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81.
82.
Zhou YP Marlen K Palma JF Schweitzer A Reilly L Gregoire FM Xu GG Blume JE Johnson JD 《The Journal of biological chemistry》2003,278(51):51316-51323
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Quantification of the effects on viral DNA synthesis of reverse transcriptase mutations conferring human immunodeficiency virus type 1 resistance to nucleoside analogues 下载免费PDF全文
Bouchonnet F Dam E Mammano F de Soultrait V Henneré G Benech H Clavel F Hance AJ 《Journal of virology》2005,79(2):812-822
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Jacques Simard Rocio Sanchez Francine Durocher Eric Rhaume Carl Turgeon Yvan Labrie Van Luu-The Farida Mebarki Yves Morel Yvan de Launoit Fernand Labrie 《The Journal of steroid biochemistry and molecular biology》1995,55(5-6):489-505
The isoenzymes of the 3β-hydroxysteroid dehydrogenase/5-ene-4-ene-isomerase (3β-HSD) gene family catalyse the transformation of all 5-ene-3β-hydroxysteroids into the corresponding 4-ene-3-keto-steroids and are responsible for the interconversion of 3β-hydroxy- and 3-keto-5-androstane steroids. The two human 3β-HSD genes and the three related pseudogenes are located on the chromosome 1p13.1 region, close to the centromeric marker D1Z5. The 3β-HSD isoenzymes prefer NAD+ to NADP+ as cofactor with the exception of the rat liver type III and mouse kidney type IV, which both prefer NADPH as cofactor for their specific 3-ketosteroid reductase activity due to the presence of Tyr36 in the rat type III and of Phe36 in mouse type IV enzymes instead of Asp36 found in other 3β-HSD isoenzymes. The rat types I and IV, bovine and guinea pig 3β-HSD proteins possess an intrinsic 17β-HSD activity psecific to 5-androstane 17β-ol steroids, thus suggesting that such “secondary” activity is specifically responsible for controlling the bioavailability of the active androgen DHT. To elucidate the molecular basis of classical form of 3β-HSD deficiency, the structures of the types I and II 3β-HSD genes in 12 male pseudohermaphrodite 3β-HSD deficient patients as well as in four female patients were analyzed. The 14 different point mutations characterized were all detected in the type II 3β-HSD gene, which is the gene predominantly expressed in the adrenals and gonads, while no mutation was detected in the type I 3β-HSD gene predominantly expressed in the placenta and peripheral tissues. The mutant type II 3β-HSD enzymes carrying mutations detected in patients affected by the salt-losing form exhibit no detectable activity in intact transfected cells, at the exception of L108W and P186L proteins, which have some residual activity (1%). Mutations found in nonsalt-loser patients have some residual activity ranging from 1 to 10% compared to the wild-type enzyme. Characterization of mutant proteins provides unique information on the structure-function relationships of the 3β-HSD superfamily. 相似文献
86.
Seven biochemical groups were found among strains previously labeledSerratia liquefaciens (groups C1ab, C1c, C1d, EB, RB, RQ, and Adc). Comparison of biochemical data with DNA relatedness data allowed the definition (or redefinition) of threeSerratia species:Serratia liquefaciens sensu stricto (group C1ab),Serratia proteamaculans (groups C1c, EB, RB, and RQ), andSerratia grimesii sp. nov. (groups C1d and Adc). Biochemical group RQ, which is genomically related toS. proteamaculans at the borderline of species level, is proposed as a new subspecies ofS. proteamaculans (Serratia proteamaculans subsp.quinovora). Group Adc (3 strains) is also ambiguously related toS. grimesii, but no other proposal is made pending additional studies. The type strains of the newly named taxa,S. grimesii andS. proteamaculans subsp.quinovora, are respectively ATCC 14460 and strain 4364 (= CIP 8195 = ATCC 33765). 相似文献
87.
Lectin receptor kinases participate in protein-protein interactions to mediate plasma membrane-cell wall adhesions in Arabidopsis 下载免费PDF全文
Gouget A Senchou V Govers F Sanson A Barre A Rougé P Pont-Lezica R Canut H 《Plant physiology》2006,140(1):81-90
Interactions between plant cell walls and plasma membranes are essential for cells to function properly, but the molecules that mediate the structural continuity between wall and membrane are unknown. Some of these interactions, which are visualized upon tissue plasmolysis in Arabidopsis (Arabidopsis thaliana), are disrupted by the RGD (arginine-glycine-aspartic acid) tripeptide sequence, a characteristic cell adhesion motif in mammals. In planta induced-O (IPI-O) is an RGD-containing protein from the plant pathogen Phytophthora infestans that can disrupt cell wall-plasma membrane adhesions through its RGD motif. To identify peptide sequences that specifically bind the RGD motif of the IPI-O protein and potentially play a role in receptor recognition, we screened a heptamer peptide library displayed in a filamentous phage and selected two peptides acting as inhibitors of the plasma membrane RGD-binding activity of Arabidopsis. Moreover, the two peptides also disrupted cell wall-plasma membrane adhesions. Sequence comparison of the RGD-binding peptides with the Arabidopsis proteome revealed 12 proteins containing amino acid sequences in their extracellular domains common with the two RGD-binding peptides. Eight belong to the receptor-like kinase family, four of which have a lectin-like extracellular domain. The lectin domain of one of these, At5g60300, recognized the RGD motif both in peptides and proteins. These results imply that lectin receptor kinases are involved in protein-protein interactions with RGD-containing proteins as potential ligands, and play a structural and signaling role at the plant cell surfaces. 相似文献
88.
Francine Z Marques Simon PR Romaine Matthew Denniff James Eales John Dormer Ingrid M Garrelds Lukasz Wojnar Katarzyna Musialik Barbara Duda-Raszewska Bartlomiej Kiszka Magdalena Duda Brian J Morris Nilesh J Samani AH Jan Danser Pawel Bogdanski Ewa Zukowska-Szczechowska Fadi J Charchar Maciej Tomaszewski 《Molecular medicine (Cambridge, Mass.)》2015,21(1):739-748
MicroRNA-181a binds to the 3′ untranslated region of messenger RNA (mRNA) for renin, a rate-limiting enzyme of the renin-angiotensin system. Our objective was to determine whether this molecular interaction translates into a clinically meaningful effect on blood pressure and whether circulating miR-181a is a measurable proxy of blood pressure. In 200 human kidneys from the TRANScriptome of renaL humAn TissuE (TRANSLATE) study, renal miR-181a was the sole negative predictor of renin mRNA and a strong correlate of circulating miR-181a. Elevated miR-181a levels correlated positively with systolic and diastolic blood pressure in TRANSLATE, and this association was independent of circulating renin. The association between serum miR-181a and systolic blood pressure was replicated in 199 subjects from the Genetic Regulation of Arterial Pressure of Humans In the Community (GRAPHIC) study. Renal immunohistochemistry and in situ hybridization showed that colocalization of miR-181a and renin was most prominent in collecting ducts where renin is not released into the systemic circulation. Analysis of 69 human kidneys characterized by RNA sequencing revealed that miR-181a was associated with downregulation of four mitochondrial pathways and upregulation of 41 signaling cascades of adaptive immunity and inflammation. We conclude that renal miR-181a has pleiotropic effects on pathways relevant to blood pressure regulation and that circulating levels of miR-181a are both a measurable proxy of renal miR-181a expression and a novel biochemical correlate of blood pressure. 相似文献
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90.
Willy J. Malaisse Abdullah Sener Francine Malaisse-Lagae 《Molecular and cellular biochemistry》1981,37(3):157-165
Summary Nutrients which stimulate insulin secretion are currently thought to initiate the series of cellular events eventually leading
to insulin release either by interacting with a stereospecific receptor system (the regulatory site hypothesis) or by acting
as a fuel (the substrate site hypothesis) in the pancreaticB-cell. The latter hypothesis is supported by a number of observations indicating that the capacity of nutrients to stimulate
insulin release is indeed highly dependent on their capacity to increase catabolic fluxes in isolated pancreatic islets. However,
these observations do not rule out the existence of nutrient receptors in islet cells. For instance, a nonmetabolized analog
of L-leucine stimulates insulin release by causing allosteric activation of glutamate dehydrogenase, which should be considered,
therefore, as a receptor for certain amino acids. Likewise, the increase in glycolytic flux, which is associated with the
process of glucose-stimulated insulin release, is attributable not solely to a mass action phenomenon but also to the activation
of phosphofructokinase by fructose 2.6-bisphosphate. The biosynthesis of this activator may involve a glucose receptor system.
The fact that certain nutrient secretagogues (e.g D-glucose and L-leucine) act in the B-cell both as substrates and enzyme
activators permits reconciliation of the substrate site and regulatory site hypotheses for insulin release. 相似文献