1z5m
From Proteopedia
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Crystal Structure Of N1-[3-[[5-bromo-2-[[3-[(1-pyrrolidinylcarbonyl)amino]phenyl]amino]-4-pyrimidinyl]amino]propyl]-2,2-dimethylpropanediamide Complexed with Human PDK1
Overview
The phosphoinositide 3-kinase/3-phosphoinositide-dependent kinase 1, (PDK1)/Akt signaling pathway plays a key role in cancer cell growth, survival, and tumor angiogenesis and represents a promising target for, anticancer drugs. Here, we describe three potent PDK1 inhibitors, BX-795, BX-912, and BX-320 (IC(50) = 11-30 nm) and their initial biological, characterization. The inhibitors blocked PDK1/Akt signaling in tumor cells, and inhibited the anchorage-dependent growth of a variety of tumor cell, lines in culture or induced apoptosis. A number of cancer cell lines with, elevated Akt activity were >30-fold more sensitive to growth inhibition by, PDK1 inhibitors in soft agar than on tissue culture plastic, consistent, with the cell survival function of the PDK1/Akt signaling pathway, which, is particularly important for unattached cells. BX-320 inhibited the, growth of LOX melanoma tumors in the lungs of nude mice after injection of, tumor cells into the tail vein. The effect of BX-320 on cancer cell growth, in vitro and in vivo indicates that PDK1 inhibitors may have clinical, utility as anticancer agents.
About this Structure
1Z5M is a Single protein structure of sequence from Homo sapiens with SO4, CL, LI8 and GOL as ligands. Active as Non-specific serine/threonine protein kinase, with EC number 2.7.11.1 Full crystallographic information is available from OCA.
Reference
Novel small molecule inhibitors of 3-phosphoinositide-dependent kinase-1., Feldman RI, Wu JM, Polokoff MA, Kochanny MJ, Dinter H, Zhu D, Biroc SL, Alicke B, Bryant J, Yuan S, Buckman BO, Lentz D, Ferrer M, Whitlow M, Adler M, Finster S, Chang Z, Arnaiz DO, J Biol Chem. 2005 May 20;280(20):19867-74. Epub 2005 Mar 16. PMID:15772071
Page seeded by OCA on Mon Nov 12 20:29:33 2007
