Literature DB >> 24825023

Phylogenetic relationships and classification of thiolases and thiolase-like proteins of Mycobacterium tuberculosis and Mycobacterium smegmatis.

Padmanabhan Anbazhagan1, Rajesh K Harijan1, Tiila R Kiema1, Neelanjana Janardan2, M R N Murthy2, Paul A M Michels3, André H Juffer1, Rik K Wierenga4.   

Abstract

Thiolases are enzymes involved in lipid metabolism. Thiolases remove the acetyl-CoA moiety from 3-ketoacyl-CoAs in the degradative reaction. They can also catalyze the reverse Claisen condensation reaction, which is the first step of biosynthetic processes such as the biosynthesis of sterols and ketone bodies. In human, six distinct thiolases have been identified. Each of these thiolases is different from the other with respect to sequence, oligomeric state, substrate specificity and subcellular localization. Four sequence fingerprints, identifying catalytic loops of thiolases, have been described. In this study genome searches of two mycobacterial species (Mycobacterium tuberculosis and Mycobacterium smegmatis), were carried out, using the six human thiolase sequences as queries. Eight and thirteen different thiolase sequences were identified in M. tuberculosis and M. smegmatis, respectively. In addition, thiolase-like proteins (one encoded in the Mtb and two in the Msm genome) were found. The purpose of this study is to classify these mostly uncharacterized thiolases and thiolase-like proteins. Several other sequences obtained by searches of genome databases of bacteria, mammals and the parasitic protist family of the Trypanosomatidae were included in the analysis. Thiolase-like proteins were also found in the trypanosomatid genomes, but not in those of mammals. In order to study the phylogenetic relationships at a high confidence level, additional thiolase sequences were included such that a total of 130 thiolases and thiolase-like protein sequences were used for the multiple sequence alignment. The resulting phylogenetic tree identifies 12 classes of sequences, each possessing a characteristic set of sequence fingerprints for the catalytic loops. From this analysis it is now possible to assign the mycobacterial thiolases to corresponding homologues in other kingdoms of life. The results of this bioinformatics analysis also show interesting differences between the distributions of M. tuberculosis and M. smegmatis thiolases over the 12 different classes.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Classification; FadA; FadA5; Lipid metabolism; Mycobacterium; Phylogenetic analysis; Sequence fingerprint; Thiolase; Tuberculosis

Mesh:

Substances:

Year:  2014        PMID: 24825023     DOI: 10.1016/j.tube.2014.03.003

Source DB:  PubMed          Journal:  Tuberculosis (Edinb)        ISSN: 1472-9792            Impact factor:   3.131


  7 in total

1.  The steroid side-chain-cleaving aldolase Ltp2-ChsH2DUF35 is a thiolase superfamily member with a radically repurposed active site.

Authors:  Rebecca Aggett; Evan Mallette; Stephanie E Gilbert; Melody A Vachon; Kurt L Schroeter; Matthew S Kimber; Stephen Y K Seah
Journal:  J Biol Chem       Date:  2019-06-16       Impact factor: 5.157

2.  Identification of Six Thiolases and Their Effects on Fatty Acid and Ergosterol Biosynthesis in Aspergillus oryzae.

Authors:  Hui Huang; Yali Niu; Qi Jin; Kunhai Qin; Li Wang; Yitong Shang; Bin Zeng; Zhihong Hu
Journal:  Appl Environ Microbiol       Date:  2022-02-09       Impact factor: 5.005

3.  FadA5 a thiolase from Mycobacterium tuberculosis: a steroid-binding pocket reveals the potential for drug development against tuberculosis.

Authors:  Christin M Schaefer; Rui Lu; Natasha M Nesbitt; Johannes Schiebel; Nicole S Sampson; Caroline Kisker
Journal:  Structure       Date:  2014-12-04       Impact factor: 5.006

4.  Crystal structure of a thiolase from Escherichia coli at 1.8 Å resolution.

Authors:  M Ithayaraja; N Janardan; Rik K Wierenga; H S Savithri; M R N Murthy
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2016-06-22       Impact factor: 1.056

5.  Structural basis for differentiation between two classes of thiolase: Degradative vs biosynthetic thiolase.

Authors:  Sukritee Bhaskar; David L Steer; Ruchi Anand; Santosh Panjikar
Journal:  J Struct Biol X       Date:  2020-01-03

Review 6.  Mutation update on ACAT1 variants associated with mitochondrial acetoacetyl-CoA thiolase (T2) deficiency.

Authors:  Elsayed Abdelkreem; Rajesh K Harijan; Seiji Yamaguchi; Rikkert K Wierenga; Toshiyuki Fukao
Journal:  Hum Mutat       Date:  2019-07-03       Impact factor: 4.878

7.  Prophage-encoded gene VpaChn25_0734 amplifies ecological persistence of Vibrio parahaemolyticus CHN25.

Authors:  Yingwei Xu; Lianzhi Yang; Yaping Wang; Zhuoying Zhu; Jizhou Yan; Si Qin; Lanming Chen
Journal:  Curr Genet       Date:  2022-01-22       Impact factor: 3.886

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.