Gerrard JA - Search Results

1

The preparation of (S)-aspartate semi-aldehyde appropriate for use in biochemical studies.

Roberts SJ, Morris JC, Dobson RC, Gerrard JA. Roberts SJ, et al. Among authors: gerrard ja. Bioorg Med Chem Lett. 2003 Jan 20;13(2):265-7. doi: 10.1016/s0960-894x(02)00923-x. Bioorg Med Chem Lett. 2003. PMID: 12482436

2

Ascorbic acid-based inhibitors of alpha-amylases.

Abell AD, Ratcliffe MJ, Gerrard J. Abell AD, et al. Bioorg Med Chem Lett. 1998 Jul 7;8(13):1703-6. doi: 10.1016/s0960-894x(98)00298-4. Bioorg Med Chem Lett. 1998. PMID: 9873419

3

Kinetic characterisation of ene-diol-based inhibitors of alpha-amylase.

Gerrard JA, Prince MJ, Abell AD. Gerrard JA, et al. Bioorg Med Chem Lett. 2000 Jul 17;10(14):1575-6. doi: 10.1016/s0960-894x(00)00288-2. Bioorg Med Chem Lett. 2000. PMID: 10915054

4

New insights into protein crosslinking via the Maillard reaction: structural requirements, the effect on enzyme function, and predicted efficacy of crosslinking inhibitors as anti-ageing therapeutics.

Miller AG, Meade SJ, Gerrard JA. Miller AG, et al. Among authors: gerrard ja. Bioorg Med Chem. 2003 Mar 20;11(6):843-52. doi: 10.1016/s0968-0896(02)00565-5. Bioorg Med Chem. 2003. PMID: 12614869

5

The role of dicarbonyl compounds in non-enzymatic crosslinking: a structure-activity study.

Meade SJ, Miller AG, Gerrard JA. Meade SJ, et al. Among authors: gerrard ja. Bioorg Med Chem. 2003 Mar 20;11(6):853-62. doi: 10.1016/s0968-0896(02)00564-3. Bioorg Med Chem. 2003. PMID: 12614870

6

Dihydrodipicolinate synthase is not inhibited by its substrate, (S)-aspartate beta-semialdehyde.

Dobson RC, Gerrard JA, Pearce FG. Dobson RC, et al. Among authors: gerrard ja. Biochem J. 2004 Feb 1;377(Pt 3):757-62. doi: 10.1042/BJ20031389. Biochem J. 2004. PMID: 14580236 Free PMC article.

7

The crystal structure of three site-directed mutants of Escherichia coli dihydrodipicolinate synthase: further evidence for a catalytic triad.

Dobson RC, Valegård K, Gerrard JA. Dobson RC, et al. Among authors: gerrard ja. J Mol Biol. 2004 Apr 23;338(2):329-39. doi: 10.1016/j.jmb.2004.02.060. J Mol Biol. 2004. PMID: 15066435

8

Dihydrodipicolinate synthase (DHDPS) from Escherichia coli displays partial mixed inhibition with respect to its first substrate, pyruvate.

Dobson RC, Griffin MD, Roberts SJ, Gerrard JA. Dobson RC, et al. Among authors: gerrard ja. Biochimie. 2004 Apr-May;86(4-5):311-5. doi: 10.1016/j.biochi.2004.03.008. Biochimie. 2004. PMID: 15194235

9

Two new irreversible inhibitors of dihydrodipicolinate synthase: diethyl (E,E)-4-oxo-2,5-heptadienedioate and diethyl (E)-4-oxo-2-heptenedioate.

Turner JJ, Healy JP, Dobson RC, Gerrard JA, Hutton CA. Turner JJ, et al. Among authors: gerrard ja. Bioorg Med Chem Lett. 2005 Feb 15;15(4):995-8. doi: 10.1016/j.bmcl.2004.12.043. Bioorg Med Chem Lett. 2005. PMID: 15686899

10

The crystal structures of native and (S)-lysine-bound dihydrodipicolinate synthase from Escherichia coli with improved resolution show new features of biological significance.

Dobson RC, Griffin MD, Jameson GB, Gerrard JA. Dobson RC, et al. Among authors: gerrard ja. Acta Crystallogr D Biol Crystallogr. 2005 Aug;61(Pt 8):1116-24. doi: 10.1107/S0907444905016318. Epub 2005 Jul 20. Acta Crystallogr D Biol Crystallogr. 2005. PMID: 16041077

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