Structure of PDB 8idr Chain B Binding Site BS01
Receptor Information
>8idr Chain B (length=144) Species:
196627
(Corynebacterium glutamicum ATCC 13032) [
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GKILLLNGPNLNMLGKREPDIYGHDTLEDVVALATAEAAKHGLEVEALQS
NHEGELIDALHNARGTHIGCVINPGGLTHTSVALLDAVKASELPTVEVHI
SNPHAREEFRHHSYISLAAVSVIAGAGIQGYRFAVDILANLKKL
Ligand information
Ligand ID
FLC
InChI
InChI=1S/C6H8O7/c7-3(8)1-6(13,5(11)12)2-4(9)10/h13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)/p-3
InChIKey
KRKNYBCHXYNGOX-UHFFFAOYSA-K
SMILES
Software
SMILES
CACTVS 3.341
OC(CC([O-])=O)(CC([O-])=O)C([O-])=O
OpenEye OEToolkits 1.5.0
C(C(=O)[O-])C(CC(=O)[O-])(C(=O)[O-])O
ACDLabs 10.04
O=C([O-])CC(O)(C([O-])=O)CC(=O)[O-]
Formula
C6 H5 O7
Name
CITRATE ANION
ChEMBL
DrugBank
ZINC
PDB chain
8idr Chain B Residue 201 [
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Receptor-Ligand Complex Structure
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PDB
8idr
Structural and Biochemical Analysis of 3-Dehydroquinate Dehydratase from Corynebacterium glutamicum.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
N75 G77 H101 I102 S103
Binding residue
(residue number reindexed from 1)
N73 G75 H99 I100 S101
Annotation score
1
Enzymatic activity
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
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Molecular Function
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Biological Process
External links
PDB
RCSB:8idr
,
PDBe:8idr
,
PDBj:8idr
PDBsum
8idr
PubMed
38151830
UniProt
O52377
|AROQ_CORGL 3-dehydroquinate dehydratase (Gene Name=aroQ)
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