An evolving hierarchical family classification for glycosyltransferases

被引:945
作者
Coutinho, PM
Deleury, E
Davies, GJ
Henrissat, B
机构
[1] CNRS, Architecture & Fonct Macromol Biol UMR6098, F-13402 Marseille 20, France
[2] Univ Aix Marseille 1, F-13402 Marseille 20, France
[3] Univ Aix Marseille 2, F-13402 Marseille 20, France
[4] Univ York, Dept Chem, Struct Biol Lab, York YO10 5YW, N Yorkshire, England
基金
英国惠康基金;
关键词
glycosyltransferases; protein families; classification; modular structure; genomic annotations;
D O I
10.1016/S0022-2836(03)00307-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Glycosyltransferases are a ubiquitous group of enzymes that catalyse the transfer of a sugar moiety from an activated sugar donor onto saccharide or non-saccharide acceptors. Although many glycosyltransferases catalyse chemically similar reactions, presumably through transition states with substantial oxocarbenium ion character, they display remarkable diversity in their donor, acceptor and product specificity and thereby generate a potentially infinite number of glycoconjugates, oligo- and polysaccharides. We have performed a comprehensive survey of glycosyltransferase-related sequences (over 7200 to date) and present here a classification of these enzymes akin to that proposed previously for glycoside hydrolases, into a hierarchical system of families, clans, and folds. This evolving classification rationalises structural and mechanistic investigation, harnesses information from a wide variety of related enzymes to inform cell biology and overcomes recurrent problems in the functional prediction of glycosyltransferase-related open-reading frames. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:307 / 317
页数:11
相关论文
共 49 条
  • [11] STRUCTURES AND MECHANISMS OF GLYCOSYL HYDROLASES
    DAVIES, G
    HENRISSAT, B
    [J]. STRUCTURE, 1995, 3 (09) : 853 - 859
  • [12] Structural enzymology of carbohydrate-active enzymes: implications for the post-genomic era
    Davies, GJ
    Henrissat, B
    [J]. BIOCHEMICAL SOCIETY TRANSACTIONS, 2002, 30 : 291 - 297
  • [13] Identification and molecular cloning of a chondroitin synthase from Pasteurella multocida type F
    DeAngelis, PL
    Padgett-McCue, AJ
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (31) : 24124 - 24129
  • [14] Identification and molecular cloning of a heparosan synthase from Pasteurella multocida type D
    DeAngelis, PL
    White, CL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (09) : 7209 - 7213
  • [15] HYDROPHOBIC CLUSTER-ANALYSIS - AN EFFICIENT NEW WAY TO COMPARE AND ANALYZE AMINO-ACID-SEQUENCES
    GABORIAUD, C
    BISSERY, V
    BENCHETRIT, T
    MORNON, JP
    [J]. FEBS LETTERS, 1987, 224 (01): : 149 - 155
  • [16] Bovine α1,3-galactosyltransferase catalytic domain structure and its relationship with ABO histo-blood group and glycosphingolipid glycosyltransferases
    Gastinel, LN
    Bignon, C
    Misra, AK
    Hindsgaul, O
    Shaper, JH
    Joziasse, DH
    [J]. EMBO JOURNAL, 2001, 20 (04) : 638 - 649
  • [17] Crystal structures of the bovine β4galactosyltransferase catalytic domain and its complex with uridine diphosphogalactose
    Gastinel, LN
    Cambillau, C
    Bourne, Y
    [J]. EMBO JOURNAL, 1999, 18 (13) : 3546 - 3557
  • [18] Crystal structure of the autocatalytic initiator of glycogen biosynthesis, glycogenin
    Gibbons, BJ
    Roach, PJ
    Hurley, TD
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2002, 319 (02) : 463 - 477
  • [19] Insights into trehalose synthesis provided by the structure of the retaining glucosyltransferase OtsA
    Gibson, RP
    Turkenburg, JP
    Charnock, SJ
    Lloyd, R
    Davies, GJ
    [J]. CHEMISTRY & BIOLOGY, 2002, 9 (12): : 1337 - 1346
  • [20] DOMAIN SEPARATION IN THE ACTIVATION OF GLYCOGEN PHOSPHORYLASE-ALPHA
    GOLDSMITH, EJ
    SPRANG, SR
    HAMLIN, R
    XUONG, NH
    FLETTERICK, RJ
    [J]. SCIENCE, 1989, 245 (4917) : 528 - 532