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5TOZ

JAK3 with covalent inhibitor PF-06651600

Summary for 5TOZ
Entry DOI10.2210/pdb5toz/pdb
DescriptorTyrosine-protein kinase JAK3, 1-{(2S,5R)-2-methyl-5-[(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino]piperidin-1-yl}propan-1-one, SULFATE ION, ... (4 entities in total)
Functional Keywordsjak3 covalent kinase, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (Human)
Cellular locationEndomembrane system ; Peripheral membrane protein : P52333
Total number of polymer chains1
Total formula weight36927.08
Authors
Vajdos, F.F. (deposition date: 2016-10-19, release date: 2016-11-09, Last modification date: 2017-11-22)
Primary citationTelliez, J.B.,Dowty, M.E.,Wang, L.,Jussif, J.,Lin, T.,Li, L.,Moy, E.,Balbo, P.,Li, W.,Zhao, Y.,Crouse, K.,Dickinson, C.,Symanowicz, P.,Hegen, M.,Banker, M.E.,Vincent, F.,Unwalla, R.,Liang, S.,Gilbert, A.M.,Brown, M.F.,Hayward, M.,Montgomery, J.,Yang, X.,Bauman, J.,Trujillo, J.I.,Casimiro-Garcia, A.,Vajdos, F.F.,Leung, L.,Geoghegan, K.F.,Quazi, A.,Xuan, D.,Jones, L.,Hett, E.,Wright, K.,Clark, J.D.,Thorarensen, A.
Discovery of a JAK3-Selective Inhibitor: Functional Differentiation of JAK3-Selective Inhibition over pan-JAK or JAK1-Selective Inhibition.
ACS Chem. Biol., 11:3442-3451, 2016
Cited by
PubMed: 27791347
DOI: 10.1021/acschembio.6b00677
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.98 Å)
Structure validation

218853

数据于2024-04-24公开中

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