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1PNL

PENICILLIN ACYLASE HAS A SINGLE-AMINO-ACID CATALYTIC CENTRE

Functional Information from GO Data
ChainGOidnamespacecontents
A0016787molecular_functionhydrolase activity
A0016811molecular_functionhydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides
A0017000biological_processantibiotic biosynthetic process
B0016787molecular_functionhydrolase activity
B0017000biological_processantibiotic biosynthetic process
Functional Information from PDB Data
site_idAC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CA B 558
ChainResidue
AGLU152
BASP73
BVAL75
BASP76
BPRO205
BASP252

site_idAC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE PAC B 559
ChainResidue
BPHE24
BSER67
BALA69
BASN241
APHE146
BSER1
BGLN23

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsACT_SITE: Nucleophile
ChainResidueDetails
BSER1

site_idSWS_FT_FI2
Number of Residues5
DetailsBINDING:
ChainResidueDetails
BASP73
BVAL75
BASP76
BPRO205
BASP252

Catalytic Information from CSA
site_idCSA1
Number of Residues3
Detailsa catalytic site defined by CSA, PubMed 11601852, 7816145, 9813130, 10331865
ChainResidueDetails
BASN241
BSER1
BALA69

site_idMCSA1
Number of Residues3
DetailsM-CSA 841
ChainResidueDetails
BSER1nucleofuge, nucleophile, proton acceptor, proton donor
BALA69electrostatic stabiliser
BASN241electrostatic stabiliser

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PDB entries from 2024-07-24

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