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3FK1

E. coli EPSP synthase (TIPS mutation) liganded with S3P and glyphosate

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0003866molecular_function3-phosphoshikimate 1-carboxyvinyltransferase activity
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0008652biological_processamino acid biosynthetic process
A0009073biological_processaromatic amino acid family biosynthetic process
A0009423biological_processchorismate biosynthetic process
A0016740molecular_functiontransferase activity
A0016765molecular_functiontransferase activity, transferring alkyl or aryl (other than methyl) groups
Functional Information from PDB Data
site_idAC1
Number of Residues16
DetailsBINDING SITE FOR RESIDUE S3P A 428
ChainResidue
ALYS22
AASP313
AASN336
ALYS340
AGPF429
AHOH514
AHOH520
AHOH612
ASER23
AARG27
AILE97
ASER169
ASER170
AGLN171
ASER197
ATYR200

site_idAC2
Number of Residues13
DetailsBINDING SITE FOR RESIDUE GPF A 429
ChainResidue
ALYS22
AASN94
AGLY96
AARG124
AGLN171
AASP313
AGLU341
AARG344
AHIS385
AARG386
ALYS411
AS3P428
AHOH631

site_idAC3
Number of Residues7
DetailsBINDING SITE FOR RESIDUE FMT A 430
ChainResidue
ALYS373
ALEU374
ASER397
AASP398
AHOH638
AHOH799
AHOH853

site_idAC4
Number of Residues5
DetailsBINDING SITE FOR RESIDUE FMT A 431
ChainResidue
ATHR5
ATHR141
ALEU143
AARG152
ATHR402

site_idAC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE FMT A 432
ChainResidue
ATHR65
ALEU66
ASER67
AARG72
AHOH475
AHOH832

site_idAC6
Number of Residues5
DetailsBINDING SITE FOR RESIDUE FMT A 433
ChainResidue
ALYS38
ATYR335
AVAL339
AHOH726
AHOH742

site_idAC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE FMT A 434
ChainResidue
AGLU300
ALEU301
APHE324
ALYS326
AHOH889

site_idAC8
Number of Residues5
DetailsBINDING SITE FOR RESIDUE FMT A 435
ChainResidue
ATHR58
AVAL62
ASER63
ATYR64
AHOH812

site_idAC9
Number of Residues5
DetailsBINDING SITE FOR RESIDUE FMT A 436
ChainResidue
ALYS38
ATYR335
AHIS363
AHOH458
AHOH488

Functional Information from PROSITE/UniProt
site_idPS00104
Number of Residues15
DetailsEPSP_SYNTHASE_1 EPSP synthase signature 1. LFlGNAGIAMRsLaA
ChainResidueDetails
ALEU90-ALA104

site_idPS00885
Number of Residues19
DetailsEPSP_SYNTHASE_2 EPSP synthase signature 2. RvKETDRLfAMateLrkVG
ChainResidueDetails
AARG338-GLY356

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsACT_SITE: Proton acceptor => ECO:0000305|PubMed:13129913
ChainResidueDetails
AASP313

site_idSWS_FT_FI2
Number of Residues7
DetailsBINDING: BINDING => ECO:0000255|HAMAP-Rule:MF_00210
ChainResidueDetails
ALYS22
AGLY96
AARG124
AGLN171
AARG344
AARG386
ALYS411

site_idSWS_FT_FI3
Number of Residues8
DetailsBINDING: BINDING => ECO:0000269|PubMed:11171958, ECO:0007744|PDB:1G6S
ChainResidueDetails
ASER23
AARG27
ASER169
ASER170
ASER197
AASP313
AASN336
ALYS340

site_idSWS_FT_FI4
Number of Residues2
DetailsSITE: Modified by bromopyruvate => ECO:0000269|PubMed:11171958
ChainResidueDetails
ACYS408
ALYS411

Catalytic Information from CSA
site_idCSA1
Number of Residues5
DetailsAnnotated By Reference To The Literature 1g6t
ChainResidueDetails
ALYS22
AASP313
ALYS411
AHIS385
AGLU341

site_idMCSA1
Number of Residues7
DetailsM-CSA 457
ChainResidueDetails
AASP49metal ligand
AASN94metal ligand
AASP313electrostatic stabiliser, proton shuttle (general acid/base)
AGLU341electrostatic stabiliser, metal ligand, proton shuttle (general acid/base)
AHIS385steric role
AARG386transition state stabiliser
ALYS411steric role

227344

PDB entries from 2024-11-13

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