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Specific inhibitors of dyneins have yet to be discovered. When they are discovered, how would they most likely affect cells?
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Reduce retrograde transport of endosomes |
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Decrease pseudopod formation in amoeboid cells |
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Increase cell size |
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Decrease contraction of skeletal muscle |
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- Describe how G proteins can alter the permeability of theplasma membrane and how they can alter the synthesis ofan intracellular mediator, such as cAMP. Give examples.To design a drug that inhibits metastasis, which of the following strategies is the WORST idea? to disrupt cadherin complexes to inhibit Rho family proteins to inhibit ARP complex O to block myosin-based contractile structureThe biomolecular interaction between protein receptors and ligands is similar to that of en- zymes and substrates, which depends in part on the shape of the protein. The shape of a protein, in turn, depends on the presence of appropriate chemical bonds in the protein. Many common medications function by altering the interactions between protein receptors and ligands, thereby interfering with the normal response of a cell to specific signals. Which of the following best describes a mechanism by which a drug might interfere with a normal cellular response? A B A medication causes the cell to become more permeable and unable to maintain the conditions that allow a normal response. с A medication interrupts the electron transport chain in a cell and makes it unable to syn- thesize sufficient ATP. D A medication enters the nucleus of a cell and alters the nucleic sequence for a specific receptor protein. A medication enters a target cell and acts as an inhibitor to an intercellular protein…
- Explain how adenyl cyclase enzymes function in signal transduction pathways. Explain how kinase enzymes function in signal transduction pathways.Below are two cell signalling pathways that work together to regulate cell growth, proliferation and ultimately the size of organs in O.Extremus. In other closely related organisms, dysfunction of these pathways has been associated with tumor growth. mTOR pathway: 1. Growth factors bind and stimulate the receptors. 2. Receptors can activate the phosphatidylinositol 3 kinase (PI3K) – Akt signaling pathway. 3. The activated Akt, a serine threonine kinase, inhibits theTSC1–TSC2 complex, allowing Rheb to activate mTORC1. 4. In parallel, amino acids activate the mTORC1 pathway through a mechanism requiring the Rag– Ragulator complex. Hippo pathway: 1. The binding of the ligand activates the receptors which activate Mst and Lats. 2. YAP activity is modulated by phosphorylation of Mst and Lats. YAP upregulates miR-29, which in turn downregulates PTEN, an inhibitor of PI(3)K and Akt. So, the two pathways crosstalk and coordinate cell number and growth. a) What purpose does this forward…Which of the situations below will enhance microtubule growth? O addition of a drug that inhibits GDP to GTP exchange on free subunits O addition of a drug that increases the dissociation of GTP-tubulin from the polymer O addition of a drug that inhibits GTP hydrolysis in subunits incorporated into the polymer O None of the above
- The pathway shown below is used by a fungus to create Arginine from a precursor starter molecule. A nonsense mutation occurs in the gene that encodes enzyme 2. This fungus is grown on media that only contains the precursor. Discuss the effects of this mutation on:(i) The function of Enzyme 2 (ii) The potential of the fungus to produce OrnithineAmoeboid cells that migrate through our tissues, such as the class of white blood cells known as neutrophils, often do so in a directed manner, triggered, for instance, by chemical signals released by pathogens such as bacteria. Directed migration in response to a chemical stimulus is known as chemotaxis. Part of an efficient chemotactic response is the ability of cells to polarize. As is the case with our structurally-polar polymers like F-actin or microtubules, polarization here refers to an asymmetry in the cells, rather than an electrical charge. In this case, it involves one part of the cell becoming the “front” (or leading edge) and another the rear. In a well-polarized, migrating cell, it’s been observed that an active form of Rac (which, in turn, can activate ARP 2/3) is concentrated towards the front of the cell, whereas an active form of Rho (which, in turn, can activate formin, inhibit ADP, and activate myosin II) is found toward the rear of the cell. Based on your…Amoeboid cells that migrate through our tissues, such as the class of white blood cells known as neutrophils, often do so in a directed manner, triggered, for instance, by chemical signals released by pathogens such as bacteria. Directed migration in response to a chemical stimulus is known as chemotaxis. Part of an efficient chemotactic response is the ability of cells to polarize. As is the case with our structurally-polar polymers like F-actin or microtubules, polarization here refers to an asymmetry in the cells, rather than an electrical charge. In this case, it involves one part of the cell becoming the “front” (or leading edge) and another the rear. In a well-polarized, migrating cell, it’s been observed that an active form of Rac (which, in turn, can activate ARP 2/3) is concentrated towards the front of the cell, whereas an active form of Rho (which, in turn, can activate formin, inhibit cofilin/ADP, and activate myosin II) is found toward the rear of the cell. Based on your…
- The most selectively toxic antibacterial agents are those that interfere with bacterial cell wall synthesis. This is because ________. Group of answer choices bacterial cell wall synthesis is easily inhibited whereas eukaryotic cell wall synthesis is more resistant to the actions of the drugs bacterial cell walls have a unique structure not found in eukaryotic host cells eukaryotic cells do not take up the drugs eukaryotic cells inactivate the drugs before they can do any damagePut the following steps for the outline of the growth factor signaling pathway in order: Map Kinase Kinase is Phosphorylated Proteins involved in gene transcription are activated Growth factor binds to its receptor in the cytoplasmic membrane Receptor recruits adaptor protein and GEF Autophosphorylation of tyrosine residues on the receptor Structural change of the receptor activates Tyrosine Kinase Map Kinase Kinase Kinase is phosphorylated Ras, a small GTPase, is activated by the exchange of GTP for GDP Map Kinase is Phosphorylated Map Kinase enters the nucleusA Simple Targeting Model describes which mechanism of cellular transport targeting? motor molecules targeted by changes in subdomain phosphatase and kinase concentrations cargo proteins targeted by changes in subdomain phosphatase and kinase concentrations random binding of cargo to cellular subdomains random binding of motor molecules to specific subcellular regions