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Wave digital adaptors for Brune, Darlington C and D, and twin-t sectionsLe, Huynh Huu 16 April 2014 (has links)
This thesis is concerned with the derivation of new wave adaptors for the Brune section, the Darlington C and De sections, and an adaptor for the Twin-T structure.
These wave adaptors have been derived by applying Martens' and Meerkötter's n-port voltage scattering matrix representation to the corresponding reference network interconnections.
The following results have been obtained:
a) The Brune, C and D adaptors are realized without any unit elements.
b) The adaptors in a0 are canonical in the number of delays.
c) All the adaptors considered may have a reflection-free port which makes cascade synthesis possible.
d) The Brune and C adaptors require six multipliers, four of which are independent and two of which are identical.
e) The D adaptor requires a total number of eleven multipliers, seven of which are independent and two pairs of which are identical.
f) The Twin-T adaptor requires ten multipliers of which seven are independent.
g) In a hardware realization, all the adaptors considered are made to have zero output after a finite time for zero input by means of a simple arithmetic procedure.
Illustrative examples of filters using these structures have been designed, and simulated on a minicomputer. Their respective impulse responses are obtained and show no granularity and/or overflow oscillations, as expected.
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Elucidating the Priming Mechanism of ClpXP Protease by Single-Domain Response Regulator CpdR in Caulobacter crescentusBarker, Kimberly E 14 November 2023 (has links) (PDF)
In Caulobacter crescentus, progression through the cell cycle is regulated by the AAA+ protease ClpXP, and there are several classes of cell-cycle substrates that require adaptors in order to be degraded. CpdR, a single domain-response regulator, binds the N-terminal domain of ClpXP and primes the protease for degradation of downstream factors (Lau et al., 2015). The ability of CpdR to bind ClpX is regulated by its phosphorylation state. In the unphosphorylated state, CpdR binds ClpXP and guides its localization to the cell pole during the swarmer to stalked transition, where CpdR is mediates degradation of substrates such as PdeA. Phosphorylation of response regulator receiver domains requires magnesium as a cofactor to stabilize the phosphorylated aspartate and reciprocally, phosphorylated receiver domains bind magnesium more effectively. While it is understood that CpdR primers ClpX for substrate degradation, the mechanism by which it does so has remained unclear. Using CollabFold, we identified putative residues involved in CpdR-ClpX binding and validated them using a BACTH screening. In vitro, we characterized the role that magnesium plays in regulating CpdR binding to ClpX. In this work, we directly test the role of magnesium in CpdR priming of ClpXP to show that magnesium may play a regulatory role in CpdR-mediated degradation, and thus binding to ClpX. We identify residues in ClpX that seem to be important for CpdR binding, which prior to this work was not clear.
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Caulobacter ClpXP Adaptor PopA’s Domain Interactions in the Adaptor Hierarchy of CtrA DegradationScudder, Thomas P 14 November 2023 (has links) (PDF)
The degradation and recycling of protein is a process essential for the maintenance and regulation of cellular function. More specifically, in Caulobacter crescentus, the ClpXP protease is responsible for driving progression through the cell cycle and protein quality control. This protease utilizes three known adaptors to selectively degrade proteins that initiate different stages of development. This thesis will elaborate on the specific binding interface on one of these adaptors, PopA, with another, RcdA, and focus in on specific residues on PopA and investigate their roles in adaptor binding and delivery of CtrA, the master regulator of Caulobacter. Finally, I will investigate the relationship between and necessity of these adaptors using a mutant PopA that does not require the presence of RcdA or the other adaptor, CpdR. The remainder of this thesis will present data that arises from these projects.
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Arranging multiple types of enzymes in defined space by modular adaptors / モジュール型アダプターを利用した複数酵素の特異的空間配置NGUYEN, MINH THANG 25 March 2019 (has links)
京都大学 / 0048 / 新制・課程博士 / 博士(エネルギー科学) / 甲第21886号 / エネ博第387号 / 新制||エネ||75(附属図書館) / 京都大学大学院エネルギー科学研究科エネルギー基礎科学専攻 / (主査)教授 森井 孝, 教授 木下 正弘, 教授 片平 正人 / 学位規則第4条第1項該当 / Doctor of Energy Science / Kyoto University / DGAM
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Role of Adaptor Proteins in MPR sorting / Funktion von Adaptorproteinen in der MPR-SortierungMedigeshi Ramarao, Guruprasad 08 May 2003 (has links)
No description available.
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Fyziologická úloha proteinu SIGIRR v časném embryonálním vývoji. / Physiological role of SIGIRR in early embryonic development.Hanusová, Zdeňka January 2012 (has links)
IL-1 receptor/Toll-like receptor (IL-1R/TLR) supefamily represents a group of proteins that share highly conserved TIR domain in their cytoplasmic region. Signal transduction mediated by TIR-containing proteins involves the activation of NF-κB transcription factor and thus the members of this superfamily play a key role in many physiological responses related to innate immune defense and inflammation. SIGIRR (single immunoglobulin IL1R-related molecule) is a recently discovered member of the IL-1R family, however it differs from the other group members by its unique structural features. SIGIRRhas been so far considered to be an 'orphan' receptor as no SIGIRR ligand has been identified yet. Moreover, SIGIRR itself is not capable to induce the NF-κB activation. Instead, SIGIRR is supposed to act as a negative regulator for IL- 1Rs/TLRs mediated inflammation. Its inhibitory function has been implemented in several signalling pathways in various cell types and tissues including the kidney, the digestive tract and the lung. Recent reports also suggest that SIGIRR could play a role in early embryonic development. The main aim of this thesis is to characterize the mechanism how SIGIRR negative regulatory function in IL-1R/TLR signalling pathway is delivered. Here we describe the establishment of...
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Model metropolitní optické sítě / Model of the metropolitan optical networkPrudík, Jiří January 2008 (has links)
The purpose of this master’s thesis is foremost to provide a simple guide how to build elements of optical metropolitan area network. The basic model consists to sequence of construction, network topology, passive and active parts. The collection contains examples of alternative technology such as Wireless LAN with different frequency. The optical network construction based on optical cable, fibres, splices, trays, adapters, connectors and active parts for example a lot of media convertor models. After that there are demonstrating type of wavelength division multiplexer used in metropolitan area network – passive planar PCL splitter. One of the passive planar splitter are used to increase optical fibre channel. At the end of the collection a simplified examples of used measurements – optical time domain reflectometry and optical fibre transmission. Contains standard protocols or reflectogram. The conclusion of this thesis summarizes costs of FTTb (Fibre To The Building) model of optical metropolitan area network in Czech republic and future contribution for society.
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