Bartlett Gail J, Borkakoti Neera, Thornton Janet M
Department of Biochemistry and Molecular Biology, University College London, Darwin Building, Gower Street, London WC1E 6BT, UK.
J Mol Biol. 2003 Aug 22;331(4):829-60. doi: 10.1016/s0022-2836(03)00734-4.
The diversity of function in some enzyme superfamilies shows that during evolution, enzymes have evolved to catalyse different reactions on the same structure scaffold. In this analysis, we examine in detail how enzymes can modify their chemistry, through a comparison of the catalytic residues and mechanisms in 27 pairs of homologous enzymes of totally different functions. We find that evolution is very economical. Enzymes retain structurally conserved residues to aid catalysis, including residues that bind catalytic metal ions and modulate cofactor chemistry. We examine the conservation of residue type and residue function in these structurally conserved residue pairs. Additionally, enzymes often retain common mechanistic steps catalyzed by structurally conserved residues. We have examined these steps in the context of their overall reactions.
一些酶超家族中的功能多样性表明,在进化过程中,酶已经进化到能够在相同的结构支架上催化不同的反应。在本分析中,我们通过比较27对功能完全不同的同源酶的催化残基和机制,详细研究了酶如何改变其化学性质。我们发现进化非常经济。酶保留结构保守的残基以辅助催化,包括结合催化金属离子和调节辅因子化学性质的残基。我们研究了这些结构保守残基对中残基类型和残基功能的保守性。此外,酶通常保留由结构保守残基催化的常见机制步骤。我们已经在其整体反应的背景下研究了这些步骤。