Structure of PDB 1ir3 Chain A Binding Site BS02
Receptor Information
>1ir3 Chain A (length=303) Species:
9606
(Homo sapiens) [
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SSVFVPDEWEVSREKITLLRELGQGSFGMVYEGNARDIIKGEAETRVAVK
TVNESASLRERIEFLNEASVMKGFTCHHVVRLLGVVSKGQPTLVVMELMA
HGDLKSYLRSLRPEAENNPGRPPPTLQEMIQMAAEIADGMAYLNAKKFVH
RDLAARNCMVAHDFTVKIGDFGMTRDIYETDYYRKGGKGLLPVRWMAPES
LKDGVFTTSSDMWSFGVVLWEITSLAEQPYQGLSNEQVLKFVMDGGYLDQ
PDNCPERVTDLMRMCWQFNPKMRPTFLEIVNLLKDDLHPSFPEVSFFHSE
ENK
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
1ir3 Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
1ir3
Crystal structure of the activated insulin receptor tyrosine kinase in complex with peptide substrate and ATP analog.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
N1137 D1150
Binding residue
(residue number reindexed from 1)
N157 D170
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D1132 A1134 R1136 N1137 D1150 E1159 L1171 P1172
Catalytic site (residue number reindexed from 1)
D152 A154 R156 N157 D170 E179 L191 P192
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:0004714
transmembrane receptor protein tyrosine kinase activity
GO:0005524
ATP binding
Biological Process
GO:0006468
protein phosphorylation
GO:0007169
cell surface receptor protein tyrosine kinase signaling pathway
Cellular Component
GO:0016020
membrane
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Biological Process
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Cellular Component
External links
PDB
RCSB:1ir3
,
PDBe:1ir3
,
PDBj:1ir3
PDBsum
1ir3
PubMed
9312016
UniProt
P06213
|INSR_HUMAN Insulin receptor (Gene Name=INSR)
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