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8TU5

Bruton's tyrosine kinase in complex with covalent inhibitor compound 27

Summary for 8TU5
Entry DOI10.2210/pdb8tu5/pdb
Related8TU3 8TU4
DescriptorTyrosine-protein kinase BTK, 1-[(1S,5S,6S)-6-methyl-6-{[(6M,8R)-6-(1-methyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrazin-4-yl]oxy}-2-azabicyclo[3.2.0]heptan-2-yl]propan-1-one (3 entities in total)
Functional Keywordskinase, transferase, transferase-inhibitor complex, transferase/inhibitor
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight33060.92
Authors
Metrick, C.M. (deposition date: 2023-08-15, release date: 2024-06-26)
Primary citationHimmelbauer, M.K.,Bajrami, B.,Basile, R.,Capacci, A.,Chen, T.,Choi, C.K.,Gilfillan, R.,Gonzalez-Lopez de Turiso, F.,Gu, C.,Hoemberger, M.,Johnson, D.S.,Jones, J.H.,Kadakia, E.,Kirkland, M.,Lin, E.Y.,Liu, Y.,Ma, B.,Magee, T.,Mantena, S.,Marx, I.E.,Metrick, C.M.,Mingueneau, M.,Murugan, P.,Muste, C.A.,Nadella, P.,Nevalainen, M.,Parker Harp, C.R.,Pattaropong, V.,Pietrasiewicz, A.,Prince, R.J.,Purgett, T.J.,Santoro, J.C.,Schulz, J.,Sciabola, S.,Tang, H.,Vandeveer, H.G.,Wang, T.,Yousaf, Z.,Helal, C.J.,Hopkins, B.T.
Discovery and Preclinical Characterization of BIIB129, a Covalent, Selective, and Brain-Penetrant BTK Inhibitor for the Treatment of Multiple Sclerosis.
J.Med.Chem., 67:8122-8140, 2024
Cited by
PubMed: 38712838
DOI: 10.1021/acs.jmedchem.4c00220
PDB entries with the same primary citation
Experimental method
Structure validation

223790

건을2024-08-14부터공개중

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