Structure of PDB 5k0k Chain B Binding Site BS01
Receptor Information
>5k0k Chain B (length=248) Species:
9606
(Homo sapiens) [
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LEDVVIDRNLLILGKILGEGGSVMEGNLKQEDGTSLKVAVKTEAACMKDF
SHPNVIRLLGVCIEMSSQGIPKPMVILPFMKYGDLHTYLLYSRLETGPKH
IPLQTLLKFMVDIALGMEYLSNRNFLHRDLAARNCMLRDDMTVCVADFPV
KWIAIESLADRVYTSKSDVWAFGVTMWEIATRGMTPYPGVQNHEMYDYLL
HGHRLKQPEDCLDELYEIMYSCWRTDPLDRPTFSVLRLQLEKLLESLP
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
5k0k Chain B Residue 903 [
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Receptor-Ligand Complex Structure
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PDB
5k0k
Design and Synthesis of Novel Macrocyclic Mer Tyrosine Kinase Inhibitors.
Resolution
2.545 Å
Binding residue
(original residue number in PDB)
N728 D741
Binding residue
(residue number reindexed from 1)
N134 D147
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D723 A725 R727 N728 D741
Catalytic site (residue number reindexed from 1)
D129 A131 R133 N134 D147
Enzyme Commision number
2.7.10.1
: receptor protein-tyrosine kinase.
Gene Ontology
Molecular Function
GO:0004672
protein kinase activity
GO:0004713
protein tyrosine kinase activity
GO:0005524
ATP binding
Biological Process
GO:0006468
protein phosphorylation
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5k0k
,
PDBe:5k0k
,
PDBj:5k0k
PDBsum
5k0k
PubMed
27994735
UniProt
Q12866
|MERTK_HUMAN Tyrosine-protein kinase Mer (Gene Name=MERTK)
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