2,835 research outputs found
Binding of nucleotides to guanylate kinase, p21<sup>ras</sup>, and nucleoside-diphosphate kinase studied by nano-electrospray mass spectrometry.
Ultrathin epitaxial Fe films in vicinal GaAs(001): A study by spin-resolved photoelectron spectroscopy
Thin epitaxial Fe films have been grown on vicinal GaAs(001) substrates and their remanent magnetic properties and the degree of substrate atom diffusion investigated using synchrotron-based photoelectron spectroscopy. The vicinal Fe films, though exhibiting greater As diffusion than their singular homologues, displayed better film quality both from the structural and the magnetic points of view. The spin-resolved valence spectra of the vicinal films resemble those for crystalline bulk Fe at lower film thicknesses than for singular films
Search for resonances in the mass distribution of jet pairs with one or two jets identified as b -jets in proton-proton collisions at s=13 TeV with the ATLAS detector
Structural characterization of the closed conformation of mouse guanylate kinase
Guanylate kinase (GMPK) is a nucleoside monophosphate kinase that catalyzes the reversible phosphoryl transfer from ATP to GMP to yield ADP and GDP. In addition to phosphorylating GMP, antiviral prodrugs such as acyclovir, ganciclovir, and carbovir and anticancer prodrugs such as the thiopurines are dependent on GMPK for their activation. Hence, structural information on mammalian GMPK could play a role in the design of improved antiviral and antineoplastic agents. Here we present the structure of the mouse enzyme in an abortive complex with the nucleotides ADP and GMP, refined at 2.1 Angstrom resolution with a final crystallographic R factor of 0.19 (R-free = 0.23). Guanylate kinase is a member of the nucleoside monophosphate (NMP) kinase family, a family of enzymes that despite having a low primary structure identity share a similar fold, which consists of three structurally distinct regions termed the CORE, LID, and NMP-binding regions. Previous studies on the yeast enzyme have shown that these parts move as rigid bodies upon substrate binding. It has been proposed that consecutive binding of substrates leads to "closing" of the active site bringing the NMP-binding and LID regions closer to each other and to the CORE region. Our structure, which is the first of any guanylate kinase with both substrates bound, supports this hypothesis. It also reveals the binding site of ATP and implicates arginines 44, 137, and 148 (in addition to the invariant P-loop lysine) as candidates for catalyzing the chemical step of the phosphoryl transfer
Isolation and Characterization of Novel BTB Domain Protein Encoding Genes from Fungal Grass Endophytes
Pasture grasses belonging to the Pooideae sub-family of the Poaceae family frequently host symbiotic fungal endophytes. These include the sexual Epichloë species and the anamorphic asexual Neotyphodium species, which are thought to have evolved from Epichloë species either by the direct loss of sexual reproduction or by interspecific hybridisation. The two key temperate pasture grasses, tall fescue (Festuca arundinacea Schreb) and perennial ryegrass (Lolium perenne L.) interact with the fungal endophytes N. coenophialum and N. lolii, respectively. Large insert genomic DNA libraries are valuable resources for the discovery and isolation of genes and their regulatory sequences, for physical mapping, map-based cloning of target genes as well as for whole genome sequencing. BTB (Bric-a-brac, tram-track, broad complex) domains are highly conserved motifs of 120 amino acids in length. The domains are rich in hydrophobic amino acids, and mediate protein-protein interaction that lead to homomeric dimerisation and in some cases heteromeric dimerisation of a large number of functionally diverse proteins. The presence of BTB domains defines a large family of genes involved in various biological processes, such as the regulation of transcription, DNA binding activity and structural organisation of macromolecular structures. Genes encoding BTB domain proteins (BDP) have previously been described in viruses, yeasts, plants, nematodes, insects, fish and mammals. However, BDP genes have not as yet been described for filamentous fungi
Foliar Expression of Candidate Genes Involved in Condensed Tannin Biosynthesis in White Clover (\u3cem\u3eTrifolium Repens\u3c/em\u3e)
Bloat disease in cattle and sheep is caused by the rapid microbial degradation of protein-rich fodder in the rumen. This leads to the production of protein foams that trap gases, causing bloat, a condition that is often fatal to livestock and costly to farmers. Condensed tannins (CTs) are phenolic polymers produced by the phenylpropanoid pathway of plants (Figure 1). CTs bind to proteins under acidic to neutral conditions, such as those present in the rumen, slowing their breakdown. A diet with a CT content of between 2% and 4% by dry weight, which is provided by some pasture legumes (e.g. Lotus corniculatus), protects livestock against bloat and improves the absorption of amino acids from the diet. White clover (Trifolium repens L.), a protein rich legume widely used in temperate regions, has virtually no CTs in leaves, although they are present in flowers
Nowcasting Aircraft Icing Conditions in the Presence of Multilayered Clouds Using Meteorological Satellite Data
Cloud properties retrieved from satellite data are used to diagnose aircraft icing threat in single layer and multilayered ice-over-liquid clouds. The algorithms are being applied in real time to the Geostationary Operational Environmental Satellite (GOES) data over the CONUS with multilayer data available over the eastern CONUS. METEOSAT data are also used to retrieve icing conditions over western Europe. The icing algorithm s methodology and validation are discussed along with future enhancements and plans. The icing risk product is available in image and digital formats on NASA Langley s Cloud and Radiation Products web site, http://wwwangler. larc.nasa.gov
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Retrievals of thick cloud optical depth from the Geoscience Laser Altimeter System (GLAS) by calibration of solar background signal
Laser beams emitted from the Geoscience Laser Altimeter System (GLAS), as well as other spaceborne laser instruments, can only penetrate clouds to a limit of a few optical depths. As a result, only optical depths of thinner clouds (< about 3 for GLAS) are retrieved from the reflected lidar signal. This paper presents a comprehensive study of possible retrievals of optical depth of thick clouds using solar background light and treating GLAS as a solar radiometer. To do so one must first calibrate the reflected solar radiation received by the photon-counting detectors of the GLAS 532-nm channel, the primary channel for atmospheric products. Solar background radiation is regarded as a noise to be subtracted in the retrieval process of the lidar products. However, once calibrated, it becomes a signal that can be used in studying the properties of optically thick clouds. In this paper, three calibration methods are presented: (i) calibration with coincident airborne and GLAS observations, (ii) calibration with coincident Geostationary Opera- tional Environmental Satellite (GOES) and GLAS observations of deep convective clouds, and (iii) cali- bration from first principles using optical depth of thin water clouds over ocean retrieved by GLAS active remote sensing. Results from the three methods agree well with each other. Cloud optical depth (COD) is retrieved from the calibrated solar background signal using a one-channel retrieval. Comparison with COD retrieved from GOES during GLAS overpasses shows that the average difference between the two retriev- als is 24%. As an example, the COD values retrieved from GLAS solar background are illustrated for a marine stratocumulus cloud field that is too thick to be penetrated by the GLAS laser. Based on this study, optical depths for thick clouds will be provided as a supplementary product to the existing operational GLAS cloud products in future GLAS data releases
Discovery, Isolation and Characterisation of Promoters from Perennial Ryegrass (\u3ci\u3eLolium Perenne\u3c/i\u3e)
The availability of a suite of promoters with a range of spatial, temporal and inducible expression patterns is of significant importance to enable targeted expression of genes of interest for molecular breeding of forage species. A range of resources and tools have been developed for promoter isolation and characterisation in perennial ryegrass (Lolium perenne L.) including genomic lambda and BAC libraries and a 15 K unigene microarray
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