Structure of PDB 2p0c Chain B Binding Site BS02

Receptor Information

>2p0c Chain B (length=248) Species: 9606 (Homo sapiens)

NKLEDVVIDRNLLILGKILGEGSVMEGNLKQEDGTSLKVAVKTMEFLSEA
ACMKDFSHPNVIRLLGVCIPKPMVILPFMKYGDLHTYLLYSRLETGPKHI
PLQTLLKFMVDIALGMEYLSNRNFLHRDLAARNCMLRDDMTVCVADFGLP
VKWIAIESLADRVYTSKSDVWAFGVTMWEIATRGMTPYPGVQNHEMYDYL
LHGHRLKQPEDCLDELYEIMYSCWRTDPLDRPTFSVLRLQLEKLLESL

Ligand information

• Ligand ID: MG
• InChI: InChI=1S/Mg/q+2
• InChIKey: JLVVSXFLKOJNIY-UHFFFAOYSA-N
• SMILES:
  ACDLabs 10.04
  OpenEye OEToolkits 1.5.0: [Mg+2]
  CACTVS 3.341: [Mg++]
• Formula: Mg
• Name: MAGNESIUM ION
• DrugBank: DB01378
• PDB chain: 2p0c Chain B Residue 6

Receptor-Ligand Complex Structure

Structure summary

• PDB: 2p0c Structural insights into the inhibited states of the Mer receptor tyrosine kinase.
• Resolution: 2.4 Å
• Binding residue (original residue number in PDB): E712 N716
• Binding residue (residue number reindexed from 1): E117 N121
• Annotation score: 1

Enzymatic activity

• Catalytic site (original residue number in PDB): D723 A725 R727 N728 D741
• Catalytic site (residue number reindexed from 1): D128 A130 R132 N133 D146
• 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

External links

• PDB: RCSB:2p0c, PDBe:2p0c, PDBj:2p0c
• PDBsum: 2p0c
• PubMed: 19028587
• UniProt: Q12866|MERTK_HUMAN Tyrosine-protein kinase Mer (Gene Name=MERTK)