Structure of PDB 2rio Chain B Binding Site BS01
Receptor Information
>2rio Chain B (length=395) Species:
4932
(Saccharomyces cerevisiae) [
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NFEQSLKNLVVSEKILGYGSSGTVVFQGSFQGRPVAVKRMLIDFCDIALM
EIKLLTESDDHPNVIRYYCSETTDRFLYIALELCNLNLQDLVESYNPISL
LRQIASGVAHLHSLKIIHRDLKPQNILVSTSSRFTADQQTGAENLRILIS
DFGLCKKLDSTSGWRAPELLEESNNLQTKRRLTRSIDIFSMGCVFYYILS
KGKHPFGDKYSRESNIIRGIFSLDEMKCLHDRSLIAEATDLISQMIDHDP
LKRPTAMKVLRHPLFWPKSKKLEFLLKVSDRLEIENRDPPSALLMKFDAG
SDFVIPSGDWTVKFDKTFMDRKYHSSKLMDLLRALRNKYHHFMDLPEDIA
ELMGPVPDGFYDYFTKRFPNLLIGVYMIVKENLSDDQILREFLYS
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
2rio Chain B Residue 2102 [
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Receptor-Ligand Complex Structure
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PDB
2rio
Structure of the dual enzyme ire1 reveals the basis for catalysis and regulation in nonconventional RNA splicing.
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
N145 D171
Binding residue
(residue number reindexed from 1)
N125 D151
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D140 K142 N145 D171 T195
Catalytic site (residue number reindexed from 1)
D120 K122 N125 D151 T161
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
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:2rio
,
PDBe:2rio
,
PDBj:2rio
PDBsum
2rio
PubMed
18191223
UniProt
P32361
|IRE1_YEAST Serine/threonine-protein kinase/endoribonuclease IRE1 (Gene Name=IRE1)
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