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4PL4

Crystal structure of murine IRE1 in complex with OICR464 inhibitor

Functional Information from GO Data
ChainGOidnamespacecontents
A0004521molecular_functionRNA endonuclease activity
A0004540molecular_functionRNA nuclease activity
A0004672molecular_functionprotein kinase activity
A0004674molecular_functionprotein serine/threonine kinase activity
A0005524molecular_functionATP binding
A0006397biological_processmRNA processing
A0006468biological_processprotein phosphorylation
A0030968biological_processendoplasmic reticulum unfolded protein response
B0004521molecular_functionRNA endonuclease activity
B0004540molecular_functionRNA nuclease activity
B0004672molecular_functionprotein kinase activity
B0004674molecular_functionprotein serine/threonine kinase activity
B0005524molecular_functionATP binding
B0006397biological_processmRNA processing
B0006468biological_processprotein phosphorylation
B0030968biological_processendoplasmic reticulum unfolded protein response
C0004521molecular_functionRNA endonuclease activity
C0004540molecular_functionRNA nuclease activity
C0004672molecular_functionprotein kinase activity
C0004674molecular_functionprotein serine/threonine kinase activity
C0005524molecular_functionATP binding
C0006397biological_processmRNA processing
C0006468biological_processprotein phosphorylation
C0030968biological_processendoplasmic reticulum unfolded protein response
D0004521molecular_functionRNA endonuclease activity
D0004540molecular_functionRNA nuclease activity
D0004672molecular_functionprotein kinase activity
D0004674molecular_functionprotein serine/threonine kinase activity
D0005524molecular_functionATP binding
D0006397biological_processmRNA processing
D0006468biological_processprotein phosphorylation
D0030968biological_processendoplasmic reticulum unfolded protein response
Functional Information from PDB Data
site_idAC1
Number of Residues6
Detailsbinding site for residue 31K A 1001
ChainResidue
ATYR772
APHE889
ATYR892
AASN906
ALYS907
AHIS910

site_idAC2
Number of Residues14
Detailsbinding site for residue ADP A 1002
ChainResidue
ALYS599
AILE642
AGLU643
ACYS645
ATHR648
ALYS690
AHIS692
AASN693
ALEU695
AASP711
AMG1004
AHIS579
AGLY580
AALA597

site_idAC3
Number of Residues3
Detailsbinding site for residue PEU A 1003
ChainResidue
ATYR772
AHIS773
AGLY776

site_idAC4
Number of Residues4
Detailsbinding site for residue MG A 1004
ChainResidue
ALYS599
AASN693
AASP711
AADP1002

site_idAC5
Number of Residues14
Detailsbinding site for residue ADP B 1001
ChainResidue
BHIS579
BGLY580
BTHR584
BVAL586
BLYS599
BGLU643
BCYS645
BTHR648
BLYS690
BHIS692
BASN693
BLEU695
BASP711
BMG1002

site_idAC6
Number of Residues4
Detailsbinding site for residue MG B 1002
ChainResidue
BHIS692
BASN693
BASP711
BADP1001

site_idAC7
Number of Residues13
Detailsbinding site for residue ADP C 1001
ChainResidue
CHIS579
CGLY580
CVAL586
CALA597
CLYS599
CILE642
CCYS645
CTHR648
CLYS690
CHIS692
CASN693
CASP711
CMG1002

site_idAC8
Number of Residues3
Detailsbinding site for residue MG C 1002
ChainResidue
CASN693
CASP711
CADP1001

site_idAC9
Number of Residues14
Detailsbinding site for residue ADP D 1001
ChainResidue
DLEU577
DGLY578
DHIS579
DGLY580
DALA581
DVAL586
DLYS599
DILE642
DGLU643
DCYS645
DLYS690
DHIS692
DASP711
DMG1002

site_idAD1
Number of Residues4
Detailsbinding site for residue MG D 1002
ChainResidue
DHIS692
DASN693
DASP711
DADP1001

Functional Information from PROSITE/UniProt
site_idPS00108
Number of Residues13
DetailsPROTEIN_KINASE_ST Serine/Threonine protein kinases active-site signature. IvHrDLKphNILL
ChainResidueDetails
AILE684-LEU696

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues384
DetailsDomain: {"description":"KEN","evidences":[{"source":"PROSITE-ProRule","id":"PRU00725","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues4
DetailsRegion: {"description":"Interacts with hydroxy-aryl-aldehyde inhibitors","evidences":[{"source":"PubMed","id":"25164867","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues4
DetailsActive site: {"description":"Proton acceptor; for protein kinase activity","evidences":[{"source":"UniProtKB","id":"P32361","evidenceCode":"ECO:0000250"},{"source":"PROSITE-ProRule","id":"PRU00159","evidenceCode":"ECO:0000255"},{"source":"PROSITE-ProRule","id":"PRU10027","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues32
DetailsBinding site: {"evidences":[{"source":"PROSITE-ProRule","id":"PRU00159","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"25164867","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"4PL5","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues4
DetailsBinding site: {"evidences":[{"source":"PROSITE-ProRule","id":"PRU00159","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"25164867","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"4PL3","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"4PL4","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"4PL5","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues24
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"25164867","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"4PL3","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"4PL4","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"4PL5","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI7
Number of Residues4
DetailsSite: {"description":"Interacts with hydroxy-aryl-aldehyde inhibitors","evidences":[{"source":"PubMed","id":"25164867","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

246333

PDB entries from 2025-12-17

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