Evolutionary and Functional Relationships in the Truncated Hemoglobin Family.

Predicting function from sequence is an important goal in current biological research, and although, broad functional assignment is possible when a protein is assigned to a family, predicting functional specificity with accuracy is not straightforward. If function is provided by key structural prope...

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Main Authors: Juan P Bustamante, Leandro Radusky, Leonardo Boechi, Darío A Estrin, Arjen Ten Have, Marcelo A Martí
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1004701
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spelling doaj-9c3063aefec5462aa27f667a2d235e862021-04-21T15:09:10ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582016-01-01121e100470110.1371/journal.pcbi.1004701Evolutionary and Functional Relationships in the Truncated Hemoglobin Family.Juan P BustamanteLeandro RaduskyLeonardo BoechiDarío A EstrinArjen Ten HaveMarcelo A MartíPredicting function from sequence is an important goal in current biological research, and although, broad functional assignment is possible when a protein is assigned to a family, predicting functional specificity with accuracy is not straightforward. If function is provided by key structural properties and the relevant properties can be computed using the sequence as the starting point, it should in principle be possible to predict function in detail. The truncated hemoglobin family presents an interesting benchmark study due to their ubiquity, sequence diversity in the context of a conserved fold and the number of characterized members. Their functions are tightly related to O2 affinity and reactivity, as determined by the association and dissociation rate constants, both of which can be predicted and analyzed using in-silico based tools. In the present work we have applied a strategy, which combines homology modeling with molecular based energy calculations, to predict and analyze function of all known truncated hemoglobins in an evolutionary context. Our results show that truncated hemoglobins present conserved family features, but that its structure is flexible enough to allow the switch from high to low affinity in a few evolutionary steps. Most proteins display moderate to high oxygen affinities and multiple ligand migration paths, which, besides some minor trends, show heterogeneous distributions throughout the phylogenetic tree, again suggesting fast functional adaptation. Our data not only deepens our comprehension of the structural basis governing ligand affinity, but they also highlight some interesting functional evolutionary trends.https://doi.org/10.1371/journal.pcbi.1004701
collection DOAJ
language English
format Article
sources DOAJ
author Juan P Bustamante
Leandro Radusky
Leonardo Boechi
Darío A Estrin
Arjen Ten Have
Marcelo A Martí
spellingShingle Juan P Bustamante
Leandro Radusky
Leonardo Boechi
Darío A Estrin
Arjen Ten Have
Marcelo A Martí
Evolutionary and Functional Relationships in the Truncated Hemoglobin Family.
PLoS Computational Biology
author_facet Juan P Bustamante
Leandro Radusky
Leonardo Boechi
Darío A Estrin
Arjen Ten Have
Marcelo A Martí
author_sort Juan P Bustamante
title Evolutionary and Functional Relationships in the Truncated Hemoglobin Family.
title_short Evolutionary and Functional Relationships in the Truncated Hemoglobin Family.
title_full Evolutionary and Functional Relationships in the Truncated Hemoglobin Family.
title_fullStr Evolutionary and Functional Relationships in the Truncated Hemoglobin Family.
title_full_unstemmed Evolutionary and Functional Relationships in the Truncated Hemoglobin Family.
title_sort evolutionary and functional relationships in the truncated hemoglobin family.
publisher Public Library of Science (PLoS)
series PLoS Computational Biology
issn 1553-734X
1553-7358
publishDate 2016-01-01
description Predicting function from sequence is an important goal in current biological research, and although, broad functional assignment is possible when a protein is assigned to a family, predicting functional specificity with accuracy is not straightforward. If function is provided by key structural properties and the relevant properties can be computed using the sequence as the starting point, it should in principle be possible to predict function in detail. The truncated hemoglobin family presents an interesting benchmark study due to their ubiquity, sequence diversity in the context of a conserved fold and the number of characterized members. Their functions are tightly related to O2 affinity and reactivity, as determined by the association and dissociation rate constants, both of which can be predicted and analyzed using in-silico based tools. In the present work we have applied a strategy, which combines homology modeling with molecular based energy calculations, to predict and analyze function of all known truncated hemoglobins in an evolutionary context. Our results show that truncated hemoglobins present conserved family features, but that its structure is flexible enough to allow the switch from high to low affinity in a few evolutionary steps. Most proteins display moderate to high oxygen affinities and multiple ligand migration paths, which, besides some minor trends, show heterogeneous distributions throughout the phylogenetic tree, again suggesting fast functional adaptation. Our data not only deepens our comprehension of the structural basis governing ligand affinity, but they also highlight some interesting functional evolutionary trends.
url https://doi.org/10.1371/journal.pcbi.1004701
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