1,297 research outputs found
Central extension of the reflection equations and an analog of Miki's formula
Two different types of centrally extended quantum reflection algebras are
introduced. Realizations in terms of the elements of the central extension of
the Yang-Baxter algebra are exhibited. A coaction map is identified. For the
special case of , a realization in terms of elements
satisfying the Zamolodchikov-Faddeev algebra - a `boundary' analog of Miki's
formula - is also proposed, providing a free field realization of
(q-Onsager) currents.Comment: 11 pages; two references added; to appear in J. Phys.
SAGA: A project to automate the management of software production systems
The project to automate the management of software production systems is described. The SAGA system is a software environment that is designed to support most of the software development activities that occur in a software lifecycle. The system can be configured to support specific software development applications using given programming languages, tools, and methodologies. Meta-tools are provided to ease configuration. Several major components of the SAGA system are completed to prototype form. The construction methods are described
A deformed analogue of Onsager's symmetry in the XXZ open spin chain
The XXZ open spin chain with general integrable boundary conditions is shown
to possess a q-deformed analogue of the Onsager's algebra as fundamental
non-abelian symmetry which ensures the integrability of the model. This
symmetry implies the existence of a finite set of independent mutually
commuting nonlocal operators which form an abelian subalgebra. The transfer
matrix and local conserved quantities, for instance the Hamiltonian, are
expressed in terms of these nonlocal operators. It follows that Onsager's
original approach of the planar Ising model can be extended to the XXZ open
spin chain.Comment: 12 pages; LaTeX file with amssymb; v2: typos corrected,
clarifications in the text; v3: minor changes in references, version to
appear in JSTA
Examining UAS Employment Expectations and Requirements
Unmanned aircraft system (UAS) technology is radically changing how organizations, such as government agencies, non-profit corporations, and companies, apply aviation resources. Unmanned aviation is supporting improved efficiency, expanded capability, and heightened reliability through an increasing number of uses relating to: a) research and development and training-education, b) event filming, c) industrial, utility, and environmental projects, d) real estate, e) construction activities, f) agricultural, g) press and media, and h) state/local emergency services. The increasing application, and subsequent operational growth, is occurring in response to maturing technology, refined operational management and permissibility, innovative concept development, demonstrated capability, enhanced supportability, and the availability of specialized education and training opportunities. Technological advancement, regulatory changes, economic development, and widespread adoption of this technology is also leading to an observable growth of related employment opportunities. The Federal Aviation Administration has indicated that there are currently 116,027 remote pilots certified to operate small UAS in the National Airspace System, with growth to almost 350,000 by 2023. The examination of current career opportunities, in connection with commonly advertised job types and the associated roles and responsibilities, could better inform future UAS curricula design and enhancement efforts. This paper and associated presentation will feature an in-depth examination of such positions to categorize type and summarize prevalent attributes, while also highlighting notable features such as popular hiring locations, salary estimation, and experience-levels. The intent is to provide a detailed summary of hiring expectations and identify potential opportunities for improving academic alignment and career development efforts
Structure of HrcQ(B)-C, a conserved component of the bacterial type III secretion systems
Type III secretion systems enable plant and animal bacterial pathogens to deliver virulence proteins into the cytosol of eukaryotic host cells, causing a broad spectrum of diseases including bacteremia, septicemia, typhoid fever, and bubonic plague in mammals, and localized lesions, systemic wilting, and blights in plants. In
addition, type III secretion systems are also required for biogenesis of the bacterial flagellum. The HrcQ(B) protein, a component of the secretion apparatus of Pseudomonas syringae with homologues in all type III systems, has a variable N-terminal and a conserved C-terminal domain (HrcQ(B)-C). Here, we report the crystal structure
of HrcQ(B)-C and show that this domain retains the ability of the full-length protein to interact with other type III components. A 3D analysis of sequence conservation patterns reveals two clusters of residues potentially involved in protein–protein interactions. Based on the analogies between HrcQ(B) and its flagellum homologues,
we propose that HrcQ(B)-C participates in the formation of
a C-ring-like assembly
Distinctive expression patterns of 185/333 genes in the purple sea urchin, Strongylocentrotus purpuratus: an unexpectedly diverse family of transcripts in response to LPS, β-1,3-glucan, and dsRNA
BACKGROUND: A diverse set of transcripts called 185/333 is strongly expressed in sea urchins responding to immune challenge. Optimal alignments of full-length 185/333 cDNAs requires the insertion of large gaps that define 25 blocks of sequence called elements. The presence or absence of individual elements also defines a specific element pattern for each message. Individual sea urchins were challenged with pathogen associated molecular patterns (PAMPs) (lipopolysaccharide, β-1,3-glucan, or double stranded RNA), and changes in the 185/333 message repertoire were followed over time. RESULTS: Each animal expressed a diverse set of 185/333 messages prior to challenge and a 0.96 kb message was the predominant size after challenge. Sequence analysis of the cloned messages indicated that the major element pattern expressed in immunoquiescent sea urchins was either C1 or E2.1. In contrast, most animals responding to lipopolysaccharide, β-1,3-glucan or injury, predominantly expressed messages of the E2 pattern. In addition to the major patterns, extensive element pattern diversity was observed among the different animals before and after challenge. Nucleotide sequence diversity of the transcripts increased in response to β-1,3-glucan, double stranded RNA and injury, whereas diversity decreased in response to LPS. CONCLUSION: These results illustrate that sea urchins appear to be able to differentiate among different PAMPs by inducing the transcription of different sets of 185/333 genes. Furthermore, animals may share a suite of 185/333 genes that are expressed in response to common pathogens, while also maintaining a large number of unique genes within the population
The Erd\H{o}s-Ko-Rado theorem for twisted Grassmann graphs
We present a "modern" approach to the Erd\H{o}s-Ko-Rado theorem for
Q-polynomial distance-regular graphs and apply it to the twisted Grassmann
graphs discovered in 2005 by van Dam and Koolen.Comment: 5 page
From Quantum Affine Symmetry to Boundary Askey-Wilson Algebra and Reflection Equation
Within the quantum affine algebra representation theory we construct linear
covariant operators that generate the Askey-Wilson algebra. It has the property
of a coideal subalgebra, which can be interpreted as the boundary symmetry
algebra of a model with quantum affine symmetry in the bulk. The generators of
the Askey-Wilson algebra are implemented to construct an operator valued -
matrix, a solution of a spectral dependent reflection equation. We consider the
open driven diffusive system where the Askey-Wilson algebra arises as a
boundary symmetry and can be used for an exact solution of the model in the
stationary state. We discuss the possibility of a solution beyond the
stationary state on the basis of the proposed relation of the Askey-Wilson
algebra to the reflection equation
Adaptive response and enlargement of dynamic range
Many membrane channels and receptors exhibit adaptive, or desensitized,
response to a strong sustained input stimulus, often supported by protein
activity-dependent inactivation. Adaptive response is thought to be related to
various cellular functions such as homeostasis and enlargement of dynamic range
by background compensation. Here we study the quantitative relation between
adaptive response and background compensation within a modeling framework. We
show that any particular type of adaptive response is neither sufficient nor
necessary for adaptive enlargement of dynamic range. In particular a precise
adaptive response, where system activity is maintained at a constant level at
steady state, does not ensure a large dynamic range neither in input signal nor
in system output. A general mechanism for input dynamic range enlargement can
come about from the activity-dependent modulation of protein responsiveness by
multiple biochemical modification, regardless of the type of adaptive response
it induces. Therefore hierarchical biochemical processes such as methylation
and phosphorylation are natural candidates to induce this property in signaling
systems.Comment: Corrected typos, minor text revision
phenix.mr_rosetta: molecular replacement and model rebuilding with Phenix and Rosetta.
The combination of algorithms from the structure-modeling field with those of crystallographic structure determination can broaden the range of templates that are useful for structure determination by the method of molecular replacement. Automated tools in phenix.mr_rosetta simplify the application of these combined approaches by integrating Phenix crystallographic algorithms and Rosetta structure-modeling algorithms and by systematically generating and evaluating models with a combination of these methods. The phenix.mr_rosetta algorithms can be used to automatically determine challenging structures. The approaches used in phenix.mr_rosetta are described along with examples that show roles that structure-modeling can play in molecular replacement
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