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4EBP

BlaC E166A Cefotaxime Acyl-Intermediate Complex

Functional Information from GO Data
ChainGOidnamespacecontents
A0005576cellular_componentextracellular region
A0005886cellular_componentplasma membrane
A0008800molecular_functionbeta-lactamase activity
A0016787molecular_functionhydrolase activity
A0017001biological_processantibiotic catabolic process
A0030655biological_processbeta-lactam antibiotic catabolic process
A0042597cellular_componentperiplasmic space
A0046677biological_processresponse to antibiotic
B0005576cellular_componentextracellular region
B0005886cellular_componentplasma membrane
B0008800molecular_functionbeta-lactamase activity
B0016787molecular_functionhydrolase activity
B0017001biological_processantibiotic catabolic process
B0030655biological_processbeta-lactam antibiotic catabolic process
B0042597cellular_componentperiplasmic space
B0046677biological_processresponse to antibiotic
C0005576cellular_componentextracellular region
C0005886cellular_componentplasma membrane
C0008800molecular_functionbeta-lactamase activity
C0016787molecular_functionhydrolase activity
C0017001biological_processantibiotic catabolic process
C0030655biological_processbeta-lactam antibiotic catabolic process
C0042597cellular_componentperiplasmic space
C0046677biological_processresponse to antibiotic
D0005576cellular_componentextracellular region
D0005886cellular_componentplasma membrane
D0008800molecular_functionbeta-lactamase activity
D0016787molecular_functionhydrolase activity
D0017001biological_processantibiotic catabolic process
D0030655biological_processbeta-lactam antibiotic catabolic process
D0042597cellular_componentperiplasmic space
D0046677biological_processresponse to antibiotic
Functional Information from PDB Data
site_idAC1
Number of Residues7
DetailsBINDING SITE FOR RESIDUE PO4 A 301
ChainResidue
ASER70
ASER130
ATHR235
ATHR237
AHOH404
BGLN110
BGLN111

site_idAC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE PO4 A 302
ChainResidue
AASP240
ATYR272
BSER99
BGLN114
AASN170
AARG171

site_idAC3
Number of Residues3
DetailsBINDING SITE FOR RESIDUE PO4 A 303
ChainResidue
AASP124
AARG128
AARG213

site_idAC4
Number of Residues1
DetailsBINDING SITE FOR RESIDUE PO4 A 304
ChainResidue
AGLU64

site_idAC5
Number of Residues7
DetailsBINDING SITE FOR RESIDUE PCZ B 301
ChainResidue
BSER70
BSER130
BTHR235
BGLY236
BTHR237
BHOH420
BHOH434

site_idAC6
Number of Residues3
DetailsBINDING SITE FOR RESIDUE PO4 B 302
ChainResidue
BASP124
BARG128
BARG213

site_idAC7
Number of Residues9
DetailsBINDING SITE FOR RESIDUE PCZ C 301
ChainResidue
CSER70
CILE105
CSER130
CTHR235
CGLY236
CTHR237
CASP240
CHOH432
DGLN111

site_idAC8
Number of Residues3
DetailsBINDING SITE FOR RESIDUE PO4 C 302
ChainResidue
CASP124
CARG128
CARG213

site_idAC9
Number of Residues8
DetailsBINDING SITE FOR RESIDUE PO4 D 301
ChainResidue
CGLN110
CGLN111
DSER70
DSER130
DTHR216
DTHR235
DGLY236
DTHR237

site_idBC1
Number of Residues3
DetailsBINDING SITE FOR RESIDUE PO4 D 302
ChainResidue
DASP124
DARG128
DARG213

site_idBC2
Number of Residues2
DetailsBINDING SITE FOR RESIDUE PO4 D 303
ChainResidue
DARG61
DGLU64

Functional Information from PROSITE/UniProt
site_idPS00146
Number of Residues16
DetailsBETA_LACTAMASE_A Beta-lactamase class-A active site. FaFCSTfKaplVAAVL
ChainResidueDetails
APHE66-LEU81

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Acyl-ester intermediate => ECO:0000269|PubMed:19251630, ECO:0000269|PubMed:20353175, ECO:0000269|PubMed:20961112
ChainResidueDetails
ASER70
BSER70
CSER70
DSER70

site_idSWS_FT_FI2
Number of Residues4
DetailsACT_SITE: Proton acceptor => ECO:0000303|PubMed:20353175, ECO:0000303|PubMed:20961112
ChainResidueDetails
AALA166
BALA166
CALA166
DALA166

site_idSWS_FT_FI3
Number of Residues8
DetailsBINDING: BINDING => ECO:0000269|PubMed:19251630, ECO:0000269|PubMed:20353175, ECO:0000269|PubMed:20961112
ChainResidueDetails
ASER130
ATHR235
BSER130
BTHR235
CSER130
CTHR235
DSER130
DTHR235

site_idSWS_FT_FI4
Number of Residues4
DetailsSITE: Increases nucleophilicity of active site Ser => ECO:0000303|PubMed:20353175, ECO:0000303|PubMed:20961112
ChainResidueDetails
ALYS73
BLYS73
CLYS73
DLYS73

site_idSWS_FT_FI5
Number of Residues4
DetailsSITE: Functions as a gatekeeper residue that regulates substrate accessibility to the enzyme active site => ECO:0000303|PubMed:24023821
ChainResidueDetails
AILE105
BILE105
CILE105
DILE105

227344

PDB entries from 2024-11-13

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