Structure of PDB 4ki7 Chain G Binding Site BS01
Receptor Information
>4ki7 Chain G (length=141) Species:
1773
(Mycobacterium tuberculosis) [
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LIVNVINGPNLGRLGRREPAVYGGTTHDELVALIEREAAELGLKAVVRQS
DSEAQLLDWIHQAADAAEPVILNAGGLTHTSVALRDACAELSAPLIEVHI
SNVHAREEFRRHSYLSPIATGVIVGLGIQGYLLALRYLAEH
Ligand information
Ligand ID
1R2
InChI
InChI=1S/C13H9NO6/c15-10-4-8(13(16)17)5-12(7-10)20-11-3-1-2-9(6-11)14(18)19/h1-7,15H,(H,16,17)
InChIKey
KGFXJYALKCBPSP-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=C(O)c2cc(Oc1cccc(c1)[N+]([O-])=O)cc(O)c2
OpenEye OEToolkits 1.7.6
c1cc(cc(c1)Oc2cc(cc(c2)O)C(=O)O)[N+](=O)[O-]
CACTVS 3.370
OC(=O)c1cc(O)cc(Oc2cccc(c2)[N+]([O-])=O)c1
Formula
C13 H9 N O6
Name
3-hydroxy-5-(3-nitrophenoxy)benzoic acid
ChEMBL
DrugBank
ZINC
ZINC000098208014
PDB chain
4ki7 Chain G Residue 201 [
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Receptor-Ligand Complex Structure
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PDB
4ki7
Design and Structural Analysis of Aromatic Inhibitors of Type II Dehydroquinase from Mycobacterium tuberculosis.
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
N12 R15 L16 Y24 N75 G77 H101 I102 S103 R112
Binding residue
(residue number reindexed from 1)
N10 R13 L14 Y22 N73 G75 H99 I100 S101 R110
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
P11 N12 R19 Y24 N75 G78 E99 H101 R108
Catalytic site (residue number reindexed from 1)
P9 N10 R17 Y22 N73 G76 E97 H99 R106
Enzyme Commision number
4.2.1.10
: 3-dehydroquinate dehydratase.
Gene Ontology
Molecular Function
GO:0003855
3-dehydroquinate dehydratase activity
GO:0016829
lyase activity
Biological Process
GO:0008652
amino acid biosynthetic process
GO:0009073
aromatic amino acid family biosynthetic process
GO:0009423
chorismate biosynthetic process
GO:0019631
quinate catabolic 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:4ki7
,
PDBe:4ki7
,
PDBj:4ki7
PDBsum
4ki7
PubMed
25234229
UniProt
P9WPX7
|AROQ_MYCTU 3-dehydroquinate dehydratase (Gene Name=aroQ)
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