Choose scaffolding proteins nuclear response cross-talk regulation of the response cellular response signal amplification termination of signal
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- Could you please help me. Make a reaction to this. Thank you so muchNeed help Intaractions of FAK kinase which directly depend on the tyrosine residue 397 (Y397) are inhibbited by a chemical compound in cancercells. Intaraction of FAK kinase with what proteins are blocked by this inhibition? (please give a listt of them all, and that's it)Break down + function Acetyichaline.(Ach) receptors (eacn Fort)
- True or False. The binding affinity between a peptide agonist and its specific G protein coupled receptor alone determines the sensitivity of a cell to the agonist peptide.Membrane Receptors and Medicine. A patient, who has a stressful job, comes in with high blood pressure. The doctor prescribes beta-blockers to the patient. Explain what beta-blockers are and how these drugs help to bring down blood pressure to normal.Please help me with this question. PLEase give me the right answer and for number 2 WRITE AT LEAST A PARAGRAPGH and dont copy from internet.
- Answer all shortly.will give a like.True or False. The binding affinity between a peptide agonist and its specific G protein coupled receptor involves certain types of chemical bonds. Explain your answer in detail.. ( please do not copy off of another source.. e.g chegg)Inducers and Inhibitors of AEP. Short peptides such as legumain stabilization and activity modulation (LSAM) domain and αvβ3 integrin could enhance the activity of AEP. LSAM domain known as the prodomain of AEP blocks substrate binding before activation. This prodomain has a helical structure and two independent peptides. One is an activation peptide (AP, K287 to N323), and the other is a LSAM domain. LSAM domain remains even after AP is cleaved and released from protease at neutral pH via electrostatic interaction. AEP without LSAM domain has a lower melting temperature than AEP with LSAM domain [77, 117]. Another short peptide, αvβ3 integrin, can directly interact with AEP, and after forming a complex, the optimal pH for AEP activity is increased from 5.5 to 6.0. It indicates that αvβ3 binding could induce conformational stabilization of AEP accompanied by deprotonated C189. αvβ3 does not directly interact with the AEP active site; however, AEP docks to the αvβ3 RGD-binding site…
- Signal Molecule- Somatostatin Receptor Name- Somatostatin receptor type 2 Draw the structure of the signal molecule (for peptides just sketch key motifs the best you can; i.e. alpha helices and beta sheets) discuss (100 words) the key features of the signaling cascade produced by reception of the signal molecule. along w/ 2-3 bullet points highlighting areas critical to signal amplification as well as basic mechanisms of signal termination. Cite one articlehow signal summation works. Can the signals just be added? Does there need to be a break in the signals?Assighment. Create a diagram which illustrates the typical signalling mechanism of action of each of the four common classes of receptor (e.g. kinase-linked receptors etc.) and possible routes of communication (autocrine etc.). Your diagram should show the specific molecules involved, the mechanisms of signal transduction and indicate the different pathways that are activated. It should include a specific example of a receptor, ligand and signalling pathway for each general class. Include as wide a variety of ligands and modes of action as you can. For each of the examples describe the mechanism of action in the form below. DO NOT use any of the ligand-receptor combinations provide to you in the Learning Materials to date - research and create a diagram for a novel pathway instead!