1vhm Citations

Structural analysis of a set of proteins resulting from a bacterial genomics project.

Abstract

The targets of the Structural GenomiX (SGX) bacterial genomics project were proteins conserved in multiple prokaryotic organisms with no obvious sequence homolog in the Protein Data Bank of known structures. The outcome of this work was 80 structures, covering 60 unique sequences and 49 different genes. Experimental phase determination from proteins incorporating Se-Met was carried out for 45 structures with most of the remainder solved by molecular replacement using members of the experimentally phased set as search models. An automated tool was developed to deposit these structures in the Protein Data Bank, along with the associated X-ray diffraction data (including refined experimental phases) and experimentally confirmed sequences. BLAST comparisons of the SGX structures with structures that had appeared in the Protein Data Bank over the intervening 3.5 years since the SGX target list had been compiled identified homologs for 49 of the 60 unique sequences represented by the SGX structures. This result indicates that, for bacterial structures that are relatively easy to express, purify, and crystallize, the structural coverage of gene space is proceeding rapidly. More distant sequence-structure relationships between the SGX and PDB structures were investigated using PDB-BLAST and Combinatorial Extension (CE). Only one structure, SufD, has a truly unique topology compared to all folds in the PDB.

Articles - 1vhm mentioned but not cited (7)

  1. Free methionine-(R)-sulfoxide reductase from Escherichia coli reveals a new GAF domain function. Lin Z, Johnson LC, Weissbach H, Brot N, Lively MO, Lowther WT. Proc Natl Acad Sci U S A 104 9597-9602 (2007)
  2. Methionine sulfoxide reductases are essential for virulence of Salmonella typhimurium. Denkel LA, Horst SA, Rouf SF, Kitowski V, Böhm OM, Rhen M, Jäger T, Bange FC. PLoS One 6 e26974 (2011)
  3. Structural and biochemical characterization of free methionine-R-sulfoxide reductase from Neisseria meningitidis. Gruez A, Libiad M, Boschi-Muller S, Branlant G. J Biol Chem 285 25033-25043 (2010)
  4. Role of the VirA histidine autokinase of Agrobacterium tumefaciens in the initial steps of pathogenesis. Lin YH, Pierce BD, Fang F, Wise A, Binns AN, Lynn DG. Front Plant Sci 5 195 (2014)
  5. The structure and interactions of SpoIISA and SpoIISB, a toxin-antitoxin system in Bacillus subtilis. Florek P, Levdikov VM, Blagova E, Lebedev AA, Škrabana R, Resetárová S, Pavelcíková P, Barak I, Wilkinson AJ. J Biol Chem 286 6808-6819 (2011)
  6. Structural and kinetic analysis of free methionine-R-sulfoxide reductase from Staphylococcus aureus: conformational changes during catalysis and implications for the catalytic and inhibitory mechanisms. Bong SM, Kwak GH, Moon JH, Lee KS, Kim HS, Kim HY, Chi YM. J Biol Chem 285 25044-25052 (2010)
  7. Crystallization and preliminary X-ray crystallographic analysis of free methionine-(R)-sulfoxide reductase from Staphylococcus aureus. Bong SM, Moon JH, Kim HY, Kim HS, Chi YM, Kim AY. Acta Crystallogr Sect F Struct Biol Cryst Commun 65 1120-1122 (2009)


Reviews citing this publication (23)

  1. Regulation of fatty acid metabolism in bacteria. Fujita Y, Matsuoka H, Hirooka K. Mol Microbiol 66 829-839 (2007)
  2. Fe-S cluster assembly pathways in bacteria. Ayala-Castro C, Saini A, Outten FW. Microbiol Mol Biol Rev 72 110-25, table of contents (2008)
  3. Mechanistic aspects of carotenoid biosynthesis. Moise AR, Al-Babili S, Wurtzel ET. Chem Rev 114 164-193 (2014)
  4. The methionine sulfoxide reductases: Catalysis and substrate specificities. Boschi-Muller S, Gand A, Branlant G. Arch Biochem Biophys 474 266-273 (2008)
  5. Beta arcades: recurring motifs in naturally occurring and disease-related amyloid fibrils. Kajava AV, Baxa U, Steven AC. FASEB J 24 1311-1319 (2010)
  6. FtsZ ring stability: of bundles, tubules, crosslinks, and curves. Huang KH, Durand-Heredia J, Janakiraman A. J Bacteriol 195 1859-1868 (2013)
  7. Looking into laminin receptor: critical discussion regarding the non-integrin 37/67-kDa laminin receptor/RPSA protein. DiGiacomo V, Meruelo D. Biol Rev Camb Philos Soc 91 288-310 (2016)
  8. The renaissance of bacillosamine and its derivatives: pathway characterization and implications in pathogenicity. Morrison MJ, Imperiali B. Biochemistry 53 624-638 (2014)
  9. Laccases of prokaryotic origin: enzymes at the interface of protein science and protein technology. Martins LO, Durão P, Brissos V, Lindley PF. Cell Mol Life Sci 72 911-922 (2015)
  10. Active site comparisons and catalytic mechanisms of the hot dog superfamily. Labonte JW, Townsend CA. Chem Rev 113 2182-2204 (2013)
  11. Lysine biosynthesis in bacteria: a metallodesuccinylase as a potential antimicrobial target. Gillner DM, Becker DP, Holz RC. J Biol Inorg Chem 18 155-163 (2013)
  12. Fe-S cluster biogenesis by the bacterial Suf pathway. Blahut M, Sanchez E, Fisher CE, Outten FW. Biochim Biophys Acta Mol Cell Res 1867 118829 (2020)
  13. Prokaryote-derived protein inhibitors of peptidases: A sketchy occurrence and mostly unknown function. Kantyka T, Rawlings ND, Potempa J. Biochimie 92 1644-1656 (2010)
  14. Iron-sulfur clusters biogenesis by the SUF machinery: close to the molecular mechanism understanding. Pérard J, Ollagnier de Choudens S. J Biol Inorg Chem 23 581-596 (2018)
  15. Conservation of the 2-keto-3-deoxymanno-octulosonic acid (Kdo) biosynthesis pathway between plants and bacteria. Smyth KM, Marchant A. Carbohydr Res 380 70-75 (2013)
  16. Structural Biology and the Design of New Therapeutics: From HIV and Cancer to Mycobacterial Infections: A Paper Dedicated to John Kendrew. Thomas SE, Mendes V, Kim SY, Malhotra S, Ochoa-Montaño B, Blaszczyk M, Blundell TL. J Mol Biol 429 2677-2693 (2017)
  17. Iron-sulphur cluster biogenesis via the SUF pathway. Bai Y, Chen T, Happe T, Lu Y, Sawyer A. Metallomics 10 1038-1052 (2018)
  18. Structure-guided identification of a laminin binding site on the laminin receptor precursor. Jamieson KV, Hubbard SR, Meruelo D. J Mol Biol 405 24-32 (2011)
  19. Structure and function of Mycobacterium tuberculosis meso-diaminopimelic acid (DAP) biosynthetic enzymes. Usha V, Lloyd AJ, Lovering AL, Besra GS. FEMS Microbiol Lett 330 10-16 (2012)
  20. Novel genetic techniques and approaches in the microbial genomics era: identification and/or validation of targets for the discovery of new antibacterial agents. Pucci MJ. Drugs R D 8 201-212 (2007)
  21. New Insight into Isoprenoids Biosynthesis Process and Future Prospects for Drug Designing in Plasmodium. Saggu GS, Pala ZR, Garg S, Saxena V. Front Microbiol 7 1421 (2016)
  22. Strained Conformations of Nucleosides in Active Sites of Nucleoside Phosphorylases. Il'icheva IA, Polyakov KM, Mikhailov SN. Biomolecules 10 E552 (2020)
  23. Interfacial Enzymes Enable Gram-Positive Microbes to Eat Fatty Acids. Radka CD. Membranes (Basel) 13 423 (2023)

Articles citing this publication (125)