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Ligands
Code Name Style Show Link
CJN ~{N}4,~{N}4-dimethyl-~{N}1-(5-propan-2-ylpyrrolo[3,2-D]pyrimidin-4-yl)cyclohexane-1,4-diamine
Non-standard Residues
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TPO Phosphothreonine
SEP Phosphoserine
Glycosylation
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Modification
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Code : 6F3G   PDBj   RCSB PDB   PDBe
Header : SIGNALING PROTEIN
Title : IRAK4 IN COMPLEX WITH inhibitor
Release Data : 2018-05-23
Compound :
mol_id molecule chains synonym
1 Interleukin-1 receptor-associated kinase 4 A IRAK-4,Renal carcinoma antigen NY-REN-64
ec: 2.7.11.1
mol_id molecule chains synonym
2 Interleukin-1 receptor-associated kinase 4 B IRAK-4,Renal carcinoma antigen NY-REN-64
ec: 2.7.11.1
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Spodoptera frugiperda  (taxid:7108)
gene: IRAK4
expression_system_common: Fall armyworm
mol_id organism_scientific organism_common expression_system
2 Homo sapiens  (taxid:9606) Human Spodoptera frugiperda  (taxid:7108)
gene: IRAK4
expression_system_common: Fall armyworm
Authors : Xue, Y., Degorce, S.L., Robb, G.R., Ferguson, A.D.
Keywords : IRAK4, kinase, inhibitor, cancer, SIGNALING PROTEIN
Exp. method : X-RAY DIFFRACTION ( 2.37 Å )
Citation :

Optimization of permeability in a series of pyrrolotriazine inhibitors of IRAK4.

Degorce, S.L.,Anjum, R.,Dillman, K.S.  et al.
(2018)  Bioorg. Med. Chem.  26 : 913 - 924

PubMed: 29398441
DOI: 10.1016/j.bmc.2018.01.008

Chain : B
UniProt : Q9NWZ3 (IRAK4_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
ATP + L-seryl-[protein] = ADP + H(+) + O-phospho-L-seryl- [protein] 2.7.11.1 -
-
ATP + L-threonyl-[protein] = ADP + H(+) + O-phospho-L- threonyl-[protein] 2.7.11.1 -
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