Evidence map›Paper›PMID 33781198›Full record

ArticleBMC genomics2021

In silico analysis of bacterial translation factors reveal distinct translation event specific pI values.

Soma Jana, Partha P Datta

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Soma JanaDepartment of Biological Sciences, Indian Institute of Science Education and Research Kolkata, Mohanpur, WB, PIN 741246, India.
Partha P DattaDepartment of Biological Sciences, Indian Institute of Science Education and Research Kolkata, Mohanpur, WB, PIN 741246, India. partha_datta@iiserkol.ac.in.ORCID http://orcid.org/0000-0002-3478-2616
Indian Institute of Science Education and Research Kolkata · IN

Funding

Indian Institute of Science Education and Research Kolkata NA
6 · The paper itself

Abstract

backgroundProtein synthesis is a cellular process that takes place through the successive translation events within the ribosome by the event-specific protein factors, namely, initiation, elongation, release, and recycling factors. In this regard, we asked the question about how similar are those translation factors to each other from a wide variety of bacteria? Hence, we did a thorough in silico study of the translation factors from 495 bacterial sp., and 4262 amino acid sequences by theoretically measuring their pI and MW values that are two determining factors for distinguishing individual proteins in 2D gel electrophoresis in experimental procedures. Then we analyzed the output from various angles.

resultsOur study revealed the fact that it's not all same, or all random, but there are distinct orders and the pI values of translation factors are translation event specific. We found that the translation initiation factors are mainly basic, whereas, elongation and release factors that interact with the inter-subunit space of the intact 70S ribosome during translation are strictly acidic across bacterial sp. These acidic elongation factors and release factors contain higher frequencies of glutamic acids. However, among all the translation factors, the translation initiation factor 2 (IF2) and ribosome recycling factor (RRF) showed variable pI values that are linked to the order of phylogeny.

conclusionsFrom the results of our study, we conclude that among all the bacterial translation factors, elongation and release factors are more conserved in terms of their pI values in comparison to initiation and recycling factors. Acidic properties of these factors are independent of habitat, nature, and phylogeny of the bacterial species. Furthermore, irrespective of the different shapes, sizes, and functions of the elongation and release factors, possession of the strictly acidic pI values of these translation factors all over the domain Bacteria indicates that the acidic nature of these factors is a necessary criterion, perhaps to interact into the partially enclosed rRNA rich inter-subunit space of the translating 70S ribosome.

Indexed as

Escherichia coliRibosomal ProteinsBacteriaComputer SimulationRibosomesRNA, RibosomalRibosomal ProteinsRNA, RibosomalIsoelectric pointMolecular weightPhylogenyRibosomeTranslationTranslation factors

Identifiers

PMID33781198
PMCPMC8008671
OpenAlexW3141796834

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.