Current Journal Issue - Volume 19 Issue 9 (September 2010)
- Evaluation and ranking of enzyme designs
- Gert Kiss, Daniela Röthlisberger, David Baker, K. N. Houk
- Published in Wiley Online Library on Jul 27, 2010
- DOI: 10.1002/pro.462 (p 1760-1773)
Abstract In 2008, a successful computational design procedure was reported that yielded active enzyme catalysts for the Kemp elimination. Here, we studied these proteins together with a set of previously unpublished inactive designs to determine the sources of activity or lack thereof, and to predict which of the designed structures are most likely to be catalytic. Methods that range from quantum mechanics (QM) on truncated model...
- The interaction of ammonia and xenon with the imidazole glycerol phosphate synthase from Thermotoga maritima as detected by NMR spectroscopy
- Christoph Liebold, Felix List, Hans Robert Kalbitzer, Reinhard Sterner, Eike Brunner
- Published in Wiley Online Library on Jun 29, 2010
- DOI: 10.1002/pro.463 (p 1774-1782)
Abstract The imidazole glycerol phosphate (ImGP) synthase from the hyperthermophilic bacterium Thermotoga maritima is a 1:1 complex of the glutaminase subunit HisH and the cyclase subunit HisF. It has been proposed that ammonia generated by HisH is transported through a channel to the active site of HisF, which generates intermediates of histidine (ImGP) and de novo biosynthesis of 5‐aminoimidazole‐4‐carboxamideribotide. Solution NMR...
L ‐Arginine hydrochloride increases the solubility of folded and unfolded recombinant plasminogen activator rPA- Alexander Tischer, Hauke Lilie, Rainer Rudolph, Christian Lange
- Published in Wiley Online Library on Jul 27, 2010
- DOI: 10.1002/pro.465 (p 1783-1795)
Abstract L‐Arginine hydrochloride (L‐ArgHCl) was found to be an effective enhancer for in vitro protein refolding more than two decades ago. A detailed understanding of the mechanism of action, by which L‐ArgHCl as co‐solvent is capable to effectively suppress protein aggregation, while protein stability is preserved, has remained elusive. Concepts for the effects of co‐solvents, which have been established over the last decades, were found to be...
- The pyruvate kinase model system, a cautionary tale for the use of osmolyte perturbations to support conformational equilibria in allostery
- Aron W. Fenton, Troy A. Johnson, Todd Holyoak
- Published in Wiley Online Library on Jul 13, 2010
- DOI: 10.1002/pro.450 (p 1796-1800)
Abstract In the study of rabbit muscle pyruvate kinase (M1‐PYK), proline has previously been used as an osmolyte in an attempt to determine a role for preexisting conformational equilibria in allosteric regulation. In this context, osmolytes are small molecules assumed to have no direct interaction with the protein. In contrast to proline's proposed role as an osmolyte, the structure of M1PYK‐Mn‐pyruvate‐proline complex reported herein...
- Crystal structure of human thioredoxin revealing an unraveled helix and exposed S‐ nitrosation site
- Andrzej Weichsel, Michelle Kem, William R. Montfort
- Published in Wiley Online Library on Jul 26, 2010
- DOI: 10.1002/pro.455 (p 1801-1806)
Abstract Thioredoxins reduce disulfide bonds and other thiol modifications in all cells using a CXXC motif. Human thioredoxin 1 is unusual in that it codes for an additional three cysteines in its 105 amino acid sequence, each of which have been implicated in other reductive activities. Cys 62 and Cys 69 are buried in the protein interior and lie at either end of a short helix (helix 3), and yet can disulfide link under oxidizing...
- Structure of human thioredoxin exhibits a large conformational change
- Gareth Hall, Jonas Emsley
- Published in Wiley Online Library on Jul 26, 2010
- DOI: 10.1002/pro.466 (p 1807-1811)
Abstract Thioredoxin is an oxidoreductase, which is ubiquitously present across phyla from humans to plants and bacteria. Thioredoxin reduces a variety of substrates through active site Cys 32, which is subsequently oxidized to form the intramolecular disulphide with Cys 35. The thioredoxin fold is known to be highly stable and conformational changes in the active site loops and residues Cys 32, Cys 35 have been characterized...
- Crystal structure of Bacillus subtilis SPP1 phage gp23.1, a putative chaperone
- David Veesler, Stéphanie Blangy, Julie Lichière, Miguel Ortiz‐Lombardía, Paulo Tavares, Valérie Campanacci, Christian Cambillau
- Published in Wiley Online Library on Jul 27, 2010
- DOI: 10.1002/pro.464 (p 1812-1816)
Abstract SPP1 is a siphophage infecting the gram‐positive bacterium Bacillus subtilis. The SPP1 tail electron microscopy (EM) reconstruction revealed that it is mainly constituted by conserved structural proteins such as the major tail proteins (gp17.1), the tape measure protein (gp18), the Distal tail protein (Dit, gp19.1), and the Tail associated lysin (gp21). A group of five small genes (22–24.1) follows in the genome but it remains to be...




