NRPS-PKS: a knowledge-based resource for analysis of NRPS/PKS megasynthases

被引:218
作者
Ansari, MZ [1 ]
Yadav, G [1 ]
Gokhale, RS [1 ]
Mohanty, D [1 ]
机构
[1] Natl Inst Immunol, New Delhi 110067, India
基金
英国惠康基金;
关键词
D O I
10.1093/nar/gkh359
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
NRPS-PKS is web-based software for analysing large multi-enzymatic, multi-domain megasynthases that are involved in the biosynthesis of pharmaceutically important natural products such as cyclosporin, rifamycin and erythromycin. NRPS-PKS has been developed based on a comprehensive analysis of the sequence and structural features of several experimentally characterized biosynthetic gene clusters. The results of these analyses have been organized as four integrated searchable databases for elucidating domain organization and substrate specificity of nonribosomal peptide synthetases and three types of polyketide synthases. These databases work as the backend of NRPS-PKS and provide the knowledge base for predicting domain organization and substrate specificity of uncharacterized NRPS/PKS clusters. Benchmarking on a large set of biosynthetic gene clusters has demonstrated that, apart from correct identification of NRPS and PKS domains, NRPS-PKS can also predict specificities of adenylation and acyltransferase domains with reasonably high accuracy. These features of NRPS-PKS make it a valuable resource for identification of natural products biosynthesized by NRPS/PKS gene clusters found in newly sequenced genomes. The training and test sets of gene clusters included in NRPS-PKS correlate information on 307 open reading frames, 2223 functional protein domains, 68 starter/extender precursors and their specific recognition motifs, and also the chemical structure of 101 natural products from four different families. NRPS-PKS is a unique resource which provides a user-friendly interface for correlating chemical structures of natural products with the domains and modules in the corresponding nonribosomal peptide synthetases or polyketide synthases. It also provides guidelines for domain/module swapping as well as site-directed mutagenesis experiments to engineer biosynthesis of novel natural products. NRPS-PKS can be accessed at http://www.nii.res.in/nrps-pks.html.
引用
收藏
页码:W405 / W413
页数:9
相关论文
共 30 条
  • [1] BASIC LOCAL ALIGNMENT SEARCH TOOL
    ALTSCHUL, SF
    GISH, W
    MILLER, W
    MYERS, EW
    LIPMAN, DJ
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) : 403 - 410
  • [2] [Anonymous], 2001, Biotechnology
  • [3] The chalcone synthase superfamily of type III polyketide synthases
    Austin, MB
    Noel, JP
    [J]. NATURAL PRODUCT REPORTS, 2003, 20 (01) : 79 - 110
  • [4] Benson DA, 2003, NUCLEIC ACIDS RES, V31, P23, DOI 10.1093/nar/gkg057
  • [5] The parallel and convergent universes of polyketide synthases and nonribosomal peptide synthetases
    Cane, DE
    Walsh, CT
    [J]. CHEMISTRY & BIOLOGY, 1999, 6 (12): : R319 - R325
  • [6] Biochemistry - Harnessing the biosynthetic code: Combinations, permutations, and mutations
    Cane, DE
    Walsh, CT
    Khosla, C
    [J]. SCIENCE, 1998, 282 (5386) : 63 - 68
  • [7] Predictive, structure-based model of amino acid recognition by nonribosomal peptide synthetase adenylation domains
    Challis, GL
    Ravel, J
    Townsend, CA
    [J]. CHEMISTRY & BIOLOGY, 2000, 7 (03): : 211 - 224
  • [8] Structural basis for the activation of phenylalanine in the non-ribosomal biosynthesis of gramicidin S
    Conti, E
    Stachelhaus, T
    Marahiel, MA
    Brick, P
    [J]. EMBO JOURNAL, 1997, 16 (14) : 4174 - 4183
  • [9] Du L, 2001, Curr Opin Drug Discov Devel, V4, P215
  • [10] Structure of chalcone synthase and the molecular basis of plant polyketide biosynthesis
    Ferrer, JL
    Jez, JM
    Bowman, ME
    Dixon, RA
    Noel, JP
    [J]. NATURE STRUCTURAL BIOLOGY, 1999, 6 (08) : 775 - 784