Structure of PDB 2akz Chain B Binding Site BS02
Receptor Information
>2akz Chain B (length=432) Species:
9606
(Homo sapiens) [
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SIEKIWAREILDSRGNPTVEVDLYTAKGLFRAAVPSGASTGIYEALELRD
GDKQRYLGKGVLKAVDHINSTIAPALISSGLSVVEQEKLDNLMLELDGTE
NKSKFGANAILGVSLAVCKAGAAERELPLYRHIAQLAGNSDLILPVPAFN
VINGGSHAGNKLAMQEFMILPVGAESFRDAMRLGAEVYHTLKGVIKDKYG
KDATNVGDEGGFAPNILENSEALELVKEAIDKAGYTEKIVIGMDVAASEF
YRDGKYDLDFKSPTDPSRYITGDQLGALYQDFVRDYPVVSIEDPFDQDDW
AAWSKFTANVGIQIVGDDLTVTNPKRIERAVEEKACNCLLLKVNQIGSVT
EAIQACKLAQENGWGVMVSHRSGETEDTFIADLVVGLCTGQIKTGAPCRS
ERLAKYNQLMRIEEELGDEARFAGHNFRNPSV
Ligand information
Ligand ID
PO4
InChI
InChI=1S/H3O4P/c1-5(2,3)4/h(H3,1,2,3,4)/p-3
InChIKey
NBIIXXVUZAFLBC-UHFFFAOYSA-K
SMILES
Software
SMILES
CACTVS 3.341
[O-][P]([O-])([O-])=O
ACDLabs 10.04
[O-]P([O-])([O-])=O
OpenEye OEToolkits 1.5.0
[O-]P(=O)([O-])[O-]
Formula
O4 P
Name
PHOSPHATE ION
ChEMBL
DrugBank
DB14523
ZINC
PDB chain
2akz Chain B Residue 1442 [
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Receptor-Ligand Complex Structure
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PDB
2akz
Fluoride inhibition of enolase: crystal structure and thermodynamics
Resolution
1.36 Å
Binding residue
(original residue number in PDB)
A1038 S1039 H1157 R1371 S1372
Binding residue
(residue number reindexed from 1)
A38 S39 H157 R371 S372
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
S1039 H1157 E1166 E1209 D1244 E1292 D1317 K1342 H1370 K1393
Catalytic site (residue number reindexed from 1)
S39 H157 E166 E209 D244 E292 D317 K342 H370 K393
Enzyme Commision number
4.2.1.11
: phosphopyruvate hydratase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0004634
phosphopyruvate hydratase activity
GO:0005515
protein binding
GO:0016829
lyase activity
GO:0046872
metal ion binding
Biological Process
GO:0006094
gluconeogenesis
GO:0006096
glycolytic process
GO:0061621
canonical glycolysis
Cellular Component
GO:0000015
phosphopyruvate hydratase complex
GO:0001917
photoreceptor inner segment
GO:0005615
extracellular space
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0005886
plasma membrane
GO:0016020
membrane
GO:0043025
neuronal cell body
GO:0043204
perikaryon
GO:0070062
extracellular exosome
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2akz
,
PDBe:2akz
,
PDBj:2akz
PDBsum
2akz
PubMed
16411755
UniProt
P09104
|ENOG_HUMAN Gamma-enolase (Gene Name=ENO2)
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