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1A82

DETHIOBIOTIN SYNTHETASE FROM ESCHERICHIA COLI, COMPLEX WITH SUBSTRATES ATP AND DIAMINOPELARGONIC ACID

Functional Information from GO Data
ChainGOidnamespacecontents
A0000287molecular_functionmagnesium ion binding
A0004141molecular_functiondethiobiotin synthase activity
A0005524molecular_functionATP binding
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0009102biological_processbiotin biosynthetic process
A0016874molecular_functionligase activity
A0042803molecular_functionprotein homodimerization activity
A0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE MG A 901
ChainResidue
ATHR16
AASP54
AGLU115
AHOH444
AATP802

site_idAC2
Number of Residues15
DetailsBINDING SITE FOR RESIDUE DNN A 801
ChainResidue
ALEU149
AGLY150
ACYS151
AILE152
AASN153
ATYR187
AHOH429
AHOH655
AHOH716
AHOH728
AATP802
ATHR11
ASER41
APRO79
AGLY118

site_idAC3
Number of Residues25
DetailsBINDING SITE FOR RESIDUE ATP A 802
ChainResidue
ATHR11
AGLU12
AVAL13
AGLY14
ALYS15
ATHR16
AVAL17
ALYS37
AASP54
AGLU115
AGLY118
AASN175
AASP176
APRO204
ATRP205
ALEU206
APRO210
AGLU211
AHOH444
AHOH710
AHOH711
AHOH714
AHOH716
ADNN801
AMG901

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsACT_SITE: ACT_SITE => ECO:0000255|HAMAP-Rule:MF_00336, ECO:0000305|PubMed:9125495
ChainResidueDetails
APRO38

site_idSWS_FT_FI2
Number of Residues1
DetailsBINDING: BINDING => ECO:0000269|PubMed:9865950, ECO:0007744|PDB:1BS1
ChainResidueDetails
AVAL13

site_idSWS_FT_FI3
Number of Residues3
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00336, ECO:0000269|PubMed:9576910, ECO:0000269|PubMed:9865950, ECO:0007744|PDB:1A82, ECO:0007744|PDB:1BS1, ECO:0007744|PDB:1DAK, ECO:0007744|PDB:1DAM
ChainResidueDetails
AVAL17
AALA55
AGLY116

site_idSWS_FT_FI4
Number of Residues1
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00336, ECO:0000269|PubMed:7669756, ECO:0000269|PubMed:9576910, ECO:0000269|PubMed:9865950, ECO:0007744|PDB:1BS1, ECO:0007744|PDB:1DAE, ECO:0007744|PDB:1DAF, ECO:0007744|PDB:1DAG, ECO:0007744|PDB:1DAH, ECO:0007744|PDB:1DAI, ECO:0007744|PDB:1DAK, ECO:0007744|PDB:1DAM
ChainResidueDetails
AGLY42

site_idSWS_FT_FI5
Number of Residues2
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00336, ECO:0000269|PubMed:7669756, ECO:0000269|PubMed:9576910, ECO:0000269|PubMed:9865950, ECO:0007744|PDB:1A82, ECO:0007744|PDB:1BS1, ECO:0007744|PDB:1DAD, ECO:0007744|PDB:1DAF, ECO:0007744|PDB:1DAG, ECO:0007744|PDB:1DAH, ECO:0007744|PDB:1DAK, ECO:0007744|PDB:1DAM
ChainResidueDetails
AASP176
ATRP205

site_idSWS_FT_FI6
Number of Residues1
DetailsBINDING: BINDING => ECO:0000269|PubMed:7669756, ECO:0000269|PubMed:9576910, ECO:0000269|PubMed:9865950, ECO:0007744|PDB:1A82, ECO:0007744|PDB:1BS1, ECO:0007744|PDB:1DAE, ECO:0007744|PDB:1DAF, ECO:0007744|PDB:1DAG, ECO:0007744|PDB:1DAH, ECO:0007744|PDB:1DAI, ECO:0007744|PDB:1DAK, ECO:0007744|PDB:1DAM
ChainResidueDetails
AMET188

site_idSWS_FT_FI7
Number of Residues1
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00336, ECO:0000269|PubMed:7669756, ECO:0000269|PubMed:9576910, ECO:0000269|PubMed:9865950, ECO:0007744|PDB:1A82, ECO:0007744|PDB:1BS1, ECO:0007744|PDB:1DAD, ECO:0007744|PDB:1DAF, ECO:0007744|PDB:1DAH, ECO:0007744|PDB:1DAK, ECO:0007744|PDB:1DAM
ChainResidueDetails
AASN212

Catalytic Information from CSA
site_idCSA1
Number of Residues4
DetailsAnnotated By Reference To The Literature 1dak
ChainResidueDetails
ALYS15
ALYS37
ATHR11
ASER41

site_idMCSA1
Number of Residues8
DetailsM-CSA 74
ChainResidueDetails
AGLU12electrostatic stabiliser
AVAL13metal ligand
ATHR16electrostatic stabiliser, hydrogen bond donor
AVAL17metal ligand
APRO38electrostatic stabiliser, hydrogen bond donor
AGLY42electrostatic stabiliser, hydrogen bond donor
AALA55metal ligand
AGLY116metal ligand

223532

PDB entries from 2024-08-07

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