Campbell Biology In Focus, Loose-leaf Edition (3rd Edition)
3rd Edition
ISBN: 9780134895727
Author: Lisa A. Urry, Michael L. Cain, Steven A. Wasserman, Peter V. Minorsky
Publisher: PEARSON
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Chapter 35, Problem 7TYU
DRAW IT Consider a pencil-shaped protein with two epitopes, Y (the “eraser” end) and Z (the “point”· end). They are recognized by antibodies A1 and A2, respectively. Draw and label a picture showing the antibodies linking proteins into a complex that could trigger endocytosis by a macrophage.
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Chapter 35 Solutions
Campbell Biology In Focus, Loose-leaf Edition (3rd Edition)
Ch. 35.1 - Pus is both a sign of infection and an indicator...Ch. 35.1 - MAKE CONNECTIONS How do the molecules that...Ch. 35.1 - Prob. 3CCCh. 35.2 - Prob. 1CCCh. 35.2 - Explain how memory cells strengthen the immune...Ch. 35.2 - WHAT IF? If both copies of a light-chain gene and...Ch. 35.3 - Prob. 1CCCh. 35.3 - Prob. 2CCCh. 35.3 - Prob. 3CCCh. 35 - Prob. 1TYU
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- Using the envelope depiction we presented in class, draw out chemical structures for thefollowing oligonucleotides. You can abbreviate the bases as Ade, Cyt, Gua, Thy, Ura. A. d(GACA)B. p(d(TATA))C. GUCUparrow_forwardTerpenesA. Provide a reasonable mechanism for the production of geranyl pyrophosphate from IPP andDMAPPB. How many molecules of IPP and how many molecules of DMAPP would you need to makefarnesyl pyrophosphatearrow_forwardDraw the enol form of Thymine, and show how this tautomer could form a Watson-Crickbase pair with Guanine. If this happened, what would be the consequence?arrow_forward
- Consider the two isoprenoid precursors IPP and DMAPP.A. Which one is more susceptible to SN1 reaction? Explain your answerB. Which is a more likely nucleophile? Explain your answerarrow_forwardDraw the structure of the anti-HIV drug AZT (zidovudine), which stops retro-viral DNAsynthesis. When AZT is taken up by cells, it is converted to AZT triphosphate. Explain how thiscompound could interfere with DNA synthesisarrow_forwardIn the mevalonate pathway, three acetyl-CoA are combined to give a C5 product, IPP.A. Write out a 5-step general acid/general base mechanism to explain how HMG-CoA isformed from 3 acetyl-CoA (Note: we are leaving out some details. The enzyme HMG-CoA actuallyuses its Cys residues to accept acetyl groups from 2 acetyl-CoA, making new thioesters and liberatingCoASH) B. Two NADPH and two H+ are required to form mevalonic acid from HMG-CoA. Circle the Hatoms that came from NADPH, and put a square around any H atoms that came from H+.C. Three ATP are used to convert mevalonic acid to IPP. Explain the role of each ATP moleculearrow_forward
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