1a0u:D (ALA86) to (ALA142) HEMOGLOBIN (VAL BETA1 MET) MUTANT | OXYGEN TRANSPORT
1a3n:A (SER3) to (HIS72) DEOXY HUMAN HEMOGLOBIN | OXYGEN TRANSPORT, HEME, RESPIRATORY PROTEIN, ERYTHROCYTE
1na6:B (SER195) to (GLY282) CRYSTAL STRUCTURE OF RESTRICTION ENDONUCLEASE ECORII MUTANT R88A | SITE-SPECIFIC RESTRICTION; MUTATION; REPLICATION, HYDROLASE
1a6i:A (GLU107) to (LEU204) TET REPRESSOR, CLASS D VARIANT | TRANSCRIPTION REGULATION, REPRESSOR, DNA-BINDING
2oif:B (SER11) to (LEU85) THE CRYSTAL STRUCTURE OF FERRIC CYANIDE BOUND BARLEY HEXACOORDINATE HEMOGLOBIN. | HEXACOORDINATE HEMOGLOBIN, BARLEY, LIGAND BINDING, NON- SYMBIOTIC, SYMBIOTIC, EVOLUTION, CONFORMATIONAL CHANGES, OXYGEN TRANSPORT, METAL BINDING PROTEIN
2oif:C (GLU12) to (LEU85) THE CRYSTAL STRUCTURE OF FERRIC CYANIDE BOUND BARLEY HEXACOORDINATE HEMOGLOBIN. | HEXACOORDINATE HEMOGLOBIN, BARLEY, LIGAND BINDING, NON- SYMBIOTIC, SYMBIOTIC, EVOLUTION, CONFORMATIONAL CHANGES, OXYGEN TRANSPORT, METAL BINDING PROTEIN
1ngk:C (SER4) to (GLY57) CRYSTALLOGRAPHIC STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS HEMOGLOBIN O | TRUNCATED HEMOGLOBIN, OXYGEN STORAGE/TRANSPORT COMPLEX
1ngk:D (SER4) to (GLY57) CRYSTALLOGRAPHIC STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS HEMOGLOBIN O | TRUNCATED HEMOGLOBIN, OXYGEN STORAGE/TRANSPORT COMPLEX
1ngk:E (SER4) to (GLY57) CRYSTALLOGRAPHIC STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS HEMOGLOBIN O | TRUNCATED HEMOGLOBIN, OXYGEN STORAGE/TRANSPORT COMPLEX
1ngk:F (SER4) to (GLY57) CRYSTALLOGRAPHIC STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS HEMOGLOBIN O | TRUNCATED HEMOGLOBIN, OXYGEN STORAGE/TRANSPORT COMPLEX
1ngk:G (SER4) to (GLY57) CRYSTALLOGRAPHIC STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS HEMOGLOBIN O | TRUNCATED HEMOGLOBIN, OXYGEN STORAGE/TRANSPORT COMPLEX
1ngk:H (SER4) to (GLY57) CRYSTALLOGRAPHIC STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS HEMOGLOBIN O | TRUNCATED HEMOGLOBIN, OXYGEN STORAGE/TRANSPORT COMPLEX
1ngk:I (SER4) to (GLY57) CRYSTALLOGRAPHIC STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS HEMOGLOBIN O | TRUNCATED HEMOGLOBIN, OXYGEN STORAGE/TRANSPORT COMPLEX
1ngk:J (SER4) to (GLY57) CRYSTALLOGRAPHIC STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS HEMOGLOBIN O | TRUNCATED HEMOGLOBIN, OXYGEN STORAGE/TRANSPORT COMPLEX
1ngk:K (SER4) to (GLY57) CRYSTALLOGRAPHIC STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS HEMOGLOBIN O | TRUNCATED HEMOGLOBIN, OXYGEN STORAGE/TRANSPORT COMPLEX
1ngk:L (SER4) to (GLY57) CRYSTALLOGRAPHIC STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS HEMOGLOBIN O | TRUNCATED HEMOGLOBIN, OXYGEN STORAGE/TRANSPORT COMPLEX
4wjg:A (LEU80) to (THR137) STRUCTURE OF T. BRUCEI HAPTOGLOBIN-HEMOGLOBIN RECEPTOR BINDING TO HUMAN HAPTOGLOBIN-HEMOGLOBIN | ENDOCYTOSIS, TRYPANOSOME, RECEPTOR
4wjg:F (LEU80) to (THR137) STRUCTURE OF T. BRUCEI HAPTOGLOBIN-HEMOGLOBIN RECEPTOR BINDING TO HUMAN HAPTOGLOBIN-HEMOGLOBIN | ENDOCYTOSIS, TRYPANOSOME, RECEPTOR
4wjg:K (LEU80) to (THR137) STRUCTURE OF T. BRUCEI HAPTOGLOBIN-HEMOGLOBIN RECEPTOR BINDING TO HUMAN HAPTOGLOBIN-HEMOGLOBIN | ENDOCYTOSIS, TRYPANOSOME, RECEPTOR
4wjg:P (LEU80) to (THR137) STRUCTURE OF T. BRUCEI HAPTOGLOBIN-HEMOGLOBIN RECEPTOR BINDING TO HUMAN HAPTOGLOBIN-HEMOGLOBIN | ENDOCYTOSIS, TRYPANOSOME, RECEPTOR
4wjg:U (LEU80) to (THR137) STRUCTURE OF T. BRUCEI HAPTOGLOBIN-HEMOGLOBIN RECEPTOR BINDING TO HUMAN HAPTOGLOBIN-HEMOGLOBIN | ENDOCYTOSIS, TRYPANOSOME, RECEPTOR
4wjg:Z (LEU80) to (THR137) STRUCTURE OF T. BRUCEI HAPTOGLOBIN-HEMOGLOBIN RECEPTOR BINDING TO HUMAN HAPTOGLOBIN-HEMOGLOBIN | ENDOCYTOSIS, TRYPANOSOME, RECEPTOR
3rut:A (THR378) to (ASP458) FXR WITH SRC1 AND GSK359 | NUCLEAR RECEPTOR, ALPHA-HELICAL SANDWICH, TRANSCRIPTION FACTOR, RXR, TRANSCRIPTION CO-FACTORS, BILE ACID, FARNESOID, TRANSCRIPTION REGULATOR
1aj8:B (LYS79) to (GLY145) CITRATE SYNTHASE FROM PYROCOCCUS FURIOSUS | HYPERTHERMOSTABLE, LYASE
4wn1:A (SER571) to (ASP634) CRYSTAL STRUCTURE OF PDE10A IN COMPLEX WITH 1-METHYL-5-(1-METHYL-3- {[4-(QUINOLIN-2-YL)PHENOXY]METHYL}-1H-PYRAZOL-4-YL)PYRIDIN-2(1H)-ONE | PHOSPHODIESTERASE, COMPLEX, INHIBITOR
4wn1:B (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A IN COMPLEX WITH 1-METHYL-5-(1-METHYL-3- {[4-(QUINOLIN-2-YL)PHENOXY]METHYL}-1H-PYRAZOL-4-YL)PYRIDIN-2(1H)-ONE | PHOSPHODIESTERASE, COMPLEX, INHIBITOR
3eid:B (THR310) to (THR366) 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
3ej1:B (VAL311) to (VAL367) CDK2/CYCLINA COMPLEXED WITH A PYRAZOLOPYRIDAZINE INHIBITOR | CDK, CYCLIN, KINASE, ATP-BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, NUCLEUS, TRANSFERASE-CELL CYCLE COMPLEX
3ej1:D (THR310) to (THR366) CDK2/CYCLINA COMPLEXED WITH A PYRAZOLOPYRIDAZINE INHIBITOR | CDK, CYCLIN, KINASE, ATP-BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, NUCLEUS, TRANSFERASE-CELL CYCLE COMPLEX
3ryt:A (SER1846) to (MET1890) THE PLEXIN A1 INTRACELLULAR REGION IN COMPLEX WITH RAC1 | PLEXIN, RASGAP, GTPASE ACTIVATING PROTEIN, RAC, SIGNALING PROTEIN
2oun:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 IN COMPLEX WITH AMP | PDE, PRODUCT BINDING, HYDROLASE
2ouq:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 IN COMPLEX WITH GMP | PDE, GMP COMPLEX, HYDROLASE
2our:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 MUTANT D674A IN COMPLEX WITH CAMP | PDE10, CAMP, SUBSTRATE SPECIFICITY, HYDROLASE
2ous:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 MUTANT D674A | PDE, HYDROLASE
2ouu:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 MUTANT D674A IN COMPLEX WITH CGMP | PDE, CGMP, SUBSTRATE SPECIFICITY, HYDROLASE
2ouv:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 MUTANT OF D564N | PDE, HYDROLASE
3eoc:B (THR310) to (GLY369) CDK2/CYCLINA COMPLEXED WITH A IMIDAZO TRIAZIN-2-AMINE | CDK, CYCLIN, ATP-BINDING, CELL CYCLE, CELL DIVISION, KINASE, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, NUCLEUS, TRANSFERASE-CELL CYCLE COMPLEX
3eoc:D (THR310) to (VAL367) CDK2/CYCLINA COMPLEXED WITH A IMIDAZO TRIAZIN-2-AMINE | CDK, CYCLIN, ATP-BINDING, CELL CYCLE, CELL DIVISION, KINASE, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, NUCLEUS, TRANSFERASE-CELL CYCLE COMPLEX
3s1j:C (ASP3) to (ILE65) CRYSTAL STRUCTURE OF ACETATE-BOUND HELL'S GATE GLOBIN I | GLOBIN, HEME, ACETATE-BOUND, AUTOXIDATION, OXYGEN TRANSPORT, OXYGEN STORAGE
1nxe:B (ILE1117) to (ILE1180) A NOVEL NADH ALLOSTERIC REGULATOR SITE IS FOUND ON THE SURFACE OF THE HEXAMERIC TYPE II PHE383ALA VARIANT OF CITRATE SYNTHASE | CITRATE SYNTHASE, NADH, ALLOSTERIC, TRANSFERASE
3eu1:A (SER3) to (LEU73) CRYSTAL STRUCTURE DETERMINATION OF GOAT HEMOGLOBIN (CAPRA HIRCUS) AT 3 ANGSTROM RESOLUTION | LOW OXYGEN AFFINITY, CAPRA HIRCUS, HEMOGLOBIN, ALLOSTERIC MECHANISM, 2,3-DIPHOSPHO GLYCERATE, OXYGEN STORAGE, OXYGEN TRANSPORT
4wz6:A (THR501) to (LYS563) HUMAN CFTR AA389-678 (NBD1), DELTAF508 WITH THREE SOLUBILIZING MUTATIONS, BOUND ATP | ATPASE, HYDROLASE, ATP/ADP BINDING, ATP BINDING PROTEIN
1bbw:A (THR327) to (GLU377) LYSYL-TRNA SYNTHETASE (LYSS) | LIGASE, AMINOACYL-TRNA SYNTHETASE, PROTEIN BIOSYNTHESIS
4x0l:A (SER4) to (HIS73) HUMAN HAPTOGLOBIN-HAEMOGLOBIN COMPLEX | HAPTOGLOBIN-HAEMOGLOBIN COMPLEX, OXYGEN TRANSPORT
1bij:A (SER3) to (HIS72) CROSSLINKED, DEOXY HUMAN HEMOGLOBIN A | HEME, ALLOSTERIC INTERMEDIATE, OXYGEN TRANSPORT, CROSSLINKED
2bkm:A (THR7) to (GLY59) CRYSTAL STRUCTURE OF THE TRUNCATED HEMOGLOBIN FROM GEOBACILLUS STEAROTHERMOPHILUS | HYPOTHETICAL PROTEIN, OXYGEN TRANSPORT, TRANSPORT, OXYGEN STORAGE
2bkz:B (VAL311) to (GLY369) STRUCTURE OF CDK2-CYCLIN A WITH PHA-404611 | TRANSFERASE/COMPLEX, PROTEIN KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, PHOSPHORYLATION, CELL DIVISION, CYCLIN, ATP-BINDING, CELL CYCLE, MITOSIS, POLYMORPHISM
2bkz:D (VAL311) to (GLY369) STRUCTURE OF CDK2-CYCLIN A WITH PHA-404611 | TRANSFERASE/COMPLEX, PROTEIN KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, PHOSPHORYLATION, CELL DIVISION, CYCLIN, ATP-BINDING, CELL CYCLE, MITOSIS, POLYMORPHISM
2peg:A (LEU81) to (GLU139) CRYSTAL STRUCTURE OF TREMATOMUS BERNACCHII HEMOGLOBIN IN A PARTIAL HEMICHROME STATE | HEMICHROME, R/TINTERMEDIATE QUATERNARY STRUCTURE, OXYGEN STORAGE/TRANSPORT COMPLEX
2bpm:B (VAL311) to (GLY369) STRUCTURE OF CDK2-CYCLIN A WITH PHA-630529 | PROTEIN KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, PHOSPHORYLATION, CELL DIVISION, CYCLIN
2bpm:D (ASN312) to (THR366) STRUCTURE OF CDK2-CYCLIN A WITH PHA-630529 | PROTEIN KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, PHOSPHORYLATION, CELL DIVISION, CYCLIN
3s65:D (PHE85) to (HIS143) STRUCTURES AND OXYGEN AFFINITIES OF CRYSTALLINE HUMAN HEMOGLOBIN C (BETA6 LYS) IN THE R2 QUATERNARY STRUCTURES | HEMOGLOBIN, ALLOSTERY, OXYGEN TRANSPORT
3f5x:B (ASN312) to (GLY369) CDK-2-CYCLIN COMPLEX WITH INDAZOLE INHIBITOR 9 BOUND AT ITS ACTIVE SITE | KINASE, PKC, PROTEIN KINASE, INHIBITOR, ATP-BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, CYCLIN, NUCLEUS, TRANSFERASE-CELL CYCLE COMPLEX
3f5x:D (ASN312) to (GLY369) CDK-2-CYCLIN COMPLEX WITH INDAZOLE INHIBITOR 9 BOUND AT ITS ACTIVE SITE | KINASE, PKC, PROTEIN KINASE, INHIBITOR, ATP-BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, CYCLIN, NUCLEUS, TRANSFERASE-CELL CYCLE COMPLEX
1bu2:A (LEU156) to (ASP210) X-RAY STRUCTURE OF A VIRAL CYCLIN FROM HERPESVIRUS SAIMIRI | CELL CYCLE REGULATION, HERPESVIRUS SAIMIRI, VIRAL CYCLIN
2pgh:D (PHE85) to (HIS143) STRUCTURE DETERMINATION OF AQUOMET PORCINE HEMOGLOBIN AT 2.8 ANGSTROM RESOLUTION | OXYGEN TRANSPORT
4xbi:A (THR8) to (GLN73) STRUCTURE OF A MALARIAL PROTEIN INVOLVED IN PROTEOSTASIS | CLP CHAPERONE, AAA+ ATPASE, REFOLDASE, PROTEIN METABOLISM, CHAPERONE
4xbi:B (THR8) to (LYS72) STRUCTURE OF A MALARIAL PROTEIN INVOLVED IN PROTEOSTASIS | CLP CHAPERONE, AAA+ ATPASE, REFOLDASE, PROTEIN METABOLISM, CHAPERONE
3fes:C (THR6) to (MSE66) CRYSTAL STRUCTURE OF THE ATP-DEPENDENT CLP PROTEASE CLPC FROM CLOSTRIDIUM DIFFICILE | ALPHA-HELICAL BUNDLES, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, ATP- BINDING, CHAPERONE, NUCLEOTIDE-BINDING, PROTEASE, ATP BINDING PROTEIN
3fes:D (SER80) to (MSE141) CRYSTAL STRUCTURE OF THE ATP-DEPENDENT CLP PROTEASE CLPC FROM CLOSTRIDIUM DIFFICILE | ALPHA-HELICAL BUNDLES, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, ATP- BINDING, CHAPERONE, NUCLEOTIDE-BINDING, PROTEASE, ATP BINDING PROTEIN
3fh2:A (THR6) to (ILE67) THE CRYSTAL STRUCTURE OF THE PROBABLE ATP-DEPENDENT PROTEASE (HEAT SHOCK PROTEIN) FROM CORYNEBACTERIUM GLUTAMICUM | PROBABLE ATP-DEPENDENT PROTEASE (HEAT SHOCK PROTEIN), STRUCTURAL GENOMICS, PSI2, MCSG, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, ATP-BINDING, CHAPERONE, HYDROLASE, NUCLEOTIDE-BINDING, PROTEASE, STRESS RESPONSE
3fh2:A (THR81) to (LEU142) THE CRYSTAL STRUCTURE OF THE PROBABLE ATP-DEPENDENT PROTEASE (HEAT SHOCK PROTEIN) FROM CORYNEBACTERIUM GLUTAMICUM | PROBABLE ATP-DEPENDENT PROTEASE (HEAT SHOCK PROTEIN), STRUCTURAL GENOMICS, PSI2, MCSG, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, ATP-BINDING, CHAPERONE, HYDROLASE, NUCLEOTIDE-BINDING, PROTEASE, STRESS RESPONSE
1oi9:B (THR310) to (GLY369) STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH A 6-CYCLOHEXYLMETHYLOXY-2-ANILINO-PURINE INHIBITOR | KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION
1oi9:D (THR310) to (GLY369) STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH A 6-CYCLOHEXYLMETHYLOXY-2-ANILINO-PURINE INHIBITOR | KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION
1oiu:B (ASN312) to (GLY369) STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH A 6-CYCLOHEXYLMETHYLOXY-2-ANILINO-PURINE INHIBITOR | KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION
1oiu:D (THR310) to (THR368) STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH A 6-CYCLOHEXYLMETHYLOXY-2-ANILINO-PURINE INHIBITOR | KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION
1oiy:B (ASN312) to (THR366) STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH A 6-CYCLOHEXYLMETHYLOXY-2-ANILINO-PURINE INHIBITOR | KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION
1oiy:D (ASN312) to (VAL367) STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH A 6-CYCLOHEXYLMETHYLOXY-2-ANILINO-PURINE INHIBITOR | KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION
1oj6:D (GLU7) to (ASN78) HUMAN BRAIN NEUROGLOBIN THREE-DIMENSIONAL STRUCTURE | NEUROGLOBIN, HEME HEXACOORDINATION, OXYGEN TRANSPORT
1cbl:A (PHE85) to (ALA142) THE 1.9 ANGSTROM STRUCTURE OF DEOXY-BETA4 HEMOGLOBIN: ANALYSIS OF THE PARTITIONING OF QUATERNARY-ASSOCIATED AND LIGAND-INDUCED CHANGES IN TERTIARY STRUCTURE | OXYGEN TRANSPORT
4i3z:B (ASN312) to (GLY369) STRUCTURE OF PCDK2/CYCLINA BOUND TO ADP AND 2 MAGNESIUM IONS | ADP AND MAGNESIUM BINDING, T160 PHOSPHORYLATION, TRANSFERASE-CELL CYCLE COMPLEX
4i3z:D (ASN312) to (GLY369) STRUCTURE OF PCDK2/CYCLINA BOUND TO ADP AND 2 MAGNESIUM IONS | ADP AND MAGNESIUM BINDING, T160 PHOSPHORYLATION, TRANSFERASE-CELL CYCLE COMPLEX
1okw:B (THR310) to (THR366) CYCLIN A BINDING GROOVE INHIBITOR AC-ARG-ARG-LEU-ASN-(M-CL-PHE)-NH2 | CELL CYCLE, COMPLEX(KINASE-CYCLIN), CYCLIN A, LIGAND EXCHANGE, PEPTIDOMIMETICS, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
1okw:D (VAL311) to (THR366) CYCLIN A BINDING GROOVE INHIBITOR AC-ARG-ARG-LEU-ASN-(M-CL-PHE)-NH2 | CELL CYCLE, COMPLEX(KINASE-CYCLIN), CYCLIN A, LIGAND EXCHANGE, PEPTIDOMIMETICS, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
1okv:B (VAL311) to (THR366) CYCLIN A BINDING GROOVE INHIBITOR H-ARG-ARG-LEU-ILE-PHE-NH2 | KINASE-CYCLIN COMPLEX, CYCLIN A, INHIBITOR, LIGAND EXCHANGE, DRUG DESIGN, PEPTIDOMIMETICS, CELL CYCLE, KINASE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
1ol1:B (VAL311) to (THR366) CYCLIN A BINDING GROOVE INHIBITOR H-CIT-CIT-LEU-ILE-(P-F-PHE)-NH2 | TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX, CELL CYCLE, KINASE-CYCLIN COMPLEX, CYCLIN A, INHIBITOR, LIGAND EXCHANGE, DRUG DESIGN, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, CELL DIVISION, MITOSIS, PHOSPHORYLATION, PEPTIDOMIMETICS
1ol2:B (VAL311) to (THR366) CYCLIN A BINDING GROOVE INHIBITOR H-ARG-ARG-LEU-ASN-(P-F-PHE)-NH2 | CELL CYCLE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX, CYCLIN A, LIGAND EXCHANGE, PEPTIDOMIMETICS, KINASE
1ol2:D (THR310) to (THR366) CYCLIN A BINDING GROOVE INHIBITOR H-ARG-ARG-LEU-ASN-(P-F-PHE)-NH2 | CELL CYCLE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX, CYCLIN A, LIGAND EXCHANGE, PEPTIDOMIMETICS, KINASE
3sl3:D (LEU326) to (ILE410) CRYSTAL STRUCTURE OF THE APO FORM OF THE CATALYTIC DOMAIN OF PDE4D2 | CATALYTIC MECHANISM, CAMP HYDROLYSIS, HYDROLASE
2c4g:B (VAL311) to (GLY369) STRUCTURE OF CDK2-CYCLIN A WITH PHA-533514 | PROTEIN KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, PHOSPHORYLATION, CELL DIVISION, CYCLIN, ATP-BINDING, CELL CYCLE, MITOSIS, NUCLEOTIDE-BINDING, POLYMORPHISM
2c4g:D (VAL311) to (GLY369) STRUCTURE OF CDK2-CYCLIN A WITH PHA-533514 | PROTEIN KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, PHOSPHORYLATION, CELL DIVISION, CYCLIN, ATP-BINDING, CELL CYCLE, MITOSIS, NUCLEOTIDE-BINDING, POLYMORPHISM
3sn7:A (LEU495) to (CYS552) HIGHLY POTENT, SELECTIVE, AND ORALLY ACTIVE PHOSPHODIESTARASE 10A INHIBITORS | HYDROLASE, HYDROLASE INHIBITOR, ZN BINDING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3sni:A (LEU495) to (CYS552) HIGHLY POTENT, SELECTIVE, AND ORALLY ACTIVE PHOSPHODIESTARASE 10A INHIBITORS | HYDROLASE, HYDROLASE INHIBITOR, ZN BINDING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1or6:A (ASP45) to (ALA105) CRYSTAL STRUCTURE OF HEMAT SENSOR DOMAIN FROM B.SUBTILIS IN THE UNLIGANDED FORM | GLOBIN FOLD, SIGNALING PROTEIN
1or6:B (GLY44) to (ALA105) CRYSTAL STRUCTURE OF HEMAT SENSOR DOMAIN FROM B.SUBTILIS IN THE UNLIGANDED FORM | GLOBIN FOLD, SIGNALING PROTEIN
2c5o:B (THR310) to (THR366) DIFFERENTIAL BINDING OF INHIBITORS TO ACTIVE AND INACTIVE CDK2 PROVIDES INSIGHTS FOR DRUG DESIGN | DIFFERENTIAL INHIBITION, TRANSFERASE, CDK2, ATP-BINDING, CELL CYCLE, CELL DIVISION, POLYMORPHISM, PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN, KINASE, MITOSIS, CYCLIN
2c5o:D (VAL311) to (THR366) DIFFERENTIAL BINDING OF INHIBITORS TO ACTIVE AND INACTIVE CDK2 PROVIDES INSIGHTS FOR DRUG DESIGN | DIFFERENTIAL INHIBITION, TRANSFERASE, CDK2, ATP-BINDING, CELL CYCLE, CELL DIVISION, POLYMORPHISM, PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN, KINASE, MITOSIS, CYCLIN
2c5n:B (THR310) to (THR366) DIFFERENTIAL BINDING OF INHIBITORS TO ACTIVE AND INACTIVE CDK2 PROVIDES INSIGHTS FOR DRUG DESIGN | DIFFERENTIAL INHIBITION, TRANSFERASE, CDK2, ATP-BINDING, CELL CYCLE, CELL DIVISION, POLYMORPHISM, PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN, KINASE, MITOSIS, CYCLIN
2c5v:B (VAL311) to (GLY369) DIFFERENTIAL BINDING OF INHIBITORS TO ACTIVE AND INACTIVE CDK2 PROVIDES INSIGHTS FOR DRUG DESIGN | ATP-BINDING, CELL CYCLE, CELL DIVISION, COMPLEX (KINASE/CYCLIN), CYCIN A, CYCLIN, DRUG DESIGN, LIGAND EXCHANGE, KINASE, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHORYLATION, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, COMPLEX (TRANSFERASE/CYCLIN)
2c5v:D (VAL311) to (GLY369) DIFFERENTIAL BINDING OF INHIBITORS TO ACTIVE AND INACTIVE CDK2 PROVIDES INSIGHTS FOR DRUG DESIGN | ATP-BINDING, CELL CYCLE, CELL DIVISION, COMPLEX (KINASE/CYCLIN), CYCIN A, CYCLIN, DRUG DESIGN, LIGAND EXCHANGE, KINASE, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHORYLATION, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, COMPLEX (TRANSFERASE/CYCLIN)
2c5x:B (VAL311) to (THR366) DIFFERENTIAL BINDING OF INHIBITORS TO ACTIVE AND INACTIVE CDK2 PROVIDES INSIGHTS FOR DRUG DESIGN | TRANSFERASE/INHIBITOR, INHIBITION, ACTIVE, INACTIVE, CDK2, CELL CYCLE, CELL DIVISION, KINASE, MITOSIS, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, ATP-BINDING, COMPLEX (TRANSFERASE/INHIBITOR)
2c5x:D (ASN312) to (THR366) DIFFERENTIAL BINDING OF INHIBITORS TO ACTIVE AND INACTIVE CDK2 PROVIDES INSIGHTS FOR DRUG DESIGN | TRANSFERASE/INHIBITOR, INHIBITION, ACTIVE, INACTIVE, CDK2, CELL CYCLE, CELL DIVISION, KINASE, MITOSIS, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, ATP-BINDING, COMPLEX (TRANSFERASE/INHIBITOR)
3spc:A (MET70) to (PRO187) INWARD RECTIFIER POTASSIUM CHANNEL KIR2.2 IN COMPLEX WITH DIOCTANOYLGLYCEROL PYROPHOSPHATE (DGPP) | PIP, MEMBRANE PROTEIN, LIPID, RECEPTOR, METAL TRANSPORT
4xlp:C (LEU193) to (LEU221) CRYSTAL STRUCTURE OF T.AQUATICUS TRANSCRIPTION INITIATION COMPLEX CONTAINING UPSTREAM FORK PROMOTER | PROTEIN-DNA COMPLEX, BACTERIAL TRANSCRIPTION INITIATION COMPLEX, TRANSCRIPTION, TRANSCRIPTION-DNA COMPLEX
4xlp:I (LEU193) to (LEU221) CRYSTAL STRUCTURE OF T.AQUATICUS TRANSCRIPTION INITIATION COMPLEX CONTAINING UPSTREAM FORK PROMOTER | PROTEIN-DNA COMPLEX, BACTERIAL TRANSCRIPTION INITIATION COMPLEX, TRANSCRIPTION, TRANSCRIPTION-DNA COMPLEX
2c6t:B (THR310) to (THR366) CRYSTAL STRUCTURE OF THE HUMAN CDK2 COMPLEXED WITH THE TRIAZOLOPYRIMIDINE INHIBITOR | SERINE/THREONINE PROTEIN KINASE, CDK2, ATP-BINDING, CELL CYCLE, MITOSIS, PHOSPHORYLATION, TRIAZOLOPYRIMIDINE INHIBITOR, COMPLEX (TRANSFERASE/CYCLIN2)
2c6t:D (THR310) to (THR366) CRYSTAL STRUCTURE OF THE HUMAN CDK2 COMPLEXED WITH THE TRIAZOLOPYRIMIDINE INHIBITOR | SERINE/THREONINE PROTEIN KINASE, CDK2, ATP-BINDING, CELL CYCLE, MITOSIS, PHOSPHORYLATION, TRIAZOLOPYRIMIDINE INHIBITOR, COMPLEX (TRANSFERASE/CYCLIN2)
1oyn:A (PRO325) to (ILE410) CRYSTAL STRUCTURE OF PDE4D2 IN COMPLEX WITH (R,S)-ROLIPRAM | PDE, CAMP, ROLIPRAM, HYDROLASE
3su8:X (GLY2083) to (GLU2129) CRYSTAL STRUCTURE OF A TRUNCATED INTRACELLULAR DOMAIN OF PLEXIN-B1 IN COMPLEX WITH RAC1 | AXON GUIDANCE, SIGNAL TRANSDUCTION, APOPTOSIS-SIGNALING PROTEIN COMPLEX
2cch:B (ASN312) to (GLY369) THE CRYSTAL STRUCTURE OF CDK2 CYCLIN A IN COMPLEX WITH A SUBSTRATE PEPTIDE DERIVED FROM CDC MODIFIED WITH A GAMMA- LINKED ATP ANALOGUE | COMPLEX(TRANSFERASE/CELL DIVISION), ATP-BINDING, CDK2, CELL CYCLE, CELL DIVISION, CYCLIN, MITOSIS, NUCLEAR PROTEIN, PEPTIDE SPECIFICITY, PHOSPHORYLATION, POLYMORPHISM, PROTEIN KINASE, RECRUITMENT, SERINE-THREONINE-PROTEIN KINASE, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE
2cch:D (ASN312) to (THR366) THE CRYSTAL STRUCTURE OF CDK2 CYCLIN A IN COMPLEX WITH A SUBSTRATE PEPTIDE DERIVED FROM CDC MODIFIED WITH A GAMMA- LINKED ATP ANALOGUE | COMPLEX(TRANSFERASE/CELL DIVISION), ATP-BINDING, CDK2, CELL CYCLE, CELL DIVISION, CYCLIN, MITOSIS, NUCLEAR PROTEIN, PEPTIDE SPECIFICITY, PHOSPHORYLATION, POLYMORPHISM, PROTEIN KINASE, RECRUITMENT, SERINE-THREONINE-PROTEIN KINASE, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE
2cci:B (THR310) to (GLY369) CRYSTAL STRUCTURE OF PHOSPHO-CDK2 CYCLIN A IN COMPLEX WITH A PEPTIDE CONTAINING BOTH THE SUBSTRATE AND RECRUITMENT SITES OF CDC6 | COMPLEX (TRANSFERASE/CELL DIVISION), PROTEIN KINASES, CELL CYCLE, RECRUITMENT, SUBSTRATE RECOGNITION, ATP-BINDING, CELL DIVISION, KINASE, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHORYLATION, SERINE/THREONINE- PROTEIN KINASE, TRANSFERASE, CYCLIN, DNA REPLICATION, NUCLEAR PROTEIN, COMPLEX
2cci:D (ASN312) to (VAL367) CRYSTAL STRUCTURE OF PHOSPHO-CDK2 CYCLIN A IN COMPLEX WITH A PEPTIDE CONTAINING BOTH THE SUBSTRATE AND RECRUITMENT SITES OF CDC6 | COMPLEX (TRANSFERASE/CELL DIVISION), PROTEIN KINASES, CELL CYCLE, RECRUITMENT, SUBSTRATE RECOGNITION, ATP-BINDING, CELL DIVISION, KINASE, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHORYLATION, SERINE/THREONINE- PROTEIN KINASE, TRANSFERASE, CYCLIN, DNA REPLICATION, NUCLEAR PROTEIN, COMPLEX
1p5e:B (ASN312) to (GLY369) THE STRUCURE OF PHOSPHO-CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR 4,5,6,7-TETRABROMOBENZOTRIAZOLE (TBS) | KINASE INHIBITOR, CDK2, TBS, CELL CYCLE
1p5e:D (THR310) to (GLY369) THE STRUCURE OF PHOSPHO-CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR 4,5,6,7-TETRABROMOBENZOTRIAZOLE (TBS) | KINASE INHIBITOR, CDK2, TBS, CELL CYCLE
4iit:C (ALA120) to (GLY210) THE PHENYLACETYL-COA MONOOXYGENASE PAAABC SUBCOMPLEX WITH PHENYLACETYL-COA | STRUCTURAL GENOMICS, MONTREAL-KINGSTON BACTERIAL STRUCTURAL GENOMICS INITIATIVE, BSGI, FERRITIN-LIKE FOLD, BACTERIAL MULTICOMPONENT MONOOXYGENASE, OXIDOREDUCTASE
2cjm:B (THR310) to (THR366) MECHANISM OF CDK INHIBITION BY ACTIVE SITE PHOSPHORYLATION: CDK2 Y15P T160P IN COMPLEX WITH CYCLIN A STRUCTURE | PHOSPHORYLATION, NUCLEOTIDE-BINDING, MITOSIS, CELL CYCLE, REGULATION, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, TRANSFERASE, CELL DIVISION, CYCLIN-DEPENDENT KINASE, COMPLEX (TRANSFERASE/CELL DIVISION)
2cjm:D (THR310) to (VAL367) MECHANISM OF CDK INHIBITION BY ACTIVE SITE PHOSPHORYLATION: CDK2 Y15P T160P IN COMPLEX WITH CYCLIN A STRUCTURE | PHOSPHORYLATION, NUCLEOTIDE-BINDING, MITOSIS, CELL CYCLE, REGULATION, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, TRANSFERASE, CELL DIVISION, CYCLIN-DEPENDENT KINASE, COMPLEX (TRANSFERASE/CELL DIVISION)
3g5u:A (SER1122) to (GLN1189) STRUCTURE OF P-GLYCOPROTEIN REVEALS A MOLECULAR BASIS FOR POLY-SPECIFIC DRUG BINDING | P-GLYCOPROTEIN, MULTIDRUG RESISTANCE, PGP, CYCLIC PEPTIDE, MEMBRANE PROTEIN
2qj0:A (GLY35) to (GLN103) STRUCTURE OF THE YEAST U-BOX-CONTAINING UBIQUITIN LIGASE UFD2P | HELICAL HAIRPIN, LIGASE
1pdu:A (ILE453) to (LYS511) LIGAND-BINDING DOMAIN OF DROSOPHILA ORPHAN NUCLEAR RECEPTOR DHR38 | NUCLEAR RECEPTOR, LIGAND-BINDING DOMAIN, HORMONE/GROWTH FACTOR RECEPTOR COMPLEX
1pdu:B (ILE453) to (LEU523) LIGAND-BINDING DOMAIN OF DROSOPHILA ORPHAN NUCLEAR RECEPTOR DHR38 | NUCLEAR RECEPTOR, LIGAND-BINDING DOMAIN, HORMONE/GROWTH FACTOR RECEPTOR COMPLEX
4iod:A (SER90) to (PRO155) PRELIMINARY STRUCTURAL INVESTIGATIONS OF A MALARIAL PROTEIN SECRETION SYSTEM. | MALARIA, AAA+ ATPASE CLPB CHAPERONE, N-TERMINAL CARGO-BINDING DOMAIN, PROTEIN TRANSLOCATION AND UNFOLDING, PARASITOPHOROUS VACUOLE, CHAPERONE
4iod:C (SER90) to (VAL154) PRELIMINARY STRUCTURAL INVESTIGATIONS OF A MALARIAL PROTEIN SECRETION SYSTEM. | MALARIA, AAA+ ATPASE CLPB CHAPERONE, N-TERMINAL CARGO-BINDING DOMAIN, PROTEIN TRANSLOCATION AND UNFOLDING, PARASITOPHOROUS VACUOLE, CHAPERONE
4iro:A (SER3) to (LYS73) CRYSTAL STRUCTURE OF T-STATE CARBONMONOXY HEMOGLOBIN FROM TREMATOMUS BERNACCHII AT PH 8.4 | GLOBIN FOLD, OXYGEN TRANSPORT
4iro:A (LEU81) to (GLU139) CRYSTAL STRUCTURE OF T-STATE CARBONMONOXY HEMOGLOBIN FROM TREMATOMUS BERNACCHII AT PH 8.4 | GLOBIN FOLD, OXYGEN TRANSPORT
1pkd:B (THR310) to (GLY369) THE CRYSTAL STRUCTURE OF UCN-01 IN COMPLEX WITH PHOSPHO- CDK2/CYCLIN A | PROTEIN KINASE-DRUG COMPLEX, TRANSFERASE/CELL CYCLE COMPLEX
2qr4:A (PHE113) to (ASN148) CRYSTAL STRUCTURE OF OLIGOENDOPEPTIDASE-F FROM ENTEROCOCCUS FAECIUM | STRUCTURAL GENOMICS, OLIGOENDOPEPTIDASE F, PSI-2, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, NYSGXRC, HYDROLASE
4xy2:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A IN COMPLEX WITH ASP9436 | PHOSPHODIESTERASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4xy2:B (GLU504) to (CYS562) CRYSTAL STRUCTURE OF PDE10A IN COMPLEX WITH ASP9436 | PHOSPHODIESTERASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2qrw:D (SER4) to (GLY57) CRYSTAL STUCTURE OF MYCOBACTERIUM TUBERCULOSIS TRHBO WG8F MUTANT | TRUNCATED HEMOGLOBIN FOLD, ALPHA HELIX, HEME, HYDROXYLATION, IRON, MEMBRANE, METAL-BINDING, OXYGEN TRANSPORT, TRANSPORT, TRANSPORT PROTEIN
2qrw:E (SER4) to (GLY57) CRYSTAL STUCTURE OF MYCOBACTERIUM TUBERCULOSIS TRHBO WG8F MUTANT | TRUNCATED HEMOGLOBIN FOLD, ALPHA HELIX, HEME, HYDROXYLATION, IRON, MEMBRANE, METAL-BINDING, OXYGEN TRANSPORT, TRANSPORT, TRANSPORT PROTEIN
2qrw:H (SER4) to (GLY57) CRYSTAL STUCTURE OF MYCOBACTERIUM TUBERCULOSIS TRHBO WG8F MUTANT | TRUNCATED HEMOGLOBIN FOLD, ALPHA HELIX, HEME, HYDROXYLATION, IRON, MEMBRANE, METAL-BINDING, OXYGEN TRANSPORT, TRANSPORT, TRANSPORT PROTEIN
2qrw:I (SER4) to (GLY57) CRYSTAL STUCTURE OF MYCOBACTERIUM TUBERCULOSIS TRHBO WG8F MUTANT | TRUNCATED HEMOGLOBIN FOLD, ALPHA HELIX, HEME, HYDROXYLATION, IRON, MEMBRANE, METAL-BINDING, OXYGEN TRANSPORT, TRANSPORT, TRANSPORT PROTEIN
2qrw:J (SER4) to (GLY57) CRYSTAL STUCTURE OF MYCOBACTERIUM TUBERCULOSIS TRHBO WG8F MUTANT | TRUNCATED HEMOGLOBIN FOLD, ALPHA HELIX, HEME, HYDROXYLATION, IRON, MEMBRANE, METAL-BINDING, OXYGEN TRANSPORT, TRANSPORT, TRANSPORT PROTEIN
2qrw:L (SER4) to (GLY57) CRYSTAL STUCTURE OF MYCOBACTERIUM TUBERCULOSIS TRHBO WG8F MUTANT | TRUNCATED HEMOGLOBIN FOLD, ALPHA HELIX, HEME, HYDROXYLATION, IRON, MEMBRANE, METAL-BINDING, OXYGEN TRANSPORT, TRANSPORT, TRANSPORT PROTEIN
4ix6:B (THR417) to (LEU468) CRYSTAL STRUCTURE OF A STT7 HOMOLOG FROM MICROMONAS ALGAE SOAKED WITH ATP | PROTEIN KINASE, CANONICAL PROTEIN KINASE FOLD, ATP BINDING, TRANSFERASE
4xzc:A (LEU231) to (ALA300) THE CRYSTAL STRUCTURE OF KUPE VIRUS NUCLEOPROTEIN | NUCLEOPROTEIN, KUPE VIRUS, RNA BINDING PROTEIN
4y0c:B (SER95) to (GLY157) THE STRUCTURE OF ARABIDOPSIS CLPT2 | CASEINOLYTIC PROTEASE, N-DOMAIN, ALPHA HELICAL BUNDLE, PLASTID, PROTEIN BINDING
4y0c:A (SER95) to (LYS154) THE STRUCTURE OF ARABIDOPSIS CLPT2 | CASEINOLYTIC PROTEASE, N-DOMAIN, ALPHA HELICAL BUNDLE, PLASTID, PROTEIN BINDING
1ptw:A (PRO325) to (ILE410) THE CRYSTAL STRUCTURE OF AMP-BOUND PDE4 SUGGESTS A MECHANISM FOR PHOSPHODIESTERASE CATALYSIS | CATALYTIC MECHANISM, CAMP HYDROLYSIS CRYSTAL STRUCTURE, BINUCLEAR CATALYSIS, HYDROLASE
1ptw:B (ASN209) to (ASP272) THE CRYSTAL STRUCTURE OF AMP-BOUND PDE4 SUGGESTS A MECHANISM FOR PHOSPHODIESTERASE CATALYSIS | CATALYTIC MECHANISM, CAMP HYDROLYSIS CRYSTAL STRUCTURE, BINUCLEAR CATALYSIS, HYDROLASE
3gou:B (PHE85) to (ALA142) CRYSTAL STRUCTURE OF DOG (CANIS FAMILIARIS) HEMOGLOBIN | HEME, OXYGEN TRANSPORT, TETRAMER, IRON, METAL-BINDING, POLYMORPHISM, TRANSPORT
3gqg:C (MET82) to (GLU139) CRYSTAL STRUCTURE AT ACIDIC PH OF THE FERRIC FORM OF THE ROOT EFFECT HEMOGLOBIN FROM TREMATOMUS BERNACCHII. | PENTACOORDINATE HIGH-SPIN FE(III) FORM, ANTACRTIC FISH HEMOGLOBIN,, ACETYLATION, HEME, IRON, METAL-BINDING, OXYGEN TRANSPORT, TRANSPORT
3gqr:E (SER81) to (LEU136) CRYSTAL STRUCTURE DETERMINATION OF CAT (FELIS SILVESTRIS CATUS) HEMOGLOBIN AT 2.4 ANGSTROM RESOLUTION | LOW OXYGEN AFFINITY, METHEMOGLOBIN, ORTHORHOMBIC, HEME, IRON, OXYGEN TRANSPORT, TRANSPORT, POLYMORPHISM, OXYGEN STORAGE
3tdl:A (SER5) to (ASP56) STRUCTURE OF HUMAN SERUM ALBUMIN IN COMPLEX WITH DAUDA | PROTEIN-DRUG COMPLEX, HUMAN SERUM ALBUMIN, MYRISTATE, DAUDA, FLUORESCENT FATTY ACID ANALOGUE, PROTEIN BINDING, TRANSPORT PROTEIN
4j72:A (PHE14) to (LEU92) CRYSTAL STRUCTURE OF POLYPRENYL-PHOSPHATE N-ACETYL HEXOSAMINE 1- PHOSPHATE TRANSFERASE | ALPHA-HELICAL MEMBRANE PROTEIN, MEMBRANE ENZYME, MAGNESIUM BINDING, UNDECAPRENYL PHOSPHATE BINDING, UDP-MURNAC-PENTAPEPTIDE BINDING, MEMBRANE, TRANSFERASE
4j72:B (ALA15) to (LEU92) CRYSTAL STRUCTURE OF POLYPRENYL-PHOSPHATE N-ACETYL HEXOSAMINE 1- PHOSPHATE TRANSFERASE | ALPHA-HELICAL MEMBRANE PROTEIN, MEMBRANE ENZYME, MAGNESIUM BINDING, UNDECAPRENYL PHOSPHATE BINDING, UDP-MURNAC-PENTAPEPTIDE BINDING, MEMBRANE, TRANSFERASE
1e9h:D (VAL311) to (VAL367) THR 160 PHOSPHORYLATED CDK2 - HUMAN CYCLIN A3 COMPLEX WITH THE INHIBITOR INDIRUBIN-5-SULPHONATE BOUND | CELL CYCLE, COMPLEX (PROTEIN KINASE/CYCLIN), KINASES, INHIBITOR, CYCLIN, COMPLEX, PHOSPHORYLATION
2r80:A (LEU80) to (THR137) PIGEON HEMOGLOBIN (OXY FORM) | OXYGEN TRANPORT/STORAGE, HEME, IRON, METAL-BINDING, OXYGEN TRANSPORT, TRANSPORT, OXYGEN BINDING
2r80:C (LEU80) to (THR137) PIGEON HEMOGLOBIN (OXY FORM) | OXYGEN TRANPORT/STORAGE, HEME, IRON, METAL-BINDING, OXYGEN TRANSPORT, TRANSPORT, OXYGEN BINDING
2dpp:B (ASP30) to (GLY88) CRYSTAL STRUCTURE OF THERMOSTABLE BACILLUS SP. RAPC8 NITRILE HYDRATASE | NITRILE HYDRATASE, COBALT, OXIDISED CYS, LYASE
2r8q:B (PHE843) to (ARG931) STRUCTURE OF LMJPDEB1 IN COMPLEX WITH IBMX | LEISHIMANIASIS, PARASITE INHIBITOR SELECTIVITY, CAMP PHOSPHODIESTERASE, HYDROLASE
3tm9:A (GLN4) to (ASN67) Y29A MUTANT OF VITREOSCILLA STERCORARIA HEMOGLOBIN | GLOBIN 8-HELIX FOLD, OXYGEN STORAGE, OXYGEN TRANSPORT
3tnw:B (THR310) to (THR366) STRUCTURE OF CDK2/CYCLIN A IN COMPLEX WITH CAN508 | CYCLIN DEPENDENT KINASE, KINASE CYCLIN, PHOSPHOTRANSFERASE, CYCLIN A, PHOSPHORYLATION AT CDK2 THREONINE 160, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
3tnw:D (THR310) to (THR366) STRUCTURE OF CDK2/CYCLIN A IN COMPLEX WITH CAN508 | CYCLIN DEPENDENT KINASE, KINASE CYCLIN, PHOSPHOTRANSFERASE, CYCLIN A, PHOSPHORYLATION AT CDK2 THREONINE 160, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
2rao:A (SER3) to (VAL70) X RAY CRYSTAL STRUCTURE OF RABBIT HEMOGLOBIN (OXY FORM) AT 2.0 ANGSTROM RESOLUTION | OXYGEN TRANPORT/STORAGE, HEME, IRON, METAL-BINDING, OXYGEN TRANSPORT, TRANSPORT, OXYGEN BINDING
3gys:C (SER81) to (LEU136) CRYSTAL STRUCTURE DETERMINATION OF CAT (FELIS SILVESTRIS CATUS) HEMOGLOBIN AT 2.9 ANGSTROM RESOLUTION | METHEMOGLOBIN, LOW-OXYGEN AFFINITY, ORTHORHOMBIC, CHROMATOGRAPHY, HEME, IRON, OXYGEN TRANSPORT, TRANSPORT, POLYMORPHISM, OXYGEN STORAGE
3gys:F (ALA86) to (HIS143) CRYSTAL STRUCTURE DETERMINATION OF CAT (FELIS SILVESTRIS CATUS) HEMOGLOBIN AT 2.9 ANGSTROM RESOLUTION | METHEMOGLOBIN, LOW-OXYGEN AFFINITY, ORTHORHOMBIC, CHROMATOGRAPHY, HEME, IRON, OXYGEN TRANSPORT, TRANSPORT, POLYMORPHISM, OXYGEN STORAGE
2ri4:C (ALA4) to (VAL70) CRYSTAL STRUCTURE DETERMINATION OF GOAT METHEMOGLOBIN AT 2.7 ANGSTROM | METHEMOGLOBIN, LOW OXYGEN AFFINITY, ALLOSTERIC MECHANISM, HEME, IRON, METAL-BINDING, POLYMORPHISM, TRANSPORT, OXYGEN STORAGE, OXYGEN TRANSPORT
3h39:A (GLY207) to (LEU246) THE COMPLEX STRUCTURE OF CCA-ADDING ENZYME WITH ATP | TRANSFERASE/RNA, NUCLEOTIDE-BINDING, NUCLEOTIDYLTRANSFERASE, RNA- BINDING, TRANSFERASE
1qmz:B (ASN312) to (THR366) PHOSPHORYLATED CDK2-CYCLYIN A-SUBSTRATE PEPTIDE COMPLEX | CELL CYCLE, COMPLEX (PROTEIN KINASE/CYCLIN), CYCLIN, CDK, PHOSPHORYLATION, SUBSTRATE COMPLEX
1qmz:D (ASN312) to (THR366) PHOSPHORYLATED CDK2-CYCLYIN A-SUBSTRATE PEPTIDE COMPLEX | CELL CYCLE, COMPLEX (PROTEIN KINASE/CYCLIN), CYCLIN, CDK, PHOSPHORYLATION, SUBSTRATE COMPLEX
1qpw:B (PHE85) to (HIS146) CRYSTAL STRUCTURE DETERMINATION OF PORCINE HEMOGLOBIN AT 1.8A RESOLUTION | X-RAY STUDY, PORCINE HEMOGLOBIN, ARTIFICIAL HUMAN BLOOD, OXYGEN TRANSPORT
1qpw:C (SER3) to (HIS72) CRYSTAL STRUCTURE DETERMINATION OF PORCINE HEMOGLOBIN AT 1.8A RESOLUTION | X-RAY STUDY, PORCINE HEMOGLOBIN, ARTIFICIAL HUMAN BLOOD, OXYGEN TRANSPORT
2uue:B (VAL311) to (VAL367) REPLACE: A STRATEGY FOR ITERATIVE DESIGN OF CYCLIN BINDING GROOVE INHIBITORS | POLYMORPHISM, CYCLIN GROOVE, CELL DIVISION, CDK2, KINASE, CYCLIN, ACTIVE, MITOSIS, INHIBITION, PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE, NONPEPTIDE, TRANSFERASE, ATP-BINDING
2uue:D (VAL311) to (GLY369) REPLACE: A STRATEGY FOR ITERATIVE DESIGN OF CYCLIN BINDING GROOVE INHIBITORS | POLYMORPHISM, CYCLIN GROOVE, CELL DIVISION, CDK2, KINASE, CYCLIN, ACTIVE, MITOSIS, INHIBITION, PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE, NONPEPTIDE, TRANSFERASE, ATP-BINDING
1qvu:A (THR109) to (SER187) CRYSTAL STRUCTURE OF THE MULTIDRUG BINDING TRANSCRIPTIONAL REPRESSOR QACR BOUND TO TWO DRUGS: ETHIDIUM AND PROFLAVINE | QACR, MULTIDRUG BINDING PROTEIN, TRANSCRIPTION, REPRESSOR, COOPERATIVE DNA BINDING
1f5q:B (LEU148) to (THR203) CRYSTAL STRUCTURE OF MURINE GAMMA HERPESVIRUS CYCLIN COMPLEXED TO HUMAN CYCLIN DEPENDENT KINASE 2 | HERPESVIRAL CYCLIN, CYCLIN DEPENDENT KINASE. PROTEIN/PROTEIN COMPLEX, TRANSFERASE
1f5q:D (LEU148) to (THR203) CRYSTAL STRUCTURE OF MURINE GAMMA HERPESVIRUS CYCLIN COMPLEXED TO HUMAN CYCLIN DEPENDENT KINASE 2 | HERPESVIRAL CYCLIN, CYCLIN DEPENDENT KINASE. PROTEIN/PROTEIN COMPLEX, TRANSFERASE
2eg5:C (LEU296) to (GLY352) THE STRUCTURE OF XANTHOSINE METHYLTRANSFERASE | SAM-DEPENDANT N-METHYLTRANSFERASE, XANTHOSINE, SAH, TRANSFERASE
2eg5:E (LEU296) to (GLY352) THE STRUCTURE OF XANTHOSINE METHYLTRANSFERASE | SAM-DEPENDANT N-METHYLTRANSFERASE, XANTHOSINE, SAH, TRANSFERASE
2eg5:G (LEU296) to (GLY352) THE STRUCTURE OF XANTHOSINE METHYLTRANSFERASE | SAM-DEPENDANT N-METHYLTRANSFERASE, XANTHOSINE, SAH, TRANSFERASE
2uxh:A (CYS124) to (SER205) TTGR IN COMPLEX WITH QUERCETIN | TRANSCRIPTION, DNA-BINDING, TETR FAMILY
2uxh:B (CYS124) to (ARG203) TTGR IN COMPLEX WITH QUERCETIN | TRANSCRIPTION, DNA-BINDING, TETR FAMILY
2uxi:A (CYS124) to (ARG203) PHLORETIN IN COMPLEX WITH TTGR | TRANSCRIPTION, DNA-BINDING, TETR FAMILY
2uxi:B (CYS124) to (SER205) PHLORETIN IN COMPLEX WITH TTGR | TRANSCRIPTION, DNA-BINDING, TETR FAMILY
1r1x:A (SER81) to (SER138) CRYSTAL STRUCTURE OF OXY-HUMAN HEMOGLOBIN BASSETT AT 2.15 ANGSTROM | HEMOGLOBIN, CARBON MONOXIDE, MUTANT, ROCHESTER, OXYGEN AFFINITY, CRYSTAL STRUCTURE, OXYGEN TRANSPORT
2uxo:A (CYS124) to (ARG203) TTGR IN COMPLEX WITH TETRACYCLINE | REPRESSOR PROTEIN, TRANSCRIPTION REGULATION, MULTIDRUG BINDING PROTEIN, TRANSCRIPTIONAL REGULATOR OF EFFLUX PUMPS, REPRESSOR, TETR FAMILY, DNA-BINDING, TRANSCRIPTION
2uxo:B (CYS124) to (ARG203) TTGR IN COMPLEX WITH TETRACYCLINE | REPRESSOR PROTEIN, TRANSCRIPTION REGULATION, MULTIDRUG BINDING PROTEIN, TRANSCRIPTIONAL REGULATOR OF EFFLUX PUMPS, REPRESSOR, TETR FAMILY, DNA-BINDING, TRANSCRIPTION
2uxp:A (CYS124) to (SER205) TTGR IN COMPLEX CHLORAMPHENICOL | TRANSCRIPTION, DNA-BINDING, TETR FAMILY
2uxp:B (CYS124) to (SER205) TTGR IN COMPLEX CHLORAMPHENICOL | TRANSCRIPTION, DNA-BINDING, TETR FAMILY
2uxu:A (CYS124) to (SER205) TTGR IN COMPLEX WITH NARINGENIN | REPRESSOR PROTEIN, TRANSCRIPTION REGULATION, MULTIDRUG BINDING PROTEIN, TRANSCRIPTIONAL REGULATOR OF EFFLUX PUMPS, REPRESSOR, TETR FAMILY, DNA-BINDING, TRANSCRIPTION
2uxu:B (CYS124) to (ARG203) TTGR IN COMPLEX WITH NARINGENIN | REPRESSOR PROTEIN, TRANSCRIPTION REGULATION, MULTIDRUG BINDING PROTEIN, TRANSCRIPTIONAL REGULATOR OF EFFLUX PUMPS, REPRESSOR, TETR FAMILY, DNA-BINDING, TRANSCRIPTION
2uzb:B (ASN312) to (GLY369) 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
2uzb:D (ASN312) to (GLY369) 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
2uzd:B (ASN312) to (VAL367) 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
2uzd:D (ASN312) to (THR366) 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
2uzl:B (ASN312) to (THR366) 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
2uzl:D (ASN312) to (THR366) 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
3ubc:G (GLN4) to (ILE65) OXYGEN-BOUND HELL'S GATE GLOBIN I BY LB NANOTEMPLATE METHOD | OXYGEN-BOUND, AUTOXIDATION, NANOTEMPLATE, LANGMUIR-BLODGETT, THIN FILMS, OXYGEN TRANSPORT
2v22:B (THR310) to (THR368) REPLACE: A STRATEGY FOR ITERATIVE DESIGN OF CYCLIN BINDING GROOVE INHIBITORS | POLYMORPHISM, CYCLIN GROOVE, CELL DIVISION, CDK2, KINASE, CYCLIN, ACTIVE, MITOSIS, INHIBITION, PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE, NONPEPTIDE, TRANSFERASE, ATP-BINDING
2v22:D (VAL311) to (THR366) REPLACE: A STRATEGY FOR ITERATIVE DESIGN OF CYCLIN BINDING GROOVE INHIBITORS | POLYMORPHISM, CYCLIN GROOVE, CELL DIVISION, CDK2, KINASE, CYCLIN, ACTIVE, MITOSIS, INHIBITION, PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE, NONPEPTIDE, TRANSFERASE, ATP-BINDING
3hht:B (ASP30) to (GLY88) A MUTANT OF THE NITRILE HYDRATASE FROM GEOBACILLUS PALLIDUS HAVING ENHANCED THERMOSTABILITY | ALPHA AND BETA PROTEINS (A+B), LYASE
1fin:B (VAL311) to (VAL367) CYCLIN A-CYCLIN-DEPENDENT KINASE 2 COMPLEX | COMPLEX (TRANSFERASE/CYCLIN), CYCLIN, CDK, PHOSPHORYLATION
1fin:D (VAL311) to (THR366) CYCLIN A-CYCLIN-DEPENDENT KINASE 2 COMPLEX | COMPLEX (TRANSFERASE/CYCLIN), CYCLIN, CDK, PHOSPHORYLATION
3ubv:G (ILE72) to (ALA132) OXYGEN-BOUND HELL'S GATE GLOBIN I BY CLASSICAL HANGING DROP | GLOBIN, OXYGEN-BOUND, AUTOXIDATION, OXYGEN, OXYGEN TRANSPORT
4yqh:A (LEU505) to (CYS562) 2-[2-(4-PHENYL-1H-IMIDAZOL-2-YL)ETHYL]QUINOXALINE (SUNOVION COMPOUND 14) CO-CRYSTALLIZED WITH PDE10A | INHIBITOR, PDE10A, CO-CRYSTAL
4yqh:B (GLU504) to (CYS562) 2-[2-(4-PHENYL-1H-IMIDAZOL-2-YL)ETHYL]QUINOXALINE (SUNOVION COMPOUND 14) CO-CRYSTALLIZED WITH PDE10A | INHIBITOR, PDE10A, CO-CRYSTAL
4ys7:A (LEU508) to (CYS562) CO-CRYSTAL STRUCTURE OF 2-[2-(5,8-DIMETHYL[1,2,4]TRIAZOLO[1,5- A]PYRAZIN-2-YL)ETHYL]-3-METHYL-3H-IMIDAZO[4,5-F]QUINOLINE (COMPOUND 39) WITH PDE10A | PDE10A, INHIBITOR, CO-CRYSTAL, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ys7:B (GLU506) to (CYS562) CO-CRYSTAL STRUCTURE OF 2-[2-(5,8-DIMETHYL[1,2,4]TRIAZOLO[1,5- A]PYRAZIN-2-YL)ETHYL]-3-METHYL-3H-IMIDAZO[4,5-F]QUINOLINE (COMPOUND 39) WITH PDE10A | PDE10A, INHIBITOR, CO-CRYSTAL, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3hm6:X (GLY2083) to (ALA2127) CRYSTAL STRUCTURE OF THE CYTOPLASMIC DOMAIN OF HUMAN PLEXIN B1 | STRUCTURAL GENOMICS CONSORTIUM, SGC, MEMBRANE, TRANSMEMBRANE, RECEPTOR, CELL MEMBRANE, GLYCOPROTEIN, PHOSPHOPROTEIN, SECRETED, SIGNALING PROTEIN
2f33:A (CYS187) to (ALA240) NMR SOLUTION STRUCTURE OF CA2+-LOADED CALBINDIN D28K | EF-HAND, CA2+-BINDING, METAL BINDING PROTEIN
1fvv:B (VAL311) to (VAL367) THE STRUCTURE OF CDK2/CYCLIN A IN COMPLEX WITH AN OXINDOLE INHIBITOR | CYCLIN-DEPENDENT KINASE, CYCLIN A, TRANSFERASE, CELL CYCLE
1fvv:D (THR310) to (THR366) THE STRUCTURE OF CDK2/CYCLIN A IN COMPLEX WITH AN OXINDOLE INHIBITOR | CYCLIN-DEPENDENT KINASE, CYCLIN A, TRANSFERASE, CELL CYCLE
1rnr:A (TYR209) to (PHE291) AUTOCATALYTIC GENERATION OF DOPA IN THE ENGINEERED PROTEIN R2 F208Y FROM ESCHERICHIA COLI RIBONUCLEOTIDE REDUCTASE AND CRYSTAL STRUCTURE OF THE DOPA-208 PROTEIN | REDUCTASE(ACTING ON CH2), OXIDOREDUCTASE
1ro6:A (SER399) to (ILE484) CRYSTAL STRUCTURE OF PDE4B2B COMPLEXED WITH ROLIPRAM (R & S) | PDE, ROLIPRAM, CRYSTAL, HYDROLASE
1ro9:A (SER399) to (ILE484) CRYSTAL STRUCTURES OF THE CATALYTIC DOMAIN OF PHOSPHODIESTERASE 4B2B COMPLEXED WITH 8-BR-AMP | PDE, 8-BR-AMP, HYDROLASE
1ror:A (SER399) to (ILE484) CRYSTAL STRUCTURES OF THE CATALYTIC DOMAIN OF PHOSPHODIESTERASE 4B2B COMPLEXED WITH AMP | PDE, AMP, HYDROLASE
1rq3:A (SER81) to (LEU136) CRYSTALLOGRAPHIC ANALYSIS OF THE INTERACTION OF NITRIC OXIDE WITH QUATERNARY-T HUMAN DEOXYHEMOGLOBIN, DEOXYHEMOGLOBIN | GLOBIN, OXYGEN STORAGE/TRANSPORT COMPLEX
1rq3:D (ALA86) to (ALA142) CRYSTALLOGRAPHIC ANALYSIS OF THE INTERACTION OF NITRIC OXIDE WITH QUATERNARY-T HUMAN DEOXYHEMOGLOBIN, DEOXYHEMOGLOBIN | GLOBIN, OXYGEN STORAGE/TRANSPORT COMPLEX
1g09:C (SER3) to (VAL70) CARBONMONOXY LIGANDED BOVINE HEMOGLOBIN PH 7.2 | BOVINE, HEMOGLOBIN, LIGANDED, CARBONMONOXY, PROTOPORPHYRIN IX, OXYGEN STORAGE/TRANSPORT COMPLEX
2vhd:A (LEU101) to (LEU163) CRYSTAL STRUCTURE OF THE DI-HAEM CYTOCHROME C PEROXIDASE FROM PSEUDOMONAS AERUGINOSA - MIXED VALENCE FORM | IRON, HEME, TRANSPORT, PEROXIDASE, METAL-BINDING, OXIDOREDUCTASE, ELECTRON TRANSPORT
3hqg:A (SER195) to (GLY282) CRYSTAL STRUCTURE OF RESTRICTION ENDONUCLEASE ECORII CATALYTIC C- TERMINAL DOMAIN IN COMPLEX WITH COGNATE DNA | RESTRICTION ENDONUCLEASE, ECORII, NUCLEOTIDE FLIPPING, PROTEIN-DNA COMPLEX, DNA RECOGNITION, ENDONUCLEASE, HYDROLASE, MAGNESIUM, NUCLEASE, RESTRICTION SYSTEM, HYDROLASE-DNA COMPLEX
1gbu:C (SER3) to (HIS72) DEOXY (BETA-(C93A,C112G)) HUMAN HEMOGLOBIN | HEMOGLOBIN, HUMAN, MUTANT, BETA-(C93A,C112G), DEOXY, DEOXY HEMOGLOBIN, OXYGEN TRANSPORT
3uuo:A (LEU505) to (CYS562) THE DISCOVERY OF POTENT, SELECTIVITY, AND ORALLY BIOAVAILABLE PYROZOLOQUINOLINES AS PDE10 INHIBITORS FOR THE TREATMENT OF SCHIZOPHRENIA | INHIBITOR COMPLEX, HYDROLASE, ZN BINDING, MG BINDING, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3hrw:A (SER3) to (LEU73) CRYSTAL STRUCTURE OF HEMOGLOBIN FROM MOUSE (MUS MUSCULUS)AT 2.8 | HEME, IRON, METAL-BINDING, OXYGEN TRANSPORT, POLYMORPHISM, TRANSPORT, PHOSPHOPROTEIN
3hrw:D (ALA86) to (HIS146) CRYSTAL STRUCTURE OF HEMOGLOBIN FROM MOUSE (MUS MUSCULUS)AT 2.8 | HEME, IRON, METAL-BINDING, OXYGEN TRANSPORT, POLYMORPHISM, TRANSPORT, PHOSPHOPROTEIN
1s56:A (SER14) to (GLY67) CRYSTAL STRUCTURE OF "TRUNCATED" HEMOGLOBIN N (HBN) FROM MYCOBACTERIUM TUBERCULOSIS, SOAKED WITH XE ATOMS | GROUP I TRUNCATED HEMOGLOBIN, OXYGEN STORAGE/TRANSPORT COMPLEX
1s5y:A (LEU81) to (GLU139) THE CRYSTAL STRUCTURE OF TREMATOMUS BERNACCHII HEMOGLOBIN OXIDIZED BY FERRICYANIDE | HEMICHROME, BIS-HISTIDINE, OXIDATION, OXYGEN STORAGE/TRANSPORT COMPLEX
1s61:A (SER14) to (GLY67) CRYSTAL STRUCTURE OF "TRUNCATED" HEMOGLOBIN N (HBN) FROM MYCOBACTERIUM TUBERCULOSIS, SOAKED WITH BUTYL-ISOCYANIDE | TRUNCATED HEMOGLOBIN, OXYGEN STORAGE/TRANSPORT COMPLEX
1s6d:A (GLN49) to (ASN95) STRUCTURE IN SOLUTION OF A METHIONINE-RICH 2S ALBUMIN PROTEIN FROM SUNFLOWER SEED | ALL HELIX, FOLDED LEAF, RIGHT-HANDED SUPERHELIX, DISULPHIDE RICH, PLANT PROTEIN
3hwk:E (ARG101) to (GLY164) CRYSTAL STRUCTURE OF METHYLCITRATE SYNTHASE FROM MYCOBACTERIUM TUBERCULOSIS | NIAID, SSGCID, STRUCTURAL GENOMICS, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, TUBERCLUOSIS, UW, SBRI, DECODE, ACYLTRANSFERASE, TRANSFERASE
2ful:A (ASN308) to (ASP354) CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF S. CEREVISIAE EIF5 | ATYPICAL HEAT MOTIF, TRANSLATION
2ful:B (ASN308) to (ASP354) CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF S. CEREVISIAE EIF5 | ATYPICAL HEAT MOTIF, TRANSLATION
2ful:C (ASN308) to (ASP354) CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF S. CEREVISIAE EIF5 | ATYPICAL HEAT MOTIF, TRANSLATION
2ful:D (ASN308) to (ASP354) CRYSTAL STRUCTURE OF THE C-TERMINAL DOMAIN OF S. CEREVISIAE EIF5 | ATYPICAL HEAT MOTIF, TRANSLATION
3hxv:A (ASN304) to (ARG368) CRYSTAL STRUCTURE OF CATALYTIC FRAGMENT OF E. COLI ALARS IN COMPLEX WITH GLYSA | AMINOACYL-TRNA SYNTHETASE, LIGASE, PROTEIN BIOSYNTHESIS, NUCLEOTIDE- BINDING, AMINO ACID-BINDING, ATP-BINDING, METAL-BINDING, ZINC-FINGER
3hxz:B (ASN304) to (ARG368) CRYSTAL STRUCTURE OF CATALYTIC FRAGMENT OF E. COLI ALARS G237A IN COMPLEX WITH ALASA | AMINOACYL-TRNA SYNTHETASE, LIGASE, PROTEIN BIOSYNTHESIS, NUCLEOTIDE- BINDING, AMINO ACID-BINDING, ATP-BINDING, METAL-BINDING, ZINC-FINGER
3hxz:C (ASN304) to (ARG368) CRYSTAL STRUCTURE OF CATALYTIC FRAGMENT OF E. COLI ALARS G237A IN COMPLEX WITH ALASA | AMINOACYL-TRNA SYNTHETASE, LIGASE, PROTEIN BIOSYNTHESIS, NUCLEOTIDE- BINDING, AMINO ACID-BINDING, ATP-BINDING, METAL-BINDING, ZINC-FINGER
3hxz:D (ASN304) to (ARG368) CRYSTAL STRUCTURE OF CATALYTIC FRAGMENT OF E. COLI ALARS G237A IN COMPLEX WITH ALASA | AMINOACYL-TRNA SYNTHETASE, LIGASE, PROTEIN BIOSYNTHESIS, NUCLEOTIDE- BINDING, AMINO ACID-BINDING, ATP-BINDING, METAL-BINDING, ZINC-FINGER
3hy0:B (ASN304) to (ARG368) CRYSTAL STRUCTURE OF CATALYTIC FRAGMENT OF E. COLI ALARS G237A IN COMPLEX WITH GLYSA | AMINOACYL-TRNA SYNTHETASE, LIGASE, PROTEIN BIOSYNTHESIS, NUCLEOTIDE- BINDING, AMINO ACID-BINDING, ATP-BINDING, METAL-BINDING, ZINC-FINGER
3hy1:A (ARG305) to (ARG368) CRYSTAL STRUCTURE OF CATALYTIC FRAGMENT OF E. COLI ALARS G237A IN COMPLEX WITH SERSA | AMINOACYL-TRNA SYNTHETASE, LIGASE, PROTEIN BIOSYNTHESIS, NUCLEOTIDE- BINDING, AMINO ACID-BINDING, ATP-BINDING, METAL-BINDING, ZINC-FINGER
2fx0:A (ARG114) to (LEU195) CRYSTAL STRUCTURE OF HLYIIR, A HEMOLYSIN II TRANSCRIPTIONAL REGULATOR | TRANSCRIPTIONAL REGULATOR, TRANSCRIPTION
3v53:A (ALA788) to (ILE839) CRYSTAL STRUCTURE OF HUMAN RBM25 | PWI, RNA-BINDING DOMAIN, RNA BINDING PROTEIN
1si4:A (LEU80) to (SER138) CRYSTAL STRUCTURE OF HUMAN HEMOGLOBIN A2 (IN R2 STATE) AT 2.2 A RESOLUTION | HEMOGLOBIN A2, BETA THALASSEMIA, OXYGEN TRANSPORT, ANTISICKLING EFFECT, OXYGEN STORAGE/TRANSPORT COMPLEX
2vpr:A (PHE110) to (LYS205) TET REPRESSOR CLASS H IN COMPLEX WITH 5A,6- ANHYDROTETRACYCLINE-MG | TRANSCRIPTION, METAL-BINDING, ANTIBIOTIC RESISTANCE, TRANSCRIPTION REGULATOR, TRANSCRIPTION REGULATION DNA-BINDING
2vro:A (ASP41) to (GLY120) CRYSTAL STRUCTURE OF ALDEHYDE DEHYDROGENASE FROM BURKHOLDERIA XENOVORANS LB400 | ALDEHYDE DEHYDROGENASE, BURKHOLDERIA XENOVORANS LB400, BENZOATE OXIDATION PATHWAY, OXIDOREDUCTASE
2vro:B (ASP41) to (GLY120) CRYSTAL STRUCTURE OF ALDEHYDE DEHYDROGENASE FROM BURKHOLDERIA XENOVORANS LB400 | ALDEHYDE DEHYDROGENASE, BURKHOLDERIA XENOVORANS LB400, BENZOATE OXIDATION PATHWAY, OXIDOREDUCTASE
1so2:C (ILE662) to (GLY708) CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 3B IN COMPLEX WITH A DIHYDROPYRIDAZINE INHIBITOR | PDE3B PHOSPHODIESTERASE, HYDROLASE
1spg:B (TYR85) to (LEU142) CARBONMONOXY HEMOGLOBIN FROM THE TELEOST FISH LEIOSTOMUS XANTHURUS | CARBON MONOXIDE, R-STATE, LEIOSTOMUS XANTHURUS, TELEOST FISH, ROOT EFFECT, GLOBIN, OXYGEN TRANSPORT
2g9x:B (THR310) to (VAL367) STRUCTURE OF THR 160 PHOSPHORYLATED CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR NU6271 | TRANSFERASE, SERINE/THREONINE PROTEIN KINASE, ATP-BINDING, CELL CYCLE, PHOSPHORYLATION, TRANSFERASE-CELL CYCLE COMPLEX
2g9x:D (ASN312) to (THR366) STRUCTURE OF THR 160 PHOSPHORYLATED CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR NU6271 | TRANSFERASE, SERINE/THREONINE PROTEIN KINASE, ATP-BINDING, CELL CYCLE, PHOSPHORYLATION, TRANSFERASE-CELL CYCLE COMPLEX
1h1p:B (ASN312) to (THR366) STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH THE INHIBITOR NU2058 | KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION
1h1p:D (THR310) to (VAL367) STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH THE INHIBITOR NU2058 | KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION
1h1q:B (VAL311) to (GLY369) STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH THE INHIBITOR NU6094 | KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION
1h1q:D (VAL311) to (THR368) STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH THE INHIBITOR NU6094 | KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION
1h1s:B (THR310) to (GLY369) STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH THE INHIBITOR NU6102 | KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION
1h24:B (THR310) to (THR366) CDK2/CYCLIN A IN COMPLEX WITH A 9 RESIDUE RECRUITMENT PEPTIDE FROM E2F | TRANSFERASE, CELL CYCLE, PROTEIN KINASE, CYCLIN, CDK2, RECRUITMENT, PEPTIDE SPECIFICITY, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL DIVISION, MITOSIS, PHOSPHORYLATION
1h24:D (ASN312) to (VAL367) CDK2/CYCLIN A IN COMPLEX WITH A 9 RESIDUE RECRUITMENT PEPTIDE FROM E2F | TRANSFERASE, CELL CYCLE, PROTEIN KINASE, CYCLIN, CDK2, RECRUITMENT, PEPTIDE SPECIFICITY, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL DIVISION, MITOSIS, PHOSPHORYLATION
1h25:B (THR310) to (THR366) CDK2/CYCLIN A IN COMPLEX WITH AN 11-RESIDUE RECRUITMENT PEPTIDE FROM RETINOBLASTOMA-ASSOCIATED PROTEIN | TRANSFERASE, CELL CYCLE, PROTEIN KINASE, CYCLIN, CDK2, RECRUITMENT, PEPTIDE SPECIFICITY
1h25:D (THR310) to (THR366) CDK2/CYCLIN A IN COMPLEX WITH AN 11-RESIDUE RECRUITMENT PEPTIDE FROM RETINOBLASTOMA-ASSOCIATED PROTEIN | TRANSFERASE, CELL CYCLE, PROTEIN KINASE, CYCLIN, CDK2, RECRUITMENT, PEPTIDE SPECIFICITY
1h26:B (ASN312) to (THR366) CDK2/CYCLIN A IN COMPLEX WITH AN 11-RESIDUE RECRUITMENT PEPTIDE FROM P53 | CELL CYCLE, PROTEIN KINASE, CYCLIN, CDK2, RECRUITMENT, PEPTIDE SPECIFICITY
1h27:B (THR310) to (THR366) CDK2/CYCLIN A IN COMPLEX WITH AN 11-RESIDUE RECRUITMENT PEPTIDE FROM P27 | CELL CYCLE, PROTEIN KINASE, CYCLIN, CDK2, RECRUITMENT, PEPTIDE SPECIFICITY, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, CELL DIVISION, MITOSIS, PHOSPHORYLATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1h27:D (VAL311) to (GLY369) CDK2/CYCLIN A IN COMPLEX WITH AN 11-RESIDUE RECRUITMENT PEPTIDE FROM P27 | CELL CYCLE, PROTEIN KINASE, CYCLIN, CDK2, RECRUITMENT, PEPTIDE SPECIFICITY, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, CELL DIVISION, MITOSIS, PHOSPHORYLATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1h28:B (ASN312) to (THR366) CDK2/CYCLIN A IN COMPLEX WITH AN 11-RESIDUE RECRUITMENT PEPTIDE FROM P107 | CELL CYCLE, PROTEIN KINASE, CYCLIN, CDK2, RECRUITMENT, PEPTIDE SPECIFICITY, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, CELL DIVISION, MITOSIS, PHOSPHORYLATION, CELL CYCLE-TRANSFERASE SUBSTRATE, CELL CYCLE-TRANSFERASE SUBSTRATE COMPLEX
1h28:D (THR310) to (THR368) CDK2/CYCLIN A IN COMPLEX WITH AN 11-RESIDUE RECRUITMENT PEPTIDE FROM P107 | CELL CYCLE, PROTEIN KINASE, CYCLIN, CDK2, RECRUITMENT, PEPTIDE SPECIFICITY, SERINE/THREONINE-PROTEIN KINASE, ATP-BINDING, CELL DIVISION, MITOSIS, PHOSPHORYLATION, CELL CYCLE-TRANSFERASE SUBSTRATE, CELL CYCLE-TRANSFERASE SUBSTRATE COMPLEX
2gkn:A (SER14) to (GLY67) CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS TRHBN, GLNE11VAL MUTANT | TRUNCATED HEMOGLOBIN; MUTANT, OXYGEN STORAGE/TRANSPORT COMPLEX
4zo5:A (LEU498) to (CYS552) PDE10 COMPLEXED WITH 4-ISOPROPOXY-2-(2-(3-(4-METHOXYPHENYL)-4-OXO-3,4- DIHYDROQUINAZOLIN-2-YL)ETHYL)ISOINDOLINE-1,3-DIONE | PHOSPHODIESTERASE INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4zo5:B (LEU498) to (CYS552) PDE10 COMPLEXED WITH 4-ISOPROPOXY-2-(2-(3-(4-METHOXYPHENYL)-4-OXO-3,4- DIHYDROQUINAZOLIN-2-YL)ETHYL)ISOINDOLINE-1,3-DIONE | PHOSPHODIESTERASE INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2gtl:A (SER8) to (THR87) LUMBRICUS ERYTHROCRUORIN AT 3.5A RESOLUTION | ANNELID ERYTHROCRUORINS, RESPIRATORY PROTEIN, HEXAGONAL BILAYER, DIHEDRAL D6 SYMMETRY, TRIPLE STRANDED HELICAL COILS, OXYGEN STORAGE/TRANSPORT COMPLEX
2gtl:E (SER8) to (THR87) LUMBRICUS ERYTHROCRUORIN AT 3.5A RESOLUTION | ANNELID ERYTHROCRUORINS, RESPIRATORY PROTEIN, HEXAGONAL BILAYER, DIHEDRAL D6 SYMMETRY, TRIPLE STRANDED HELICAL COILS, OXYGEN STORAGE/TRANSPORT COMPLEX
2gtl:I (SER8) to (THR87) LUMBRICUS ERYTHROCRUORIN AT 3.5A RESOLUTION | ANNELID ERYTHROCRUORINS, RESPIRATORY PROTEIN, HEXAGONAL BILAYER, DIHEDRAL D6 SYMMETRY, TRIPLE STRANDED HELICAL COILS, OXYGEN STORAGE/TRANSPORT COMPLEX
1taz:A (THR271) to (ASP335) CATALYTIC DOMAIN OF HUMAN PHOSPHODIESTERASE 1B | PDE1B, HYDROLASE
1hab:A (SER3) to (HIS72) CROSSLINKED HAEMOGLOBIN | HEME, OXYGEN TRANSPORT, RESPIRATORY PROTEIN, ERYTHROCYTE
1hbs:G (LEU83) to (THR137) REFINED CRYSTAL STRUCTURE OF DEOXYHEMOGLOBIN S. I. RESTRAINED LEAST-SQUARES REFINEMENT AT 3.0-ANGSTROMS RESOLUTION | OXYGEN TRANSPORT
2hco:A (SER81) to (THR137) THE STRUCTURE OF HUMAN CARBONMONOXY HAEMOGLOBIN AT 2.7 ANGSTROMS RESOLUTION | OXYGEN TRANSPORT
4lkq:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 WITH FRAGMENT ZT017 | FRAGMENT SCREENING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2wey:A (LEU505) to (CYS562) HUMAN PDE-PAPAVERINE COMPLEX OBTAINED BY LIGAND SOAKING OF CROSS-LINKED PROTEIN CRYSTALS | METAL-BINDING, CROSS-LINKING, PHOSPHOPROTEIN, PHOSPHODIESTERASE, ALLOSTERIC ENZYME, CGMP, CAMP, ZINC, HYDROLASE, CYTOPLASM, MAGNESIUM, PAPAVERINE, POLYMORPHISM, CGMP-BINDING, CAMP-BINDING, NUCLEOTIDE-BINDING, ALTERNATIVE SPLICING
2whb:B (THR310) to (VAL367) TRUNCATION AND OPTIMISATION OF PEPTIDE INHIBITORS OF CDK2, CYCLIN A THROUGH STRUCTURE GUIDED DESIGN | CDK2, KINASE, CYCLIN, ACTIVE, NUCLEUS, MITOSIS, SERINE/THREONINE-PROTEIN KINASE, CYTOPLASM, INHIBITION, CELL CYCLE, ATP-BINDING, CELL DIVISION, PHOSPHOPROTEIN, NUCLEOTIDE-BINDING, TRANSFERASE, POLYMORPHISM, BETA-PEPTIDE, CYCLIN GROOVE
2whb:D (VAL311) to (THR366) TRUNCATION AND OPTIMISATION OF PEPTIDE INHIBITORS OF CDK2, CYCLIN A THROUGH STRUCTURE GUIDED DESIGN | CDK2, KINASE, CYCLIN, ACTIVE, NUCLEUS, MITOSIS, SERINE/THREONINE-PROTEIN KINASE, CYTOPLASM, INHIBITION, CELL CYCLE, ATP-BINDING, CELL DIVISION, PHOSPHOPROTEIN, NUCLEOTIDE-BINDING, TRANSFERASE, POLYMORPHISM, BETA-PEPTIDE, CYCLIN GROOVE
4llp:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 WITH FRAGMENT ZT401 | FRAGMENT SCREENING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4lm1:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 WITH FRAGMENT ZT450 | FRAGMENT SCREENING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4lm4:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 WITH FRAGMENT ZT902 | FRAGMENT SCREENING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2hjd:A (PRO16) to (LEU93) CRYSTAL STRUCTURE OF A SECOND QUORUM SENSING ANTIACTIVATOR TRAM2 FROM A. TUMEFACIENS STRAIN A6 | 4 HELIX COILED COIL, SIGNALING PROTEIN
2wih:B (VAL311) to (GLY369) STRUCTURE OF CDK2-CYCLIN A WITH PHA-848125 | CELL CYCLE, ATP-BINDING, TRANSFERASE, POLYMORPHISM, PHOSPHORYLATION, NUCLEOTIDE-BINDING, CELL DIVISION, SERINE/THREONINE-PROTEIN 2 KINASE, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, MITOSIS
2wih:D (ASN312) to (VAL367) STRUCTURE OF CDK2-CYCLIN A WITH PHA-848125 | CELL CYCLE, ATP-BINDING, TRANSFERASE, POLYMORPHISM, PHOSPHORYLATION, NUCLEOTIDE-BINDING, CELL DIVISION, SERINE/THREONINE-PROTEIN 2 KINASE, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, MITOSIS
2hq5:B (ASN113) to (SER187) CRYSTAL STRUCTURE OF MULTIDRUG BINDING PROTEIN QACR FROM STAPHYLOCOCCUS AUREUS COCRYSTALLIZED WITH COMPOUND DB359 | MULTIDRUG RECOGNITION, DB359, QACR, MULTIDRUG BINDING PROTEIN, TRANSCRIPTION
2wlk:A (GLY32) to (ARG137) STRUCTURE OF THE ATP-SENSITIVE INWARD RECTIFIER POTASSIUM CHANNEL FROM MAGNETOSPIRILLUM MAGNETOTACTICUM | INTEGRAL MEMBRANE PROTEIN, IONIC CHANNEL, METAL TRANSPORT, ION TRANSPORT, TRANSPORT
2wlk:B (GLY32) to (ARG137) STRUCTURE OF THE ATP-SENSITIVE INWARD RECTIFIER POTASSIUM CHANNEL FROM MAGNETOSPIRILLUM MAGNETOTACTICUM | INTEGRAL MEMBRANE PROTEIN, IONIC CHANNEL, METAL TRANSPORT, ION TRANSPORT, TRANSPORT
2wma:B (THR310) to (GLY369) STRUCTURAL AND THERMODYNAMIC CONSEQUENCES OF CYCLIZATION OF PEPTIDE LIGANDS FOR THE RECRUITMENT SITE OF CYCLIN A | CELL CYCLE, CELL DIVISION, ANTI-ONCOGENE, SERINE/THREONINE-PROTEIN KINASE, PHOSPHORYLATION, NUCLEOTIDE-BINDING, TRANSCRIPTION REGULATION, CHROMATIN REGULATOR, RECRUITMENT, TRANSCRIPTION, NUCLEUS, MITOSIS, ATP-BINDING, TRANSFERASE
2wma:D (THR310) to (THR366) STRUCTURAL AND THERMODYNAMIC CONSEQUENCES OF CYCLIZATION OF PEPTIDE LIGANDS FOR THE RECRUITMENT SITE OF CYCLIN A | CELL CYCLE, CELL DIVISION, ANTI-ONCOGENE, SERINE/THREONINE-PROTEIN KINASE, PHOSPHORYLATION, NUCLEOTIDE-BINDING, TRANSCRIPTION REGULATION, CHROMATIN REGULATOR, RECRUITMENT, TRANSCRIPTION, NUCLEUS, MITOSIS, ATP-BINDING, TRANSFERASE
2wmb:B (THR310) to (GLY369) STRUCTURAL AND THERMODYNAMIC CONSEQUENCES OF CYCLIZATION OF PEPTIDE LIGANDS FOR THE RECRUITMENT SITE OF CYCLIN A | CELL CYCLE, CELL DIVISION, ANTI-ONCOGENE, SERINE/THREONINE-PROTEIN KINASE, PHOSPHORYLATION, NUCLEOTIDE-BINDING, TRANSCRIPTION REGULATION, CHROMATIN REGULATOR, RECRUITMENT, TRANSCRIPTION, NUCLEUS, MITOSIS, ATP-BINDING, TRANSFERASE
2wmb:D (THR310) to (GLY369) STRUCTURAL AND THERMODYNAMIC CONSEQUENCES OF CYCLIZATION OF PEPTIDE LIGANDS FOR THE RECRUITMENT SITE OF CYCLIN A | CELL CYCLE, CELL DIVISION, ANTI-ONCOGENE, SERINE/THREONINE-PROTEIN KINASE, PHOSPHORYLATION, NUCLEOTIDE-BINDING, TRANSCRIPTION REGULATION, CHROMATIN REGULATOR, RECRUITMENT, TRANSCRIPTION, NUCLEUS, MITOSIS, ATP-BINDING, TRANSFERASE
3vyg:B (GLU66) to (GLN124) CRYSTAL STRUCTURE OF THIOCYANATE HYDROLASE MUTANT R136W | THIOCYANATE HYDROLASE, CYSTEINE-SULFENIC ACID, CYSTEINE-SULFIC ACID, METALLOENZYME, HYDROLASE
1idr:A (SER14) to (GLY67) CRYSTAL STRUCTURE OF THE TRUNCATED-HEMOGLOBIN-N FROM MYCOBACTERIUM TUBERCULOSIS | TRUNCATED HEMOGLOBIN FOLD, OXYGEN STORAGE/TRANSPORT COMPLEX
2wv1:A (ARG114) to (THR196) CRYSTAL STRUCTURE OF THE HLYIIR MUTANT PROTEIN WITH RESIDUES 169-186 SUBSTITUTED BY A LINKER CONTAINING TWO THROMBIN SITES | TRANSCRIPTION, TRANSCRIPTION REGULATION, TETR FAMILY
2wv1:B (PHE126) to (THR196) CRYSTAL STRUCTURE OF THE HLYIIR MUTANT PROTEIN WITH RESIDUES 169-186 SUBSTITUTED BY A LINKER CONTAINING TWO THROMBIN SITES | TRANSCRIPTION, TRANSCRIPTION REGULATION, TETR FAMILY
4m1m:A (SER1122) to (LEU1186) CORRECTED STRUCTURE OF MOUSE P-GLYCOPROTEIN | ATP-BINDING CASSETTE TRANSPORTER, MULTIDRUG EFFLUX, ADENOSINE TRIPHOSPHATE, MERCURATED CYSTEINES, PLASMA MEMBRANE, HYDROLASE
2i40:B (VAL311) to (THR366) CDK2/CYCLIN A COMPLEXED WITH A THIOPHENE CARBOXAMIDE INHIBITOR | CDK2, CYCLIN, KINASE, TRANSFERASE-CELL CYCLE COMPLEX
2i40:D (VAL311) to (THR366) CDK2/CYCLIN A COMPLEXED WITH A THIOPHENE CARBOXAMIDE INHIBITOR | CDK2, CYCLIN, KINASE, TRANSFERASE-CELL CYCLE COMPLEX
4m2q:A (THR45) to (THR93) CRYSTAL STRUCTURE OF NON-MYRISTOYLATED RECOVERIN WITH CYSTEINE-39 OXIDIZED TO SULFENIC ACID | CALCIUM BINDING PROTEIN, EF HAND, NEURONAL CALCIUM SENSING (NCS) FAMILY PROTEIN, INHIBITS RHODOPSIN KINASE, RHODOPSIN KINASE, RETINA, METAL BINDING PROTEIN
4m4b:A (SER3) to (HIS72) HUMAN HEMOGLOBIN NITROETHANE MODIFIED | R-STATE, HUMAN HEMOGLOBIN, NITROETHANE MODIFIED, OXYGEN TRANSPORT
1uor:A (GLU16) to (THR83) X-RAY STUDY OF RECOMBINANT HUMAN SERUM ALBUMIN. PHASES DETERMINED BY MOLECULAR REPLACEMENT METHOD, USING LOW RESOLUTION STRUCTURE MODEL OF TETRAGONAL FORM OF HUMAN SERUM ALBUMIN | PLASMA PROTEIN, METAL-BINDING PROTEIN
2wxv:B (THR310) to (GLY369) STRUCTURE OF CDK2-CYCLIN A WITH A PYRAZOLO(4,3-H) QUINAZOLINE-3-CARBOXAMIDE INHIBITOR | NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE, TRANSFERASE, KINASE, CYCLIN
2wxv:D (ASN312) to (GLY369) STRUCTURE OF CDK2-CYCLIN A WITH A PYRAZOLO(4,3-H) QUINAZOLINE-3-CARBOXAMIDE INHIBITOR | NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE, TRANSFERASE, KINASE, CYCLIN
2iek:A (GLU111) to (THR199) NEW CRYSTAL FORM OF TRANSCRIPTIONAL REGULATOR TM1030 FROM THERMOTOGA MARITIMA | TRANSCRIPTIONAL REGULATOR; TETR FAMILY, TRANSCRIPTION
1urc:B (THR310) to (THR366) CYCLIN A BINDING GROOVE INHIBITOR ACE-ARG-LYS-LEU-PHE-GLY | TRANSFERASE-INHIBITOR COMPLEX, INHIBITOR, LIGAND EXCHANGE, DRUG DESIGN, PEPTIDOMIMETICS
1urc:D (ASN312) to (THR366) CYCLIN A BINDING GROOVE INHIBITOR ACE-ARG-LYS-LEU-PHE-GLY | TRANSFERASE-INHIBITOR COMPLEX, INHIBITOR, LIGAND EXCHANGE, DRUG DESIGN, PEPTIDOMIMETICS
2ig3:B (ASN7) to (MET57) CRYSTAL STRUCTURE OF GROUP III TRUNCATED HEMOGLOBIN FROM CAMPYLOBACTER JEJUNI | TRUNCATED HEMOGLOBIN, 2-ON-2 GLOBIN, OXYGEN STORAGE-TRANSPORT COMPLEX
5ab8:A (SER14) to (GLY67) HIGH RESOLUTION X-RAY STRUCTURE OF THE N-TERMINAL TRUNCATED FORM (RESIDUES 1-11) OF MYCOBACTERIUM TUBERCULOSIS HBN | OXYGEN TRANSPORT, TRUNCATED HEMOGLOBINS, 2/2 HEMOGLOBINS, GLOBIN DYNAMICS, BACTERIAL GLOBINS, HEME/LIGAND TUNNELING, NO DIOXYGENASE
3wcw:A (ILE4) to (PHE77) THE STRUCTURE OF A DEOXYGENATED 400 KDA HEMOGLOBIN PROVIDES A MORE ACCURATE DESCRIPTION OF THE COOPERATIVE MECHANISM OF GIANT HEMOGLOBINS: MG BOUND FORM | GLOBIN FOLD, OXYGEN TRANSPORT, OXYGEN BINDING, BLOOD
3wcw:D (SER5) to (ILE79) THE STRUCTURE OF A DEOXYGENATED 400 KDA HEMOGLOBIN PROVIDES A MORE ACCURATE DESCRIPTION OF THE COOPERATIVE MECHANISM OF GIANT HEMOGLOBINS: MG BOUND FORM | GLOBIN FOLD, OXYGEN TRANSPORT, OXYGEN BINDING, BLOOD
3wdc:A (THR6) to (ILE66) N-TERMINAL DOMAIN OF MYCOBACTERIUM TUBERCULOSIS CLPC1 BOUND TO CYCLOMARIN A | CHAPERONE, CHAPERONE-ANTIMICROBIAL PROTEIN COMPLEX
3wdd:A (THR6) to (ILE66) MUTANT N-TERMINAL DOMAIN OF MYCOBACTERIUM TUBERCULOSIS CLPC1, F2Y, BOUND TO CYCLOMARIN A | CHAPERONE, CHAPERONE-ANTIMICROBIAL PROTEIN COMPLEX
3wde:A (THR6) to (ILE66) MUTANT N-TERMINAL DOMAIN OF MYCOBACTERIUM TUBERCULOSIS CLPC1, F80Y, BOUND TO CYCLOMARIN A | CHAPERONE, CHAPERONE-ANTIMICROBIAL PROTEIN COMPLEX
1ixe:A (ALA76) to (GLY141) CRYSTAL STRUCTURE OF CITRATE SYNTHASE FROM THERMUS THERMOPHILUS HB8 | ENZYME-PRODUCTS COMPLEX, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, STRUCTURAL GENOMICS, LYASE
1ixe:B (ALA76) to (GLY141) CRYSTAL STRUCTURE OF CITRATE SYNTHASE FROM THERMUS THERMOPHILUS HB8 | ENZYME-PRODUCTS COMPLEX, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, STRUCTURAL GENOMICS, LYASE
1ixe:C (ALA76) to (GLY141) CRYSTAL STRUCTURE OF CITRATE SYNTHASE FROM THERMUS THERMOPHILUS HB8 | ENZYME-PRODUCTS COMPLEX, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, STRUCTURAL GENOMICS, LYASE
1ixe:D (ALA76) to (GLY141) CRYSTAL STRUCTURE OF CITRATE SYNTHASE FROM THERMUS THERMOPHILUS HB8 | ENZYME-PRODUCTS COMPLEX, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, STRUCTURAL GENOMICS, LYASE
3wi2:A (GLU506) to (CYS562) CRYSTAL STRUCTURE OF PDE10A IN COMPLEX WITH INHIBITOR | PHOSPHODIESTERASE, CGMP BINDING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3wi2:B (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A IN COMPLEX WITH INHIBITOR | PHOSPHODIESTERASE, CGMP BINDING, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1v29:B (ASP30) to (GLY88) CRYSTAL STRUCTURE OF NITRILE HYDRATASE FROM A THERMOPHILE BACILLUS SMITHII | NHASE, BACILLUS SMITHII, LYASE
1j40:E (SER81) to (LEU136) DIRECT OBSERVATION OF PHOTOLYSIS-INDUCED TERTIARY STRUCTURAL CHANGES IN HUMAN HAEMOGLOBIN; CRYSTAL STRUCTURE OF ALPHA(NI)-BETA(FE-CO) HEMOGLOBIN (LASER UNPHOTOLYSED) | TERTIARY STRUCTURE CHANGES, CRYSTAL PHOTOLYSIS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, STRUCTURAL GENOMICS, OXYGEN STORAGE/TRANSPORT COMPLEX
1j41:E (SER81) to (LEU136) DIRECT OBSERVATION OF PHOTOLYSIS-INDUCED TERTIARY STRUCTURAL CHANGES IN HUMAN HAEMOGLOBIN; CRYSTAL STRUCTURE OF ALPHA(NI)-BETA(FE) HEMOGLOBIN (LASER PHOTOLYSED) | TERTIARY STRUCTURE CHANGES, CRYSTAL PHOTOLYSIS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, STRUCTURAL GENOMICS, OXYGEN STORAGE/TRANSPORT COMPLEX
1j41:G (SER81) to (THR137) DIRECT OBSERVATION OF PHOTOLYSIS-INDUCED TERTIARY STRUCTURAL CHANGES IN HUMAN HAEMOGLOBIN; CRYSTAL STRUCTURE OF ALPHA(NI)-BETA(FE) HEMOGLOBIN (LASER PHOTOLYSED) | TERTIARY STRUCTURE CHANGES, CRYSTAL PHOTOLYSIS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, STRUCTURAL GENOMICS, OXYGEN STORAGE/TRANSPORT COMPLEX
1j7w:C (LEU80) to (LEU136) CRYSTAL STRUCTURE OF DEOXY HBBETAYQ, A SITE DIRECTED MUTANT OF HBA | GLOBIN, OXYGEN STORAGE/TRANSPORT COMPLEX
2iw6:B (THR310) to (THR366) STRUCTURE OF HUMAN THR160-PHOSPHO CDK2-CYCLIN A COMPLEXED WITH A BISANILINOPYRIMIDINE INHIBITOR | PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE COMPLEX, KINASE, MITOSIS, CELL CYCLE, TRANSFERASE, ATP-BINDING
2iw6:D (THR310) to (THR366) STRUCTURE OF HUMAN THR160-PHOSPHO CDK2-CYCLIN A COMPLEXED WITH A BISANILINOPYRIMIDINE INHIBITOR | PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE COMPLEX, KINASE, MITOSIS, CELL CYCLE, TRANSFERASE, ATP-BINDING
2iw8:B (THR310) to (GLY369) STRUCTURE OF HUMAN THR160-PHOSPHO CDK2-CYCLIN A F82H-L83V- H84D MUTANT WITH AN O6-CYCLOHEXYLMETHYLGUANINE INHIBITOR | PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE COMPLEX, KINASE, MITOSIS, CELL CYCLE, TRANSFERASE
2iw9:B (THR310) to (GLY369) STRUCTURE OF HUMAN THR160-PHOSPHO CDK2-CYCLIN A COMPLEXED WITH A BISANILINOPYRIMIDINE INHIBITOR | PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE COMPLEX, KINASE, MITOSIS, CELL CYCLE, TRANSFERASE
2iw9:D (THR310) to (THR368) STRUCTURE OF HUMAN THR160-PHOSPHO CDK2-CYCLIN A COMPLEXED WITH A BISANILINOPYRIMIDINE INHIBITOR | PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE COMPLEX, KINASE, MITOSIS, CELL CYCLE, TRANSFERASE
3j3r:B (PRO82) to (LEU142) STRUCTURAL DYNAMICS OF THE MECA-CLPC COMPLEX REVEALED BY CRYO-EM | CLPC, MECA, AAA+ ATPASE, PROTEIN UNFOLDING, CHAPERONE
3j3r:E (THR81) to (LEU142) STRUCTURAL DYNAMICS OF THE MECA-CLPC COMPLEX REVEALED BY CRYO-EM | CLPC, MECA, AAA+ ATPASE, PROTEIN UNFOLDING, CHAPERONE
3woi:A (GLN430) to (SER502) CRYSTAL STRUCTURE OF THE DAP BII (S657A) | CHYMOTRYPSIN FOLD, S46 PEPTIDASE, HYDROLASE
3j3s:B (PRO82) to (LEU142) STRUCTURAL DYNAMICS OF THE MECA-CLPC COMPLEX REVEALED BY CRYO-EM | CLPC, MECA, AAA+ ATPASE, PROTEIN UNFOLDING, CHAPERONE
3j3s:B (SER343) to (GLY399) STRUCTURAL DYNAMICS OF THE MECA-CLPC COMPLEX REVEALED BY CRYO-EM | CLPC, MECA, AAA+ ATPASE, PROTEIN UNFOLDING, CHAPERONE
3j3s:C (THR81) to (GLY143) STRUCTURAL DYNAMICS OF THE MECA-CLPC COMPLEX REVEALED BY CRYO-EM | CLPC, MECA, AAA+ ATPASE, PROTEIN UNFOLDING, CHAPERONE
3j3s:E (THR81) to (LEU142) STRUCTURAL DYNAMICS OF THE MECA-CLPC COMPLEX REVEALED BY CRYO-EM | CLPC, MECA, AAA+ ATPASE, PROTEIN UNFOLDING, CHAPERONE
3j3s:E (SER343) to (PRO410) STRUCTURAL DYNAMICS OF THE MECA-CLPC COMPLEX REVEALED BY CRYO-EM | CLPC, MECA, AAA+ ATPASE, PROTEIN UNFOLDING, CHAPERONE
3j3s:F (THR81) to (LEU142) STRUCTURAL DYNAMICS OF THE MECA-CLPC COMPLEX REVEALED BY CRYO-EM | CLPC, MECA, AAA+ ATPASE, PROTEIN UNFOLDING, CHAPERONE
3j3t:B (PRO82) to (LEU142) STRUCTURAL DYNAMICS OF THE MECA-CLPC COMPLEX REVEALED BY CRYO-EM | CLPC, MECA, AAA+ ATPASE, PROTEIN UNFOLDING, CHAPERONE
3j3t:B (LEU354) to (SER406) STRUCTURAL DYNAMICS OF THE MECA-CLPC COMPLEX REVEALED BY CRYO-EM | CLPC, MECA, AAA+ ATPASE, PROTEIN UNFOLDING, CHAPERONE
3j3t:D (PRO82) to (LEU142) STRUCTURAL DYNAMICS OF THE MECA-CLPC COMPLEX REVEALED BY CRYO-EM | CLPC, MECA, AAA+ ATPASE, PROTEIN UNFOLDING, CHAPERONE
3j3t:F (PRO82) to (LEU142) STRUCTURAL DYNAMICS OF THE MECA-CLPC COMPLEX REVEALED BY CRYO-EM | CLPC, MECA, AAA+ ATPASE, PROTEIN UNFOLDING, CHAPERONE
3j3u:D (PRO82) to (LEU141) STRUCTURAL DYNAMICS OF THE MECA-CLPC COMPLEX REVEALED BY CRYO-EM | CLPC, MECA, AAA+ ATPASE, PROTEIN UNFOLDING, CHAPERONE
2xdn:A (ILE126) to (ARG203) TRANSCRIPTION FACTOR TTGR H67A MUTANT | TRANSCRIPTION, TRANSCRIPTION REGULATION, TETR FAMILY
2xdn:C (CYS124) to (SER205) TRANSCRIPTION FACTOR TTGR H67A MUTANT | TRANSCRIPTION, TRANSCRIPTION REGULATION, TETR FAMILY
2xdn:D (CYS124) to (ARG203) TRANSCRIPTION FACTOR TTGR H67A MUTANT | TRANSCRIPTION, TRANSCRIPTION REGULATION, TETR FAMILY
4mqc:A (SER81) to (SER138) CARBONMONOXY STRUCTURE OF HEMOGLOBIN EVANS ALPHAV62MBETAWT | OXYGEN-TRANSPORT, AUTOOXIDATION, OXYGEN TRANSPORT
2xge:A (GLU107) to (LEU204) CRYSTAL STRUCTURE OF A DESIGNED HETERODIMERIC VARIANT T-A(A) B OF THE TETRACYCLINE REPRESSOR | CHIMERA, TRANSCRIPTION, TRANSCRIPTION REGULATION, ANTIBIOTIC RESISTANCE
2xge:B (GLU107) to (LEU204) CRYSTAL STRUCTURE OF A DESIGNED HETERODIMERIC VARIANT T-A(A) B OF THE TETRACYCLINE REPRESSOR | CHIMERA, TRANSCRIPTION, TRANSCRIPTION REGULATION, ANTIBIOTIC RESISTANCE
3ws9:A (LEU508) to (CYS562) CRYSTAL STRUCTURE OF PDE10A IN COMPLEX WITH A BENZIMDAZOLE INHIBITOR | PHOSPHODIESTERASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3ws9:B (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A IN COMPLEX WITH A BENZIMDAZOLE INHIBITOR | PHOSPHODIESTERASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4mrw:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 WITH FRAGMENT ZT0120 (7-CHLOROQUINOLIN-4- OL) | FRAGMENT SCREENING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3ws8:B (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A IN COMPLEX WITH A BENZIMIDAZOLE INHIBITOR | PHOSPHODIESTERASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4mrz:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 WITH FRAGMENT ZT0429 (4-METHYL-3- NITROPYRIDIN-2-AMINE) | FRAGMENT SCREENING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4ms0:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 WITH FRAGMENT ZT0443 (6-CHLOROPYRIMIDINE- 2,4-DIAMINE) | FRAGMENT SCREENING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4msa:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 WITH FRAGMENT ZT0449 (5-NITRO-1H- BENZIMIDAZOLE) | FRAGMENT SCREENING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4mse:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 WITH FRAGMENT ZT1597 (2-({[(2S)-2-METHYL- 2,3-DIHYDRO-1,3-BENZOTHIAZOL-5-YL]OXY}METHYL)QUINOLINE) | FRAGMENT SCREENING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4msh:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 WITH FRAGMENT ZT0143 ((2S)-4-CHLORO-2,3- DIHYDRO-1,3-BENZOTHIAZOL-2-AMINE) | FRAGMENT SCREENING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4msh:B (LEU508) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 WITH FRAGMENT ZT0143 ((2S)-4-CHLORO-2,3- DIHYDRO-1,3-BENZOTHIAZOL-2-AMINE) | FRAGMENT SCREENING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3wtg:A (LYS82) to (LEU136) CRYSTAL STRUCTURE OF EMU (DROMAIUS NOVAEHOLLANDIAE) HEMOGLOBIN AT 2.3 ANGSTROM RESOLUTION | HEMOGLOBIN, OXYGEN AFFINITY, AVIAN, OXYGEN TRANSPORT, OXYGEN
1jst:D (THR310) to (GLY369) PHOSPHORYLATED CYCLIN-DEPENDENT KINASE-2 BOUND TO CYCLIN A | COMPLEX (PROTEIN KINASE-CYCLIN), CYCLIN, CDK, PHOSPHORYLATION, COMPLEX (PROTEIN KINASE-CYCLIN) COMPLEX
1jsu:B (VAL311) to (THR366) P27(KIP1)/CYCLIN A/CDK2 COMPLEX | COMPLEX (TRANSFERASE/CYCLIN/INHIBITOR), KINASE, CELL CYCLE, CELL DIVISION, CDK, CYCLIN, INHIBITOR
5axp:B (LEU495) to (CYS552) CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF PDE10A COMPLEXED WITH 1- (2-FLUORO-4-(2-OXO-1,3-OXAZOLIDIN-3-YL)PHENYL)-5-METHOXY-3-(1-PHENYL- 1H-PYRAZOL-5-YL)PYRIDAZIN-4(1H)-ONE | HYDROLASE/HYDROLASE INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5axq:A (ASN562) to (ASP624) CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF PDE10A COMPLEXED WITH HIGHLY POTENT AND BRAIN-PENETRANT PDE10A INHIBITOR WITH 2-OXINDOLE SCAFFOLD | HYDROLASE/HYDROLASE INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5axq:B (LEU498) to (CYS552) CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF PDE10A COMPLEXED WITH HIGHLY POTENT AND BRAIN-PENETRANT PDE10A INHIBITOR WITH 2-OXINDOLE SCAFFOLD | HYDROLASE/HYDROLASE INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1jt6:A (THR109) to (SER187) CRYSTAL STRUCTURE OF THE MULTIDRUG BINDING PROTEIN QACR BOUND TO DEQUALINIUM | MUTLIDRUG BINDING RECOGNITION, QACR, MULITDRUG RESISTANCE, S. AUREUS, TRANSCRIPTION
1vyw:D (ASN312) to (VAL367) STRUCTURE OF CDK2/CYCLIN A WITH PNU-292137 | TRANSFERASE/COMPLEX, PROTEIN KINASE/COMPLEX, PROTEIN KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, PHOSPHORYLATION, CELL DIVISION, CYCLIN
4myh:C (ARG108) to (PHE254) STRUCTURE OF THE GLUTATHIONE BOUND MITOCHONDRIAL ABC TRANSPORTER, ATM1 | ABC TRANSPORTER, MEMBRANE TRANSPORT, MITOCHONDRIAL INNER MEMBRANE, GLUTATHIONE, TRANSPORT PROTEIN
3wyk:B (LEU495) to (CYS552) CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF PDE10A COMPLEXED WITH 3- (1-PHENYL-1H-PYRAZOL-5-YL)-1-(3-(TRIFLUOROMETHYL)PHENYL)PYRIDAZIN- 4(1H)-ONE | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3wyl:B (LEU495) to (CYS552) CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF PDE10A COMPLEXED WITH 5- METHOXY-3-(1-PHENYL-1H-PYRAZOL-5-YL)-1-(3-(TRIFLUOROMETHYL)PHENYL) PYRIDAZIN-4(1H)-ONE | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3wym:B (LEU495) to (CYS552) CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF PDE10A COMPLEXED WITH 1- (2-FLUORO-4-(1H-PYRAZOL-1-YL)PHENYL)-5-METHOXY-3-(1-PHENYL-1H- PYRAZOL-5-YL)PYRIDAZIN-4(1H)-ONE | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2xpu:A (TYR110) to (LEU204) TETR(D) IN COMPLEX WITH ANHYDROTETRACYCLINE. | TRANSCRIPTION, TRANSCRIPTION REGULATOR, HELIX-TURN-HELIX, METAL COORDINATION
5b16:A (HIS1084) to (THR1129) X-RAY STRUCTURE OF DROSHA IN COMPLEX WITH THE C-TERMINAL TAIL OF DGCR8. | ENDONUCLEASE, RNASE III, TRIMERIC COMPLEX, ZINC FINGER, HYDROLASE
5b4k:B (LEU495) to (CYS552) CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN PDE10A COMPLEXED WITH N-(4-((5-METHYL-5H-PYRROLO[3,2-D]PYRIMIDIN-4-YL)OXY)PHENYL)-1H- BENZIMIDAZOL-2-AMINE | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5b4l:B (LEU495) to (CYS552) CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF HUMAN PDE10A COMPLEXED WITH 1-(CYCLOPROPYLMETHYL)-5-(2-(2,3-DIHYDRO-1H-IMIDAZO[1,2- A]BENZIMIDAZOL-1-YL)ETHOXY)-3-(1-PHENYL-1H-PYRAZOL-5-YL)PYRIDAZIN- 4(1H)-ONE | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4n7n:G (PRO4) to (HIS72) CAPTURING THE HAEMOGLOBIN ALLOSTERIC TRANSITION IN A SINGLE CRYSTAL FORM; CRYSTAL STRUCTURE OF FULL-LIGANDED HUMAN HAEMOGLOBIN WITH PHOSPHATE AT 2.75 A RESOLUTION. | HAEMOGLOBIN, ALLOSTERIC PATHWAY, TRANSPORT PROTEIN
4n7n:K (SER3) to (HIS72) CAPTURING THE HAEMOGLOBIN ALLOSTERIC TRANSITION IN A SINGLE CRYSTAL FORM; CRYSTAL STRUCTURE OF FULL-LIGANDED HUMAN HAEMOGLOBIN WITH PHOSPHATE AT 2.75 A RESOLUTION. | HAEMOGLOBIN, ALLOSTERIC PATHWAY, TRANSPORT PROTEIN
3zfi:A (LYS55) to (LEU116) RAP1A PROTEIN (SMA2260) FROM SERRATIA MARCESCENS | TRANSPORT PROTEIN, BACTERIAL IMMUNITY, 2260 PROTEIN, T6SS, TYPE VI SECRETION SYSTEM, SELF-RESISTANCE PROTEIN
3zfz:B (LYS28) to (LEU73) CRYSTAL STRUCTURE OF CEFTAROLINE ACYL-PBP2A FROM MRSA WITH NON-COVALENTLY BOUND CEFTAROLINE AND MURAMIC ACID AT ALLOSTERIC SITE OBTAINED BY SOAKING | HYDROLASE, PENICILLIN BINDING PROTEINS, MRSA, ALLOSTERIC SITE, B- LACTAM ANTIBIOTICS
3zg0:B (ASP27) to (LEU73) CRYSTAL STRUCTURE OF CEFTAROLINE ACYL-PBP2A FROM MRSA WITH NON-COVALENTLY BOUND CEFTAROLINE AND MURAMIC ACID AT ALLOSTERIC SITE OBTAINED BY COCRYSTALLIZATION | HYDROLASE, MRSA, ALLOSTERIC SITE, B-LACTAM ANTIBIOTICS
3zg5:B (ASP27) to (GLY74) CRYSTAL STRUCTURE OF PBP2A FROM MRSA IN COMPLEX WITH PEPTIDOGLYCAN ANALOGUE AT ALLOSTERIC | HYDROLASE, PENICILLIN BINDING PROTEINS, ALLOSTERIC SITE, B- LACTAM ANTIBIOTICS
1w98:B (VAL232) to (SER293) THE STRUCTURAL BASIS OF CDK2 ACTIVATION BY CYCLIN E | CELL CYCLE, TRANSFERASE
2jk3:A (GLY124) to (LEU184) CRYSTAL STRUCTURE OF THE HLYIIR MUTANT PROTEIN WITH RESIDUES 169-186 SUBSTITUTED BY GSSGSSG LINKER | DNA-BINDING PROTEIN, TRANSCRIPTION REGULATION, DNA-BINDING, TETR FAMILY, TRANSCRIPTION, TRANSCRIPTIONAL REGULATOR
2jk3:B (SER112) to (THR185) CRYSTAL STRUCTURE OF THE HLYIIR MUTANT PROTEIN WITH RESIDUES 169-186 SUBSTITUTED BY GSSGSSG LINKER | DNA-BINDING PROTEIN, TRANSCRIPTION REGULATION, DNA-BINDING, TETR FAMILY, TRANSCRIPTION, TRANSCRIPTIONAL REGULATOR
2xyk:A (THR7) to (GLY62) GROUP II 2-ON-2 HEMOGLOBIN FROM THE PLANT PATHOGEN AGROBACTERIUM TUMEFACIENS | OXYGEN STORAGE-TRANSPORT COMPLEX, 2/2 HEMOGLOBIN
2xyk:B (THR7) to (GLY62) GROUP II 2-ON-2 HEMOGLOBIN FROM THE PLANT PATHOGEN AGROBACTERIUM TUMEFACIENS | OXYGEN STORAGE-TRANSPORT COMPLEX, 2/2 HEMOGLOBIN
1kd2:B (PHE85) to (ALA142) CRYSTAL STRUCTURE OF HUMAN DEOXYHEMOGLOBIN IN ABSENCE OF ANY ANIONS | HUMAN DEOXY HEMOGLOBIN, HIGH O2 AFFINITY T STATE, CHLORIDE BINDING SITES, ALLOSTERIC ANION BINDING SITES, HYDRATION, OXYGEN STORAGE/TRANSPORT COMPLEX
2y52:A (LEU42) to (GLY120) CRYSTAL STRUCTURE OF E496A MUTANT OF THE BOX PATHWAY ENCODED ALDH FROM BURKHOLDERIA XENOVORANS LB400 | OXIDOREDUCTASE
2y52:B (ASP41) to (GLY120) CRYSTAL STRUCTURE OF E496A MUTANT OF THE BOX PATHWAY ENCODED ALDH FROM BURKHOLDERIA XENOVORANS LB400 | OXIDOREDUCTASE
2y51:A (LEU42) to (GLY120) CRYSTAL STRUCTURE OF E167A MUTANT OF THE BOX PATHWAY ENCODED ALDH FROM BURKHOLDERIA XENOVORANS LB400 | OXIDOREDUCTASE
2y51:B (LEU42) to (GLY120) CRYSTAL STRUCTURE OF E167A MUTANT OF THE BOX PATHWAY ENCODED ALDH FROM BURKHOLDERIA XENOVORANS LB400 | OXIDOREDUCTASE
2y53:A (ASP41) to (GLY120) CRYSTAL STRUCTURE OF E257Q MUTANT OF THE BOX PATHWAY ENCODED ALDH FROM BURKHOLDERIA XENOVORANS LB400 | OXIDOREDUCTASE, NADP, NUCLEOTIDE-BINDING
2y53:B (LEU42) to (GLY120) CRYSTAL STRUCTURE OF E257Q MUTANT OF THE BOX PATHWAY ENCODED ALDH FROM BURKHOLDERIA XENOVORANS LB400 | OXIDOREDUCTASE, NADP, NUCLEOTIDE-BINDING
2y5d:A (LEU42) to (GLY120) CRYSTAL STRUCTURE OF C296A MUTANT OF THE BOX PATHWAY ENCODED ALDH FROM BURKHOLDERIA XENOVORANS LB400 | OXIDOREDUCTASE
5c1w:A (LEU495) to (CYS552) PDE10 COMPLEXED WITH 4,6-DICHLORO-2-CYCLOPROPYL-5-METHYL-PYRIMIDINE | PHOSPHODIESTERASE, INHIBITOR, COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5c28:B (LEU495) to (CYS552) PDE10 COMPLEXED WITH 6-CHLORO-2-CYCLOPROPYL-5-METHYL-PYRIMIDIN-4-AMINE | PHOSPHODIESTERASE, INHIBITOR, COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5c2a:A (GLU494) to (CYS552) PDE10 COMPLEXED WITH 6-CHLORO-2-CYCLOPROPYL-N-[(2,4-DIMETHYLTHIAZOL-5- YL)METHYL]-5-METHYL-PYRIMIDIN-4-AMINE | PHOSPHODIESTERASE, INHIBITOR, COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5c2h:A (LEU495) to (CYS552) PDE10 COMPLEXED WITH 6-CHLORO-N-[(2,4-DIMETHYLTHIAZOL-5-YL)METHYL]-5- METHYL-2-[3-(2-QUINOLYL)PROPOXY]PYRIMIDIN-4-AMINE | PHOSPHODIESTERASE, INHIBITOR, COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3zrj:A (SER88) to (HIS147) COMPLEX OF CLPV N-DOMAIN WITH VIPB PEPTIDE | CHAPERONE-PEPTIDE COMPLEX, HSP100 PROTEINS, AAA+ PROTEINS, T6SS, SECRETION, VIRULENCE
3zrj:B (SER88) to (HIS147) COMPLEX OF CLPV N-DOMAIN WITH VIPB PEPTIDE | CHAPERONE-PEPTIDE COMPLEX, HSP100 PROTEINS, AAA+ PROTEINS, T6SS, SECRETION, VIRULENCE
4npv:A (THR271) to (ASP335) CRYSTAL STRUCTURE OF HUMAN PDE1B BOUND TO INHIBITOR 7A (6,7,8- TRIMETHOXY-N-(PENTAN-3-YL)QUINAZOLIN-4-AMINE) | HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4npw:A (THR271) to (ASP335) CRYSTAL STRUCTURE OF HUMAN PDE1B BOUND TO INHIBITOR 19A (7,8- DIMETHOXY-N-[(2S)-1-(3-METHYL-1H-PYRAZOL-5-YL)PROPAN-2-YL]QUINAZOLIN- 4-AMINE) | HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
1ksf:X (ASN3) to (THR65) CRYSTAL STRUCTURE OF CLPA, AN HSP100 CHAPERONE AND REGULATOR OF CLPAP PROTEASE: STRUCTURAL BASIS OF DIFFERENCES IN FUNCTION OF THE TWO AAA+ ATPASE DOMAINS | CLPA, AAA+, ATPASES, ATP-DEPENDENT PROTEASE, CHAPERONES, CRYSTAL STRUCTURE, HYDROLASE, LIGAND BINDING PROTEIN
4nyi:S (THR605) to (GLU649) APPROACH FOR TARGETING RAS WITH SMALL MOLECULES THAT ACTIVATE SOS- MEDIATED NUCLEOTIDE EXCHANGE | RAS SOS COMPLEX, SIGNAL TRANSDUCTION, RAF, PI3K, POLY-PETIDE, CYTOSOL, SIGNALING PROTEIN
4nyj:S (THR605) to (GLU649) APPROACH FOR TARGETING RAS WITH SMALL MOLECULES THAT ACTIVATE SOS- MEDIATED NUCLEOTIDE EXCHANGE | GTPASE, SIGNALING TRANSDUCTION, RAF, RALGDS, PI3K, CYTOSOL, SIGNALING PROTEIN
1xd4:A (THR605) to (GLU649) CRYSTAL STRUCTURE OF THE DH-PH-CAT MODULE OF SON OF SEVENLESS (SOS) | NUCLEOTIDE EXCHANGE FACTOR, RAS, CDC25, RAS EXCHANGER MOTIF (REM), DBL HOMOLOGY(DH), PLECKSTRIN HOMOLOGY (PH), SIGNALING PROTEIN
1xd4:B (THR605) to (GLU649) CRYSTAL STRUCTURE OF THE DH-PH-CAT MODULE OF SON OF SEVENLESS (SOS) | NUCLEOTIDE EXCHANGE FACTOR, RAS, CDC25, RAS EXCHANGER MOTIF (REM), DBL HOMOLOGY(DH), PLECKSTRIN HOMOLOGY (PH), SIGNALING PROTEIN
2np5:D (SER135) to (GLN189) CRYSTAL STRUCTURE OF A TRANSCRIPTIONAL REGULATOR (RHA1_RO04179) FROM RHODOCOCCUS SP. RHA1. | TETR FAMILY, TRANSCRIPTIONAL REGULATOR, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, TRANSCRIPTION
4a0c:C (ARG469) to (LEU535) STRUCTURE OF THE CAND1-CUL4B-RBX1 COMPLEX | TRANSCRIPTION, LIGASE, UBIQUITIN, CELL CYCLE, DNA DAMAGE REPAIR
4a0c:E (ARG469) to (LEU535) STRUCTURE OF THE CAND1-CUL4B-RBX1 COMPLEX | TRANSCRIPTION, LIGASE, UBIQUITIN, CELL CYCLE, DNA DAMAGE REPAIR
4a0l:E (ARG469) to (LEU535) STRUCTURE OF DDB1-DDB2-CUL4B-RBX1 BOUND TO A 12 BP ABASIC SITE CONTAINING DNA-DUPLEX | LIGASE-DNA-BINDING PROTEIN-DNA COMPLEX
4a0l:H (ARG469) to (LEU535) STRUCTURE OF DDB1-DDB2-CUL4B-RBX1 BOUND TO A 12 BP ABASIC SITE CONTAINING DNA-DUPLEX | LIGASE-DNA-BINDING PROTEIN-DNA COMPLEX
3jxi:D (ARG137) to (ARG172) CRYSTAL STRUCTURE OF THE CHICKEN TRPV4 ANKYRIN REPEAT DOMAIN | ANKYRIN REPEATS, ANK REPEAT, ION TRANSPORT, IONIC CHANNEL, RECEPTOR, TRANSMEMBRANE, TRANSPORT, MEMBRANE PROTEIN
1la6:A (LEU81) to (GLU139) THE CRYSTAL STRUCTURE OF TREMATOMUS NEWNESI HEMOGLOBIN IN A PARTIAL HEMICHROME STATE | HEMICHROME, BISHISTIDINE COMPLEX, OXYGEN STORAGE/TRANSPORT COMPLEX
4odc:A (LEU82) to (GLU140) CRYSTAL STRUCTURE OF TREMATOMUS BERNACCHII HEMOGLOBIN IN A PARTIALLY CYANIDED STATE | ALPHA PROTEIN, GLOBIN FOLD, OXYGEN TRANSPORT, OXYGEN TRANSPORT- PROTEIN BINDING COMPLEX
1lfy:B (PHE85) to (ALA142) OXY HEMOGLOBIN (84% RELATIVE HUMIDITY) | HEMOGLOBIN, T STATE, HUMIDITY, ENVIRONMENT, OXYGEN STORAGE/TRANSPORT COMPLEX
4oic:B (GLN211) to (VAL264) CRYSTAL STRUCTRUAL OF A SOLUBLE PROTEIN | START FOLD, PYL-PHOSPHATASES COMPLEX, ABA SIGNALING PATHWAY, HORMONE RECEPTOR-HYDROLASE COMPLEX
2z6n:B (ALA86) to (LEU143) CRYSTAL STRUCTURE OF CARBONMONOXY HEMOGLOBIN D FROM THE ALDABRA GIANT TORTOISE, GEOCHELONE GIGANTEA | HEMOGLOBIN D, REPTILIA, THE ALDABRA GIANT TORTOISE, GEOCHELONE GIGANTEA, HEME, IRON, METAL-BINDING, OXYGEN TRANSPORT, TRANSPORT, TRANSPORT PROTEIN
1xq5:A (LEU82) to (GLU139) MET-PERCH HEMOGLOBIN AT 1.9A | FISH HEMOGLOBIN, RAPID OXIDATION, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, PSI, CESG, CENTER FOR EUKARYOTIC STRUCTURAL GENOMICS, OXYGEN STORAGE/TRANSPORT COMPLEX
2zj5:A (GLU411) to (ASN466) ARCHAEAL DNA HELICASE HJM COMPLEXED WITH ADP IN FORM 1 | RECA FOLD, ATP-BINDING, HELICASE, HYDROLASE, NUCLEOTIDE- BINDING
2zlu:A (SER3) to (HIS72) HORSE METHEMOGLOBIN HIGH SALT, PH 7.0 (88% RELATIVE HUMIDITY) | PROTEIN HYDRATION, ALLOSTERIC TRANSITIONS, VARIABILITY IN QUATERNARY STRUCTURE, SOLVENT CONTENT AND CRYSTAL STRUCTURE, WATER-MEDIATED TRANSFORMATION, HEME, IRON, METAL-BINDING, OXYGEN TRANSPORT, POLYMORPHISM, TRANSPORT, OXYGEN STORAGE
5cyi:B (ASN312) to (THR366) CDK2/CYCLIN A COVALENT COMPLEX WITH 6-(CYCLOHEXYLMETHOXY)-N-(4- (VINYLSULFONYL)PHENYL)-9H-PURIN-2-AMINE (NU6300) | CDK2 CYCLIN A COVALENT INHIBITOR VINYLSULPHONE, TRANSFERASE
5cyi:D (ASN312) to (THR366) CDK2/CYCLIN A COVALENT COMPLEX WITH 6-(CYCLOHEXYLMETHOXY)-N-(4- (VINYLSULFONYL)PHENYL)-9H-PURIN-2-AMINE (NU6300) | CDK2 CYCLIN A COVALENT INHIBITOR VINYLSULPHONE, TRANSFERASE
1xxt:D (ALA86) to (ALA142) THE T-TO-T HIGH TRANSITIONS IN HUMAN HEMOGLOBIN: WILD-TYPE DEOXY HB A (LOW SALT, ONE TEST SET) | HEMOGLOBIN TETRAMER, GLOBIN FOLD, TRANSPORT PROTEIN
3khw:B (ILE559) to (ASP605) CRYSTAL STRUCTURE OF THE LARGE C-TERMINAL DOMAIN OF POLYMERASE BASIC PROTEIN 2 FROM INFLUENZA VIRUS A/MEXICO/INDRE4487/2009(H1N1) | STRUCTURAL GENOMICS, PB2 C-TERMINAL DOMAIN, SWINE FLU, H1N1, NIAID, MRNA CAPPING, MRNA PROCESSING, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, SSGCID, VIRAL PROTEIN
2zrt:H (LYS112) to (ASP169) CRYSTAL STRUCTURE OF ZN2+-BOUND FORM OF DES3-23ALG-2 | PENTA-EF-HAND PROTEIN, CALCIUM-BINDING PROTEIN, APOPTOSIS, CALCIUM, ENDOPLASMIC RETICULUM, MEMBRANE, NUCLEUS, POLYMORPHISM
1xz5:D (ALA86) to (ALA142) T-TO-THIGH QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: ALPHAL91A DEOXY LOW-SALT | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1xzu:D (ALA86) to (ALA142) T-TO-THIGH QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: ALPHAD94G DEOXY LOW-SALT | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1xzv:D (ALA86) to (ALA142) T-TO-THIGH QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: ALPHAP95A DEOXY LOW-SALT | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1y09:D (ALA86) to (HIS143) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: ALPHAN97A DEOXY LOW-SALT | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1y0t:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAV1M DEOXY LOW-SALT (1 TEST SET) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1mbx:A (THR81) to (SER139) CRYSTAL STRUCTURE ANALYSIS OF CLPSN WITH TRANSITION METAL ION BOUND | PROTEIN BINDING, ADAPTORS, HSP100/CLP CHAPERONE, AAA+ FAMILY, ATP- DEPENDENT PROTEASE
1y0w:D (ALA86) to (ALA142) T-TO-THIGH QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAV1M DEOXY LOW-SALT (10 TEST SETS) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
3kkc:D (VAL55) to (HIS116) THE CRYSTAL STRUCTURE OF TETR TRANSCRIPTIONAL REGULATOR FROM STREPTOCOCCUS AGALACTIAE 2603V | APC20805, TETR, STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, DNA-BINDING, TRANSCRIPTION, TRANSCRIPTION REGULATION
1y22:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAV33A DEOXY LOW-SALT (1 TEST SET) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1y2z:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAV34G DEOXY LOW-SALT (1 TEST SET) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1y31:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAY35A DEOXY LOW-SALT (1 TEST SET) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1y35:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAY35F DEOXY LOW-SALT (1 TEST SET) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
4ael:A (LEU505) to (CYS562) PDE10A IN COMPLEX WITH THE INHIBITOR AZ5 | HYDROLASE, HIT-TO-LEAD, ENZYME INHIBITOR, NAPHTYRIDINE
4ael:B (LEU505) to (CYS562) PDE10A IN COMPLEX WITH THE INHIBITOR AZ5 | HYDROLASE, HIT-TO-LEAD, ENZYME INHIBITOR, NAPHTYRIDINE
1y45:A (SER81) to (THR137) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAP36A DEOXY LOW-SALT (10 TEST SETS) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1y45:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAP36A DEOXY LOW-SALT (10 TEST SETS) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1y4f:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAW37A DEOXY LOW-SALT (10 TEST SETS) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1y4g:C (SER3) to (HIS72) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAW37G DEOXY LOW-SALT (10 TEST SETS) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1y4g:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAW37G DEOXY LOW-SALT (10 TEST SETS) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
4p15:A (THR81) to (ASN144) STRUCTURE OF THE CLPC N-TERMINAL DOMAIN FROM AN ALKALIPHILIC BACILLUS LEHENSIS G1 SPECIES | HEAT-SHOCK PROTEIN, CLPC, BACILLUS, ALKALOPHILIC, HYDROLASE
1y4q:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAF42A DEOXY LOW-SALT (1 TEST SET) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1y4r:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAF45A DEOXY LOW-SALT (1 TEST SET) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1y4v:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAC93A DEOXY LOW-SALT (1 TEST SET) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1y5f:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAL96A DEOXY LOW-SALT (1 TEST SET) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1y5j:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAH97A DEOXY LOW-SALT (1 TEST SET) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1y7c:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAP100A DEOXY LOW-SALT (1 TEST SET) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1y7d:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAP100G DEOXY LOW-SALT (1 TEST SET) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1y7g:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAN102A DEOXY LOW-SALT (1 TEST SET) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1y7z:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAN108A DEOXY LOW-SALT (1 TEST SET) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1y83:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAY145G DEOXY LOW-SALT (1 TEST SET) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1y8k:C (SER3) to (HIS72) HORSE METHEMOGLOBIN LOW SALT, PH 7.0 (88% RELATIVE HUMIDITY) | AQUO METHEMOGLOBIN, QUARTERNARY ASSOCIATION, ALLOSTERIC TRANSITION, PROTEIN HYDRATION, OXYGEN STORAGE/TRANSPORT COMPLEX
1y8w:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: ALPHAR92A OXY (2MM IHP, 20% PEG) (10 TEST SETS) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1ye0:C (PRO4) to (HIS72) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAV33A OXY (2MM IHP, 20% PEG) (1 TEST SET) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1ye0:D (PHE85) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAV33A OXY (2MM IHP, 20% PEG) (1 TEST SET) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1ye1:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAY35A OXY (2MM IHP, 20% PEG) (1 TEST SET) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1yen:A (SER3) to (HIS72) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAP36A OXY (2MM IHP, 20% PEG) (10 TEST SETS) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1yen:D (ALA86) to (HIS143) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAP36A OXY (2MM IHP, 20% PEG) (10 TEST SETS) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1yeo:A (LEU80) to (THR137) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAW37A OXY (10 TEST SETS) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1yeo:B (PHE85) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAW37A OXY (10 TEST SETS) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1yeq:C (SER3) to (HIS72) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAW37Y OXY (10 TEST SETS) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
3a59:C (LEU80) to (THR137) STRUCTURE OF HEMOGLOBIN FROM FLIGHTLESS BIRD (STRUTHIO CAMELUS) | OSTRICH, STRUTHIO CAMELUS, HEMOGLOBIN, HEME, IRON, METAL- BINDING, OXYGEN TRANSPORT, POLYMORPHISM, TRANSPORT, OXYGEN STORAGE
4ajd:A (LEU505) to (CYS562) IDENTIFICATION AND STRUCTURAL CHARACTERIZATION OF PDE10 FRAGMENT INHIBITORS | HYDROLASE
4ajd:D (LEU505) to (CYS562) IDENTIFICATION AND STRUCTURAL CHARACTERIZATION OF PDE10 FRAGMENT INHIBITORS | HYDROLASE
4ajg:A (GLU504) to (CYS562) IDENTIFICATION AND STRUCTURAL CHARACTERIZATION OF PDE10 FRAGMENT INHIBITORS | HYDROLASE
1yg5:C (SER3) to (HIS72) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAW37H OXY (2MM IHP, 20% PEG) (10 TEST SETS) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1yg5:C (LEU80) to (ARG141) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: BETAW37H OXY (2MM IHP, 20% PEG) (10 TEST SETS) | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
4ajm:A (LEU505) to (CYS562) DEVELOPMENT OF A PLATE-BASED OPTICAL BIOSENSOR METHODOLOGY TO IDENTIFY PDE10 FRAGMENT INHIBITORS | HYDROLASE
4ajm:D (LEU505) to (CYS562) DEVELOPMENT OF A PLATE-BASED OPTICAL BIOSENSOR METHODOLOGY TO IDENTIFY PDE10 FRAGMENT INHIBITORS | HYDROLASE
1yh9:D (PHE85) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: HBA OXY (2MM IHP, 20% PEG) (10 TEST SETS) | HEMOGLOBIN, GLOBIN, TRANSPORT PROTEIN
1yhe:A (LEU80) to (THR137) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: HBA OXY (5.0MM IHP, 20% PEG) (10 TEST SETS) | HEMOGLOBIN, GLOBIN, TRANSPORT PROTEIN
1yhe:D (ALA86) to (ALA142) T-TO-T(HIGH) QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: HBA OXY (5.0MM IHP, 20% PEG) (10 TEST SETS) | HEMOGLOBIN, GLOBIN, TRANSPORT PROTEIN
1mwr:A (GLU29) to (LEU73) STRUCTURE OF SEMET PENICILLIN BINDING PROTEIN 2A FROM METHICILLIN RESISTANT STAPHYLOCOCCUS AUREUS STRAIN 27R (TRIGONAL FORM) AT 2.45 A RESOLUTION. | PENICILLIN BINDING PROTEIN, BETA-LACTAM, D, D- TRANSPEPTIDASE, D-CARBOXYPEPTIDASE, BIOSYNTHETIC PROTEIN
1mwu:B (ASP27) to (LEU73) STRUCTURE OF METHICILLIN ACYL-PENICILLIN BINDING PROTEIN 2A FROM METHICILLIN RESISTANT STAPHYLOCOCCUS AUREUS STRAIN 27R AT 2.60 A RESOLUTION. | PENICILLIN BINDING PROTEIN, BETA-LACTAM, D,D-TRANSPEPTIDASE, D,D- CARBOXYPEPTIDASE, METHICILLIN, BIOSYNTHETIC PROTEIN
5dcs:A (PRO189) to (GLN282) R2-LIKE LIGAND-BINDING OXIDASE WITH AEROBICALLY RECONSTITUTED MN/FE COFACTOR (LONG SOAK) | R2-LIKE LIGAND-BINDING OXIDASE, DIIRON COFACTOR, RIBONUCLEOTIDE REDUCTASE R2 SUBUNIT FOLD, METALLOPROTEIN OXIDOREDUCTASE, OXIDOREDUCTASE
3kz9:C (SER13) to (PRO58) CRYSTAL STRUCTURE OF THE MASTER TRANSCRIPTIONAL REGULATOR, SMCR, IN VIBRIO VULNIFICUS PROVIDES INSIGHT INTO ITS DNA RECOGNITION MECHANISM | VIBRIO VULNIFICUS, SMCR, TRANSCRIPTIONAL REGULATOR, QUORUM SENSING, DNA-BINDING, TRANSCRIPTION REGULATION, TRANSCRIPTION REGULATOR
1n2x:A (ALA164) to (ASN216) CRYSTAL STRUCTURE ANALYSIS OF TM0872, A PUTATIVE SAM- DEPENDENT METHYLTRANSFERASE, COMPLEXED WITH SAM | SAM-DEPENDENT METHYLTRANSFERASE FOLD, PROTEIN-SAM METHYL DONOR COMPLEX, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG
3kzi:V (ARG81) to (LEU152) CRYSTAL STRUCTURE OF MONOMERIC FORM OF CYANOBACTERIAL PHOTOSYSTEM II | ELECTRON TRANSPORT PHOTOSYSTEM, PS II, PS2, MEMBRANE COMPLEX, TRANSMEMBRANE ALPHA-HELIX, IRON, METAL-BINDING, PHOTOSYNTHESIS, PHOTOSYSTEM II, THYLAKOID, HEME, REACTION CENTER, MANGANESE, ELECTRON TRANSPORT
5dh5:B (LEU495) to (CYS552) PDE10 COMPLEXED WITH N-[(1-METHYLPYRAZOL-4-YL)METHYL]-5-[[(1S,2S)-2- (2-PYRIDYL)CYCLOPROPYL]METHOXY]PYRAZOLO[1,5-A]PYRIMIDIN-7-AMINE | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
3aev:A (TYR137) to (TYR170) CRYSTAL STRUCTURE OF A/EIF2ALPHA-ADIM2P-RRNA COMPLEX FROM PYROCOCCUS HORIKOSHII OT3 | PROTEINS-RRNA COMPLEX, 16S RRNA, RNA-BINDING, RNA PROCESSING, INITIATION FACTOR, PROTEIN BIOSYNTHESIS, TRANSLATION-RNA BINDING PROTEIN-RNA COMPLEX
1yzi:A (SER3) to (HIS72) A NOVEL QUATERNARY STRUCTURE OF HUMAN CARBONMONOXY HEMOGLOBIN | HEMOGLOBIN, ALLOSTERIC, QUATERNARY, HIGH AFFINITY, RELAXED, TENSE, OXYGEN STORAGE/TRANSPORT COMPLEX
1zkn:A (PRO325) to (ILE410) STRUCTURE OF PDE4D2-IBMX | PROTEIN-INHIBITOR COMPLEX, INHIBITOR SELECTIVITY, HYDROLASE
4at7:B (ALA218) to (ASN263) CRYSTAL STRUCTURE OF THE NF90-NF45 DIMERISATION DOMAIN COMPLEX | TRANSCRIPTION, DRPB76, NFAR, ILF3, ILF2, TEMPLATE-FREE NUCLEOTIDYLTRANSFERASE FOLD
4at9:A (ASP194) to (VAL253) CRYSTAL STRUCTURE OF THE NF90-NF45 DIMERISATION DOMAIN COMPLEX WITH UTP | IMMUNE SYSTEM, DRPB76, NFAR, ILF3, ILF2, TEMPLATE-FREE NUCLEOTIDYLTRANSFERASE FOLD
4at9:B (ALA218) to (ASN263) CRYSTAL STRUCTURE OF THE NF90-NF45 DIMERISATION DOMAIN COMPLEX WITH UTP | IMMUNE SYSTEM, DRPB76, NFAR, ILF3, ILF2, TEMPLATE-FREE NUCLEOTIDYLTRANSFERASE FOLD
4atb:B (ALA218) to (ALA262) CRYSTAL STRUCTURE OF THE NF90-NF45 DIMERISATION DOMAIN COMPLEX WITH CTP | IMMUNE SYSTEM, TEMPLATE-FREE NUCLEOTIDYL TRANSFERASE FOLD
4atb:D (ALA218) to (ALA262) CRYSTAL STRUCTURE OF THE NF90-NF45 DIMERISATION DOMAIN COMPLEX WITH CTP | IMMUNE SYSTEM, TEMPLATE-FREE NUCLEOTIDYL TRANSFERASE FOLD
4q4j:A (TYR11) to (ARG132) STRUCTURE OF CROSSLINKED TM287/288_S498C_S520C MUTANT | ABC EXPORTER, MULTIDRUG EFFLUX, ABC TRANSPORTER, MEMBRANE TRANSPORTER, HYDROLASE-TRANSPORT PROTEIN COMPLEX
5e29:A (SER81) to (THR137) CRYSTAL STRUCTURE OF DEOXYGENATED HEMOGLOBIN IN COMPLEX WITH AN ALLOSTERIC EFFECTOR AND NITRIC OXIDE | HEMOGLOBIN, RIGHT-SHIFTER, NITRIC OXIDE, OXYGEN TRANSPORT
3aq6:B (THR6) to (GLY59) CRYSTAL STRUCTURE OF TRUNCATED HEMOGLOBIN FROM TETRAHYMENA PYRIFORMIS, FE(III) FORM | 2/2 FOLD HEMOGLOBIN, NITRIC OXIDE DETOXIFICATION, OXYGEN BINDING
5e83:C (SER3) to (HIS72) CRYSTAL STRUCTURE OF CARBONMONOXY HEMOGLOBIN S (LIGANDED SICKLE CELL HEMOGLOBIN) COMPLEXED WITH GBT440, CO-CRYSTALLIZATION EXPERIMENT | MUTANT HUMAN HEMOGLOBIN S[BETAE6V], R2 QUATERNARY STATE, OXYGEN TRANSPORT
5ecf:F (LYS94) to (PHE154) LIGAND BINDING DOMAIN 1 OF PENICILLIUM MARNEFFEI MP1 PROTEIN COMPLEXED WITH ARACHIDONIC ACIDS | LBD1, ARACHIDONIC ACID, LIPID BINDING PROTEIN
5ecf:I (LYS94) to (SER155) LIGAND BINDING DOMAIN 1 OF PENICILLIUM MARNEFFEI MP1 PROTEIN COMPLEXED WITH ARACHIDONIC ACIDS | LBD1, ARACHIDONIC ACID, LIPID BINDING PROTEIN
5edi:B (ARG510) to (CYS562) HUMAN PDE10A, 6-CHLORO-5,8-DIMETHYL-2-[2-(2-METHYL-5-PYRROLIDIN-1-YL- 2H-[1,2,4]TRIAZOL-3-YL)-ETHYL]-[1,2,4]TRIAZOLO[1,5-A]PYRIDINE, 2.20A, H3, RFREE=23.5% | PHOSPHODIESTERASE, PDE10, HYDROLASE
4qg2:D (GLU193) to (ILE272) CRYSTAL STRUCTURE OF THE TETRAMERIC GTP/DATP/ATP-BOUND SAMHD1 (RN206) MUTANT CATALYTIC CORE | DEOXYNUCLEOSIDE TRIPHOSPHATE TRIPHOSPHOHYDROLASE, 2'-DEOXYADENOSINE- 5'-TRIPHOSPHATE, GUANOSINE-5'-TRIPHOSPHATE, HIV RESTRICTION FACTOR, DNTPASE, HYDROLASE
5ee4:C (SER3) to (HIS72) THE CRYSTAL STRUCTURE OF HPUA FROM KINGELLA DENITRIFICANS IN COMPLEX WITH HUMAN HAEMOGLOBIN | OUTER MEMBRANE, RECEPTOR, BETA BARREL, METAL TRANSPORT
4qko:G (LYS4) to (GLY80) THE CRYSTAL STRUCTURE OF THE PYOCIN S2 NUCLEASE DOMAIN, IMMUNITY PROTEIN COMPLEX AT 1.8 ANGSTROMS | HNH NUCLEASE DOMAIN, COLICIN NUCLEASE IMMUNITY PROTEIN COMPLEX, BACTERIOCIN, BACTERIAL CYTOTOXIN, ANTIMICROBIAL PROTEIN
3b75:D (ALA86) to (HIS143) CRYSTAL STRUCTURE OF GLYCATED HUMAN HAEMOGLOBIN | HEMOGLOBIN, GLYCATION, R STATE, R2 STATE, ACETYLATION, DISEASE MUTATION, GLYCOPROTEIN, HEME, IRON, METAL-BINDING, OXYGEN TRANSPORT, POLYMORPHISM, TRANSPORT, HYPOTENSIVE AGENT, PYRUVATE, S-NITROSYLATION, VASOACTIVE, TRANSPORT PROTEIN, OXYGEN BINDING
3b75:S (SER81) to (VAL135) CRYSTAL STRUCTURE OF GLYCATED HUMAN HAEMOGLOBIN | HEMOGLOBIN, GLYCATION, R STATE, R2 STATE, ACETYLATION, DISEASE MUTATION, GLYCOPROTEIN, HEME, IRON, METAL-BINDING, OXYGEN TRANSPORT, POLYMORPHISM, TRANSPORT, HYPOTENSIVE AGENT, PYRUVATE, S-NITROSYLATION, VASOACTIVE, TRANSPORT PROTEIN, OXYGEN BINDING
3md2:A (THR108) to (ASP156) CRYSTAL STRUCTURE OF THE MATRIX PROTEIN 1 FROM INFLUENZA A VIRUS (A/CALIFORNIA/04/2009 (H1N1)) | SWINE FLU, H1N1, INFLUENZA A VIRUS, M1, VIRAL PROTEIN
3md2:B (THR108) to (ASP156) CRYSTAL STRUCTURE OF THE MATRIX PROTEIN 1 FROM INFLUENZA A VIRUS (A/CALIFORNIA/04/2009 (H1N1)) | SWINE FLU, H1N1, INFLUENZA A VIRUS, M1, VIRAL PROTEIN
3md2:C (THR108) to (ASP156) CRYSTAL STRUCTURE OF THE MATRIX PROTEIN 1 FROM INFLUENZA A VIRUS (A/CALIFORNIA/04/2009 (H1N1)) | SWINE FLU, H1N1, INFLUENZA A VIRUS, M1, VIRAL PROTEIN
3md2:D (THR108) to (ASP156) CRYSTAL STRUCTURE OF THE MATRIX PROTEIN 1 FROM INFLUENZA A VIRUS (A/CALIFORNIA/04/2009 (H1N1)) | SWINE FLU, H1N1, INFLUENZA A VIRUS, M1, VIRAL PROTEIN
4bbr:B (VAL283) to (PHE322) STRUCTURE OF RNA POLYMERASE II-TFIIB COMPLEX | TRANSCRIPTION, RNA POLYMERASE, TFIIB
4bbx:A (GLU494) to (CYS552) DISCOVERY OF A POTENT, SELECTIVE AND ORALLY ACTIVE PDE10A INHIBITOR FOR THE TREATMENT OF SCHIZOPHRENIA | PHOSPHODIESTERASE INHIBITOR, INHIBITOR COMPLEX, HYDROLASE, ZINC BINDING, MAGNESIUM BINDING
4bcn:B (ASN312) to (GLY369) STRUCTURE OF CDK2 IN COMPLEX WITH CYCLIN A AND A 2-AMINO-4- HETEROARYL-PYRIMIDINE INHIBITOR | TRANSFERASE-CELL CYCLE COMPLEX, CDK-CYCLIN COMPLEX, CYCLIN-INHIBITOR, STRUCTURE-BASED DRUG DESIGN
4bcn:D (THR310) to (VAL367) STRUCTURE OF CDK2 IN COMPLEX WITH CYCLIN A AND A 2-AMINO-4- HETEROARYL-PYRIMIDINE INHIBITOR | TRANSFERASE-CELL CYCLE COMPLEX, CDK-CYCLIN COMPLEX, CYCLIN-INHIBITOR, STRUCTURE-BASED DRUG DESIGN
4bcp:B (THR310) to (GLY369) STRUCTURE OF CDK2 IN COMPLEX WITH CYCLIN A AND A 2-AMINO-4- HETEROARYL-PYRIMIDINE INHIBITOR | TRANSFERASE-CELL CYCLE COMPLEX, CDK-CYCLIN COMPLEX, CYCLIN-INHIBITOR, STRUCTURE-BASED DRUG DESIGN
4bcp:D (THR310) to (THR366) STRUCTURE OF CDK2 IN COMPLEX WITH CYCLIN A AND A 2-AMINO-4- HETEROARYL-PYRIMIDINE INHIBITOR | TRANSFERASE-CELL CYCLE COMPLEX, CDK-CYCLIN COMPLEX, CYCLIN-INHIBITOR, STRUCTURE-BASED DRUG DESIGN
4bcq:B (THR310) to (THR368) STRUCTURE OF CDK2 IN COMPLEX WITH CYCLIN A AND A 2-AMINO-4- HETEROARYL-PYRIMIDINE INHIBITOR | TRANSFERASE-CELL CYCLE COMPLEX, CDK-CYCLIN COMPLEX, CYCLIN A, CYCLIN- DEPENDENT KINASE 2, STRUCTURE-BASED DRUG DESIGN
4bcq:D (THR310) to (VAL367) STRUCTURE OF CDK2 IN COMPLEX WITH CYCLIN A AND A 2-AMINO-4- HETEROARYL-PYRIMIDINE INHIBITOR | TRANSFERASE-CELL CYCLE COMPLEX, CDK-CYCLIN COMPLEX, CYCLIN A, CYCLIN- DEPENDENT KINASE 2, STRUCTURE-BASED DRUG DESIGN
4bgd:A (LEU916) to (GLU985) CRYSTAL STRUCTURE OF BRR2 IN COMPLEX WITH THE JAB1/MPN DOMAIN OF PRP8 | TRANSCRIPTION, SPLICEOSOME, RNA HELICASE, U5 SNRNP, RETINITIS PIGMENTOSA
3bht:B (THR310) to (GLY369) STRUCTURE OF PHOSPHORYLATED THR160 CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR MERIOLIN 3 | SER/THR PROTEIN KINASE, TRANSFERASE, PHOSPHORYLATION, CELL CYCLE, ATP-BINDING, CELL DIVISION, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, CYCLIN
3bht:D (THR310) to (GLY369) STRUCTURE OF PHOSPHORYLATED THR160 CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR MERIOLIN 3 | SER/THR PROTEIN KINASE, TRANSFERASE, PHOSPHORYLATION, CELL CYCLE, ATP-BINDING, CELL DIVISION, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, CYCLIN
5eui:A (LEU80) to (SER138) STRUCTURE OF PREDICTED ANCESTRAL PIKA HEMOGLOBIN | HEMOGLOBIN, PIKA, OXYGEN-TRANSPORT, RECOMBINANT, OXYGEN TRANSPORT
3mqt:P (ASN65) to (LEU117) CRYSTAL STRUCTURE OF A MANDELATE RACEMASE/MUCONATE LACTONIZING ENZYME FROM SHEWANELLA PEALEANA | PSI-II, NYSGXRC, MANDELATE RACEMASE, MUCONATE LACTONIZING ENZYME, STRUCTURAL GENOMICS, PROTEIN STRUCTURE INITIATIVE, NEW YORK SGX RESEARCH CENTER FOR STRUCTURAL GENOMICS, ISOMERASE
3bj1:A (LEU82) to (GLU139) MET-PERCH HEMOGLOBIN AT PH 5.7 | HEMOGLOBIN, AUTOOXIDATION, HEME LOSS, OXYGEN STORAGE/TRANSPORT, OXYGEN BINDING
3bj1:C (LEU82) to (GLU139) MET-PERCH HEMOGLOBIN AT PH 5.7 | HEMOGLOBIN, AUTOOXIDATION, HEME LOSS, OXYGEN STORAGE/TRANSPORT, OXYGEN BINDING
3bj2:A (LEU82) to (GLU139) MET-PERCH HEMOGLOBIN AT PH 6.3 | HEMOGLOBIN, AUTOOXIDATION, HEME LOSS, OXYGEN STORAGE/TRANSPORT, OXYGEN BINDING
3bj2:C (LEU82) to (GLU139) MET-PERCH HEMOGLOBIN AT PH 6.3 | HEMOGLOBIN, AUTOOXIDATION, HEME LOSS, OXYGEN STORAGE/TRANSPORT, OXYGEN BINDING
3bj3:C (LEU82) to (GLU139) MET-PERCH HEMOGLOBIN AT PH 8.0 | HEMOGLOBIN, AUTOOXIDATION, HEME LOSS, OXYGEN STORAGE/TRANSPORT, OXYGEN BINDING
4bl2:B (ASP27) to (LEU73) CRYSTAL STRUCTURE OF PBP2A CLINICAL MUTANT E150K FROM MRSA | HYDROLASE, PENICILLIN BINDING PROTEINS, B-LACTUM ANTIBIOTICS
5exd:F (LYS235) to (VAL303) CRYSTAL STRUCTURE OF OXALATE OXIDOREDUCTASE FROM MOORELLA THERMOACETICA BOUND WITH CARBOXY-DI-OXIDO-METHYL-TPP (COOM-TPP) INTERMEDIATE | OXALATE, OXIDOREDUCTASE, OFOR, THIAMINE
3bom:A (THR82) to (ALA138) CRYSTAL STRUCTURE OF TROUT HEMOGLOBIN AT 1.35 ANGSTROM RESOLUTION | FISH HEMOGLOBIN, STRUCTURAL GENOMICS COMMUNITY REQUEST, PROTEIN STRUCTURE INITIATIVE, PSI-2, CENTER FOR EUKARYOTIC STRUCTURAL GENOMICS, CESG, HEME, IRON, METAL-BINDING, OXYGEN TRANSPORT, TRANSPORT, OXYGEN STORAGE/TRANSPORT, OXYGEN STORAGE-TRANSPORT COMPLEX
3bom:B (VAL86) to (GLY143) CRYSTAL STRUCTURE OF TROUT HEMOGLOBIN AT 1.35 ANGSTROM RESOLUTION | FISH HEMOGLOBIN, STRUCTURAL GENOMICS COMMUNITY REQUEST, PROTEIN STRUCTURE INITIATIVE, PSI-2, CENTER FOR EUKARYOTIC STRUCTURAL GENOMICS, CESG, HEME, IRON, METAL-BINDING, OXYGEN TRANSPORT, TRANSPORT, OXYGEN STORAGE/TRANSPORT, OXYGEN STORAGE-TRANSPORT COMPLEX
3bom:D (VAL86) to (ARG144) CRYSTAL STRUCTURE OF TROUT HEMOGLOBIN AT 1.35 ANGSTROM RESOLUTION | FISH HEMOGLOBIN, STRUCTURAL GENOMICS COMMUNITY REQUEST, PROTEIN STRUCTURE INITIATIVE, PSI-2, CENTER FOR EUKARYOTIC STRUCTURAL GENOMICS, CESG, HEME, IRON, METAL-BINDING, OXYGEN TRANSPORT, TRANSPORT, OXYGEN STORAGE/TRANSPORT, OXYGEN STORAGE-TRANSPORT COMPLEX
3bqi:A (ALA1500) to (PHE1555) STRUCTURE OF A CHONDROITIN SULPHATE BINDING DBL3X FROM A VAR2CSA ENCODED PFEMP1 PROTEIN | MALARIA, PREGNANCY, PFEMP1, VAR2CSA, DBL3X, CHONDROITIN SULPHATE, CELL ADHESION
3bqk:A (LYS1515) to (ASN1556) STRUCTURE OF A CHONDROITIN SULPHATE BINDING DBL3X FROM A VAR2CSA ENCODED PFEMP1 PROTEIN IN COMPLEX WITH SULPHATE | MALARIA, PREGNANCY, VAR2CSA ENCODED PFEMP1 PROTEIN, DBL3X DOMAIN, CHONDROITIN SULPHATE A, CELL ADHESION
3br2:A (THR109) to (SER187) CRYSTAL STRUCTURE OF THE COMPLEX OF DEQUALINIUM BOUND TO QACR(E120Q), A MUTANT OF A MULTIDRUG BINDING TRANSCRIPTIONAL REPRESSOR | QACR, MULTIDRUG RESISTANCE, TETR, DEQUALINIUM, DNA-BINDING, PLASMID, REPRESSOR, TRANSCRIPTION, TRANSCRIPTION REGULATION
3btj:A (THR109) to (SER187) CRYSTAL STRUCTURE OF QACR(E58Q) BOUND TO DEQUALINIUM | QACR, MULTIDRUG BINDING, DEQUALINIUM, BIVALENT DRUG, DNA- BINDING, PLASMID, REPRESSOR, TRANSCRIPTION, TRANSCRIPTION REGULATION
3my5:B (ASN312) to (GLY369) CDK2/CYCLINA IN COMPLEX WITH DRB | CDK, CYCLIN, INHIBITOR, DRB, TRANSFERASE-PROTEIN BINDING-INHIBITOR COMPLEX
3my5:D (THR310) to (VAL367) CDK2/CYCLINA IN COMPLEX WITH DRB | CDK, CYCLIN, INHIBITOR, DRB, TRANSFERASE-PROTEIN BINDING-INHIBITOR COMPLEX
4r6i:A (ASN335) to (ASN390) ATXA PROTEIN, A VIRULENCE REGULATOR FROM BACILLUS ANTHRACIS. | STRUCTURAL GENOMICS, IDP01169, ATXA, TRANSCRIPTIONAL ACTIVATOR, VIRULENCE REGULATOR, DNA BINDING, NIAID, NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID, TRANSCRIPTION
4r6i:B (ASN335) to (LYS388) ATXA PROTEIN, A VIRULENCE REGULATOR FROM BACILLUS ANTHRACIS. | STRUCTURAL GENOMICS, IDP01169, ATXA, TRANSCRIPTIONAL ACTIVATOR, VIRULENCE REGULATOR, DNA BINDING, NIAID, NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES, CSGID, TRANSCRIPTION
4bzb:D (VAL378) to (TYR432) CRYSTAL STRUCTURE OF THE TETRAMERIC DGTP-BOUND SAMHD1 MUTANT CATALYTIC CORE | HYDROLASE, HIV RESTRICTION FACTOR, DNTPASE
4c0a:A (LEU482) to (SER546) ARF1(DELTA1-17)IN COMPLEX WITH BRAG2 SEC7-PH DOMAIN | PROTEIN TRANSPORT, ENDOCYTOSIS
4c0a:B (LEU482) to (SER546) ARF1(DELTA1-17)IN COMPLEX WITH BRAG2 SEC7-PH DOMAIN | PROTEIN TRANSPORT, ENDOCYTOSIS
4c0a:E (LEU482) to (SER546) ARF1(DELTA1-17)IN COMPLEX WITH BRAG2 SEC7-PH DOMAIN | PROTEIN TRANSPORT, ENDOCYTOSIS
4c0a:F (LEU482) to (SER546) ARF1(DELTA1-17)IN COMPLEX WITH BRAG2 SEC7-PH DOMAIN | PROTEIN TRANSPORT, ENDOCYTOSIS
4r8z:A (LEU155) to (HIS220) CRYSTAL STRUCTURE OF PA4781 HD-GYP DOMAIN FROM PSEUDOMONAS AERUGINOSA AT 2.2A RESOLUTION SHOWING A BI-METALLIC NI ION CENTER | BIMETALLIC, C-DI-GMP, PDE, PHOSPHDIESTERASE, CYCLIC-DI-GMP, BIOFILM, HYDROLASE
4c0z:L (THR87) to (SER147) THE N-TERMINAL DOMAIN OF THE STREPTOCOCCUS PYOGENES PILUS TIP ADHESIN CPA | CELL ADHESION, THIOESTER-DOMAIN, PILUS
4c1i:B (CYS636) to (CYS695) SELECTIVE INHIBITORS OF PDE2, PDE9, AND PDE10: MODULATORS OF ACTIVITY OF THE CENTRAL NERVOUS SYSTEM | HYDROLASE, HYDROLASE INHIBITOR COMPLEX
3cml:A (GLY1499) to (PHE1555) CRYSTAL STRUCTURE OF THE DBL3X DOMAIN OF THE PLASMODIUM FALCIPURUM VAR2CSA PROTEIN | DBL3X, VAR2CSA, CHONDROITIN-SULFATE BINDING DOMAIN, MEMBRANE PROTEIN
4cad:I (SER123) to (ARG217) MECHANISM OF FARNESYLATED CAAX PROTEIN PROCESSING BY THE INTEGRAL MEMBRANE PROTEASE RCE1 | PROTEIN BINDING, INTEGRAL MEMBRANE PROTEASE, MONOCLONAL ANTIBODY FAB FRAGMENT
4cei:B (ALA823) to (ALA906) CRYSTAL STRUCTURE OF ADPNP-BOUND ADDAB WITH A FORKED DNA SUBSTRATE | HYDROLASE-DNA COMPLEX, HELICASE-NUCLEASE, BACTERIAL PROTEINS, BINDING SITES, DNA BREAKS, DOUBLE-STRANDED, DNA HELICASES, DNA REPAIR, SINGLE-STRANDED, DNA- BINDING PROTEINS, DEOXYRIBONUCLEASES, EXODEOXYRIBONUCLEASE V, EXODEOXYRIBONUCLEASES, HOMOLOGOUS RECOMBINATION
4cfm:B (ASN312) to (GLY369) STRUCTURE-BASED DESIGN OF C8-SUBSTITUTED O6- CYCLOHEXYLMETHOXYGUANINE CDK1 AND 2 INHIBITORS. | CELL CYCLE, CYCLIN DEPENDENT KINASES, STRUCTURE-BASED DRUG DESIGN, CONFORMATIONAL RESTRAINT, REVERSED BINDING MODE
4cfm:D (ASN312) to (GLY369) STRUCTURE-BASED DESIGN OF C8-SUBSTITUTED O6- CYCLOHEXYLMETHOXYGUANINE CDK1 AND 2 INHIBITORS. | CELL CYCLE, CYCLIN DEPENDENT KINASES, STRUCTURE-BASED DRUG DESIGN, CONFORMATIONAL RESTRAINT, REVERSED BINDING MODE
4cfn:B (THR310) to (GLY369) STRUCTURE-BASED DESIGN OF C8-SUBSTITUTED O6-CYCLOHEXYLMETHOXYGUANINE CDK1 AND 2 INHIBITORS. | CELL CYCLE, CYCLIN DEPENDENT KINASES, STRUCTURE-BASED DRUG DESIGN, CONFORMATIONAL RESTRAINT, REVERSED BINDING MODE
4cfn:D (ASN312) to (THR366) STRUCTURE-BASED DESIGN OF C8-SUBSTITUTED O6-CYCLOHEXYLMETHOXYGUANINE CDK1 AND 2 INHIBITORS. | CELL CYCLE, CYCLIN DEPENDENT KINASES, STRUCTURE-BASED DRUG DESIGN, CONFORMATIONAL RESTRAINT, REVERSED BINDING MODE
4cfv:B (ASN312) to (THR366) STRUCTURE-BASED DESIGN OF C8-SUBSTITUTED O6- CYCLOHEXYLMETHOXYGUANINE CDK1 AND 2 INHIBITORS. | TRANSFERASE, CYCLIN DEPENDENT KINASES, STRUCTURE-BASED DRUG DESIGN, CONFORMATIONAL RESTRAINT, REVERSED BINDING MODE
4cfv:D (THR310) to (THR366) STRUCTURE-BASED DESIGN OF C8-SUBSTITUTED O6- CYCLOHEXYLMETHOXYGUANINE CDK1 AND 2 INHIBITORS. | TRANSFERASE, CYCLIN DEPENDENT KINASES, STRUCTURE-BASED DRUG DESIGN, CONFORMATIONAL RESTRAINT, REVERSED BINDING MODE
4cfw:B (ASN312) to (GLY369) STRUCTURE-BASED DESIGN OF C8-SUBSTITUTED O6- CYCLOHEXYLMETHOXYGUANINE CDK1 AND 2 INHIBITORS. | CELL CYCLE, STRUCTURE-BASED DRUG DESIGN, CONFORMATIONAL RESTRAINT, REVERSED BINDING MODE
4cfw:D (ASN312) to (GLY369) STRUCTURE-BASED DESIGN OF C8-SUBSTITUTED O6- CYCLOHEXYLMETHOXYGUANINE CDK1 AND 2 INHIBITORS. | CELL CYCLE, STRUCTURE-BASED DRUG DESIGN, CONFORMATIONAL RESTRAINT, REVERSED BINDING MODE
4cfx:B (ASN312) to (THR368) STRUCTURE-BASED DESIGN OF C8-SUBSTITUTED O6-CYCLOHEXYLMETHOXYGUANINE CDK1 AND 2 INHIBITORS. | CELL CYCLE, STRUCTURE-BASED DRUG DESIGN, CONFORMATIONAL RESTRAINT, REVERSED BINDING MODE
4cfx:D (VAL311) to (VAL367) STRUCTURE-BASED DESIGN OF C8-SUBSTITUTED O6-CYCLOHEXYLMETHOXYGUANINE CDK1 AND 2 INHIBITORS. | CELL CYCLE, STRUCTURE-BASED DRUG DESIGN, CONFORMATIONAL RESTRAINT, REVERSED BINDING MODE
4cjn:B (ASP27) to (LEU73) CRYSTAL STRUCTURE OF PBP2A FROM MRSA IN COMPLEX WITH QUINAZOLINONE LIGAND | HYDROLASE, IMMUNE SYSTEM, ALLOSTERIC SITE
3cuz:A (ALA448) to (ILE514) ATOMIC RESOLUTION STRUCTURES OF ESCHERICHIA COLI AND BACILLIS ANTHRACIS MALATE SYNTHASE A: COMPARISON WITH ISOFORM G AND IMPLICATIONS FOR STRUCTURE BASED DRUG DESIGN | MALATE SYNTHASE, TIM BARREL, CYTOPLASM, GLYOXYLATE BYPASS, TRANSFERASE, TRICARBOXYLIC ACID CYCLE
3cv2:A (ALA448) to (SER517) ATOMIC RESOLUTION STRUCTURES OF ESCHERICHIA COLI AND BACILLIS ANTHRACIS MALATE SYNTHASE A: COMPARISON WITH ISOFORM G AND IMPLICATIONS FOR STRUCTURE BASED DRUG DESIGN | MALATE SYNTHASE, TIM BARREL, CYTOPLASM, GLYOXYLATE BYPASS, TRANSFERASE, TRICARBOXYLIC ACID CYCLE
3cv2:B (ALA448) to (SER517) ATOMIC RESOLUTION STRUCTURES OF ESCHERICHIA COLI AND BACILLIS ANTHRACIS MALATE SYNTHASE A: COMPARISON WITH ISOFORM G AND IMPLICATIONS FOR STRUCTURE BASED DRUG DESIGN | MALATE SYNTHASE, TIM BARREL, CYTOPLASM, GLYOXYLATE BYPASS, TRANSFERASE, TRICARBOXYLIC ACID CYCLE
3d17:A (SER3) to (ALA71) A TRIPLY LIGATED CRYSTAL STRUCTURE OF RELAXED STATE HUMAN HEMOGLOBIN | LIGANDED, RELAXED, TRIPLY LIGATED, LIGAND UPTAKE, LIGAND CHANNEL, ACETYLATION, DISEASE MUTATION, GLYCATION, GLYCOPROTEIN, HEME, IRON, METAL-BINDING, OXYGEN TRANSPORT, POLYMORPHISM, TRANSPORT, HYPOTENSIVE AGENT, PYRUVATE, S- NITROSYLATION, VASOACTIVE, OXYGEN BINDING
3d1k:A (LEU81) to (GLU139) R/T INTERMEDIATE QUATERNARY STRUCTURE OF AN ANTARCTIC FISH HEMOGLOBIN IN AN ALPHA(CO)-BETA(PENTACOORDINATE) STATE | ANTARCTIC FISH HEMOGLOBIN, INTERMEDIATE R/T QUATERNARY STRUCTURE, OXIDATION PATHWAY, HEME, IRON, METAL-BINDING, OXYGEN TRANSPORT, TRANSPORT, ACETYLATION, OXYGEN BINDING
4cpk:B (LYS28) to (LEU73) CRYSTAL STRUCTURE OF PBP2A DOUBLE CLINICAL MUTANT N146K- E150K FROM MRSA | HYDROLASE, PENICILLIN-BINDING PROTEIN, MRSA, ALLOSTERIC SITE
3d3m:B (LEU730) to (VAL784) THE CRYSTAL STRUCTURE OF THE C-TERMINAL REGION OF DEATH ASSOCIATED PROTEIN 5(DAP5) | HEAT REPEAT DOMAIN, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, ISRAEL STRUCTURAL PROTEOMICS CENTER, ISPC, ACETYLATION, INITIATION FACTOR, PHOSPHOPROTEIN, PROTEIN BIOSYNTHESIS, REPRESSOR, TRANSLATION REGULATION
3odq:A (SER3) to (HIS72) STRUCTURE OF A CRYSTAL FORM OF HUMAN METHEMOGLOBIN INDICATIVE OF FIBER FORMATION | STRUCTURAL GENOMICS, PSI-2, PROTEIN STRUCTURE INITIATIVE, CENTER FOR HIGH-THROUGHPUT STRUCTURAL BIOLOGY, CHTSB, OXYGEN TRANSPORT, OXYGEN BINDING, HEME GROUP, RED BLOOD CELLS
3dhr:G (SER3) to (HIS72) CRYSTAL STRUCTURE DETERMINATION OF METHEMOGLOBIN FROM PIGEON AT 2 ANGSTROM RESOLUTION (COLUMBA LIVIA) | AVIAN HEMOGLOBIN, METHEMOGLOBIN, TRICLINIC, HEME, IRON, METAL-BINDING, OXYGEN TRANSPORT, TRANSPORT, OXYGEN STORAGE
3dhr:G (LEU80) to (THR137) CRYSTAL STRUCTURE DETERMINATION OF METHEMOGLOBIN FROM PIGEON AT 2 ANGSTROM RESOLUTION (COLUMBA LIVIA) | AVIAN HEMOGLOBIN, METHEMOGLOBIN, TRICLINIC, HEME, IRON, METAL-BINDING, OXYGEN TRANSPORT, TRANSPORT, OXYGEN STORAGE
3dhw:F (LYS51) to (ILE115) CRYSTAL STRUCTURE OF METHIONINE IMPORTER METNI | ABC-TRANSPORTER, METHIONINE UPTAKE TRANSPORTER, MEMBRANE PROTEIN, AMINO-ACID TRANSPORT, INNER MEMBRANE, TRANSMEMBRANE, ATP-BINDING, HYDROLASE, NUCLEOTIDE-BINDING, MEMBRANE PROTEIN-HYDROLASE COMPLEX
3oo5:A (SER81) to (LEU136) R-STATE HUMAN HEMOGLOBIN: NITRIHEME MODIFIED | NITRITE, R-STATE HUMAN HEMOGLOBIN, NITRIHEME, OXYGEN TRANSPORT
3dog:B (THR310) to (GLY369) STRUCTURE OF THR 160 PHOSPHORYLATED CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR N-&-N1 | SER/THR PROTEIN KINASE; TRANSFERASE; PHOSPHORYLATION; CELL CYCLE, ATP-BINDING, CELL CYCLE, CELL DIVISION, KINASE, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, CYCLIN, CYTOPLASM, NUCLEUS
3dog:D (THR310) to (GLY369) STRUCTURE OF THR 160 PHOSPHORYLATED CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR N-&-N1 | SER/THR PROTEIN KINASE; TRANSFERASE; PHOSPHORYLATION; CELL CYCLE, ATP-BINDING, CELL CYCLE, CELL DIVISION, KINASE, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, CYCLIN, CYTOPLASM, NUCLEUS
4tz0:A (GLU509) to (ASN564) DEAD-BOX HELICASE MSS116 BOUND TO SSRNA AND GDP-BEF | DEAD-BOX, RNA HELICASE, HYDROLASE, RNA BINDING PROTEIN-RNA COMPLEX
4tz6:A (GLU509) to (ASN564) DEAD-BOX HELICASE MSS116 BOUND TO SSRNA AND UDP-BEF | DEAD-BOX, RNA HELICASE, HYDROLASE, RNA BINDING PROTEIN-RNA COMPLEX
4dmv:A (ASN410) to (GLN454) CRYSTAL STRUCTURE OF THE GT DOMAIN OF CLOSTRIDIUM DIFFICILE TOXIN A | TRANSFERASE
3e3j:C (GLU42) to (ASP130) CRYSTAL STRUCTURE OF AN INTERMEDIATE COMPLEX OF T7 RNAP AND 8NT OF RNA | T7 RNA POLYMERASE, DNA-DIRECTED RNA POLYMERASE, TRANSCRIPTION, NUCLEOTIDYLTRANSFERASE, TRANSFERASE, TRANSFERASE/RNA/DNA COMPLEX
3e3j:B (GLU42) to (ASP130) CRYSTAL STRUCTURE OF AN INTERMEDIATE COMPLEX OF T7 RNAP AND 8NT OF RNA | T7 RNA POLYMERASE, DNA-DIRECTED RNA POLYMERASE, TRANSCRIPTION, NUCLEOTIDYLTRANSFERASE, TRANSFERASE, TRANSFERASE/RNA/DNA COMPLEX
5hss:B (PHE50) to (CYS101) LINALOOL DEHYDRATASE/ISOMERASE: LDI WITH MONOTERPENE SUBSTRATE | LINALOOL DEHYDRATASE/ISOMERASE, ALPHA6 ALPHA6 BARREL FOLD, MYRCENE, GERANIOL, LYASE
5hss:E (PHE50) to (MET99) LINALOOL DEHYDRATASE/ISOMERASE: LDI WITH MONOTERPENE SUBSTRATE | LINALOOL DEHYDRATASE/ISOMERASE, ALPHA6 ALPHA6 BARREL FOLD, MYRCENE, GERANIOL, LYASE
5hu6:A (SER4) to (HIS73) STRUCTURE OF THE T. BRUCEI HAPTOGLOBIN-HAEMOGLOBIN RECEPTOR BOUND TO HUMAN HAPTOLGOBIN-HAEMOGLOBIN | TRYPANOSOME HAPTOGLOBIN-HAEMOGLOBIN, TRANSPORT PROTEIN
4ubl:A (GLU351) to (HIS435) KINETIC CRYSTALLOGRAPHY OF ALPHA_E7-CARBOXYLESTERSE FROM LUCILLA CUPRINA - ABSORBED X-RAY DOSE 9.26 MGY | ALPHA/BETA HYDROLASE FOLD, CARBOXYLESTERASE, HYDROLASE
3phw:C (CYS40) to (SER95) OTU DOMAIN OF CRIMEAN CONGO HEMORRHAGIC FEVER VIRUS IN COMPLEX WITH UBIQUITIN | OTU DOMAIN, DE-UBIQUITINASE, DE-ISGYLASE, HYDROLASE-RIBOSOMAL PROTEIN COMPLEX
5if1:B (VAL311) to (GLY369) CRYSTAL STRUCTURE APO CDK2/CYCLIN A | ANTINEOPLASTIC AGENTS, CYCLIN-DEPENDENT KINASES, DOSE-RESPONSE RELATIONSHIP, DRUG, DRUG DISCOVERY, HELA CELLS, MOLECULAR STRUCTURE, NEOPLASMS, PROTEIN KINASE INHIBITORS, PYRIMIDINES, STRUCTURE- ACTIVITY RELATIONSHIP, STRUCTURE-KINETICS RELATIONSHIP, SULFOXIDES, BIOPHYSICAL ASSAYS, TUMOR, HUMANS, TRANSFERASE
5if1:D (VAL311) to (VAL367) CRYSTAL STRUCTURE APO CDK2/CYCLIN A | ANTINEOPLASTIC AGENTS, CYCLIN-DEPENDENT KINASES, DOSE-RESPONSE RELATIONSHIP, DRUG, DRUG DISCOVERY, HELA CELLS, MOLECULAR STRUCTURE, NEOPLASMS, PROTEIN KINASE INHIBITORS, PYRIMIDINES, STRUCTURE- ACTIVITY RELATIONSHIP, STRUCTURE-KINETICS RELATIONSHIP, SULFOXIDES, BIOPHYSICAL ASSAYS, TUMOR, HUMANS, TRANSFERASE
4usc:B (ALA14) to (ALA90) CRYSTAL STRUCTURE OF PEROXIDASE FROM PALM TREE CHAMAEROPS EXCELSA | OXIDOREDUCTASE, PLANT PEROXIDASE, GLYCOSYLATION
4e99:A (GLU17) to (THR76) HUMAN SERUM ALBUMIN COMPLEX WITH PERFLUOROOCTANE SULFONATE POTASSIUM | PLASMA PROTEIN, TRANSPORTER, DRUG BINDING, EXTRACELLULAR, TRANSPORT PROTEIN
4uur:A (THR23) to (GLY78) COLD-ADAPTED TRUNCATED HEMOGLOBIN FROM THE ANTARCTIC MARINE BACTERIUM PSEUDOALTEROMONAS HALOPLANKTIS TAC125 | OXIDOREDUCTASE
4eoi:B (THR310) to (THR366) THR 160 PHOSPHORYLATED CDK2 K89D, Q131E - HUMAN CYCLIN A3 COMPLEX WITH THE INHIBITOR RO3306 | PROTEIN KINASE, CELL CYCLE, PHOSPHORYLATION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4eoj:B (THR310) to (THR366) THR 160 PHOSPHORYLATED CDK2 H84S, Q85M, K89D - HUMAN CYCLIN A3 COMPLEX WITH ATP | PROTEIN KINASE, CELL CYCLE, COMPLEX, PHOSPHORYLATION, TRANSFERASE
4eok:B (THR310) to (THR366) THR 160 PHOSPHORYLATED CDK2 H84S, Q85M, K89D - HUMAN CYCLIN A3 COMPLEX WITH THE INHIBITOR NU6102 | PROTEIN KINASE, CELL CYCLE, PHOSPHORYLATION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4eol:B (THR310) to (GLY369) THR 160 PHOSPHORYLATED CDK2 H84S, Q85M, K89D - HUMAN CYCLIN A3 COMPLEX WITH THE INHIBITOR RO3306 | PROTEIN KINASE, CELL CYCLE, PHOSPHORYLATION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4eol:D (THR310) to (GLY369) THR 160 PHOSPHORYLATED CDK2 H84S, Q85M, K89D - HUMAN CYCLIN A3 COMPLEX WITH THE INHIBITOR RO3306 | PROTEIN KINASE, CELL CYCLE, PHOSPHORYLATION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4eom:B (THR310) to (GLY369) THR 160 PHOSPHORYLATED CDK2 H84S, Q85M, Q131E - HUMAN CYCLIN A3 COMPLEX WITH ATP | PROTEIN KINASE, CELL CYCLE, COMPLEX, PHOSPHORYLATION, TRANSFERASE
4eom:D (THR310) to (GLY369) THR 160 PHOSPHORYLATED CDK2 H84S, Q85M, Q131E - HUMAN CYCLIN A3 COMPLEX WITH ATP | PROTEIN KINASE, CELL CYCLE, COMPLEX, PHOSPHORYLATION, TRANSFERASE
4eoo:B (THR310) to (GLY369) THR 160 PHOSPHORYLATED CDK2 Q131E - HUMAN CYCLIN A3 COMPLEX WITH ATP | PROTEIN KINASE, CELL CYCLE, COMPLEX, PHOSPHORYLATION, TRANSFERASE
4eop:B (THR310) to (GLY369) THR 160 PHOSPHORYLATED CDK2 Q131E - HUMAN CYCLIN A3 COMPLEX WITH THE INHIBITOR RO3306 | PROTEIN KINASE, CELL CYCLE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4eop:D (THR310) to (THR366) THR 160 PHOSPHORYLATED CDK2 Q131E - HUMAN CYCLIN A3 COMPLEX WITH THE INHIBITOR RO3306 | PROTEIN KINASE, CELL CYCLE, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4eoq:D (THR310) to (THR366) THR 160 PHOSPHORYLATED CDK2 WT - HUMAN CYCLIN A3 COMPLEX WITH ATP | PROTEIN KINASE, CELL CYCLE, COMPLEX, PHOSPHORYLATION, TRANSFERASE
4eor:B (THR310) to (THR366) THR 160 PHOSPHORYLATED CDK2 WT - HUMAN CYCLIN A3 COMPLEX WITH THE INHIBITOR NU6102 | PROTEIN KINASE, CELL CYCLE, PHOSPHORYLATION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4eor:D (THR310) to (THR366) THR 160 PHOSPHORYLATED CDK2 WT - HUMAN CYCLIN A3 COMPLEX WITH THE INHIBITOR NU6102 | PROTEIN KINASE, CELL CYCLE, PHOSPHORYLATION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4eos:D (THR310) to (GLY369) THR 160 PHOSPHORYLATED CDK2 WT - HUMAN CYCLIN A3 COMPLEX WITH THE INHIBITOR RO3306 | PROTEIN KINASE, CELL CYCLE, PHOSPHORYLATION, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
5ivk:A (PHE355) to (HIS435) THE ALPHA-ESTERASE-7 CARBOXYLESTERASE, E3, FROM THE BLOWFLY LUCILIA CUPRINA: PHOSPHORYLATED-ENZYME ENSEMBLE REFINEMENT | CARBOXYLESTERASE, ORGANOPHOSPHATE, PROTEIN DYNAMICS, ACETYLCHOLINESTERASE, HYDROLASE
4f4o:A (SER3) to (HIS72) STRUCTURE OF THE HAPTOGLOBIN-HAEMOGLOBIN COMPLEX | GLOBIN FOLD, SERINE PROTEASE FOLD, COMPLEMENT CONTROL PROTEIN, HAEMOGLOBIN SCAVENGING, OXYGEN STORAGE-TRANSPORT COMPLEX, OXYGEN TRANSPORT-TRANSPORT PROTEIN COMPLEX
4f4o:G (SER3) to (HIS72) STRUCTURE OF THE HAPTOGLOBIN-HAEMOGLOBIN COMPLEX | GLOBIN FOLD, SERINE PROTEASE FOLD, COMPLEMENT CONTROL PROTEIN, HAEMOGLOBIN SCAVENGING, OXYGEN STORAGE-TRANSPORT COMPLEX, OXYGEN TRANSPORT-TRANSPORT PROTEIN COMPLEX
4f4o:K (PHE85) to (HIS143) STRUCTURE OF THE HAPTOGLOBIN-HAEMOGLOBIN COMPLEX | GLOBIN FOLD, SERINE PROTEASE FOLD, COMPLEMENT CONTROL PROTEIN, HAEMOGLOBIN SCAVENGING, OXYGEN STORAGE-TRANSPORT COMPLEX, OXYGEN TRANSPORT-TRANSPORT PROTEIN COMPLEX
3qhr:B (ASN312) to (THR366) STRUCTURE OF A PCDK2/CYCLINA TRANSITION-STATE MIMIC | KINASE CATALYTIC DOMAIN, PROTEIN KINASE, CYCLIN, PHOSPHORYLATED THR- 160, TRANSFERASE-PROTEIN BINDING COMPLEX
3qhr:D (ASN312) to (GLY369) STRUCTURE OF A PCDK2/CYCLINA TRANSITION-STATE MIMIC | KINASE CATALYTIC DOMAIN, PROTEIN KINASE, CYCLIN, PHOSPHORYLATED THR- 160, TRANSFERASE-PROTEIN BINDING COMPLEX
4f70:B (PRO155) to (VAL208) CRYSTAL STRUCTURE OF HUMAN CDK8/CYCC IN COMPLEX WITH COMPOUND 4 (1-[3- TERT-BUTYL-1-(4-METHYLPHENYL)-1H-PYRAZOL-5-YL]-3-[2-(MORPHOLIN-4-YL) ETHYL]UREA) | PROTEIN KINASE COMPLEX, PROTEROS, TRANSFERASE-TRANSCRIPTION-INHIBITOR COMPLEX
4fby:V (ARG81) to (LEU146) FS X-RAY DIFFRACTION OF PHOTOSYSTEM II | PHOTOSYSTEM, PS II, PS2, MEMBRANE COMPLEX, TRANSMEMBRANE ALPHA-HELIX, PHOTOSYNTHESIS, X-RAY FREE ELECTRON LASER, PHOTOSYSTEM II, REACTION CENTER, IRON, MANGANESE, LIGHT HARVESTING, ELECTRON TRANSPORT, WATER OXIDATION, THYLAKOID MEMBRANE
4fcb:A (LEU495) to (CYS552) POTENT AND SELECTIVE PHOSPHODIESTERASE 10A INHIBITORS | BINDING SITES, CYCLIC AMP, CYCLIC GMP,LIGANDS, PHOSPHODIESTERASE INHIBITORS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4fcd:A (LEU495) to (CYS552) POTENT AND SELECTIVE PHOSPHODIESTERASE 10A INHIBITORS | BINDING SITES, CYCLIC AMP, CYCLIC GMP, HUMANS, HYDROLYSIS, LIGANDS, PHOSPHODIESTERASE INHIBITORS, PHOSPHORIC DIESTER HYDROLASES, RECOMBINANT PROTEINS, STRUCTURE-ACTIVITY RELATIONSHIP, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
3qz5:H (TRP29) to (GLU77) CRYSTAL STRUCTURE OF CO-TYPE NITRILE HYDRATASE ALPHA-E168Q FROM PSEUDOMONAS PUTIDA. | NITRILE HYDRATASE, CO, COBALT, CYSTEINE SULFINIC ACID, LYASE
3qz9:H (TRP29) to (GLU77) CRYSTAL STRUCTURE OF CO-TYPE NITRILE HYDRATASE BETA-Y215F FROM PSEUDOMONAS PUTIDA. | NITRILE HYDRATASE, CO, COBALT, CYSTEINE SULFINIC ACID, LYASE
4g6b:B (HIS114) to (ILE180) THREE DIMENSIONAL STRUCTURE ANALYSIS OF THE TYPE II CITRATE SYNTHASE FROM E.COLI | CITRATE SYNTHASE, TRANSFERASE
5k9r:B (GLU494) to (CYS552) PDE10A WITH IMIDAZOPYRAZINE INHIBITOR | HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4gg4:A (PRO665) to (GLY710) CRYSTAL STRUCTURE OF THE TAL EFFECTOR DHAX3 BOUND TO SPECIFIC DNA-RNA HYBRID | TANDEM REPEAT, TAL EFFECTOR, SEQUENCE SPECIFIC DNA BINDING PROTEIN, DNA DUPLEX, DNA-RNA HYBRID, DNA BINDING PROTEIN-DNA-RNA COMPLEX
5knn:G (GLY321) to (PHE382) EVOLUTIONARY GAIN OF ALANINE MISCHARGING TO NON-COGNATE TRNAS WITH A G4:U69 BASE PAIR | TRNA SYNTHETASE, LIGASE
5tj5:A (THR411) to (TYR479) ATOMIC MODEL FOR THE MEMBRANE-EMBEDDED MOTOR OF A EUKARYOTIC V-ATPASE | ROTARY ATPASE, VACUOLAR-TYPE ATPASE, ELECTRON CRYOMICROSCOPY, VO REGION, MEMBRANE PROTEIN, MOTOR PROTEIN
6hbw:C (SER3) to (HIS72) CRYSTAL STRUCTURE OF DEOXY-HUMAN HEMOGLOBIN BETA6 GLU->TRP | OXYGEN TRANSPORT, HEMOGLOBIN, OXYGEN STORAGE/TRANSPORT COMPLEX
3ecn:B (SER534) to (ILE595) CRYSTAL STRUCTURE OF PDE8A CATALYTIC DOMAIN IN COMPLEX WITH IBMX | IBMX, PDE8A CATALYTIC DOMAIN, REFOLDING, ALTERNATIVE SPLICING, CAMP, HYDROLASE, MAGNESIUM, MANGANESE, METAL- BINDING
1aj9:A (SER3) to (HIS72) R-STATE HUMAN CARBONMONOXYHEMOGLOBIN ALPHA-A53S | OXYGEN TRANSPORT, HEMOGLOBIN, MUTANT, ALPHA-A53S, CARBOXYHEMOGLOBIN, CARBONMONOXIDE, CARBONMONOXYHEMOGLOBIN, CARBONMONOXY
2oup:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A | PDE10, HYDROLASE
2ouy:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 MUTANT D564A IN COMPLEX WITH CAMP. | PDE, SUBSTRATE SPECIFICITY, CAMP, HYDROLASE
1nvv:S (THR605) to (GLU649) STRUCTURAL EVIDENCE FOR FEEDBACK ACTIVATION BY RASGTP OF THE RAS-SPECIFIC NUCLEOTIDE EXCHANGE FACTOR SOS | PROTO-ONCOGENE, GTP-BINDING, GUANINE-NUCLEOTIDE RELEASING FACTOR, SIGNALING PROTEIN
1o1m:A (SER225) to (LEU280) DEOXY HEMOGLOBIN (A-GLYGLYGLY-C:V1M,L29F,H58Q B,D:V1M,V67W) | HEME, OXYGEN DELIVERY VEHICLE, BLOOD SUBSTITUTE, OXYGEN STORAGE/TRANSPORT COMPLEX
1bz0:C (SER81) to (LEU136) HEMOGLOBIN A (HUMAN, DEOXY, HIGH SALT) | OXYGEN TRANSPORT, OXYGEN STORAGE/TRANSPORT COMPLEX
1ogu:B (ASN312) to (THR366) STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH A 2-ARYLAMINO-4-CYCLOHEXYLMETHYL-5-NITROSO-6-AMINOPYRIMIDINE INHIBITOR | KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION
1ogu:D (THR310) to (THR368) STRUCTURE OF HUMAN THR160-PHOSPHO CDK2/CYCLIN A COMPLEXED WITH A 2-ARYLAMINO-4-CYCLOHEXYLMETHYL-5-NITROSO-6-AMINOPYRIMIDINE INHIBITOR | KINASE, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, ATP- BINDING, CELL CYCLE, CELL DIVISION, MITOSIS, PHOSPHORYLATION
4ii5:B (ASN312) to (GLY369) STRUCTURE OF PCDK2/CYCLINA BOUND TO ADP AND 1 MAGNESIUM ION | ADP AND MAGNESIUM BINDING, T160 PHOSPHORYLATION, TRANSFERASE-CELL CYCLE COMPLEX
4ii5:D (ASN312) to (GLY369) STRUCTURE OF PCDK2/CYCLINA BOUND TO ADP AND 1 MAGNESIUM ION | ADP AND MAGNESIUM BINDING, T160 PHOSPHORYLATION, TRANSFERASE-CELL CYCLE COMPLEX
4irf:A (SER90) to (LYS151) PRELIMINARY STRUCTURAL INVESTIGATIONS OF A MALARIAL PROTEIN SECRETION SYSTEM | MALARIA, AAA+ ATPASE CLPB CHAPERONE, N-TERMINAL CARGO-BINDING DOMAIN, PROTEIN TRANSLOCATION AND UNFOLDING, PARASITOPHOROUS VACUOLE, CHAPERONE
4irf:B (SER90) to (LYS151) PRELIMINARY STRUCTURAL INVESTIGATIONS OF A MALARIAL PROTEIN SECRETION SYSTEM | MALARIA, AAA+ ATPASE CLPB CHAPERONE, N-TERMINAL CARGO-BINDING DOMAIN, PROTEIN TRANSLOCATION AND UNFOLDING, PARASITOPHOROUS VACUOLE, CHAPERONE
1e08:E (PRO28) to (LEU79) STRUCTURAL MODEL OF THE [FE]-HYDROGENASE/CYTOCHROME C553 COMPLEX COMBINING NMR AND SOFT-DOCKING | HYDROGENASE, CYTOCHROME C553, ELECTRON TRANSFER COMPLEX
4y2b:A (ASP190) to (THR251) CO-CRYSTAL STRUCTURE OF 3-ETHYL-2-(ISOPROPYLAMINO)-7-(PYRIDIN-3-YL) THIENO[3,2-D]PYRIMIDIN-4(3H)-ONE BOUND TO PDE7A | PHOSPHODIESTERASE, PDE7A, CAMP, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4j34:A (LYS249) to (TYR289) CRYSTAL STRUCTURE OF KYNURENINE 3-MONOOXYGENASE - TRUNCATED AT POSITION 394 PLUS HIS TAG CLEAVED. | MONOOXYGENASE KYNURENINE HIS CLEAVED, OXIDOREDUCTASE
2r1h:B (VAL86) to (GLY143) MET-TROUT IV HEMOGLOBIN AT PH 6.3 | TROUT HEMOGLOBIN, AUTOXIDATION, HEMIN LOSS, HEME POCKET, IRON, METAL- BINDING, OXYGEN TRANSPORT, TRANSPORT, OXYGEN BINDING
2r1h:C (THR82) to (GLU139) MET-TROUT IV HEMOGLOBIN AT PH 6.3 | TROUT HEMOGLOBIN, AUTOXIDATION, HEMIN LOSS, HEME POCKET, IRON, METAL- BINDING, OXYGEN TRANSPORT, TRANSPORT, OXYGEN BINDING
2r1h:D (VAL86) to (ARG144) MET-TROUT IV HEMOGLOBIN AT PH 6.3 | TROUT HEMOGLOBIN, AUTOXIDATION, HEMIN LOSS, HEME POCKET, IRON, METAL- BINDING, OXYGEN TRANSPORT, TRANSPORT, OXYGEN BINDING
1qi8:A (SER81) to (LEU136) DEOXYGENATED STRUCTURE OF A DISTAL POCKET HEMOGLOBIN MUTANT | HEMOGLOBIN, BLOOD SUBSTITUTE, LOW NO REACTIVITY, OXYGEN STORAGE/TRANSPORT COMPLEX
4yji:A (SER314) to (ALA364) THE CRYSTAL STRUCTURE OF A BACTERIAL ARYL ACYLAMIDASE BELONGING TO THE AMIDASE SIGNATURE (AS) ENZYMES FAMILY | AMIDASE, HYDROLASE
3u4q:B (GLU822) to (ALA906) STRUCTURE OF ADDAB-DNA COMPLEX AT 2.8 ANGSTROMS | HELICASE, NUCLEASE, DOUBLE STRAND DNA REPAIR, PROTEIN-DNA COMPLEX, HYDROLASE-DNA COMPLEX
2efd:A (GLY23) to (LEU90) ARA7/ATVPS9A | GEF, GTPASE, VPS9, RAB5, NUCLEOTIDE, TRANSPORT PROTEIN
1fpm:B (GLU204) to (LYS256) MONOVALENT CATION BINDING SITES IN N10-FORMYLTETRAHYDROFOLATE SYNTHETASE FROM MOORELLA THERMOACETICA | MONOVALENT CATION, THERMOSTABLE, TETRAMER, LIGASE
3ui7:A (GLU504) to (CYS562) DISCOVERY OF ORALLY ACTIVE PYRAZOLOQUINOLINE AS A POTENT PDE10 INHIBITOR FOR THE MANAGEMENT OF SCHIZOPHRENIA | INHIBITOR COMPLEX, HYDROLASE, ZN BINDING, MG BINDING, HYDROLASE- HYDROLASE INHIBITOR COMPLEX
4yzf:A (VAL383) to (GLY455) CRYSTAL STRUCTURE OF THE ANION EXCHANGER DOMAIN OF HUMAN ERYTHROCYTE BAND 3 | IMMUNE SYSTEM, HUMAN MEMBRANE PROTEIN, ANION EXCHANGER, ERYTHROCYTES
4yzf:B (VAL383) to (GLY455) CRYSTAL STRUCTURE OF THE ANION EXCHANGER DOMAIN OF HUMAN ERYTHROCYTE BAND 3 | IMMUNE SYSTEM, HUMAN MEMBRANE PROTEIN, ANION EXCHANGER, ERYTHROCYTES
4yzf:C (VAL383) to (GLY455) CRYSTAL STRUCTURE OF THE ANION EXCHANGER DOMAIN OF HUMAN ERYTHROCYTE BAND 3 | IMMUNE SYSTEM, HUMAN MEMBRANE PROTEIN, ANION EXCHANGER, ERYTHROCYTES
4yzf:D (VAL383) to (GLY455) CRYSTAL STRUCTURE OF THE ANION EXCHANGER DOMAIN OF HUMAN ERYTHROCYTE BAND 3 | IMMUNE SYSTEM, HUMAN MEMBRANE PROTEIN, ANION EXCHANGER, ERYTHROCYTES
2vkd:B (CYS395) to (LYS455) CRYSTAL STRUCTURE OF THE CATALYTIC DOMAIN OF LETHAL TOXIN FROM CLOSTRIDIUM SORDELLII IN COMPLEX WITH UDP-GLC AND MANGANESE ION | TOXIN, GLYCOSYLTRANSFERASE
4zds:B (LYS245) to (ALA299) CRYSTAL STRUCTURE OF CORE DNA BINDING DOMAIN OF ARABIDOPSIS THALIANA TRANSCRIPTION FACTOR ETHYLENE-INSENSITIVE 3 | DNA BINDING DOMAIN TRANSCRIPTION FACTOR, TRANSCRIPTION ACTIVATOR
1gy3:D (ASN312) to (VAL367) PCDK2/CYCLIN A IN COMPLEX WITH MGADP, NITRATE AND PEPTIDE SUBSTRATE | TRANSFERASE-TRANSFERASE SUBSTRATE COMPLEX, CELL CYCLE REGULATORY PROTEIN KINASE, THR160-PHOSPHO-CYCLIN DEPENDENT PROTEIN KINASE 2 IN ASSOCIATION WITH CYCLIN A, TRANSFERASE- TRANSFERASE SUBSTRATE COMPLEX
1hba:D (ALA86) to (ALA142) HIGH-RESOLUTION X-RAY STUDY OF DEOXYHEMOGLOBIN ROTHSCHILD 37BETA TRP-> ARG: A MUTATION THAT CREATES AN INTERSUBUNIT CHLORIDE-BINDING SITE | OXYGEN TRANSPORT
1hbb:D (ALA86) to (ALA142) HIGH-RESOLUTION X-RAY STUDY OF DEOXYHEMOGLOBIN ROTHSCHILD 37BETA TRP-> ARG: A MUTATION THAT CREATES AN INTERSUBUNIT CHLORIDE-BINDING SITE | OXYGEN TRANSPORT
2w72:D (ALA86) to (ALA142) DEOXYGENATED STRUCTURE OF A DISTAL SITE HEMOGLOBIN MUTANT PLUS XE | IRON, HEME, GLYCATION, TRANSPORT, ACETYLATION, PHOSPHOPROTEIN, PACKING DEFECTS, DISEASE MUTATION, DISTAL SITE POINT MUTATION, OXYGEN TRANSPORT, HYDROPHOBIC CAVITIES, POLYMORPHISM, GLYCOPROTEIN, METAL-BINDING
4llj:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 WITH FRAGMENT ZT214 | FRAGMENT SCREENING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4llk:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 WITH FRAGMENT ZT217 | FRAGMENT SCREENING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4llx:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 WITH FRAGMENT ZT434 | FRAGMENT SCREENING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4lm0:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 WITH FRAGMENT ZT448 | FRAGMENT SCREENING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4lm2:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 WITH FRAGMENT ZT462 | FRAGMENT SCREENING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4lm3:A (LEU505) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 WITH FRAGMENT ZT464 | FRAGMENT SCREENING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
2wip:B (VAL311) to (GLY369) STRUCTURE OF CDK2-CYCLIN A COMPLEXED WITH 8-ANILINO-1- METHYL-4,5-DIHYDRO-1H-PYRAZOLO[4,3-H] QUINAZOLINE-3- CARBOXYLIC ACID | CELL CYCLE, ATP-BINDING, TRANSFERASE, POLYMORPHISM, PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN 2 KINASE, SERINE/THREONINE-PROTEIN KINASE, CELL DIVISION, PHOSPHOPROTEIN, PROTEIN KINASE, KINASE, CYCLIN, NUCLEUS, MITOSIS, CYTOPLASM
2wip:D (VAL311) to (GLY369) STRUCTURE OF CDK2-CYCLIN A COMPLEXED WITH 8-ANILINO-1- METHYL-4,5-DIHYDRO-1H-PYRAZOLO[4,3-H] QUINAZOLINE-3- CARBOXYLIC ACID | CELL CYCLE, ATP-BINDING, TRANSFERASE, POLYMORPHISM, PHOSPHORYLATION, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN 2 KINASE, SERINE/THREONINE-PROTEIN KINASE, CELL DIVISION, PHOSPHOPROTEIN, PROTEIN KINASE, KINASE, CYCLIN, NUCLEUS, MITOSIS, CYTOPLASM
2wpa:B (VAL311) to (GLY369) OPTIMISATION OF 6,6-DIMETHYL PYRROLO 3,4-C PYRAZOLES: IDENTIFICATION OF PHA-793887, A POTENT CDK INHIBITOR SUITABLE FOR INTRAVENOUS DOSING | SERINE/THREONINE-PROTEIN 2 KINASE, CYCLIN, MITOSIS, CELL CYCLE, TRANSFERASE, ATP-BINDING, PHOSPHOPROTEIN,
2wpa:D (ASN312) to (GLY369) OPTIMISATION OF 6,6-DIMETHYL PYRROLO 3,4-C PYRAZOLES: IDENTIFICATION OF PHA-793887, A POTENT CDK INHIBITOR SUITABLE FOR INTRAVENOUS DOSING | SERINE/THREONINE-PROTEIN 2 KINASE, CYCLIN, MITOSIS, CELL CYCLE, TRANSFERASE, ATP-BINDING, PHOSPHOPROTEIN,
5a4j:B (GLU203) to (LYS255) CRYSTAL STRUCTURE OF FTHFS1 FROM T.ACETOXYDANS RE1 | LIGASE, PROTEIN
5a4j:D (GLU203) to (LYS255) CRYSTAL STRUCTURE OF FTHFS1 FROM T.ACETOXYDANS RE1 | LIGASE, PROTEIN
2i2z:A (GLU6) to (ASP56) HUMAN SERUM ALBUMIN COMPLEXED WITH MYRISTATE AND ASPIRIN | PLASMA PROTEIN, METAL-BINDING, LIPID-BINDING, LIPID BINDING PROTEIN
2x1n:D (THR310) to (THR366) TRUNCATION AND OPTIMISATION OF PEPTIDE INHIBITORS OF CDK2, CYCLIN A THROUGH STRUCTURE GUIDED DESIGN | INHIBITION, TRANSFERASE, SERINE/THREONINE-PROTEIN KINASE, CELL CYCLE, CELL DIVISION
4msc:A (GLU504) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 WITH FRAGMENT ZT1595 (2-[(QUINOLIN-7- YLOXY)METHYL]QUINOLINE) | FRAGMENT SCREENING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4msn:A (GLU504) to (CYS562) CRYSTAL STRUCTURE OF PDE10A2 WITH FRAGMENT ZT0451 (8-NITROQUINOLINE) | FRAGMENT SCREENING, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
4n7p:A (PRO4) to (HIS72) CAPTURING THE HAEMOGLOBIN ALLOSTERIC TRANSITION IN A SINGLE CRYSTAL FORM; CRYSTAL STRUCTURE OF HALF-LIGANDED HUMAN HAEMOGLOBIN WITHOUT PHOSPHATE AT 2.8 A RESOLUTION. | HYBRID HAEMOGLOBIN, ALLOSTERIC PATHWAY, TRANSPORT PROTEIN
2y0j:A (LEU498) to (CYS552) TRIAZOLOQUINAZOLINES AS A NOVEL CLASS OF PHOSPHODIESTERASE 10A (PDE10A) INHIBITORS, PART 2, LEAD-OPTIMISATION. | HYDROLASE
2y0j:B (LEU495) to (CYS552) TRIAZOLOQUINAZOLINES AS A NOVEL CLASS OF PHOSPHODIESTERASE 10A (PDE10A) INHIBITORS, PART 2, LEAD-OPTIMISATION. | HYDROLASE
2k77:A (THR7) to (ILE68) NMR SOLUTION STRUCTURE OF THE BACILLUS SUBTILIS CLPC N- DOMAIN | HSP100/CLP/AAA+, N-DOMAIN, REPEAT, N-CLPCR, CHAPERONE/PROTEASE, COMPETENCE, CHAPERONE, PROTEIN BINDING
2k77:A (THR81) to (LEU142) NMR SOLUTION STRUCTURE OF THE BACILLUS SUBTILIS CLPC N- DOMAIN | HSP100/CLP/AAA+, N-DOMAIN, REPEAT, N-CLPCR, CHAPERONE/PROTEASE, COMPETENCE, CHAPERONE, PROTEIN BINDING
4nkx:D (LYS227) to (ASN321) HUMAN STEROIDOGENIC CYTOCHROME P450 17A1 MUTANT A105L WITH SUBSTRATE PROGESTERONE | HEME PROTEIN, MONOOXYGENASE, STEROID 17ALPHA-HYDROXYLASE, STEROID C17,20 LYASE, NADPH-CYTOCHROME P450 REDUCTASE, CYTOCHROME B5, ENDOPLASMIC RETICULUM MEMBRANE, OXIDOREDUCTASE, LYASE
5c2e:A (GLU494) to (CYS552) PDE10 COMPLEXED WITH6-CHLORO-N-[(2,4-DIMETHYLTHIAZOL-5-YL)METHYL]-5- METHYL-2-[2-(2-PYRIDYL)ETHOXY]PYRIMIDIN-4-AMINE | PHOSPHODIESTERASE, INHIBITOR, COMPLEX, HYDROLASE-HYDROLASE INHIBITOR COMPLEX
5c2g:A (ASP422) to (GLY456) GWS1B RUBISCO: FORM II RUBISCO DERIVED FROM UNCULTIVATED GALLIONELLACEA SPECIES (CABP-BOUND). | RUBISCO, HEXAMER, METAGENOMICS, LYASE
5c2g:B (ASP422) to (GLY456) GWS1B RUBISCO: FORM II RUBISCO DERIVED FROM UNCULTIVATED GALLIONELLACEA SPECIES (CABP-BOUND). | RUBISCO, HEXAMER, METAGENOMICS, LYASE
1khy:A (THR7) to (LEU71) THE CRYSTAL STRUCTURE OF CLPB N TERMINAL DOMAIN, IMPLICATION TO THE PEPTIDE BINDING FUNCTION OF CLPB | ALPHA HELIX, CHAPERONE
1khy:A (GLN85) to (GLN142) THE CRYSTAL STRUCTURE OF CLPB N TERMINAL DOMAIN, IMPLICATION TO THE PEPTIDE BINDING FUNCTION OF CLPB | ALPHA HELIX, CHAPERONE
1khy:B (THR7) to (LEU71) THE CRYSTAL STRUCTURE OF CLPB N TERMINAL DOMAIN, IMPLICATION TO THE PEPTIDE BINDING FUNCTION OF CLPB | ALPHA HELIX, CHAPERONE
1khy:B (GLN85) to (GLN142) THE CRYSTAL STRUCTURE OF CLPB N TERMINAL DOMAIN, IMPLICATION TO THE PEPTIDE BINDING FUNCTION OF CLPB | ALPHA HELIX, CHAPERONE
3zri:A (SER88) to (HIS147) N-DOMAIN OF CLPV FROM VIBRIO CHOLERAE | CHAPERONE, HSP100 PROTEINS, AAA+ PROTEINS, T6SS, SECRETION, VIRULENCE
5csd:C (LYS94) to (PHE154) LIGAND BINDING DOMAIN 2 OF PENICILLIUM MARNEFFEI MP1 PROTEIN IN COMPLEX WITH ARACHIDONIC ACIDS | ARACHIDONIC ACID, LIGAND BINDING DOMAIN, LIPID BINDING PROTEIN
1xl6:A (LEU34) to (ARG137) INTERMEDIATE GATING STRUCTURE 2 OF THE INWARDLY RECTIFYING K+ CHANNEL KIRBAC3.1 | INTEGRAL MEMBRANE PROTEIN, ION CHANNEL, INWARDLY RECTIFYING K+ CHANNEL, METAL TRANSPORT
1xl6:B (LEU34) to (THR136) INTERMEDIATE GATING STRUCTURE 2 OF THE INWARDLY RECTIFYING K+ CHANNEL KIRBAC3.1 | INTEGRAL MEMBRANE PROTEIN, ION CHANNEL, INWARDLY RECTIFYING K+ CHANNEL, METAL TRANSPORT
4aam:A (LEU123) to (VAL186) MACA WILD-TYPE MIXED-VALENCE | OXIDOREDUCTASE, MULTIHEME CYTOCHROMES, CONFORMATIONAL REARRANGEMENT
1xz7:D (ALA86) to (ALA142) T-TO-THIGH QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: ALPHAR92A DEOXY LOW-SALT | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
1y0c:D (ALA86) to (ALA142) T-TO-THIGH QUATERNARY TRANSITIONS IN HUMAN HEMOGLOBIN: ALPHAY140F DEOXY LOW-SALT | HEMOGLOBIN MUTANT, GLOBIN, TRANSPORT PROTEIN
2zzg:A (ALA363) to (GLY445) CRYSTAL STRUCTURE OF ALANYL-TRNA SYNTHETASE IN COMPLEX WITH 5''-O-(N-(L-ALANYL)-SULFAMYOXYL) ADENINE WITHOUT OLIGOMERIZATION DOMAIN | LIGASE, HYDROLASE
2zzg:B (ALA363) to (GLY445) CRYSTAL STRUCTURE OF ALANYL-TRNA SYNTHETASE IN COMPLEX WITH 5''-O-(N-(L-ALANYL)-SULFAMYOXYL) ADENINE WITHOUT OLIGOMERIZATION DOMAIN | LIGASE, HYDROLASE
4ph0:A (SER143) to (CYS202) CAPSID PROTEIN FROM BOVINE LEUKEMIA VIRUS | RETROVIRAL CAPSID, ALL ALPHA
4ph0:E (SER143) to (CYS202) CAPSID PROTEIN FROM BOVINE LEUKEMIA VIRUS | RETROVIRAL CAPSID, ALL ALPHA
1yvt:A (SER81) to (LEU136) THE HIGH SALT (PHOSPHATE) CRYSTAL STRUCTURE OF CO HEMOGLOBIN E (GLU26LYS) AT PHYSIOLOGICAL PH (PH 7.35) | HEMOGLOBIN E OXYGEN TRANSPORT BETA THALASSEMIA PHYSIOLOGICAL, TRANSPORT PROTEIN
3lhq:A (MET123) to (CYS205) DNA-BINDING TRANSCRIPTIONAL REPRESSOR ACRR FROM SALMONELLA TYPHIMURIUM. | STRUCTURAL GENOMICS, IDP02616, CSGID, DNA-BINDING, TRANSCRIPTION, REPRESSOR, ACRR, TRANSCRIPTION REGULATION, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES
3lhq:B (MET123) to (CYS205) DNA-BINDING TRANSCRIPTIONAL REPRESSOR ACRR FROM SALMONELLA TYPHIMURIUM. | STRUCTURAL GENOMICS, IDP02616, CSGID, DNA-BINDING, TRANSCRIPTION, REPRESSOR, ACRR, TRANSCRIPTION REGULATION, CENTER FOR STRUCTURAL GENOMICS OF INFECTIOUS DISEASES
5e57:B (ALA131) to (GLY199) CRYSTAL STRUCTURE OF MYCOBACTERIUM SMEGMATIS AMTR | HTH DNA BINDING MOTIF, LIGAND BINDING DOMAIN, TETR, NITROGEN REGULATION, TRANSLATION
5e6p:A (LEU1792) to (LEU1835) PLEXINB2 CYTOPLASMIC REGION/PDZ-RHOGEF PDZ DOMAIN COMPLEX | PLEXIN, PDZ, PDZ-RHOGEF, COMPLEX, SIGNALING PROTEIN
4qfy:D (VAL378) to (TYR432) CRYSTAL STRUCTURE OF THE TETRAMERIC DGTP/DCTP-BOUND SAMHD1 (RN206) MUTANT CATALYTIC CORE | DEOXYNUCLEOSIDE TRIPHOSPHATE TRIPHOSPHOHYDROLASE, 2'-DEOXYNUCLEOTIDE- 5'-TRIPHOSPHATE, HIV RESTRICTION FACTOR, DNTPASE, HYDROLASE
4bcm:D (THR310) to (ALA363) STRUCTURE OF CDK2 IN COMPLEX WITH CYCLIN A AND A 2-AMINO-4- HETEROARYL-PYRIMIDINE INHIBITOR | TRANSFERASE-CELL CYCLE COMPLEX, CDK-CYCLIN COMPLEX, STRUCTURE-BASED DRUG DESIGN
4bco:B (THR310) to (THR366) STRUCTURE OF CDK2 IN COMPLEX WITH CYCLIN A AND A 2-AMINO-4- HETEROARYL-PYRIMIDINE INHIBITOR | TRANSFERASE-CELL CYCLE COMPLEX, CDK-CYCLIN COMPLEX, CYCLIN-INHIBITOR, STRUCTURE-BASED DRUG DESIGN
4bco:D (THR310) to (GLY369) STRUCTURE OF CDK2 IN COMPLEX WITH CYCLIN A AND A 2-AMINO-4- HETEROARYL-PYRIMIDINE INHIBITOR | TRANSFERASE-CELL CYCLE COMPLEX, CDK-CYCLIN COMPLEX, CYCLIN-INHIBITOR, STRUCTURE-BASED DRUG DESIGN
3bhu:B (THR310) to (GLY369) STRUCTURE OF PHOSPHORYLATED THR160 CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR MERIOLIN 5 | SER/THR PROTEIN KINASE, TRANSFERASE, PHOSPHORYLATION, CELL CYCLE, ATP-BINDING, CELL DIVISION, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, CYCLIN
3bhu:D (THR310) to (THR366) STRUCTURE OF PHOSPHORYLATED THR160 CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR MERIOLIN 5 | SER/THR PROTEIN KINASE, TRANSFERASE, PHOSPHORYLATION, CELL CYCLE, ATP-BINDING, CELL DIVISION, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, SERINE/THREONINE-PROTEIN KINASE, CYCLIN
3bhv:B (THR310) to (GLY369) STRUCTURE OF PHOSPHORYLATED THR160 CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR VARIOLIN B | SER/THR PROTEIN KINASE, TRANSFERASE, PHOSPHORYLATION, CELL CYCLE, ATP-BINDING, CELL DIVISION, MITOSIS, NUCLEOTIDE- BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE- PROTEIN KINASE, CYCLIN
3bql:A (LYS1515) to (PHE1555) STRUCTURE OF A CHONDROITIN SULPHATE BINDING DBL3X DOMAIN FROM A VAR2CSA ENCODED PFEMP1 PROTEIN | MALAIRA, PREGANACY, VAR2CSA ENCODED PFEMP1 PROTEIN DBL3X DOMAIN, CHONDROITIN SULPHATE A, CELL ADHESION
3ciu:A (SER3) to (HIS72) SITE-SELECTIVE GLYCOSYLATION OF CYSTEINE-93 BETA ON THE SURFACE OF BOVINE HEMOGLOBIN AND ITS APPLICATION AS A NOVEL OXYGEN THERAPEUTIC | HEMOGLOBIN, GLYCOSYLATION, SITE-SELECTIVE, OXYGEN CARRIER, BLOOD SUBSTITUTE, HEME, IRON, OXYGEN TRANSPORT, POLYMORPHISM, TRANSPORT, OXYGEN BINDING
3ciu:D (PHE85) to (ALA142) SITE-SELECTIVE GLYCOSYLATION OF CYSTEINE-93 BETA ON THE SURFACE OF BOVINE HEMOGLOBIN AND ITS APPLICATION AS A NOVEL OXYGEN THERAPEUTIC | HEMOGLOBIN, GLYCOSYLATION, SITE-SELECTIVE, OXYGEN CARRIER, BLOOD SUBSTITUTE, HEME, IRON, OXYGEN TRANSPORT, POLYMORPHISM, TRANSPORT, OXYGEN BINDING
3cpz:A (GLY1499) to (ASN1556) CRYSTAL STRUCTURE OF VAR2CSA DBL3X DOMAIN IN THE PRESENCE OF DODECASACCHARIDE OF CSA | DBL3X, VAR2CSA, CHONDROITIN SULPHATE A (CSA), PREGNANCY- ASSOCIATED MALARIA, MEMBRANE PROTEIN
4cfu:B (THR310) to (THR366) STRUCTURE-BASED DESIGN OF C8-SUBSTITUTED O6- CYCLOHEXYLMETHOXYGUANINE CDK1 AND 2 INHIBITORS. | TRANSFERASE, STRUCTURE-BASED DRUG DESIGN, CONFORMATIONAL RESTRAINT, REVERSED BINDING MODE
4cfu:D (THR310) to (GLY369) STRUCTURE-BASED DESIGN OF C8-SUBSTITUTED O6- CYCLOHEXYLMETHOXYGUANINE CDK1 AND 2 INHIBITORS. | TRANSFERASE, STRUCTURE-BASED DRUG DESIGN, CONFORMATIONAL RESTRAINT, REVERSED BINDING MODE
3dbl:C (SER303) to (ASN386) STRUCTURAL DISSECTION OF A GATING MECHANISM PREVENTING MISACTIVATION OF UBIQUITIN BY NEDD8'S E1 (APPBP1- UBA3ARG190WT-NEDD8ALA72GLN) | CELL CYCLE, ACTIVATING ENZYME, APOPTOSIS, MEMBRANE, UBL CONJUGATION PATHWAY, ATP-BINDING, LIGASE, NUCLEOTIDE- BINDING, POLYMORPHISM, NUCLEUS
3dcu:A (THR378) to (ASP458) FXR WITH SRC1 AND GSK8062 | FXR, NUCLEAR RECEPTOR, GW4064, ALPHA-HELICAL SANDWICH, ACTIVATOR, ALTERNATIVE SPLICING, DNA-BINDING, METAL-BINDING, NUCLEUS, RECEPTOR, REPRESSOR, TRANSCRIPTION REGULATION, ZINC, ZINC-FINGER, ACYLTRANSFERASE, CHROMOSOMAL REARRANGEMENT, PHOSPHOPROTEIN, POLYMORPHISM, PROTO-ONCOGENE, TRANSFERASE, UBL CONJUGATION, TRANSCRIPTION/TRANSCRIPTION ACTIVATOR COMPLEX
4to5:B (CYS205) to (ILE272) STRUCTURE BASIS OF CELLULAR DNTP REGULATION, SAMHD1-GTP-DTTP-DCTP COMPLEX | SAMHD1, HIV, RESTRICTION FACTOR, DNTPASE, DNTP REGULATION, HOST PATHOGEN INTERACTION, HYDROLASE
3ddp:D (ILE311) to (THR368) STRUCTURE OF PHOSPHORYLATED THR160 CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR CR8 | SER/THR PROTEIN KINASE; PHOSPHORYLATION; CELL CYCLE, ATP- BINDING, CELL DIVISION, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, CYCLIN, CYTOPLASM, NUCLEUS, TRANSFERASE/CELL CYCLE COMPLEX
3ddq:B (THR310) to (GLY369) STRUCTURE OF PHOSPHORYLATED THR160 CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR ROSCOVITINE | SER/THR PROTEIN KINASE; TRANSFERASE; PHOSPHORYLATION; CELL CYCLE, ATP-BINDING, CELL CYCLE, CELL DIVISION, KINASE, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, CYCLIN, CYTOPLASM, NUCLEUS, TRANSFERASE/CELL CYCLE COMPLEX
3ddq:D (THR310) to (THR368) STRUCTURE OF PHOSPHORYLATED THR160 CDK2/CYCLIN A IN COMPLEX WITH THE INHIBITOR ROSCOVITINE | SER/THR PROTEIN KINASE; TRANSFERASE; PHOSPHORYLATION; CELL CYCLE, ATP-BINDING, CELL CYCLE, CELL DIVISION, KINASE, MITOSIS, NUCLEOTIDE-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SERINE/THREONINE-PROTEIN KINASE, CYCLIN, CYTOPLASM, NUCLEUS, TRANSFERASE/CELL CYCLE COMPLEX
3our:A (HIS300) to (SER342) CRYSTAL STRUCTURE OF COMPLEX BETWEEN EIIA AND A NOVEL PYRUVATE DECARBOXYLASE | EXHIBIT NO HYDROLASE ACTIVITY1, LYASE-TRANSFERASE COMPLEX
3our:C (HIS300) to (SER342) CRYSTAL STRUCTURE OF COMPLEX BETWEEN EIIA AND A NOVEL PYRUVATE DECARBOXYLASE | EXHIBIT NO HYDROLASE ACTIVITY1, LYASE-TRANSFERASE COMPLEX
3our:E (HIS300) to (SER342) CRYSTAL STRUCTURE OF COMPLEX BETWEEN EIIA AND A NOVEL PYRUVATE DECARBOXYLASE | EXHIBIT NO HYDROLASE ACTIVITY1, LYASE-TRANSFERASE COMPLEX
4u8u:D (ILE4) to (LEU77) THE CRYSTALLOGRAPHIC STRUCTURE OF THE GIANT HEMOGLOBIN FROM GLOSSOSCOLEX PAULISTUS AT 3.2 A RESOLUTION. | ERYTHROCRUORINS, GLOSSOSCOLEX PAULISTUS, GIANT EXTRACELLULAR HEMOGLOBIN, OXYGEN STORAGE-TRANSPORT COMPLEX
4u8u:H (ILE4) to (LEU77) THE CRYSTALLOGRAPHIC STRUCTURE OF THE GIANT HEMOGLOBIN FROM GLOSSOSCOLEX PAULISTUS AT 3.2 A RESOLUTION. | ERYTHROCRUORINS, GLOSSOSCOLEX PAULISTUS, GIANT EXTRACELLULAR HEMOGLOBIN, OXYGEN STORAGE-TRANSPORT COMPLEX
4u8u:L (ILE4) to (LEU77) THE CRYSTALLOGRAPHIC STRUCTURE OF THE GIANT HEMOGLOBIN FROM GLOSSOSCOLEX PAULISTUS AT 3.2 A RESOLUTION. | ERYTHROCRUORINS, GLOSSOSCOLEX PAULISTUS, GIANT EXTRACELLULAR HEMOGLOBIN, OXYGEN STORAGE-TRANSPORT COMPLEX
4u8u:S (ILE4) to (LEU77) THE CRYSTALLOGRAPHIC STRUCTURE OF THE GIANT HEMOGLOBIN FROM GLOSSOSCOLEX PAULISTUS AT 3.2 A RESOLUTION. | ERYTHROCRUORINS, GLOSSOSCOLEX PAULISTUS, GIANT EXTRACELLULAR HEMOGLOBIN, OXYGEN STORAGE-TRANSPORT COMPLEX
4u8u:W (ILE4) to (LEU77) THE CRYSTALLOGRAPHIC STRUCTURE OF THE GIANT HEMOGLOBIN FROM GLOSSOSCOLEX PAULISTUS AT 3.2 A RESOLUTION. | ERYTHROCRUORINS, GLOSSOSCOLEX PAULISTUS, GIANT EXTRACELLULAR HEMOGLOBIN, OXYGEN STORAGE-TRANSPORT COMPLEX
4u8u:a (ILE4) to (LEU77) THE CRYSTALLOGRAPHIC STRUCTURE OF THE GIANT HEMOGLOBIN FROM GLOSSOSCOLEX PAULISTUS AT 3.2 A RESOLUTION. | ERYTHROCRUORINS, GLOSSOSCOLEX PAULISTUS, GIANT EXTRACELLULAR HEMOGLOBIN, OXYGEN STORAGE-TRANSPORT COMPLEX
4u8u:h (ILE4) to (LEU77) THE CRYSTALLOGRAPHIC STRUCTURE OF THE GIANT HEMOGLOBIN FROM GLOSSOSCOLEX PAULISTUS AT 3.2 A RESOLUTION. | ERYTHROCRUORINS, GLOSSOSCOLEX PAULISTUS, GIANT EXTRACELLULAR HEMOGLOBIN, OXYGEN STORAGE-TRANSPORT COMPLEX
4u8u:l (ILE4) to (LEU77) THE CRYSTALLOGRAPHIC STRUCTURE OF THE GIANT HEMOGLOBIN FROM GLOSSOSCOLEX PAULISTUS AT 3.2 A RESOLUTION. | ERYTHROCRUORINS, GLOSSOSCOLEX PAULISTUS, GIANT EXTRACELLULAR HEMOGLOBIN, OXYGEN STORAGE-TRANSPORT COMPLEX
4u8u:p (ILE4) to (LEU77) THE CRYSTALLOGRAPHIC STRUCTURE OF THE GIANT HEMOGLOBIN FROM GLOSSOSCOLEX PAULISTUS AT 3.2 A RESOLUTION. | ERYTHROCRUORINS, GLOSSOSCOLEX PAULISTUS, GIANT EXTRACELLULAR HEMOGLOBIN, OXYGEN STORAGE-TRANSPORT COMPLEX
5jdo:C (SER4) to (HIS73) T. CONGOLENSE HAPTOGLOBIN-HAEMOGLOBIN RECEPTOR IN COMPLEX WITH HAEMOGLOBIN | TRYPANOSOME, HAPTOGLOBIN-HAEMOGLOBIN RECEPTOR, HAEMOGLOBIN, EPIMASTIGOTE, OXYGEN TRANSPORT
5jdo:D (ALA87) to (ALA143) T. CONGOLENSE HAPTOGLOBIN-HAEMOGLOBIN RECEPTOR IN COMPLEX WITH HAEMOGLOBIN | TRYPANOSOME, HAPTOGLOBIN-HAEMOGLOBIN RECEPTOR, HAEMOGLOBIN, EPIMASTIGOTE, OXYGEN TRANSPORT
5jdo:E (SER4) to (HIS73) T. CONGOLENSE HAPTOGLOBIN-HAEMOGLOBIN RECEPTOR IN COMPLEX WITH HAEMOGLOBIN | TRYPANOSOME, HAPTOGLOBIN-HAEMOGLOBIN RECEPTOR, HAEMOGLOBIN, EPIMASTIGOTE, OXYGEN TRANSPORT
5jdo:E (LEU81) to (TYR141) T. CONGOLENSE HAPTOGLOBIN-HAEMOGLOBIN RECEPTOR IN COMPLEX WITH HAEMOGLOBIN | TRYPANOSOME, HAPTOGLOBIN-HAEMOGLOBIN RECEPTOR, HAEMOGLOBIN, EPIMASTIGOTE, OXYGEN TRANSPORT
5jdo:F (ALA87) to (ALA143) T. CONGOLENSE HAPTOGLOBIN-HAEMOGLOBIN RECEPTOR IN COMPLEX WITH HAEMOGLOBIN | TRYPANOSOME, HAPTOGLOBIN-HAEMOGLOBIN RECEPTOR, HAEMOGLOBIN, EPIMASTIGOTE, OXYGEN TRANSPORT
4fx3:B (THR310) to (VAL367) CRYSTAL STRUCTURE OF THE CDK2/CYCLIN A COMPLEX WITH OXINDOLE INHIBITOR | COMPLEX (TRANSFERASE-CYCLIN), TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX
4fx3:D (VAL311) to (VAL367) CRYSTAL STRUCTURE OF THE CDK2/CYCLIN A COMPLEX WITH OXINDOLE INHIBITOR | COMPLEX (TRANSFERASE-CYCLIN), TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX