Structure of PDB 3ujr Chain B Binding Site BS01
Receptor Information
>3ujr 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
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
3ujr Chain B Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
3ujr
Structures of asymmetric complexes of human neuron specific enolase with resolved substrate and product and an analogous complex with two inhibitors indicate subunit interaction and inhibitor cooperativity.
Resolution
1.4 Å
Binding residue
(original residue number in PDB)
D244 E292 D317
Binding residue
(residue number reindexed from 1)
D244 E292 D317
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
S39 H157 E166 E209 D244 E292 D317 K342 H370 K393
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:3ujr
,
PDBe:3ujr
,
PDBj:3ujr
PDBsum
3ujr
PubMed
22437160
UniProt
P09104
|ENOG_HUMAN Gamma-enolase (Gene Name=ENO2)
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