Structure of PDB 4mh7 Chain B Binding Site BS01
Receptor Information
>4mh7 Chain B (length=255) Species:
9606
(Homo sapiens) [
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LEDVVIDRNLLILGKILGEGSVMEGNLKQEDGTSLKVAVKTMKLDNSSQR
EIEEFLSEAACMKDFSHPNVIRLLGVCIEPMVILPFMKYGDLHTYLLYSR
LETGPKHIPLQTLLKFMVDIALGMEYLSNRNFLHRDLAARNCMLRDDMTV
CVADFPVKWIAIESLADRVYTSKSDVWAFGVTMWEIATRGMTPYPGVQNH
EMYDYLLHGHRLKQPEDCLDELYEIMYSCWRTDPLDRPTFSVLRLQLEKL
LESLP
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
4mh7 Chain B Residue 905 [
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Receptor-Ligand Complex Structure
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PDB
4mh7
Discovery of Mer specific tyrosine kinase inhibitors for the treatment and prevention of thrombosis.
Resolution
2.51 Å
Binding residue
(original residue number in PDB)
S686 L688 P692 K693
Binding residue
(residue number reindexed from 1)
S99 L101 P105 K106
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D723 A725 R727 N728 D741
Catalytic site (residue number reindexed from 1)
D136 A138 R140 N141 D154
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
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Biological Process
External links
PDB
RCSB:4mh7
,
PDBe:4mh7
,
PDBj:4mh7
PDBsum
4mh7
PubMed
24219778
UniProt
Q12866
|MERTK_HUMAN Tyrosine-protein kinase Mer (Gene Name=MERTK)
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