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Page 1
Identification of novel potent hydroxamic acid inhibitors of peptidyl deformylase and the importance of the hydroxamic acid functionality on inhibition.
Thorarensen A, Deibel MR Jr, Rohrer DC, Vosters AF, Yem AW, Marshall VD, Lynn JC, Bohanon MJ, Tomich PK, Zurenko GE, Sweeney MT, Jensen RM, Nielsen JW, Seest EP, Dolak LA. Thorarensen A, et al. Among authors: vosters af. Bioorg Med Chem Lett. 2001 Jun 4;11(11):1355-8. doi: 10.1016/s0960-894x(01)00242-6. Bioorg Med Chem Lett. 2001. PMID: 11378353
Crystal structure of type II peptide deformylase from Staphylococcus aureus.
Baldwin ET, Harris MS, Yem AW, Wolfe CL, Vosters AF, Curry KA, Murray RW, Bock JH, Marshall VP, Cialdella JI, Merchant MH, Choi G, Deibel MR Jr. Baldwin ET, et al. Among authors: vosters af. J Biol Chem. 2002 Aug 23;277(34):31163-71. doi: 10.1074/jbc.M202750200. Epub 2002 Jun 4. J Biol Chem. 2002. PMID: 12048187 Free article.
Co-crystallization of Staphylococcus aureus peptide deformylase (PDF) with potent inhibitors.
Harris MS, Bock JH, Choi G, Cialdella JS, Curry KA, Deibel MR Jr, Jacobsen EJ, Marshall VP, Murray RW Jr, Vosters AF, Wolfe CL, Yem AW, Baldwin ET. Harris MS, et al. Among authors: vosters af. Acta Crystallogr D Biol Crystallogr. 2002 Dec;58(Pt 12):2153-6. doi: 10.1107/s090744490201569x. Epub 2002 Nov 23. Acta Crystallogr D Biol Crystallogr. 2002. PMID: 12454484
Purification and characterization of heterodimeric human immunodeficiency virus type 1 (HIV-1) reverse transcriptase produced by in vitro processing of p66 with recombinant HIV-1 protease.
Chattopadhyay D, Evans DB, Deibel MR Jr, Vosters AF, Eckenrode FM, Einspahr HM, Hui JO, Tomasselli AG, Zurcher-Neely HA, Heinrikson RL, et al. Chattopadhyay D, et al. Among authors: vosters af. J Biol Chem. 1992 Jul 15;267(20):14227-32. J Biol Chem. 1992. PMID: 1378437 Free article.
11 results