Structure of PDB 3p23 Chain C Binding Site BS01
Receptor Information
>3p23 Chain C (length=390) Species:
9606
(Homo sapiens) [
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TSVVIVGKISFCPKDVLGHGAEGTIVYRGMFDNRDVAVKRILPECFSFAD
REVQLLRESDEHPNVIRYFCTEKDRQFQYIAIELCAATLQEYVEQKDFAH
LGLEPITLLQQTTSGLAHLHSLNIVHRDLKPHNILISMPNAHGKIKAMIS
DFGLCKKSGVPGTEGWIAPEMLSEDNPTYTVDIFSAGCVFYYVISEGSHP
FGKSLQRQANILLGACSLDCLHPEKHEDVIARELIEKMIAMDPQKRPSAK
HVLKHPFFWSLEKQLQFFQDVSDRIEKESLDGPIVKQLERGGRAVVKMDW
RENITVPLQTDLRKFRTYKGGSVRDLLRAMRNKKHHYRELPAEVRETLGT
LPDDFVCYFTSRFPHLLAHTYRAMELCSHERLFQPYYFHE
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
3p23 Chain C Residue 1001 [
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Receptor-Ligand Complex Structure
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PDB
3p23
Structure of the Ire1 autophosphorylation complex and implications for the unfolded protein response.
Resolution
2.7 Å
Binding residue
(original residue number in PDB)
H692 D711
Binding residue
(residue number reindexed from 1)
H132 D151
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D688 K690 N693 D711 T734
Catalytic site (residue number reindexed from 1)
D128 K130 N133 D151 T163
Enzyme Commision number
2.7.11.1
: non-specific serine/threonine protein kinase.
3.1.26.-
Gene Ontology
Molecular Function
GO:0004521
RNA endonuclease activity
GO:0004540
RNA nuclease activity
GO:0004672
protein kinase activity
GO:0004674
protein serine/threonine kinase activity
GO:0005524
ATP binding
Biological Process
GO:0006397
mRNA processing
GO:0006468
protein phosphorylation
GO:0030968
endoplasmic reticulum unfolded protein response
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Molecular Function
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Biological Process
External links
PDB
RCSB:3p23
,
PDBe:3p23
,
PDBj:3p23
PDBsum
3p23
PubMed
21317875
UniProt
O75460
|ERN1_HUMAN Serine/threonine-protein kinase/endoribonuclease IRE1 (Gene Name=ERN1)
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