Structure of PDB 4riw Chain D Binding Site BS02
Receptor Information
>4riw Chain D (length=297) Species:
9606
(Homo sapiens) [
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LVEPLTPSGEAPNQALLRILKETEFKKIKVLGSGAFGTVYKGLWIPEGEK
VKIPVAIKELREATSPKANKEILDEAYVMASVDNPHVCRLLGICLTSTVQ
LITQLMPFGCLLDYVREHKDNIGSQYLLNWCVQIAKGMNYLEDRRLVHRD
LAARNVLVKTPQHVKITDFGLAKLLGAEEKEYHAEGGKVPIKWMALESIL
HRIYTHQSDVWSYGVTVWELMTFGSKPYDGIPASEISSILEKGERLPQPP
ICTIDVYMIMRKCWMIDADSRPKFRELIIEFSKMARDPQRYLVIQGD
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
4riw Chain D Residue 1002 [
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Receptor-Ligand Complex Structure
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PDB
4riw
Structural analysis of the EGFR/HER3 heterodimer reveals the molecular basis for activating HER3 mutations.
Resolution
3.1 Å
Binding residue
(original residue number in PDB)
N818 D831
Binding residue
(residue number reindexed from 1)
N155 D168
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D813 A815 R817 N818 D831 G850
Catalytic site (residue number reindexed from 1)
D150 A152 R154 N155 D168 G187
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
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Molecular Function
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Biological Process
External links
PDB
RCSB:4riw
,
PDBe:4riw
,
PDBj:4riw
PDBsum
4riw
PubMed
25468994
UniProt
P00533
|EGFR_HUMAN Epidermal growth factor receptor (Gene Name=EGFR)
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