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PDBsum entry 1y91

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Transferase PDB id
1y91
Contents
Protein chain
286 a.a.
Ligands
CT9
Waters ×190

References listed in PDB file
Key reference
Title Structure-Guided design of pyrazolo[1,5-A]pyrimidines as inhibitors of human cyclin-Dependent kinase 2.
Authors D.S.Williamson, M.J.Parratt, J.F.Bower, J.D.Moore, C.M.Richardson, P.Dokurno, A.D.Cansfield, G.L.Francis, R.J.Hebdon, R.Howes, P.S.Jackson, A.M.Lockie, J.B.Murray, C.L.Nunns, J.Powles, A.Robertson, A.E.Surgenor, C.J.Torrance.
Ref. Bioorg Med Chem Lett, 2005, 15, 863-867. [DOI no: 10.1016/j.bmcl.2004.12.073]
PubMed id 15686876
Abstract
The protein structure guided design of a series of pyrazolo[1,5-a]pyrimidines with high potency for human cyclin-dependent kinase 2 (CDK2) is described. Some examples were shown to inhibit the growth of human colon tumour cells, were equipotent for CDK1 and were selective against GSK-3beta and other kinases.
PROCHECK
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