Structure of PDB 8idr Chain D Binding Site BS01
Receptor Information
>8idr Chain D (length=145) Species:
196627
(Corynebacterium glutamicum ATCC 13032) [
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PGKILLLNGPNLNMLGKREPDIYGHDTLEDVVALATAEAAKHGLEVEALQ
SNHEGELIDALHNARGTHIGCVINPGGLTHTSVALLDAVKASELPTVEVH
ISNPHAREEFRHHSYISLAAVSVIAGAGIQGYRFAVDILANLKKL
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 D 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)
R19 Y24 N75 G77 H81 H101 I102 S103
Binding residue
(residue number reindexed from 1)
R18 Y23 N74 G76 H80 H100 I101 S102
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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