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1.
Acta Crystallogr D Biol Crystallogr ; 70(Pt 12): 3266-72, 2014 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-25478844

RESUMO

The 1.8 Šresolution neutron structure of deuterated type III antifreeze protein in which the methyl groups of leucine and valine residues are selectively protonated is presented. Comparison between this and the 1.85 Šresolution neutron structure of perdeuterated type III antifreeze protein indicates that perdeuteration improves the visibility of solvent molecules located in close vicinity to hydrophobic residues, as cancellation effects between H atoms of the methyl groups and nearby heavy-water molecules (D2O) are avoided.


Assuntos
Proteínas Anticongelantes Tipo III/química , Proteínas de Peixes/química , Difração de Nêutrons/métodos , Perciformes , Animais , Deutério/química , Modelos Moleculares , Perciformes/metabolismo , Prótons , Solventes/química , Água/química
2.
Protein Expr Purif ; 101: 42-53, 2014 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-24927643

RESUMO

This study investigated the structural and biophysical characteristics of GumB and GumC, two Xanthomonas campestris membrane proteins that are involved in xanthan biosynthesis. Xanthan is an exopolysaccharide that is thought to be a virulence factor that contributes to bacterial in planta growth. It also is one of the most important industrial biopolymers. The first steps of xanthan biosynthesis are well understood, but the polymerization and export mechanisms remain unclear. For this reason, the key proteins must be characterized to better understand these processes. Here we characterized, by biochemical and biophysical techniques, GumB, the outer membrane polysaccharide export protein, and GumC, the polysaccharide co-polymerase protein of the xanthan biosynthesis system. Our results suggested that recombinant GumB is a tetrameric protein in solution. On the other hand, we observed that both native and recombinant GumC present oligomeric conformation consistent with dimers and higher-order oligomers. The transmembrane segments of GumC are required for GumC expression and/or stability. These initial results provide a starting point for additional studies that will clarify the roles of GumB and GumC in the xanthan polymerization and export processes and further elucidate their functions and mechanisms of action.


Assuntos
Proteínas da Membrana Bacteriana Externa/genética , Proteínas de Bactérias/metabolismo , Proteínas de Transporte/genética , Proteínas de Membrana Transportadoras/metabolismo , Xanthomonas campestris/enzimologia , Sequência de Aminoácidos , Proteínas da Membrana Bacteriana Externa/análise , Proteínas da Membrana Bacteriana Externa/química , Proteínas de Bactérias/genética , Proteínas de Transporte/análise , Proteínas de Transporte/química , Proteínas de Membrana Transportadoras/genética , Polissacarídeos Bacterianos/biossíntese , Proteólise , Proteínas Recombinantes de Fusão/análise , Proteínas Recombinantes de Fusão/química , Proteínas Recombinantes de Fusão/genética , Xanthomonas campestris/genética , Xanthomonas campestris/metabolismo
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