Literature DB >> 14999012

Het-PDB Navi.: a database for protein-small molecule interactions.

Akihiro Yamaguchi1, Kei Iida, Nobuaki Matsui, Shirou Tomoda, Kei Yura, Mitiko Go.   

Abstract

The genomes of more than 100 species have been sequenced, and the biological functions of encoded proteins are now actively being researched. Protein function is based on interactions between proteins and other molecules. One approach to assuming protein function based on genomic sequence is to predict interactions between an encoded protein and other molecules. As a data source for such predictions, knowledge regarding known protein-small molecule interactions needs to be compiled. We have, therefore, surveyed interactions between proteins and other molecules in Protein Data Bank (PDB), the protein three-dimensional (3D) structure database. Among 20,685 entries in PDB (April, 2003), 4,189 types of small molecules were found to interact with proteins. Biologically relevant small molecules most often found in PDB were metal ions, such as calcium, zinc, and magnesium. Sugars and nucleotides were the next most common. These molecules are known to act as cofactors for enzymes and/or stabilizers of proteins. In each case of interactions between a protein and small molecule, we found preferred amino acid residues at the interaction sites. These preferences can be the basis for predicting protein function from genomic sequence and protein 3D structures. The data pertaining to these small molecules were collected in a database named Het-PDB Navi., which is freely available at http://daisy.nagahama-i-bio.ac.jp/golab/hetpdbnavi.html and linked to the official PDB home page.

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Year:  2004        PMID: 14999012     DOI: 10.1093/jb/mvh009

Source DB:  PubMed          Journal:  J Biochem        ISSN: 0021-924X            Impact factor:   3.387


  13 in total

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3.  HemeBIND: a novel method for heme binding residue prediction by combining structural and sequence information.

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4.  Domain-based small molecule binding site annotation.

Authors:  Kevin A Snyder; Howard J Feldman; Michel Dumontier; John J Salama; Christopher W V Hogue
Journal:  BMC Bioinformatics       Date:  2006-03-17       Impact factor: 3.169

5.  Binding MOAD, a high-quality protein-ligand database.

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6.  Structural and functional analyses of Barth syndrome-causing mutations and alternative splicing in the tafazzin acyltransferase domain.

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7.  Distinct Conformation of ATP Molecule in Solution and on Protein.

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Journal:  Biophysics (Nagoya-shi)       Date:  2013-01-18

8.  GIANT: pattern analysis of molecular interactions in 3D structures of protein-small ligand complexes.

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Journal:  BMC Bioinformatics       Date:  2014-01-14       Impact factor: 3.169

9.  AS-ALPS: a database for analyzing the effects of alternative splicing on protein structure, interaction and network in human and mouse.

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10.  Glycoconjugate Data Bank: Structures--an annotated glycan structure database and N-glycan primary structure verification service.

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