310 research outputs found

    Ethyl 7-oxo-3,5-diphenyl-1,4-diazepane-2-carboxyl­ate

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    The title compound, C20H22N2O3, crystallizes with two independent mol­ecules in the asymmetric unit. In both mol­ecules, the diazepane rings adopt chair conformations. The mean planes of the diazepane rings in the two molecules form dihedral angles of 71.6 (4)/40.3 (5) and 75.9 (5)/58.6 (7)° with the neighbouring benzene rings. The carbonyl-group O atoms deviate significantly from the diazepane rings, by 0.685 (14) and 0.498 (13) Å. The eth­oxy­carbonyl groups show conformational difference between two mol­ecules, as reflected in the orientation of the carbonyl O atoms and the C—C—O—C torsion angle of −179.0 (2)° in one mol­ecule and 73.2 (2)° in the other. In one molecule there is a short N—H⋯O contact that generates an S(5) ring motif. In the crystal, N—H⋯O inter­actions generate R 2 2(8) graph-set motifs and C—H⋯O inter­actions generate R 2 2(10) and R 2 2(14) graph-set motifs. C—H⋯π inter­actions also occur

    Transactions in Relaxed Memory Architectures

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    The integration of transactions into hardware relaxed memory architectures is a topic of current research both in industry and academia. In this paper, we provide a general architectural framework for the introduction of transactions into models of relaxed memory in hardware, including the sc, tso, armv8 and ppc models. Our framework incorporates flexible and expressive forms of transaction aborts and execution that have hitherto been in the realm of software transactional memory. In contrast to software transactional memory, we account for the characteristics of relaxed memory as a restricted form of distributed system, without a notion of global time. We prove abstraction theorems to demonstrate that the programmer API matches the intuitions and expectations about transactions

    Chaperone-Mediated Protein Disaggregation Triggers Proteolytic Clearance of Intra-nuclear Protein Inclusions

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    The formation of insoluble inclusions in the cytosol and nucleus is associated with impaired protein homeostasis and is a hallmark of several neurodegenerative diseases. Due to the absence of the autophagic machinery, nuclear protein aggregates require a solubilization step preceding degradation by the 26S proteasome. Using yeast, we identify a nuclear protein quality control pathway required for the clearance of protein aggregates. The nuclear J-domain protein Apj1 supports protein disaggregation together with Hsp70 but independent of the canonical disaggregase Hsp104. Disaggregation mediated by Apj1/Hsp70 promotes turnover rather than refolding. A loss of Apj1 activity uncouples disaggregation from proteasomal turnover, resulting in accumulation of toxic soluble protein species. Endogenous substrates of the Apj1/Hsp70 pathway include both nuclear and cytoplasmic proteins, which aggregate inside the nucleus upon proteotoxic stress. These findings demonstrate the coordinated activity of the Apj1/Hsp70 disaggregation system with the 26S proteasome in facilitating the clearance of toxic inclusions inside the nucleus

    Diethyl [benzyl­amino­(1,3-diphenyl-1H-pyrazol-4-­yl)meth­yl]phospho­nate

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    In the title compound, C27H30N3O3P, the pyrazole ring is essentially planar [maximum deviation = 0.002 (2) Å] and it forms dihedral angles of 9.3 (1) and 40.2 (1)°, respectively, with the phenyl rings attached to the N and C atoms. In the crystal, pairs of centrosymmetrically related mol­ecules are linked into dimers by N—H⋯O hydrogen bonds

    Ethyl 2-(7-oxo-3,5-diphenyl-1,4-diaze­pan-2-yl)acetate

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    In the title compound, C21H24N2O3, the diazepane ring adopts a chair conformation. The central diazepane ring forms dihedral angles 67.80 (7) and 72.29 (5)° with the two benzene rings. The eth­oxy­carbonyl group is disordered over two conformations with site-occupancy factors of 0.643 (5) and 0.357 (5). In the crystal, inversion dimers linked by pairs of N—H⋯O hydrogen bonds generate R 2 2(8) loops

    Revealing genetic variation in mini core germplasm of urdbean (Vigna mungo (L.) Hepper)

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    A set of 47 urdbean genotypes including 12 promising varieties and 34 popular land races and a popular OUAT variety “Ujala” (standard check) were characterized for genetic variation based on molecular markers and morpho-economic traits. The molecular marker- based genotyping revealed a tremendous higher level of polymorphism (97.05%) with high average PIC (polymorphic information content) value (0.75). ISSR 1357 was considered highly informative that revealed the highest PIC (0.87) and marker index value (MI:5.25). An 840 bp allele (band) was characteristic to Kantapada local - A, Kendrapada local-D, and Nayagarh local - C. Such genotype- specific finger-printing may serve for reliable varietal characterization and elimination of duplicates. The test genotypes were grouped into six distinct clusters. TU 10-13, LBG 623, TAU 1, OBG 33, LBG 17 and PU 31 were highly divergent. PU 31 had inherent high yield potential (˃5.0q/ha) with known YMV resistance. The above divergent high yielding test genotypes may serve as candidate varieties for further genetic improvement using recombination breeding

    Revealing genetic variation in mini core germplasm of urdbean (Vigna mungo (L.) Hepper)

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    91-99A set of 47 urdbean genotypes including 12 promising varieties and 34 popular land races and a popular OUAT variety “Ujala” (standard check) were characterized for genetic variation based on molecular markers and morpho-economic traits. The molecular marker- based genotyping revealed a tremendous higher level of polymorphism (97.05%) with high average PIC (polymorphic information content) value (0.75). ISSR 1357 was considered highly informative that revealed the highest PIC (0.87) and marker index value (MI:5.25). An 840 bp allele (band) was characteristic to Kantapada local - A, Kendrapada local-D, and Nayagarh local - C. Such genotype- specific finger-printing may serve for reliable varietal characterization and elimination of duplicates. The test genotypes were grouped into six distinct clusters. TU 10-13, LBG 623, TAU 1, OBG 33, LBG 17 and PU 31 were highly divergent. PU 31 had inherent high yield potential (˃5.0q/ha) with known YMV resistance. The above divergent high yielding test genotypes may serve as candidate varieties for further genetic improvement using recombination breeding

    Studies on soil fertility status of coffee growing regions in Wayanad district

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    Top soil in Wayanad region is prone to disturbance and erosion, as the coffee growers’ practice scraping, scuffling and cover digging. It isnecessary to conserve the inherent fertility of top soil by minimum disturbance during farming operations. Otherwise soil deterioration can become one of the major constraints for crop production in the present day exploitative cultivation of plantation crops. It is well known that nutrient availability is influenced by their distribution in the soil as well as other soil characteristics. Soil fertility is the key to meet the nutrient requirement of the crops. Soil test based nutrient management will increase the crop productivity there by helping to save the fertility. The study, carried out to understand the fertility status of the coffee soils, revealed a higher acidity (98%) with deficiencies of calcium (32%), magnesium (96%) and boron (31%) limiting the coffee productivity in the district. The coffee area in the district is strongly acidic (69%) due to lack of liming and continuous use of acid producing fertilizers. Fifty per cent of soil sampleswere high in phosphorus which in turn impair the nutrient balance and affects micronutrient absorption by plants. Deficiency of calcium and magnesium affects uptake of other nutrients which upsets cellular functions. In coffee, boron deficiency will reduce the productivity by affecting flowering and fruit set. Amelioration of soil acidity and optimal use of major, secondary and micronutrients are must to enhance coffee productivity in the district. Application of manures and fertilizers based on soil test values will save the fertilizers and also sustain the soil health. Integrated management of plant nutrients is essential to achieve sustainable coffee crop production
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