Structure of PDB 5ta6 Chain A Binding Site BS02
Receptor Information
>5ta6 Chain A (length=294) Species:
9606
(Homo sapiens) [
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AKEIPEVLVDPRSRRRYVRGRFLGKGGFAKCFEISDADTKEVFAGKIVPK
SLLLKPHQREKMSMEISIHRSLAHQHVVGFHGFFEDNDFVFVVLELCRRR
SLLELHKRRKALTEPEARYYLRQIVLGCQYLHRNRVIHRDLKLGNLFLNE
DLEVKIGDFGLATKVEYDGERKKVLCGTPNYIAPEVLSKKGHSFEVDVWS
IGCIMYTLLVGKPPFETSCLKETYLRIKKNEYSIPKHINPVAASLIQKML
QTDPTARPTINELLNDEFFTSGYIPARLPITCLTIPPRFSIAPS
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
5ta6 Chain A Residue 1001 [
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Receptor-Ligand Complex Structure
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PDB
5ta6
Structure-based design and SAR development of 5,6-dihydroimidazolo[1,5-f]pteridine derivatives as novel Polo-like kinase-1 inhibitors.
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
H93 C212
Binding residue
(residue number reindexed from 1)
H57 C176
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D176 K178 G180 N181 D194 T214
Catalytic site (residue number reindexed from 1)
D140 K142 G144 N145 D158 T178
Enzyme Commision number
2.7.11.21
: polo kinase.
Gene Ontology
Molecular Function
GO:0004672
protein kinase activity
GO:0005524
ATP binding
Biological Process
GO:0006468
protein phosphorylation
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Molecular Function
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Biological Process
External links
PDB
RCSB:5ta6
,
PDBe:5ta6
,
PDBj:5ta6
PDBsum
5ta6
PubMed
28169164
UniProt
P53350
|PLK1_HUMAN Serine/threonine-protein kinase PLK1 (Gene Name=PLK1)
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