Structure of PDB 4yi7 Chain A Binding Site BS01
Receptor Information
>4yi7 Chain A (length=331) Species:
62977
(Acinetobacter baylyi ADP1) [
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RANIQQALNHITKNIHLTQAQMEDVMRSIMQGEATEAQIGALMMGLRMKG
ESIDEITAAARVMRELAIKIDVSDIQYLVDIVGTGGDNLFNVSTASSFVI
AAAGATIAKHGNRSSDLLEQAGINLDLDMQQTERCIREMGVGFLFAMKYA
VGPRRELGIRSIFNLLGPLTNPAGVKRFVIGVFSDELCRPIAEVMKQLGA
EHVMVVHSKDGLDEISLASQTYIAELKNGEVTEWVLNPEDVNIPSQTLSG
LIVEDSNASLKLIKDALGRKKSDIGEKAANMIALNAGAGIYVSGLATSYK
QGVALAHDIIYGGQALEKMSILSEFTKALKE
Ligand information
Ligand ID
BE2
InChI
InChI=1S/C7H7NO2/c8-6-4-2-1-3-5(6)7(9)10/h1-4H,8H2,(H,9,10)
InChIKey
RWZYAGGXGHYGMB-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
Nc1ccccc1C(O)=O
ACDLabs 10.04
O=C(O)c1ccccc1N
OpenEye OEToolkits 1.5.0
c1ccc(c(c1)C(=O)O)N
Formula
C7 H7 N O2
Name
2-AMINOBENZOIC ACID
ChEMBL
CHEMBL14173
DrugBank
DB04166
ZINC
ZINC000000047985
PDB chain
4yi7 Chain A Residue 400 [
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Receptor-Ligand Complex Structure
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PDB
4yi7
Substrate inhibition of protein in tryptophan biosynthesis pathway redirects flux to aromatic catabolism in Acinetobacter baylyi ADP1.
Resolution
1.853 Å
Binding residue
(original residue number in PDB)
V81 G82 H111 R168 G181
Binding residue
(residue number reindexed from 1)
V82 G83 H110 R154 G167
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
V81
Catalytic site (residue number reindexed from 1)
V82
Enzyme Commision number
2.4.2.18
: anthranilate phosphoribosyltransferase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0004048
anthranilate phosphoribosyltransferase activity
GO:0016757
glycosyltransferase activity
GO:0016763
pentosyltransferase activity
GO:0046872
metal ion binding
Biological Process
GO:0000162
tryptophan biosynthetic process
Cellular Component
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4yi7
,
PDBe:4yi7
,
PDBj:4yi7
PDBsum
4yi7
PubMed
UniProt
P00500
|TRPD_ACIAD Anthranilate phosphoribosyltransferase (Gene Name=trpD)
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