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Ligands
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9T6 4-[[(1s,3r)-5-oxidanyl-2-adamantyl]amino]-1h-pyrrolo[2,3-B]pyridine-5-carboxamide
Non-standard Residues
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Code : 6AAM   PDBj   RCSB PDB   PDBe
Header : TRANSFERASE/INHIBITOR
Title : Crystal structure of TYK2 in complex with peficitinib
Release Data : 2018-08-15
Compound :
mol_id molecule chains
1 Non-receptor tyrosine-protein kinase TYK2 A
ec: 2.7.10.2
mutation: D1023N, I1114L,K972A,E971A,Q969A,C936A,C1142A
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Spodoptera frugiperda  (taxid:7108)
gene: TYK2
Authors : Nomura, N., Tomimoto, Y.
Keywords : protein kinase, TRANSFERASE-INHIBITOR complex
Exp. method : X-RAY DIFFRACTION ( 1.98 Å )
Citation :

Discovery and structural characterization of peficitinib (ASP015K) as a novel and potent JAK inhibitor

Hamaguchi, H.,Amano, Y.,Moritomo, A.  et al.
(2018)  Bioorg. Med. Chem.  26 : 4971 - 4983

PubMed: 30145050
DOI: 10.1016/j.bmc.2018.08.005

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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