Browner MF - Search Results

1

Flexibility of the NSAID binding site in the structure of human cyclooxygenase-2.

Luong C, Miller A, Barnett J, Chow J, Ramesha C, Browner MF. Luong C, et al. Among authors: browner mf. Nat Struct Biol. 1996 Nov;3(11):927-33. doi: 10.1038/nsb1196-927. Nat Struct Biol. 1996. PMID: 8901870

2

Crystal structures of MMP-1 and -13 reveal the structural basis for selectivity of collagenase inhibitors.

Lovejoy B, Welch AR, Carr S, Luong C, Broka C, Hendricks RT, Campbell JA, Walker KA, Martin R, Van Wart H, Browner MF. Lovejoy B, et al. Among authors: browner mf. Nat Struct Biol. 1999 Mar;6(3):217-21. doi: 10.1038/6657. Nat Struct Biol. 1999. PMID: 10074939

3

Rational design of 6-methylsulfonylindoles as selective cyclooxygenase-2 inhibitors.

Campbell JA, Bordunov V, Broka CA, Browner MF, Kress JM, Mirzadegan T, Ramesha C, Sanpablo BF, Stabler R, Takahara P, Villasenor A, Walker KA, Wang JH, Welch M, Weller P. Campbell JA, et al. Among authors: browner mf. Bioorg Med Chem Lett. 2004 Sep 20;14(18):4741-5. doi: 10.1016/j.bmcl.2004.06.075. Bioorg Med Chem Lett. 2004. PMID: 15324899

4

The crystal structure of JNK2 reveals conformational flexibility in the MAP kinase insert and indicates its involvement in the regulation of catalytic activity.

Shaw D, Wang SM, Villaseñor AG, Tsing S, Walter D, Browner MF, Barnett J, Kuglstatter A. Shaw D, et al. Among authors: browner mf. J Mol Biol. 2008 Nov 21;383(4):885-93. doi: 10.1016/j.jmb.2008.08.086. Epub 2008 Sep 10. J Mol Biol. 2008. PMID: 18801372

5

X-ray crystal structure of JNK2 complexed with the p38alpha inhibitor BIRB796: insights into the rational design of DFG-out binding MAP kinase inhibitors.

Kuglstatter A, Ghate M, Tsing S, Villaseñor AG, Shaw D, Barnett JW, Browner MF. Kuglstatter A, et al. Among authors: browner mf. Bioorg Med Chem Lett. 2010 Sep 1;20(17):5217-20. doi: 10.1016/j.bmcl.2010.06.157. Epub 2010 Jul 23. Bioorg Med Chem Lett. 2010. PMID: 20655210

6

Insights into the conformational flexibility of Bruton's tyrosine kinase from multiple ligand complex structures.

Kuglstatter A, Wong A, Tsing S, Lee SW, Lou Y, Villaseñor AG, Bradshaw JM, Shaw D, Barnett JW, Browner MF. Kuglstatter A, et al. Among authors: browner mf. Protein Sci. 2011 Feb;20(2):428-36. doi: 10.1002/pro.575. Protein Sci. 2011. PMID: 21280133 Free PMC article.

7

Partial activation of muscle phosphorylase by replacement of serine 14 with acidic residues at the site of regulatory phosphorylation.

Buchbinder JL, Luong CB, Browner MF, Fletterick RJ. Buchbinder JL, et al. Among authors: browner mf. Biochemistry. 1997 Jul 1;36(26):8039-44. doi: 10.1021/bi9704820. Biochemistry. 1997. PMID: 9201951

8

Discovery of S-[5-amino-1-(4-fluorophenyl)-1H-pyrazol-4-yl]-[3-(2,3-dihydroxypropoxy)phenyl]methanone (RO3201195), an orally bioavailable and highly selective inhibitor of p38 MAP kinase.

Goldstein DM, Alfredson T, Bertrand J, Browner MF, Clifford K, Dalrymple SA, Dunn J, Freire-Moar J, Harris S, Labadie SS, La Fargue J, Lapierre JM, Larrabee S, Li F, Papp E, McWeeney D, Ramesha C, Roberts R, Rotstein D, San Pablo B, Sjogren EB, So OY, Talamas FX, Tao W, Trejo A, Villasenor A, Welch M, Welch T, Weller P, Whiteley PE, Young K, Zipfel S. Goldstein DM, et al. Among authors: browner mf. J Med Chem. 2006 Mar 9;49(5):1562-75. doi: 10.1021/jm050736c. J Med Chem. 2006. PMID: 16509574

9

Cutting Edge: IL-1 receptor-associated kinase 4 structures reveal novel features and multiple conformations.

Kuglstatter A, Villaseñor AG, Shaw D, Lee SW, Tsing S, Niu L, Song KW, Barnett JW, Browner MF. Kuglstatter A, et al. Among authors: browner mf. J Immunol. 2007 Mar 1;178(5):2641-5. doi: 10.4049/jimmunol.178.5.2641. J Immunol. 2007. PMID: 17312103

10

Purification of glycogen phosphorylase isozymes by metal-affinity chromatography.

Luong CB, Browner MF, Fletterick RJ, Haymore BL. Luong CB, et al. Among authors: browner mf. J Chromatogr. 1992 Dec 11;584(1):77-84. doi: 10.1016/0378-4347(92)80011-e. J Chromatogr. 1992. PMID: 1487518

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