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1DPM

THREE-DIMENSIONAL STRUCTURE OF THE ZINC-CONTAINING PHOSPHOTRIESTERASE WITH BOUND SUBSTRATE ANALOG DIETHYL 4-METHYLBENZYLPHOSPHONATE

Functional Information from GO Data
ChainGOidnamespacecontents
A0004063molecular_functionaryldialkylphosphatase activity
A0005886cellular_componentplasma membrane
A0008270molecular_functionzinc ion binding
A0009056biological_processcatabolic process
A0016787molecular_functionhydrolase activity
A0016788molecular_functionhydrolase activity, acting on ester bonds
A0046872molecular_functionmetal ion binding
B0004063molecular_functionaryldialkylphosphatase activity
B0005886cellular_componentplasma membrane
B0008270molecular_functionzinc ion binding
B0009056biological_processcatabolic process
B0016787molecular_functionhydrolase activity
B0016788molecular_functionhydrolase activity, acting on ester bonds
B0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE ZN A 800
ChainResidue
AHIS55
AHIS57
AASP301
AZN801
AFMT902
AHOH909

site_idAC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE ZN A 801
ChainResidue
AZN800
AEBP900
AFMT902
AHOH909
AHIS55
AHIS201
AHIS230

site_idAC3
Number of Residues6
DetailsBINDING SITE FOR RESIDUE ZN B 802
ChainResidue
BHIS55
BHIS57
BASP301
BZN803
BFMT904
BHOH924

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE ZN B 803
ChainResidue
BHIS201
BHIS230
BZN802
BEBP902
BFMT904
BHOH924

site_idAC5
Number of Residues7
DetailsBINDING SITE FOR RESIDUE EBP A 900
ChainResidue
ATRP131
AHIS201
AHIS257
ALEU271
AASP301
AMET317
AZN801

site_idAC6
Number of Residues4
DetailsBINDING SITE FOR RESIDUE EBP A 901
ChainResidue
AARG152
AGLN155
ATYR156
BPHE51

site_idAC7
Number of Residues8
DetailsBINDING SITE FOR RESIDUE EBP B 902
ChainResidue
BTRP131
BHIS201
BHIS257
BLEU271
BASP301
BMET317
BZN803
BHOH924

site_idAC8
Number of Residues4
DetailsBINDING SITE FOR RESIDUE EBP B 903
ChainResidue
AGLU71
BGLN155
BTYR156
BARG164

site_idAC9
Number of Residues8
DetailsBINDING SITE FOR RESIDUE FMT A 902
ChainResidue
AHIS55
AHIS57
ALYS169
AHIS201
AHIS230
AZN800
AZN801
AHOH909

site_idBC1
Number of Residues8
DetailsBINDING SITE FOR RESIDUE FMT B 904
ChainResidue
BHIS55
BHIS57
BLYS169
BHIS201
BHIS230
BZN802
BZN803
BHOH924

Functional Information from PROSITE/UniProt
site_idPS01322
Number of Residues9
DetailsPHOSPHOTRIESTERASE_1 Phosphotriesterase family signature 1. GfTLtHEHI
ChainResidueDetails
AGLY50-ILE58

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues10
DetailsBINDING: BINDING => ECO:0000269|PubMed:7794910, ECO:0007744|PDB:1DPM, ECO:0007744|PDB:1EYW, ECO:0007744|PDB:1EZ2, ECO:0007744|PDB:1HZY, ECO:0007744|PDB:2O4M, ECO:0007744|PDB:2O4Q, ECO:0007744|PDB:2OB3, ECO:0007744|PDB:2OQL
ChainResidueDetails
AHIS55
BASP301
AHIS57
AHIS201
AHIS230
AASP301
BHIS55
BHIS57
BHIS201
BHIS230

site_idSWS_FT_FI2
Number of Residues2
DetailsBINDING: via carbamate group => ECO:0000269|PubMed:7794910, ECO:0007744|PDB:1DPM, ECO:0007744|PDB:1EYW, ECO:0007744|PDB:1EZ2, ECO:0007744|PDB:1HZY, ECO:0007744|PDB:2O4M, ECO:0007744|PDB:2O4Q, ECO:0007744|PDB:2OB3, ECO:0007744|PDB:2OQL
ChainResidueDetails
ALYS169
BLYS169

site_idSWS_FT_FI3
Number of Residues2
DetailsMOD_RES: N6-carboxylysine => ECO:0000255|PROSITE-ProRule:PRU00679, ECO:0000269|PubMed:7794910, ECO:0007744|PDB:1DPM, ECO:0007744|PDB:1EYW, ECO:0007744|PDB:1EZ2, ECO:0007744|PDB:1HZY, ECO:0007744|PDB:2O4M, ECO:0007744|PDB:2O4Q, ECO:0007744|PDB:2OB3, ECO:0007744|PDB:2OQL
ChainResidueDetails
ALYS169
BLYS169

Catalytic Information from CSA
site_idCSA1
Number of Residues3
DetailsAnnotated By Reference To The Literature 1ez2
ChainResidueDetails
AHIS254
AASP233
AASP301

site_idCSA2
Number of Residues3
DetailsAnnotated By Reference To The Literature 1ez2
ChainResidueDetails
BHIS254
BASP233
BASP301

site_idMCSA1
Number of Residues8
DetailsM-CSA 159
ChainResidueDetails
AHIS55metal ligand
AHIS57metal ligand
ALYS169metal ligand
AHIS201metal ligand
AHIS230metal ligand
AASP233hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
AHIS254hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor, proton relay
AASP301hydrogen bond acceptor, hydrogen bond donor, metal ligand, proton acceptor, proton donor

site_idMCSA2
Number of Residues8
DetailsM-CSA 159
ChainResidueDetails
BHIS55metal ligand
BHIS57metal ligand
BLYS169metal ligand
BHIS201metal ligand
BHIS230metal ligand
BASP233hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
BHIS254hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor, proton relay
BASP301hydrogen bond acceptor, hydrogen bond donor, metal ligand, proton acceptor, proton donor

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PDB entries from 2024-07-10

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