Functional annotation by identification of local surface similarities:: a novel tool for structural genomics -: art. no. 194

被引:28
作者
Ferrè, F
Ausiello, G
Zanzoni, A
Helmer-Citterich, M
机构
[1] Boston Coll, Dept Biol, Chestnut Hill, MA 02167 USA
[2] Univ Roma Tor Vergata, Dept Biol, Ctr Mol Bioinformat, I-00173 Rome, Italy
关键词
D O I
10.1186/1471-2105-6-194
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Protein function is often dependent on subsets of solvent-exposed residues that may exist in a similar three-dimensional configuration in non homologous proteins thus having different order and/or spacing in the sequence. Hence, functional annotation by means of sequence or fold similarity is not adequate for such cases. Results: We describe a method for the function-related annotation of protein structures by means of the detection of local structural similarity with a library of annotated functional sites. An automatic procedure was used to annotate the function of local surface regions. Next, we employed a sequence-independent algorithm to compare exhaustively these functional patches with a larger collection of protein surface cavities. After tuning and validating the algorithm on a dataset of well annotated structures, we applied it to a list of protein structures that are classified as being of unknown function in the Protein Data Bank. By this strategy, we were able to provide functional clues to proteins that do not show any significant sequence or global structural similarity with proteins in the current databases. Conclusion: This method is able to spot structural similarities associated to function-related similarities, independently on sequence or fold resemblance, therefore is a valuable tool for the functional analysis of uncharacterized proteins. Results are available at http:// cbm. bio. uniroma2. it/ surface/ structuralGenomics. html.
引用
收藏
页数:14
相关论文
共 64 条
  • [1] Analysis of zinc binding sites in protein crystal structures
    Alberts, IL
    Nadassy, K
    Wodak, SJ
    [J]. PROTEIN SCIENCE, 1998, 7 (08) : 1700 - 1716
  • [2] SCOP database in 2004: refinements integrate structure and sequence family data
    Andreeva, A
    Howorth, D
    Brenner, SE
    Hubbard, TJP
    Chothia, C
    Murzin, AG
    [J]. NUCLEIC ACIDS RESEARCH, 2004, 32 : D226 - D229
  • [3] [Anonymous], 1995, J MOL GRAPH
  • [4] [Anonymous], P 5 INT C MOL STRUCT
  • [5] pdbFun: mass selection and fast comparison of annotated PDB residues
    Ausiello, G
    Zanzoni, A
    Peluso, D
    Via, A
    Helmer-Citterich, M
    [J]. NUCLEIC ACIDS RESEARCH, 2005, 33 : W133 - W137
  • [6] Structural insights into protein-metal ion partnerships
    Barondeau, DP
    Getzoff, ED
    [J]. CURRENT OPINION IN STRUCTURAL BIOLOGY, 2004, 14 (06) : 765 - 774
  • [7] The Protein Data Bank
    Berman, HM
    Battistuz, T
    Bhat, TN
    Bluhm, WF
    Bourne, PE
    Burkhardt, K
    Iype, L
    Jain, S
    Fagan, P
    Marvin, J
    Padilla, D
    Ravichandran, V
    Schneider, B
    Thanki, N
    Weissig, H
    Westbrook, JD
    Zardecki, C
    [J]. ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 2002, 58 : 899 - 907
  • [8] Inferring functional relationships of proteins from local sequence and spatial surface patterns
    Binkowski, TA
    Adamian, L
    Liang, J
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2003, 332 (02) : 505 - 526
  • [9] The SWISS-PROT protein knowledgebase and its supplement TrEMBL in 2003
    Boeckmann, B
    Bairoch, A
    Apweiler, R
    Blatter, MC
    Estreicher, A
    Gasteiger, E
    Martin, MJ
    Michoud, K
    O'Donovan, C
    Phan, I
    Pilbout, S
    Schneider, M
    [J]. NUCLEIC ACIDS RESEARCH, 2003, 31 (01) : 365 - 370
  • [10] The Gene Ontology Annotation (GOA) Database: sharing knowledge in Uniprot with Gene Ontology
    Camon, E
    Magrane, M
    Barrell, D
    Lee, V
    Dimmer, E
    Maslen, J
    Binns, D
    Harte, N
    Lopez, R
    Apweiler, R
    [J]. NUCLEIC ACIDS RESEARCH, 2004, 32 : D262 - D266