» Articles » PMID: 29383564

Large Scale Analyses and Visualization of Adaptive Amino Acid Changes Projects

Overview
Journal Interdiscip Sci
Specialty Biology
Date 2018 Feb 1
PMID 29383564
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

When changes at few amino acid sites are the target of selection, adaptive amino acid changes in protein sequences can be identified using maximum-likelihood methods based on models of codon substitution (such as codeml). Although such methods have been employed numerous times using a variety of different organisms, the time needed to collect the data and prepare the input files means that tens or hundreds of coding regions are usually analyzed. Nevertheless, the recent availability of flexible and easy to use computer applications that collect relevant data (such as BDBM) and infer positively selected amino acid sites (such as ADOPS), means that the entire process is easier and quicker than before. However, the lack of a batch option in ADOPS, here reported, still precludes the analysis of hundreds or thousands of sequence files. Given the interest and possibility of running such large-scale projects, we have also developed a database where ADOPS projects can be stored. Therefore, this study also presents the B+ database, which is both a data repository and a convenient interface that looks at the information contained in ADOPS projects without the need to download and unzip the corresponding ADOPS project file. The ADOPS projects available at B+ can also be downloaded, unzipped, and opened using the ADOPS graphical interface. The availability of such a database ensures results repeatability, promotes data reuse with significant savings on the time needed for preparing datasets, and effortlessly allows further exploration of the data contained in ADOPS projects.

Citing Articles

The Josephin domain (JD) containing proteins are predicted to bind to the same interactors: Implications for spinocerebellar ataxia type 3 (SCA3) studies using mutants.

Sousa E Silva R, Sousa A, Vieira J, Vieira C Front Mol Neurosci. 2023; 16:1140719.

PMID: 37008788 PMC: 10050893. DOI: 10.3389/fnmol.2023.1140719.


The evolution of vitamin C biosynthesis and transport in animals.

Duque P, Vieira C, Bastos B, Vieira J BMC Ecol Evol. 2022; 22(1):84.

PMID: 35752765 PMC: 9233358. DOI: 10.1186/s12862-022-02040-7.


The identification of the Rosa S-locus and implications on the evolution of the Rosaceae gametophytic self-incompatibility systems.

Vieira J, Pimenta J, Gomes A, Laia J, Rocha S, Heitzler P Sci Rep. 2021; 11(1):3710.

PMID: 33580108 PMC: 7881130. DOI: 10.1038/s41598-021-83243-8.


Predicting Specificities Under the Non-self Gametophytic Self-Incompatibility Recognition Model.

Vieira J, Rocha S, Vazquez N, Lopez-Fernandez H, Fdez-Riverola F, Reboiro-Jato M Front Plant Sci. 2019; 10:879.

PMID: 31379893 PMC: 6649718. DOI: 10.3389/fpls.2019.00879.

References
1.
Khan M, Ryden A, Chowdhury M, Hasan M, Kazi J . Maximum likelihood analysis of mammalian p53 indicates the presence of positively selected sites and higher tumorigenic mutations in purifying sites. Gene. 2011; 483(1-2):29-35. DOI: 10.1016/j.gene.2011.05.011. View

2.
Yang W, Bielawski J, Yang Z . Widespread adaptive evolution in the human immunodeficiency virus type 1 genome. J Mol Evol. 2003; 57(2):212-21. DOI: 10.1007/s00239-003-2467-9. View

3.
Vieira J, Santos R, Ferreira S, Vieira C . Inferences on the number and frequency of S-pollen gene (SFB) specificities in the polyploid Prunus spinosa. Heredity (Edinb). 2008; 101(4):351-8. DOI: 10.1038/hdy.2008.60. View

4.
Zhang Y, Yu Z . The first evidence of positive selection in peptidoglycan recognition protein (PGRP) genes of Crassostrea gigas. Fish Shellfish Immunol. 2013; 34(5):1352-5. DOI: 10.1016/j.fsi.2013.01.018. View

5.
Jiggins F, Kim K . A screen for immunity genes evolving under positive selection in Drosophila. J Evol Biol. 2007; 20(3):965-70. DOI: 10.1111/j.1420-9101.2007.01305.x. View