The Short-chain Dehydrogenase/Reductase Engineering Database (SDRED): A classification and analysis system for a highly diverse enzyme family

被引:33
|
作者
Graeff, Maike [1 ]
Buchholz, Patrick C. F. [1 ]
Stockinger, Peter [1 ]
Bommarius, Bettina [2 ]
Bommarius, Andreas S. [2 ]
Pleiss, Juergen [1 ]
机构
[1] Univ Stuttgart, Inst Biochem & Tech Biochem, Stuttgart, Germany
[2] Georgia Inst Technol, Dept Chem & Biomol Engn, Atlanta, GA 30332 USA
关键词
protein family database; SDR; SDRED; sequence network; sequence-function-relationship; ALCOHOL-DEHYDROGENASE; STRUCTURAL INSIGHT; SEARCH; REDUCTASES; SUBSTITUTION; SUPERFAMILY; REDUCTION; SUBSTRATE; ALIGNMENT; SEQUENCE;
D O I
10.1002/prot.25666
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
The Short-chain Dehydrogenases/Reductases Engineering Database (SDRED) covers one of the largest known protein families (168 150 proteins). Assignment to the superfamilies of Classical and Extended SDRs was achieved by global sequence similarity and by identification of family-specific sequence motifs. Two standard numbering schemes were established for Classical and Extended SDRs that allow for the determination of conserved amino acid residues, such as cofactor specificity determining positions or superfamily specific sequence motifs. The comprehensive sequence dataset of the SDRED facilitates the refinement of family-specific sequence motifs. The glycine-rich motifs for Classical and Extended SDRs were refined to improve the precision of superfamily classification. In each superfamily, the majority of sequences formed a tightly connected sequence network and belonged to a large homologous family. Despite their different sequence motifs and their different sequence length, the two sequence networks of Classical and Extended SDRs are not separate, but connected by edges at a threshold of 40% sequence similarity, indicating that all SDRs belong to a large, connected network. The SDRED is accessible at https://sdred.biocatnet.de/.
引用
下载
收藏
页码:443 / 451
页数:9
相关论文
共 48 条
  • [31] Crystallographic structure determination and analysis of a potential short-chain dehydrogenase/reductase (SDR) from multi-drug resistant Acinetobacter baumannii
    Ghafoori, Seyed Mohammad
    Abdollahpour, Soha
    Shirmast, Paniz
    Forwood, Jade K.
    PLOS ONE, 2023, 18 (08):
  • [32] Biochemical and structural characterization of recombinant short-chain NAD(H)-dependent dehydrogenase/reductase from Sulfolobus acidocaldarius highly enantioselective on diaryl diketone benzil
    Angela Pennacchio
    Vincenzo Sannino
    Giosuè Sorrentino
    Mosè Rossi
    Carlo A. Raia
    Luciana Esposito
    Applied Microbiology and Biotechnology, 2013, 97 : 3949 - 3964
  • [33] Biochemical and structural characterization of recombinant short-chain NAD(H)-dependent dehydrogenase/reductase from Sulfolobus acidocaldarius highly enantioselective on diaryl diketone benzil
    Pennacchio, Angela
    Sannino, Vincenzo
    Sorrentino, Giosue
    Rossi, Mose
    Raia, Carlo A.
    Esposito, Luciana
    APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2013, 97 (09) : 3949 - 3964
  • [34] Medium- and short-chain dehydrogenase/reductase gene and protein familiesThe SDR superfamily: functional and structural diversity within a family of metabolic and regulatory enzymes
    K. L. Kavanagh
    H. Jörnvall
    B. Persson
    U. Oppermann
    Cellular and Molecular Life Sciences, 2008, 65
  • [35] Structure-based phylogenetic analysis of short-chain alcohol dehydrogenases and reclassification of the 17beta-hydroxysteroid dehydrogenase family
    Breitling, R
    Laubner, D
    Adamski, J
    MOLECULAR BIOLOGY AND EVOLUTION, 2001, 18 (12) : 2154 - 2161
  • [36] Properties of short-chain dehydrogenase/reductase RalR1: Characterization of purified enzyme, its orientation in the microsomal membrane, and distribution in human tissues and cell lines
    Belyaeva, OV
    Stetsenko, AV
    Nelson, P
    Kedishvili, NY
    BIOCHEMISTRY, 2003, 42 (50) : 14838 - 14845
  • [37] PURIFICATION AND STRUCTURAL CHARACTERIZATION OF PLACENTAL NAD+-LINKED 15-HYDROXYPROSTAGLANDIN DEHYDROGENASE - THE PRIMARY STRUCTURE REVEALS THE ENZYME TO BELONG TO THE SHORT-CHAIN ALCOHOL-DEHYDROGENASE FAMILY
    KROOK, M
    MAREKOV, L
    JORNVALL, H
    BIOCHEMISTRY, 1990, 29 (03) : 738 - 743
  • [38] SDR7-6, a short-chain alcohol dehydrogenase/reductase family protein, regulates light-dependent cell death and defence responses in rice
    Zheng, Yanmei
    Zhu, Yongsheng
    Mao, Xiaohui
    Jiang, Minrong
    Wei, Yidong
    Lian, Ling
    Xu, Huibin
    Chen, Liping
    Xie, Huaan
    Lu, Guodong
    Zhang, Jianfu
    MOLECULAR PLANT PATHOLOGY, 2022, 23 (01) : 78 - 91
  • [39] Characterization and regulation of an airway epithelial cell-specific novel gene which belongs to the short-chain alcohol dehydrogenase/reductase (SDR) gene family.
    Di, YP
    Soref, CM
    Zhao, YH
    Wu, R
    AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1999, 159 (03) : A37 - A37
  • [40] A unique catalytic triad revealed by the crystal structure of APE0912, a short-chain dehydrogenase/reductase family protein from Aerapyrum pernix K1
    Yamamura, Akihiro
    Ichimura, Takefumi
    Mimoto, Futa
    Ohtsuka, Jun
    Miyazono, Ken-Ichi
    Okai, Masahiko
    Kamo, Masayuki
    Lee, Woo-Cheol
    Nagata, Koji
    Tanokura, Masaru
    PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2008, 70 (04) : 1640 - 1645