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1GZE

Structure of the Clostridium botulinum C3 exoenzyme (L177C mutant)

Functional Information from GO Data
ChainGOidnamespacecontents
A0005576cellular_componentextracellular region
A0016740molecular_functiontransferase activity
A0016757molecular_functionglycosyltransferase activity
A0016763molecular_functionpentosyltransferase activity
A0016779molecular_functionnucleotidyltransferase activity
A1990404molecular_functionNAD+-protein mono-ADP-ribosyltransferase activity
B0005576cellular_componentextracellular region
B0016740molecular_functiontransferase activity
B0016757molecular_functionglycosyltransferase activity
B0016763molecular_functionpentosyltransferase activity
B0016779molecular_functionnucleotidyltransferase activity
B1990404molecular_functionNAD+-protein mono-ADP-ribosyltransferase activity
C0005576cellular_componentextracellular region
C0016740molecular_functiontransferase activity
C0016757molecular_functionglycosyltransferase activity
C0016763molecular_functionpentosyltransferase activity
C0016779molecular_functionnucleotidyltransferase activity
C1990404molecular_functionNAD+-protein mono-ADP-ribosyltransferase activity
D0005576cellular_componentextracellular region
D0016740molecular_functiontransferase activity
D0016757molecular_functionglycosyltransferase activity
D0016763molecular_functionpentosyltransferase activity
D0016779molecular_functionnucleotidyltransferase activity
D1990404molecular_functionNAD+-protein mono-ADP-ribosyltransferase activity
Functional Information from PDB Data
site_idAC1
Number of Residues3
DetailsBINDING SITE FOR RESIDUE HG A1248
ChainResidue
APHE49
ACYS177
AMET215

site_idAC2
Number of Residues3
DetailsBINDING SITE FOR RESIDUE HG B1247
ChainResidue
BPHE49
BCYS177
BMET215

site_idAC3
Number of Residues3
DetailsBINDING SITE FOR RESIDUE HG C1252
ChainResidue
CPHE49
CCYS177
CMET215

site_idAC4
Number of Residues2
DetailsBINDING SITE FOR RESIDUE HG D1247
ChainResidue
DPHE49
DCYS177

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues796
DetailsDomain: {"description":"TR mART core","evidences":[{"source":"PROSITE-ProRule","id":"PRU01340","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues12
DetailsActive site: {"evidences":[{"source":"PROSITE-ProRule","id":"PRU01340","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues52
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"12029083","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"16177825","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues4
DetailsSite: {"description":"Transition state stabilizer"}
ChainResidueDetails

Catalytic Information from CSA
site_idCSA1
Number of Residues1
DetailsAnnotated By Reference To The Literature 1g24
ChainResidueDetails
AGLU214

site_idCSA2
Number of Residues1
DetailsAnnotated By Reference To The Literature 1g24
ChainResidueDetails
BGLU214

site_idCSA3
Number of Residues1
DetailsAnnotated By Reference To The Literature 1g24
ChainResidueDetails
CGLU214

site_idCSA4
Number of Residues1
DetailsAnnotated By Reference To The Literature 1g24
ChainResidueDetails
DGLU214

site_idMCSA1
Number of Residues2
DetailsM-CSA 824
ChainResidueDetails
ASER174electrostatic stabiliser, polar interaction
AGLU214electrostatic stabiliser, polar interaction, proton acceptor, proton donor

site_idMCSA2
Number of Residues2
DetailsM-CSA 824
ChainResidueDetails
BSER174electrostatic stabiliser, polar interaction
BGLU214electrostatic stabiliser, polar interaction, proton acceptor, proton donor

site_idMCSA3
Number of Residues2
DetailsM-CSA 824
ChainResidueDetails
CSER174electrostatic stabiliser, polar interaction
CGLU214electrostatic stabiliser, polar interaction, proton acceptor, proton donor

site_idMCSA4
Number of Residues2
DetailsM-CSA 824
ChainResidueDetails
DSER174electrostatic stabiliser, polar interaction
DGLU214electrostatic stabiliser, polar interaction, proton acceptor, proton donor

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PDB entries from 2025-12-24

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