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Nucleotide binding database NBDB – a collection of sequence motifs with specific protein-ligand interactions
NBDB database describes protein motifs, elementary functional loops (EFLs) that are involved in binding of nucleotide-containing ligands and other biologically relevant cofactors/coenzymes, including ATP, AMP, ATP, GMP, GDP, GTP, CTP, PAP, PPS, FMN, FAD(H), NAD(H), NADP, cAMP, cGMP, c-di-AMP and c-d...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4702817/ https://www.ncbi.nlm.nih.gov/pubmed/26507856 http://dx.doi.org/10.1093/nar/gkv1124 |
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author | Zheng, Zejun Goncearenco, Alexander Berezovsky, Igor N. |
author_facet | Zheng, Zejun Goncearenco, Alexander Berezovsky, Igor N. |
author_sort | Zheng, Zejun |
collection | PubMed |
description | NBDB database describes protein motifs, elementary functional loops (EFLs) that are involved in binding of nucleotide-containing ligands and other biologically relevant cofactors/coenzymes, including ATP, AMP, ATP, GMP, GDP, GTP, CTP, PAP, PPS, FMN, FAD(H), NAD(H), NADP, cAMP, cGMP, c-di-AMP and c-di-GMP, ThPP, THD, F-420, ACO, CoA, PLP and SAM. The database is freely available online at http://nbdb.bii.a-star.edu.sg. In total, NBDB contains data on 249 motifs that work in interactions with 24 ligands. Sequence profiles of EFL motifs were derived de novo from nonredundant Uniprot proteome sequences. Conserved amino acid residues in the profiles interact specifically with distinct chemical parts of nucleotide-containing ligands, such as nitrogenous bases, phosphate groups, ribose, nicotinamide, and flavin moieties. Each EFL profile in the database is characterized by a pattern of corresponding ligand–protein interactions found in crystallized ligand–protein complexes. NBDB database helps to explore the determinants of nucleotide and cofactor binding in different protein folds and families. NBDB can also detect fragments that match to profiles of particular EFLs in the protein sequence provided by user. Comprehensive information on sequence, structures, and interactions of EFLs with ligands provides a foundation for experimental and computational efforts on design of required protein functions. |
format | Online Article Text |
id | pubmed-4702817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-47028172016-01-07 Nucleotide binding database NBDB – a collection of sequence motifs with specific protein-ligand interactions Zheng, Zejun Goncearenco, Alexander Berezovsky, Igor N. Nucleic Acids Res Database Issue NBDB database describes protein motifs, elementary functional loops (EFLs) that are involved in binding of nucleotide-containing ligands and other biologically relevant cofactors/coenzymes, including ATP, AMP, ATP, GMP, GDP, GTP, CTP, PAP, PPS, FMN, FAD(H), NAD(H), NADP, cAMP, cGMP, c-di-AMP and c-di-GMP, ThPP, THD, F-420, ACO, CoA, PLP and SAM. The database is freely available online at http://nbdb.bii.a-star.edu.sg. In total, NBDB contains data on 249 motifs that work in interactions with 24 ligands. Sequence profiles of EFL motifs were derived de novo from nonredundant Uniprot proteome sequences. Conserved amino acid residues in the profiles interact specifically with distinct chemical parts of nucleotide-containing ligands, such as nitrogenous bases, phosphate groups, ribose, nicotinamide, and flavin moieties. Each EFL profile in the database is characterized by a pattern of corresponding ligand–protein interactions found in crystallized ligand–protein complexes. NBDB database helps to explore the determinants of nucleotide and cofactor binding in different protein folds and families. NBDB can also detect fragments that match to profiles of particular EFLs in the protein sequence provided by user. Comprehensive information on sequence, structures, and interactions of EFLs with ligands provides a foundation for experimental and computational efforts on design of required protein functions. Oxford University Press 2016-01-04 2015-10-26 /pmc/articles/PMC4702817/ /pubmed/26507856 http://dx.doi.org/10.1093/nar/gkv1124 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Database Issue Zheng, Zejun Goncearenco, Alexander Berezovsky, Igor N. Nucleotide binding database NBDB – a collection of sequence motifs with specific protein-ligand interactions |
title | Nucleotide binding database NBDB – a collection of sequence motifs with specific protein-ligand interactions |
title_full | Nucleotide binding database NBDB – a collection of sequence motifs with specific protein-ligand interactions |
title_fullStr | Nucleotide binding database NBDB – a collection of sequence motifs with specific protein-ligand interactions |
title_full_unstemmed | Nucleotide binding database NBDB – a collection of sequence motifs with specific protein-ligand interactions |
title_short | Nucleotide binding database NBDB – a collection of sequence motifs with specific protein-ligand interactions |
title_sort | nucleotide binding database nbdb – a collection of sequence motifs with specific protein-ligand interactions |
topic | Database Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4702817/ https://www.ncbi.nlm.nih.gov/pubmed/26507856 http://dx.doi.org/10.1093/nar/gkv1124 |
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