S)-4-(2-(2,2-DIFLUORO-2-(PIPERIDIN-2-YL)ETHYLAMINO) ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME THIOLATE ENZYME, INHIBITOR, OXIDOREDUCTASE
3nlw:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3S,4S)-4-(2-(2,2-DIFLUORO-2-(PIPERIDIN-2-YL)ETHYLAMINO) ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME THIOLATE ENZYME, INHIBITOR, OXIDOREDUCTASE
3nlx:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2- (2,2-DIFLUORO-2-(3-FLUOROPHENYL)ETHYLAMINO) ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME THIOLATE ENZYME, INHIBITOR, OXIDOREDUCTASE
3nlx:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2- (2,2-DIFLUORO-2-(3-FLUOROPHENYL)ETHYLAMINO) ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME THIOLATE ENZYME, INHIBITOR, OXIDOREDUCTASE
3nly:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2- (2,2-DIFLUORO-2-(4-FLUOROPHENYL)ETHYLAMINO) ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME THIOLATE ENZYME, INHIBITOR, OXIDOREDUCTASE
3nly:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2- (2,2-DIFLUORO-2-(4-FLUOROPHENYL)ETHYLAMINO) ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME THIOLATE ENZYME, INHIBITOR, OXIDOREDUCTASE
3nlz:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-(2,2-DIFLUORO-2-PHENYLETHYLAMINO)ETHOXY) PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME THIOLATE ENZYME, INHIBITOR, OXIDOREDUCTASE
3nlz:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-(2,2-DIFLUORO-2-PHENYLETHYLAMINO)ETHOXY) PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME THIOLATE ENZYME, INHIBITOR, OXIDOREDUCTASE
3nm0:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-(2,2-DIFLUORO-2-PHENYLETHYLAMINO)ETHOXY) PYRROLIDIN-3-YL)METHYL)-4-METHYL-3,4,5,6-TETRAHYDROPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME THIOLATE ENZYME INHIBITOR, OXIDOREDUCTASE
3nm0:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-(2,2-DIFLUORO-2-PHENYLETHYLAMINO)ETHOXY) PYRROLIDIN-3-YL)METHYL)-4-METHYL-3,4,5,6-TETRAHYDROPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME THIOLATE ENZYME INHIBITOR, OXIDOREDUCTASE
5fok:A (GLY597) to (GLN623) CRYSTAL STRUCTURE OF THE SIDEROPHORE RECEPTOR PIUA FROM PSEUDOMONAS AERUGINOSA | METAL TRANSPORT, TONB-DEPENDENT RECEPTOR, SIDEROPHORE RECEPTOR, OUTER-MEMBRANE PROTEIN
4c8f:D (LEU89) to (GLN97) MOUSE ZNRF3 ECTODOMAIN CRYSTAL FORM IV | LIGASE, WNT, RNF43, LGR4, LGR5, LGR6, RSPO, R-SPONDIN, R-SPO, RSPO1, RSPO2, RSPO3, RSPO4, RECEPTOR, MEMBRANE, SIGNALLING
3nny:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 6-(((3R,4R)-4-(2-(3-FLUOROPHENETHYLAMINO)ETHOXY)PYRROLIDIN-3- YL)METHYL)PYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, INHIBITOR, OXIDOREDUCTASE
3nny:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 6-(((3R,4R)-4-(2-(3-FLUOROPHENETHYLAMINO)ETHOXY)PYRROLIDIN-3- YL)METHYL)PYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, INHIBITOR, OXIDOREDUCTASE
3nnz:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 6-(((3S,4S)-4-(2-(3-FLUOROPHENETHYLAMINO)ETHOXY)PYRROLIDIN-3- YL)METHYL)PYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, INHIBITOR, OXIDOREDUCTASE
3nnz:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 6-(((3S,4S)-4-(2-(3-FLUOROPHENETHYLAMINO)ETHOXY)PYRROLIDIN-3- YL)METHYL)PYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, INHIBITOR, OXIDOREDUCTASE
4cam:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-FLUOROPHENETHYLAMINO)METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cam:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-FLUOROPHENETHYLAMINO)METHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cap:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-(2-(3-(3-FLUOROPHENYL(PROPYLAMINO)METHYL) )QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4cap:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-(2-(3-(3-FLUOROPHENYL(PROPYLAMINO)METHYL) )QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4can:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-(2-(3-FLUOROBENZYLAMINO)ETHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4can:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-(2-(3-FLUOROBENZYLAMINO)ETHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cao:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-(2-(3-(3-FLUOROPHENYL(PROPYLAMINO)ETHYL)) QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4cao:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-(2-(3-(3-FLUOROPHENYL(PROPYLAMINO)ETHYL)) QUINOLIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4car:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-FLUOROPHENETHYLAMINO)METHYL) QUINOLIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4car:B (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-FLUOROPHENETHYLAMINO)METHYL) QUINOLIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
3nol:A (ILE26) to (ASP40) CRYSTAL STRUCTURE OF ZYMOMONAS MOBILIS GLUTAMINYL CYCLASE (TRIGONAL FORM) | BETA-PROPELLER, GLUTAMINYL CYCLASE, CYCLOTRANSFERASE, PYROGLUTAMATE, TRANSFERASE
4cbb:D (ILE313) to (PRO327) APO FORM OF BETAINE ALDEHYDE DEHYDROGENASE FROM PSEUDOMONAS AERUGINOSA | OXIDOREDUCTASE, ALDEHYDE OXIDATION
3npf:A (SER127) to (LYS136) CRYSTAL STRUCTURE OF A PUTATIVE DIPEPTIDYL-PEPTIDASE VI (BACOVA_00612) FROM BACTEROIDES OVATUS AT 1.72 A RESOLUTION | STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, HYDROLASE
3npf:B (SER127) to (LYS136) CRYSTAL STRUCTURE OF A PUTATIVE DIPEPTIDYL-PEPTIDASE VI (BACOVA_00612) FROM BACTEROIDES OVATUS AT 1.72 A RESOLUTION | STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, HYDROLASE
4cdt:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-FLUOROPHENETHYLAMINO)ETHYL)QUINOLIN- 2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cdt:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-FLUOROPHENETHYLAMINO)ETHYL)QUINOLIN- 2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
3nuk:A (GLU396) to (ILE408) THE CRYSTAL STRUCTURE OF THE W169Y MUTANT OF ALPHA-GLUCOSIDASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174 | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, (BETA/ALPHA)8 BARREL, GLYCOSYLE HYDROLYSIS, HYDROLASE
3num:A (ASP315) to (TYR325) SUBSTRATE INDUCED REMODELING OF THE ACTIVE SITE REGULATES HTRA1 ACTIVITY | SERINE PROTEASE, DEGP, HTRA, PROTEASE, HYDROLASE
3cq8:A (PRO35) to (ASP51) TERNARY COMPLEX OF THE L415F MUTANT RB69 EXO(-)POLYMERASE | B FAMILY POLYMERASE FOLD, DNA REPLICATION, DNA-BINDING, DNA-DIRECTED DNA POLYMERASE, EXONUCLEASE, HYDROLASE, NUCLEASE, NUCLEOTIDYLTRANSFERASE, TRANSFERASE, TRANSFERASE-DNA COMPLEX
3nvq:A (PHE55) to (GLY70) MOLECULAR MECHANISM OF GUIDANCE CUE RECOGNITION | BETA-PROPELLER, SIGNALING, SIGNALING PROTEIN-PROTEIN BINDING COMPLEX
3nvq:E (PHE55) to (GLY70) MOLECULAR MECHANISM OF GUIDANCE CUE RECOGNITION | BETA-PROPELLER, SIGNALING, SIGNALING PROTEIN-PROTEIN BINDING COMPLEX
3cr0:A (GLU298) to (GLY308) WEE1 KINASE COMPLEX WITH INHIBITOR PD259_809 | KINASE DOMAIN, INHIBITOR COMPLEX, TRANSFERASE
4cft:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-FLUOROPHENETHYLAMINO)ETHYL) QUINOLIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cft:B (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-FLUOROPHENETHYLAMINO)ETHYL) QUINOLIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4rqt:A (HIS35) to (HIS48) ALCOHOL DEHYDROGENASE CRYSTAL STRUCTURE | ROSSMANN FOLD, ALCOHOL DEHYDROGENASE, OXIDOREDUCTASE
4rqu:A (HIS35) to (LEU46) ALCOHOL DEHYDROGENASE CRYSTAL STRUCTURE IN COMPLEX WITH NAD | ROSSMANN FOLD, ALCOHOL DEHYDROGENASE, NAD, OXIDOREDUCTASE
4rqu:B (HIS35) to (LEU46) ALCOHOL DEHYDROGENASE CRYSTAL STRUCTURE IN COMPLEX WITH NAD | ROSSMANN FOLD, ALCOHOL DEHYDROGENASE, NAD, OXIDOREDUCTASE
4cfx:C (ASN3) to (THR14) STRUCTURE-BASED DESIGN OF C8-SUBSTITUTED O6-CYCLOHEXYLMETHOXYGUANINE CDK1 AND 2 INHIBITORS. | CELL CYCLE, STRUCTURE-BASED DRUG DESIGN, CONFORMATIONAL RESTRAINT, REVERSED BINDING MODE
3nw8:B (VAL574) to (GLN584) GLYCOPROTEIN B FROM HERPES SIMPLEX VIRUS TYPE 1, Y179S MUTANT, HIGH-PH | ENVELOPE GLYCOPROTEIN, MEMBRANE FUSION, VIRAL PROTEIN, GLYCOPROTEIN B, HERPESVIRUS 1, HSV-1, MEMBRANE
3nw8:D (ASP110) to (GLN126) GLYCOPROTEIN B FROM HERPES SIMPLEX VIRUS TYPE 1, Y179S MUTANT, HIGH-PH | ENVELOPE GLYCOPROTEIN, MEMBRANE FUSION, VIRAL PROTEIN, GLYCOPROTEIN B, HERPESVIRUS 1, HSV-1, MEMBRANE
4rs4:B (PRO288) to (ASP298) CRYSTAL STRUCTURE AND MUTATIONAL ANALYSIS OF THE ENDORIBONUCLEASE FROM HUMAN CORONAVIRUS 229E | ENDORIBONUCLEASE, HYDROLASE
3nwx:B (ASP30) to (GLY49) X-RAY STRUCTURE OF ESTER CHEMICAL ANALOGUE [O-ILE50,O-ILE50']HIV-1 PROTEASE COMPLEXED WITH KVS-1 INHIBITOR | BETA-BARREL, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3nxg:C (GLU25) to (GLU46) JC POLYOMAVIRUS VP1 | BETA-SANDWICH JELLY ROLL, VIRAL PROTEIN
3nxd:E (GLU25) to (GLU46) JC POLYOMAVIRUS VP1 IN COMPLEX WITH LSTC | BETA-SANDWICH WITH JELLY ROLL TOPOLOGY, MAJOR CAPSID PROTEIN, VIRAL PROTEIN
5fvo:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(2-(5-(3-METHOXYPROPYLAMINO)PYRIDIN-3-YL) ETHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5fvq:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(2-(5-(4-METHYLPIPERAZIN-1-YL) PYRIDIN-3-YL)ETHYL)PYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5fvq:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(2-(5-(4-METHYLPIPERAZIN-1-YL) PYRIDIN-3-YL)ETHYL)PYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4rtd:A (GLY520) to (GLY545) ESCHERICHIA COLI ALPHA-2-MACROGLOBULIN ACTIVATED BY PORCINE ELASTASE | THIOESTER DOMAIN, MACROGLOBULIN, LIPID BINDING PROTEIN
5fvs:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(2-(5-(3-(METHYLAMINO)PROPYL) PYRIDIN-3-YL)ETHYL)PYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5fvs:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(2-(5-(3-(METHYLAMINO)PROPYL) PYRIDIN-3-YL)ETHYL)PYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5fvv:A (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(2-(5-(1-METHYLPIPERIDIN-4-YL) PYRIDIN-3-YL)ETHYL)PYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE
5fvv:B (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(2-(5-(1-METHYLPIPERIDIN-4-YL) PYRIDIN-3-YL)ETHYL)PYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE
5fvw:A (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(2-(5-(3-(METHYLAMINO)PROPYL) PYRIDIN-3-YL)ETHYL)PYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE
5fvw:B (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(2-(5-(3-(METHYLAMINO)PROPYL) PYRIDIN-3-YL)ETHYL)PYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE
5fvz:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(2-(5-(3-(DIMETHYLAMINO)PROPYL) PYRIDIN-3-YL)ETHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5fvx:A (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH 6-(2-(5-(3-(DIMETHYLAMINO)PROPYL) PYRIDIN-3-YL)ETHYL)-4-METHYLPYRIDIN- 2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE
5fvy:B (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(2-(5-(4-METHYLPIPERAZIN- 1-YL)PYRIDIN-3-YL)ETHYL)PYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5fw0:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(2-(5-((2-METHOXYETHYL)(METHYL)AMINO) PYRIDIN-3-YL)ETHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5fw0:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(2-(5-((2-METHOXYETHYL)(METHYL)AMINO) PYRIDIN-3-YL)ETHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
3nz2:C (SER60) to (GLU69) CRYSTAL STRUCTURE OF HEXAPEPTIDE-REPEAT CONTAINING-ACETYLTRANSFERASE VCA0836 COMPLEXED WITH ACETYL CO ENZYME A FROM VIBRIO CHOLERAE O1 BIOVAR ELTOR | STRUCTURAL GENOMICS, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID, BETA-HELIX, METHYLTRANSFERASE, TRANSFERASE
5fww:A (VAL1051) to (ARG1060) WNT MODULATOR KREMEN IN COMPLEX WITH DKK1 (CRD2) AND LRP6 (PE3PE4) | SIGNALING PROTEIN, WNT, CELL SURFACE, SIGNALLING, MEMBRANE PROTEIN
4rvx:A (ASP30) to (GLY49) CRYSTAL STRUCTURE OF MULTIDRUG-RESISTANT CLINICAL ISOLATE A02 HIV-1 PROTEASE IN COMPLEX WITH NON-PEPTIDIC INHIBITOR, GRL079 | HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, HIV-1 PROTEASE- INHIBITOR COMPLEX, GRL079, NON-PEPTIDIC PROTEASE INHIBITOR
3o0w:A (TYR306) to (VAL313) STRUCTURAL BASIS OF CARBOHYDRATE RECOGNITION BY CALRETICULIN | JELLY ROLL FOLD, CHAPERONE, CARBOHYDRATE BINDING; CALCIUM BINDING
3o14:A (GLY0) to (ASP14) CRYSTAL STRUCTURE OF AN ANTI-ECFSIGMA FACTOR, CHRR (MAQU_0586) FROM MARINOBACTER AQUAEOLEI VT8 AT 1.70 A RESOLUTION | CHRR, CUPIN, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-BIOLOGY, GENE REGULATION
4rwl:B (LEU478) to (ALA488) CRYSTAL STRUCTURE OF FGFR1 (C488A, C584C) IN COMPLEX WITH 6-(7-((1- AMINOCYCLOPROPYL) METHOXY)-6-METHOXYQUINOLIN-4-YLOXY)-N-METHYL-1- NAPHTHAMIDE (E3810) | RECEPTOR TYROSINE KINASE, GATEKEEPER MUTATION, PROTO-ONCOGENE, KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4s1t:A (PRO288) to (ASP298) CRYSTAL STRUCTURE OF THE MUTANT I26A/N52A OF THE ENDORIBONUCLEASE FROM HUMAN CORONAVIRUS 229E | HCOV-229E, ENDORIBONUCLEASE, TRIMERIC NSP15, DOUBLE MUTATION, HYDROLASE
4s1t:B (PRO288) to (ASP298) CRYSTAL STRUCTURE OF THE MUTANT I26A/N52A OF THE ENDORIBONUCLEASE FROM HUMAN CORONAVIRUS 229E | HCOV-229E, ENDORIBONUCLEASE, TRIMERIC NSP15, DOUBLE MUTATION, HYDROLASE
4s1t:C (PRO288) to (ASP298) CRYSTAL STRUCTURE OF THE MUTANT I26A/N52A OF THE ENDORIBONUCLEASE FROM HUMAN CORONAVIRUS 229E | HCOV-229E, ENDORIBONUCLEASE, TRIMERIC NSP15, DOUBLE MUTATION, HYDROLASE
4s1t:D (PRO288) to (ASP298) CRYSTAL STRUCTURE OF THE MUTANT I26A/N52A OF THE ENDORIBONUCLEASE FROM HUMAN CORONAVIRUS 229E | HCOV-229E, ENDORIBONUCLEASE, TRIMERIC NSP15, DOUBLE MUTATION, HYDROLASE
4s1t:E (PRO288) to (ASP298) CRYSTAL STRUCTURE OF THE MUTANT I26A/N52A OF THE ENDORIBONUCLEASE FROM HUMAN CORONAVIRUS 229E | HCOV-229E, ENDORIBONUCLEASE, TRIMERIC NSP15, DOUBLE MUTATION, HYDROLASE
4s1t:F (PRO288) to (ASP298) CRYSTAL STRUCTURE OF THE MUTANT I26A/N52A OF THE ENDORIBONUCLEASE FROM HUMAN CORONAVIRUS 229E | HCOV-229E, ENDORIBONUCLEASE, TRIMERIC NSP15, DOUBLE MUTATION, HYDROLASE
5g0n:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE D597N MUTANT HEME DOMAIN IN COMPLEX WITH N1-(5-(2-(6-AMINO-4- METHYLPYRIDIN-2-YL)ETHYL)PYRIDIN-3-YL)-N1,N2- DIMETHYLETHANE-1,2-DIAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5g0n:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE D597N MUTANT HEME DOMAIN IN COMPLEX WITH N1-(5-(2-(6-AMINO-4- METHYLPYRIDIN-2-YL)ETHYL)PYRIDIN-3-YL)-N1,N2- DIMETHYLETHANE-1,2-DIAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5g0o:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE D597N MUTANT HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(2-(5-(4- METHYLPIPERAZIN-1-YL)PYRIDIN-3-YL)ETHYL)PYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5g0o:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE D597N MUTANT HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(2-(5-(4- METHYLPIPERAZIN-1-YL)PYRIDIN-3-YL)ETHYL)PYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5g0p:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE M336V D597N MUTANT HEME DOMAIN IN COMPLEX WITH 6-(2-(5-(3-(DIMETHYLAMINO) PROPYL)PYRIDIN-3-YL)ETHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5g0p:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE M336V D597N MUTANT HEME DOMAIN IN COMPLEX WITH 6-(2-(5-(3-(DIMETHYLAMINO) PROPYL)PYRIDIN-3-YL)ETHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
3o9d:B (ASP30) to (GLY49) CRYSTAL STRUCTURE OF WILD-TYPE HIV-1 PROTEASE IN COMPLEX WITH KD19 | HIV-1 PROTEASE, DRUG RESISTANCE, DRUG DESIGN, PROTEASE INHIBITORS, AIDS, ASPARTYL PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3o9h:B (ASP30) to (GLY49) CRYSTAL STRUCTURE OF WILD-TYPE HIV-1 PROTEASE IN COMPLEX WITH KD26 | HIV-1 PROTEASE, DRUG RESISTANCE, DRUG DESIGN, PROTEASE INHIBITORS, AIDS, ASPARTYL PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3o9i:A (ASP30) to (ILE50) CRYSTAL STRUCTURE OF WILD-TYPE HIV-1 PROTEASE IN COMPLEX WITH AF61 | HIV-1 PROTEASE, DRUG RESISTANCE, DRUG DESIGN, PROTEASE INHIBITORS, AIDS, ASPARTYL PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3oae:A (TYR27) to (THR39) CRYSTAL STRUCTURE OF HPV16 L1 PENTAMER BOUND TO HEPARIN OLIGOSACCHARIDES | JELLY ROLL, CAPSID PROTEIN, RECEPTOR HSPG, VIRUS CAPSID, VIRAL PROTEIN
3oae:C (TYR27) to (THR39) CRYSTAL STRUCTURE OF HPV16 L1 PENTAMER BOUND TO HEPARIN OLIGOSACCHARIDES | JELLY ROLL, CAPSID PROTEIN, RECEPTOR HSPG, VIRUS CAPSID, VIRAL PROTEIN
3oae:D (TYR27) to (THR39) CRYSTAL STRUCTURE OF HPV16 L1 PENTAMER BOUND TO HEPARIN OLIGOSACCHARIDES | JELLY ROLL, CAPSID PROTEIN, RECEPTOR HSPG, VIRUS CAPSID, VIRAL PROTEIN
3oae:E (TYR27) to (THR39) CRYSTAL STRUCTURE OF HPV16 L1 PENTAMER BOUND TO HEPARIN OLIGOSACCHARIDES | JELLY ROLL, CAPSID PROTEIN, RECEPTOR HSPG, VIRUS CAPSID, VIRAL PROTEIN
4ctq:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (R)-6-(2-AMINO-2-(3-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL) ETHYL)PHENYL)ETHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4ctq:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (R)-6-(2-AMINO-2-(3-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL) ETHYL)PHENYL)ETHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4ctp:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-6-(2-AMINO-2-(3-(2-(6-AMINO-4- METHYLPYRIDIN-2-YL)ETHYL)PHENYL)ETHYL)-4-METHYLPYRIDIN-2- AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4ctp:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-6-(2-AMINO-2-(3-(2-(6-AMINO-4- METHYLPYRIDIN-2-YL)ETHYL)PHENYL)ETHYL)-4-METHYLPYRIDIN-2- AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4ctr:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 2-(6-AMINO-4-METHYLPYRIDIN-2-YL)-1-(3-(2-( 6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL )PHENYL)ETHAN-1-OL | OXIDOREDUCTASE, INHIBITOR COMPLEX
4ctr:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 2-(6-AMINO-4-METHYLPYRIDIN-2-YL)-1-(3-(2-( 6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL )PHENYL)ETHAN-1-OL | OXIDOREDUCTASE, INHIBITOR COMPLEX
4ctt:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-6-(2-AMINO-2-(3-(2-(4-METHYLPYRIDIN-2-YL) ETHYL)PHENYL)ETHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4ctt:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-6-(2-AMINO-2-(3-(2-(4-METHYLPYRIDIN-2-YL) ETHYL)PHENYL)ETHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4ctu:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(3-AMINO-2-(3-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL) ETHYL)PHENYL)PROPYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4ctu:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(3-AMINO-2-(3-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL) ETHYL)PHENYL)PROPYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4ctv:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(3-AMINO-2-(6-(2-(6-AMINO-4- METHYLPYRIDIN-2-YL)ETHYL)PYRIDIN-2-YL)PROPYL)-4- METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4ctv:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(3-AMINO-2-(6-(2-(6-AMINO-4- METHYLPYRIDIN-2-YL)ETHYL)PYRIDIN-2-YL)PROPYL)-4- METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4ctw:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (R)-6-(3-AMINO-2-(5-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL) ETHYL)PYRIDIN-3-YL)PROPYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4ctw:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (R)-6-(3-AMINO-2-(5-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL) ETHYL)PYRIDIN-3-YL)PROPYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4ctx:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-6-(3-AMINO-2-(5-(2-(6-AMINO-4- METHYLPYRIDIN-2-YL)ETHYL)PYRIDIN-3-YL)PROPYL)-4- METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4ctx:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (S)-6-(3-AMINO-2-(5-(2-(6-AMINO-4- METHYLPYRIDIN-2-YL)ETHYL)PYRIDIN-3-YL)PROPYL)-4- METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cu0:B (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (R)-6-(3-AMINO-2-(5-(2-(6-AMINO-4- METHYLPYRIDIN-2-YL)ETHYL)PYRIDIN-3-YL)PROPYL)-4- METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cu1:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-[(2S)-3-AMINO-2-{5-[2-(6-AMINO- 4-METHYLPYRIDIN-2-YL)ETHYL]PYRIDIN-3-YL}PROPYL]-4- METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cu1:B (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-[(2S)-3-AMINO-2-{5-[2-(6-AMINO- 4-METHYLPYRIDIN-2-YL)ETHYL]PYRIDIN-3-YL}PROPYL]-4- METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cun:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (9AS)-2-AMINO-9A-METHYL-8,9,9A,10- TETRAHYDROBENZO[G]PTERIDINE-4,6(3H,7H)-DIONE | OXIDOREDUCTASE, COFACTOR ANALOG COMPLEX
4cvg:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN (H4B-FREE) SUPPLEMENTED WITH 50UM ZN ACETATE AND WITH POOR BINDING OF 6-ACETYL-2-AMINO-7,7-DIMETHYL-7,8-DIHYDROPTERIDIN-4(3H)-ONE. | OXIDOREDUCTASE, COFACTOR ANALOG COMPLEX
3da0:B (GLY93) to (LYS100) CRYSTAL STRUCTURE OF A CLEAVED FORM OF A CHIMERIC RECEPTOR BINDING PROTEIN FROM LACTOCOCCAL PHAGES SUBSPECIES TP901-1 AND P2 | LACTOCOCCAL PHAGE P2, LACTOCOCCAL PHAGE TP901-1 RECEPTOR BINDING PROTEIN, VIRAL PROTEIN
3da0:C (GLY93) to (LYS100) CRYSTAL STRUCTURE OF A CLEAVED FORM OF A CHIMERIC RECEPTOR BINDING PROTEIN FROM LACTOCOCCAL PHAGES SUBSPECIES TP901-1 AND P2 | LACTOCOCCAL PHAGE P2, LACTOCOCCAL PHAGE TP901-1 RECEPTOR BINDING PROTEIN, VIRAL PROTEIN
3ode:B (LYS108) to (GLU116) HUMAN PARP-1 ZINC FINGER 2 (ZN2) BOUND TO DNA | PROTEIN-DNA COMPLEX, PARP ZINC FINGER, DNA BINDING PROTEIN-DNA COMPLEX
3oe7:V (GLU68) to (GLY80) STRUCTURE OF FOUR MUTANT FORMS OF YEAST F1 ATPASE: GAMMA-I270T | ATP SYNTHASE, ATP PHOSPHATASE, F1F0 ATPASE, ATP SYNTHESIS, ADP, PO4, MITOCHONDRIA, HYDROLASE
4cww:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(((3R,4R)-4-((5-(4- METHYLPYRIDIN-2-YL)PENTYL)OXY)PYRROLIDIN-3-YL)METHYL) PYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4cwy:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(5-(((3R,4R)-4-((6-AMINO-4- METHYLPYRIDIN-2-YL)METHYL)PYRROLIDIN-3-YL)OXY)PENTYL)-4- METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4cx0:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE Y477A MUTANT HEME DOMAIN IN COMPLEX WITH 6-((((3S, 5R)-5-(((6- AMINO-4-METHYLPYRIDIN-2-YL)METHOXY)METHYL)PYRROLIDIN-3-YL) OXY)METHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cx0:B (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE Y477A MUTANT HEME DOMAIN IN COMPLEX WITH 6-((((3S, 5R)-5-(((6- AMINO-4-METHYLPYRIDIN-2-YL)METHOXY)METHYL)PYRROLIDIN-3-YL) OXY)METHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cx1:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE L111A MUTANT HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(((3R,4R)-4-( (5-(4-METHYLPYRIDIN-2-YL)PENTYL)OXY)PYRROLIDIN-3-YL)METHYL) PYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cx1:B (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE L111A MUTANT HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(((3R,4R)-4-( (5-(4-METHYLPYRIDIN-2-YL)PENTYL)OXY)PYRROLIDIN-3-YL)METHYL) PYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cx2:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(5-(((3R,4R)-4-((6-AMINO-4- METHYLPYRIDIN-2-YL)METHYL)PYRROLIDIN-3-YL)OXY)PENTYL)-4- METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cx3:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE M336V D597N MUTANT HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(((3R,4R)-4-( (5-(PYRIDIN-2-YL)PENTYL)OXY)PYRROLIDIN-3-YL)METHYL)PYRIDIN- 2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cx3:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE M336V D597N MUTANT HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(((3R,4R)-4-( (5-(PYRIDIN-2-YL)PENTYL)OXY)PYRROLIDIN-3-YL)METHYL)PYRIDIN- 2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cx4:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE M336V D597N MUTANT HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(((3R,4R)-4-( (5-(4-METHYLPYRIDIN-2-YL)PENTYL)OXY)PYRROLIDIN-3-YL)METHYL) PYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cx4:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE M336V D597N MUTANT HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(((3R,4R)-4-( (5-(4-METHYLPYRIDIN-2-YL)PENTYL)OXY)PYRROLIDIN-3-YL)METHYL) PYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cx5:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE H341L MUTANT HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(((3R,4R)-4-( (5-(PYRIDIN-2-YL)PENTYL)OXY)PYRROLIDIN-3-YL)METHYL)PYRIDIN- 2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cx5:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE H341L MUTANT HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(((3R,4R)-4-( (5-(PYRIDIN-2-YL)PENTYL)OXY)PYRROLIDIN-3-YL)METHYL)PYRIDIN- 2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cx6:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE H341L MUTANT HEME DOMAIN IN COMPLEX WITH 6-((((3S, 5R)-5-(((6- AMINO-4-METHYLPYRIDIN-2-YL)METHOXY)METHYL)PYRROLIDIN-3-YL) OXY)METHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4cx6:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE H341L MUTANT HEME DOMAIN IN COMPLEX WITH 6-((((3S, 5R)-5-(((6- AMINO-4-METHYLPYRIDIN-2-YL)METHOXY)METHYL)PYRROLIDIN-3-YL) OXY)METHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
3oeh:N (GLU68) to (GLY80) STRUCTURE OF FOUR MUTANT FORMS OF YEAST F1 ATPASE: BETA-V279F | ATP SYNTHASE, ATP PHOSPHATASE, F1F0 ATPASE, ATP SYNTHESIS, HYDROLASE, ADP, PO4, MITOCHONDRIA
4cyl:A (GLU411) to (SER423) TOMOGRAPHIC SUBVOLUME AVERAGE OF EFF-1 FUSOGEN ON EXTRACELLULAR VESICLES | CELL ADHESION, CELL-CELL FUSION, EXTRACELLULAR FUSION, MEMBRANE FUSION, PRE-FUSION STATE
3dfl:A (GLN59) to (LEU81) CRYSTAL STRUCTURE OF HUMAN PROSTASIN COMPLEXED TO 4- GUANIDINOBENZOIC ACID | PROSTASIN, SERINE PROTEASE, GLYCOPROTEIN, HYDROLASE, MEMBRANE, SECRETED, TRANSMEMBRANE, ZYMOGEN
5gib:B (GLN15) to (SER37) SUCCINIC ACID BOUND TRYPSIN CRYSTALLIZED AS DIMER | TRYPSIN, DIMER, SUCCINIC ACID, HYDROLASE
3oh3:A (HIS561) to (ASN570) PROTEIN STRUCTURE OF USP FROM L. MAJOR BOUND TO URIDINE-5'-DIPHOSPHATE -ARABINOSE | LEFT HANDED BETA HELIX, ROSSMANN FOLD, UDP SUGAR PYROPHOSPHORYLASE, TRANSFERASE
4d1n:A (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS HEME DOMAIN WITH L-ARG BOUND | OXIDOREDUCTASE
4d1n:B (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS HEME DOMAIN WITH L-ARG BOUND | OXIDOREDUCTASE
4d1n:C (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS HEME DOMAIN WITH L-ARG BOUND | OXIDOREDUCTASE
4d1n:D (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS HEME DOMAIN WITH L-ARG BOUND | OXIDOREDUCTASE
4d1o:A (PRO93) to (GLY101) STRUCTURE OF HUMAN ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN WITH L-ARG BOUND | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE,
4d1p:A (PRO93) to (GLY101) STRUCTURE OF HUMAN ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-((((3S, 5R)-5-(((6-AMINO-4- METHYLPYRIDIN-2-YL)METHOXY)METHYL)PYRROLIDIN-3-YL)OXY) METHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE,
5gm0:A (ASN52) to (VAL60) TL-GAL WITH LACTOSE | CARBOHYDRATES, TOXASCARIS LEONINA, GALECTIN, SUGAR BINDING PROTEIN
3ojv:D (MET149) to (SER157) CRYSTAL STRUCTURE OF FGF1 COMPLEXED WITH THE ECTODOMAIN OF FGFR1C EXHIBITING AN ORDERED LIGAND SPECIFICITY-DETERMINING BETAC'-BETAE LOOP | BETA TREFOIL MOTIF, IMMUNOGLOBULIN-LIKE DOMAIN, GROWTH FACTOR, GROWTH FACTOR RECEPTOR, EXTRACELLULAR, CYTOKINE-SIGNALING PROTEIN COMPLEX
3ojy:C (GLY29) to (SER38) CRYSTAL STRUCTURE OF HUMAN COMPLEMENT COMPONENT C8 | MACPF, LIPOCALIN, COMPLEMENT, IMMUNE SYSTEM
5gmf:A (ARG545) to (LEU557) CRYSTAL STRUCTURE OF MONKEY TLR7 IN COMPLEX WITH GUANOSINE AND POLYU | IMMUNE SYSTEM, TLR7, INNATE IMMUNITY, SSRNA RECOGNITON, IMMUNE SYSTEM-RNA COMPLEX
5gmf:B (ARG545) to (LEU557) CRYSTAL STRUCTURE OF MONKEY TLR7 IN COMPLEX WITH GUANOSINE AND POLYU | IMMUNE SYSTEM, TLR7, INNATE IMMUNITY, SSRNA RECOGNITON, IMMUNE SYSTEM-RNA COMPLEX
5gmf:C (ARG545) to (LEU557) CRYSTAL STRUCTURE OF MONKEY TLR7 IN COMPLEX WITH GUANOSINE AND POLYU | IMMUNE SYSTEM, TLR7, INNATE IMMUNITY, SSRNA RECOGNITON, IMMUNE SYSTEM-RNA COMPLEX
5gmf:D (ARG545) to (LEU557) CRYSTAL STRUCTURE OF MONKEY TLR7 IN COMPLEX WITH GUANOSINE AND POLYU | IMMUNE SYSTEM, TLR7, INNATE IMMUNITY, SSRNA RECOGNITON, IMMUNE SYSTEM-RNA COMPLEX
4d2y:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (1R,2R)-2-(3-FLUOROBENZYL)-N-{2-[2-(1H-IMIDAZOL- 1-YL)PYRIMIDIN-4-YL]ETHYL}CYCLOPROPANAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4d2y:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (1R,2R)-2-(3-FLUOROBENZYL)-N-{2-[2-(1H-IMIDAZOL- 1-YL)PYRIMIDIN-4-YL]ETHYL}CYCLOPROPANAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4d2z:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (1S,2S)-2-(3-FLUOROBENZYL)-N-{2-[2-(1H-IMIDAZOL- 1-YL)PYRIMIDIN-4-YL]ETHYL} CYCLOPROPANAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4d2z:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (1S,2S)-2-(3-FLUOROBENZYL)-N-{2-[2-(1H-IMIDAZOL- 1-YL)PYRIMIDIN-4-YL]ETHYL} CYCLOPROPANAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4d30:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL) ETHYL-3-(PYRIDIN-3-YL)PROPAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4d30:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL) ETHYL-3-(PYRIDIN-3-YL)PROPAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4d31:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL)-N-( 3-CYANOBENZYL)ETHAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4d31:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL)-N-( 3-CYANOBENZYL)ETHAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4d32:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 3-(3-FLUOROPHENYL)-N-2-(2-(5-METHYL-1H- IMIDAZOL-1-YL)PYRIMIDIN-4-YL)ETHYLPROPAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4d32:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 3-(3-FLUOROPHENYL)-N-2-(2-(5-METHYL-1H- IMIDAZOL-1-YL)PYRIMIDIN-4-YL)ETHYLPROPAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4d3b:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N1-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL)-N2- (3-FLUOROPHENETHYL)ETHANE-1,2-DIAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4d3b:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N1-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL)-N2- (3-FLUOROPHENETHYL)ETHANE-1,2-DIAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4d37:B (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-{[(1R,2R)-2-(3-FLUOROPHENYL)CYCLOPROPYL] ETHYL}-2-[2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL]ETHANAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4d3a:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 3-(3-FLUOROPHENYL)-N-2-(2-(5-METHYL- 1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL)ETHYLPROPAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4twn:A (ASN620) to (GLU631) HUMAN EPHA3 KINASE DOMAIN IN COMPLEX WITH BIRB796 | TRANSFERASE/TRANSFERASE INHIBITOR, TRANSFERASE
3dqr:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NOS D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH A INHIBITOR (+-)-N1-{CIS-4'-[(6"-AMINOPYRIDIN- 2"-YL)METHYL]PYRROLIDIN-3'-YL}ETHANE-1,2-DIAMINE | NITRIC OXIDE SYNTHASE HEME ENZYME INHIBITOR, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3dqr:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NOS D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH A INHIBITOR (+-)-N1-{CIS-4'-[(6"-AMINOPYRIDIN- 2"-YL)METHYL]PYRROLIDIN-3'-YL}ETHANE-1,2-DIAMINE | NITRIC OXIDE SYNTHASE HEME ENZYME INHIBITOR, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
4d7o:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(4-(((3-FLUOROPHENETHYL)AMINO)METHYL) PHENYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4d7o:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(4-(((3-FLUOROPHENETHYL)AMINO)METHYL) PHENYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
3dr4:C (LEU4) to (LEU14) GDP-PEROSAMINE SYNTHASE K186A MUTANT FROM CAULOBACTER CRESCENTUS WITH BOUND SUGAR LIGAND | PEROSAMINE, DEOXYSUGAR, PYRIDOXAL PHOSPHATE, ASPARTATE AMINOTRANSFERASE, O-ANTIGEN
3dr4:D (PRO5) to (LEU14) GDP-PEROSAMINE SYNTHASE K186A MUTANT FROM CAULOBACTER CRESCENTUS WITH BOUND SUGAR LIGAND | PEROSAMINE, DEOXYSUGAR, PYRIDOXAL PHOSPHATE, ASPARTATE AMINOTRANSFERASE, O-ANTIGEN
3dr7:A (LEU4) to (LEU14) GDP-PEROSAMINE SYNTHASE FROM CAULOBACTER CRESCENTUS WITH BOUND GDP-3-DEOXYPEROSAMINE | PEROSAMINE, PYRIDOXAL PHOSPHATE, O-ANTIGEN, LIPOPOLYSACCHARIDE, ASPARTATE AMINOTRANSFERASE, DEOXYSUGAR
3dr7:B (PRO5) to (LEU14) GDP-PEROSAMINE SYNTHASE FROM CAULOBACTER CRESCENTUS WITH BOUND GDP-3-DEOXYPEROSAMINE | PEROSAMINE, PYRIDOXAL PHOSPHATE, O-ANTIGEN, LIPOPOLYSACCHARIDE, ASPARTATE AMINOTRANSFERASE, DEOXYSUGAR
3dr7:C (PRO5) to (LEU14) GDP-PEROSAMINE SYNTHASE FROM CAULOBACTER CRESCENTUS WITH BOUND GDP-3-DEOXYPEROSAMINE | PEROSAMINE, PYRIDOXAL PHOSPHATE, O-ANTIGEN, LIPOPOLYSACCHARIDE, ASPARTATE AMINOTRANSFERASE, DEOXYSUGAR
3dr7:D (PRO5) to (LEU14) GDP-PEROSAMINE SYNTHASE FROM CAULOBACTER CRESCENTUS WITH BOUND GDP-3-DEOXYPEROSAMINE | PEROSAMINE, PYRIDOXAL PHOSPHATE, O-ANTIGEN, LIPOPOLYSACCHARIDE, ASPARTATE AMINOTRANSFERASE, DEOXYSUGAR
5h8h:B (LEU7) to (PRO22) STRUCTURE OF THE HUMAN GLUN1/GLUN2A LBD IN COMPLEX WITH GNE3419 | GLUN1, GLUN2A, NMDA, RECEPTOR, TRANSPORT PROTEIN
5h8n:B (LEU7) to (PRO22) STRUCTURE OF THE HUMAN GLUN1/GLUN2A LBD IN COMPLEX WITH NAM | GLUN1, GLUN2A, NMDA, RECEPTOR, TRANSPORT PROTEIN
5h8q:B (LEU7) to (PRO22) STRUCTURE OF THE HUMAN GLUN1/GLUN2A LBD IN COMPLEX WITH GNE8324 | GLUN1, GLUN2A, NMDA, RECEPTOR, TRANSPORT PROTEIN
4dbf:A (GLY44) to (ALA56) CRYSTAL STRUCTURES OF CG1458 | OXALOACETATE DECARBOXYLASE, ISOMERASE
4u30:A (GLN30) to (VAL53) HUMAN MESOTRYPSIN COMPLEXED WITH BIKUNIN KUNITZ DOMAIN 2 | SERINE PROTEASE, PROTEASE INHIBITOR, PROTEIN-PROTEIN INTERACTION, PROTEIN DEGRADATION, PROTEOLYSIS, SUBSTRATE SPECIFICITY, ENZYME KINETICS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5hca:C (TYR301) to (TYR308) GLOBULAR DOMAIN OF THE ENTAMOEBA HISTOLYTICA CALRETICULIN IN COMPLEX WITH GLUCOSE | CHAPERONE, LEGUME LECTIN DOMAIN, SUGAR BINDING PROTEIN
5hca:B (TYR301) to (TYR308) GLOBULAR DOMAIN OF THE ENTAMOEBA HISTOLYTICA CALRETICULIN IN COMPLEX WITH GLUCOSE | CHAPERONE, LEGUME LECTIN DOMAIN, SUGAR BINDING PROTEIN
3otr:B (GLY376) to (GLU389) 2.75 ANGSTROM CRYSTAL STRUCTURE OF ENOLASE 1 FROM TOXOPLASMA GONDII | STRUCTURAL GENOMICS, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID, ALPHA-BETA BARREL, TIM BARREL, ENOLASE 1 LIKE N- TERMINAL DOMAIN, 2-PHOSPHO-D-GLYCERATE HYDROLASE, LYASE
4u43:A (PHE25) to (THR35) MAP4K4 IN COMPLEX WITH INHIBITOR (COMPOUND 6) | KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4u4b:A (ILE140) to (GLU160) CRYSTAL STRUCTURE OF PECTATE LYASE PEL3 FROM PECTOBACTERIUM CAROTOVORUM WITH ONE MONOMER IN THE A.U. | PROTEIN SECRETION, BACTERIAL PATHOGENESIS, LYASE
4dg4:A (GLN30) to (VAL53) HUMAN MESOTRYPSIN-S39Y COMPLEXED WITH BOVINE PANCREATIC TRYPSIN INHIBITOR (BPTI) | HUMAN MESOTRYPSIN, CANONICAL INHIBITOR, BPTI, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4dg4:G (GLN30) to (VAL53) HUMAN MESOTRYPSIN-S39Y COMPLEXED WITH BOVINE PANCREATIC TRYPSIN INHIBITOR (BPTI) | HUMAN MESOTRYPSIN, CANONICAL INHIBITOR, BPTI, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3ozc:A (GLY105) to (MET119) CRYSTAL STRUCTURE OF HUMAN 5'-DEOXY-5'-METHYLADENOSINE PHOSPHORYLASE IN COMPLEX WITH PCL-PHENYLTHIODADMEIMMA | 5'-METHYLTHIOADENOSINE,PHOSPHORYLASE,MTAP,PCL-PHENYLTHIODADMEIMMA, TRANSFERASE
5hie:A (GLN456) to (SER467) BRAF KINASE DOMAIN B3AC LOOP DELETION MUTANT IN COMPLEX WITH DABRAFENIB | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
5hj0:A (MET103) to (GLN115) CRYSTAL STRUCTURE OF MIS18 'YIPPEE-LIKE' DOMAIN | CENTROMERE, MIS18, LIGASE
5hj0:B (MET103) to (GLN115) CRYSTAL STRUCTURE OF MIS18 'YIPPEE-LIKE' DOMAIN | CENTROMERE, MIS18, LIGASE
5hj0:C (MET103) to (GLN115) CRYSTAL STRUCTURE OF MIS18 'YIPPEE-LIKE' DOMAIN | CENTROMERE, MIS18, LIGASE
4u5z:I (ASN37) to (THR54) TRICHODYSPLASIA SPINULOSA-ASSOCIATED POLYOMAVIRUS (TSPYV) VP1 | VIRAL COAT PROTEIN, JELLY-ROLL FOLD, GLYCAN BINDING, VIRAL PROTEIN
4djo:B (ASP30) to (GLY49) CRYSTAL STRUCTURE OF WILD-TYPE HIV-1 PROTEASE IN COMPLEX WITH MKP56 | HIV-1 PROTEASE, DRUG RESISTANCE, DRUG DESIGN, PROTEASE INHIBITORS, AIDS, ASPARTYL PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5hjo:A (PRO298) to (PHE307) MURINE ENDOPLASMIC RETICULUM ALPHA-GLUCOSIDASE II WITH BOUND SUBSTRATE ANALOGUE | ENZYME GLYCOSYL HYDROLASE, GH31, QUALITY CONTROL EXOGLYCOSIDASE, HYDROLASE
5hjo:C (PRO298) to (PHE307) MURINE ENDOPLASMIC RETICULUM ALPHA-GLUCOSIDASE II WITH BOUND SUBSTRATE ANALOGUE | ENZYME GLYCOSYL HYDROLASE, GH31, QUALITY CONTROL EXOGLYCOSIDASE, HYDROLASE
5hjr:A (PRO298) to (PHE307) MURINE ENDOPLASMIC RETICULUM ALPHA-GLUCOSIDASE II WITH BOUND COVALENT INTERMEDIATE | ENZYME GLYCOSYL HYDROLASE GH31 QUALITY CONTROL EXOGLYCOSIDASE, HYDROLASE
3e16:B (GLN30) to (LEU53) X-RAY STRUCTURE OF HUMAN PROSTASIN IN COMPLEX WITH BENZOXAZOLE WARHEAD PEPTIDOMIMIC, LYSINE IN P3 | PROSTASIN, HCAP-1, CHANNEL ACTIVATING PROTEASE, INHIBITOR, ENAC, BENZOXAZOLE, CELL MEMBRANE, GLYCOPROTEIN, HYDROLASE, MEMBRANE, PROTEASE, SECRETED, SERINE PROTEASE, TRANSMEMBRANE, ZYMOGEN
3e1x:B (GLN30) to (LEU53) THE CRYSTAL STRUCTURE OF APO PROSTASIN AT 1.7 ANGSTROMS RESOLUTION | PROSTASIN, ENAC, HCAP-1, CHANNEL ACTIVATING PROTEASE, CELL MEMBRANE, GLYCOPROTEIN, HYDROLASE, MEMBRANE, PROTEASE, SECRETED, SERINE PROTEASE, TRANSMEMBRANE, ZYMOGEN
5htg:A (GLU3) to (ASP15) STRUCTURE OF APO P1 FORM OF CANDIDA ALBICANS FKBP12 | FKBP12, PATHOGENIC FUNGI, CALCINEURIN, ISOMERASE
5htg:B (GLU3) to (ASP15) STRUCTURE OF APO P1 FORM OF CANDIDA ALBICANS FKBP12 | FKBP12, PATHOGENIC FUNGI, CALCINEURIN, ISOMERASE
4uch:A (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH 3-(((2-((2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL) ETHYL)AMINO)METHYL)BENZONITRILE | OXIDOREDUCTASE
4uch:B (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH 3-(((2-((2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL) ETHYL)AMINO)METHYL)BENZONITRILE | OXIDOREDUCTASE
4dtn:A (PRO35) to (ASP51) RB69 DNA POLYMERASE TERNARY COMPLEX WITH DATP OPPOSITE AN ABASIC SITE AND DDA/DT AS THE PENULTIMATE BASE-PAIR | ABASIC SITE, THF, RB69POL, DATP, TRANSFERASE-DNA COMPLEX
4dto:A (PRO35) to (ASP51) RB69 DNA POLYMERASE TERNARY COMPLEX WITH DCTP OPPOSITE AN ABASIC SITE AND DDA/DT AS THE PENULTIMATE BASE-PAIR | ABASIC SITE, THF, RB69POL, DATP, TRANSFERASE-DNA COMPLEX
4dtp:A (PRO35) to (ASP51) RB69 DNA POLYMERASE TERNARY COMPLEX WITH DGTP OPPOSITE AN ABASIC SITE AND DDA/DT AS THE PENULTIMATE BASE-PAIR | ABASIC SITE, THF, RB69POL, DGTP, TRANSFERASE-DNA COMPLEX
4dtr:A (PRO35) to (ASP51) RB69 DNA POLYMERASE TERNARY COMPLEX WITH DATP OPPOSITE AN ABASIC SITE AND DDC/DG AS THE PENULTIMATE BASE-PAIR | ABASIC SITE, THF, RB69POL, DTTP, TRANSFERASE-DNA COMPLEX
4dur:A (VAL7) to (PHE15) THE X-RAY CRYSTAL STRUCTURE OF FULL-LENGTH TYPE II HUMAN PLASMINOGEN | SERINE PROTEASE, FIBRINOLYSIS, HYDROLASE
4ugz:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N1-(3-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL) ETHYL)PHENYL)-N1,N2-DIMETHYLETHANE-1,2-DIAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4ugz:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N1-(3-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL) ETHYL)PHENYL)-N1,N2-DIMETHYLETHANE-1,2-DIAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4uh0:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N1-(6-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL) ETHYL)PYRIDIN-2-YL)-N1,N2-DIMETHYLETHANE-1,2-DIAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4uh0:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N1-(6-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL) ETHYL)PYRIDIN-2-YL)-N1,N2-DIMETHYLETHANE-1,2-DIAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4uh1:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N1-(5-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL) ETHYL)PYRIDIN-3-YL)-N1,N2-DIMETHYLETHANE-1,2-DIAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4uh1:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N1-(5-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL) ETHYL)PYRIDIN-3-YL)-N1,N2-DIMETHYLETHANE-1,2-DIAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4uh2:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N1-(3-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL)- 5-(TRIFLUOROMETHYL)PHENYL)-N1,N2-DIMETHYLETHANE-1,2-DIAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4uh2:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N1-(3-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL)- 5-(TRIFLUOROMETHYL)PHENYL)-N1,N2-DIMETHYLETHANE-1,2-DIAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4uh3:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N1-(3-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL) ETHYL)-5-FLUOROPHENYL)-N1,N2-DIMETHYLETHANE-1,2-DIAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4uh3:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N1-(3-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL) ETHYL)-5-FLUOROPHENYL)-N1,N2-DIMETHYLETHANE-1,2-DIAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4uh4:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 3-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL)- 5-(METHYL(2-(METHYLAMINO)ETHYL)AMINO)BENZONITRILE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4uh4:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 3-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL)- 5-(METHYL(2-(METHYLAMINO)ETHYL)AMINO)BENZONITRILE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4uh5:A (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH N1-(5-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL) PYRIDIN-3-YL)-N1,N2-DIMETHYLETHANE-1,2-DIAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE
4uh5:B (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH N1-(5-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL) PYRIDIN-3-YL)-N1,N2-DIMETHYLETHANE-1,2-DIAMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE
4uh6:A (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH 3-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL)-5-( METHYL(2-(METHYLAMINO)ETHYL)AMINO)BENZONITRILE | OXIDOREDUCTASE
4uh6:B (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH 3-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL)-5-( METHYL(2-(METHYLAMINO)ETHYL)AMINO)BENZONITRILE | OXIDOREDUCTASE
4uha:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 3-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL) ETHYL)-5-(METHYL(2-(METHYLAMINO)ETHYL)AMINO)BENZONITRILE | OXIDOREDUCTASE, INHIBITOR COMPLEX
3pha:A (GLU396) to (ILE408) THE CRYSTAL STRUCTURE OF THE W169Y MUTANT OF ALPHA-GLUCOSIDASE (GH31 FAMILY) FROM RUMINOCOCCUS OBEUM ATCC 29174 IN COMPLEX WITH ACARBOSE | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, STRUCTURALCOMPLEX, MCSG, MIDWEST CENTER FOR STRUCTURAL GENOMICS, HYDROLASE, (BETA/ALPHA)8-BARREL, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4uhv:B (SER194) to (VAL219) THE STRUCTURE OF VGRG1, THE NEEDLE TIP OF THE BACTERIAL TYPE VI SECRETION SYSTEM | STRUCTURAL PROTEIN, VGRG1, VIRULENCE, TOXIN, EFFECTOR, PUNCTURING DEVICE, SPIKE, T6SS, P. AERUGINOSA
5i2k:B (LEU7) to (PRO22) STRUCTURE OF THE HUMAN GLUN1/GLUN2A LBD IN COMPLEX WITH 7-{[ETHYL(4- FLUOROPHENYL)AMINO]METHYL}-N,2-DIMETHYL-5-OXO-5H-[1,3]THIAZOLO[3,2- A]PYRIMIDINE-3-CARBOXAMIDE (COMPOUND 19) | GLUN1, GLUN2A, RECEPTOR, NMDA, TRANSPORT PROTEIN
5i2n:B (LEU7) to (PRO22) STRUCTURE OF THE HUMAN GLUN1/GLUN2A LBD IN COMPLEX WITH N-ETHYL-7-{[2- FLUORO-3-(TRIFLUOROMETHYL)PHENYL]METHYL}-2-METHYL-5-OXO-5H-[1, 3]THIAZOLO[3,2-A]PYRIMIDINE-3-CARBOXAMIDE (COMPOUND 29) | NMDA, RECEPTOR, GLUTAMATE, CHANNEL, TRANSPORT PROTEIN
5i3o:A (GLN50) to (GLY61) CRYSTAL STRUCTURE OF BMP-2-INDUCIBLE KINASE IN COMPLEX WITH AN INDAZOLE INHIBITOR | TRANSFERASE, PROTEIN KINASE DOMAIN, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
5i3r:A (GLN50) to (GLY61) CRYSTAL STRUCTURE OF BMP-2-INDUCIBLE KINASE IN COMPLEX WITH AN INDAZOLE INHIBITOR | TRANSFERASE, PROTEIN KINASE DOMAIN, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
5i3r:B (GLN50) to (GLY61) CRYSTAL STRUCTURE OF BMP-2-INDUCIBLE KINASE IN COMPLEX WITH AN INDAZOLE INHIBITOR | TRANSFERASE, PROTEIN KINASE DOMAIN, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
5i56:A (LYS7) to (PRO21) AGONIST-BOUND GLUN1/GLUN2A AGONIST BINDING DOMAINS WITH TCN201 | NMDA RECEPTOR, ANTAGONIST, TRANSPORT PROTEIN, RECEPTOR
5i57:A (SER3) to (PRO21) GLUTAMATE- AND GLYCINE-BOUND GLUN1/GLUN2A AGONIST BINDING DOMAINS | NMDA RECEPTOR, ANTAGONIST, TRANSPORT PROTEIN, RECEPTOR
5i59:A (THR4) to (PRO21) GLUTAMATE- AND GLYCINE-BOUND GLUN1/GLUN2A AGONIST BINDING DOMAINS WITH MPX 007 | NMDA RECEPTOR, ANTAGONIST, TRANSPORT PROTEIN, RECEPTOR
4umt:A (TYR10) to (GLY20) STRUCTURE OF MELK IN COMPLEX WITH INHIBITORS | TRANSFERASE, FRAGMENT BASED DRUG DESIGN
3plb:A (GLN30) to (SER54) BOVINE TRYPSIN VARIANT X(TRIPLEILE227) IN COMPLEX WITH SMALL MOLECULE INHIBITOR | TRYPSIN-LIKE SERINE PROTEASE, PROTEIN BINDING, DUODENUM, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3pne:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-((2,2-DIFLUORO-2-(3-CHLOROPHENYL)ETHYL)AMINO) ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | HEME ENZYME, INHIBITOR, OXIDOREDUCTASE-INHIBITOR COMPLEX
3pne:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-((2,2-DIFLUORO-2-(3-CHLOROPHENYL)ETHYL)AMINO) ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | HEME ENZYME, INHIBITOR, OXIDOREDUCTASE-INHIBITOR COMPLEX
3pnf:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-((2,2-DIFLUORO-2-(2-CHLOROPHENYL)ETHYL)AMINO) ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | HEME ENZYME, INHIBITOR, OXIDOREDUCTASE-INHIBITOR COMPLEX
3pnf:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-((2,2-DIFLUORO-2-(2-CHLOROPHENYL)ETHYL)AMINO) ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | HEME ENZYME, INHIBITOR, OXIDOREDUCTASE-INHIBITOR COMPLEX
3png:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-((2-FLUORO-2-(3-FLUOROPHENYL)ETHYL)AMINO) ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | HEME ENZYME, INHIBITOR, OXIDOREDUCTASE-INHIBITOR COMPLEX
3png:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-((2-FLUORO-2-(3-FLUOROPHENYL)ETHYL)AMINO) ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | HEME ENZYME, INHIBITOR, OXIDOREDUCTASE-INHIBITOR COMPLEX
3pnh:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-((2-FLUORO-2-(3-FLUOROPHENYL) ETHYL) AMINO)ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | HEME ENZYME, INHIBITOR, OXIDOREDUCTASE-INHIBITOR COMPLEX
4upd:B (GLY61) to (CYS72) OPEN CONFORMATION OF O. PICEAE STEROL ESTERASE MUTANT I544W | HYDROLASE
3poc:A (GLU396) to (ILE408) THE CRYSTAL STRUCTURE OF THE D307A MUTANT OF ALPHA-GLUCOSIDASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174 IN COMPLEX WITH ACARBOSE | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, MULTI-DOMAIN, ALPHA- GLUCOSIDASE, CYTOPLASMIC, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4upn:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N,N''-{[(2S)-3-AMINOPROPANE-1,2-DIYL] BIS(OXYMETHANEDIYLBENZENE-3,1-DIYL)}DITHIOPHENE-2-CARBOXIMIDAMIDE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4upn:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N,N''-{[(2S)-3-AMINOPROPANE-1,2-DIYL] BIS(OXYMETHANEDIYLBENZENE-3,1-DIYL)}DITHIOPHENE-2-CARBOXIMIDAMIDE | OXIDOREDUCTASE, INHIBITOR COMPLEX
3pos:A (TYR306) to (VAL313) CRYSTAL STRUCTURE OF THE GLOBULAR DOMAIN OF HUMAN CALRETICULIN | LEGUME LECTIN FOLD, CNX/CRT FAMILY, MULTI-FUNCTIONAL, CHAPERONE, CARBOHYDRATE BINDING, PEPTIDE BINDING, MULTI-COMPARTMENTAL
3pos:B (TYR306) to (VAL313) CRYSTAL STRUCTURE OF THE GLOBULAR DOMAIN OF HUMAN CALRETICULIN | LEGUME LECTIN FOLD, CNX/CRT FAMILY, MULTI-FUNCTIONAL, CHAPERONE, CARBOHYDRATE BINDING, PEPTIDE BINDING, MULTI-COMPARTMENTAL
3pos:C (TYR306) to (VAL313) CRYSTAL STRUCTURE OF THE GLOBULAR DOMAIN OF HUMAN CALRETICULIN | LEGUME LECTIN FOLD, CNX/CRT FAMILY, MULTI-FUNCTIONAL, CHAPERONE, CARBOHYDRATE BINDING, PEPTIDE BINDING, MULTI-COMPARTMENTAL
4upp:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N'-[4-[[(2S,4R)-4-[3-[(C-THIOPHEN-2- YLCARBONIMIDOYL)AMINO]PHENOXY]PYRROLIDIN-2- YL]METHOXY]PHENYL]THIOPHENE-2-CARBOXIMIDAMIDE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4upp:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N'-[4-[[(2S,4R)-4-[3-[(C-THIOPHEN-2- YLCARBONIMIDOYL)AMINO]PHENOXY]PYRROLIDIN-2- YL]METHOXY]PHENYL]THIOPHENE-2-CARBOXIMIDAMIDE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4upo:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-[3-({[(3S,5S)-5-{[(3-{[(Z)-IMINO(THIOPHEN- 2-YL)METHYL]AMINO}BENZYL)OXY]METHYL}PYRROLIDIN-3-YL]OXY} METHYL)PHENYL]THIOPHENE-2-CARBOXIMIDAMIDE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4upo:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-[3-({[(3S,5S)-5-{[(3-{[(Z)-IMINO(THIOPHEN- 2-YL)METHYL]AMINO}BENZYL)OXY]METHYL}PYRROLIDIN-3-YL]OXY} METHYL)PHENYL]THIOPHENE-2-CARBOXIMIDAMIDE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4upq:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N',N'-{[(2R)-3-AMINOPROPANE-1,2-DIYL] BIS(OXYMETHANEDIYLBENZENE-3,1-DIYL)}DITHIOPHENE-2-CARBOXIMIDAMIDE | OXIDOREDUCTASE, INHIBITOR COMPLEX
3pow:A (TYR306) to (VAL313) CRYSTAL STRUCTURE OF THE GLOBULAR DOMAIN OF HUMAN CALRETICULIN | LEGUME LECTIN FOLD, CNX/CRT FAMILY, MULTI-FUNCTIONAL, CARBOHYDRATE BINDING, PEPTIDE BINDING, MULTI-COMPARTMENTAL, CHAPERONE
3pp0:A (ALA710) to (LYS724) CRYSTAL STRUCTURE OF THE KINASE DOMAIN OF HUMAN HER2 (ERBB2). | KINASE DOMAIN, ANTI-ONCOGENE, ATP-BINDING, CELL CYCLE, DISEASE MUTATION, GLYCOPROTEIN, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, RECEPTOR, SECRETED, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE, TYROSINE KINASE INHIBITOR, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX
3ppu:B (ALA58) to (PRO73) CRYSTAL STRUCTURE OF THE GLUTATHIONE-S-TRANSFERASE XI FROM PHANEROCHAETE CHRYSOSPORIUM | GST FOLD, TRANSFERASE
4e4n:A (LEU875) to (HIS885) JAK1 KINASE (JH1 DOMAIN) IN COMPLEX WITH COMPOUND 49 | O-PHOSPHOTYROSINE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4ur9:B (GLN10) to (ASP20) STRUCTURE OF LIGAND BOUND GLYCOSYLHYDROLASE | HYDROLASE
5ied:A (PRO298) to (PHE307) MURINE ENDOPLASMIC RETICULUM ALPHA-GLUCOSIDASE II WITH CASTANOSPERMINE | ENZYME GLYCOSYL HYDROLASE GH31 QUALITY CONTROL EXOGLYCOSIDASE, HYDROLASE
4e6r:B (GLY158) to (VAL169) CRYSTAL STRUCTURE OF A CYTOPLASMIC PROTEIN NCK2 (NCK2) FROM HOMO SAPIENS AT 2.20 A RESOLUTION | SH3 DOMAIN, PROTEIN BINDING, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI- BIOLOGY, SUGAR BINDING PROTEIN
4uta:B (LYS47) to (GLU62) CRYSTAL STRUCTURE OF DENGUE 2 VIRUS ENVELOPE GLYCOPROTEIN IN COMPLEX WITH THE FAB FRAGMENT OF THE BROADLY NEUTRALIZING HUMAN ANTIBODY EDE1 C8 | IMMUNE SYSTEM-VIRAL PROTEIN COMPLEX, VIRAL PROTEIN, MEMBRANE FUSION, CLASS 2 FUSION PROTEIN, DENGUE VIRUS, BROADLY NEUTRALIZING ANTIBODY
4utc:A (CYS285) to (LEU294) CRYSTAL STRUCTURE OF DENGUE 2 VIRUS ENVELOPE GLYCOPROTEIN | VIRAL PROTEIN, MEMBRANE FUSION, CLASS 2 FUSION PROTEIN,
4utc:B (THR48) to (GLU62) CRYSTAL STRUCTURE OF DENGUE 2 VIRUS ENVELOPE GLYCOPROTEIN | VIRAL PROTEIN, MEMBRANE FUSION, CLASS 2 FUSION PROTEIN,
4eax:B (ASP16) to (THR27) MOUSE NGF IN COMPLEX WITH LYSO-PS | LYSO-PS, PHOSPHOLIPID, HORMONE
4eax:D (ASP16) to (THR27) MOUSE NGF IN COMPLEX WITH LYSO-PS | LYSO-PS, PHOSPHOLIPID, HORMONE
3puv:A (VAL298) to (GLN309) CRYSTAL STRUCTURE OF AN OUTWARD-FACING MBP-MALTOSE TRANSPORTER COMPLEX BOUND TO ADP-VO4 | ATP BINDING CASSETTE, NUCLEOTIDE BINDING DOMAIN, SUBSTRATE BINDING PROTEIN, ABC TRANSPORTER, IMPORTER, ATPASE, ATP BINDING, MALTODEXTRIN BINDING, TRANSMEMBRANE INTEGRAL MEMBRANE, HYDROLASE- TRANSPORT PROTEIN COMPLEX
4ehz:A (LEU875) to (HIS885) THE JAK1 KINASE DOMAIN IN COMPLEX WITH INHIBITOR | KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4ej8:B (ASP30) to (GLY48) APO HIV PROTEASE (PR) DIMER IN CLOSED FORM WITH FRAGMENT 1F1 IN THE OUTSIDE/TOP OF FLAP | APO PROTEASE, ALLOSTERY, FRAGMENT BINDING, CLOSED FORM, HYDROLASE
4ejr:B (ASN176) to (LEU192) CRYSTAL STRUCTURE OF MAJOR CAPSID PROTEIN S DOMAIN FROM RABBIT HEMORRHAGIC DISEASE VIRUS | VIRAL PROTEIN, CAPSID PROTEIN
4eog:A (LEU123) to (GLY136) CRYSTAL STRUCTURE OF CSX1 OF PYROCOCCUS FURIOSUS | BETA-HAIRPIN, NUCLEIC ACID BINDING PROTEIN, RNA BINDING, DNA BINDING PROTEIN
5ire:C (ARG57) to (CYS74) THE CRYO-EM STRUCTURE OF ZIKA VIRUS | ZIKA VIRUS, VIRUS
3q3w:B (MSE1) to (GLY9) ISOPROPYLMALATE ISOMERASE SMALL SUBUNIT FROM CAMPYLOBACTER JEJUNI. | STRUCTURAL GENOMICS, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID, ISOPROPYLMALATE, ISOMERASE, TRANSFERASE
3q4u:A (ILE208) to (ARG218) CRYSTAL STRUCTURE OF THE ACVR1 KINASE DOMAIN IN COMPLEX WITH LDN- 193189 | STRUCTURAL GENOMICS CONSORTIUM, SGC, PROTEIN KINASE, TRANSFERASE
4uwb:A (ARG477) to (ALA488) FIBROBLAST GROWTH FACTOR RECEPTOR 1 KINASE IN COMPLEX WITH JK-P5 | TRANSFERASE
3q7j:B (MET1) to (ASP13) ENGINEERED THERMOPLASMA ACIDOPHILUM F3 FACTOR MIMICS HUMAN AMINOPEPTIDASE N (APN) AS A TARGET FOR ANTICANCER DRUG DEVELOPMENT | TRF3, INHIBITOR FBO, AMINOPEPTIDASE, INHIBITOR BINDING, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3q99:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE IN THE FERRIC STATE IN COMPLEX WITH N~5~-[(3-(ETHYLSULFANYL)PROPANIMIDOYL]-L-ORNITHINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, OXIDOREDUCTASE, INHIBITOR, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3q99:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE IN THE FERRIC STATE IN COMPLEX WITH N~5~-[(3-(ETHYLSULFANYL)PROPANIMIDOYL]-L-ORNITHINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, OXIDOREDUCTASE, INHIBITOR, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3q9a:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE IN THE FERRIC STATE IN COMPLEX WITH N-5-[2-(ETHYLSULFANYL)ETHANIMIDOYL]-L-ORNITHINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, OXIDOREDUCTASE, INHIBITOR, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3q9a:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE IN THE FERRIC STATE IN COMPLEX WITH N-5-[2-(ETHYLSULFANYL)ETHANIMIDOYL]-L-ORNITHINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, OXIDOREDUCTASE, INHIBITOR, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4eux:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(5-(((3R,4R)-4-((6-AMINO-4-METHYLPYRIDIN-2-YL)METHYL) PYRROLIDIN-3-YL)OXY)PENTYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4eux:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(5-(((3R,4R)-4-((6-AMINO-4-METHYLPYRIDIN-2-YL)METHYL) PYRROLIDIN-3-YL)OXY)PENTYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
4exw:D (TYR125) to (ARG132) THE STRUCTURE OF DDRB FROM DEINOCOCCUS: A NEW FOLD FOR SINGLE-STRANDED DNA BINDING PROTEINS. | ANTI-PARALLEL BETA-BARREL, PENTAMER, DNA BINDING, DNA ANNEALING, DNA BINDING PROTEIN
3qcw:A (PRO300) to (THR314) STRUCTURE OF NEUREXIN 1 ALPHA (DOMAINS LNS1-LNS6), NO SPLICE INSERTS | SYNAPTIC ADHESION MOLECULE, CELL ADHESION
3qcw:A (VAL740) to (GLN756) STRUCTURE OF NEUREXIN 1 ALPHA (DOMAINS LNS1-LNS6), NO SPLICE INSERTS | SYNAPTIC ADHESION MOLECULE, CELL ADHESION
3qcw:B (PRO300) to (THR314) STRUCTURE OF NEUREXIN 1 ALPHA (DOMAINS LNS1-LNS6), NO SPLICE INSERTS | SYNAPTIC ADHESION MOLECULE, CELL ADHESION
3qcw:B (VAL740) to (GLN756) STRUCTURE OF NEUREXIN 1 ALPHA (DOMAINS LNS1-LNS6), NO SPLICE INSERTS | SYNAPTIC ADHESION MOLECULE, CELL ADHESION
3qei:A (PRO35) to (ASP51) RB69 DNA POLYMERASE (L561A/S565G/Y567A) TERNARY COMPLEX WITH DCTP OPPOSITE DIFLUOROTOLUENE NUCLEOSIDE | DIFLUOROTOLUENE NUCLEOSIDE,DCTP, TRIPLE MUTANT, TRANSFERASE-DNA COMPLEX
3qep:A (PRO35) to (ASP51) RB69 DNA POLYMERASE (L561A/S565G/Y567A) TERNARY COMPLEX WITH DTTP OPPOSITE DIFLUOROTOLUENE NUCLEOSIDE | DIFLUOROTOLUENE NUCLEOSIDE, DTTP, TRIPLE MUTANT, TRANSFERASE-DNA COMPLEX
3qer:A (PRO35) to (ASP51) RB69 DNA POLYMERASE (L561A/S565G/Y567A) TERNARY COMPLEX WITH DATP OPPOSITE DIFLUOROTOLUENE NUCLEOSIDE | DIFLUOROTOLUENE NUCLEOSIDE, DATP, TRIPLE MUTANT, TRANSFERASE-DNA COMPLEX
3qet:A (PRO35) to (ASP51) RB69 DNA POLYMERASE (L561A/S565G/Y567A) TERNARY COMPLEX WITH DTTP OPPOSITE DT | DIFLUOROTOLUENE NUCLEOSIDE, DTTP/DT, TRIPLE MUTANT, TRANSFERASE-DNA COMPLEX
4f23:C (GLY318) to (GLY336) INFLUENZA A VIRUS HEMAGGLUTININ H16 HA0 STRUCTURE WITH AN ALPHA-HELIX CONFORMATION IN THE CLEAVAGE SITE: A POTENTIAL DRUG TARGET | HEMAGGLUTININ, SIALIC ACID, GLYCOLYSATION, MEMBRANE, VIRAL PROTEIN
5iz7:A (THR47) to (GLU62) CRYO-EM STRUCTURE OF THERMALLY STABLE ZIKA VIRUS STRAIN H/PF/2013 | VIRAL PROTEIN, FLAVIVIRUS, GLYCOPROTEIN, ZIKA VIRUS, VIRUS
4f75:B (ASP30) to (GLY49) CRYSTAL STRUCTURE OF ACTIVE HIV-1 PROTEASE IN COMPLEX WITH THE N TERMINAL PRODUCT OF THE SUBSTRATE RH-IN | HIV-1 PROTEASE, SUBSTRATE COMPLEX, AIDS, PRODUCT COMPLEX, ASPARTYL PROTEASE, HYDROLASE, HYDROLASE-HYDROLASE PRODUCT COMPLEX
3qnn:A (PRO35) to (ASP51) RB69 DNA POLYMERASE (Y567A) TERNARY COMPLEX WITH DGT OPPOSITE 3TCO | 3TCO, DGTP, Y567A, TRANSFERASE-DNA COMPLEX
4fbx:A (ASP38) to (GLY48) COMPLEX STRUCTURE OF HUMAN PROTEIN KINASE CK2 CATALYTIC SUBUNIT CRYSTALLIZED IN THE PRESENCE OF A BISUBSTRATE INHIBITOR | PROTEIN KINASE FOLD, PROTEIN PHOSPHORYLATION, BISUBSTRATE INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4fd3:E (TRP105) to (TYR113) CRYSTAL STRUCTURE OF APO-FORMED YMTOAR1 | SHORT-CHAIN ALCOHOL DEHYDROGENASE (SDR) FAMILY, FATTY ACID BIOSYNTHESIS, NADPH, COFACTOR, MITOCHONDRION, OXIDOREDUCTASE
3qpr:A (ALA367) to (GLY379) HK97 PROHEAD I ENCAPSIDATING INACTIVE VIRALLY ENCODED PROTEASE | VIRUS PROCAPSID PARTICLES, VIRUS
3qq1:D (THR227) to (GLU235) CRYSTAL STRUCTURE OF A DOUBLE MUTANT [A58P, DEL(N59)] OF 3-DEOXY-D- MANNO-OCTULOSONATE 8-PHOSPHATE SYNTHASE (KDO8PS) FROM NEISSERIA MENINGITIDIS | MANNO-OCTULOSONATE, SYNTHASE, LIPOPOLYSACCHARIDE, KDOP, KDO8 KDOPS, KDO8PS, TIM BARREL, BIOSYNTHESIS, TRANSFERASE, LYASE, LIPOPOLYSACCHARIDE BIOSYNTHESIS
3qre:A (PHE66) to (ILE116) CRYSTAL STRUCTURE OF AN ENOYL-COA HYDRATASE ECHA12_1 FROM MYCOBACTERIUM MARINUM | STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, SSGCID, MYCOBACTERIUM, TUBERCULOSIS, ENOYL-COA, COENZYME A, HYDRATASE, FATTY ACID METABOLISM, OPPORTUNISTIC INFECTIONS IN HUMANS, ASSOCIATED WITH SWIMMING, FISH-TANK, LYASE
4feh:A (GLY301) to (ASN309) MYCOBACTERIUM TUBERCULOSIS DPRE1 - HEXAGONAL CRYSTAL FORM | ALPHA+BETA, OXIDOREDUCTASE, DECAPRENYLPHOSPHORYL-BETA-D-RIBOSE
4v3u:A (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH N-2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL)ETHYL- 3-(PYRIDIN-3-YL)PROPAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE
4v3u:B (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH N-2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL)ETHYL- 3-(PYRIDIN-3-YL)PROPAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE
4v3u:C (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH N-2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL)ETHYL- 3-(PYRIDIN-3-YL)PROPAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE
4v3u:D (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH N-2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL)ETHYL- 3-(PYRIDIN-3-YL)PROPAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE
4v3v:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(2-(1H-IMIDAZOL-1-YL)-4-PYRIMIDYLMETHYL)- 3-(3-FLUOROPHENYL)PROPAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4v3v:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(2-(1H-IMIDAZOL-1-YL)-4-PYRIMIDYLMETHYL)- 3-(3-FLUOROPHENYL)PROPAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4v3w:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL)-N-( 3-FLUOROPHENETHYL)ETHAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4v3w:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL)-N-( 3-FLUOROPHENETHYL)ETHAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4v3x:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL) ETHYL-3-(3-FLUOROPHENYL)PROPAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4v3x:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL) ETHYL-3-(3-FLUOROPHENYL)PROPAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4v3y:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL) ETHYL-3-(3-CHLOROPHENYL)PROPAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4v3y:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL) ETHYL-3-(3-CHLOROPHENYL)PROPAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4v3z:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL)-N-( 2-(3-FLUOROPHENYL)CYCLOPROPYLMETHYL)ETHAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4v3z:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL)-N-( 2-(3-FLUOROPHENYL)CYCLOPROPYLMETHYL)ETHAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
3qy9:C (LYS173) to (GLY186) THE CRYSTAL STRUCTURE OF DIHYDRODIPICOLINATE REDUCTASE FROM STAPHYLOCOCCUS AUREUS | ROSSMANN FOLD, REDUCTASE, NADH, NADPH, DIHYDRODIPICOLINATE, OXIDOREDUCTASE
4fi1:A (ASP39) to (LYS50) CRYSTAL STRUCTURE OF SCCK2 ALPHA IN COMPLEX WITH ATP | PROTEIN-ATP COMPLEX, PROTEIN KINASE, PHOSPHORYLATION, TRANSFERASE
4fj8:A (PRO35) to (ASP51) RB69 DNA POLYMERASE TERNARY COMPLEX WITH DCTP/DT | DCTP/DT, RB69, RB69POL, QUADRUPLE, TRANSFERASE-DNA COMPLEX
3r05:A (PRO300) to (THR314) STRUCTURE OF NEUREXIN 1 ALPHA (DOMAINS LNS1-LNS6), WITH SPLICE INSERT SS3 | SYNAPTIC ADHESION MOLECULE, CELL ADHESION
3r05:B (PRO300) to (THR314) STRUCTURE OF NEUREXIN 1 ALPHA (DOMAINS LNS1-LNS6), WITH SPLICE INSERT SS3 | SYNAPTIC ADHESION MOLECULE, CELL ADHESION
4fjh:A (PRO35) to (ASP51) RB69 DNA POLYMERASE TERNARY COMPLEX WITH DGTP/DC | DGTP/DC, RB69, RB69POL, QUADRUPLE, TRANSFERASE-DNA COMPLEX
3r2j:A (CYS18) to (ILE30) CRYSTAL STRUCTURE OF PNC1 FROM L. INFANTUM IN COMPLEX WITH NICOTINATE | ALPHA/BETA-HYDROLASE-LIKE, NICOTINAMIDASE, CYTOPLASMIC, HYDROLASE
4fjx:A (PRO35) to (ASP51) RB69 DNA POLYMERASE TERNARY COMPLEX WITH DATP/DG | DATP/DG, RB69, RB69 POL, QUADRUPLE, TRANSFERASE-DNA COMPLEX
4fk0:A (PRO35) to (ASP51) RB69 DNA POLYMERASE TERNARY COMPLEX WITH DCTP/DG | DCTP/DG, RB69, RB69 POL, QUADRUPLE, TRANSFERASE-DNA COMPLEX
4fk2:A (PRO35) to (ASP51) RB69 DNA POLYMERASE TERNARY COMPLEX WITH DTTP/DG | DTTP/DG, RB69, RB69 POL, QUADRUPLE, TRANSFERASE-DNA COMPLEX
4fk4:A (PRO35) to (ASP51) RB69 DNA POLYMERASE TERNARY COMPLEX WITH DGTP/DG | DGTP/DG, RB69, RB69 POL, QUADRUPLE, TRANSFERASE-DNA COMPLEX
5j9h:A (GLY666) to (ILE677) CRYSTAL STRUCTURE OF GLYCOPROTEIN C FROM PUUMALA VIRUS IN THE POST- FUSION CONFORMATION (PH 8.0) | HANTAVIRUS, MEMBRANE FUSION, CONFORMATIONAL CHANGES, ENVELOPED VIRUSES, VIRUS ENTRY, VIRAL PROTEIN
5jb1:A (TYR27) to (GLY46) PSEUDO-ATOMIC STRUCTURE OF HUMAN PAPILLOMAVIRUS TYPE 59 L1 VIRUS-LIKE PARTICLE | CAPSID, T=7 ICOSAHEDRAL, VIRUS-LIKE PARTICLE, VIRUS
5je5:A (ASP148) to (ASN165) CRYSTAL STRUCTURE OF BURKHOLDERIA GLUMAE TOXA WITH BOUND S- ADENOSYLHOMOCYSTEINE (SAH) AND 1-DEMETHYLTOXOFLAVIN | N-METHYLTRANSFERASE, S-ADENOSYLMETHIONINE (SAM), PRODUCT, COMPLEX, TRANSFERASE
4fob:A (ILE1116) to (ALA1126) CRYSTAL STRUCTURE OF HUMAN ANAPLASTIC LYMPHOMA KINASE IN COMPLEX WITH ACYLIMINOBENZIMIDAZOLE INHIBITOR 1 | RECEPTOR TYROSINE KINASE, INHIBITOR, CRIZOTINIB, NEUROBLASTOMA, CD246, PHOSPHOTRANSFERASE, NPM-ALK, EML4-ALK, IN SITU PROTEOLYSIS, TRANSFERASE-INHIBITOR COMPLEX
3rg0:A (TYR306) to (VAL313) STRUCTURAL AND FUNCTIONAL RELATIONSHIPS BETWEEN THE LECTIN AND ARM DOMAINS OF CALRETICULIN | BETA-SANDWICH, CHAPERONE, MONOGLUCOSYLATED PROTEINS BINDING, CARBOHYDRATE BINDING, CALCIUM BINDING, ENDOPLASMIC RETICULUM
5jlv:D (ASP554) to (HIS564) RECEPTOR BINDING DOMAIN OF BOTULINUM NEUROTOXIN A IN COMPLEX WITH HUMAN GLYCOSYLATED SV2C | GLYCOSYLATION, BOTULINUM NEUROTOXIN, RECEPTOR BINDING DOMAIN, HYDROLASE
5jmc:B (SER555) to (HIS564) RECEPTOR BINDING DOMAIN OF BOTULINUM NEUROTOXIN A IN COMPLEX WITH RAT SV2C | HYDROLASE
5jmc:D (ASP554) to (HIS564) RECEPTOR BINDING DOMAIN OF BOTULINUM NEUROTOXIN A IN COMPLEX WITH RAT SV2C | HYDROLASE
5jmc:F (ASP554) to (HIS564) RECEPTOR BINDING DOMAIN OF BOTULINUM NEUROTOXIN A IN COMPLEX WITH RAT SV2C | HYDROLASE
3rhx:B (LEU478) to (ALA488) CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF FGFR1 KINASE IN COMPLEX WITH ARQ 069 | FGFR1 KINASE, FGFR2 KINASE, INACTIVE CONFORMATION, KINASE-INHIBITOR COMPLEX, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4fvc:A (HIS50) to (GLY59) HMOB STRUCTURE WITH HEME | FERREDOXIN-FOLD, HEME OXIGENASE, HEME, OXIDOREDUCTASE
4fvc:B (HIS50) to (GLY59) HMOB STRUCTURE WITH HEME | FERREDOXIN-FOLD, HEME OXIGENASE, HEME, OXIDOREDUCTASE
4fvc:C (HIS50) to (GLY59) HMOB STRUCTURE WITH HEME | FERREDOXIN-FOLD, HEME OXIGENASE, HEME, OXIDOREDUCTASE
4fvc:D (HIS50) to (GLY59) HMOB STRUCTURE WITH HEME | FERREDOXIN-FOLD, HEME OXIGENASE, HEME, OXIDOREDUCTASE
4fvc:E (HIS50) to (GLY59) HMOB STRUCTURE WITH HEME | FERREDOXIN-FOLD, HEME OXIGENASE, HEME, OXIDOREDUCTASE
4fvc:F (HIS50) to (GLY59) HMOB STRUCTURE WITH HEME | FERREDOXIN-FOLD, HEME OXIGENASE, HEME, OXIDOREDUCTASE
3rik:A (LEU383) to (PRO401) THE ACID BETA-GLUCOSIDASE ACTIVE SITE EXHIBITS PLASTICITY IN BINDING 3,4,5,6-TETRAHYDROXYAZEPANE-BASED INHIBITORS: IMPLICATIONS FOR PHARMACOLOGICAL CHAPERONE DESIGN FOR GAUCHER DISEASE | TIM-BARREL, LYSOSOMAL HYDROLASE, HYDROLASE, GLYCOSYLATION, LYSOSOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3rik:B (LEU383) to (PRO401) THE ACID BETA-GLUCOSIDASE ACTIVE SITE EXHIBITS PLASTICITY IN BINDING 3,4,5,6-TETRAHYDROXYAZEPANE-BASED INHIBITORS: IMPLICATIONS FOR PHARMACOLOGICAL CHAPERONE DESIGN FOR GAUCHER DISEASE | TIM-BARREL, LYSOSOMAL HYDROLASE, HYDROLASE, GLYCOSYLATION, LYSOSOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4fvw:A (GLY325) to (GLY333) STRUCTURE OF RAT NNOS HEME DOMAIN IN COMPLEX WITH N(OMEGA)-METHOXY-L- ARGININE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, SUBSTRATE ANALOG
4fvw:B (GLY325) to (GLY333) STRUCTURE OF RAT NNOS HEME DOMAIN IN COMPLEX WITH N(OMEGA)-METHOXY-L- ARGININE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, SUBSTRATE ANALOG
4fvx:A (GLY325) to (GLY333) STRUCTURE OF RAT NNOS HEME DOMAIN IN COMPLEX WITH N(OMEGA)-ETHOXY-L- ARGININE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, SUBSTRATE ANALOG
4fvx:B (GLY325) to (GLY333) STRUCTURE OF RAT NNOS HEME DOMAIN IN COMPLEX WITH N(OMEGA)-ETHOXY-L- ARGININE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, SUBSTRATE ANALOG
4fvy:A (GLY325) to (GLY333) STRUCTURE OF RAT NNOS HEME DOMAIN IN COMPLEX WITH N(OMEGA)-HYDROXY- N(OMEGA)-METHYL-L-ARGININE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, SUBSTRATE ANALOG
4fvy:B (GLY325) to (GLY333) STRUCTURE OF RAT NNOS HEME DOMAIN IN COMPLEX WITH N(OMEGA)-HYDROXY- N(OMEGA)-METHYL-L-ARGININE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, SUBSTRATE ANALOG
4fvz:A (GLY325) to (GLY333) STRUCTURE OF RAT NNOS HEME DOMAIN IN COMPLEX WITH N(OMEGA)-METHYL- N(OMEGA)-METHOXY-L-ARGININE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, SUBSTRATE ANALOG
4fvz:B (GLY325) to (GLY333) STRUCTURE OF RAT NNOS HEME DOMAIN IN COMPLEX WITH N(OMEGA)-METHYL- N(OMEGA)-METHOXY-L-ARGININE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, SUBSTRATE ANALOG
3rio:A (GLY36) to (ASP45) CRYSTAL STRUCTURE OF GLCT CAT-PRDI | TWISTED BETA SHEET, FOUR HELIX BUNDLE, TRANSCRIPTIONAL ANTITERMINATION, TRANSCRIPTION
4fw0:A (GLY325) to (GLY333) STRUCTURE OF RAT NNOS HEME DOMAIN IN COMPLEX WITH N(DELTA)-METHYL- N(OMEGA)-HYDROXY-L-ARGININE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, SUBSTRATE ANALOG
4fw0:B (GLY325) to (GLY333) STRUCTURE OF RAT NNOS HEME DOMAIN IN COMPLEX WITH N(DELTA)-METHYL- N(OMEGA)-HYDROXY-L-ARGININE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, SUBSTRATE ANALOG
5jty:A (LYS7) to (PRO21) GLUTAMATE- AND DCKA-BOUND GLUN1/GLUN2A AGONIST BINDING DOMAINS WITH MPX-007 | NMDA RECEPTOR, ANTAGONIST, TRANSPORT PROTEIN, RECEPTOR
5jty:B (SER10) to (ASP24) GLUTAMATE- AND DCKA-BOUND GLUN1/GLUN2A AGONIST BINDING DOMAINS WITH MPX-007 | NMDA RECEPTOR, ANTAGONIST, TRANSPORT PROTEIN, RECEPTOR
5kcb:A (LYS69) to (ALA93) THE STRUCTURE OF SAV2435 BOUND TO ETHIDIUM BROMIDE | GYRI-LIKE DOMATIN, MULTI-DRUG RECOGNITION, UNKNOWN FUNCTION
5kcj:B (LEU7) to (PRO22) STRUCTURE OF THE HUMAN GLUN1/GLUN2A LBD IN COMPLEX WITH GNE6901 | GRIN1, GRIN2A, NMDA RECEPTOR, GLYCINE, GLUTAMATE, TRANSPORT PROTEIN
4gel:A (SER204) to (THR222) CRYSTAL STRUCTURE OF ZUCCHINI | PIRNA, PHOSPHOLIPASE D, NUCLEASE, HYDROLASE
4gfp:A (ASP2) to (GLU14) 2.7 ANGSTROM RESOLUTION STRUCTURE OF 3-PHOSPHOSHIKIMATE 1- CARBOXYVINYLTRANSFERASE (AROA) FROM COXIELLA BURNETII IN A SECOND CONFORMATIONAL STATE | STRUCTURAL GENOMICS, NIAID, NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID, 3-PHOSPHOSHIKIMATE 1-CARBOXYVINYLTRANSFERASE ACTIVITY, TRANSFERASE
4gh7:A (GLY29) to (GLY38) CRYSTAL STRUCTURE OF ANTICALIN N7A IN COMPLEX WITH ONCOFETAL FIBRONECTIN FRAGMENT FN7B8 | LIPOCALIN, ANTICALIN, HUMAN FIBRONECTIN, FN TYPE III DOMAIN, ONCOFETAL FIBRONECTIN SPLICE VARIANT P02751-7, LIPOCALIN-BASED BINDING PROTEIN, EXTRA-DOMAIN B, EIIIB, ED-B, EXTRACELLULAR MATRIX, PROTEIN BINDING
4go2:B (MET734) to (PRO748) CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE IN COMPLEX WITH THIO-NADP | ALDEHYDE DEHYDROGENASE, FDH, OXIDOREDUCTASE
4gqe:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (5E)-5-[(N-TERT-BUTOXYCARBAMIMIDOYL)IMINO]-L-NORVALINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, SUBSTRATE ANALOG
4gqe:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (5E)-5-[(N-TERT-BUTOXYCARBAMIMIDOYL)IMINO]-L-NORVALINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, SUBSTRATE ANALOG
5kr2:B (ASP30) to (ILE50) PROTEASE PR5-SQV | HIV-1 PROTEASE, E35D, SALT-BRIDGE INTERACTION, NATURAL POLYMORPHISM, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5l2y:H (GLN30) to (VAL53) FACTOR VIIA IN COMPLEX WITH THE INHIBITOR 1-[(2R,15R)-2-[(1-AMINO-4- FLUOROISOQUINOLIN-6-YL)AMINO]-4,15,20-TRIMETHYL-3,12-DIOXO-13-OXA-4, 11-DIAZATRICYCLO[14.2.2.1~6,10~]HENICOSA-1(18),6,8,10(21),16,19- HEXAEN-7-YL] CYCLOBUTANE-1-CARBOXYLIC ACID | GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM-BINDING, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5l2z:H (GLN30) to (VAL53) FACTOR VIIA IN COMPLEX WITH THE INHIBITOR 1-[(2R,15R)-2-[(1-AMINO-4- FLUOROISOQUINOLIN-6-YL)AMINO]-4,15,17-TRIMETHYL-3,12-DIOXO-13-OXA-4, 11-DIAZATRICYCLO[14.2.2.1~6,10~]HENICOSA-1(18),6(21),7,9,16,19- HEXAEN-7-YL]CYCLOHEXANE-1-CARBOXYLIC ACID | GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM-BINDING, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5l56:A (VAL305) to (GLN320) PLEXIN A1 FULL EXTRACELLULAR REGION, DOMAINS 1 TO 10, TO 4 ANGSTROM | RECEPTOR, SIGNALING, AXON GUIDANCE, SIGNALING PROTEIN
5l59:A (VAL305) to (GLN320) PLEXIN A1 FULL EXTRACELLULAR REGION, DOMAINS 1 TO 10, TO 6 ANGSTROM, SPACEGROUP P2(1) | RECEPTOR, SIGNALING, AXON GUIDANCE, SIGNALING PROTEIN
5l59:B (VAL305) to (GLN320) PLEXIN A1 FULL EXTRACELLULAR REGION, DOMAINS 1 TO 10, TO 6 ANGSTROM, SPACEGROUP P2(1) | RECEPTOR, SIGNALING, AXON GUIDANCE, SIGNALING PROTEIN
5l5c:A (VAL305) to (GLN320) PLEXIN A1 FULL EXTRACELLULAR REGION, DOMAINS 1 TO 10, TO 6 ANGSTROM, SPACEGROUP P4(3)2(1)2 | RECEPTOR, SIGNALING, AXON GUIDANCE, SIGNALING PROTEIN
5l73:B (PHE648) to (ASP666) MAM DOMAIN OF HUMAN NEUROPILIN-1 | MAM DOMAIN, DIMERISATION DOMAIN, NEUROPILIN, SIGNALING PROTEIN
5lk5:A (TYR306) to (VAL313) CRYSTAL STRUCTURE OF THE GLOBULAR DOMAIN OF HUMAN CALRETICULIN MUTANT D71K | CALCIUM-BINDING PROTEIN
5lk5:B (TYR306) to (VAL313) CRYSTAL STRUCTURE OF THE GLOBULAR DOMAIN OF HUMAN CALRETICULIN MUTANT D71K | CALCIUM-BINDING PROTEIN
5lk5:C (TYR306) to (VAL313) CRYSTAL STRUCTURE OF THE GLOBULAR DOMAIN OF HUMAN CALRETICULIN MUTANT D71K | CALCIUM-BINDING PROTEIN
5lk5:D (TYR306) to (VAL313) CRYSTAL STRUCTURE OF THE GLOBULAR DOMAIN OF HUMAN CALRETICULIN MUTANT D71K | CALCIUM-BINDING PROTEIN
5lk5:E (TYR306) to (VAL313) CRYSTAL STRUCTURE OF THE GLOBULAR DOMAIN OF HUMAN CALRETICULIN MUTANT D71K | CALCIUM-BINDING PROTEIN
5lk5:F (TYR306) to (VAL313) CRYSTAL STRUCTURE OF THE GLOBULAR DOMAIN OF HUMAN CALRETICULIN MUTANT D71K | CALCIUM-BINDING PROTEIN
5lk5:G (TYR306) to (VAL313) CRYSTAL STRUCTURE OF THE GLOBULAR DOMAIN OF HUMAN CALRETICULIN MUTANT D71K | CALCIUM-BINDING PROTEIN
5lk5:H (TYR306) to (VAL313) CRYSTAL STRUCTURE OF THE GLOBULAR DOMAIN OF HUMAN CALRETICULIN MUTANT D71K | CALCIUM-BINDING PROTEIN
5lk5:I (TYR306) to (VAL313) CRYSTAL STRUCTURE OF THE GLOBULAR DOMAIN OF HUMAN CALRETICULIN MUTANT D71K | CALCIUM-BINDING PROTEIN
5m3m:G (VAL132) to (ALA142) FREE MONOMERIC RNA POLYMERASE I AT 4.0A RESOLUTION | RNA POLYMERASE I, TRANSCRIPTION
5tp9:B (LEU7) to (PRO22) STRUCTURE OF THE HUMAN GLUN1/GLUN2A LBD IN COMPLEX WITH COMPOUND 2 (GNE9178) | NMDA RECEPTOR, GLUTAMATE, GLYCINE, CALCIUM CHANNEL, MEMBRANE, TRANSPORT PROTEIN
8nse:A (PRO95) to (GLY103) BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE, NNA COMPLEX | NITRIC OXIDE SYNTHASE, HEME PROTEIN, TETRAHYDROBIOPTERIN, OXIDOREDUCTASE
9est:A (GLN30) to (MET53) STRUCTURAL STUDY OF PORCINE PANCREATIC ELASTASE COMPLEXED WITH 7- AMINO-3-(2-BROMOETHOXY)-4-CHLOROISOCOUMARIN AS A NONREACTIVATABLE DOUBLY COVALENT ENZYME-INHIBITOR COMPLEX | HYDROLASE(SERINE PROTEINASE)
2aw3:B (THR339) to (ASP356) X-RAY STUDIES ON MALTODEXTRIN PHOSPHORYLASE COMPLEXES: RECOGNITION OF SUBSTRATES AND CATHALITIC MECHANISM OF PHOSPHORYLASE FAMILY | MALTOPENTAOSE, CARBOHYDRATE RECOGNITION, PHOSPHORYLASE MECHANISM, TERNARY COMPLEXES WITH NATURAL AND INHIBITORY SUBSTRATES, TRANSFERASE
4h96:A (THR147) to (PRO160) CANDIDA ALBICANS DIHYDROFOLATE REDUCTASE COMPLEXED WITH NADPH AND 5- {3-[3-(2,3-DIHYDRO-1,4-BENZODIOXIN-6-YL)-5-METHOXYPHENYL]PROP-1-YN-1- YL}-6-ETHYLPYRIMIDINE-2,4-DIAMINE (UCP1018) | ANTIFUNGAL AGENTS, CANDIDA ALBICANS, DRUG DESIGN, ENZYME INHIBITORS, FUNGAL PROTEINS, TETRAHYDROFOLATE DEHYDROGENASE, OXIDOREDUCTASE- OXIDOREDUCTASE INHIBITOR COMPLEX
1nxd:4 (SER164) to (PHE175) CRYSTAL STRUCTURE OF MNMN CONCANAVALIN A | LECTIN, METAL BINDING PROTEIN
4wwq:B (HIS426) to (ARG435) APO STRUCTURE OF THE GRB7 SH2 DOMAIN | SRC HOMOLOGY DOMAIN, PHOSPHOTYROSINE BINDING POCKET, SIGNALING PROTEIN
4x14:A (LEU27) to (GLU46) JC MAD-1 POLYOMAVIRUS VP1 IN COMPLEX WITH GM1 OLIGOSACCHARIDE | BETA-SANDWICH, JELLY-ROLL, VIRAL MAJOR CAPSID PROTEIN, GLYCAN, VIRAL PROTEIN
2bm7:A (ASP141) to (GLY161) THE STRUCTURE OF MFPA (RV3361C, P3221 CRYSTAL FORM). THE PENTAPEPTIDE REPEAT PROTEIN FROM MYCOBACTERIUM TUBERCULOSIS FOLDS AS A RIGHT-HANDED QUADRILATERAL BETA- HELIX. | PENTAPEPTIDE REPEAT PROTEIN, FLUROQUINOLONE RESISTANCE, DNA GYRASE, DNA MIMICRY, RIGHT-HANDED QUADRILATERAL BETA-HELIX
4x8x:B (ILE203) to (ARG211) CRYSTAL STRUCTURE OF DSCAM1 ISOFORM 1.9, N-TERMINAL FOUR IG DOMAINS | IG FOLD, CELL ADHESION
3sa3:A (ASP30) to (GLY49) CRYSTAL STRUCTURE OF WILD-TYPE HIV-1 PROTEASE IN COMPLEX WITH AG23 | HIV-1 PROTEASE, DRUG RESISTANCE, DRUG DESIGN, PROTEASE INHIBITORS, AIDS, ASPARTYL PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3sa3:B (ASP30) to (GLY49) CRYSTAL STRUCTURE OF WILD-TYPE HIV-1 PROTEASE IN COMPLEX WITH AG23 | HIV-1 PROTEASE, DRUG RESISTANCE, DRUG DESIGN, PROTEASE INHIBITORS, AIDS, ASPARTYL PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1by3:A (SER581) to (LYS611) FHUA FROM E. COLI | FHUA, MEMBRANE PROTEIN, LIGAND-GATED, IRON TRANSPORT
2phu:B (ASN41) to (PHE52) PTEROCARPUS ANGOLENSIS LECTIN IN COMPLEX WITH MAN-8D1D3 | LECTIN, CARBOHYDRATE, HIGH MANNOSE, SUGAR BINDING PROTEIN
4hzc:D (GLN151) to (SER162) CRYSTAL STRUCTURE OF SERINE ACETYLTRANSFERASE FROM BRUCELLA ABORTUS STRAIN S19 | CYSTEINE BIOSYNTHESIS, ACETYLTRANSFERASE, LEFT HANDED BETA-HELICAL (LBH) DOMAIN, TRANSFERASE
4hzf:A (HIS20) to (GLN33) STRUCTURE OF THE WILD TYPE CATABOLITE GENE ACTIVATOR PROTEIN | CAP DIMER, DNA BINDING, TRANSCRIPTION
1c4r:A (ARG105) to (THR119) THE STRUCTURE OF THE LIGAND-BINDING DOMAIN OF NEUREXIN 1BETA: REGULATION OF LNS DOMAIN FUNCTION BY ALTERNATIVE SPLICING | LECTIN-LIKE, NEUROBIOLOGY, CELL-CELL ADHESION, CELL-CELL RECOGNITION, ALTERNATIVE SPLICING, MEMBRANE PROTEIN
1c4r:B (ARG105) to (THR119) THE STRUCTURE OF THE LIGAND-BINDING DOMAIN OF NEUREXIN 1BETA: REGULATION OF LNS DOMAIN FUNCTION BY ALTERNATIVE SPLICING | LECTIN-LIKE, NEUROBIOLOGY, CELL-CELL ADHESION, CELL-CELL RECOGNITION, ALTERNATIVE SPLICING, MEMBRANE PROTEIN
1c4r:C (ARG105) to (THR119) THE STRUCTURE OF THE LIGAND-BINDING DOMAIN OF NEUREXIN 1BETA: REGULATION OF LNS DOMAIN FUNCTION BY ALTERNATIVE SPLICING | LECTIN-LIKE, NEUROBIOLOGY, CELL-CELL ADHESION, CELL-CELL RECOGNITION, ALTERNATIVE SPLICING, MEMBRANE PROTEIN
1c4r:D (ARG105) to (THR119) THE STRUCTURE OF THE LIGAND-BINDING DOMAIN OF NEUREXIN 1BETA: REGULATION OF LNS DOMAIN FUNCTION BY ALTERNATIVE SPLICING | LECTIN-LIKE, NEUROBIOLOGY, CELL-CELL ADHESION, CELL-CELL RECOGNITION, ALTERNATIVE SPLICING, MEMBRANE PROTEIN
1c4r:E (ARG105) to (THR119) THE STRUCTURE OF THE LIGAND-BINDING DOMAIN OF NEUREXIN 1BETA: REGULATION OF LNS DOMAIN FUNCTION BY ALTERNATIVE SPLICING | LECTIN-LIKE, NEUROBIOLOGY, CELL-CELL ADHESION, CELL-CELL RECOGNITION, ALTERNATIVE SPLICING, MEMBRANE PROTEIN
1c4r:F (ARG105) to (THR119) THE STRUCTURE OF THE LIGAND-BINDING DOMAIN OF NEUREXIN 1BETA: REGULATION OF LNS DOMAIN FUNCTION BY ALTERNATIVE SPLICING | LECTIN-LIKE, NEUROBIOLOGY, CELL-CELL ADHESION, CELL-CELL RECOGNITION, ALTERNATIVE SPLICING, MEMBRANE PROTEIN
1c4r:G (ARG105) to (THR119) THE STRUCTURE OF THE LIGAND-BINDING DOMAIN OF NEUREXIN 1BETA: REGULATION OF LNS DOMAIN FUNCTION BY ALTERNATIVE SPLICING | LECTIN-LIKE, NEUROBIOLOGY, CELL-CELL ADHESION, CELL-CELL RECOGNITION, ALTERNATIVE SPLICING, MEMBRANE PROTEIN
1c4r:H (ARG105) to (THR119) THE STRUCTURE OF THE LIGAND-BINDING DOMAIN OF NEUREXIN 1BETA: REGULATION OF LNS DOMAIN FUNCTION BY ALTERNATIVE SPLICING | LECTIN-LIKE, NEUROBIOLOGY, CELL-CELL ADHESION, CELL-CELL RECOGNITION, ALTERNATIVE SPLICING, MEMBRANE PROTEIN
4xhg:A (LYS8) to (SER19) STRUCTURE OF C. GLABRATA HRR25 BOUND TO ADP (FORMATE CONDITION) | CASEIN KINASE, MONOPOLIN, TRANSFERASE
4i3v:H (LEU318) to (THR332) STRUCTURE OF PHOSPHONOACETALDEHYDE DEHYDROGENASE IN COMPLEX WITH PHOSPHONOACETALDEHYDE AND COFACTOR NAD+ | ALDEHYDE DEHYDROGENASE, PHOSPHONATE CATABOLISM, OXIDOREDUCTASE
4i3x:A (LEU318) to (THR332) STRUCTURE OF PHOSPHONOACETALDEHYDE DEHYDROGENASE IN COMPLEX WITH PHOSPHONOACETATE AND COFACTOR NAD+ | ALDEHYDE DEHYDROGENASE, PHOSPHONATE CATABOLISM, OXIDOREDUCTASE
4i3x:D (LEU318) to (THR332) STRUCTURE OF PHOSPHONOACETALDEHYDE DEHYDROGENASE IN COMPLEX WITH PHOSPHONOACETATE AND COFACTOR NAD+ | ALDEHYDE DEHYDROGENASE, PHOSPHONATE CATABOLISM, OXIDOREDUCTASE
4i3x:G (LEU318) to (THR332) STRUCTURE OF PHOSPHONOACETALDEHYDE DEHYDROGENASE IN COMPLEX WITH PHOSPHONOACETATE AND COFACTOR NAD+ | ALDEHYDE DEHYDROGENASE, PHOSPHONATE CATABOLISM, OXIDOREDUCTASE
1oke:B (LYS47) to (GLU62) CRYSTAL STRUCTURE OF THE DENGUE 2 VIRUS ENVELOPE PROTEIN IN COMPLEX WITH N-OCTYL-BETA-D-GLUCOSIDE | VIRAL PROTEIN, MEMBRANE FUSION, FLAVIVIRUS, FUSION PEPTIDE, VIRAL PROTEIN, LOW-PH CONFORMATIONAL CHANGE, CLASS 2 FUSION PROTEIN
3sjk:A (LYS130) to (ASN139) CRYSTAL STRUCTURE OF THE C147A MUTANT 3C FROM ENTEROVIRUS 71 | CHYMOTRYPSIN-LIKE FOLD, PROTEASE, HYDROLASE
1om4:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NOS HEME DOMAIN WITH L-ARGININE BOUND | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME
1om4:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NOS HEME DOMAIN WITH L-ARGININE BOUND | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME
3spy:A (PRO35) to (ASP51) RB69 DNA POLYMERASE(L415A/L561A/S565G/Y567A) TERNARY COMPLEX WITH DUPCPP OPPOSITE DA | DUPCPP, QUADRUPLE MUTANT, TRANSFERASE-DNA COMPLEX
3svp:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-((2,2-DIFLUORO-2-(3-CHLORO-5-FLUOROPHENYL) ETHYL)AMINO)ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3svp:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3R,4R)-4-(2-((2,2-DIFLUORO-2-(3-CHLORO-5-FLUOROPHENYL) ETHYL)AMINO)ETHOXY)PYRROLIDIN-3-YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4ihg:A (ASN99) to (ASP107) CHASING ACYL CARRIER PROTEIN THROUGH A CATALYTIC CYCLE OF LIPID A PRODUCTION | LEFT HANDED BETA HELIX, LPXD, ACYLTRANSFERASE, LIPID A, PROTEIN- PROTEIN COMPLEX, ACP RECOGNITION DOMAIN, ACP MEDIATED PRODUCT RELEASE, TRANSFERASE-LIPID BINDING PROTEIN COMPLEX
1p6l:A (PRO95) to (GLY103) BOVINE ENDOTHELIAL NOS HEME DOMAIN WITH L-N(OMEGA)-NITROARGININE-2,4- L-DIAMINOBUTYRIC AMIDE BOUND | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME
1p6m:A (PRO95) to (GLY103) BOVINE ENDOTHELIAL NOS HEME DOMAIN WITH (4S)-N-(4-AMINO-5- [AMINOETHYL]AMINOPENTYL)-N'-NITROGUANIDINE BOUND | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE, HEME-ENZYME
1d8m:A (GLY138) to (SER145) CRYSTAL STRUCTURE OF MMP3 COMPLEXED WITH A HETEROCYCLE- BASED INHIBITOR | MIXED ALPHA BETA STRUCTURE, ZINC PROTEASE, INHIBITED, HYDROLASE
4ims:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6,6'-((5-(3-AMINOPROPYL)-1,3-PHENYLENE)BIS(ETHANE-2,1-DIYL)) BIS(4-METHYLPYRIDIN-2-AMINE) | OXIDOREDUCTASE NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4ims:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6,6'-((5-(3-AMINOPROPYL)-1,3-PHENYLENE)BIS(ETHANE-2,1-DIYL)) BIS(4-METHYLPYRIDIN-2-AMINE) | OXIDOREDUCTASE NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4imu:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE IN COMPLEX WITH 6,6'- ((5-(AMINOMETHYL)-1,3-PHENYLENE)BIS(ETHANE-2,1-DIYL))BIS(4- METHYLPYRIDIN-2-AMINE) | OXIDOREDUCTASE NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4imu:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE IN COMPLEX WITH 6,6'- ((5-(AMINOMETHYL)-1,3-PHENYLENE)BIS(ETHANE-2,1-DIYL))BIS(4- METHYLPYRIDIN-2-AMINE) | OXIDOREDUCTASE NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4ip7:B (VAL214) to (PRO224) STRUCTURE OF THE S12D VARIANT OF HUMAN LIVER PYRUVATE KINASE IN COMPLEX WITH CITRATE AND FBP. | KINASE, GLYCOLYSIS, ALLOSTERIC, PHOSPHORYLATION MIMIC, LIVER, TRANSFERASE
4ip7:D (GLU210) to (SER217) STRUCTURE OF THE S12D VARIANT OF HUMAN LIVER PYRUVATE KINASE IN COMPLEX WITH CITRATE AND FBP. | KINASE, GLYCOLYSIS, ALLOSTERIC, PHOSPHORYLATION MIMIC, LIVER, TRANSFERASE
4ish:H (GLN30) to (VAL53) STRUCTURE OF FACTOR VIIA IN COMPLEX WITH THE INHIBITOR BMS-593214 ALSO KNOWN AS 2'-[(6R,6AR,11BR)-2-CARBAMIMIDOYL-6,6A,7,11B-TETRAHYDRO-5H- INDENO[2,1-C]QUINOLIN-6-YL]-5'-HYDROXY-4'-METHOXYBIPHENYL-4- CARBOXYLIC ACID | GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM-BINDING, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4ivc:A (LEU875) to (HIS885) JAK1 KINASE (JH1 DOMAIN) IN COMPLEX WITH THE INHIBITOR (TRANS-4-{2- [(1R)-1-HYDROXYETHYL]IMIDAZO[4,5-D]PYRROLO[2,3-B]PYRIDIN-1(6H)- YL}CYCLOHEXYL)ACETONITRILE | PROTEIN KINASE, PHOSPHO TRANSFER, PHOSPHO TYROSINE, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
1du3:E (TRP154) to (ASN166) CRYSTAL STRUCTURE OF TRAIL-SDR5 | TRAIL, DR5, COMPLEX, APOPTOSIS
1du3:K (TRP154) to (ASN166) CRYSTAL STRUCTURE OF TRAIL-SDR5 | TRAIL, DR5, COMPLEX, APOPTOSIS
2qtv:A (SER443) to (PRO452) STRUCTURE OF SEC23-SAR1 COMPLEXED WITH THE ACTIVE FRAGMENT OF SEC31 | COPII COAT, VESICULAR TRANSPORT, CYTOPLASM, CYTOPLASMIC VESICLE, ENDOPLASMIC RETICULUM, ER-GOLGI TRANSPORT, GOLGI APPARATUS, MEMBRANE, METAL-BINDING, PROTEIN TRANSPORT, UBL CONJUGATION, ZINC, GTP-BINDING, HYDROLASE, NUCLEOTIDE- BINDING, PHOSPHORYLATION, WD REPEAT
1dzl:A (TYR27) to (GLY46) L1 PROTEIN OF HUMAN PAPILLOMAVIRUS 16 | VIRUS, ICOSAHEDRAL
2d3s:A (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN WITH TN-ANTIGEN | LEGUME LECTIN, GLYCOSYLATED PROTEIN, AGGLUTININ, TN-ANTIGEN, SUGAR BINDING PROTEIN
2d3s:D (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN WITH TN-ANTIGEN | LEGUME LECTIN, GLYCOSYLATED PROTEIN, AGGLUTININ, TN-ANTIGEN, SUGAR BINDING PROTEIN
2r16:A (VAL741) to (GLN756) CRYSTAL STRUCTURE OF BOVINE NEUREXIN 1 ALPHA LNS/LG DOMAIN 4 (WITH NO SPLICE INSERT) | BETA-SANDWICH, CELL ADHESION, SPLICING
1e6h:A (GLY51) to (ASP62) A-SPECTRIN SH3 DOMAIN A11V, M25I, V44I, V58L MUTANTS | SH3-DOMAIN, CYTOSKELETON, CALMODULIN-BINDING, ACTIN-BINDING
2r5j:L (TYR27) to (SER39) PENTAMER STRUCTURE OF MAJOR CAPSID PROTEIN L1 OF HUMAN PAPILLOMA VIRUS TYPE 35 | HPV35, CAPSID, PENTAMER, STRUCTURE, TYPE SPECIFIC EPITOPE, CAPSID PROTEIN, LATE PROTEIN, VIRION, VIRAL PROTEIN
2r5j:O (TYR27) to (SER39) PENTAMER STRUCTURE OF MAJOR CAPSID PROTEIN L1 OF HUMAN PAPILLOMA VIRUS TYPE 35 | HPV35, CAPSID, PENTAMER, STRUCTURE, TYPE SPECIFIC EPITOPE, CAPSID PROTEIN, LATE PROTEIN, VIRION, VIRAL PROTEIN
1ebz:A (ASP30) to (GLY49) HIV-1 PROTEASE IN COMPLEX WITH THE INHIBITOR BEA388 | DIMER, PROTEIN-INHIBITOR COMPLEX, HYDROLASE/HYDROLASE INHIBITOR COMPLEX
1ec2:A (ASP30) to (GLY49) HIV-1 PROTEASE IN COMPLEX WITH THE INHIBITOR BEA428 | DIMER, PROTEIN-INHIBITOR COMPLEX, HYDROLASE/HYDROLASE INHIBITOR COMPLEX
3gu8:A (TYR13) to (GLN23) CRYSTAL STRUCTURE OF DAPKL93G WITH N6-CYCLOPENTYLADENOSINE | GATEKEEPER MUTANT, ALTERNATIVE SPLICING, ANK REPEAT, APOPTOSIS, ATP-BINDING, CALMODULIN-BINDING, CYTOPLASM, KINASE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE
3gxd:B (LEU383) to (PRO401) CRYSTAL STRUCTURE OF APO ACID-BETA-GLUCOSIDASE PH 4.5 | HYDROLASE, ALTERNATIVE INITIATION, DISEASE MUTATION, DISULFIDE BOND, GAUCHER DISEASE, GLYCOPROTEIN, GLYCOSIDASE, ICHTHYOSIS, LIPID METABOLISM, LYSOSOME, MEMBRANE, SPHINGOLIPID METABOLISM
3gxm:B (LEU383) to (PRO401) CRYSTAL STRUCTURE OF ACID-BETA-GLUCOSIDASE AT PH 4.5, PHOSPHATE CRYSTALLIZATION CONDITION | HYDROLASE, ALTERNATIVE INITIATION, DISEASE MUTATION, DISULFIDE BOND, GAUCHER DISEASE, GLYCOPROTEIN, GLYCOSIDASE, ICHTHYOSIS, LIPID METABOLISM, LYSOSOME, MEMBRANE, SPHINGOLIPID METABOLISM
2dtw:B (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH 2ME-O-D- GALACTOSE | LEGUME LECTIN, GLYCOSYLATED PROTEIN, AGGLUTININ, SUGAR BINDING PROTEIN
2dtw:C (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH 2ME-O-D- GALACTOSE | LEGUME LECTIN, GLYCOSYLATED PROTEIN, AGGLUTININ, SUGAR BINDING PROTEIN
2dtw:D (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH 2ME-O-D- GALACTOSE | LEGUME LECTIN, GLYCOSYLATED PROTEIN, AGGLUTININ, SUGAR BINDING PROTEIN
2rgp:A (LEU703) to (LYS716) STRUCTURE OF EGFR IN COMPLEX WITH HYDRAZONE, A POTENT DUAL INHIBITOR | KINASE DOMAIN, ALTERNATIVE SPLICING, ANTI-ONCOGENE, ATP- BINDING, CELL CYCLE, DISEASE MUTATION, GLYCOPROTEIN, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, RECEPTOR, SECRETED, TRANSFERASE, TRANSMEMBRANE, TYROSINE- PROTEIN KINASE, UBL CONJUGATION
3tvz:A (HIS56) to (GLY65) STRUCTURE OF BACILLUS SUBTILIS HMOB | PUTATIVE MONOOXYGENASE, ABM FAMILY, FERREDOXIN FOLD, MONOOXYGENASE, OXIDOREDUCTASE
3tvz:B (HIS56) to (GLY65) STRUCTURE OF BACILLUS SUBTILIS HMOB | PUTATIVE MONOOXYGENASE, ABM FAMILY, FERREDOXIN FOLD, MONOOXYGENASE, OXIDOREDUCTASE
3tvz:C (HIS56) to (GLY65) STRUCTURE OF BACILLUS SUBTILIS HMOB | PUTATIVE MONOOXYGENASE, ABM FAMILY, FERREDOXIN FOLD, MONOOXYGENASE, OXIDOREDUCTASE
1eyq:B (PHE89) to (SER102) CHALCONE ISOMERASE AND NARINGENIN | CHALCONE ISOMERASE, FLAVONOID, ISOMERASE
3tyo:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3S,4S)-4-(2-((FURAN-2-YLMETHYL)AMINO)ETHOXY)PYRROLIDIN-3- YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3tyo:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((3S,4S)-4-(2-((FURAN-2-YLMETHYL)AMINO)ETHOXY)PYRROLIDIN-3- YL)METHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR BINDING, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4jsh:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-((3-(PIPERIDIN-4-YLMETHOXY)PHENOXY)METHYL)PYRIDIN-2- AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4jsh:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-((3-(PIPERIDIN-4-YLMETHOXY)PHENOXY)METHYL)PYRIDIN-2- AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4jsj:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((5-(((3-FLUOROPHENETHYL)AMINO)METHYL)PYRIDIN-3-YL)OXY) METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4jsj:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(((5-(((3-FLUOROPHENETHYL)AMINO)METHYL)PYRIDIN-3-YL)OXY) METHYL)-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
2e7t:A (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH A BLOOD GROUP TRISACCHARIDE | LECTIN, SUGAR BINDING PROTEIN, JELLY ROLL
2e7t:C (ILE109) to (PRO117) CRYSTAL STRUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH A BLOOD GROUP TRISACCHARIDE | LECTIN, SUGAR BINDING PROTEIN, JELLY ROLL
4jyu:H (GLN30) to (VAL53) STRUCTURE OF FACTOR VIIA IN COMPLEX WITH THE INHIBITOR (2R)-2-[(1- AMINOISOQUINOLIN-6-YL)AMINO]-2-[3-ETHOXY-4-(PROPAN-2-YLOXY)PHENYL]-N- (PHENYLSULFONYL)ETHANAMIDE | GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM-BINDING, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4jzf:H (GLN30) to (VAL53) STRUCTURE OF FACTOR VIIA IN COMPLEX WITH THE INHIBITOR 2-{2-[(3- CARBAMOYLPHENYL)CARBAMOYL]-6-METHOXYPYRIDIN-3-YL}-5-{[(2S)-1-HYDROXY- 3,3-DIMETHYLBUTAN-2-YL]CARBAMOYL}BENZOIC ACID | GLYCOPROTEIN, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM BINDING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1fm7:A (PHE89) to (SER102) CHALCONE ISOMERASE COMPLEXED WITH 5-DEOXYFLAVANONE | NATURAL PRODUCT BIOSYNTHESIS, PLANT ENZYME, CHALCONE, DIFFUSION- LIMITED, ISOMERASE
1fm7:B (PHE89) to (SER102) CHALCONE ISOMERASE COMPLEXED WITH 5-DEOXYFLAVANONE | NATURAL PRODUCT BIOSYNTHESIS, PLANT ENZYME, CHALCONE, DIFFUSION- LIMITED, ISOMERASE
4k5e:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (R)-1,2-BIS((2-AMINO-4-METHYLPYRIDIN-6-YL)-METHOXY)-PROPAN-3- AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4k5e:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH (R)-1,2-BIS((2-AMINO-4-METHYLPYRIDIN-6-YL)-METHOXY)-PROPAN-3- AMINE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
1fop:A (PRO95) to (GLY103) BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH L- ARG AND NO(H4B-BOUND) | ALPHA-BETA FOLD, NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE
3hm7:B (ASP5) to (THR15) CRYSTAL STRUCTURE OF ALLANTOINASE FROM BACILLUS HALODURANS C-125 | ALLANTOINASE, METALLO-DEPENDENT HYDROLASE, PROTEIN STRUCTURE INITIATIVE, PSI-2, NEW YORK STRUCTURAL GENOMIX RESEARCH CONSORTIUM, NYSGXRC, STRUCTURAL GENOMICS, DNA-BINDING, HYDROLASE, METAL-BINDING, PURINE METABOLISM, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS
1rf5:A (MET1) to (ILE13) STRUCTURAL STUDIES OF STREPTOCOCCUS PNEUMONIAE EPSP SYNTHASE IN UNLIGANDED STATE | SHIKIMATE PATHWAY, EPSP SYNTHASE, S3P, GLYPHOSATE, PEP, S. PNEUMONIAE, TRANSFERASE
1rf5:B (MET1) to (ILE13) STRUCTURAL STUDIES OF STREPTOCOCCUS PNEUMONIAE EPSP SYNTHASE IN UNLIGANDED STATE | SHIKIMATE PATHWAY, EPSP SYNTHASE, S3P, GLYPHOSATE, PEP, S. PNEUMONIAE, TRANSFERASE
1rgs:A (PHE152) to (GLN165) REGULATORY SUBUNIT OF CAMP DEPENDENT PROTEIN KINASE | REGULATORY SUBUNIT, KINASE
4k8f:A (ARG24) to (GLY37) STRUCTURE OF THE HEME DOMAIN OF COOA FROM RHODOSPIRILLUM RUBRUM | HEME PROTEIN, COOA TRANSCRIPTION FACTOR, TRANSCRIPTION
4k8f:C (ARG24) to (GLY37) STRUCTURE OF THE HEME DOMAIN OF COOA FROM RHODOSPIRILLUM RUBRUM | HEME PROTEIN, COOA TRANSCRIPTION FACTOR, TRANSCRIPTION
1fu6:A (GLN9) to (ASP17) NMR STRUCTURE OF THE N-SH2 DOMAIN OF THE P85 SUBUNIT OF PI3- KINASE | CENTRAL BETA-SHEET WITH TWO FLANKING ALPHA-HELICES, PROTEIN BINDING
2f61:A (LEU383) to (PRO401) CRYSTAL STRUCTURE OF PARTIALLY DEGLYCOSYLATED ACID BETA-GLUCOSIDASE | ALPHA/BETA, TIM BARREL, IMMUNOGLOBULIN FOLD, HYDROLASE
2f61:B (LEU383) to (PRO401) CRYSTAL STRUCTURE OF PARTIALLY DEGLYCOSYLATED ACID BETA-GLUCOSIDASE | ALPHA/BETA, TIM BARREL, IMMUNOGLOBULIN FOLD, HYDROLASE
4kch:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N,N'-([1,1'-BIPHENYL]-3,3'-DIYL)BIS(THIOPHENE-2-CARBOXIMIDAMIDE) | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4kch:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N,N'-([1,1'-BIPHENYL]-3,3'-DIYL)BIS(THIOPHENE-2-CARBOXIMIDAMIDE) | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4kcq:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(4-(2-(ETHYL(3-(THIOPHENE-2-CARBOXIMIDAMIDO)BENZYL) AMINO)ETHYL)PHENYL)THIOPHENE-2-CARBOXIMIDAMIDE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4kcq:B (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(4-(2-(ETHYL(3-(THIOPHENE-2-CARBOXIMIDAMIDO)BENZYL) AMINO)ETHYL)PHENYL)THIOPHENE-2-CARBOXIMIDAMIDE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4kcr:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(3-(((3-FLUOROPHENETHYL)AMINO)METHYL)PHENYL)THIOPHENE- 2-CARBOXIMIDAMIDE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4kcr:B (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N-(3-(((3-FLUOROPHENETHYL)AMINO)METHYL)PHENYL)THIOPHENE- 2-CARBOXIMIDAMIDE | NITRIC OXIDE SYNTHASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
4kcu:A (ARG171) to (LEU180) PYRUVATE KINASE (PYK) FROM TRYPANOSOMA BRUCEI SOAKED WITH D-MALATE | PYRUVATE KINASE, DECARBOXYLASE, TRANSFERASE
2f9g:A (ASP12) to (ALA23) CRYSTAL STRUCTURE OF FUS3 PHOSPHORYLATED ON TYR182 | MAP KINASE, TRANSFERASE
2fcp:A (GLN617) to (PHE631) FERRIC HYDROXAMATE UPTAKE RECEPTOR (FHUA) FROM E.COLI | TONB-DEPENDENT RECEPTOR, INTEGRAL OUTER MEMBRANE PROTEIN, FERRICHROME-IRON RECEPTOR, ACTIVE TRANSPORT, IRON TRANSPORT PROTEIN, MEMBRANE PROTEIN
4kfq:B (LEU6) to (PRO21) CRYSTAL STRUCTURE OF THE NMDA RECEPTOR GLUN1 LIGAND BINDING DOMAIN IN COMPLEX WITH 1-THIOXO-1,2-DIHYDRO-[1,2,4]TRIAZOLO[4,3-A]QUINOXALIN- 4(5H)-ONE | MEMBRANE PROTEIN, LIGAND BINDING DOMAIN, IONOTROPIC GLUTAMATE RECEPTOR
4khw:A (PRO35) to (ASP51) TERNARY COMPLEX OF RB69 MUTANT L415F WITH RIBONUCLEOTIDE AT -2 POSITION | RIBONUCLEOTIDE, TRANSFERASE-DNA COMPLEX
2fkl:B (ASP177) to (PRO188) STRUCTURE OF THE ALZHEIMER'S AMYLOID PRECURSOR PROTEIN (APP) COPPER BINDING DOMAIN (RESIDUES 126- 189 OF APP) | ALPHA-BETA TWO-LAYERED SANDWICH, METAL BINDING PROTEIN
3hsp:A (GLY325) to (GLY333) TERNARY STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE WITH NHA AND NO BOUND(2) | NITRIC OXIDE SYNTHASE HEME ENZYME DIATOMIC LIGAND, CALMODULIN- BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3hsp:B (GLY325) to (GLY333) TERNARY STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE WITH NHA AND NO BOUND(2) | NITRIC OXIDE SYNTHASE HEME ENZYME DIATOMIC LIGAND, CALMODULIN- BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
2frp:G (ALA367) to (GLY379) BACTERIOPHAGE HK97 EXPANSION INTERMEDIATE IV | BACTERIOPHAGE, HK97, CAPSID PROTEIN, EXPANSION INTERMEDIATE, ICOSAHEDRAL VIRUS
2fsy:G (ALA367) to (GLY379) BACTERIOPHAGE HK97 PEPSIN-TREATED EXPANSION INTERMEDIATE IV | BACTERIOPHAGE, HK97, CAPSID PROTEIN, EXPANSION INTERMEDIATE, ICOSAHEDRAL VIRUS
2ft1:G (ALA367) to (GLY379) BACTERIOPHAGE HK97 HEAD II | BACTERIOPHAGE, HK97, CAPSID PROTEIN, MATURE CAPSID, ICOSAHEDRAL VIRUS
2fte:G (ALA367) to (GLY379) BACTERIOPHAGE HK97 EXPANSION INTERMEDIATE IV | BACTERIOPHAGE, HK97, CAPSID PROTEIN, EXPANSION INTERMEDIATE, VIRUS/VIRAL PROTEIN COMPLEX
2fty:D (ASP5) to (ALA16) CRYSTAL STRUCTURE OF DIHYDROPYRIMIDINASE FROM SACCHAROMYCES KLUYVERI | ALPHA/BETA BARREL, BETA-SANDWICH, HYDROLASE
4kp5:A (PRO100) to (SER108) CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH 2-CHLORO-4-[(PYRIMIDIN-2-YLSULFANYL) ACETYL]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4kp5:C (PRO100) to (SER108) CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH 2-CHLORO-4-[(PYRIMIDIN-2-YLSULFANYL) ACETYL]BENZENESULFONAMIDE | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE, METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
3v4v:B (GLN83) to (PRO91) CRYSTAL STRUCTURE OF A4B7 HEADPIECE COMPLEXED WITH FAB ACT-1 AND RO0505376 | CELL ADHESION, MADCAM-1, MEMBRANE
3v4v:D (GLN83) to (PRO91) CRYSTAL STRUCTURE OF A4B7 HEADPIECE COMPLEXED WITH FAB ACT-1 AND RO0505376 | CELL ADHESION, MADCAM-1, MEMBRANE
1sg3:A (ALA91) to (ASP101) STRUCTURE OF ALLANTOICASE | ALLANTOICASE, JELLY ROLL, HEXAMER, HYDROLASE
2vnt:A (LYS-2) to (LEU6) UROKINASE-TYPE PLASMINOGEN ACTIVATOR INHIBITOR COMPLEX WITH A 1-(7-SULPHOAMIDOISOQUINOLINYL)GUANIDINE | UPA, INHIBITOR COMPLEX, HYDROLASE
1gog:A (LYS223) to (MET233) NOVEL THIOETHER BOND REVEALED BY A 1.7 ANGSTROMS CRYSTAL STRUCTURE OF GALACTOSE OXIDASE | OXIDOREDUCTASE(OXYGEN(A))
4zhh:B (GLY29) to (GLY38) SIDEROCALIN-MEDIATED RECOGNITION AND CELLULAR UPTAKE OF ACTINIDES | METAL BINDING PROTEIN-INHIBITOR COMPLEX
3i7l:A (GLY393) to (PRO405) CRYSTAL STRUCTURE OF DDB1 IN COMPLEX WITH THE H-BOX MOTIF OF DDB2 | DDB1, DDB2, H-BOX MOTIF, CYTOPLASM, DNA DAMAGE, DNA REPAIR, DNA-BINDING, HOST-VIRUS INTERACTION, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, UBL CONJUGATION, UBL CONJUGATION PATHWAY, ALTERNATIVE SPLICING, DISEASE MUTATION, WD REPEAT, XERODERMA PIGMENTOSUM
1t2x:A (LYS223) to (MET233) GLACTOSE OXIDASE C383S MUTANT IDENTIFIED BY DIRECTED EVOLUTION | 7 BLADE BETA PROPELLER, C383S MUTANT FORM, MUTANT FORM OF COPPER CONTAINING ENZYME, OXIDOREDUCTASE
4zma:H (GLN30) to (VAL53) CRYSTAL STRUCTURE OF A FVIIA-TRYPSIN CHIMERA (ST) IN COMPLEX WITH SOLUBLE TISSUE FACTOR | FUSION PROTEIN, TRYPSIN-FOLD, PROTEIN-PROTEIN COMPLEX, HYDROLASE
2w35:A (ASP105) to (LEU114) STRUCTURES OF ENDONUCLEASE V WITH DNA REVEAL INITIATION OF DEAMINATED ADENINE REPAIR | HYPOXANTHINE, ENDONUCLEASE, ENDONUCLEASEV, HYDROLASE, INOSINE, DNA DAMAGE, DNA REPAIR
2w35:B (ASP105) to (LEU114) STRUCTURES OF ENDONUCLEASE V WITH DNA REVEAL INITIATION OF DEAMINATED ADENINE REPAIR | HYPOXANTHINE, ENDONUCLEASE, ENDONUCLEASEV, HYDROLASE, INOSINE, DNA DAMAGE, DNA REPAIR
3iom:A (GLY131) to (LEU142) CRYSTAL STRUCTURE OF PURINE NUCLEOSIDE PHOSPHORYLASE FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH 2'-DEOXYGUANOSINE | PURINE NUCLEOSIDE PHOSPHORYLASE, MYCOBACTERIUM TUBERCULOSIS, 2 - DEOXYGUANOSINE, GLYCOSYLTRANSFERASE, TRANSFERASE
3iom:B (GLN132) to (LEU142) CRYSTAL STRUCTURE OF PURINE NUCLEOSIDE PHOSPHORYLASE FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH 2'-DEOXYGUANOSINE | PURINE NUCLEOSIDE PHOSPHORYLASE, MYCOBACTERIUM TUBERCULOSIS, 2 - DEOXYGUANOSINE, GLYCOSYLTRANSFERASE, TRANSFERASE
1u46:B (LEU117) to (GLU130) CRYSTAL STRUCTURE OF THE UNPHOSPHORYLATED KINASE DOMAIN OF THE TYROSINE KINASE ACK1 | TYROSINE KINASE, TRANSFERASE
2hx3:A (GLY325) to (GLY333) RAT NNOS HEME DOMAIN COMPLEXED WITH (4S)-N-{4-AMINO-5-[(2-AMINOETHYL)- HYDROXYAMINO]-PENTYL}-N'-NITROGUANIDINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, INHIBITOR, OXIDOREDUCTASE
2hx3:A (GLN464) to (ASN476) RAT NNOS HEME DOMAIN COMPLEXED WITH (4S)-N-{4-AMINO-5-[(2-AMINOETHYL)- HYDROXYAMINO]-PENTYL}-N'-NITROGUANIDINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, INHIBITOR, OXIDOREDUCTASE
2hx3:B (GLY325) to (GLY333) RAT NNOS HEME DOMAIN COMPLEXED WITH (4S)-N-{4-AMINO-5-[(2-AMINOETHYL)- HYDROXYAMINO]-PENTYL}-N'-NITROGUANIDINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, INHIBITOR, OXIDOREDUCTASE
2i7g:A (PRO157) to (PRO166) CRYSTAL STRUCTURE OF MONOOXYGENASE FROM AGROBACTERIUM TUMEFACIENS | ALPHA-BETA, TIM BARREL, HELIX-BUNDLE, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, OXIDOREDUCTASE
2i7g:B (PRO157) to (PRO166) CRYSTAL STRUCTURE OF MONOOXYGENASE FROM AGROBACTERIUM TUMEFACIENS | ALPHA-BETA, TIM BARREL, HELIX-BUNDLE, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, OXIDOREDUCTASE
5af7:A (VAL175) to (ASP188) 3-SULFINOPROPIONYL-COENZYME A (3SP-COA) DESULFINASE FROM ADVENELLA MIMIGARDEFORDENSIS DPN7T: CRYSTAL STRUCTURE AND FUNCTION OF A DESULFINASE WITH AN ACYL-COA DEHYDROGENASE FOLD. NATIVE CRYSTAL STRUCTURE | HYDROLASE, DESULFINASE, ACYL-COA DEHYDROGENASE, 3-SULFINOPROPIONYL- COENZYME A, FLAVIN ADENINE DINUCLEOTIDE
2itj:B (ASN153) to (TYR162) ORIGIN BINDING DOMAIN OF THE SV40 LARGE T ANTIGEN (RESIDUES 131-259). P212121 CRYSTAL FORM | DNA BINDING PROTEIN
2x8f:B (LEU216) to (ARG222) NATIVE STRUCTURE OF ENDO-1,5-ALPHA-L-ARABINANASES FROM BACILLUS SUBTILIS | HYDROLASE
1jc9:A (PHE192) to (ASP200) TACHYLECTIN 5A FROM TACHYPLEUS TRIDENTATUS (JAPANESE HORSESHOE CRAB) | LECTIN, FIBRINOGEN RELATED, SUGAR BINDING PROTEIN
1jd0:A (PRO102) to (SER110) CRYSTAL STRUCTURE OF THE EXTRACELLULAR DOMAIN OF HUMAN CARBONIC ANHYDRASE XII COMPLEXED WITH ACETAZOLAMIDE | EXTRACELLULAR DOMAIN, HUMAN CARBONIC ANHYDRASE XII, BITOPIC MEMBRANE PROTEIN, TYPE I MEMBRANE PROTEIN, LYASE
1jd0:B (PRO102) to (SER110) CRYSTAL STRUCTURE OF THE EXTRACELLULAR DOMAIN OF HUMAN CARBONIC ANHYDRASE XII COMPLEXED WITH ACETAZOLAMIDE | EXTRACELLULAR DOMAIN, HUMAN CARBONIC ANHYDRASE XII, BITOPIC MEMBRANE PROTEIN, TYPE I MEMBRANE PROTEIN, LYASE
2xb6:C (ARG105) to (THR119) REVISITED CRYSTAL STRUCTURE OF NEUREXIN1BETA-NEUROLIGIN4 COMPLEX | ALPHA-BETA-HYDROLASE FOLD, AUTISM, CONFORMATIONAL REARRANGEMENT, CELL ADHESION
2xb6:C (ASN278) to (VAL288) REVISITED CRYSTAL STRUCTURE OF NEUREXIN1BETA-NEUROLIGIN4 COMPLEX | ALPHA-BETA-HYDROLASE FOLD, AUTISM, CONFORMATIONAL REARRANGEMENT, CELL ADHESION
2xb6:D (ARG105) to (THR119) REVISITED CRYSTAL STRUCTURE OF NEUREXIN1BETA-NEUROLIGIN4 COMPLEX | ALPHA-BETA-HYDROLASE FOLD, AUTISM, CONFORMATIONAL REARRANGEMENT, CELL ADHESION
2xb6:D (ASN278) to (VAL288) REVISITED CRYSTAL STRUCTURE OF NEUREXIN1BETA-NEUROLIGIN4 COMPLEX | ALPHA-BETA-HYDROLASE FOLD, AUTISM, CONFORMATIONAL REARRANGEMENT, CELL ADHESION
2j3m:B (LEU384) to (LYS404) PROLYL-TRNA SYNTHETASE FROM ENTEROCOCCUS FAECALIS COMPLEXED WITH ATP, MANGANESE AND PROLINOL | BACTERIAL-TYPE PROLYL-TRNA SYNTHETASE, CLASS II AMINOACYL- TRNA SYNTHETASE, EDITING, TRANSLATION, ATP + L-PROLINE + TRNA (PRO) GIVES AMP + PPI + L-PROLYL-TRNA(PRO), LIGASE
2xja:A (ARG60) to (LEU67) STRUCTURE OF MURE FROM M.TUBERCULOSIS WITH DIPEPTIDE AND ADP | LIGASE, PEPTIDOGLYCAN, PEPTIDASE LIGASE
5b04:E (ASN371) to (LYS381) CRYSTAL STRUCTURE OF THE EUKARYOTIC TRANSLATION INITIATION FACTOR 2B FROM SCHIZOSACCHAROMYCES POMBE | COMPLEX, TRANSLATION
1w5v:A (ASP30) to (GLY49) HIV-1 PROTEASE IN COMPLEX WITH FLUORO SUBSTITUTED DIOL- BASED C2-SYMMETRIC INHIBITOR | HYDROLASE/HYDROLASE INHIBITOR, HYDROLASE, DIMER, PROTEIN-INHIBITOR COMPLEX
2xt2:A (GLY159) to (ARG179) STRUCTURE OF THE PENTAPEPTIDE REPEAT PROTEIN ALBG, A RESISTANCE FACTOR FOR THE TOPOISOMERASE POISON ALBICIDIN. | CELL CYCLE, RIGHT HANDED QUADRILATERAL BETA HELIX
2xt2:B (ALA89) to (GLU97) STRUCTURE OF THE PENTAPEPTIDE REPEAT PROTEIN ALBG, A RESISTANCE FACTOR FOR THE TOPOISOMERASE POISON ALBICIDIN. | CELL CYCLE, RIGHT HANDED QUADRILATERAL BETA HELIX
1waf:B (ARG27) to (ASP51) DNA POLYMERASE FROM BACTERIOPHAGE RB69 | NUCLEOTIDYLTRANSFERASE, RB69 DNA POLYMERASE (GP43)
4nff:A (GLN30) to (THR54) HUMAN KALLIKREIN-RELATED PEPTIDASE 2 IN COMPLEX WITH PPACK | CHYMOTRYPSIN-LIKE PROTEASE, ZINC BINDING, EXTRACELLULAR, HYDROLASE
2jv0:A (LYS48) to (GLY57) SET DOMAIN OF RIZ1 TUMOR SUPPRESSOR (PRDM2) | SET DOMAIN, PR DOMAIN, RIZ1, PRDM2, PROTEIN LYSINE METHYLTRANSFERASE, HISTONE LYSINE METHYLTRANSFERASE, HKMT, ACTIVATOR, ALTERNATIVE INITIATION, DNA-BINDING, METAL-BINDING, NUCLEUS, PHOSPHORYLATION, TRANSCRIPTION, TRANSCRIPTION REGULATION, ZINC-FINGER
4nmk:F (LEU314) to (PRO329) THERMOSTABLE ALDEHYDE DEHYDROGENASE FROM PYROBACULUM SP. CRYSTALLIZED IN MICROGRAVITY (COMPLEX WITH NADP+) | ALDEHYDE OXIDATION, NADP REDUCTION, INTRACELLULAR, OXIDOREDUCTASE
5c4x:C (ILE41) to (THR56) CRYSTAL STRUCTURE OF A TRANSCRIBING RNA POLYMERASE II COMPLEX REVEALS A COMPLETE TRANSCRIPTION BUBBLE | PROTEIN-DNA COMPLEX, RNA POLYMERASE II, TRANSCRIBING COMPLEX, TRANSCRIPTION BUBBLE, TRANSFERASE-RNA-DNA COMPLEX
2mo1:A (MET1) to (GLU12) BACKBONE 1H, 13C, AND 15N CHEMICAL SHIFT ASSIGNMENTS FOR COLD SHOCK PROTEIN, TACSP WITH DT7 | COLD SHOCK PROTEIN, THERMUS AQUATICUS, PROTEIN STABILITY, PROTEIN BINDING, DNA BINDING PROTEIN
1kt0:A (GLY147) to (TYR159) STRUCTURE OF THE LARGE FKBP-LIKE PROTEIN, FKBP51, INVOLVED IN STEROID RECEPTOR COMPLEXES | FKBP-LIKE PPIASE, TPR REPEATS, ISOMERASE
2nph:B (ASP1030) to (ILE1050) CRYSTAL STRUCTURE OF HIV1 PROTEASE IN SITU PRODUCT COMPLEX | ANTI-PARALLEL BETA SHEET, HYDROLASE
2nrb:D (ASP466) to (PRO475) C28S MUTANT OF SUCCINYL-COA:3-KETOACID COA TRANSFERASE FROM PIG HEART | ALPHA/BETA PROTEIN, TRANSFERASE
2nst:A (THR206) to (ALA220) CRYSTAL STRUCTURE OF PECTIN METHYLESTERASE D178A MUTANT IN COMPLEX WITH HEXASACCHARIDE II | MICHAELIS COMPLEX, HYDROLASE
2nst:B (THR206) to (ALA220) CRYSTAL STRUCTURE OF PECTIN METHYLESTERASE D178A MUTANT IN COMPLEX WITH HEXASACCHARIDE II | MICHAELIS COMPLEX, HYDROLASE
2nt1:A (LEU383) to (PRO401) STRUCTURE OF ACID-BETA-GLUCOSIDASE AT NEUTRAL PH | ACID-BETA-GLUCOSIDASE, CEREZYME, GLUCOSYLCERAMIDE, GAUCHER DISEASE, HYDROLASE
2nt1:D (LEU383) to (PRO401) STRUCTURE OF ACID-BETA-GLUCOSIDASE AT NEUTRAL PH | ACID-BETA-GLUCOSIDASE, CEREZYME, GLUCOSYLCERAMIDE, GAUCHER DISEASE, HYDROLASE
3jta:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN THE FERROUS STATE COMPLEXED WITH N~5~-[4-(METHYLSULFANYL) BUTANIMIDOYL]-L-ORNITHINE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE ENZYME, SUBSTRATE- ANALOGUE INHIBITOR, THIOETHER HEME LIGAND, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
3jta:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN THE FERROUS STATE COMPLEXED WITH N~5~-[4-(METHYLSULFANYL) BUTANIMIDOYL]-L-ORNITHINE | NITRIC OXIDE SYNTHASE, HEME-THIOLATE ENZYME, SUBSTRATE- ANALOGUE INHIBITOR, THIOETHER HEME LIGAND, ALTERNATIVE SPLICING, CALMODULIN-BINDING, CELL MEMBRANE, CELL PROJECTION, FAD, FMN, HEME, IRON, MEMBRANE, METAL-BINDING, NADP, OXIDOREDUCTASE
1xge:B (ALA100) to (SER118) DIHYDROOROTASE FROM ESCHERICHIA COLI: LOOP MOVEMENT AND COOPERATIVITY BETWEEN SUBUNITS | TIM BARREL, HYDROLASE
3jwv:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE R349A MUTANT HEME DOMAIN IN COMPLEX WITH N1-{(3'S,4'R)-4'-[(6"-AMINO-4"-METHYLPYRIDIN- 2"-YL)METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL)ETHANE-1,2- DIAMINE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jwv:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE R349A MUTANT HEME DOMAIN IN COMPLEX WITH N1-{(3'S,4'R)-4'-[(6"-AMINO-4"-METHYLPYRIDIN- 2"-YL)METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL)ETHANE-1,2- DIAMINE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jx0:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE D597N MUTANT HEME DOMAIN IN COMPLEX WITH N1-{(3'S,4'S)-4'-[(6"-AMINO-4"-METHYLPYRIDIN- 2"-YL)METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL)ETHANE-1,2- DIAMINE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jx0:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE D597N MUTANT HEME DOMAIN IN COMPLEX WITH N1-{(3'S,4'S)-4'-[(6"-AMINO-4"-METHYLPYRIDIN- 2"-YL)METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL)ETHANE-1,2- DIAMINE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jx4:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH N1-{(3'R,4'S)-4'-[(6"-AMINO-4"- METHYLPYRIDIN-2"-YL)METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL) ETHANE-1,2-DIAMINE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3jx4:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH N1-{(3'R,4'S)-4'-[(6"-AMINO-4"- METHYLPYRIDIN-2"-YL)METHYL]PYRROLIDIN-3'-YL}-N2-(3'-FLUOROPHENETHYL) ETHANE-1,2-DIAMINE | HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
4a3r:A (GLY360) to (GLU373) CRYSTAL STRUCTURE OF ENOLASE FROM BACILLUS SUBTILIS. | LYASE, GLYCOLYSIS, DEGRADOSOME
4a3r:C (GLY360) to (GLU373) CRYSTAL STRUCTURE OF ENOLASE FROM BACILLUS SUBTILIS. | LYASE, GLYCOLYSIS, DEGRADOSOME
4a3r:D (GLY360) to (GLU373) CRYSTAL STRUCTURE OF ENOLASE FROM BACILLUS SUBTILIS. | LYASE, GLYCOLYSIS, DEGRADOSOME
1xjw:B (GLU101) to (ASN111) THE STRUCTURE OF E. COLI ASPARTATE TRANSCARBAMOYLASE Q137A MUTANT IN THE R-STATE | ALLOSTERIC ENZYME, POLAR CONTACTS, ELECTROSTATICS, SMALL ANGLE X-RAY SCATTERING, DOMAIN CLOSURE, INTERSUBUNIT INTERACTIONS, TRANSFERASE- TRANSFERASE REGULATOR COMPLEX
4oj6:A (GLY395) to (GLY404) CRYSTAL STRUCTURE OF A PUTATIVE TAILSPIKE PROTEIN (TSP1, ORF210) FROM ESCHERICHIA COLI O157:H7 BACTERIOHAGE CBA120; SE-MET PROTEIN | PARALLEL BETA HELIX, PUTATIVE ENDO-GLYCOSIDASE, BACTERIAL POLYSACCHARIDE, PHAGE BASEPLATE, PHAGE TAIL, VIRAL PROTEIN
4oj6:B (GLY395) to (GLY404) CRYSTAL STRUCTURE OF A PUTATIVE TAILSPIKE PROTEIN (TSP1, ORF210) FROM ESCHERICHIA COLI O157:H7 BACTERIOHAGE CBA120; SE-MET PROTEIN | PARALLEL BETA HELIX, PUTATIVE ENDO-GLYCOSIDASE, BACTERIAL POLYSACCHARIDE, PHAGE BASEPLATE, PHAGE TAIL, VIRAL PROTEIN
4oj6:C (GLY395) to (GLY404) CRYSTAL STRUCTURE OF A PUTATIVE TAILSPIKE PROTEIN (TSP1, ORF210) FROM ESCHERICHIA COLI O157:H7 BACTERIOHAGE CBA120; SE-MET PROTEIN | PARALLEL BETA HELIX, PUTATIVE ENDO-GLYCOSIDASE, BACTERIAL POLYSACCHARIDE, PHAGE BASEPLATE, PHAGE TAIL, VIRAL PROTEIN
4a63:A (THR119) to (THR130) CRYSTAL STRUCTURE OF THE P73-ASPP2 COMPLEX AT 2.6A RESOLUTION | CELL CYCLE, TP53BP2, TUMOUR SUPPRESSOR, ANKYRINS, APOPTOSIS REGULATORY PROTEINS
4a63:E (THR119) to (THR130) CRYSTAL STRUCTURE OF THE P73-ASPP2 COMPLEX AT 2.6A RESOLUTION | CELL CYCLE, TP53BP2, TUMOUR SUPPRESSOR, ANKYRINS, APOPTOSIS REGULATORY PROTEINS
4a63:G (THR119) to (THR130) CRYSTAL STRUCTURE OF THE P73-ASPP2 COMPLEX AT 2.6A RESOLUTION | CELL CYCLE, TP53BP2, TUMOUR SUPPRESSOR, ANKYRINS, APOPTOSIS REGULATORY PROTEINS
4a63:I (THR119) to (THR130) CRYSTAL STRUCTURE OF THE P73-ASPP2 COMPLEX AT 2.6A RESOLUTION | CELL CYCLE, TP53BP2, TUMOUR SUPPRESSOR, ANKYRINS, APOPTOSIS REGULATORY PROTEINS
4a63:K (THR119) to (THR130) CRYSTAL STRUCTURE OF THE P73-ASPP2 COMPLEX AT 2.6A RESOLUTION | CELL CYCLE, TP53BP2, TUMOUR SUPPRESSOR, ANKYRINS, APOPTOSIS REGULATORY PROTEINS
2zmk:C (ILE109) to (PRO117) CRYSTL STRUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH GAL- ALPHA-1,4-GAL-BETA-ETHYLENE | LEGUME LECTIN, SUGAR BINDING PROTEIN, SUGAR SPECIFICITY, GLYCOPROTEIN, LECTIN
2zmk:D (ILE109) to (PRO117) CRYSTL STRUCTURE OF BASIC WINGED BEAN LECTIN IN COMPLEX WITH GAL- ALPHA-1,4-GAL-BETA-ETHYLENE | LEGUME LECTIN, SUGAR BINDING PROTEIN, SUGAR SPECIFICITY, GLYCOPROTEIN, LECTIN
1m9u:A (GLN30) to (LEU53) CRYSTAL STRUCTURE OF EARTHWORM FIBRINOLYTIC ENZYME COMPONENT A FROM EISENIA FETIDA | HYDROLASE, SERINE PROTEASE (ELASTASE-LIKE), FIBRINOLYTIC ENZYME
1m9u:B (GLN30) to (LEU53) CRYSTAL STRUCTURE OF EARTHWORM FIBRINOLYTIC ENZYME COMPONENT A FROM EISENIA FETIDA | HYDROLASE, SERINE PROTEASE (ELASTASE-LIKE), FIBRINOLYTIC ENZYME
1m9u:C (GLN30) to (LEU53) CRYSTAL STRUCTURE OF EARTHWORM FIBRINOLYTIC ENZYME COMPONENT A FROM EISENIA FETIDA | HYDROLASE, SERINE PROTEASE (ELASTASE-LIKE), FIBRINOLYTIC ENZYME
1mdo:A (ASP9) to (MSE18) CRYSTAL STRUCTURE OF ARNB AMINOTRANSFERASE WITH PYRIDOMINE 5' PHOSPHATE | TYPE 1 AMINOTRANSFERASE FOLD, TRANSFERASE
1y20:A (LEU6) to (PRO21) CRYSTAL STRUCTURE OF THE NR1 LIGAND-BINDING CORE IN COMPLEX WITH ACPC | PROTEIN-LIGAND COMPLEX; LIGAND-BINDING COMPLEX, LIGAND BINDING PROTEIN
5d41:A (LEU703) to (LYS716) EGFR KINASE DOMAIN IN COMPLEX WITH MUTANT SELECTIVE ALLOSTERIC INHIBITOR | ALLOSTERIC INHIBITOR, EGFR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
1mmv:A (GLY325) to (GLY333) RAT NEURONAL NOS HEME DOMAIN WITH NG-PROPYL-L-ARGININE BOUND | NITRIC OXIDE SYNTHASE, OXYDOREDUCTASE, HEME-ENZYME, OXIDOREDUCTASE
1mmv:B (GLY325) to (GLY333) RAT NEURONAL NOS HEME DOMAIN WITH NG-PROPYL-L-ARGININE BOUND | NITRIC OXIDE SYNTHASE, OXYDOREDUCTASE, HEME-ENZYME, OXIDOREDUCTASE
1y8t:C (ASP156) to (PRO166) CRYSTAL STRUCTURE OF RV0983 FROM MYCOBACTERIUM TUBERCULOSIS- PROTEOLYTICALLY ACTIVE FORM | SERINE PROTEASE, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, TB STRUCTURAL GENOMICS CONSORTIUM, TBSGC, UNKNOWN FUNCTION
3a2o:B (ASP130) to (GLY149) CRYSTAL STRUCTURE OF HIV-1 PROTEASE COMPLEXED WITH KNI-1689 | HIV-1 PROTEASE, INHIBITOR, ASPARTYL PROTEASE, HYDROLASE, PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1mv8:B (THR426) to (ILE434) 1.55 A CRYSTAL STRUCTURE OF A TERNARY COMPLEX OF GDP-MANNOSE DEHYDROGENASE FROM PSUEDOMONAS AERUGINOSA | ROSSMANN FOLD, DOMAIN-SWAPPED DIMER, ENZYME COMPLEX WITH COFACTOR AND PRODUCT, OXIDOREDUCTASE
1mv8:D (THR426) to (ILE434) 1.55 A CRYSTAL STRUCTURE OF A TERNARY COMPLEX OF GDP-MANNOSE DEHYDROGENASE FROM PSUEDOMONAS AERUGINOSA | ROSSMANN FOLD, DOMAIN-SWAPPED DIMER, ENZYME COMPLEX WITH COFACTOR AND PRODUCT, OXIDOREDUCTASE
5dep:F (ARG7) to (ALA17) STRUCTURE OF PSEUDOMONAS AERUGINOSA LPXA IN COMPLEX WITH UDP-GLCNAC | ACYLTRANSFERASE CATALYTIC DOMAIN, FATTY ACIDS, LIPID A, SUBSTRATE SPECIFICITY, URIDINE DIPHOSPHATE N-ACETYLGLUCOSAMINE, HYDROCARBON RULERS, TRANSFERASE
5dl6:A (ASP144) to (HIS155) CRYSTAL STRUCTURE OF ACINETOBACTER BAUMANNII OCCAB2 | OUTER MEMBRANE PROTEIN, BETA-BARREL, ANTIBIOTIC UPTAKE ACINETOBACTER, MEMBRANE PROTEIN
4pot:B (GLU37) to (PRO54) STRUCTURE OF HUMAN POLYOMAVIRUS 9 VP1 PENTAMER IN COMPLEX WITH N- GLYCOLYLNEURAMINIC ACID CONTAINING 3'-SIALYLLACTOSAMINE | JELLY ROLL FOLD, CAPSID FORMATION, RECEPTOR INTERACTION, CARBOHYDRATE, SIALYLOLIGOSACCHARIDE, VIRAL COAT PROTEIN, VIRAL PROTEIN
5dra:A (THR189) to (ASP198) T3284 LOOP VARIANT OF BETA1 | SYNTHETIC PROTEIN, LOOP DESIGN, DE NOVO PROTEIN
1zap:A (LEU38) to (PRO67) SECRETED ASPARTIC PROTEASE FROM C. ALBICANS | ASPARTIC PROTEASE, SECRETED, CANDIDA ALBICANS
4q0l:B (PRO100) to (SER108) CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLE, LYASE-LYASE INHIBITOR COMPLEX
4q0l:C (PRO100) to (SER108) CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLE, LYASE-LYASE INHIBITOR COMPLEX
4q0l:D (PRO100) to (SER108) CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLE, LYASE-LYASE INHIBITOR COMPLEX
4q2w:A (GLY63) to (ASP74) CRYSTAL STRUCTURE OF PNEUMOCOCCAL PEPTIDOGLYCAN HYDROLASE LYTB | ALL-BETA MODULE, GH73, HYDROLASE
1zru:A (GLY192) to (LYS199) STRUCTURE OF THE LACTOPHAGE P2 RECEPTOR BINDING PROTEIN IN COMPLEX WITH GLYCEROL | 3 DOMAINS: BETA BARREL, BETA PRISM, BETA BARREL, STRUCTURAL GENOMICS, STRUCTURAL PROTEOMICS IN EUROPE, SPINE, VIRAL PROTEIN
1zru:B (GLY192) to (LYS199) STRUCTURE OF THE LACTOPHAGE P2 RECEPTOR BINDING PROTEIN IN COMPLEX WITH GLYCEROL | 3 DOMAINS: BETA BARREL, BETA PRISM, BETA BARREL, STRUCTURAL GENOMICS, STRUCTURAL PROTEOMICS IN EUROPE, SPINE, VIRAL PROTEIN
1zru:C (GLY192) to (LYS199) STRUCTURE OF THE LACTOPHAGE P2 RECEPTOR BINDING PROTEIN IN COMPLEX WITH GLYCEROL | 3 DOMAINS: BETA BARREL, BETA PRISM, BETA BARREL, STRUCTURAL GENOMICS, STRUCTURAL PROTEOMICS IN EUROPE, SPINE, VIRAL PROTEIN
5e5k:B (ASP30) to (GLY49) JOINT X-RAY/NEUTRON STRUCTURE OF HIV-1 PROTEASE TRIPLE MUTANT (V32I, I47V,V82I) WITH DARUNAVIR AT PH 4.3 | PROTEASE DRUG RESISTANT MUTANT INHIBITOR COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2a2c:A (PRO448) to (GLU457) X-RAY STRUCTURE OF HUMAN N-ACETYL GALACTOSAMINE KINASE COMPLEXED WITH MG-ADP AND N-ACETYL GALACTOSAMINE 1- PHOSPHATE | KINASE, GALACTOKINASE, , TRANSFERASE
3lzj:A (PRO35) to (ASP51) RB69 DNA POLYMERASE (Y567A) TERNARY COMPLEX WITH DCTP OPPOSITE 7,8- DIHYDRO-8-OXOGUANINE | DNA POLYMERASE, REPLICATION FIDELITY, 7,8-DIHYDRO-8-OXOGUANINE, POLYMERASE-DNA-DNTP TERNARY COMPLEX, TRANSFERASE-DNA COMPLEX
5ecj:A (ASP79) to (ARG93) CRYSTAL STRUCTURE OF MONOBODY MB(S4) BOUND TO PRDM14 IN COMPLEX WITH MTGR1 | TRANSFERASE, PROTEIN BINDING, GENE REGULATION-TRANSCRIPTION COMPLEX
5ecj:B (ASP79) to (ARG93) CRYSTAL STRUCTURE OF MONOBODY MB(S4) BOUND TO PRDM14 IN COMPLEX WITH MTGR1 | TRANSFERASE, PROTEIN BINDING, GENE REGULATION-TRANSCRIPTION COMPLEX
4qjo:A (PRO100) to (SER108) CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4qjo:B (PRO100) to (SER108) CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4qjo:C (PRO100) to (SER108) CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
4qjo:D (PRO100) to (SER108) CRYSTAL STRUCTURE OF CATALYTIC DOMAIN OF HUMAN CARBONIC ANHYDRASE ISOZYME XII WITH INHIBITOR | DRUG DESIGN, CARBONIC ANHYDRASE, BENZENESULFONAMIDE,METAL-BINDING, LYASE-LYASE INHIBITOR COMPLEX
3b8j:A (GLY202) to (ILE236) Q191A MUTANT OF DEGS-DELTAPDZ | DEGS, PROTEASE, PERIPLASMIC STRESS SENSOR, HTRA, ALLOSTERIC ACTIVATION, HYDROLASE, SERINE PROTEASE
3be2:A (ARG833) to (ALA844) CRYSTAL STRUCTURE OF THE VEGFR2 KINASE DOMAIN IN COMPLEX WITH A BENZAMIDE INHIBITOR | ANGIOGENESIS, RECEPTOR TYROSINE KINASE, ATP-BINDING, DEVELOPMENTAL PROTEIN, DIFFERENTIATION, GLYCOPROTEIN, HOST- VIRUS INTERACTION, IMMUNOGLOBULIN DOMAIN, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHORYLATION, POLYMORPHISM, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE
4bg7:A (GLN4) to (ASP15) BACTERIOPHAGE T5 HOMOLOG OF THE EUKARYOTIC TRANSCRIPTION COACTIVATOR PC4 IMPLICATED IN RECOMBINATION-DEPENDENT DNA REPLICATION | REPLICATION, RECOMBINATION, REPAIR, TRANSCRIPTION, SSB
5ew3:A (LEU834) to (ALA844) HUMAN VASCULAR ENDOTHELIAL GROWTH FACTOR RECEPTOR 2 (KDR) KINASE DOMAIN IN COMPLEX WITH AAL993 | KDR, KINASE DOMAIN, ATP-BINDING SITE, VEGFR2 INHIBITORS, TRANSFERASE
3n04:B (GLU396) to (ILE408) THE CRYSTAL STRUCTURE OF THE ALPHA-GLUCOSIDASE (FAMILY 31) FROM RUMINOCOCCUS OBEUM ATCC 29174 | STRUCTURAL GENOMICS, PSI-2,PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, HYDROLASE
3bx7:A (GLY29) to (GLY38) ENGINEERED HUMAN LIPOCALIN 2 (LCN2) IN COMPLEX WITH THE EXTRACELLULAR DOMAIN OF HUMAN CTLA-4 | PROTEIN DESIGN, PROTEIN-PROTEIN COMPLEX, GLYCOPROTEIN, IMMUNOGLOBULIN DOMAIN, POLYMORPHISM, TRANSMEMBRANE PROTEIN, DE NOVO PROTEIN, PROTEIN BINDING
4r2x:F (ASP103) to (LEU113) UNIQUE CONFORMATION OF URIDINE AND ASYMMETRY OF THE HEXAMERIC MOLECULE REVEALED IN THE HIGH-RESOLUTION STRUCTURES OF SHEWANELLA ONEIDENSIS URIDINE PHOSPHORYLASE IN THE FREE FORM AND IN COMPLEX WITH URIDINE | URIDINE PHOSPHORYLASE, TRANSFERASE
3n5p:A (PRO95) to (GLY103) STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 4-(2-(6-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL)PYRIDIN-2-YL) ETHYL)-6-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n5v:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-(3-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL)PHENETHYL)-6- METHYLPYRIDIN-2-AMINE | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n5v:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-(3-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL)PHENETHYL)-6- METHYLPYRIDIN-2-AMINE | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n5x:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-(2-(5-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL)PYRIDIN-3-YL) ETHYL)-6-METHYLPYRIDIN-2-AMINE | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n5x:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-(2-(5-(2-(6-AMINO-4-METHYLPYRIDIN-2-YL)ETHYL)PYRIDIN-3-YL) ETHYL)-6-METHYLPYRIDIN-2-AMINE | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n5y:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6,6'-(2,2'-(PYRIDINE-2,6-DIYL)BIS(ETHANE-2,1-DIYL))BIS(4- METHYLPYRIDIN-2-AMINE) | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n5y:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6,6'-(2,2'-(PYRIDINE-2,6-DIYL)BIS(ETHANE-2,1-DIYL))BIS(4- METHYLPYRIDIN-2-AMINE) | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n61:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH 6,6'-(2,2'-(PYRIDINE-3,5-DIYL)BIS(ETHANE-2,1- DIYL))BIS(4-METHYLPYRIDIN-2-AMINE) | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n61:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH 6,6'-(2,2'-(PYRIDINE-3,5-DIYL)BIS(ETHANE-2,1- DIYL))BIS(4-METHYLPYRIDIN-2-AMINE) | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n64:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE D597N MUTANT HEME DOMAIN IN COMPLEX WITH 6,6'-(2,2'-(5-AMINO-1,3-PHENYLENE)BIS(ETHANE-2,1- DIYL))BIS(4-METHYLPYRIDIN-2-AMINE) | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n64:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE D597N MUTANT HEME DOMAIN IN COMPLEX WITH 6,6'-(2,2'-(5-AMINO-1,3-PHENYLENE)BIS(ETHANE-2,1- DIYL))BIS(4-METHYLPYRIDIN-2-AMINE) | HEME ENZYME, NITRIC OXIDE SYNTHASE, SUBSTRATE INHIBITOR, ZN BINDING', OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n67:A (PRO95) to (GLY103) STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE N368D/V106M DOUBLE MUTANT HEME DOMAIN COMPLEXED WITH 6,6'-(2,2'-(5-AMINO-1,3-PHENYLENE) BIS(ETHANE-2,1-DIYL))BIS(4-METHYLPYRIDIN-2-AMINE) | NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n6a:A (PRO95) to (GLY103) STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE N368D/V106M DOUBLE MUTANT HEME DOMAIN COMPLEXED WITH 4-(2-(5-(2-(6-AMINO-4- METHYLPYRIDIN-2-YL)ETHYL)PYRIDIN-3-YL)ETHYL)-6-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE, OXIDOREDUCTASE-OXIDOREDUCTASE INHIBITOR COMPLEX
3n82:C (ARG329) to (PRO343) T244A MUTANT OF HUMAN MITOCHONDRIAL ALDEHYDE DEHYDROGENASE, NADH COMPLEX | OXIDOREDUCTASE, ALDH, ROSSMANN FOLD
3nb2:A (SER275) to (ASN284) CRYSTAL STRUCTURE OF E. COLI O157:H7 EFFECTOR PROTEIN NLEL | SECRETED EFFECTOR PROTEIN, PENTAPEPTIDE, HECT DOMAIN, HECT E3 UBIQUITIN LIGASE, LIGASE
5fl1:A (SER617) to (ALA626) STRUCTURE OF A HYDROLASE WITH AN INHIBITOR | HYDROLASE
3ckh:A (GLN67) to (GLU92) CRYSTAL STRUCTURE OF EPH A4 RECEPTOR | EPH RECEPTOR, ATP-BINDING, GLYCOPROTEIN, KINASE, MEMBRANE, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, TRANSFERASE, TRANSMEMBRANE, TYROSINE-PROTEIN KINASE
3nld:A (PRO95) to (GLY103) STRUCTURE OF ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN COMPLEXED WITH 6-{{(3'S,4'S)-3'-[2"-(3'''-FLUOROPHENETHYLAMINO) ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, HEME ENZYME, SUBSTRATE INHIBITOR, OXIDOREDUCTASE
3nlo:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE R349A MUTANT HEME DOMAIN IN COMPLEX WITH 6-{{(3'S,4'R)-3'-[2"-(3'''-FLUOROPHENETHYLAMINO) ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR, HEME ENZYME, OXIDOREDUCTASE
3nln:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE R349A MUTANT HEME DOMAIN IN COMPLEX WITH 6-{{(3'R,4'S)-3'-[2"-(3'''-FLUOROPHENETHYLAMINO) ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR, HEME ENZYME, OXIDOREDUCTASE
3nln:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE R349A MUTANT HEME DOMAIN IN COMPLEX WITH 6-{{(3'R,4'S)-3'-[2"-(3'''-FLUOROPHENETHYLAMINO) ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN-2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR, HEME ENZYME, OXIDOREDUCTASE
3nlr:A (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH 6-{{(3'R,4'S)-3'-[2"-(3'''- FLUOROPHENETHYLAMINO)ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN- 2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR, HEME ENZYME, OXIDOREDUCTASE
3nlr:B (GLY325) to (GLY333) STRUCTURE OF NEURONAL NITRIC OXIDE SYNTHASE D597N/M336V MUTANT HEME DOMAIN IN COMPLEX WITH 6-{{(3'R,4'S)-3'-[2"-(3'''- FLUOROPHENETHYLAMINO)ETHOXY]PYRROLIDIN-4'-YL}METHYL}-4-METHYLPYRIDIN- 2-AMINE | NITRIC OXIDE SYNTHASE, INHIBITOR, HEME ENZYME, OXIDOREDUCTASE
5fob:B (GLU1566) to (SER1573) CRYSTAL STRUCTURE OF HUMAN COMPLEMENT C3B IN COMPLEX WITH SMALLPOX INHIBITOR OF COMPLEMENT (SPICE) | LIPID BINDING PROTEIN, COMPLEMENT SYSTEM, IMMUNE SYSTEM, PLASMA PROTEIN, REGULATORS OF COMPLEMENT ACTIVITY, COFACTOR ACTIVITY, DECAY ACCELERATING ACTIVITY, IMMUNE EVASION
4c9e:E (LEU89) to (HIS99) MOUSE ZNRF3 ECTODOMAIN IN COMPLEX WITH XENOPUS RSPO2 FU1- FU2 (SELENO MET) CRYSTAL FORM II | LIGASE-SIGNALING PROTEIN COMPLEX, WNT, RNF43, LGR4, LGR5, LGR6, RSPO, R-SPO, RSPO1, RSPO3, RSPO4, RECEPTOR, MEMBRANE, SIGNALLING
4caq:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-CHLOROPHENETHYLAMINO)ETHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4caq:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 7-((3-CHLOROPHENETHYLAMINO)ETHYL)QUINOLIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4rl8:A (GLY121) to (ARG135) CRYSTAL STRUCTURE OF THE COG4313 OUTER MEMBRANE CHANNEL FROM PSEUDOMONAS PUTIDA F1 | BETA BARREL, CHANNEL, BACTERIAL OUTER MEMBRANE, MEMBRANE PROTEIN
4rl8:D (GLY14) to (ALA32) CRYSTAL STRUCTURE OF THE COG4313 OUTER MEMBRANE CHANNEL FROM PSEUDOMONAS PUTIDA F1 | BETA BARREL, CHANNEL, BACTERIAL OUTER MEMBRANE, MEMBRANE PROTEIN
5fvr:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(2-(5-(1-METHYLPIPERIDIN-4-YL) PYRIDIN-3-YL)ETHYL)PYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5fvr:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(2-(5-(1-METHYLPIPERIDIN-4-YL) PYRIDIN-3-YL)ETHYL)PYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5fvp:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-[2-(5-MORPHOLIN-4-YLPYRIDIN-3-YL) ETHYL]PYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5fvp:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-[2-(5-MORPHOLIN-4-YLPYRIDIN-3-YL) ETHYL]PYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5fvt:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(2-(5-(3-(DIMETHYLAMINO)PROPYL)PYRIDIN- 3-YL)ETHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5fvt:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH 6-(2-(5-(3-(DIMETHYLAMINO)PROPYL)PYRIDIN- 3-YL)ETHYL)-4-METHYLPYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
5fvu:A (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(2-(5-(4-METHYLPIPERAZIN-1-YL) PYRIDIN-3-YL)ETHYL)PYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE
5fvu:B (GLY330) to (GLY338) STRUCTURE OF HUMAN NNOS R354A G357D MUTANT HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(2-(5-(4-METHYLPIPERAZIN-1-YL) PYRIDIN-3-YL)ETHYL)PYRIDIN-2-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE
4rvi:C (ASP30) to (ILE50) CRYSTAL STRUCTURE OF MULTIDRUG-RESISTANT CLINICAL ISOLATE A02 HIV-1 PROTEASE IN COMPLEX WITH NON-PEPTIDIC INHIBITOR, GRL0519 | HIV-1 PROTEASE-INHIBITOR COMPLEX, GRL0519, G52, PROTEASE INHIBITOR, NON-PEPTIDIC PROTEASE INHIBITOR, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4rvi:D (ASP30) to (GLY49) CRYSTAL STRUCTURE OF MULTIDRUG-RESISTANT CLINICAL ISOLATE A02 HIV-1 PROTEASE IN COMPLEX WITH NON-PEPTIDIC INHIBITOR, GRL0519 | HIV-1 PROTEASE-INHIBITOR COMPLEX, GRL0519, G52, PROTEASE INHIBITOR, NON-PEPTIDIC PROTEASE INHIBITOR, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3o0x:A (TYR306) to (VAL313) STRUCTURAL BASIS OF CARBOHYDRATE RECOGNITION BY CALRETICULIN | JELLY ROLL FOLD, CHAPERONE, CARBOHYDRATE BINDING; CALCIUM BINDING
3o0x:B (TYR306) to (VAL313) STRUCTURAL BASIS OF CARBOHYDRATE RECOGNITION BY CALRETICULIN | JELLY ROLL FOLD, CHAPERONE, CARBOHYDRATE BINDING; CALCIUM BINDING
4tll:A (LEU398) to (PRO413) CRYSTAL STRUCTURE OF GLUN1/GLUN2B NMDA RECEPTOR, STRUCTURE 1 | NEUROTRANSMITTER RECEPTOR, NMDA RECEPTOR, GLUN1/GLUN2B, MEMBRANE PROTEIN, ION CHANNEL, SIGNALING PROTEIN
4cvl:A (ALA23) to (THR30) PAMURF IN COMPLEX WITH AMP-PNP | LIGASE, MURF,
4cwz:B (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE Y477A MUTANT HEME DOMAIN IN COMPLEX WITH 4-METHYL-6-(((3R,4R)-4-( (5-(4-METHYLPYRIDIN-2-YL)PENTYL)OXY)PYRROLIDIN-3-YL)METHYL) PYRIDIN-2-AMINE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4czs:B (SER164) to (PHE175) DISCOVERY OF GLYCOMIMETIC LIGANDS VIA GENETICALLY-ENCODED LIBRARY OF PHAGE DISPLAYING MANNOSE-PEPTIDES | SUGAR BINDING PROTEIN
4d2t:D (TYR10) to (GLY18) STRUCTURE OF MELK IN COMPLEX WITH INHIBITORS | TRANSFERASE, FRAGMENT BASED DRUG DESIGN, KINASE
4d39:A (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL)-N- (3-CYANOBENZYL)ETHAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
4d39:B (PRO95) to (GLY103) STRUCTURE OF BOVINE ENDOTHELIAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH2-(2-(1H-IMIDAZOL-1-YL)PYRIMIDIN-4-YL)-N- (3-CYANOBENZYL)ETHAN-1-AMINE | OXIDOREDUCTASE, NITRIC OXIDE SYNTHASE, INHIBITOR COMPLEX
3dqs:B (PRO95) to (GLY103) STRUCTURE OF ENDOTHELIAL NOS HEME DOMAIN IN COMPLEX WITH A INHIBITOR (+-)-N1-{CIS-4'-[(6"-AMINO-4"-METHYLPYRIDIN-2"-YL)METHYL]PYRROLIDIN- 3'-YL}-N2-(4'-CHLOROBENZYL)ETHANE-1,2-DIAMINE | NITRIC OXIDE SYNTHASE HEME ENZYME INHIBITOR, BLOOD COAGULATION, CALMODULIN-BINDING, CYTOSKELETON, FAD, FMN, GOLGI APPARATUS, HEME, IRON, LIPOPROTEIN, MEMBRANE, METAL-BINDING, MYRISTATE, NADP, OXIDOREDUCTASE, PALMITATE, PHOSPHOPROTEIN
5h8f:B (LYS8) to (PRO22) STRUCTURE OF THE APO HUMAN GLUN1/GLUN2A LBD | GLUN1, GLUN2A, NMDA, RECEPTOR, TRANSPORT PROTEIN
5h9o:A (PRO298) to (PHE307) COMPLEX OF MURINE ENDOPLASMIC RETICULUM ALPHA-GLUCOSIDASE II WITH D- GLUCOSE | ENZYME GLYCOSYL HYDROLASE GH31 QUALITY CONTROL EXOGLYCOSIDASE, HYDROLASE
5h9o:C (PRO298) to (PHE307) COMPLEX OF MURINE ENDOPLASMIC RETICULUM ALPHA-GLUCOSIDASE II WITH D- GLUCOSE | ENZYME GLYCOSYL HYDROLASE GH31 QUALITY CONTROL EXOGLYCOSIDASE, HYDROLASE
5hez:B (HIS848) to (ASN859) JAK2 KINASE (JH1 DOMAIN) MUTANT P1057A IN COMPLEX WITH TG101209 | PROTEIN KINASE, INHIBITOR, MUTATION, TYK2, SURROGATE, P1104A, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
5hez:D (HIS848) to (ASN859) JAK2 KINASE (JH1 DOMAIN) MUTANT P1057A IN COMPLEX WITH TG101209 | PROTEIN KINASE, INHIBITOR, MUTATION, TYK2, SURROGATE, P1104A, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4dqc:A (ASP30) to (GLY49) CRYSTAL STRUCTURE OF (G16C/L38C) HIV-1 PROTEASE IN COMPLEX WITH DRV | HIV-1 PROTEASE, DRUG RESISTANCE, DRUG DESIGN, PROTEASE INHIBITORS, AIDS, ASPARTYL PROTEASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4upm:A (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N',N'-{[(2R)-3-AMINOPROPANE-1,2-DIYL] BIS(OXYMETHANEDIYLBENZENE-3,1-DIYL)}DITHIOPHENE-2-CARBOXIMIDAMIDE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4upm:B (GLY325) to (GLY333) STRUCTURE OF RAT NEURONAL NITRIC OXIDE SYNTHASE HEME DOMAIN IN COMPLEX WITH N',N'-{[(2R)-3-AMINOPROPANE-1,2-DIYL] BIS(OXYMETHANEDIYLBENZENE-3,1-DIYL)}DITHIOPHENE-2-CARBOXIMIDAMIDE | OXIDOREDUCTASE, INHIBITOR COMPLEX
4e3s:A (PRO35) to (ASP51) RB69 DNA POLYMERASE TERNARY COMPLEX WITH DQTP OPPOSITE DT | DQTP, RB69POL, TRANSFERASE-DNA COMPLEX
4e4g:A (GLY365) to (PRO373) CRYSTAL STRUCTURE OF PUTATIVE METHYLMALONATE-SEMIALDEHYDE DEHYDROGENASE FROM SINORHIZOBIUM MELILOTI 1021 | STRUCTURAL GENOMICS, CRYSTAL STRUCTURE,PROTEIN STRUCTURE INITIATIVE, NYSGRC, PSI-BIOLOGY, NEW YORK STRUCTURAL GENOMICS RESEARCH CONSORTIUM, OXIDOREDUCTASE
3psb:B (TRP450) to (GLN461) FURO[2,3-C]PYRIDINE-BASED INDANONE OXIMES AS POTENT AND SELECTIVE B- RAF INHIBITORS | KINASE, ATP-BINDING, CARDIOMYOPATHY, DISEASE MUTATION, METAL-BINDING, NUCLEOTIDE-BINDING, PHORBOL-ESTER BINDING, PHOSPHOPROTEIN, PROTO- ONCOGENE, SERINE/THREONINE-PROTEIN KINASE, ZINC-FINGER, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX
3pvk:A (LEU38) to (PRO67) SECRETED ASPARTIC PROTEASE 2 IN COMPLEX WITH BENZAMIDINE | HYDROLASE
3pwc:A (GLN30) to (SER54) BOVINE TRYPSIN VARIANT X(TRIPLEGLU217ILE227) IN COMPLEX WITH SMALL MOLECULE INHIBITOR | TRYPSIN-LIKE SERINE PROTEASE, HYDROLASE, PROTEIN BINDING, DUODENUM, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4es5:D (THR329) to (GLU341) CRYSTAL STRUCTURE OF THE CAP-BINDING DOMAIN OF POLYMERASE BASIC PROTEIN 2 FROM INFLUENZA VIRUS A/BAR-HEADED GS/QINGHAI/15C/2005 (H5N1) WITH BOUND M7GTP | CAP-BINDING PROTEIN, TRANSCRIPTION
4f73:A (ASP30) to (ILE50) CRYSTAL STRUCTURE OF ACTIVE HIV-1 PROTEASE IN COMPLEX WITH THE N TERMINAL PRODUCT OF CA-P2 CLEAVAGE SITE | HIV-1 PROTEASE, SUBSTRATE COMPLEX, AIDS, PRODUCT COMPLEX, ASPARTYL PROTEASE, HYDROLASE, HYDROLASE-HYDROLASE PRODUCT COMPLEX
3qo6:A (ASP269) to (PRO279) CRYSTAL STRUCTURE ANALYSIS OF THE PLANT PROTEASE DEG1 | PROTEASE, HTRA, PH-SENSOR, HYDROLASE, PHOTOSYNTHESIS
3qo6:C (ASP269) to (PRO279) CRYSTAL STRUCTURE ANALYSIS OF THE PLANT PROTEASE DEG1 | PROTEASE, HTRA, PH-SENSOR, HYDROLASE, PHOTOSYNTHESIS
4v2y:C (THR109) to (PRO122) CEREBLON ISOFORM 4 FROM MAGNETOSPIRILLUM GRYPHISWALDENSE IN COMPLEX WITH THALIDOMIDE | SIGNALING PROTEIN, TERATOGENICITY, AROMATIC CAGE
4v2z:C (GLN108) to (PRO122) CEREBLON ISOFORM 4 FROM MAGNETOSPIRILLUM GRYPHISWALDENSE IN COMPLEX WITH POMALIDOMIDE | SIGNALING PROTEIN, TERATOGENICITY, AROMATIC CAGE, CC-4047, POMALYST
4fjg:A (PRO35) to (ASP51) RB69 DNA POLYMERASE TERNARY COMPLEX WITH DATP/DC | DATP/DC, RB69, RB69POL, QUADRUPLE, TRANSFERASE-DNA COMPLEX
4fji:A (PRO35) to (ASP51) RB69 DNA POLYMERASE TERNARY COMPLEX WITH DCTP/DC | DCTP/DC, RB69, RB69POL, QUADRUPLE, TRANSFERASE-DNA COMPLEX
3r2b:A (LEU52) to (SER67) MK2 KINASE BOUND TO COMPOUND 5B | KINASE DOMAIN WITH BOUND INHIBITOR, KINASE DOMAIN, PHOSPHOTRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
3r2b:B (LEU52) to (SER67) MK2 KINASE BOUND TO COMPOUND 5B | KINASE DOMAIN WITH BOUND INHIBITOR, KINASE DOMAIN, PHOSPHOTRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
3r2b:C (LEU52) to (SER67) MK2 KINASE BOUND TO COMPOUND 5B | KINASE DOMAIN WITH BOUND INHIBITOR, KINASE DOMAIN, PHOSPHOTRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
3r2b:D (LEU52) to (SER67) MK2 KINASE BOUND TO COMPOUND 5B | KINASE DOMAIN WITH BOUND INHIBITOR, KINASE DOMAIN, PHOSPHOTRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
3r2b:F (LEU52) to (SER67) MK2 KINASE BOUND TO COMPOUND 5B | KINASE DOMAIN WITH BOUND INHIBITOR, KINASE DOMAIN, PHOSPHOTRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
3r2b:I (LEU52) to (SER67) MK2 KINASE BOUND TO COMPOUND 5B | KINASE DOMAIN WITH BOUND INHIBITOR, KINASE DOMAIN, PHOSPHOTRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
3r2b:J (LEU52) to (SER67) MK2 KINASE BOUND TO COMPOUND 5B | KINASE DOMAIN WITH BOUND INHIBITOR, KINASE DOMAIN, PHOSPHOTRANSFERASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
3rhp:D (MET734) to (PRO748) CRYSTAL STRUCTURE OF THE C707A MUTANT OF THE C-TERMINAL DOMAIN OF 10'FORMYLTETRAHYDROFOLATE DEHYDROGENASE | FDH, OXIDOREDUCTASE
3ril:B (LEU383) to (PRO401) THE ACID BETA-GLUCOSIDASE ACTIVE SITE EXHIBITS PLASTICITY IN BINDING 3,4,5,6-TETRAHYDROXYAZEPANE-BASED INHIBITORS: IMPLICATIONS FOR PHARMACOLOGICAL CHAPERONE DESIGN FOR GAUCHER DISEASE | TIM-BARREL, LYSOSOMAL HYDROLASE, HYDROLASE, GLYCOSYLATION, LYSOSOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3ril:D (LEU383) to (PRO401) THE ACID BETA-GLUCOSIDASE ACTIVE SITE EXHIBITS PLASTICITY IN BINDING 3,4,5,6-TETRAHYDROXYAZEPANE-BASED INHIBITORS: IMPLICATIONS FOR PHARMACOLOGICAL CHAPERONE DESIGN FOR GAUCHER DISEASE | TIM-BARREL, LYSOSOMAL HYDROLASE, HYDROLASE, GLYCOSYLATION, LYSOSOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5k1s:B (GLY77) to (GLN88) CRYSTAL STRUCTURE OF AIBC | MEDIUM CHAIN REDUCTASE, ISOVALERATE, HEXAHISTIDINE TAG, TEV-PROTEASE RECOGNITION SEQUENCE, OXIDOREDUCTASE
4gdi:E (SER89) to (PRO99) A SUBTYPE N10 NEURAMINIDASE-LIKE PROTEIN OF A/LITTLE YELLOW-SHOULDERED BAT/GUATEMALA/164/2009 | INFLUENZA VIRUS, NEURAMINIDASE-LIKE, N10, BETA-PROPELLER, ECTODOMAIN, VIRAL PROTEIN
5kdt:B (LEU7) to (LYS21) STRUCTURE OF THE HUMAN GLUN1/GLUN2A LBD IN COMPLEX WITH GNE0723 | NMDA, RECEPTOR, GLUTAMATE, CHANNEL, TRANSPORT PROTEIN
5l30:H (GLN30) to (VAL53) FACTOR VIIA IN COMPLEX WITH THE INHIBITOR (2R,15R)-2-[(1- AMINOISOQUINOLIN-6-YL)AMINO]-4,15,17-TRIMETHYL-7-[1-(1H-TETRAZOL-5- YL)CYCLOPROPYL]-13-OXA-4,11-DIAZATRICYCLO[14.2.2.1~6,10~]HENICOSA- 1(18),6(21),7,9,16,19-HEXAENE-3,12-DIONE | GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM-BINDING, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
5syn:D (GLY207) to (PRO214) COCRYSTAL STRUCTURE OF THE HUMAN ACYL PROTEIN THIOESTERASE 2 WITH AN ISOFORM-SELECTIVE INHIBITOR, ML349 | HYDROLASE, INHIBITOR, THIOESTERASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5tpa:B (LEU7) to (LYS21) STRUCTURE OF THE HUMAN GLUN1/GLUN2A LBD IN COMPLEX WITH COMPOUND 9 (GNE3500) | NMDA RECEPTOR, GLUTAMATE, GLYCINE, CALCIUM CHANNEL, MEMBRANE, TRANSPORT PROTEIN