SuperCYP: a comprehensive database on Cytochrome P450 enzymes including a tool for analysis of CYP-drug interactions

被引:193
作者
Preissner, Saskia [1 ]
Kroll, Katharina [1 ]
Dunkel, Mathias [1 ]
Senger, Christian [2 ]
Goldsobel, Gady [1 ]
Kuzman, Daniel [1 ]
Guenther, Stefan [1 ]
Winnenburg, Rainer [3 ]
Schroeder, Michael [3 ]
Preissner, Robert [1 ]
机构
[1] Charite, Inst Physiol, Struct Bioinformat Grp, D-14197 Berlin, Germany
[2] Heidelberg Univ, Dept Internal Med Clin Pharmacol & Pharmacoepidem, Heidelberg, Germany
[3] Tech Univ Dresden, Ctr Biotechnol, Dresden, Germany
关键词
PROTEIN DATA-BANK; BINDING SITES; PREDICTION; DISCOVERY; SYSTEM; GENES; P450;
D O I
10.1093/nar/gkp970
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
Much of the information on the Cytochrome P450 enzymes (CYPs) is spread across literature and the internet. Aggregating knowledge about CYPs into one database makes the search more efficient. Text mining on 57 CYPs and drugs led to a mass of papers, which were screened manually for facts about metabolism, SNPs and their effects on drug degradation. Information was put into a database, which enables the user not only to look up a particular CYP and all metabolized drugs, but also to check tolerability of drug-cocktails and to find alternative combinations, to use metabolic pathways more efficiently. The SuperCYP database contains 1170 drugs with more than 3800 interactions including references. Approximately 2000 SNPs and mutations are listed and ordered according to their effect on expression and/or activity. SuperCYP (http://bioinformatics.charite.de/supercyp) is a comprehensive resource focused on CYPs and drug metabolism. Homology-modeled structures of the CYPs can be downloaded in PDB format and related drugs are available as MOL-files. Within the resource, CYPs can be aligned with each other, drug-cocktails can be 'mixed', SNPs, protein point mutations, and their effects can be viewed and corresponding PubMed IDs are given. SuperCYP is meant to be a platform and a starting point for scientists and health professionals for furthering their research.
引用
收藏
页码:D237 / D243
页数:7
相关论文
共 31 条
  • [1] The SWISS-MODEL workspace: a web-based environment for protein structure homology modelling
    Arnold, K
    Bordoli, L
    Kopp, J
    Schwede, T
    [J]. BIOINFORMATICS, 2006, 22 (02) : 195 - 201
  • [2] Effective therapeutic dosage of antipsychotic medications in patients with psychotic symptoms: Is there a racial difference?
    Bakare M.O.
    [J]. BMC Research Notes, 1 (1)
  • [3] Genotypes for the cytochrome P450 enzymes CYP2D6 and CYP2C19 in human longevity - Role of CYP2D6 and CYP2C19 in longevity
    Bathum, L
    Andersen-Ranberg, K
    Boldsen, J
    Brosen, K
    Jeune, B
    [J]. EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1998, 54 (05) : 427 - 430
  • [4] The Protein Data Bank
    Berman, HM
    Westbrook, J
    Feng, Z
    Gilliland, G
    Bhat, TN
    Weissig, H
    Shindyalov, IN
    Bourne, PE
    [J]. NUCLEIC ACIDS RESEARCH, 2000, 28 (01) : 235 - 242
  • [5] GEOGRAPHICAL INTERRACIAL DIFFERENCES IN POLYMORPHIC DRUG OXIDATION - CURRENT STATE OF KNOWLEDGE OF CYTOCHROMES P450 (CYP) 2D6 AND 2C19
    BERTILSSON, L
    [J]. CLINICAL PHARMACOKINETICS, 1995, 29 (03) : 192 - 209
  • [6] Dell H, 1998, Methods Mol Biol, V107, P381
  • [7] Resolution of multiple substrate binding sites in cytochrome P450 3A4: The stoichiometry of the enzyme-substrate complexes probed by FRET and Job's titration
    Fernando, H
    Halpert, JR
    Davydov, DR
    [J]. BIOCHEMISTRY, 2006, 45 (13) : 4199 - 4209
  • [8] The Cytochrome P450 Engineering Database: a navigation and prediction tool for the cytochrome P450 protein family
    Fischer, Markus
    Knoll, Michael
    Sirim, Demet
    Wagner, Florian
    Funke, Sonja
    Pleiss, Juergen
    [J]. BIOINFORMATICS, 2007, 23 (15) : 2015 - 2017
  • [9] Flockhart DA, 2000, CHILD ADOL PSYCH CL, V9, P43
  • [10] Geer LY, 2009, NUCL ACIDS RES