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6YAT

Crystal structure of STK4 (MST1) in complex with compound 6

Summary for 6YAT
Entry DOI10.2210/pdb6yat/pdb
DescriptorSerine/threonine-protein kinase 4, (2R)-3-(cyclohexylamino)-2-hydroxypropane-1-sulfonic acid, GLYCEROL, ... (5 entities in total)
Functional Keywordskinase, kinase inhibitor, mst1, stk4, hippo pathway, chemical probe, structural genomics, structural genomics consortium, sgc, transferase
Biological sourceHomo sapiens (Human)
Total number of polymer chains2
Total formula weight73135.32
Authors
Chaikuad, A.,Bata, N.,Limpert, A.S.,Lambert, L.J.,Bakas, N.A.,Cosford, N.D.P.,Knapp, S.,Structural Genomics Consortium (SGC) (deposition date: 2020-03-13, release date: 2020-04-29, Last modification date: 2024-01-24)
Primary citationBata, N.,Chaikuad, A.,Bakas, N.A.,Limpert, A.S.,Lambert, L.J.,Sheffler, D.J.,Berger, L.M.,Liu, G.,Yuan, C.,Wang, L.,Peng, Y.,Dong, J.,Celeridad, M.,Layng, F.,Knapp, S.,Cosford, N.D.P.
Inhibitors of the Hippo Pathway Kinases STK3/MST2 and STK4/MST1 Have Utility for the Treatment of Acute Myeloid Leukemia.
J.Med.Chem., 65:1352-1369, 2022
Cited by
PubMed: 34807584
DOI: 10.1021/acs.jmedchem.1c00804
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.58 Å)
Structure validation

222926

数据于2024-07-24公开中

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