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Ligands
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0X6 2,6-dichloro-4-cyano-N-{2-[(cyclopropylcarbonyl)amino]pyridin-4-yl}benzamide
Non-standard Residues
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Glycosylation
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Code : 4GII   PDBj   RCSB PDB   PDBe
Header : TRANSFERASE/TRANSFERASE INHIBITOR
Title : Tyk2 (JH1) in complex with 2,6-dichloro-4-cyano-N-{2-[(cyclopropylcarbonyl)amino]pyridin-4-yl}benzamide
Release Data : 2013-05-29
Compound :
mol_id molecule chains
1 Non-receptor tyrosine-protein kinase TYK2 A
ec: 2.7.10.2
fragment: Kinase domain, UNP residues 885-1176
mutation: C936A,Q969A,E971A,K972A,D1023N,C1142A
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Spodoptera frugiperda  (taxid:7108)
gene: TYK2
expression_system_common: Fall armyworm
Authors : Ultsch, M.H.
Keywords : Aminopyridine, Benzamide, Kinase, Enzyme inhibitor, Tyrosine Kinase, ATP Binding, TRANSFERASE-TRANSFERASE INHIBITOR complex
Exp. method : X-RAY DIFFRACTION ( 2.31 Å )
Citation :

Lead Optimization of a 4-Aminopyridine Benzamide Scaffold To Identify Potent, Selective, and Orally Bioavailable TYK2 Inhibitors.

Liang, J.,van Abbema, A.,Balazs, M.  et al.
(2013)  J.Med.Chem.  56 : 4521 - 4536

PubMed: 23668484
DOI: 10.1021/jm400266t

Chain : A
UniProt : P29597 (TYK2_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
ATP + L-tyrosyl-[protein] = ADP + H(+) + O-phospho-L-tyrosyl- [protein] 2.7.10.2 PubMed:10542297, PubMed:7526154
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