Structure of PDB 5moe Chain B Binding Site BS03
Receptor Information
>5moe Chain B (length=323) Species:
9606
(Homo sapiens) [
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PVPSRARVYTDVNTHRPSEYWDYESHVVEWGNQDDYQLVRKLGRGKYSEV
FEAINITNNEKVVVKILKPVKKKKIKREIKILENLRGGPNIITLADIVKD
PVSRTPALVFEHVNNTDFKQLYQTLTDYDIRFYMYEILKALDYCHSMGIM
HRDVKPHNVMIDHEHRKLRLIDWGLAEFYHPGQEYNVRVASRYFKGPELL
VDYQMYDYSLDMWSLGCMLASMIFRKEPFFHGHDNYDQLVRIAKVLGTED
LYDYIDKYNIELDPRFNDILGRHSRKRWERFVHSENQHLVSPEALDFLDK
LLRYDHQSRLTAREAMEHPYFYT
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
5moe Chain B Residue 403 [
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Receptor-Ligand Complex Structure
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PDB
5moe
A fragment-based approach leading to the discovery of a novel binding site and the selective CK2 inhibitor CAM4066.
Resolution
1.89 Å
Binding residue
(original residue number in PDB)
N161 D175
Binding residue
(residue number reindexed from 1)
N158 D172
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D156 K158 N161 D175 P184 S194
Catalytic site (residue number reindexed from 1)
D153 K155 N158 D172 P181 S191
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
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Molecular Function
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Biological Process
External links
PDB
RCSB:5moe
,
PDBe:5moe
,
PDBj:5moe
PDBsum
5moe
PubMed
28495381
UniProt
P68400
|CSK21_HUMAN Casein kinase II subunit alpha (Gene Name=CSNK2A1)
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