Usages in wwPDB of concept: c_1061
nUsages: 353; SSE string: HEEE
2oaj:A   (ALA857) to   (VAL887)  CRYSTAL STRUCTURE OF SRO7 FROM S. CEREVISIAE  |   WD40 REPEAT, BETA PROPELLER, ENDOCYTOSIS/EXOCYTOSIS COMPLEX 
1n8w:B   (ASN213) to   (GLU246)  BIOCHEMICAL AND STRUCTURAL STUDIES OF MALATE SYNTHASE FROM MYCOBACTERIUM TUBERCULOSIS  |   MALATE SYNTHASE, GLYOXYLATE PATHWAY, MYCOBACTERIUM TUBERCULOSIS, MALATE, COENZYME A, GLCB, GLYOXYLATE, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, TB STRUCTURAL GENOMICS CONSORTIUM, TBSGC, LYASE 
1a41:A   (GLU141) to   (HIS177)  TYPE 1-TOPOISOMERASE CATALYTIC FRAGMENT FROM VACCINIA VIRUS  |   TYPE 1B TOPOISOMERASE, ISOMERASE 
3rwr:B   (LYS565) to   (GLU614)  CRYSTAL STRUCTURE OF THE HUMAN XRCC4-XLF COMPLEX  |   COMPLEX-FILAMENT, NON-HOMOLOGOUS END-JOINING, DNA AND PROTEIN BINDING, DNA BINDING PROTEIN-PROTEIN BINDING COMPLEX 
1nqy:A   (THR143) to   (GLY179)  THE STRUCTURE OF A COA PYROPHOSPHATASE FROM D. RADIODURANS  |   NUDIX, PYROPHOSPHATASE, DR1184, COA, HYDROLASE 
3elz:C    (PRO24) to    (PHE63)  CRYSTAL STRUCTURE OF ZEBRAFISH ILEAL BILE ACID-BINDIN PROTEIN COMPLEXED WITH CHOLIC ACID (CRYSTAL FORM A).  |   ILEAL BILE ACID-BINDING PROTEIN, ZEBRAFISH (DANIO RERIO), CHOLIC ACID, LIPID-BINDING, TRANSPORT, LIPID BINDING PROTEIN 
2bj0:C   (VAL158) to   (LYS202)  CRYSTAL STRUCTURE OF ACHBP FROM BULINUS TRUNCATUS REVALS THE CONSERVED STRUCTURAL SCAFFOLD AND SITES OF VARIATION IN NICOTINIC ACETYLCHOLINE RECEPTORS  |   3D-STRUCTURE, GLYCOPROTEIN, GLYCPROTEIN, IGG FOLD, IMMUNOGLOBULIN DOMAIN, PENTAMER, SIGNAL 
4hnp:E    (PHE19) to    (LYS60)  CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH VINYLKETONE CARMAPHYCIN ANALOGUE VNK1  |   PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4hnp:S    (PHE19) to    (LYS60)  CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH VINYLKETONE CARMAPHYCIN ANALOGUE VNK1  |   PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4x6z:T    (PHE20) to    (LYS61)  YEAST 20S PROTEASOME IN COMPLEX WITH PR-VI MODULATOR  |   20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE 
3s9i:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 2-4-DIOXO-4-PHENYLBUTANOIC ACID INHIBITOR  |   INHIBITOR COMPLEX, STRUCTURAL GENOMICS, MYCOBACTERIUM TUBERCULOSIS STRUCTURAL PROTEOMICS PROJECT, XMTB, MALATE SYNTHASE, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
4hrc:E    (PHE19) to    (LYS60)  CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE CARMAPHYCIN ANALOGUE 3  |   PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4hrc:S    (PHE19) to    (LYS60)  CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH EPOXYKETONE CARMAPHYCIN ANALOGUE 3  |   PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4hrd:E    (PHE19) to    (LYS60)  CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH THE NATURAL PRODUCT CARMAPHYCIN A  |   PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4hrd:S    (PHE19) to    (LYS60)  CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH THE NATURAL PRODUCT CARMAPHYCIN A  |   PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3faw:A  (SER1056) to  (ALA1100)  CRYSTAL STRUCTURE OF THE GROUP B STREPTOCOCCUS PULLULANASE SAP  |   TIM BARREL, BETA BARREL, HYDROLASE, CELL WALL, PEPTIDOGLYCAN-ANCHOR, SECRETED 
3s9z:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 4-(2-BROMOPHENYL)-2,4-DIOXOBUTANOIC ACID INHIBITOR  |   INHIBITOR COMPLEX, STRUCTURAL GENOMICS, MYCOBACTERIUM TUBERCULOSIS STRUCTURAL PROTEOMICS PROJECT, XMTB, MALATE SYNTHASE, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
3fax:A  (SER1056) to  (ASN1099)  THE CRYSTAL STRUCTURE OF GBS PULLULANASE SAP IN COMPLEX WITH MALTOTETRAOSE  |   TIM BARREL, ALPHA AMYLASE DOMAIN, PULLULANASE DOMAIN, HYDROLASE, CELL WALL, PEPTIDOGLYCAN-ANCHOR, SECRETED 
3sad:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 4-(2-MEHTYLPHENYL)-2,4-DIOXOBUTANOIC ACID INHIBITOR  |   INHIBITOR COMPLEX, STRUCTURAL GENOMICS, MYCOBACTERIUM TUBERCULOSIS STRUCTURAL PROTEOMICS PROJECT, XMTB, MALATE SYNTHASE, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
3saz:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 4-(3-BROMOPHENYL)-2,4-DIOXOBUTANOIC ACID INHIBITOR  |   INHIBITOR COMPLEX, STRUCTURAL GENOMICS, MYCOBACTERIUM TUBERCULOSIS STRUCTURAL PROTEOMICS PROJECT, XMTB, MALATE SYNTHASE, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
3sb0:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 4-(2-CHLORO-6-FLUORO-3-METHYLPHENYL)-2,4-DIOXOBUTANOIC ACID INHIBITOR  |   INHIBITOR COMPLEX, STRUCTURAL GENOMICS, MYCOBACTERIUM TUBERCULOSIS STRUCTURAL PROTEOMICS PROJECT, XMTB, MALATE SYNTHASE, TRANSFERASE- TRANSFERASE INHIBITOR COMPLEX 
4hu4:A   (ARG541) to   (PRO590)  CRYSTAL STRUCTURE OF EAL DOMAIN OF THE E. COLI DOSP - DIMERIC FORM  |   EAL DOMAIN; CYCLIC DI-GMP PHOSPHODIESTERASE; TIM-BARREL; ECDOS; DIRECT OXYGEN SENSOR, SIGNALING PROTEIN,HYDROLASE 
2phb:A    (GLY25) to    (THR54)  AN ORALLY EFFICACIOUS FACTOR XA INHIBITOR  |   FXA COAGULATION FACTOR INHIBITOR, BLOOD CLOTTING 
3sdi:E    (PHE22) to    (LYS65)  STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 20  |   20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3sdk:S    (PHE22) to    (LYS65)  STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 34  |   20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4i3c:B    (PRO27) to    (PHE69)  CRYSTAL STRUCTURE OF FLUORESCENT PROTEIN UNAG N57Q MUTANT  |   FLUORESCENT PROTEIN, BILIRUBIN BINDING PROTEIN, LIPOCALIN, BETA BARREL, CYTOSOL 
3shj:E    (GLN23) to    (LYS65)  PROTEASOME IN COMPLEX WITH HYDROXYUREA DERIVATIVE HU10  |   UBIQUITIN, DRUG DEVELOPMENT, CANCER, IMMUNOLOGY, PROTEIN DEGRADATION, UNFOLDED PROTEIN SUBSTRATES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3shj:S    (GLN23) to    (LYS65)  PROTEASOME IN COMPLEX WITH HYDROXYUREA DERIVATIVE HU10  |   UBIQUITIN, DRUG DEVELOPMENT, CANCER, IMMUNOLOGY, PROTEIN DEGRADATION, UNFOLDED PROTEIN SUBSTRATES, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1opb:A    (PHE27) to    (PHE64)  THE CRYSTAL STRUCTURES OF HOLO-AND APO-CELLULAR RETINOL BINDING PROTEIN II  |   RETINOL TRANSPORT 
1opb:B    (PHE27) to    (ASP63)  THE CRYSTAL STRUCTURES OF HOLO-AND APO-CELLULAR RETINOL BINDING PROTEIN II  |   RETINOL TRANSPORT 
1opb:C    (PHE27) to    (ASP63)  THE CRYSTAL STRUCTURES OF HOLO-AND APO-CELLULAR RETINOL BINDING PROTEIN II  |   RETINOL TRANSPORT 
1p69:A   (ASN520) to   (TRP563)  STRUCTURAL BASIS FOR VARIATION IN ADENOVIRUS AFFINITY FOR THE CELLULAR RECEPTOR CAR (P417S MUTANT)  |   VIRUS, VIRAL PROTEIN, VIRAL PROTEIN/RECEPTOR COMPLEX 
1d8c:A   (THR212) to   (ASP243)  MALATE SYNTHASE G COMPLEXED WITH MAGNESIUM AND GLYOXYLATE  |   ALPHA-BETA BARREL, TIM BARREL, GLYOXYLATE CYCLE, ENOLIZATION, CONDENSATION, CONCERTED ACID-BASE CATALYSIS, LYASE 
1p8d:A   (ILE309) to   (SER336)  X-RAY CRYSTAL STRUCTURE OF LXR LIGAND BINDING DOMAIN WITH 24(S),25- EPOXYCHOLESTEROL  |   LXR, EPOXYCHOLESTEROL, NUCLEAR RECEPTOR, STEROID RECEPTOR, LIVER X RECEPTOR, TRANSCRIPTION, MEMBRANE PROTEIN-PROTEIN BINDING COMPLEX 
1p9k:A    (LYS40) to    (ALA79)  THE SOLUTION STRUCTURE OF YBCJ FROM E. COLI REVEALS A RECENTLY DISCOVERED ALFAL MOTIF INVOLVED IN RNA-BINDING  |   ALFAL MOTIF, RNA-BINDING PROTEIN, E.COLI, MONTREAL-KINGSTON BACTERIAL STRUCTURAL GENOMICS INITIATIVE, BSGI, STRUCTURAL GENOMICS, RNA BINDING PROTEIN 
4inr:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH THE VINYL SULFONE LU102  |   UPS, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, NTN HYDROLASE, NON- LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4inr:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH THE VINYL SULFONE LU102  |   UPS, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, NTN HYDROLASE, NON- LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3gj4:C    (HIS30) to    (THR66)  CRYSTAL STRUCTURE OF HUMAN RANGDP-NUP153ZNF3 COMPLEX  |   G PROTEIN, GDP, RAN, NUP153, NUCLEAR PORE, ZINC FINGER, ACETYLATION, CYTOPLASM, GTP-BINDING, HOST-VIRUS INTERACTION, ISOPEPTIDE BOND, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, PROTEIN TRANSPORT, TRANSPORT, UBL CONJUGATION, DNA-BINDING, METAL-BINDING, MRNA TRANSPORT, NUCLEAR PORE COMPLEX, TRANSLOCATION, ZINC, ZINC- FINGER, TRANSPORT PROTEIN 
3gj5:A    (HIS30) to    (THR66)  CRYSTAL STRUCTURE OF HUMAN RANGDP-NUP153ZNF4 COMPLEX  |   G PROTEIN, GDP, RAN, NUP153, NUCLEAR PORE, ZINC FINGER, ACETYLATION, CYTOPLASM, GTP-BINDING, HOST-VIRUS INTERACTION, ISOPEPTIDE BOND, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, PROTEIN TRANSPORT, TRANSPORT, UBL CONJUGATION, DNA-BINDING, METAL-BINDING, MRNA TRANSPORT, NUCLEAR PORE COMPLEX, TRANSLOCATION, ZINC, ZINC- FINGER, TRANSPORT PROTEIN 
3gj5:C    (HIS30) to    (THR66)  CRYSTAL STRUCTURE OF HUMAN RANGDP-NUP153ZNF4 COMPLEX  |   G PROTEIN, GDP, RAN, NUP153, NUCLEAR PORE, ZINC FINGER, ACETYLATION, CYTOPLASM, GTP-BINDING, HOST-VIRUS INTERACTION, ISOPEPTIDE BOND, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, PROTEIN TRANSPORT, TRANSPORT, UBL CONJUGATION, DNA-BINDING, METAL-BINDING, MRNA TRANSPORT, NUCLEAR PORE COMPLEX, TRANSLOCATION, ZINC, ZINC- FINGER, TRANSPORT PROTEIN 
3gj8:A    (HIS30) to    (THR66)  CRYSTAL STRUCTURE OF HUMAN RANGDP-NUP153ZNF34 COMPLEX  |   G PROTEIN, GDP, RAN, NUP153, NUCLEAR PORE, ZINC FINGER, ACETYLATION, CYTOPLASM, GTP-BINDING, HOST-VIRUS INTERACTION, ISOPEPTIDE BOND, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, PROTEIN TRANSPORT, TRANSPORT, UBL CONJUGATION, DNA-BINDING, METAL-BINDING, MRNA TRANSPORT, NUCLEAR PORE COMPLEX, TRANSLOCATION, ZINC, ZINC- FINGER, TRANSPORT PROTEIN 
3gj8:C    (HIS30) to    (THR66)  CRYSTAL STRUCTURE OF HUMAN RANGDP-NUP153ZNF34 COMPLEX  |   G PROTEIN, GDP, RAN, NUP153, NUCLEAR PORE, ZINC FINGER, ACETYLATION, CYTOPLASM, GTP-BINDING, HOST-VIRUS INTERACTION, ISOPEPTIDE BOND, NUCLEOTIDE-BINDING, NUCLEUS, PHOSPHOPROTEIN, POLYMORPHISM, PROTEIN TRANSPORT, TRANSPORT, UBL CONJUGATION, DNA-BINDING, METAL-BINDING, MRNA TRANSPORT, NUCLEAR PORE COMPLEX, TRANSLOCATION, ZINC, ZINC- FINGER, TRANSPORT PROTEIN 
3gpj:E    (GLN23) to    (LYS65)  CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH SYRINGOLIN B  |   PROTEASOME, VIRULENCE, UBIQUITIN, CANCER THERAPY, IMMUNOLOGY, CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN 
3gpj:S    (GLN23) to    (LYS65)  CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH SYRINGOLIN B  |   PROTEASOME, VIRULENCE, UBIQUITIN, CANCER THERAPY, IMMUNOLOGY, CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN 
3gpw:E    (PHE22) to    (LYS65)  CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH SALINOSPORAMIDE DERIVATIVES: IRREVERSIBLE INHIBITOR LIGAND  |   PROTEASOME, UBIQUITIN, CANCER THERAPY, IMMUNOLOGY, TIME- DEPENDENT ELIMINATION OF A DEFINED LEAVING GROUP, CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN 
3gpw:S    (PHE22) to    (LYS65)  CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH SALINOSPORAMIDE DERIVATIVES: IRREVERSIBLE INHIBITOR LIGAND  |   PROTEASOME, UBIQUITIN, CANCER THERAPY, IMMUNOLOGY, TIME- DEPENDENT ELIMINATION OF A DEFINED LEAVING GROUP, CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN 
3tcq:A   (SER107) to   (LEU158)  CRYSTAL STRUCTURE OF MATRIX PROTEIN VP40 FROM EBOLA VIRUS SUDAN  |   SEATTLE STRUCTURAL GENOMICS CENTERS FOR INFECTIOUS DISEASE, SSGCID, EBOLA, SEBOV, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, MATRIX PROTEIN, VIRAL PROTEIN 
4y69:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAD-EP  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4y69:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAD-EP  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4y6a:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-PAD-EP  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4y6a:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-PAD-EP  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4y6v:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH AC-PAE-EP  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4j5x:B   (ALA279) to   (ALA312)  CRYSTAL STRUCTURE OF THE SR12813-BOUND PXR/RXRALPHA LBD HETEROTETRAMER COMPLEX  |   PREGNANE X RECEPTOR, RETINOID X RECEPTOR ALPHA, LIGAND BINDING DOMAIN, NUCLEAR RECEPTOR, SR12813, ALPHA HELICAL SANDWICH, UNIQUE INTERMOLECULAR BETA-SHEET DIMERIZATION, XENOBIOTIC SENSING, UPREGULATION OF DRUG METABOLISM ENZYMES, RETINOIC ACID-BINDING PROTEIN 
4j70:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH THE BELACTOSIN DERIVATIVE 3E  |   PROTEASOME, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, BETA-LACTONE, NTN HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4j70:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH THE BELACTOSIN DERIVATIVE 3E  |   PROTEASOME, DRUG DISCOVERY, IRREVERSIBLE INHIBITION, BETA-LACTONE, NTN HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4y84:E    (GLN20) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH N3-A(4,4-F2P)NLL-EP  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS 
4y84:S    (GLN20) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH N3-A(4,4-F2P)NLL-EP  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS 
4y8g:E    (GLN20) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH N3-APNLL-EP  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS 
4y8g:S    (GLN20) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH N3-APNLL-EP  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS 
4y8h:E    (GLN20) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH N3-APAL-EP  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS 
4y8h:S    (GLN20) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH N3-APAL-EP  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, INHIBITOR, BINDING ANALYSIS 
4y8n:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA7-DELTA7_CTER MUTANT IN COMPLEX WITH AC-PAE- EP  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
4y8s:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-LAE-EP  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
4y8s:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-LAE-EP  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
4y8t:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-PAE-EP  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
4y8t:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA2-H116D MUTANT IN COMPLEX WITH AC-PAE-EP  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
4ya0:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA2-H116E MUTANT IN COMPLEX WITH AC-PAE-EP  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
4ya0:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA2-H116E MUTANT IN COMPLEX WITH AC-PAE-EP  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
4ya1:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA2-H116N MUTANT  |   HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4ya1:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA2-H116N MUTANT  |   HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4ya4:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA2-H114D MUTANT  |   HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4ya4:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA2-H114D MUTANT  |   HYDROLASE, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4jf5:A   (SER192) to   (LEU230)  STRUCTURE OF OXA-23 AT PH 4.1  |   BETA-LACTAMASE, HYDROLASE 
1qfg:A   (GLY636) to   (ASN693)  E. COLI FERRIC HYDROXAMATE RECEPTOR (FHUA)  |   TONB-DEPENDENT RECEPTOR, INTEGRAL OUTER MEMBRANE PROTEIN, FERRICHROME-IRON RECEPTOR, ACTIVE TRANSPORT, IRON TRANSPORT PROTEIN, LIPOPOLYSACCHARIDE, METAL TRANSPORT 
1f2t:A    (GLY35) to   (LYS101)  CRYSTAL STRUCTURE OF ATP-FREE RAD50 ABC-ATPASE  |   DNA DOUBLE-STRAND BREAK REPAIR, ABC ATPASE, REPLICATION 
1f2u:A    (GLY35) to   (GLY105)  CRYSTAL STRUCTURE OF RAD50 ABC-ATPASE  |   DNA DOUBLE-STRAND BREAK REPAIR, ABC-ATPASE, REPLICATION 
1f2u:C    (GLY35) to   (LYS101)  CRYSTAL STRUCTURE OF RAD50 ABC-ATPASE  |   DNA DOUBLE-STRAND BREAK REPAIR, ABC-ATPASE, REPLICATION 
4jsq:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH THE DIMERIZED LINEAR MIMETIC OF TMC-95A - YCP:4E  |   UPS, PROTEASOME, DRUG DISCOVERY, NON-COVALENT REVERSIBLE INHIBITION, BIVALENCE, TMC-95A DERIVATIVES, NTN HYDROLASE, NON-LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4jsq:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH THE DIMERIZED LINEAR MIMETIC OF TMC-95A - YCP:4E  |   UPS, PROTEASOME, DRUG DISCOVERY, NON-COVALENT REVERSIBLE INHIBITION, BIVALENCE, TMC-95A DERIVATIVES, NTN HYDROLASE, NON-LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4jsu:E    (GLN20) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH THE DIMERIZED LINEAR MIMETIC OF TMC-95A - YCP:3A  |   UPS, PROTEASOME, DRUG DISCOVERY, NON-COVALENT REVERSIBLE INHIBITION, BIVALENCE, TMC-95A DERIVATIVES, NTN HYDROLASE, NON-LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4jsu:S    (GLN20) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH THE DIMERIZED LINEAR MIMETIC OF TMC-95A - YCP:3A  |   UPS, PROTEASOME, DRUG DISCOVERY, NON-COVALENT REVERSIBLE INHIBITION, BIVALENCE, TMC-95A DERIVATIVES, NTN HYDROLASE, NON-LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2e8y:B   (SER623) to   (ALA663)  CRYSTAL STRUCTURE OF PULLULANASE TYPE I FROM BACILLUS SUBTILIS STR. 168  |   MULTIPLE DOMAIN, BETA-ALPHA-BARREL, ALPHA-AMYLASE-FAMILY, HYDROLASE 
2e8z:B   (SER623) to   (ALA663)  CRYSTAL STRUCTURE OF PULLULANASE TYPE I FROM BACILLUS SUBTILIS STR. 168 COMPLEXED WITH ALPHA-CYCLODEXTRIN  |   MULTIPLE DOMAIN, BETA-ALPHA-BARREL, ALPHA-AMYLASE-FAMILY, ALPHA- CYCLODEXTRIN, HYDROLASE 
4jt0:E    (GLN20) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH THE DIMERIZED LINEAR MIMETIC OF TMC-95A - YCP:4A  |   UPS, PROTEASOME, DRUG DISCOVERY, NON-COVALENT REVERSIBLE INHIBITION, BIVALENCE, TMC-95A DERIVATIVES, NTN HYDROLASE, NON-LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4jt0:S    (GLN20) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH THE DIMERIZED LINEAR MIMETIC OF TMC-95A - YCP:4A  |   UPS, PROTEASOME, DRUG DISCOVERY, NON-COVALENT REVERSIBLE INHIBITION, BIVALENCE, TMC-95A DERIVATIVES, NTN HYDROLASE, NON-LYSOSOMAL PROTEIN BREAKDOWN, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
2ei6:A    (GLY25) to    (THR54)  FACTOR XA IN COMPLEX WITH THE INHIBITOR (-)-CIS-N1-[(5- CHLOROINDOL-2-YL)CARBONYL]-N2-[(5-METHYL-4,5,6,7- TETRAHYDROTHIAZOLO[5,4-C]PYRIDIN-2-YL)CARBONYL]-1,2- CYCLOHEXANEDIAMINE  |   GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM- BINDING 
2ei7:A    (GLY25) to    (THR54)  FACTOR XA IN COMPLEX WITH THE INHIBITOR TRANS-N1-[(5- CHLOROINDOL-2-YL)CARBONYL]-N2-[(5-METHYL-4,5,6,7- TETRAHYDROTHIAZOLO[5,4-C]PYRIDIN-2-YL)CARBONYL]-1,2- CYCLOHEXANEDIAMINE  |   GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM- BINDING 
2ei8:A    (GLY25) to    (THR54)  FACTOR XA IN COMPLEX WITH THE INHIBITOR (1S,2R,4S)-N1-[(5- CHLOROINDOL-2-YL)CARBONYL]-4-(N,N-DIMETHYLCARBAMOYL)-N2- [(5-METHYL-4,5,6,7-TETRAHYDROTHIAZOLO[5,4-C]PYRIDIN-2-YL) CARBONYL]-1,2-CYCLOHEXANEDIAMINE  |   GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM- BINDING 
1fi1:A   (GLY636) to   (ASN693)  FHUA IN COMPLEX WITH LIPOPOLYSACCHARIDE AND RIFAMYCIN CGP4832  |   OUTER MEMBRANE PROTEIN; TONB-DEPENDENT RECEPTOR; FHUA; SIDEROPHORE RECEPTOR; INTEGRAL MEMBRANE PROTEIN; LIPOPOLYSACCHARIDE; RIFAMYCIN CGP 4832; BETA-BARREL; ANTIBIOTIC, METAL TRANSPORT 
2exn:A    (CYS42) to    (PRO70)  SOLUTION STRUCTURE FOR THE PROTEIN CODED BY GENE LOCUS BB0938 OF BORDETELLA BRONCHISEPTICA. NORTHEAST STRUCTURAL GENOMICS TARGET BOR11.  |   BETA BARREL CONTAINING FOLD; AUTOSTRUCTURE; AUTOASSIGN; NMR STRUCTURE; BOR11, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, NORTHEAST STRUCTURAL GENOMICS CONSORTIUM, NESG, UNKNOWN FUNCTION 
2f16:E    (PHE22) to    (LYS65)  CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH BORTEZOMIB  |   BETA-SANDWICH FLANKED BY HELICES, COMPLEX STRUCTURE COVALENTLY BOUND TO THE SYNTHETIC INIHIBTOR BORTEZOMIB, HYDROLASE 
2f16:S    (PHE22) to    (LYS65)  CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH BORTEZOMIB  |   BETA-SANDWICH FLANKED BY HELICES, COMPLEX STRUCTURE COVALENTLY BOUND TO THE SYNTHETIC INIHIBTOR BORTEZOMIB, HYDROLASE 
4yw4:A   (PRO139) to   (SER172)  STREPTOCOCCUS PNEUMONIAE SIALIDASE NANC  |   SIALIDASE, NEURAMINIDASE, NANC, CBM40, HYDROLASE 
4yw4:B   (PRO139) to   (SER172)  STREPTOCOCCUS PNEUMONIAE SIALIDASE NANC  |   SIALIDASE, NEURAMINIDASE, NANC, CBM40, HYDROLASE 
4yx7:E    (PRO33) to    (LEU69)  COMPLEX OF SPAO(SPOA1,2) AND ORGB(APAR)::T4LYSOZYME FUSION PROTEIN  |   TYPE III SECRETION SYSTEM, PROTEIN TRANSPORT 
3un4:E    (GLN20) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH PR-957 (MORPHOLINE)  |   PROTEASOME, ANTIGEN PRESENTATION, DRUG DEVELOPMENT, PROTEIN DEGRADATION, HYDROLASE -HYDROLASE-INHIBITOR COMPLEX, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
3un4:S    (GLN20) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH PR-957 (MORPHOLINE)  |   PROTEASOME, ANTIGEN PRESENTATION, DRUG DEVELOPMENT, PROTEIN DEGRADATION, HYDROLASE -HYDROLASE-INHIBITOR COMPLEX, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
3un8:E    (GLN20) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH PR-957 (EPOXIDE)  |   PROTEASOME, ANTIGEN PRESENTATION, DRUG DEVELOPMENT, PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBTIOR COMPLEX 
1g5w:A    (PHE27) to    (SER63)  SOLUTION STRUCTURE OF HUMAN HEART-TYPE FATTY ACID BINDING PROTEIN  |   NMR SPECTROSCOPY, PROTEIN-LIGAND INTERACTIONS, SELECTED-FIT BINDING, LIPID BINDING PROTEIN 
1g65:S    (GLN23) to    (LYS65)  CRYSTAL STRUCTURE OF EPOXOMICIN:20S PROTEASOME REVEALS A MOLECULAR BASIS FOR SELECTIVITY OF ALPHA,BETA-EPOXYKETONE PROTEASOME INHIBITORS  |   PROTEASOME, EPOXOMICIN, UBIQUITIN, NTN-HYDOLASE, PROTEASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
1ryp:F    (GLN21) to    (LYS61)  CRYSTAL STRUCTURE OF THE 20S PROTEASOME FROM YEAST AT 2.4 ANGSTROMS RESOLUTION  |   MULTICATALYTIC PROTEINASE, 20S PROTEASOME, PROTEIN DEGRADATION, ANTIGEN PROCESSING, HYDROLASE, PROTEASE 
1ryp:T    (GLN21) to    (LYS61)  CRYSTAL STRUCTURE OF THE 20S PROTEASOME FROM YEAST AT 2.4 ANGSTROMS RESOLUTION  |   MULTICATALYTIC PROTEINASE, 20S PROTEASOME, PROTEIN DEGRADATION, ANTIGEN PROCESSING, HYDROLASE, PROTEASE 
2fgz:A   (ASP966) to  (ILE1013)  CRYSTAL STRUCTURE ANALYSIS OF APO PULLULANASE FROM KLEBSIELLA PNEUMONIAE  |   MULTIPLE DOMAIN, BETA-ALPHA-BARREL, ALPHA-AMYLASE-FAMILY, HYDROLASE 
2fh6:A   (ASP966) to  (ILE1013)  CRYSTAL STRUCTURE ANALYSIS OF KLEBSIELLA PNEUMONIAE PULLULANASE COMPLEXED WITH GLUCOSE  |   MULTIPLE DOMAIN, BETA-ALPHA-BARREL, ALPHA-AMYLASE-FAMILY, COMPLEX WITH GLUCOSE, HYDROLASE 
2fh8:A   (ASP966) to  (ILE1013)  CRYSTAL STRUCTURE ANALYSIS OF KLEBSIELLA PNEUMONIAE PULLULANASE COMPLEXED WITH ISOMALTOSE  |   MULTIPLE DOMAIN, BETA-ALPHA-BARREL, ALPHA-AMYLASE-FAMILY, COMPLEX WITH ISOMALTOSE, HYDROLASE 
2fhc:A   (ASP966) to  (ILE1013)  CRYSTAL STRUCTURE ANALYSIS OF KLEBSIELLA PNEUMONIAE PULLULANASE COMPLEXED WITH MALTOTRIOSE  |   MULTIPLE DOMAIN, BETA-ALPHA-BARREL, ALPHA-AMYLASE-FAMILY, COMPLEX WITH MALTOTRIOSE, HYDROLASE 
2fhf:A   (ASP966) to  (ILE1013)  CRYSTAL STRUCTURE ANALYSIS OF KLEBSIELLA PNEUMONIAE PULLULANASE COMPLEXED WITH MALTOTETRAOSE  |   MULTIPLE DOMAIN, BETA-ALPHA-BARREL, ALPHA-AMYLASE-FAMILY, COMPLEX WITH MALTOTETRAOSE, HYDROLASE 
2ftb:A    (ASN29) to    (PHE62)  CRYSTAL STRUCTURE OF AXOLOTL (AMBYSTOMA MEXICANUM) LIVER BILE ACID-BINDING PROTEIN BOUND TO OLEIC ACID  |   LIVER BILE ACID-BINDING PROTEIN, LIVER BASIC FATTY ACID- BINDING PROTEIN, AXOLOTL, OLEIC ACID, BABP, LB-FABP, LIPID BINDING PROTEIN 
4koo:B   (LYS169) to   (PRO210)  CRYSTAL STRUCTURE OF WHY1 FROM ARABIDOPSIS THALIANA  |   PLANT, WHIRLY, SINGLE-STRANDED DNA BINDING PROTEIN, DNA BINDING PROTEIN 
4koo:C   (LYS169) to   (PRO210)  CRYSTAL STRUCTURE OF WHY1 FROM ARABIDOPSIS THALIANA  |   PLANT, WHIRLY, SINGLE-STRANDED DNA BINDING PROTEIN, DNA BINDING PROTEIN 
4koo:D   (LYS169) to   (PRO210)  CRYSTAL STRUCTURE OF WHY1 FROM ARABIDOPSIS THALIANA  |   PLANT, WHIRLY, SINGLE-STRANDED DNA BINDING PROTEIN, DNA BINDING PROTEIN 
4koq:A   (LYS173) to   (PRO214)  CRYSTAL STRUCTURE OF WHY3 FROM ARABIDOPSIS THALIANA  |   PLANT, WHIRLY, SINGLE-STRANDED DNA BINDING PROTEIN, DNA BINDING PROTEIN 
3hye:E    (PHE22) to    (LYS65)  CRYSTAL STRUCTURE OF 20S PROTEASOME IN COMPLEX WITH HYDROXYLATED SALINOSPORAMIDE  |   CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, PROTEASOME, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN 
3hye:S    (PHE22) to    (LYS65)  CRYSTAL STRUCTURE OF 20S PROTEASOME IN COMPLEX WITH HYDROXYLATED SALINOSPORAMIDE  |   CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, PROTEASOME, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN 
3i2m:X    (LYS27) to    (ASN64)  THE CRYSTAL STRUCTURE OF PF-8, THE DNA POLYMERASE ACCESSORY SUBUNIT FROM KAPOSI S SARCOMA-ASSOCIATED HERPESVIRUS  |   PROCESSIVITY, REPLICATION 
1smp:A   (SER413) to   (ILE459)  CRYSTAL STRUCTURE OF A COMPLEX BETWEEN SERRATIA MARCESCENS METALLO-PROTEASE AND AN INHIBITOR FROM ERWINIA CHRYSANTHEMI  |   COMPLEX (METALLOPROTEASE/INHIBITOR) 
4ktr:A    (ALA26) to    (THR60)  CRYSTAL STRUCTURE OF 2-O-ALPHA-GLUCOSYLGLYCEROL PHOSPHORYLASE IN COMPLEX WITH ISOFAGOMINE AND GLYCEROL  |   (ALPHA/ALPHA)6 BARREL, PHOSPHORYLASE, TRANSFERASE 
3vcf:B   (LEU219) to   (PHE249)  SSV1 INTEGRASE C-TERMINAL CATALYTIC DOMAIN (174-335AA)  |   CATALYZES SITE-SPECIFIC INTEGRATION, RECOMBINATION 
2g7b:A    (VAL26) to    (PHE65)  CRYSTAL STRUCTURE OF THE R132K:R111L:L121E MUTANT OF CELLULAR RETINOIC ACID BINDING PROTEIN TYPE II IN COMPLEX WITH ALL-TRANS-RETINAL AT 1.18 ANGSTROMS RESOLUTION  |   CRABPII, RETINOIC ACID, RETINOIDS, BETA BARREL, CRYSTALLOGRAPHY, X-RAY, HIGH RESOLUTION, SCHIFF BASE, PROTONATED SCHIFF BASE, RETINAL, TRANSPORT PROTEIN 
1h2c:A   (SER107) to   (LEU158)  EBOLA VIRUS MATRIX PROTEIN VP40 N-TERMINAL DOMAIN IN COMPLEX WITH RNA (HIGH-RESOLUTION VP40[55-194] VARIANT).  |   VIRUS/VIRAL PROTEIN, FILOVIRUS, EBOLA VIRUS, MATRIX PROTEIN VP40, ASSEMBLY, BUDDING 
1h2d:B   (SER107) to   (LEU158)  EBOLA VIRUS MATRIX PROTEIN VP40 N-TERMINAL DOMAIN IN COMPLEX WITH RNA (LOW-RESOLUTION VP40[31-212] VARIANT).  |   VIRUS/VIRAL PROTEIN, FILOVIRUS, EBOLA VIRUS, MATRIX PROTEIN VP40, ASSEMBLY, BUDDING 
3iez:B  (GLN1499) to  (ILE1537)  CRYSTAL STRUCTURE OF THE RASGAP C-TERMINAL (RGC) DOMAIN OF IQGAP2  |   GAP, STRUCTURAL GENOMICS CONSORTIUM, SGC, ALTERNATIVE SPLICING, CALMODULIN-BINDING, PHOSPHOPROTEIN, POLYMORPHISM, SIGNALING PROTEIN 
2gpl:E    (PHE22) to    (LYS65)  TMC-95 BASED BIPHENYL-ETHER MACROCYCLES: SPECIFIC PROTEASOME INHIBITORS  |   PROTEASOMAL SUBUNIT FOLD REPRESENTS AN ANTIPARALLEL BETA- SHEET FLANKED BY HELICES; NTN-HYDROLASE 
2gpl:S    (PHE22) to    (LYS65)  TMC-95 BASED BIPHENYL-ETHER MACROCYCLES: SPECIFIC PROTEASOME INHIBITORS  |   PROTEASOMAL SUBUNIT FOLD REPRESENTS AN ANTIPARALLEL BETA- SHEET FLANKED BY HELICES; NTN-HYDROLASE 
2gq3:B   (ASN213) to   (GLU246)  MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH MAGNESIUM, MALATE, AND COENZYME A  |   TIM BARREL, COENZYME A, TRANSFERASE 
2grx:A   (GLY636) to   (ASN693)  CRYSTAL STRUCTURE OF TONB IN COMPLEX WITH FHUA, E. COLI OUTER MEMBRANE RECEPTOR FOR FERRICHROME  |   BETA BARREL, OUTER MEMBRANE, HETEROCOMPLEX, INTER-PROTEIN BETA SHEET, PROTEIN-PROTEIN, METAL TRANSPORT 
2grx:B   (GLY636) to   (ASN693)  CRYSTAL STRUCTURE OF TONB IN COMPLEX WITH FHUA, E. COLI OUTER MEMBRANE RECEPTOR FOR FERRICHROME  |   BETA BARREL, OUTER MEMBRANE, HETEROCOMPLEX, INTER-PROTEIN BETA SHEET, PROTEIN-PROTEIN, METAL TRANSPORT 
4ld8:A   (SER107) to   (LEU158)  CRYSTAL STRUCTURE OF DIMERIC SUDAN VIRUS VP40  |   VIRAL MATRIX PROTEIN, MATRIX ASSEMBLY, VIRAL BUDDING, VIRAL TRANSCRIPTION REGULATION, VIRAL PROTEIN 
4ldb:A   (SER107) to   (LEU158)  CRYSTAL STRUCTURE OF EBOLA VIRUS VP40 DIMER  |   VIRAL MATRIX PROTEIN, VIRAL BUDDING, ASSEMBLY, VIRAL TRANSCRIPTION REGULATION, VIRAL PROTEIN 
4ldb:B   (SER107) to   (LEU158)  CRYSTAL STRUCTURE OF EBOLA VIRUS VP40 DIMER  |   VIRAL MATRIX PROTEIN, VIRAL BUDDING, ASSEMBLY, VIRAL TRANSCRIPTION REGULATION, VIRAL PROTEIN 
4ldb:C   (SER107) to   (LEU158)  CRYSTAL STRUCTURE OF EBOLA VIRUS VP40 DIMER  |   VIRAL MATRIX PROTEIN, VIRAL BUDDING, ASSEMBLY, VIRAL TRANSCRIPTION REGULATION, VIRAL PROTEIN 
4ldb:D   (SER107) to   (LEU158)  CRYSTAL STRUCTURE OF EBOLA VIRUS VP40 DIMER  |   VIRAL MATRIX PROTEIN, VIRAL BUDDING, ASSEMBLY, VIRAL TRANSCRIPTION REGULATION, VIRAL PROTEIN 
4ldd:B   (SER107) to   (LEU158)  CRYSTAL STRUCTURE OF EBOLA VIRUS VP40 HEXAMER  |   EBOLAVIRUS MATRIX ASSEMBLY, VIRAL PROTEIN 
4ldd:C   (SER107) to   (LEU158)  CRYSTAL STRUCTURE OF EBOLA VIRUS VP40 HEXAMER  |   EBOLAVIRUS MATRIX ASSEMBLY, VIRAL PROTEIN 
4ldd:A   (SER107) to   (LEU158)  CRYSTAL STRUCTURE OF EBOLA VIRUS VP40 HEXAMER  |   EBOLAVIRUS MATRIX ASSEMBLY, VIRAL PROTEIN 
4ldm:A   (SER107) to   (LEU158)  CRYSTAL STRUCTURE OF AN RNA-FREE VP40 OCTAMERIC RING  |   EBOLAVIRUS MATRIX PROTEIN, RNA BINDING RING, VIRAL TRANSCRIPTION REGULATION, VIRAL PROTEIN 
2gys:B     (THR3) to    (ASN42)  2.7 A STRUCTURE OF THE EXTRACELLULAR DOMAINS OF THE HUMAN BETA COMMON RECEPTOR INVOLVED IN IL-3, IL-5, AND GM-CSF SIGNALLING  |   DIMER OF INTERLOCKING CHAINS OF FIBRONECTIN-III DOMAINS, FOUR FIBRONECTIN-III DOMAINS PER CHAIN, SIGNALING PROTEIN, CYTOKINE 
3vnf:A    (PRO13) to    (ASN50)  STRUCTURE OF THE EBOLAVIRUS PROTEIN VP24 FROM SUDAN  |   EBOLAVIRUS, INTERFERON ANTAGONIST, VP24, STAT1, ZAIRE, SUDAN, RESTON, VP35, KARYOPHERIN ALPHA, IFN RESPONSE PATHWAY, VIRAL PROTEIN 
4zzg:F    (GLN21) to    (LYS61)  YEAST 20S PROTEASOME IN COMPLEX WITH BLM-PEP ACTIVATOR  |   20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE 
4zzg:T    (GLN21) to    (LYS61)  YEAST 20S PROTEASOME IN COMPLEX WITH BLM-PEP ACTIVATOR  |   20S PROTEASOME, LOW-MOLECULAR MASS ACTIVATORS, ALLOSTERIC REGULATION, HYDROLASE 
3vst:C   (ALA165) to   (ASN200)  THE COMPLEX STRUCTURE OF XYLC WITH TRIS  |   GLYCOSIDE HYDROLASE, BETA-XYLOSIDASE, PRODUCT INHIBITION, HYDROLASE 
4lp7:C    (PRO45) to    (ASN91)  CRYSTAL STRUCTURE OF THE HUMAN METAPNEUMOVIRUS MATRIX PROTEIN  |   TWISTED BETA SANDWICH, VIRAL MATRIX, LIPID BINDING, CALCIUM BINDING PROTEIN 
4lqi:E    (PHE22) to    (LYS65)  YEAST 20S PROTEASOME IN COMPLEX WITH VIBRALACTONE  |   BETA-LACTONE, INHIBITOR, NATURAL PRODUCT, TARGET IDENTIFICATION, NTN- PROTEASE, CELLULAR PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4lqi:S    (PHE22) to    (LYS65)  YEAST 20S PROTEASOME IN COMPLEX WITH VIBRALACTONE  |   BETA-LACTONE, INHIBITOR, NATURAL PRODUCT, TARGET IDENTIFICATION, NTN- PROTEASE, CELLULAR PROTEIN DEGRADATION, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4ltc:E    (PHE19) to    (LYS60)  CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH ENONE CARMAPHYCIN ANALOGUE 6  |   PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4ltc:S    (PHE19) to    (LYS60)  CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH ENONE CARMAPHYCIN ANALOGUE 6  |   PROTEASOME, INHIBITOR, CARMAPHYCIN, EPOXYKETONE, VINYLKETONE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
1u5i:A   (ASN117) to   (ASP155)  CRYSTAL STRUCTURE ANALYSIS OF RAT M-CALPAIN MUTANT LYS10 THR  |   CALPAIN, SULFHYDRYL PROTEASE, CRYSTAL STRUCTURE, HYDROLASE 
1uqw:B   (GLY152) to   (LYS180)  CRYSTAL STRUCTURE OF YLIB PROTEIN FROM ESCHERICHIA COI  |   ZN BINDING PROTEIN, TRANSPORT, LIPOPROTEIN, BACTERIAL TARGETS AT IGS-CNRS, FRANCE, BIGS, STRUCTURAL GENOMICS 
1iv8:A   (ASP135) to   (PRO162)  CRYSTAL STRUCTURE OF MALTOOLIGOSYL TREHALOSE SYNTHASE  |   TREHALOSE SYNTHASE, BETA ALPHA BARREL, INTRAMOLECULAR TRANSGLUCOSYLATION, ISOMERASE 
1v7v:A   (ASN166) to   (PHE204)  CRYSTAL STRUCTURE OF VIBRIO PROTEOLYTICUS CHITOBIOSE PHOSPHORYLASE  |   BETA-SANDWICH, (ALPHA/ALPHA)6 BARREL, TRANSFERASE 
1v7w:A   (ASN166) to   (PHE204)  CRYSTAL STRUCTURE OF VIBRIO PROTEOLYTICUS CHITOBIOSE PHOSPHORYLASE IN COMPLEX WITH GLCNAC  |   BETA-SANDWICH, (ALPHA/ALPHA)6 BARREL, TRANSFERASE 
1v7x:A   (ASN166) to   (PHE204)  CRYSTAL STRUCTURE OF VIBRIO PROTEOLYTICUS CHITOBIOSE PHOSPHORYLASE IN COMPLEX WITH GLCNAC AND SULFATE  |   BETA-SANDWICH, (ALPHA/ALPHA)6 BARREL, TRANSFERASE 
1jd2:E    (PHE22) to    (LYS65)  CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME:TMC-95A COMPLEX: A NON- COVALENT PROTEASOME INHIBITOR  |   BETA-SANDWICH, PROTEASOME:INHIBITOR COMPLEX, HYDROLASE, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
3wtf:A    (THR73) to   (PRO113)  STRUCTURE OF PAXX  |   DNA REPAIR, SCAFFOLD, IMMUNE SYSTEM 
2j94:A    (GLY25) to    (THR54)  CRYSTAL STRUCTURE OF A HUMAN FACTOR XA INHIBITOR COMPLEX  |   GAMMA- CARBOXYGLUTAMIC ACID, SERINE PROTEASE, EGF-LIKE DOMAIN, BLOOD COAGULATION, POLYMORPHISM, GLYCOPROTEIN, HYDROXYLATION, GAMMA-CARBOXYGLUTAMIC ACID, CALCIUM, ZYMOGEN, COMPLEX, PROTEASE, HYDROLASE 
5az4:B   (GLU667) to   (PHE717)  CRYSTAL STRUCTURE OF A 79KDA FRAGMENT OF FLGE, THE HOOK PROTEIN FROM CAMPYLOBACTER JEJUNI  |   FLAGELLUM, HOOK, UNIVERSAL JOINT, MOTOR PROTEIN 
1w1w:A    (SER40) to   (ILE121)  SC SMC1HD:SCC1-C COMPLEX, ATPGS  |   COHESIN, CHROMOSOME SEGREGATION, CELL ADHESION, KLEISIN, MITOSIS, CELL CYCLE 
1w1w:D    (GLY38) to   (ILE121)  SC SMC1HD:SCC1-C COMPLEX, ATPGS  |   COHESIN, CHROMOSOME SEGREGATION, CELL ADHESION, KLEISIN, MITOSIS, CELL CYCLE 
1kac:A   (ASN520) to   (TRP563)  KNOB DOMAIN FROM ADENOVIRUS SEROTYPE 12 IN COMPLEX WITH DOMAIN 1 OF ITS CELLULAR RECEPTOR CAR  |   ADHESION PROTEIN RECEPTOR COMPLEX, VIRAL PROTEIN/RECEPTOR COMPLEX 
2k62:A    (ILE28) to    (THR63)  NMR SOLUTION STRUCTURE OF THE SUPRAMOLECULAR ADDUCT BETWEEN A LIVER CYTOSOLIC BILE ACID BINDING PROTEIN AND A BILE ACID-BASED GD(III)-CHELATE  |   HEPATOSPECIFIC CONTRAST AGENT, HADDOCK, GD(III) BILE ACID ADDUCT, ACETYLATION, CYTOPLASM, LIPID-BINDING, TRANSPORT, LIPID BINDING PROTEIN 
1wu1:A    (GLY25) to    (THR54)  FACTOR XA IN COMPLEX WITH THE INHIBITOR 4-[(5-CHLOROINDOL-2-YL) SULFONYL]-2-(2-METHYLPROPYL)-1-[[5-(PYRIDIN-4-YL) PYRIMIDIN-2- YL]CARBONYL]PIPERAZINE  |   GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM-BINDING 
1kgl:A    (VAL27) to    (PHE64)  SOLUTION STRUCTURE OF CELLULAR RETINOL BINDING PROTEIN TYPE- I IN COMPLEX WITH ALL-TRANS-RETINOL  |   BETA BARREL, RETINOID CARRIER, HOLO FORM, NMR SPECTROSCOPY, 15N ISOTOPE ENRICHMENT, LIPID BINDING PROTEIN 
5c7v:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 1H-PYRROLE-2-CARBOXYLIC ACID  |   FRAGMENT, COMPLEX, INHIBITOR, TRANSFERASE 
5c9u:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 2-(2-(2,4-DICHLOROPHENYL)HYDRAZINYL)-2-OXOACETIC ACID  |   FRAGMENT, COMPLEX, ACETYL-TRANSFERASE, TRANSFERASE 
5c9w:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH (Z)-N-(2-BROMOPHENYL)-2-(HYDROXYIMINO)ACETAMIDE  |   FRAGMENT, COMPLEX, OXIDOREDUCTASE 
5cak:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 2-HYDROXY-3-(1H-INDOL-3-YL)PROPANOIC ACID  |   FRAGMENT, COMPLEX, ACETYLTRANSFERASE, TRANSFERASE 
5cbb:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 5-(3H-INDOL-3-YLIDENE)-2,5-DIHYDRO-1H-PYRAZOLE-3- CARBOXYLATE  |   FRAGMENT, COMPLEX, ACETYLTRANSFERASE, TRANSFERASE 
5cbi:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 5-CHLORO-2-HYDROXYBENZONITRILE  |   FRAGMENT, COMPLEX, ACETYLTRANSFERASE, TRANSFERASE 
5cbj:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 3-(PHENYLTHIO)ACRYLIC ACID  |   COMPLEX, FRAGMENT, TRANSFERASE 
5cc3:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 6-BROMO-1H-INDOLE-2-CARBOXYLIC ACID  |   COMPLEX, FRAGMENT, TRANSFERASE 
5cc5:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 1H-INDOLE-3-CARBOXYLIC ACID  |   COMPLEX, FRAGMENT, TRANSFERASE 
5cc7:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 1H-INDOLE-6-CARBOXYLIC ACID  |   COMPLEX, FRAGMENT, TRANSFERASE 
5ccz:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 3-(4-FLUOROPHENYL)-4-METHYL-1H-PYRAZOL-5-AMINE  |   FRAGMENT, COMPLEX, ACETYLTRANSFERASE, TRANSFERASE 
2nub:A   (LYS120) to   (PRO165)  STRUCTURE OF AQUIFEX AEOLICUS ARGONUATE  |   RNASEH, ARGONAUTE, RIBONUCLEASE, RNAI, RISC, SIGNALING PROTEIN 
2yoc:A   (ASP954) to  (ILE1001)  CRYSTAL STRUCTURE OF PULA FROM KLEBSIELLA OXYTOCA  |   HYDROLASE, GLYCOSYL HYDROLASE, TYPE 2 SECRETION SYSTEMS 
2yoc:B   (ASP954) to  (ILE1001)  CRYSTAL STRUCTURE OF PULA FROM KLEBSIELLA OXYTOCA  |   HYDROLASE, GLYCOSYL HYDROLASE, TYPE 2 SECRETION SYSTEMS 
5cew:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 2-(PYRIDIN-4-YL)THIAZOLIDINE-4-CARBOXYLIC ACID  |   COMPLEX, FRAGMENT, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5cjm:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 4H-THIENO[3,2-B]PYRROLE-5-CARBOXYLIC ACID  |   FRAGMENT, COMPLEX, ACETYLTRANSFERASE, TRANSFERASE 
2z0l:A   (GLY103) to   (PRO147)  CRYSTAL STRUCTURE OF EBV-DNA POLYMERASE ACCESSORY PROTEIN BMRF1  |   ALPHA/BETA PROTEIN, ACTIVATOR, DNA-BINDING, EARLY PROTEIN, NUCLEUS, TRANSCRIPTION, TRANSCRIPTION REGULATION, REPLICATION, STRUCTURAL GENOMICS, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI 
2zcy:E    (GLN23) to    (LYS65)  YEAST 20S PROTEASOME:SYRINGOLIN A-COMPLEX  |   ALPHA/BETA SANDWICH, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, PROTEASOME, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN 
2zcy:S    (GLN23) to    (LYS65)  YEAST 20S PROTEASOME:SYRINGOLIN A-COMPLEX  |   ALPHA/BETA SANDWICH, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, PROTEASOME, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN 
1m4z:A     (THR4) to    (GLY51)  CRYSTAL STRUCTURE OF THE N-TERMINAL BAH DOMAIN OF ORC1P  |   DNA REPLICATION, TRANSCRIPTIONAL SILENCING, CHROMATIN, BAH DOMAIN, GENE REGULATION 
4aby:A    (GLU62) to   (ARG124)  CRYSTAL STRUCTURE OF DEINOCOCCUS RADIODURANS RECN HEAD DOMAIN  |   HYDROLASE, DNA REPAIR, DOUBLE STRAND BREAK REPAIR, ATPASE, NUCLEOTIDE BINDING DOMAIN 
4aby:C    (GLU62) to   (ARG124)  CRYSTAL STRUCTURE OF DEINOCOCCUS RADIODURANS RECN HEAD DOMAIN  |   HYDROLASE, DNA REPAIR, DOUBLE STRAND BREAK REPAIR, ATPASE, NUCLEOTIDE BINDING DOMAIN 
4aby:D    (GLU62) to   (ALA123)  CRYSTAL STRUCTURE OF DEINOCOCCUS RADIODURANS RECN HEAD DOMAIN  |   HYDROLASE, DNA REPAIR, DOUBLE STRAND BREAK REPAIR, ATPASE, NUCLEOTIDE BINDING DOMAIN 
1mdw:B   (GLU118) to   (ASP155)  CRYSTAL STRUCTURE OF CALCIUM-BOUND PROTEASE CORE OF CALPAIN II REVEALS THE BASIS FOR INTRINSIC INACTIVATION  |   CALPAIN CYSTEINE PROTEASE FOLD, TWO COOPERATIVE CALCIUM SITES, HELIX INSTABILITY, TRYPTOPHAN-BASED ACTIVE SITE BLOCKAGE, HYDROLASE 
4ad8:A    (GLU62) to   (SER126)  CRYSTAL STRUCTURE OF A DELETION MUTANT OF DEINOCOCCUS RADIODURANS RECN  |   DNA BINDING PROTEIN, DNA REPAIR, ATPASE DOMAIN 
5d0t:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA5-D166N MUTANT IN COMPLEX WITH MG132  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
5d0t:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA5-D166N MUTANT IN COMPLEX WITH MG132  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
5d0w:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA5-T1S MUTANT  |   HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
5d0w:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA5-T1S MUTANT  |   HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
5d0x:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA5-T1S MUTANT IN COMPLEX WITH BORTEZOMIB  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
5d0x:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA5-T1S MUTANT IN COMPLEX WITH BORTEZOMIB  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
1mx8:A    (ASN26) to    (GLY67)  TWO HOMOLOGOUS RAT CELLULAR RETINOL-BINDING PROTEINS DIFFER IN LOCAL STRUCTURE AND FLEXIBILITY  |   BETA-BARREL, HELIX-TURN-HELIX, VITAMIN A, RETONOL BINDING, TRANSPORT, LIPID BINDING PROTEIN 
5dac:A    (THR41) to   (THR113)  ATP-GAMMA-S BOUND RAD50 FROM CHAETOMIUM THERMOPHILUM IN COMPLEX WITH DNA  |   ATPASE, ATPYS BOUND, HYDROLASE 
5dac:B    (THR41) to   (THR113)  ATP-GAMMA-S BOUND RAD50 FROM CHAETOMIUM THERMOPHILUM IN COMPLEX WITH DNA  |   ATPASE, ATPYS BOUND, HYDROLASE 
3kzt:A   (GLY112) to   (PRO148)  CRYSTAL STRUCTURE OF PROTEIN OF UNKNOWN FUNCTION (NP_812423.1) FROM BACTEROIDES THETAIOTAOMICRON VPI-5482 AT 2.10 A RESOLUTION  |   PROTEIN OF UNKNOWN FUNCTION, STRUCTURAL GENOMICS, JOINT CENTER FOR STRUCTURAL GENOMICS, JCSG, PROTEIN STRUCTURE INITIATIVE, PSI-2, UNKNOWN FUNCTION 
5dki:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH ALKYNE-PI  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, TARGET DELIVERY, PROTEASOME, INHIBITOR, BINDING ANALYSIS 
5dki:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH ALKYNE-PI  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, TARGET DELIVERY, PROTEASOME, INHIBITOR, BINDING ANALYSIS 
5dkj:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH OCTREOTIDE-PI  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, TARGET DELIVERY, PROTEASOME, INHIBITOR, BINDING ANALYSIS 
5dkj:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH OCTREOTIDE-PI  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, TARGET DELIVERY, PROTEASOME, INHIBITOR, BINDING ANALYSIS 
5drc:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 2-HYDROXY-4-(1H-INDOL-3-YL)-4-OXOBUT-2-ENOIC ACID  |   ACETYLTRANSFERASE, TRANSFERASE 
5dri:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 2-HYDROXY-4-(1H-INDOL-5-YL)-4-OXOBUT-2-ENOIC ACID INHIBITOR  |   ACETYLTRANSFERASE, TRANSFERASE 
5dx7:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 5-(5-CHLOROTHIOPHEN-2-YL)ISOXAZOLE-3-CARBOXYLIC ACID  |   ACETYLTRANSFERASE, TRANSFERASE 
4q1s:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH KENDOMYCIN  |   PROTEASOME, NATURAL PRODUCT, QUINONE METHIDE, COVALENT BINDING, EXOSITE, HYDROLASE-TOXIN COMPLEX 
4q1s:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME IN COMPLEX WITH KENDOMYCIN  |   PROTEASOME, NATURAL PRODUCT, QUINONE METHIDE, COVALENT BINDING, EXOSITE, HYDROLASE-TOXIN COMPLEX 
4q46:A   (SER444) to   (ASN484)  THE SECOND STRUCTURE OF INFLUENZA B PB2 CAP-BINDING DOMAIN COMPLEX WITH GDP  |   CAP BINDING, VIRAL PROTEIN 
4q6u:A     (HIS0) to    (LYS26)  CRYSTAL STRUCTURE OF A PUTATIVE UNCHARACTERIZED PROTEIN FROM MYCOBACTERIUM TUBERCULOSIS  |   SEATTLE STRUCTURAL GENOICS FOR INFECTIOUS DISEASE, MYCOBACTERIUM TUBERCULOSIS, STRUCTURAL GENOMICS, SSGCID, SEATTLE STRUCTURAL GENOMICS CENTER FOR INFECTIOUS DISEASE, UNKNOWN FUNCTION 
3auy:A    (SER39) to    (LYS99)  CRYSTAL STRUCTURE OF RAD50 BOUND TO ADP  |   DNA REPAIR, ABC TRANSPORTER ATPASE DOMAIN-LIKE, P-LOOP CONTAINING NUCLEOSIDE TRIPHOSPHATE HYDROLASES, MRE11, RECOMBINATION 
3auy:B    (SER39) to    (LYS99)  CRYSTAL STRUCTURE OF RAD50 BOUND TO ADP  |   DNA REPAIR, ABC TRANSPORTER ATPASE DOMAIN-LIKE, P-LOOP CONTAINING NUCLEOSIDE TRIPHOSPHATE HYDROLASES, MRE11, RECOMBINATION 
5ecv:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 2-HYDROXY-4-(4-METHYL-1H-INDOL-5-YL)-4-OXOBUT-2-ENOIC ACID  |   TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
4qgw:B    (VAL26) to    (ASN64)  CRYSTAL STURCTURE OF THE R132K:R111L:L121D MUTANT OF CELLULAR RETINOIC ACID BINDING PROTEINII COMPLEXED WITH A SYNTHETIC LIGAND (MEROCYANINE) AT 1.77 ANGSTROM RESOLUTION  |   PROTEIN ENGINEERING, PROTEIN FLUORESCENCE, MEROCYANINE DYES FOR FLUORESCENT PROTEIN LABELING, FLUORESCENT PROTEIN TAG, MEROCYANINE PROTONATED SCHIFF BASE IMINIUM, PROTEIN BINDING 
4qls:E    (GLN20) to    (LYS60)  YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 11  |   PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4qls:S    (GLN20) to    (LYS60)  YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 11  |   PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4qlu:E    (PHE19) to    (LYS60)  YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 9  |   PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4qlu:S    (PHE19) to    (LYS60)  YCP IN COMPLEX WITH TRIPEPTIDIC EPOXYKETONE INHIBITOR 9  |   PROTEASOME, EPOXYKETONE, IMMUNOPROTEASOME INHIBITOR, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3mg4:E    (PHE22) to    (LYS65)  STRUCTURE OF YEAST 20S PROTEASOME WITH COMPOUND 1  |   20S PROTEASOME, HYDROLASE 
3mg4:S    (PHE22) to    (LYS65)  STRUCTURE OF YEAST 20S PROTEASOME WITH COMPOUND 1  |   20S PROTEASOME, HYDROLASE 
3mg6:S    (GLN23) to    (LYS65)  STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 6  |   20S PROTEASOME, HYDROLASE 
3mg8:S    (GLN23) to    (LYS65)  STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 16  |   20S PROTEASOME, HYDROLASE 
4be7:B   (LEU129) to   (LYS168)  MUTANT (K220R) OF THE HSDR SUBUNIT OF THE ECOR124I RESTRICTION ENZYME IN COMPLEX WITH ATP  |   HYDROLASE, DNA RESTRICTION, DNA MODIFICATION 
4qux:E    (PHE19) to    (LYS60)  YCP BETA5-A49T-MUTANT  |   CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE 
4qux:S    (PHE19) to    (LYS60)  YCP BETA5-A49T-MUTANT  |   CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE 
4quy:E    (PHE19) to    (LYS60)  YCP BETA5-A49S-MUTANT  |   CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE 
4quy:S    (PHE19) to    (LYS60)  YCP BETA5-A49S-MUTANT  |   CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE 
4qv6:E    (GLN20) to    (LYS60)  YCP BETA5-A49V MUTANT  |   CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE 
4qv6:S    (GLN20) to    (LYS60)  YCP BETA5-A49V MUTANT  |   CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE 
4qv9:E    (GLN20) to    (LYS60)  YCP BETA5-C63F MUTANT  |   CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE 
4qv9:S    (GLN20) to    (LYS60)  YCP BETA5-C63F MUTANT  |   CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE 
4qvl:E    (PHE19) to    (LYS60)  YCP IN COMPLEX WITH BORTEZOMIB  |   CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4qvl:S    (PHE19) to    (LYS60)  YCP IN COMPLEX WITH BORTEZOMIB  |   CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4qvm:E    (PHE19) to    (LYS60)  YCP BETA5-M45A MUTANT IN COMPLEX WITH BORTEZOMIB  |   CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4qvm:S    (PHE19) to    (LYS60)  YCP BETA5-M45A MUTANT IN COMPLEX WITH BORTEZOMIB  |   CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4qvw:E    (PHE19) to    (LYS60)  YCP BETA5-A49S-MUTANT IN COMPLEX WITH BORTEZOMIB  |   CANCER, PROTEASOME, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
4qvw:S    (PHE19) to    (LYS60)  YCP BETA5-A49S-MUTANT IN COMPLEX WITH BORTEZOMIB  |   CANCER, PROTEASOME, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
4qw0:E    (PHE19) to    (LYS60)  YCP BETA5-A49T-A50V-DOUBLE MUTANT IN COMPLEX WITH BORTEZOMIB  |   CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4qw0:S    (PHE19) to    (LYS60)  YCP BETA5-A49T-A50V-DOUBLE MUTANT IN COMPLEX WITH BORTEZOMIB  |   CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4r02:E    (PHE19) to    (LYS60)  YCP IN COMPLEX WITH BSC4999 (ALPHA-KETO PHENYLAMIDE)  |   CANCER, PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, REVERSIBLE COVALENT LIGAND, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3n1k:A   (SER145) to   (PRO186)  CRYSTAL STRUCTURE OF A STWHY2-CERE32 COMPLEX  |   SINGLE-STRANDED DNA BINDING PROTEIN, PLANT, WHIRLY, PROTEIN-DNA COMPLEX, DNA BINDING PROTEIN-DNA COMPLEX 
3n1l:A   (SER145) to   (PRO186)  CRYSTAL STRUCTURE OF A STWHY2-RCERE32 COMPLEX  |   SINGLE-STRANDED DNA BINDING PROTEIN, PLANT, WHIRLY, PROTEIN-DNA COMPLEX, DNA BINDING PROTEIN-DNA COMPLEX 
5f9t:B   (PRO139) to   (SER172)  CRYSTAL STRUCTURE OF STREPTOCOCCUS PNEUMONIAE NANC, COVALENT COMPLEX WITH A FLUORINATED NEU5AC DERIVATIVE  |   SIALIDASE, NEURAMINIDASE, COVALENT INTERMEDIATE, CBM40, HYDROLASE 
4r17:E    (GLN20) to    (LYS60)  LIGAND-INDUCED AZIRIDINE-FORMATION AT SUBUNIT BETA5 OF THE YEAST 20S PROTEASOME  |   PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, UMPOLUNG, CROSSLINK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4r17:S    (GLN20) to    (LYS60)  LIGAND-INDUCED AZIRIDINE-FORMATION AT SUBUNIT BETA5 OF THE YEAST 20S PROTEASOME  |   PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, UMPOLUNG, CROSSLINK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4r18:E    (GLN20) to    (LYS60)  LIGAND-INDUCED LYS33-THR1 CROSSLINKING AT SUBUNIT BETA5 OF THE YEAST 20S PROTEASOME  |   PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, UMPOLUNG, CROSSLINK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4r18:S    (GLN20) to    (LYS60)  LIGAND-INDUCED LYS33-THR1 CROSSLINKING AT SUBUNIT BETA5 OF THE YEAST 20S PROTEASOME  |   PROTEASOME, DRUG DEVELOPMENT, BINDING ANALYSIS, UMPOLUNG, CROSSLINK, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4c21:A   (GLU418) to   (LEU462)  L-FUCOSE ISOMERASE IN COMPLEX WITH FUCITOL  |   FUCOSE PROCESSING, ISOMERASE 
4c47:B    (LYS28) to   (SER118)  SALMONELLA ENTERICA TRIMERIC LIPOPROTEIN SADB  |   CELL ADHESION, BACTERIAL ADHESION, MEMBRANE TRAFFICKING, MEMBRANE INSERTION, AUTOTRANSPORT, POLAR CORE RESIDUES 
3nzj:E    (PHE22) to    (LYS65)  CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH LIGAND 2A  |   UBIQUITIN, PROTEIN DEGRADATION, N-TERMINAL NUCLEOPHILIC HYDROLASE, 19S REGULATORY PARTICLE, UBIQUITIN-TAGGED SUBSTRATES, CYTOSOL, NUCLEUS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3nzj:S    (PHE22) to    (LYS65)  CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH LIGAND 2A  |   UBIQUITIN, PROTEIN DEGRADATION, N-TERMINAL NUCLEOPHILIC HYDROLASE, 19S REGULATORY PARTICLE, UBIQUITIN-TAGGED SUBSTRATES, CYTOSOL, NUCLEUS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3nzw:E    (PHE22) to    (LYS65)  CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH 2B  |   UBIQUITIN, PROTEIN DEGRADATION, N-TERMINAL NUCLEOPHILIC HYDROLASE, 19S REGULATORY PARTICLE, UBIQUITIN-TAGGED SUBSTRATES, CYTOSOL, NUCLEUS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3nzw:S    (PHE22) to    (LYS65)  CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH 2B  |   UBIQUITIN, PROTEIN DEGRADATION, N-TERMINAL NUCLEOPHILIC HYDROLASE, 19S REGULATORY PARTICLE, UBIQUITIN-TAGGED SUBSTRATES, CYTOSOL, NUCLEUS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3d29:E    (GLN23) to    (LYS65)  PROTEASOME INHIBITION BY FELLUTAMIDE B  |   ANTI-PARALLEL BETA-SHEET STRUCTURE FLANKED BY ALPHA-HELICES, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, PROTEASOME, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN 
3d29:S    (GLN23) to    (LYS65)  PROTEASOME INHIBITION BY FELLUTAMIDE B  |   ANTI-PARALLEL BETA-SHEET STRUCTURE FLANKED BY ALPHA-HELICES, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, PROTEASOME, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN 
4cvw:A   (THR775) to   (VAL827)  STRUCTURE OF THE BARLEY LIMIT DEXTRINASE-LIMIT DEXTRINASE INHIBITOR COMPLEX  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, STARCH DEBRANCHING ENZYME, GLYCOSIDE HYDROLASE FAMILY 13, PULLULANASE, CEREAL-TYPE INHIBITOR, CM-PROTEIN, ENDOGENOUS INHIBITOR 
4cvw:B   (THR775) to   (VAL827)  STRUCTURE OF THE BARLEY LIMIT DEXTRINASE-LIMIT DEXTRINASE INHIBITOR COMPLEX  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, STARCH DEBRANCHING ENZYME, GLYCOSIDE HYDROLASE FAMILY 13, PULLULANASE, CEREAL-TYPE INHIBITOR, CM-PROTEIN, ENDOGENOUS INHIBITOR 
3oeu:S    (PHE22) to    (LYS65)  STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 24  |   20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3oev:S    (PHE22) to    (LYS65)  STRUCTURE OF YEAST 20S OPEN-GATE PROTEASOME WITH COMPOUND 25  |   20S PROTEASOME, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4cyv:C   (SER187) to   (LEU236)  STRUCTURE OF THE A_MALLARD_SWEDEN_51_2002 H10 AVIAN HAEMMAGLUTININ  |   VIRAL PROTEIN 
4cyz:A   (SER187) to   (LEU236)  STRUCTURE OF THE A_MALLARD_SWEDEN_51_2002 H10 AVIAN HAEMMAGLUTININ IN COMPLEX WITH AVIAN RECEPTOR ANALOG LSTA  |   VIRAL PROTEIN 
4cyz:E   (THR188) to   (LEU236)  STRUCTURE OF THE A_MALLARD_SWEDEN_51_2002 H10 AVIAN HAEMMAGLUTININ IN COMPLEX WITH AVIAN RECEPTOR ANALOG LSTA  |   VIRAL PROTEIN 
4d00:A   (SER180) to   (LEU229)  HAEMAGGLUTININ OF H10N8 INFLUENZA VIRUS ISOLATED FROM HUMANS IN COMPLEX WITH HUMAN RECEPTOR ANALOGUE 6'SLN  |   VIRAL PROTEIN, H10N8, INFLUENZA, SIALIC ACID, GLYCOPROTEIN, VIRUS RECEPTOR, AVIAN FLU, SIALYLLACTOSAMINE, LSTA 
4d00:C   (SER180) to   (LEU229)  HAEMAGGLUTININ OF H10N8 INFLUENZA VIRUS ISOLATED FROM HUMANS IN COMPLEX WITH HUMAN RECEPTOR ANALOGUE 6'SLN  |   VIRAL PROTEIN, H10N8, INFLUENZA, SIALIC ACID, GLYCOPROTEIN, VIRUS RECEPTOR, AVIAN FLU, SIALYLLACTOSAMINE, LSTA 
4d00:E   (SER180) to   (LEU229)  HAEMAGGLUTININ OF H10N8 INFLUENZA VIRUS ISOLATED FROM HUMANS IN COMPLEX WITH HUMAN RECEPTOR ANALOGUE 6'SLN  |   VIRAL PROTEIN, H10N8, INFLUENZA, SIALIC ACID, GLYCOPROTEIN, VIRUS RECEPTOR, AVIAN FLU, SIALYLLACTOSAMINE, LSTA 
3dgv:C    (TYR29) to    (GLY67)  CRYSTAL STRUCTURE OF THROMBIN ACTIVATABLE FIBRINOLYSIS INHIBITOR (TAFI)  |   BLOOD COAGULATION, FIBRINOLYSIS, CARBOXYPEPTIDASE, PROTEIN STABILITY, GLYCOPROTEIN, HYDROLASE, METAL-BINDING, METALLOPROTEASE, PROTEASE, SECRETED, ZYMOGEN 
4d4t:A    (PRO44) to    (CYS91)  RSV MATRIX PROTEIN  |   VIRAL PROTEIN 
5gxh:A    (PRO76) to   (ALA106)  THE STRUCTURE OF THE GEMIN5 WD40 DOMAIN WITH AAUUUUUG  |   SNRNP ASSEMBLY, SNRNA, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, RNA BINDING PROTEIN-RNA COMPLEX 
5gxi:A    (PRO76) to   (ALA106)  STRUCUTRE OF THE GEMIN5 WD40 DOMAIN IN COMPLEX WITH AAUUUUUGAG  |   SNRNP ASSEMBLY, SNRNA, STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, RNA BINDING PROTEIN-RNA COMPLEX 
5h1k:B    (PRO76) to   (ALA106)  CRYSTAL STRUCTURE OF WD40 REPEAT DOMAINS OF GEMIN5 IN COMPLEX WITH 13- NT U4 SNRNA FRAGMENT  |   WD REPEAT, GEMIN5, SMN, RNA BINDING, U4 SNRNA, SPLICING-RNA COMPLEX 
5h1l:A    (PRO76) to   (ALA106)  CRYSTAL STRUCTURE OF WD40 REPEAT DOMAINS OF GEMIN5 IN COMPLEX WITH 7- NT U4 SNRNA FRAGMENT  |   WD REPEAT, GEMIN5, SMN, U4 SNRNA, RNA BINDING, SPLICING-RNA COMPLEX 
5h8m:A   (ASN213) to   (PRO245)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE C619A, G459A MUTANT IN COMPLEX WITH PRODUCT MALATE  |   TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5h8p:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN APO FORM  |   FRAGMENT, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5h8u:B   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS WILD-TYPE MALATE SYNTHASE IN COMPLEX WITH PRODUCT MALATE  |   TRANSFERASE 
3dy3:E    (GLN23) to    (LYS65)  CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH THE EPIMER FORM OF SPIROLACTACYSTIN  |   PROTEASOME, INHIBITOR, PROTEIN DEGRADATION, UBIQUITIN- PROTEASOME-PATHWAY, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN 
3dy3:S    (GLN23) to    (LYS65)  CRYSTAL STRUCTURE OF YEAST 20S PROTEASOME IN COMPLEX WITH THE EPIMER FORM OF SPIROLACTACYSTIN  |   PROTEASOME, INHIBITOR, PROTEIN DEGRADATION, UBIQUITIN- PROTEASOME-PATHWAY, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN 
3e2e:A   (ALA691) to   (LYS741)  CRYSTAL STRUCTURE OF AN INTERMEDIATE COMPLEX OF T7 RNAP AND 7NT OF RNA  |   T7 RNA POLYMERASE, DNA-DIRECTED RNA POLYMERASE, TRANSCRIPTION, NUCLEOTIDYLTRANSFERASE, TRANSFERASE, TRANSFERASE-RNA-DNA COMPLEX 
3e3j:C   (VAL693) to   (LYS741)  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 
3pjt:B   (ASP409) to   (ALA461)  STRUCTURE OF PSEUDOMONAS FLUORESCENCE LAPD EAL DOMAIN COMPLEXED WITH C-DI-GMP, C2221  |   TIM BARREL, C-DI-GMP RECEPTOR, LYASE 
4eu2:F    (PHE20) to    (LYS61)  CRYSTAL STRUCTURE OF 20S PROTEASOME WITH NOVEL INHIBITOR K-7174  |   PROTEASOME INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4eu2:T    (PHE20) to    (LYS61)  CRYSTAL STRUCTURE OF 20S PROTEASOME WITH NOVEL INHIBITOR K-7174  |   PROTEASOME INHIBITOR, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3qc5:X   (ASN567) to   (ASP593)  GSPB  |   CARBOHYDRATE/SUGAR BINDING, SUGAR BINDING PROTEIN 
4eza:A    (GLN24) to    (ASN61)  CRYSTAL STRUCTURE OF THE ATYPICAL PHOSPHOINOSITIDE (API) BINDING DOMAIN OF IQGAP2  |   GAP, STRUCTURAL GENOMICS CONSORTIUM, SGC, SIGNALING PROTEIN 
4eza:B    (GLN24) to    (ILE62)  CRYSTAL STRUCTURE OF THE ATYPICAL PHOSPHOINOSITIDE (API) BINDING DOMAIN OF IQGAP2  |   GAP, STRUCTURAL GENOMICS CONSORTIUM, SGC, SIGNALING PROTEIN 
3qks:A    (GLY35) to   (LYS101)  MRE11 RAD50 BINDING DOMAIN BOUND TO RAD50  |   RECA-LIKE FOLD, COILED-COILS, ATPASE, EXONUCLEASE, ENDONUCLEASE, ATP BINDING, DNA BINDING, REPLICATION 
3qkt:B    (GLY35) to   (GLY105)  RAD50 ABC-ATPASE WITH ADJACENT COILED-COIL REGION IN COMPLEX WITH AMP- PNP  |   RECA-LIKE FOLD, COILED-COILS, ATPASE, ATP BINDING, DNA BINDING, MRE11, REPLICATION 
3qku:A    (GLY35) to   (LYS101)  MRE11 RAD50 BINDING DOMAIN IN COMPLEX WITH RAD50 AND AMP-PNP  |   RECA-LIKE FOLD, COILED-COILS, ATPASE, EXONUCLEASE, ENDONUCLEASE, ATP BINDING, DNA BINDING, REPLICATION 
3qku:B    (GLY35) to   (GLY105)  MRE11 RAD50 BINDING DOMAIN IN COMPLEX WITH RAD50 AND AMP-PNP  |   RECA-LIKE FOLD, COILED-COILS, ATPASE, EXONUCLEASE, ENDONUCLEASE, ATP BINDING, DNA BINDING, REPLICATION 
3r1x:B    (ALA84) to   (GLY118)  CRYSTAL STRUCTURE OF 2-OXO-3-DEOXYGALACTONATE KINASE FROM KLEBSIELLA PNEUMONIAE  |   STRUCTURAL GENOMICS, PSI-BIOLOGY, MIDWEST CENTER FOR STRUCTURAL GENOMICS, MCSG, 2-OXO-3-DEOXYGALACTONATE KINASE, 2-DEHYDRO-3- DEOXYGALACTONOKINASE, 2-KETO-3-DEOXYGALACTONATE KINASE, DELEY- DOUDOROFF PATHWAY, TRANSFERASE 
3r9y:A   (SER145) to   (THR188)  CRYSTAL STRUCTURE OF STWHY2 K67A (FORM I)  |   STWHY2, SINGLE-STRANDED DNA BINDING PROTEIN, PLANT, POTATO, WHIRLY, MITOCHONDRIA, DNA BINDING PROTEIN 
4fpg:A    (ALA95) to   (SER128)  CRYSTAL STRUCTURE OF THE NANB SIALIDASE FROM STREPTOCOCCUS PNEUMONIAE IN COMPLEX WITH 2-[(3-HYDROXYBENZYL)AMMONIO]ETHANESULFONATE  |   HYDROLASE, INTRAMOLECULAR TRANS-SIALIDASE, GLYCOSIDASE, DRUG DESIGN, NEURAMINIDASE, HYDROLASE-INHIBITOR COMPLEX 
4g1m:B   (CYS435) to   (PRO464)  RE-REFINEMENT OF ALPHA V BETA 3 STRUCTURE  |   PROTEIN BINDING 
5l5b:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133)  |   HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
5l5b:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133)  |   HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
5l5d:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH ONX 0914  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
5l5d:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH ONX 0914  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
5l5h:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH PR-924  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
5l5h:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH PR-924  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
5l5i:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 9  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
5l5i:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 9  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
5l61:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (99- 132) IN COMPLEX WITH EPOXYKETONE INHIBITOR 14  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
5l61:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (99- 132) IN COMPLEX WITH EPOXYKETONE INHIBITOR 14  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
5l62:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 16  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
5l62:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 16  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
5l65:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH CARFILZOMIB  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
5l69:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 16  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
5l69:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 16  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
5l6c:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 18  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
5l6c:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME WITH MOUSE BETA5I (1-138) AND MOUSE BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 18  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
5l8o:B    (SER25) to    (PHE64)  CRYSTAL STRUCTURE OF HUMAN FABP6 IN COMPLEX WITH CHOLATE  |   FABP6, FATTY ACID BINDING PROTEIN 6, ILEAL BILE ACID BINDING PROTEIN, I-BABP, ILEAL, GASTROTROPIN, FRAGMENTS, CHOLATE, LIPID BINDING PROTEIN 
5t8g:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 2-OXO-4-((THIOPHENE-2-CARBONYL)OXY)BUTANOIC ACID  |   TRANSFERASE, INHIBITOR, TRANSFERASE-TRANSFERASE INHIBITOR COMPLEX 
5tee:A    (PRO76) to   (LEU107)  CRYSTAL STRUCTURE OF GEMIN5 WD40 REPEATS IN APO FORM  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, SPLICING 
5tef:A    (PRO76) to   (ALA106)  CRYSTAL STRUCTURE OF GEMIN5 WD40 REPEATS IN COMPLEX WITH M7GPPPG  |   STRUCTURAL GENOMICS, STRUCTURAL GENOMICS CONSORTIUM, SGC, SPLICING 
1n8i:A   (ASN213) to   (ASP244)  BIOCHEMICAL AND STRUCTURAL STUDIES OF MALATE SYNTHASE FROM MYCOBACTERIUM TUBERCULOSIS  |   MALATE SYNTHASE, GLYOXYLATE PATHWAY, MYCOBACTERIUM TUBERCULOSIS, ACETYL COENZYME A, ISOCITRATE LYASE, PERSISTENCE, GLCB, STRUCTURAL GENOMICS, PSI, PROTEIN STRUCTURE INITIATIVE, TB STRUCTURAL GENOMICS CONSORTIUM, TBSGC 
2p95:A    (GLY25) to    (THR54)  FACTOR XA IN COMPLEX WITH THE INHIBITOR 5-CHLORO-N-((1R,2S)- 2-(4-(2-OXOPYRIDIN-1(2H)-YL)BENZAMIDO) CYCLOPENTYL) THIOPHENE-2-CARBOXAMIDE  |   GLYCOPROTEIN, HYDROLASE, SERINE PROTEASE, PLASMA, BLOOD COAGULATION FACTOR, PROTEIN INHIBITOR COMPLEX, CALCIUM- BINDING 
2qre:C   (ARG491) to   (ASP540)  CRYSTAL STRUCTURE OF THE ADENYLATE SENSOR FROM AMP-ACTIVATED PROTEIN KINASE IN COMPLEX WITH 5-AMINOIMIDAZOLE-4-CARBOXAMIDE 1-BETA-D- RIBOFURANOTIDE (ZMP)  |   AMPK, 5-AMINOIMIDAZOLE-4-CARBOXAMIDE 1-BETA-D-RIBOFURANOTIDE, ZMP, AICAR PHOSPHATE, ATP-BINDING, KINASE, NUCLEOTIDE-BINDING, SERINE/THREONINE-PROTEIN KINASE, TRANSFERASE, CBS DOMAIN 
3gpt:E    (GLN23) to    (LYS65)  CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH SALINOSPORAMIDE DERIVATIVES: SLOW SUBSTRATE LIGAND  |   PROTEASOME, UBIQUITIN, CANCER THERAPY, INHIBITOR, IMMUNOLOGY, TIME DEPENDENT LEAVING GROUP ELIMINATION, CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN 
3gpt:S    (GLN23) to    (LYS65)  CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH SALINOSPORAMIDE DERIVATIVES: SLOW SUBSTRATE LIGAND  |   PROTEASOME, UBIQUITIN, CANCER THERAPY, INHIBITOR, IMMUNOLOGY, TIME DEPENDENT LEAVING GROUP ELIMINATION, CYTOPLASM, HYDROLASE, NUCLEUS, PHOSPHOPROTEIN, PROTEASE, THREONINE PROTEASE, ISOPEPTIDE BOND, UBL CONJUGATION, ZYMOGEN 
3tdd:E    (PHE22) to    (LYS65)  CRYSTAL STRUCTURE OF YEAST CP IN COMPLEX WITH BELACTOSIN C  |   UBIQUITIN, INHIBITOR, PROTEASOME, DRUG DEVELOPMENT, PRIMED SUBSTRATE BINDING CHANNEL, BETA-SANDWICH FLANKED BY ALPHA-HELICES, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3tdd:S    (PHE22) to    (LYS65)  CRYSTAL STRUCTURE OF YEAST CP IN COMPLEX WITH BELACTOSIN C  |   UBIQUITIN, INHIBITOR, PROTEASOME, DRUG DEVELOPMENT, PRIMED SUBSTRATE BINDING CHANNEL, BETA-SANDWICH FLANKED BY ALPHA-HELICES, HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4ya5:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA2-H114D MUTANT IN COMPLEX WITH AC-PAE-EP  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
4yw2:B   (PRO139) to   (SER172)  CRYSTAL STRUCTURE OF STREPTOCOCCUS PNEUMONIAE NANC, COMPLEX 6'SL  |   SIALIDASE, NEURAMINIDASE, 6'SL, CBM40, HYDROLASE 
2fcp:A   (GLY634) to   (ASN691)  FERRIC HYDROXAMATE UPTAKE RECEPTOR (FHUA) FROM E.COLI  |   TONB-DEPENDENT RECEPTOR, INTEGRAL OUTER MEMBRANE PROTEIN, FERRICHROME-IRON RECEPTOR, ACTIVE TRANSPORT, IRON TRANSPORT PROTEIN, MEMBRANE PROTEIN 
2fhb:A   (ASP966) to  (ILE1013)  CRYSTAL STRUCTURE ANALYSIS OF KLEBSIELLA PNEUMONIAE PULLULANASE COMPLEXED WITH MALTOSE  |   MULTIPLE DOMAIN, BETA-ALPHA-BARREL, ALPHA-AMYLASE-FAMILY, COMPLEX WITH MALTOSE, HYDROLASE 
2vqp:A    (PRO44) to    (CYS91)  STRUCTURE OF THE MATRIX PROTEIN FROM HUMAN RESPIRATORY SYNCYTIAL VIRUS  |   VIRAL PROTEIN, VIRAL MATRIX PROTEIN, PERIPHERAL MEMBRANE PROTEIN, RSV, VIRION, MATRIX PROTEIN, ENVELOPE PROTEIN 
2vqp:A   (THR182) to   (ASP225)  STRUCTURE OF THE MATRIX PROTEIN FROM HUMAN RESPIRATORY SYNCYTIAL VIRUS  |   VIRAL PROTEIN, VIRAL MATRIX PROTEIN, PERIPHERAL MEMBRANE PROTEIN, RSV, VIRION, MATRIX PROTEIN, ENVELOPE PROTEIN 
3v9x:A     (GLY9) to    (HIS61)  CRYSTAL STRUCTURE OF RNASE T IN COMPLEX WITH A PREFERRED SSDNA (AAA) WITH TWO MG IN THE ACTIVE SITE  |   DEDD NUCLEASES FAMILY, EXO-NUCLEASE, HYDROLASE-DNA COMPLEX 
2gcj:C   (GLN278) to   (GLN321)  CRYSTAL STRUCTURE OF THE POB3 MIDDLE DOMAIN  |   CHROMATIN, FACT, DOUBLE PH DOMAIN, REPLICATION 
1ik9:A    (LYS63) to   (ARG107)  CRYSTAL STRUCTURE OF A XRCC4-DNA LIGASE IV COMPLEX  |   DNA END JOINING, DOUBLE-STRAND BREAK REPAIR, V(D)J RECOMBINATION, PROTEIN-PROTEIN COMPLEX, COILED COIL, GENE REGULATION/LIGASE COMPLEX 
5b0v:B    (PRO95) to   (ILE146)  CRYSTAL STRUCTURE OF MARBURG VIRUS VP40 DIMER  |   MARBURG VIRUS, VIRUS ASSEMBLY PROTEIN, IMMUNOSUPPRESSION, FILOVIRUS, VIRAL PROTEIN 
3zgx:A    (ASN39) to   (LEU113)  CRYSTAL STRUCTURE OF THE KLEISIN-N SMC INTERFACE IN PROKARYOTIC CONDENSIN  |   CELL CYCLE 
5bxl:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA2-G170A MUTANT  |   HYDROLASE, IMMUNODEFICIENCY, PROTEASOME, MUTANT, ASSEMBLY DEFECT 
5bxl:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA2-G170A MUTANT  |   HYDROLASE, IMMUNODEFICIENCY, PROTEASOME, MUTANT, ASSEMBLY DEFECT 
2lba:A    (PRO24) to    (ASP66)  SOLUTION STRUCTURE OF CHICKEN ILEAL BABP IN COMPLEX WITH GLYCOCHENODEOXYCHOLIC ACID  |   ILEAL BILE ACID BINDING PROTEIN, LIPID BINDING PROTEIN 
1x3l:A    (PRO23) to    (GLU46)  CRYSTAL STRUCTURE OF THE PH0495 PROTEIN FROM PYROCOCCCUS HORIKOSHII OT3  |   STRUCTURAL GENOMICS, RIKEN STRUCTURAL GENOMICS/PROTEOMICS INITIATIVE, RSGI, NPPSFA, NATIONAL PROJECT ON PROTEIN STRUCTURAL AND FUNCTIONAL ANALYSES, TRANSFERASE 
5c9x:A   (ASN213) to   (GLU246)  CRYSTAL STRUCTURE OF MYCOBACTERIUM TUBERCULOSIS MALATE SYNTHASE IN COMPLEX WITH 2,4-DICHLORO-5-FLUOROBENZOIC ACID  |   FRAGMENT, COMPLEX, TRANSFERASE 
5cj0:A    (LYS63) to   (ARG107)  CRYSTAL STRUCTURE OF AMINO ACIDS 1631-1692 OF MYH7  |   MYOSIN, COILED-COIL, MOTOR PROTEIN 
3bdm:E    (GLN23) to    (LYS65)  YEAST 20S PROTEASOME:GLIDOBACTIN A-COMPLEX  |   PROTEASOME, UBIQUITIN, PROTEOLYSIS, PATHOGEN, VIRULENCE FACTOR, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN 
3bdm:S    (GLN23) to    (LYS65)  YEAST 20S PROTEASOME:GLIDOBACTIN A-COMPLEX  |   PROTEASOME, UBIQUITIN, PROTEOLYSIS, PATHOGEN, VIRULENCE FACTOR, CYTOPLASM, HYDROLASE, NUCLEUS, PROTEASE, THREONINE PROTEASE, UBL CONJUGATION, PHOSPHOPROTEIN, ZYMOGEN 
4qw3:E    (PHE19) to    (LYS60)  YCP BETA5-C63F MUTANT IN COMPLEX WITH BORTEZOMIB  |   CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4qw3:S    (PHE19) to    (LYS60)  YCP BETA5-C63F MUTANT IN COMPLEX WITH BORTEZOMIB  |   CANCER, PROTEASOME, BORTEZOMIB, DRUG RESISTANCE, BINDING ANALYSIS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3n1h:A   (SER145) to   (PRO186)  CRYSTAL STRUCTURE OF STWHY2  |   STWHY2, SINGLE-STRANDED DNA BINDING PROTEIN, PLANT, POTATO, WHIRLY, DNA BINDING PROTEIN 
5fgh:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) IN COMPLEX WITH MG132  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
5fgh:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME BETA5-K33A MUTANT (PROPEPTIDE EXPRESSED IN TRANS) IN COMPLEX WITH MG132  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
3nzx:E    (PHE22) to    (LYS65)  CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH LIGAND 2C  |   UBIQUITIN, PROTEIN DEGRADATION, N-TERMINAL NUCLEOPHILIC HYDROLASE, 19S REGULATORY PARTICLE, UBIQUITIN-TAGGED SUBSTRATES, CYTOSOL, NUCLEUS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
3nzx:S    (PHE22) to    (LYS65)  CRYSTAL STRUCTURE OF THE YEAST 20S PROTEASOME IN COMPLEX WITH LIGAND 2C  |   UBIQUITIN, PROTEIN DEGRADATION, N-TERMINAL NUCLEOPHILIC HYDROLASE, 19S REGULATORY PARTICLE, UBIQUITIN-TAGGED SUBSTRATES, CYTOSOL, NUCLEUS, HYDROLASE-HYDROLASE INHIBITOR COMPLEX 
4fpe:A    (ALA95) to   (SER128)  CRYSTAL STRUCTURE OF THE NANB SIALIDASE FROM STREPTOCOCCUS PNEUMONIAE IN COMPLEX WITH 2-[(4-METHOXYBENZYL)AMMONIO]ETHANESULFONATE  |   HYDROLASE, INTRAMOLECULAR TRANS-SIALIDASE, GLYCOSIDASE, DRUG DESIGN, NEURAMINIDASE, HYDROLASE-INHIBITOR COMPLEX 
4fzg:E    (PHE19) to    (LYS60)  20S YEAST PROTEASOME IN COMPLEX WITH GLIDOBACTIN  |   UBIQUITIN, PROTEASOME, DRUG DEVELOPMENT, INHIBITOR, NATURAL PRODUCT, N-TERMINAL NUCLEOPHILIC HYDROLASE, PROTEIN DEGRADATION, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
4fzg:S    (PHE19) to    (LYS60)  20S YEAST PROTEASOME IN COMPLEX WITH GLIDOBACTIN  |   UBIQUITIN, PROTEASOME, DRUG DEVELOPMENT, INHIBITOR, NATURAL PRODUCT, N-TERMINAL NUCLEOPHILIC HYDROLASE, PROTEIN DEGRADATION, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
4gk7:E    (PHE22) to    (LYS63)  YEAST 20S PROTEASOME IN COMPLEX WITH THE SYRINGOLIN-GLIDOBACTIN CHIMERA  |   PROTEASOME, CANCER, PROTEIN DEGRADATION, INHIBITION, NATURAL PRODUCT DERIVATIVE, NTN-HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, 12-MEMBERED DIPEPTIDE-MACROLACTAM 
4gk7:S    (PHE22) to    (LYS63)  YEAST 20S PROTEASOME IN COMPLEX WITH THE SYRINGOLIN-GLIDOBACTIN CHIMERA  |   PROTEASOME, CANCER, PROTEIN DEGRADATION, INHIBITION, NATURAL PRODUCT DERIVATIVE, NTN-HYDROLASE, HYDROLASE-HYDROLASE INHIBITOR COMPLEX, 12-MEMBERED DIPEPTIDE-MACROLACTAM 
5l5r:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138;V31M) AND HUMAN BETA6 (97-111; 118-133)  |   HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
5l5r:S    (GLN20) to    (LYS60)  YEAST 20S PROTEASOME WITH HUMAN BETA5I (1-138;V31M) AND HUMAN BETA6 (97-111; 118-133)  |   HYDROLASE COMPLEX, PROTEASOME, MUTANT, BINDING ANALYSIS, HYDROLASE- HYDROLASE INHIBITOR COMPLEX 
5l63:E    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 17  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS 
5l63:S    (PHE19) to    (LYS60)  YEAST 20S PROTEASOME WITH HUMAN BETA5C (1-138) AND HUMAN BETA6 (97- 111; 118-133) IN COMPLEX WITH EPOXYKETONE INHIBITOR 17  |   HYDROLASE-HYDROLASE INHIBITOR COMPLEX, PROTEASOME, MUTANT, INHIBITOR, BINDING ANALYSIS