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1RW8

Crystal Structure of TGF-beta receptor I kinase with ATP site inhibitor

Summary for 1RW8
Entry DOI10.2210/pdb1rw8/pdb
DescriptorTGF-beta receptor type I, 3-(4-FLUOROPHENYL)-2-(6-METHYLPYRIDIN-2-YL)-5,6-DIHYDRO-4H-PYRROLO[1,2-B]PYRAZOLE (3 entities in total)
Functional Keywordstgf-beta receptor i, protein kinase, transferase
Biological sourceHomo sapiens (human)
Cellular locationMembrane; Single-pass type I membrane protein: P36897
Total number of polymer chains1
Total formula weight34744.90
Authors
Zhang, F.,Sawyer, J.S. (deposition date: 2003-12-16, release date: 2005-02-01, Last modification date: 2023-08-23)
Primary citationSawyer, J.S.,Beight, D.W.,Britt, K.S.,Anderson, B.D.,Campbell, R.M.,Goodson Jr., T.,Herron, D.K.,Li, H.Y.,McMillen, W.T.,Mort, N.,Parsons, S.,Smith, E.C.,Wagner, J.R.,Yan, L.,Zhang, F.,Yingling, J.M.
Synthesis and activity of new aryl- and heteroaryl-substituted 5,6-dihydro-4H-pyrrolo[1,2-b]pyrazole inhibitors of the transforming growth factor-beta type I receptor kinase domain.
Bioorg.Med.Chem.Lett., 14:3581-3584, 2004
Cited by
PubMed: 15177479
DOI: 10.1016/j.bmcl.2004.04.007
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.4 Å)
Structure validation

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数据于2024-04-24公开中

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