Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

1DAF

DETHIOBIOTIN SYNTHETASE COMPLEXED WITH 7-(CARBOXYAMINO)-8-AMINO-NONANOIC ACID, ADP, AND CALCIUM

Functional Information from GO Data
ChainGOidnamespacecontents
A0000166molecular_functionnucleotide binding
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 Residues6
DetailsBINDING SITE FOR RESIDUE CA A 227
ChainResidue
AASP54
AADP226
AHOH363
AHOH370
AHOH374
AHOH380

site_idAC2
Number of Residues14
DetailsBINDING SITE FOR RESIDUE DSD A 225
ChainResidue
ASER41
AALA117
AGLY118
AGLY150
ACYS151
AILE152
AASN153
ATYR187
AHOH230
AHOH285
AHOH286
ATHR11
ALYS37
AALA40

site_idAC3
Number of Residues19
DetailsBINDING SITE FOR RESIDUE ADP A 226
ChainResidue
AGLU12
AVAL13
AGLY14
ALYS15
ATHR16
AVAL17
AASP54
AGLU115
AASN175
AASP176
APRO204
ALEU206
APRO210
AGLU211
ACA227
AHOH286
AHOH363
AHOH367
AHOH369

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
ATHR11electrostatic stabiliser
AGLU12metal ligand
ALYS15electrostatic stabiliser, hydrogen bond donor
ATHR16metal ligand
ALYS37electrostatic stabiliser, hydrogen bond donor
ASER41electrostatic stabiliser, hydrogen bond donor
AASP54metal ligand
AGLU115metal ligand

237735

PDB entries from 2025-06-18

PDB statisticsPDBj update infoContact PDBjnumon