2gm1

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Crystal structure of the mitotic kinesin eg5 in complex with mg-adp and n-(3-aminopropyl)-n-((3-benzyl-5-chloro-4-oxo-3,4-dihydropyrrolo[2,1-f][1,2,4]triazin-2-yl)(cyclopropyl)methyl)-4-methylbenzamide

File:2gm1.gif


2gm1, resolution 2.30Å

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OverviewOverview

Synthesis and SAR of substituted pyrrolotriazine-4-one analogues as Eg5, inhibitors are described. Many of these analogues displayed potent, inhibitory activities in the Eg5 ATPase and A2780 cell proliferation, assays. In addition, pyrrolotriazine-4-one analogue 26 demonstrated in, vivo efficacy in an iv P388 murine leukemia model. Both NMR and X-ray, crystallographic studies revealed that these analogues bind to an, allosteric site on the Eg5 protein.

About this StructureAbout this Structure

2GM1 is a Single protein structure of sequence from Homo sapiens with MG, 2AZ and ADP as ligands. Full crystallographic information is available from OCA.

ReferenceReference

Synthesis and SAR of pyrrolotriazine-4-one based Eg5 inhibitors., Kim KS, Lu S, Cornelius LA, Lombardo LJ, Borzilleri RM, Schroeder GM, Sheng C, Rovnyak G, Crews D, Schmidt RJ, Williams DK, Bhide RS, Traeger SC, McDonnell PA, Mueller L, Sheriff S, Newitt JA, Pudzianowski AT, Yang Z, Wild R, Lee FY, Batorsky R, Ryder JS, Ortega-Nanos M, Shen H, Gottardis M, Roussell DL, Bioorg Med Chem Lett. 2006 Aug 1;16(15):3937-42. Epub 2006 May 30. PMID:16730979

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