Structure of PDB 5lxm Chain A Binding Site BS02
Receptor Information
>5lxm Chain A (length=267) Species:
9606
(Homo sapiens) [
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RQWALEDFEIGRPLGKGKFGNVYLAREKQSKFILALKVLFKAQLEKAGVE
HQLRREVEIQSHLRHPNILRLYGYFHDATRVYLILEYAPLGTVYRELQKL
SKFDEQRTATYITELANALSYCHSKRVIHRDIKPENLLLGSAGELKIADF
GWSVHAPSSRRTTLAGTLDYLPPEMIEGRMHDEKVDLWSLGVLCYEFLVG
KPPFEANTYQETYKRISRVEFTFPDFVTEGARDLISRLLKHNPSQRPMLR
EVLEHPWITANSSKPSN
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
5lxm Chain A Residue 509 [
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Receptor-Ligand Complex Structure
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PDB
5lxm
A TPX2 Proteomimetic Has Enhanced Affinity for Aurora-A Due to Hydrocarbon Stapling of a Helix.
Resolution
2.08 Å
Binding residue
(original residue number in PDB)
N261 D274
Binding residue
(residue number reindexed from 1)
N136 D149
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D256 K258 E260 N261 D274 T292
Catalytic site (residue number reindexed from 1)
D131 K133 E135 N136 D149 T167
Enzyme Commision number
2.7.11.1
: non-specific serine/threonine protein kinase.
Gene Ontology
Molecular Function
GO:0004672
protein kinase activity
GO:0005524
ATP binding
Biological Process
GO:0000212
meiotic spindle organization
GO:0000226
microtubule cytoskeleton organization
GO:0000278
mitotic cell cycle
GO:0006468
protein phosphorylation
GO:0007052
mitotic spindle organization
GO:0007098
centrosome cycle
GO:0007100
mitotic centrosome separation
GO:0051321
meiotic cell cycle
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Molecular Function
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Biological Process
External links
PDB
RCSB:5lxm
,
PDBe:5lxm
,
PDBj:5lxm
PDBsum
5lxm
PubMed
27775325
UniProt
O14965
|AURKA_HUMAN Aurora kinase A (Gene Name=AURKA)
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