Journal Issue - Volume 18 Issue 4 (April 2009)
In This Issue
- Published in Wiley Interscience on Mar 25, 2009
- DOI: 10.1002/pro.99 (p n/a-n/a)
Interactive graphics return to protein science
- Arthur G. Palmer, Brian W. Matthews
- Published in Wiley Interscience on Mar 25, 2009
- DOI: 10.1002/pro.103 (p 677-677)
Domain swapping in the kinase superfamily: OSR1 joins the mix
- Ying Li, Arthur G. Palmer
- Published in Wiley Interscience on Mar 20, 2009
- DOI: 10.1002/pro.98 (p 678-681)
In memoriam: Reflections on Fred Richards (1925–2009)
- Robert L. Baldwin
- Published in Wiley Interscience on Feb 12, 2009
- DOI: 10.1002/pro.81 (p 682-685)
A novel topology for representing protein folds
- Mark R. Segal
- Published in Wiley Interscience on Feb 18, 2009
- DOI: 10.1002/pro.90 (p 686-693)
Abstract Various topologies for representing 3D protein structures have been advanced for purposes ranging from prediction of folding rates to ab initio structure prediction. Examples include relative contact order, Delaunay tessellations, and backbone torsion angle distributions. Here, we introduce a new topology based on a novel means for operationalizing 3D proximities with respect to the underlying chain. The measure involves...
Aegerolysins: Structure, function, and putative biological role
- Sabina Berne, Ljerka Lah, Kristina Sepčić
- Published in Wiley Interscience on Feb 12, 2009
- DOI: 10.1002/pro.85 (p 694-706)
Abstract Aegerolysins, discovered in fungi, bacteria and plants, are highly similar proteins with interesting biological properties. Certain aegerolysins possess antitumoral, antiproliferative, and antibacterial activities. Further possible medicinal applications include their use in the prevention of atherosclerosis, or as vaccines. Additional biotechnological value of fungal aegerolysins lies in their involvement in development,...
Computational studies of H5N1 influenza virus resistance to oseltamivir
- Nick X. Wang, Jie J. Zheng
- Published in Wiley Interscience on Feb 10, 2009
- DOI: 10.1002/pro.77 (p 707-715)
Abstract Influenza A (H5N1) virus is one of the world's greatest pandemic threats. Neuraminidase (NA) inhibitors, oseltamivir and zanamivir, prevent the spread of influenza, but drug‐resistant viruses have reduced their effectiveness. Resistance depends on the binding properties of NA‐drug complexes. Key residue mutations within the active site of NA glycoproteins diminish binding, thereby resulting in drug resistance. We performed...
Structural characterization of unphosphorylated STAT5a oligomerization equilibrium in solution by small‐angle X‐ray scattering
- Pau Bernadó, Yolanda Pérez, Jascha Blobel, Juan Fernández‐Recio, Dmitri I. Svergun, Miquel Pons
- Published in Wiley Interscience on Feb 10, 2009
- DOI: 10.1002/pro.83 (p 716-726)
Abstract Signal transducer and activator of transcription (STAT) proteins play a crucial role in the activation of gene transcription in response to extracellular stimuli. The regulation and activity of these proteins require a complex rearrangement of the domains. According to the established models, based on crystallographic data, STATs convert from a basal antiparallel inactive dimer into a parallel active one following...
Engineering a G protein‐coupled receptor for structural studies: Stabilization of the BLT1 receptor ground state
- Aimée Martin, Marjorie Damian, Michel Laguerre, Joseph Parello, Bernard Pucci, Laurence Serre, Sophie Mary, Jacky Marie, Jean‐Louis Banères
- Published in Wiley Interscience on Jan 06, 2009
- DOI: 10.1002/pro.55 (p 727-734)
Abstract Structural characterization of membrane proteins is hampered by their instability in detergent solutions. We modified here a G protein‐coupled receptor, the BLT1 receptor of leukotriene B4, to stabilize it in vitro. For this, we introduced a metal‐binding site connecting the third and sixth transmembrane domains of the receptor. This modification was intended to restrain the activation‐associated relative movement of these helices that...
Δ98Δ, a minimalist model of antiparallel β‐sheet proteins based on intestinal fatty acid binding protein
- Lucrecia María Curto, Julio Javier Caramelo, Gisela Raquel Franchini, José María Delfino
- Published in Wiley Interscience on Jan 22, 2009
- DOI: 10.1002/pro.71 (p 735-746)
Abstract The design of β‐barrels has always been a formidable challenge for de novo protein design. For instance, a persistent problem is posed by the intrinsic tendency to associate given by free edges. From the opposite standpoint provided by the redesign of natural motifs, we believe that the intestinal fatty acid binding protein (IFABP) framework allows room for intervention, giving rise to abridged forms from which lessons on...
Structural and functional characterization of TRI3 trichothecene 15‐ Fusarium sporotrichioides
- Graeme S. Garvey, Susan P. McCormick, Nancy J. Alexander, Ivan Rayment
- Published in Wiley Interscience on Mar 16, 2009
- DOI: 10.1002/pro.80 (p 747-761)
Abstract Fusarium head blight is a devastating disease of cereal crops whose worldwide incidence is increasing and at present there is no satisfactory way of combating this pathogen or its associated toxins. There is a wide variety of trichothecene mycotoxins and they all contain a 12,13‐epoxytrichothecene skeleton but differ in their substitutions. Indeed, there is considerable variation in the toxin profile across the numerous...
Redesign of a protein–peptide interaction: Characterization and applications
- Meredith E. Jackrel, Roberto Valverde, Lynne Regan
- Published in Wiley Interscience on Feb 12, 2009
- DOI: 10.1002/pro.75 (p 762-774)
Abstract The design of protein–peptide interactions has a wide array of practical applications and also reveals insight into the basis for molecular recognition. Here, we present the redesign of a tetratricopeptide repeat (TPR) protein scaffold, along with its corresponding peptide ligand. We show that the binding properties of these protein–peptide pairs can be understood, quantitatively, using straightforward chemical...
Opposite allosteric mechanisms in TetR and CAP
- Jennifer E. Seedorff, Michael E. Rodgers, Robert Schleif
- Published in Wiley Interscience on Feb 10, 2009
- DOI: 10.1002/pro.88 (p 775-781)
Abstract Regulation of the DNA binding affinity of an oligomeric protein can be considered to consist of an intrinsic component, in which the affinity of an individual DNA‐binding domain is modulated in response to effector binding, and an extrinsic component, in which the relative position of the protein's two DNA‐binding domains are altered so that they can or cannot contact both half‐site operators simultaneously. We demonstrated...
Structure of dystrophia myotonica protein kinase
- Jonathan M. Elkins, Ann Amos, Frank H. Niesen, Ashley C.W. Pike, Oleg Fedorov, Stefan Knapp
- Published in Wiley Interscience on Feb 10, 2009
- DOI: 10.1002/pro.82 (p 782-791)
Abstract Dystrophia myotonica protein kinase (DMPK) is a serine/threonine kinase composed of a kinase domain and a coiled‐coil domain involved in the multimerization. The crystal structure of the kinase domain of DMPK bound to the inhibitor bisindolylmaleimide VIII (BIM‐8) revealed a dimeric enzyme associated by a conserved dimerization domain. The affinity of dimerisation suggested that the kinase domain alone is insufficient for...
9,10‐Anthraquinone hinders β‐aggregation: How does a small molecule interfere with Aβ‐peptide amyloid fibrillation?
- Marino Convertino, Riccardo Pellarin, Marco Catto, Angelo Carotti, Amedeo Caflisch
- Published in Wiley Interscience on Feb 10, 2009
- DOI: 10.1002/pro.87 (p 792-800)
Abstract Amyloid aggregation is linked to a number of neurodegenerative syndromes, the most prevalent one being Alzheimer's disease. In this pathology, the β‐amyloid peptides (Aβ) aggregate into oligomers, protofibrils, and fibrils and eventually into plaques, which constitute the characteristic hallmark of Alzheimer's disease. Several low‐molecular‐weight compounds able to impair the Aβ aggregation process have been recently...




