Structure of PDB 6ao5 Chain A Binding Site BS02
Receptor Information
>6ao5 Chain A (length=321) Species:
9606
(Homo sapiens) [
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DVLEKLGEGSYGSVFKAIHVVAIKQDLQEIIKEISIMQQCDSPYVVKYYG
SYFLWIVMEYCGAGSVSDIIRLRNKTLIEDEIATILKSTLKGLEYLHFMR
KIHRNIKAGNILLNTEGHAKLADFGVAVIGTPFWMAPEVIQEIGYNCVAD
IWSLGITSIEMAEGKPPYADIHPMRAIFMIPTNPPPTFRKPELWSDDFTD
FVKKCLVKNPEQRATATQLLQHPFIKNAKPVSILRDLITEAMEIKAKRHE
EQQRELEEEENWKVPQDGDFDFLKNLSLEELQMRLKALDPMMEREIEELR
QRYTAKRQPILDAMDAKKRRQ
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
6ao5 Chain A Residue 502 [
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Receptor-Ligand Complex Structure
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PDB
6ao5
SAV1 promotes Hippo kinase activation through antagonizing the PP2A phosphatase STRIPAK.
Resolution
2.955 Å
Binding residue
(original residue number in PDB)
N151 D164
Binding residue
(residue number reindexed from 1)
N110 D123
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
N146 K148 G150 N151 D164 T184
Catalytic site (residue number reindexed from 1)
N105 K107 G109 N110 D123 T131
Enzyme Commision number
2.7.11.1
: non-specific serine/threonine protein kinase.
Gene Ontology
Molecular Function
GO:0004672
protein kinase activity
GO:0004674
protein serine/threonine kinase activity
GO:0005524
ATP binding
Biological Process
GO:0006468
protein phosphorylation
GO:0007165
signal transduction
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Molecular Function
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Biological Process
External links
PDB
RCSB:6ao5
,
PDBe:6ao5
,
PDBj:6ao5
PDBsum
6ao5
PubMed
29063833
UniProt
Q13188
|STK3_HUMAN Serine/threonine-protein kinase 3 (Gene Name=STK3)
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