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8FLG

Bruton's tyrosine kinase in complex with an orthosteric inhibitor

Summary for 8FLG
Entry DOI10.2210/pdb8flg/pdb
DescriptorTyrosine-protein kinase BTK, DIMETHYL SULFOXIDE, N~2~-(3-chlorophenyl)-N-[(3R)-1-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperidin-3-yl]glycinamide, ... (4 entities in total)
Functional Keywordstyrosine protein kinase btk, ligase, transferase-inhibitor complex, transferase/inhibitor
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight34359.85
Authors
Metrick, C.M.,Marcotte, D.J. (deposition date: 2022-12-21, release date: 2023-03-01)
Primary citationVandeveer, G.H.,Arduini, R.M.,Baker, D.P.,Barry, K.,Bohnert, T.,Bowden-Verhoek, J.K.,Conlon, P.,Cullen, P.F.,Guan, B.,Jenkins, T.J.,Liao, S.Y.,Lin, L.,Liu, Y.T.,Marcotte, D.,Mertsching, E.,Metrick, C.M.,Negrou, E.,Powell, N.,Scott, D.,Silvian, L.F.,Hopkins, B.T.
Discovery of structural diverse reversible BTK inhibitors utilized to develop a novel in vivo CD69 and CD86 PK/PD mouse model.
Bioorg.Med.Chem.Lett., 80:129108-129108, 2023
Cited by
PubMed: 36538993
DOI: 10.1016/j.bmcl.2022.129108
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.2 Å)
Structure validation

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