Grygon CA - Search Results

1

Assembly of major histocompatibility complex (MHC) class II transcription factors: association and promoter recognition of RFX proteins.

Burd AL, Ingraham RH, Goldrick SE, Kroe RR, Crute JJ, Grygon CA. Burd AL, et al. Among authors: grygon ca. Biochemistry. 2004 Oct 12;43(40):12750-60. doi: 10.1021/bi030262o. Biochemistry. 2004. PMID: 15461447

2

Discovery and characterization of a substrate selective p38alpha inhibitor.

Davidson W, Frego L, Peet GW, Kroe RR, Labadia ME, Lukas SM, Snow RJ, Jakes S, Grygon CA, Pargellis C, Werneburg BG. Davidson W, et al. Among authors: grygon ca. Biochemistry. 2004 Sep 21;43(37):11658-71. doi: 10.1021/bi0495073. Biochemistry. 2004. PMID: 15362850

3

Determination of affinities for lck SH2 binding peptides using a sensitive fluorescence assay: comparison between the pYEEIP and pYQPQP consensus sequences reveals context-dependent binding specificity.

Cousins-Wasti RC, Ingraham RH, Morelock MM, Grygon CA. Cousins-Wasti RC, et al. Among authors: grygon ca. Biochemistry. 1996 Dec 24;35(51):16746-52. doi: 10.1021/bi9620868. Biochemistry. 1996. PMID: 8988011

4

Interaction between the SH2 domains of ZAP-70 and the tyrosine-based activation motif 1 sequence of the zeta subunit of the T-cell receptor.

Labadia ME, Jakes S, Grygon CA, Greenwood DJ, Schembri-King J, Lukas SM, Warren TC, Ingraham RH. Labadia ME, et al. Among authors: grygon ca. Arch Biochem Biophys. 1997 Jun 1;342(1):117-25. doi: 10.1006/abbi.1997.0118. Arch Biochem Biophys. 1997. PMID: 9185620

5

Agonist versus antagonist induce distinct thermodynamic modes of co-factor binding to the glucocorticoid receptor.

Kroe RR, Baker MA, Brown MP, Farrow NA, Gautschi E, Hopkins JL, LaFrance RR, Kronkaitis A, Freeman D, Thomson D, Nabozny G, Grygon CA, Labadia ME. Kroe RR, et al. Among authors: grygon ca. Biophys Chem. 2007 Jul;128(2-3):156-64. doi: 10.1016/j.bpc.2007.03.013. Epub 2007 Apr 5. Biophys Chem. 2007. PMID: 17466438

6

Herpes simplex virus helicase-primase inhibitors are active in animal models of human disease.

Crute JJ, Grygon CA, Hargrave KD, Simoneau B, Faucher AM, Bolger G, Kibler P, Liuzzi M, Cordingley MG. Crute JJ, et al. Among authors: grygon ca. Nat Med. 2002 Apr;8(4):386-91. doi: 10.1038/nm0402-386. Nat Med. 2002. PMID: 11927945

7

Amino acid substitutions in HIV-1 reverse transcriptase with corresponding residues from HIV-2. Effect on kinetic constants and inhibition by non-nucleoside analogs.

Bacolla A, Shih CK, Rose JM, Piras G, Warren TC, Grygon CA, Ingraham RH, Cousins RC, Greenwood DJ, Richman D, et al. Bacolla A, et al. Among authors: grygon ca. J Biol Chem. 1993 Aug 5;268(22):16571-7. J Biol Chem. 1993. PMID: 7688367 Free article.

8

Characterization of the allosteric inhibition of a protein-protein interaction by mass spectrometry.

Davidson W, Hopkins JL, Jeanfavre DD, Barney KL, Kelly TA, Grygon CA. Davidson W, et al. Among authors: grygon ca. J Am Soc Mass Spectrom. 2003 Jan;14(1):8-13. doi: 10.1016/S1044-0305(02)00706-7. J Am Soc Mass Spectrom. 2003. PMID: 12504329 Free article.

9

Binding site elucidation of hydantoin-based antagonists of LFA-1 using multidisciplinary technologies: evidence for the allosteric inhibition of a protein--protein interaction.

Last-Barney K, Davidson W, Cardozo M, Frye LL, Grygon CA, Hopkins JL, Jeanfavre DD, Pav S, Qian C, Stevenson JM, Tong L, Zindell R, Kelly TA. Last-Barney K, et al. Among authors: grygon ca. J Am Chem Soc. 2001 Jun 20;123(24):5643-50. doi: 10.1021/ja0104249. J Am Chem Soc. 2001. PMID: 11403595

10

Design and synthesis of dipeptide nitriles as reversible and potent Cathepsin S inhibitors.

Ward YD, Thomson DS, Frye LL, Cywin CL, Morwick T, Emmanuel MJ, Zindell R, McNeil D, Bekkali Y, Girardot M, Hrapchak M, DeTuri M, Crane K, White D, Pav S, Wang Y, Hao MH, Grygon CA, Labadia ME, Freeman DM, Davidson W, Hopkins JL, Brown ML, Spero DM. Ward YD, et al. Among authors: grygon ca. J Med Chem. 2002 Dec 5;45(25):5471-82. doi: 10.1021/jm020209i. J Med Chem. 2002. PMID: 12459015

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