Structure of PDB 1eua Chain A Binding Site BS01
Receptor Information
>1eua Chain A (length=213) Species:
562
(Escherichia coli) [
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MKNWKTSAESILTTGPVVPVIVVKKLEHAVPMAKALVAGGVRVLEVTLRT
ECAVDAIRAIAKEVPEAIVGAGTVLNPQQLAEVTEAGAQFAISPGLTEPL
LKAATEGTIPLIPGISTVSELMLGMDYGLKEFKFFPAEANGGVKALQAIA
GPFSQVRFCPTGGISPANYRDYLALKSVLCIGGSWLVPADALEAGDYDRI
TKLAREAVEGAKL
Ligand information
Ligand ID
PYR
InChI
InChI=1S/C3H4O3/c1-2(4)3(5)6/h1H3,(H,5,6)
InChIKey
LCTONWCANYUPML-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.385
CC(=O)C(O)=O
OpenEye OEToolkits 1.7.6
CC(=O)C(=O)O
ACDLabs 12.01
O=C(C(=O)O)C
Formula
C3 H4 O3
Name
PYRUVIC ACID
ChEMBL
CHEMBL1162144
DrugBank
DB00119
ZINC
ZINC000001532517
PDB chain
1eua Chain A Residue 2101 [
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Receptor-Ligand Complex Structure
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PDB
1eua
Covalent intermediate trapped in 2-keto-3-deoxy-6- phosphogluconate (KDPG) aldolase structure at 1.95-A resolution.
Resolution
1.95 Å
Binding residue
(original residue number in PDB)
E45 T73 I92 K133
Binding residue
(residue number reindexed from 1)
E45 T73 I92 K133
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
E45 R49 K133
Catalytic site (residue number reindexed from 1)
E45 R49 K133
Enzyme Commision number
4.1.2.14
: 2-dehydro-3-deoxy-phosphogluconate aldolase.
4.1.3.16
: 4-hydroxy-2-oxoglutarate aldolase.
Gene Ontology
Molecular Function
GO:0008675
2-dehydro-3-deoxy-phosphogluconate aldolase activity
GO:0008700
(R,S)-4-hydroxy-2-oxoglutarate aldolase activity
GO:0008948
oxaloacetate decarboxylase activity
GO:0016829
lyase activity
GO:0016833
oxo-acid-lyase activity
GO:0042802
identical protein binding
GO:0106009
(4S)-4-hydroxy-2-oxoglutarate aldolase activity
Biological Process
GO:0009255
Entner-Doudoroff pathway through 6-phosphogluconate
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0016020
membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1eua
,
PDBe:1eua
,
PDBj:1eua
PDBsum
1eua
PubMed
11274385
UniProt
P0A955
|ALKH_ECOLI KHG/KDPG aldolase (Gene Name=eda)
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