Davies GJ - Search Results

1

Selective Fluorogenic β-Glucocerebrosidase Substrates for Convenient Analysis of Enzyme Activity in Cell and Tissue Homogenates.

Deen MC, Proceviat C, Shan X, Wu L, Shen DL, Davies GJ, Vocadlo DJ. Deen MC, et al. Among authors: davies gj. ACS Chem Biol. 2020 Apr 17;15(4):824-829. doi: 10.1021/acschembio.9b01044. Epub 2020 Mar 16. ACS Chem Biol. 2020. PMID: 32109051 Free article.

2

Catalysis by hen egg-white lysozyme proceeds via a covalent intermediate.

Vocadlo DJ, Davies GJ, Laine R, Withers SG. Vocadlo DJ, et al. Among authors: davies gj. Nature. 2001 Aug 23;412(6849):835-8. doi: 10.1038/35090602. Nature. 2001. PMID: 11518970 Free article.

3

Structure and mechanism of a bacterial beta-glucosaminidase having O-GlcNAcase activity.

Dennis RJ, Taylor EJ, Macauley MS, Stubbs KA, Turkenburg JP, Hart SJ, Black GN, Vocadlo DJ, Davies GJ. Dennis RJ, et al. Among authors: davies gj. Nat Struct Mol Biol. 2006 Apr;13(4):365-71. doi: 10.1038/nsmb1079. Epub 2006 Mar 26. Nat Struct Mol Biol. 2006. PMID: 16565725

4

Functional analysis of a group A streptococcal glycoside hydrolase Spy1600 from family 84 reveals it is a beta-N-acetylglucosaminidase and not a hyaluronidase.

Sheldon WL, Macauley MS, Taylor EJ, Robinson CE, Charnock SJ, Davies GJ, Vocadlo DJ, Black GW. Sheldon WL, et al. Among authors: davies gj. Biochem J. 2006 Oct 15;399(2):241-7. doi: 10.1042/BJ20060307. Biochem J. 2006. PMID: 16822234 Free PMC article.

5

Inhibition of O-GlcNAcase by a gluco-configured nagstatin and a PUGNAc-imidazole hybrid inhibitor.

Shanmugasundaram B, Debowski AW, Dennis RJ, Davies GJ, Vocadlo DJ, Vasella A. Shanmugasundaram B, et al. Among authors: davies gj. Chem Commun (Camb). 2006 Nov 13;(42):4372-4. doi: 10.1039/b612154c. Epub 2006 Sep 29. Chem Commun (Camb). 2006. PMID: 17057847

6

Analysis of PUGNAc and NAG-thiazoline as transition state analogues for human O-GlcNAcase: mechanistic and structural insights into inhibitor selectivity and transition state poise.

Whitworth GE, Macauley MS, Stubbs KA, Dennis RJ, Taylor EJ, Davies GJ, Greig IR, Vocadlo DJ. Whitworth GE, et al. Among authors: davies gj. J Am Chem Soc. 2007 Jan 24;129(3):635-44. doi: 10.1021/ja065697o. J Am Chem Soc. 2007. PMID: 17227027

7

A 1-acetamido derivative of 6-epi-valienamine: an inhibitor of a diverse group of beta-N-acetylglucosaminidases.

Scaffidi A, Stubbs KA, Dennis RJ, Taylor EJ, Davies GJ, Vocadlo DJ, Stick RV. Scaffidi A, et al. Among authors: davies gj. Org Biomol Chem. 2007 Sep 21;5(18):3013-9. doi: 10.1039/b709681j. Epub 2007 Aug 15. Org Biomol Chem. 2007. PMID: 17728868

8

Structure of an O-GlcNAc transferase homolog provides insight into intracellular glycosylation.

Martinez-Fleites C, Macauley MS, He Y, Shen DL, Vocadlo DJ, Davies GJ. Martinez-Fleites C, et al. Among authors: davies gj. Nat Struct Mol Biol. 2008 Jul;15(7):764-5. doi: 10.1038/nsmb.1443. Epub 2008 Jun 8. Nat Struct Mol Biol. 2008. PMID: 18536723

9

Mechanistic insights into glycosidase chemistry.

Vocadlo DJ, Davies GJ. Vocadlo DJ, et al. Among authors: davies gj. Curr Opin Chem Biol. 2008 Oct;12(5):539-55. doi: 10.1016/j.cbpa.2008.05.010. Curr Opin Chem Biol. 2008. PMID: 18558099 Review.

10

A potent mechanism-inspired O-GlcNAcase inhibitor that blocks phosphorylation of tau in vivo.

Yuzwa SA, Macauley MS, Heinonen JE, Shan X, Dennis RJ, He Y, Whitworth GE, Stubbs KA, McEachern EJ, Davies GJ, Vocadlo DJ. Yuzwa SA, et al. Among authors: davies gj. Nat Chem Biol. 2008 Aug;4(8):483-90. doi: 10.1038/nchembio.96. Epub 2008 Jun 29. Nat Chem Biol. 2008. PMID: 18587388

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