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The organization of domains in proteins obeys Menzerath-Altmann’s law of language
BACKGROUND: The combination of domains in multidomain proteins enhances their function and structure but lengthens the molecules and increases their cost at cellular level. METHODS: The dependence of domain length on the number of domains a protein holds was surveyed for a set of 60 proteomes repres...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531524/ https://www.ncbi.nlm.nih.gov/pubmed/26260760 http://dx.doi.org/10.1186/s12918-015-0192-9 |
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author | Shahzad, Khuram Mittenthal, Jay E. Caetano-Anollés, Gustavo |
author_facet | Shahzad, Khuram Mittenthal, Jay E. Caetano-Anollés, Gustavo |
author_sort | Shahzad, Khuram |
collection | PubMed |
description | BACKGROUND: The combination of domains in multidomain proteins enhances their function and structure but lengthens the molecules and increases their cost at cellular level. METHODS: The dependence of domain length on the number of domains a protein holds was surveyed for a set of 60 proteomes representing free-living organisms from all kingdoms of life. Distributions were fitted using non-linear functions and fitted parameters interpreted with a formulation of decreasing returns. RESULTS: We find that domain length decreases with increasing number of domains in proteins, following the Menzerath-Altmann (MA) law of language. Highly significant negative correlations exist for the set of proteomes examined. Mathematically, the MA law expresses as a power law relationship that unfolds when molecular persistence P is a function of domain accretion. P holds two terms, one reflecting the matter-energy cost of adding domains and extending their length, the other reflecting how domain length and number impinges on information and biophysics. The pattern of diminishing returns can therefore be explained as a frustrated interplay between the strategies of economy, flexibility and robustness, matching previously observed trade-offs in the domain makeup of proteomes. Proteomes of Archaea, Fungi and to a lesser degree Plants show the largest push towards molecular economy, each at their own economic stratum. Fungi increase domain size in single domain proteins while reinforcing the pattern of diminishing returns. In contrast, Metazoa, and to lesser degrees Protista and Bacteria, relax economy. Metazoa achieves maximum flexibility and robustness by harboring compact molecules and complex domain organization, offering a new functional vocabulary for molecular biology. CONCLUSIONS: The tendency of parts to decrease their size when systems enlarge is universal for language and music, and now for parts of macromolecules, extending the MA law to natural systems. |
format | Online Article Text |
id | pubmed-4531524 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45315242015-08-12 The organization of domains in proteins obeys Menzerath-Altmann’s law of language Shahzad, Khuram Mittenthal, Jay E. Caetano-Anollés, Gustavo BMC Syst Biol Research Article BACKGROUND: The combination of domains in multidomain proteins enhances their function and structure but lengthens the molecules and increases their cost at cellular level. METHODS: The dependence of domain length on the number of domains a protein holds was surveyed for a set of 60 proteomes representing free-living organisms from all kingdoms of life. Distributions were fitted using non-linear functions and fitted parameters interpreted with a formulation of decreasing returns. RESULTS: We find that domain length decreases with increasing number of domains in proteins, following the Menzerath-Altmann (MA) law of language. Highly significant negative correlations exist for the set of proteomes examined. Mathematically, the MA law expresses as a power law relationship that unfolds when molecular persistence P is a function of domain accretion. P holds two terms, one reflecting the matter-energy cost of adding domains and extending their length, the other reflecting how domain length and number impinges on information and biophysics. The pattern of diminishing returns can therefore be explained as a frustrated interplay between the strategies of economy, flexibility and robustness, matching previously observed trade-offs in the domain makeup of proteomes. Proteomes of Archaea, Fungi and to a lesser degree Plants show the largest push towards molecular economy, each at their own economic stratum. Fungi increase domain size in single domain proteins while reinforcing the pattern of diminishing returns. In contrast, Metazoa, and to lesser degrees Protista and Bacteria, relax economy. Metazoa achieves maximum flexibility and robustness by harboring compact molecules and complex domain organization, offering a new functional vocabulary for molecular biology. CONCLUSIONS: The tendency of parts to decrease their size when systems enlarge is universal for language and music, and now for parts of macromolecules, extending the MA law to natural systems. BioMed Central 2015-08-11 /pmc/articles/PMC4531524/ /pubmed/26260760 http://dx.doi.org/10.1186/s12918-015-0192-9 Text en © Shahzad et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Shahzad, Khuram Mittenthal, Jay E. Caetano-Anollés, Gustavo The organization of domains in proteins obeys Menzerath-Altmann’s law of language |
title | The organization of domains in proteins obeys Menzerath-Altmann’s law of language |
title_full | The organization of domains in proteins obeys Menzerath-Altmann’s law of language |
title_fullStr | The organization of domains in proteins obeys Menzerath-Altmann’s law of language |
title_full_unstemmed | The organization of domains in proteins obeys Menzerath-Altmann’s law of language |
title_short | The organization of domains in proteins obeys Menzerath-Altmann’s law of language |
title_sort | organization of domains in proteins obeys menzerath-altmann’s law of language |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4531524/ https://www.ncbi.nlm.nih.gov/pubmed/26260760 http://dx.doi.org/10.1186/s12918-015-0192-9 |
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