Hepatitis C databases, principles and utility to researchers

被引:30
作者
Kuiken, C
Mizokarni, M
Deleage, G
Yusim, K
Peni, F
Shin-I, T
Charaway, C
Tao, N
Crisan, D
Grando, D
Dalwani, A
Geourjon, C
Agraxwal, A
Combet, C
机构
[1] Los Alamos Natl Lab, Theoret Biol & Biophys Grp, Los Alamos, NM 87545 USA
[2] Nagoya City Univ, Grad Sch Med Sci, Dept Clin Mol Informat Med, Kawasumi, Mizuho Nagoya, Japan
[3] Inst Biol & Chim Prot, CNRS, UCBL, UMR5086,IFR128 BioSci Lyon Gerland 7, Lyon, France
关键词
D O I
10.1002/hep.21162
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Part of the effort to develop hepatitis C-specific drugs and vaccines is the study of genetic variability of all publicly available HCV sequences. Three HCV databases are currently available to aid this effort and to provide additional insight into the basic biology, immunology, and evolution of the virus. The Japanese HCV database (http://s2as02.genes.nig.ac.jp) gives access to a genomic mapping of sequences as well as their phylogenetic relationships. The European HCV database (http://euhcvdb.ibcp.fr) offers access to a computer-annotated set of sequences and molecular models of HCV proteins and focuses on protein sequence, structure and fimction analysis. The HCV database at the Los Alamos National Laboratory in the United States (http://hcv.lanl.gov) provides access to a manually annotated sequence database and a database of immunological epitopes which contains concise descriptions of experimental results. In this paper, we briefly describe each of these databases and their associated websites and tools, and give some examples of their use in furthering HCV research.
引用
收藏
页码:1157 / 1165
页数:9
相关论文
共 31 条
  • [1] THE NATURAL-HISTORY OF COMMUNITY-ACQUIRED HEPATITIS-C IN THE UNITED-STATES
    ALTER, MJ
    MARGOLIS, HS
    KRAWCZYNSKI, K
    JUDSON, FN
    MARES, A
    ALEXANDER, WJ
    HU, PY
    MILLER, JK
    GERBER, MA
    SAMPLINER, RE
    MEEKS, EL
    BEACH, MJ
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1992, 327 (27) : 1899 - 1905
  • [2] Subcellular localization and topology of the p7 polypeptide of hepatitis C virus
    Carrère-Kremer, S
    Montpellier-Pala, C
    Cocquerel, L
    Wychowski, C
    Penin, F
    Dubuisson, J
    [J]. JOURNAL OF VIROLOGY, 2002, 76 (08) : 3720 - 3730
  • [3] NPS@:: Network Protein Sequence Analysis
    Combet, C
    Blanchet, C
    Geourjon, C
    Deléage, G
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 2000, 25 (03) : 147 - 150
  • [4] Geno3D:: automatic comparative molecular modelling of protein
    Combet, C
    Jambon, M
    Deléage, G
    Geourjon, C
    [J]. BIOINFORMATICS, 2002, 18 (01) : 213 - 214
  • [5] Combet Christophe, 2004, Appl Bioinformatics, V3, P237, DOI 10.2165/00822942-200403040-00005
  • [6] Farci P, 2000, SEMIN LIVER DIS, V20, P103
  • [7] HIGGINS DG, 1992, COMPUT APPL BIOSCI, V8, P15
  • [8] Hoofnagle JH, 1997, HEPATOLOGY S1, V26, p15S
  • [9] A new bioinformatic approach to detect common 3D sites in protein structures
    Jambon, M
    Imberty, A
    Deléage, G
    Geourjon, C
    [J]. PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2003, 52 (02) : 137 - 145
  • [10] Differences in hepatitis C virus core protein processing among genotypes 1 and 2
    Kato, T
    Miyamoto, M
    Date, T
    Furusaka, A
    Hiramoto, J
    Nagayama, K
    Tsai, N
    Mizokami, M
    Wakita, T
    [J]. HEPATOLOGY RESEARCH, 2004, 30 (04) : 204 - 209