Literature DB >> 18171028

At the periphery of the amidohydrolase superfamily: Bh0493 from Bacillus halodurans catalyzes the isomerization of D-galacturonate to D-tagaturonate.

Tinh T Nguyen1, Shoshana Brown, Alexander A Fedorov, Elena V Fedorov, Patricia C Babbitt, Steven C Almo, Frank M Raushel.   

Abstract

The amidohydrolase superfamily is a functionally diverse set of enzymes that catalyzes predominantly hydrolysis reactions involving sugars, nucleic acids, amino acids, and organophosphate esters. One of the most divergent members of this superfamily, uronate isomerase from Escherichia coli, catalyzes the isomerization of d-glucuronate to d-fructuronate and d-galacturonate to d-tagaturonate and is the only uronate isomerase in this organism. A gene encoding a putative uronate isomerase in Bacillus halodurans (Bh0705) was identified based on sequence similarity to uronate isomerases from other organisms. Kinetic evidence indicates that Bh0705 is relatively specific for the isomerization of d-glucuronate to d-fructuronate, confirming this functional assignment. Despite a low sequence identity to all other characterized uronate isomerases, phylogenetic and network-based analysis suggests that a second gene in this organism, Bh0493, is also a uronate isomerase, although it is an outlier in the group, with <20% sequence identity to any other characterized uronate isomerase from another species. The elucidation of the X-ray structure at a resolution of 2.0 A confirms that Bh0493 is a member of the amidohydrolase superfamily with conserved residues common to other members of the uronate isomerase family. Functional characterization of this protein shows that unlike Bh0705, Bh0493 can utilize both d-glucuronate and d-galacturonate as substrates. In B. halodurans, Bh0705 is found in an operon for the metabolism of d-glucuronate, whereas Bh0493 is in an operon for the metabolism of d-galacturonate. These results provide the first identification of a uronate isomerase that operates in a pathway distinct from that for d-glucuronate. While most organisms that contain this pathway have only one gene for a uronate isomerase, sequence analysis and operon context show that five other organisms also appear to have two genes and one organism appears to have three genes for this activity.

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Year:  2008        PMID: 18171028     DOI: 10.1021/bi7017738

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  18 in total

1.  Structure-based function discovery of an enzyme for the hydrolysis of phosphorylated sugar lactones.

Authors:  Dao Feng Xiang; Peter Kolb; Alexander A Fedorov; Chengfu Xu; Elena V Fedorov; Tamari Narindoshivili; Howard J Williams; Brian K Shoichet; Steven C Almo; Frank M Raushel
Journal:  Biochemistry       Date:  2012-02-15       Impact factor: 3.162

2.  Functional identification and structure determination of two novel prolidases from cog1228 in the amidohydrolase superfamily .

Authors:  Dao Feng Xiang; Yury Patskovsky; Chengfu Xu; Alexander A Fedorov; Elena V Fedorov; Abby A Sisco; J Michael Sauder; Stephen K Burley; Steven C Almo; Frank M Raushel
Journal:  Biochemistry       Date:  2010-08-10       Impact factor: 3.162

3.  Annotating enzymes of uncertain function: the deacylation of D-amino acids by members of the amidohydrolase superfamily.

Authors:  Jennifer A Cummings; Alexander A Fedorov; Chengfu Xu; Shoshana Brown; Elena Fedorov; Patricia C Babbitt; Steven C Almo; Frank M Raushel
Journal:  Biochemistry       Date:  2009-07-14       Impact factor: 3.162

4.  Target selection and annotation for the structural genomics of the amidohydrolase and enolase superfamilies.

Authors:  Ursula Pieper; Ranyee Chiang; Jennifer J Seffernick; Shoshana D Brown; Margaret E Glasner; Libusha Kelly; Narayanan Eswar; J Michael Sauder; Jeffrey B Bonanno; Subramanyam Swaminathan; Stephen K Burley; Xiaojing Zheng; Mark R Chance; Steven C Almo; John A Gerlt; Frank M Raushel; Matthew P Jacobson; Patricia C Babbitt; Andrej Sali
Journal:  J Struct Funct Genomics       Date:  2009-02-14

5.  Using sequence similarity networks for visualization of relationships across diverse protein superfamilies.

Authors:  Holly J Atkinson; John H Morris; Thomas E Ferrin; Patricia C Babbitt
Journal:  PLoS One       Date:  2009-02-03       Impact factor: 3.240

6.  Functional identification of incorrectly annotated prolidases from the amidohydrolase superfamily of enzymes.

Authors:  Dao Feng Xiang; Yury Patskovsky; Chengfu Xu; Amanda J Meyer; J Michael Sauder; Stephen K Burley; Steven C Almo; Frank M Raushel
Journal:  Biochemistry       Date:  2009-05-05       Impact factor: 3.162

7.  Functional annotation of two new carboxypeptidases from the amidohydrolase superfamily of enzymes.

Authors:  Dao Feng Xiang; Chengfu Xu; Desigan Kumaran; Ann C Brown; J Michael Sauder; Stephen K Burley; Subramanyam Swaminathan; Frank M Raushel
Journal:  Biochemistry       Date:  2009-06-02       Impact factor: 3.162

Review 8.  Exploiting structural classifications for function prediction: towards a domain grammar for protein function.

Authors:  Benoît H Dessailly; Oliver C Redfern; Alison Cuff; Christine A Orengo
Journal:  Curr Opin Struct Biol       Date:  2009-04-22       Impact factor: 6.809

9.  The mechanism of the reaction catalyzed by uronate isomerase illustrates how an isomerase may have evolved from a hydrolase within the amidohydrolase superfamily.

Authors:  Tinh T Nguyen; Alexander A Fedorov; Lakenya Williams; Elena V Fedorov; Yingchun Li; Chengfu Xu; Steven C Almo; Frank M Raushel
Journal:  Biochemistry       Date:  2009-09-22       Impact factor: 3.162

10.  Origin of saxitoxin biosynthetic genes in cyanobacteria.

Authors:  Ahmed Moustafa; Jeannette E Loram; Jeremiah D Hackett; Donald M Anderson; F Gerald Plumley; Debashish Bhattacharya
Journal:  PLoS One       Date:  2009-06-01       Impact factor: 3.240

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