Qyestion 1: If a cell has an adequate supply of adenine nucleotides but requires more guanine nucleotides for protein synthesis: 1. Glutamine-PRPP amidotransferase will not be fully inhibited. 2. AMP will be a feedback inhibitor of the condensation of IMP with aspartate. 3. ATP will stimulate the production of GMP from IMP. 4. ATP will inhibit nucleoside diphosphate reductase. A. 1, 2, and 3 B. 2 and 4 C. 1, 2, 3, and 4 D. 1 and 3
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- BIOMOLECULES - Please answer the questions properly. - Multiple choice Qyestion 1 : If a cell has an adequate supply of adenine nucleotides but requires more guanine nucleotides for protein synthesis: 1. Glutamine-PRPP amidotransferase will not be fully inhibited. 2. AMP will be a feedback inhibitor of the condensation of IMP with aspartate. 3. ATP will stimulate the production of GMP from IMP. 4. ATP will inhibit nucleoside diphosphate reductase. A. 1, 2, and 3 B. 2 and 4 C. 1, 2, 3, and 4 D. 1 and 3BIOMOLECULES - Please answer the questions properly. - Multiple choice 1. In human beings, what is the major control of de novo pyrimidine nucleotide synthesis? A. substrate availability B. feedback inhibition of glutamine-PRPP amidotransferase C. competitive inhibition of carbamoyl phosphate synthetase II D. availability of N-acetyl glutamate 2. In patients with Lesch Nyhan Syndrome, purine nucleotides are overproduced and over excreted. The hypoxanthine analogue Allopurinol, which effectively treats gout , has no effect on the severe neurological symptoms of Lesch- Nyhan patients because it does not? A. decrease de novo pyrimidine synthesis B. increase PRPP levels (Phosphoribosyl pyrophosphate) C. Decrease urate synthesis D. decrease de novo purine synthesisme (1).docx BIU A A- are they different? 3. What are three ways that 2-deoxystreptamine (2-DOS) aminoglycosides can inhibit protein synthesis? 4. Chloramphenicol: a. Where does this drug bind? b. How does it inhibit protein synthesis?
- BIOMOLECULES - Please answer the questions properly. - Multiple choice 1. In human beings, what is the major control of de novo pyrimidine nucleotide synthesis? A. substrate availability B. feedback inhibition of glutamine-PRPP amidotransferase C. competitive inhibition of carbamoyl phosphate synthetase II D. availability of N-acetyl glutamate 2. In patients with Lesch Nyhan Syndrome, purine nucleotides are overproduced and over excreted. The hypoxanthine analogue Allopurinol, which effectively treats gout , has no effect on the severe neurological symptoms of Lesch- Nyhan patients because it does not? A. decrease de novo pyrimidine synthesis B. increase PRPP levels (Phosphoribosyl pyrophosphate) C. Decrease urate synthesis D. decrease de novo purine synthesisBIOMOLECULES - Please answer the questions properly. - Multiple choice Allopurinol is an inhibitor of xanthine oxidase. Administration of allopurinol to a patient with gout and normal HG-PRT levels would be expected to lead to all of the following EXCEPT: A. decreased de novo synthesis of IMP B. increased xanthine in the blood C. increased levels of PRPP D. decreased urate in the urine 2. Which of the following unique attributes creates a steroid? A. 1 carboxyl group B. 4-fused carbon rings C. 2-fused oxygen molecules D. 3-fused hydrogen chainsBIOMOLECULES - MULTIPLE CHOICE - Please answer properly QUESTION : In human beings, what is the major control of de novo pyrimidine nucleotide synthesis? A. substrate availability B. competitive inhibition of carbamoyl phosphate synthetase II C. feedback inhibition of glutamine-PRPP amidotransferase D. vailability of N-acetyl glutamate
- Need help, please. Drop down answer list choices from left to right. 1. The first set of drop down answer choices are ATP, AMP, cAMP, GTP, GDP, or PP1. 2. The second set of drop down answer choices are activation or inhibition. 3. The third set of drop down answer choices are phosphorylation or dephosphorylation. 4. The fourth set of drop down answer choices are PKA, PP1, GS, or PFK1. 5. The fifth set of drop down answer choices are phosphorylation or dephosphorylation. 6. The sixth set of drop down answer choices are PFK-1, PFK-2, FBase-1, or FBase-2. 7. The seventh set of drop down answer choices are increased activity, decreased activity, or no change in activity.BIOMOLECULES - Please answer the questions properly. - Multiple choice 1. Major controls of de novo AMP synthesis include: 1. allosteric inhibition by GMP. 2. allosteric inhibition by AMP. 3. availability of PRPP. 4. stimulation by GTP A. 1, 2, and 3 B. 1, 2, 3, and 4 C. 2 and 4 D. 1 and 3I. Active site analysis. Below is a diagram of a putative active site for Monoamine oxidase. As we learned, the purpose of tertiary structure is to form a scaffold so you can orient just a few amino acids in the right orientation to promote binding and/or catalysis. The position where this occurs is the active site. The amino acid architecture of an active site is designed to bind substrates. Amino acid side chains are capable of hydrogen bonding, ionic and hydrophobic interactions. Fill in each amino acid that you think is suitable for interacting with the part of the substrate it is closest to. Assume the pH will be at 7.0 a.a.#1 a.a.#2 a.a.#6 HO Lond NH₂ НО a.a.#5 OH a.a.#3 a.a.#4
- Question:- Explain why withholding galactose from the diet of galactosaemia patients has no effects on their synthesis of glycoprotein.IX. Insulin, a hormone vital in blood sugar regulation and having a polypeptide chain with disulfide linkages, loses its regulatory activity when heated at nearly 100°C for 5-10 minutes. Explain the molecular basis of this observed thermal property of insulin relative to its native structure and function. I--P CO HI F. sum21.ex1.137 Accessibility Mo 日- Which of the following molecules generally possesses a complex shape that allows the molecule to function as tools and machinery that essentially do all the work within a living cell? 15. A. triglycerides B. proteins C. carbohydrate D. A and Bare correct. 16. Which of the following molecules is NOT involved in cell-to-cell signaling? A nroctaalandine Give %00% kidomi 56°F 近 Insert F8 F6 & %24 8. K 2 G oW N M
