Chemistry, 28.06.2019 19:20 ilovebeans25423
Give two reasons to explain why a proline residue in the middle of an α-helix is predicted to be destabilizing to the helical structure. check all tha apply. a. pro does not have the α−nh group that acts as a stabilizing h-bond donor in the middle of the helix. b. pro is nonpolar amino acid that does not connect turns of the α-helix. c. pro is nonpolar amino acid that destabilizes polar core of the protein. d. insertion of pro gives an exceptional conformational rigidity to the protein chain chain. e. pro is not able to adopt the ideal ϕ and ψ angles for an α -helix.
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Chemistry, 22.06.2019 09:50
Achemist has dissolved a certain substance in water. the chemist knows that more of the substance could be dissolved into the water before it stops dissolving. therefore
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Chemistry, 22.06.2019 11:50
Calculate the molarity of each of the following solutions. part a) 0.12 mol of lino3 in 5.5 l of solution part b) 60.7 g c2h6o in 2.48 l of solution part c) 14.2 mg ki in 100 ml of solution
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Chemistry, 22.06.2019 14:20
Which statement explains why the bonds between non metals tend to be covalent? the bonds are found to be nondirectional they have large differences in electronegativity they have small differences in electronegativity they have ions that produce an electrostatic pull
Answers: 1
Give two reasons to explain why a proline residue in the middle of an α-helix is predicted to be des...
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