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1MZC

Co-Crystal Structure Of Human Farnesyltransferase With Farnesyldiphosphate and Inhibitor Compound 33a

Summary for 1MZC
Entry DOI10.2210/pdb1mzc/pdb
Related1JCQ 1LD7 1LD8
Related PRD IDPRD_900003
DescriptorProtein Farnesyltransferase alpha Subunit, Protein Farnesyltransferase beta Subunit, beta-D-fructofuranose-(2-1)-alpha-D-glucopyranose, ... (7 entities in total)
Functional Keywordsalpha-alpha barrel, inhibitor, ftase, pftase, fpp, caax, ras, transferase
Biological sourceHomo sapiens (human)
More
Total number of polymer chains2
Total formula weight94948.87
Authors
Primary citationDeSolms, S.J.,Ciccarone, T.M.,MacTough, S.C.,Shaw, A.W.,Buser, C.A.,Ellis-Hutchings, M.,Fernandes, C.,Hamilton, K.A.,Huber, H.E.,Kohl, N.E.,Lobell, R.B.,Robinson, R.G.,Tsou, N.N.,Walsh, E.S.,Graham, S.L.,Beese, L.S.,Taylor, J.S.
Dual Protein Farnesyltransferase-Geranylgeranyltransferase-I Inhibitors as Potential Cancer Chemotherapeutic Agents.
J.Med.Chem., 46:2973-2984, 2003
Cited by
PubMed: 12825937
DOI: 10.1021/jm020587n
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2 Å)
Structure validation

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