Literature DB >> 31658388

Structural diversity in the Mycobacteria DUF3349 superfamily.

Garry W Buchko1,2,3, Jan Abendroth1,4, John I Robinson1,4, Isabelle Q Phan1,5, Peter J Myler1,5,6,7, Thomas E Edwards1,4.   

Abstract

A protein superfamily with a "Domain of Unknown Function,", DUF3349 (PF11829), is present predominately in Mycobacterium and Rhodococcus bacterial species suggesting that these proteins may have a biological function unique to these bacteria. We previously reported the inaugural structure of a DUF3349 superfamily member, n class="Species">Mycobacterium tuberculosis Rv0543c. Here, we report the structures determined for three additional DUF3349 proteins: Mycobacterium smegmatis MSMEG_1063 and MSMEG_1066 and Mycobacterium abscessus MAB_3403c. Like Rv0543c, the NMR solution structure of MSMEG_1063 revealed a monomeric five α-helix bundle with a similar overall topology. Conversely, the crystal structure of MSMEG_1066 revealed a five α-helix protein with a strikingly different topology and a tetrameric quaternary structure that was confirmed by size exclusion chromatography. The NMR solution structure of a fourth member of the DUF3349 superfamily, MAB_3403c, with 18 residues missing at the N-terminus, revealed a monomeric α-helical protein with a folding topology similar to the three C-terminal helices in the protomer of the MSMEG_1066 tetramer. These structures, together with a GREMLIN-based bioinformatics analysis of the DUF3349 primary amino acid sequences, suggest two subfamilies within the DUF3349 family. The division of the DUF3349 into two distinct subfamilies would have been lost if structure solution had stopped with the first structure in the DUF3349 family, highlighting the insights generated by solving multiple structures within a protein superfamily. Future studies will determine if the structural diversity at the tertiary and quaternary levels in the DUF3349 protein superfamily have functional roles in Mycobacteria and Rhodococcus species with potential implications for structure-based drug discovery.
© 2019 The Protein Society.

Entities:  

Keywords:  NMR spectrometry; circular dichroism; structural genomics; structure-based drug discovery; tuberculosis

Mesh:

Substances:

Year:  2019        PMID: 31658388      PMCID: PMC7020984          DOI: 10.1002/pro.3758

Source DB:  PubMed          Journal:  Protein Sci        ISSN: 0961-8368            Impact factor:   6.725


  53 in total

1.  Reduced-dimensionality NMR spectroscopy for high-throughput protein resonance assignment.

Authors:  Thomas Szyperski; Deok C Yeh; Dinesh K Sukumaran; Hunter N B Moseley; Gaetano T Montelione
Journal:  Proc Natl Acad Sci U S A       Date:  2002-06-11       Impact factor: 11.205

2.  Substructure solution with SHELXD.

Authors:  Thomas R Schneider; George M Sheldrick
Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2002-09-28

3.  Coot: model-building tools for molecular graphics.

Authors:  Paul Emsley; Kevin Cowtan
Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2004-11-26

4.  Using circular dichroism collected as a function of temperature to determine the thermodynamics of protein unfolding and binding interactions.

Authors:  Norma J Greenfield
Journal:  Nat Protoc       Date:  2006       Impact factor: 13.491

5.  Structural diversity in the Mycobacteria DUF3349 superfamily.

Authors:  Garry W Buchko; Jan Abendroth; John I Robinson; Isabelle Q Phan; Peter J Myler; Thomas E Edwards
Journal:  Protein Sci       Date:  2019-11-21       Impact factor: 6.725

6.  Cytosolic expression, solution structures, and molecular dynamics simulation of genetically encodable disulfide-rich de novo designed peptides.

Authors:  Garry W Buchko; Surya V S R K Pulavarti; Victor Ovchinnikov; Elizabeth A Shaw; Stephen A Rettie; Peter J Myler; Martin Karplus; Thomas Szyperski; David Baker; Christopher D Bahl
Journal:  Protein Sci       Date:  2018-09       Impact factor: 6.725

7.  High-resolution crystal structure of a hepatitis B virus replication inhibitor bound to the viral core protein.

Authors:  Klaus Klumpp; Angela M Lam; Christine Lukacs; Robert Vogel; Suping Ren; Christine Espiritu; Ruth Baydo; Kateri Atkins; Jan Abendroth; Guochun Liao; Andrey Efimov; George Hartman; Osvaldo A Flores
Journal:  Proc Natl Acad Sci U S A       Date:  2015-11-23       Impact factor: 11.205

8.  TALOS+: a hybrid method for predicting protein backbone torsion angles from NMR chemical shifts.

Authors:  Yang Shen; Frank Delaglio; Gabriel Cornilescu; Ad Bax
Journal:  J Biomol NMR       Date:  2009-06-23       Impact factor: 2.835

Review 9.  Molecular genetics of Mycobacterium tuberculosis pathogenesis.

Authors:  Josephine E Clark-Curtiss; Shelley E Haydel
Journal:  Annu Rev Microbiol       Date:  2003       Impact factor: 15.500

10.  Immobilized metal-affinity chromatography protein-recovery screening is predictive of crystallographic structure success.

Authors:  Ryan Choi; Angela Kelley; David Leibly; Stephen Nakazawa Hewitt; Alberto Napuli; Wesley Van Voorhis
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2011-08-13
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  1 in total

1.  Structural diversity in the Mycobacteria DUF3349 superfamily.

Authors:  Garry W Buchko; Jan Abendroth; John I Robinson; Isabelle Q Phan; Peter J Myler; Thomas E Edwards
Journal:  Protein Sci       Date:  2019-11-21       Impact factor: 6.725

  1 in total

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