AffinDB: a freely accessible database of affinities for protein-ligand complexes from the PDB

被引:76
|
作者
Block, Peter [1 ]
Sotriffer, Christoph A. [1 ]
Dramburg, Ingo [1 ]
Klebe, Gerhard [1 ]
机构
[1] Univ Marburg, Dept Pharmaceut Chem, D-35032 Marburg, Germany
关键词
D O I
10.1093/nar/gkj039
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
AffinDB is a database of affinity data for structurally resolved protein-ligand complexes from the Protein Data Bank (PDB). It is freely accessible at http://www.agklebe.de/affinity. Affinity data are collected from the scientific literature, both from primary sources describing the original experimental work of affinity determination and from secondary references which report affinity values determined by others. AffinDB currently contains over 730 affinity entries covering more than 450 different protein-ligand complexes. Besides the affinity value, PDB summary information and additional data are provided, including the experimental conditions of the affinity measurement (if available in the corresponding reference); 2D drawing, SMILES code and molecular weight of the ligand; links to other databases, and bibliographic information. AffinDB can be queried by PDB code or by any combination of affinity range, temperature and pH value of the measurement, ligand molecular weight, and publication data (author, journal and year). Search results can be saved as tabular reports in text files. The database is supposed to be a valuable resource for researchers interested in biomolecular recognition and the development of tools for correlating structural data with affinities, as needed, for example, in structure-based drug design.
引用
收藏
页码:D522 / D526
页数:5
相关论文
共 50 条
  • [1] PDB-ligand: an interactive clustering tool for protein-ligand complexes in PDB
    Shin, JM
    Cho, DH
    Im, SY
    Ha, SY
    Yoon, JH
    Han, CK
    FEBS JOURNAL, 2005, 272 : 104 - 104
  • [2] BindingDB: a web-accessible database of experimentally determined protein-ligand binding affinities
    Liu, Tiqing
    Lin, Yuhmei
    Wen, Xin
    Jorissen, Robert N.
    Gilson, Michael K.
    NUCLEIC ACIDS RESEARCH, 2007, 35 : D198 - D201
  • [3] Drawing the PDB: Protein-Ligand Complexes in Two Dimensions
    Stierand, Katrin
    Rarey, Matthias
    ACS MEDICINAL CHEMISTRY LETTERS, 2010, 1 (09): : 540 - 545
  • [4] The PDBbind database: Collection of binding affinities for protein-ligand complexes with known three-dimensional structures
    Wang, RX
    Fang, XL
    Lu, YP
    Wang, SM
    JOURNAL OF MEDICINAL CHEMISTRY, 2004, 47 (12) : 2977 - 2980
  • [5] sc-PDB-Frag: A Database of Protein-Ligand Interaction Patterns for Bioisosteric Replacements
    Desaphy, Jeremy
    Rognan, Didier
    JOURNAL OF CHEMICAL INFORMATION AND MODELING, 2014, 54 (07) : 1908 - 1918
  • [6] Chalcogen Bonding in Protein-Ligand Complexes: PDB Survey and Quantum Mechanical Calculations
    Kriz, Kristian
    Fanfrlik, Jindrich
    Lepsik, Martin
    CHEMPHYSCHEM, 2018, 19 (19) : 2540 - 2548
  • [7] Calculation of protein-ligand binding affinities
    Gilson, Michael K.
    Zhou, Huan-Xiang
    ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE, 2007, 36 : 21 - 42
  • [8] Leveraging nonstructural data to predict structures and affinities of protein-ligand complexes
    Paggi, Joseph M.
    Belk, Julia A.
    Hollingsworth, Scott A.
    Villanueva, Nicolas
    Powers, Alexander S.
    Clark, Mary J.
    Chemparathy, Augustine G.
    Tynan, Jonathan E.
    Lau, Thomas K.
    Sunahara, Roger K.
    Dror, Ron O.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2021, 118 (51)
  • [9] Accurate prediction of binding modes and binding affinities of protein-ligand complexes
    Friesner, RA
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2005, 230 : U1282 - U1283
  • [10] Collection of binding affinities for protein-ligand complexes with known 3-D structures: The PDBbind database.
    Wang, RX
    Fang, XL
    Lu, YP
    Yang, CY
    Wang, SM
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2004, 228 : U527 - U527