BioLiP: a semi-manually curated database for biologically relevant ligand-protein interactions

被引:526
作者
Yang, Jianyi [1 ]
Roy, Ambrish [1 ]
Zhang, Yang [1 ]
机构
[1] Univ Michigan, Dept Computat Med & Bioinformat, Ann Arbor, MI 48109 USA
基金
美国国家科学基金会;
关键词
BINDING-SITES; RESIDUES; PREDICTION; RESOURCE;
D O I
10.1093/nar/gks966
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
BioLiP (http://zhanglab.ccmb.med.umich.edu/BioLiP/) is a semi-manually curated database for biologically relevant ligand-protein interactions. Establishing interactions between protein and biologically relevant ligands is an important step toward understanding the protein functions. Most ligand-binding sites prediction methods use the protein structures from the Protein Data Bank (PDB) as templates. However, not all ligands present in the PDB are biologically relevant, as small molecules are often used as additives for solving the protein structures. To facilitate template-based ligand-protein docking, virtual ligand screening and protein function annotations, we develop a hierarchical procedure for assessing the biological relevance of ligands present in the PDB structures, which involves a four-step biological feature filtering followed by careful manual verifications. This procedure is used for BioLiP construction. Each entry in BioLiP contains annotations on: ligand-binding residues, ligand-binding affinity, catalytic sites, Enzyme Commission numbers, Gene Ontology terms and cross-links to the other databases. In addition, to facilitate the use of BioLiP for function annotation of uncharacterized proteins, a new consensus-based algorithm COACH is developed to predict ligand-binding sites from protein sequence or using 3D structure. The BioLiP database is updated weekly and the current release contains 204 223 entries.
引用
收藏
页码:D1096 / D1103
页数:8
相关论文
共 29 条
[11]   ProtChemSI: a network of protein-chemical structural interactions [J].
Kalinina, Olga V. ;
Wichmann, Oliver ;
Apic, Gordana ;
Russell, Robert B. .
NUCLEIC ACIDS RESEARCH, 2012, 40 (D1) :D549-D553
[12]   KEGG for integration and interpretation of large-scale molecular data sets [J].
Kanehisa, Minoru ;
Goto, Susumu ;
Sato, Yoko ;
Furumichi, Miho ;
Tanabe, Mao .
NUCLEIC ACIDS RESEARCH, 2012, 40 (D1) :D109-D114
[13]   BSP-SLIM: A blind low-resolution ligand-protein docking approach using predicted protein structures [J].
Lee, Hui Sun ;
Zhang, Yang .
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2012, 80 (01) :93-110
[14]   BindingDB: a web-accessible database of experimentally determined protein-ligand binding affinities [J].
Liu, Tiqing ;
Lin, Yuhmei ;
Wen, Xin ;
Jorissen, Robert N. ;
Gilson, Michael K. .
NUCLEIC ACIDS RESEARCH, 2007, 35 :D198-D201
[15]   FireDB - a database of functionally important residues from proteins of known structure [J].
Lopez, Gonzalo ;
Valencia, A. ;
Tress, M. .
NUCLEIC ACIDS RESEARCH, 2007, 35 :D219-D223
[16]   PROTEIN-DNA RECOGNITION [J].
PABO, CO ;
SAUER, RT .
ANNUAL REVIEW OF BIOCHEMISTRY, 1984, 53 :293-321
[17]   The Catalytic Site Atlas: a resource of catalytic sites and residues identified in enzymes using structural data [J].
Porter, CT ;
Bartlett, GJ ;
Thornton, JM .
NUCLEIC ACIDS RESEARCH, 2004, 32 :D129-D133
[18]   FunFOLD: an improved automated method for the prediction of ligand binding residues using 3D models of proteins [J].
Roche, Daniel B. ;
Tetchner, Stuart J. ;
McGuffin, Liam J. .
BMC BIOINFORMATICS, 2011, 12
[19]   The RCSB Protein Data Bank: redesigned web site and web services [J].
Rose, Peter W. ;
Beran, Bojan ;
Bi, Chunxiao ;
Bluhm, Wolfgang F. ;
Dimitropoulos, Dimitris ;
Goodsell, David S. ;
Prlic, Andreas ;
Quesada, Martha ;
Quinn, Gregory B. ;
Westbrook, John D. ;
Young, Jasmine ;
Yukich, Benjamin ;
Zardecki, Christine ;
Berman, Helen M. ;
Bourne, Philip E. .
NUCLEIC ACIDS RESEARCH, 2011, 39 :D392-D401
[20]   COFACTOR: an accurate comparative algorithm for structure-based protein function annotation [J].
Roy, Ambrish ;
Yang, Jianyi ;
Zhang, Yang .
NUCLEIC ACIDS RESEARCH, 2012, 40 (W1) :W471-W477