Structure of PDB 4y12 Chain A Binding Site BS03
Receptor Information
>4y12 Chain A (length=322) Species:
83332
(Mycobacterium tuberculosis H37Rv) [
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RAPDIDPLEALMTNPVVPESKRFCWNCGRPVGRSDSETKGASEGWCPYCG
SPYSFLPQLNPGDIVAGQYEVKGCIAHGGLGWIYLALDRNVNGRPVVLKG
LVHSGDAEAQAMAMAERQFLAEVVHPSIVQIFNFVEHTDRHGDPVGYIVM
EYVGGQSLKRSKGQKLPVAEAIAYLLEILPALSYLHSIGLVYNDLKPENI
MLTEEQLKLIDLGAVSRINSFGYLYGTPGFQAPEIVRTGPTVATDIYTVG
RTLAALTLDLPTRNGRYVDGLPEDDPVLKTYDSYGRLLRRAIDPDPRQRF
TTAEEMSAQLTGVLREVVAQDT
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
4y12 Chain A Residue 503 [
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Receptor-Ligand Complex Structure
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PDB
4y12
Molecular Basis of the Activity and the Regulation of the Eukaryotic-like S/T Protein Kinase PknG from Mycobacterium tuberculosis.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
N281 D293
Binding residue
(residue number reindexed from 1)
N199 D211
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D276 K278 N281 D293 T309
Catalytic site (residue number reindexed from 1)
D194 K196 N199 D211 T227
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:0006468
protein phosphorylation
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:4y12
,
PDBe:4y12
,
PDBj:4y12
PDBsum
4y12
PubMed
25960409
UniProt
P9WI73
|PKNG_MYCTU Serine/threonine-protein kinase PknG (Gene Name=pknG)
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