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MALISAM: a database of structurally analogous motifs in proteins
MALISAM (manual alignments for structurally analogous motifs) represents the first database containing pairs of structural analogs and their alignments. To find reliable analogs, we developed an approach based on three ideas. First, an insertion together with a part of the evolutionary core of one d...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Oxford University Press
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2238938/ https://www.ncbi.nlm.nih.gov/pubmed/17855399 http://dx.doi.org/10.1093/nar/gkm698 |
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author | Cheng, Hua Kim, Bong-Hyun Grishin, Nick V. |
author_facet | Cheng, Hua Kim, Bong-Hyun Grishin, Nick V. |
author_sort | Cheng, Hua |
collection | PubMed |
description | MALISAM (manual alignments for structurally analogous motifs) represents the first database containing pairs of structural analogs and their alignments. To find reliable analogs, we developed an approach based on three ideas. First, an insertion together with a part of the evolutionary core of one domain family (a hybrid motif) is analogous to a similar motif contained within the core of another domain family. Second, a motif at an interface, formed by secondary structural elements (SSEs) contributed by two or more domains or subunits contacting along that interface, is analogous to a similar motif present in the core of a single domain. Third, an artificial protein obtained through selection from random peptides or in sequence design experiments not biased by sequences of a particular homologous family, is analogous to a structurally similar natural protein. Each analogous pair is superimposed and aligned manually, as well as by several commonly used programs. Applications of this database may range from protein evolution studies, e.g. development of remote homology inference tools and discriminators between homologs and analogs, to protein-folding research, since in the absence of evolutionary reasons, similarity between proteins is caused by structural and folding constraints. The database is publicly available at http://prodata.swmed.edu/malisam. |
format | Text |
id | pubmed-2238938 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22389382008-02-12 MALISAM: a database of structurally analogous motifs in proteins Cheng, Hua Kim, Bong-Hyun Grishin, Nick V. Nucleic Acids Res Articles MALISAM (manual alignments for structurally analogous motifs) represents the first database containing pairs of structural analogs and their alignments. To find reliable analogs, we developed an approach based on three ideas. First, an insertion together with a part of the evolutionary core of one domain family (a hybrid motif) is analogous to a similar motif contained within the core of another domain family. Second, a motif at an interface, formed by secondary structural elements (SSEs) contributed by two or more domains or subunits contacting along that interface, is analogous to a similar motif present in the core of a single domain. Third, an artificial protein obtained through selection from random peptides or in sequence design experiments not biased by sequences of a particular homologous family, is analogous to a structurally similar natural protein. Each analogous pair is superimposed and aligned manually, as well as by several commonly used programs. Applications of this database may range from protein evolution studies, e.g. development of remote homology inference tools and discriminators between homologs and analogs, to protein-folding research, since in the absence of evolutionary reasons, similarity between proteins is caused by structural and folding constraints. The database is publicly available at http://prodata.swmed.edu/malisam. Oxford University Press 2008-01 2007-09-12 /pmc/articles/PMC2238938/ /pubmed/17855399 http://dx.doi.org/10.1093/nar/gkm698 Text en © 2007 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Cheng, Hua Kim, Bong-Hyun Grishin, Nick V. MALISAM: a database of structurally analogous motifs in proteins |
title | MALISAM: a database of structurally analogous motifs in proteins |
title_full | MALISAM: a database of structurally analogous motifs in proteins |
title_fullStr | MALISAM: a database of structurally analogous motifs in proteins |
title_full_unstemmed | MALISAM: a database of structurally analogous motifs in proteins |
title_short | MALISAM: a database of structurally analogous motifs in proteins |
title_sort | malisam: a database of structurally analogous motifs in proteins |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2238938/ https://www.ncbi.nlm.nih.gov/pubmed/17855399 http://dx.doi.org/10.1093/nar/gkm698 |
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