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1XVU

Crystal Structure of CaiB mutant D169A in complex with Coenzyme A

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0005737cellular_componentcytoplasm
A0008410molecular_functionCoA-transferase activity
A0008735molecular_functionL-carnitine CoA-transferase activity
A0009437biological_processcarnitine metabolic process
A0016740molecular_functiontransferase activity
A0016782molecular_functiontransferase activity, transferring sulphur-containing groups
A0042413biological_processcarnitine catabolic process
Functional Information from PDB Data
site_idAC1
Number of Residues19
DetailsBINDING SITE FOR RESIDUE COA A 501
ChainResidue
AALA25
AARG103
AARG104
APRO138
AALA139
AMET200
AASN316
AHOH520
AHOH524
AHOH534
AHOH588
AASN45
ALEU71
AASN72
AILE73
APHE74
AALA95
ASER96
ALYS97

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsACT_SITE: Nucleophile => ECO:0000255|HAMAP-Rule:MF_01050, ECO:0000305|PubMed:15518548
ChainResidueDetails
AALA169

site_idSWS_FT_FI2
Number of Residues2
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_01050, ECO:0000269|PubMed:15518548
ChainResidueDetails
ALYS97
AARG104

Catalytic Information from CSA
site_idCSA1
Number of Residues1
DetailsAnnotated By Reference To The Literature 1xvt
ChainResidueDetails
AALA169

site_idMCSA1
Number of Residues1
DetailsM-CSA 531
ChainResidueDetails
AALA169covalently attached, electrofuge, electrophile, nucleofuge, nucleophile

223532

PDB entries from 2024-08-07

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