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Essential Cell Biology 5th edition

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A:10 Answers

Figure A4−4

ANSWER 4–5

Figure A4−5

curly

See Figure A4–5.

mild reduction

oxidation

straight

substrate

mirror image

ECB5 EA4.04/A4.04

of substrate

active site

of enzyme

active site

of enzyme

ANSWER 4–6

A. Feedback inhibition from Z that affects the reaction

B → C would increase the flow through the B → X →

Y → Z pathway, because the conversion of B to C is

inhibited. Thus, the more Z there is, the more production

ECB5 EA4.05/A4.05

of Z would be stimulated. This is likely to result in an

uncontrolled “runaway” amplification of this pathway.

B. Feedback inhibition from Z affecting Y → Z would only

inhibit the production of Z. In this scheme, however, X

and Y would still be made at normal rates, even though

both of these intermediates are no longer needed at this

level. This pathway is therefore less efficient than the

one shown in Figure 4−42.

C. If Z is a positive regulator of the step B → X, then the

more Z there is, the more B will be converted to X and

therefore shunted into the pathway producing more Z.

This would result in a runaway amplification similar to

that described for (A).

D. If Z is a positive regulator of the step B → C, then

accumulation of Z leads to a redirection of the pathway

to make more C. This is a second possible way, in

addition to that shown in the figure, to balance the

distribution of compounds into the two branches of the

pathway.

ANSWER 4–7 Both nucleotide binding and

phosphorylation can induce allosteric changes in proteins.

These can have a multitude of consequences, such as

altered enzyme activity, drastic shape changes, and changes

in affinity for other proteins or small molecules. Both

mechanisms are quite versatile. An advantage of nucleotide

binding is the fast rate with which a small nucleotide

can diffuse to the protein; the shape changes that

accompany the function of motor proteins, for example,

require quick nucleotide replenishment. If the different

conformational states of a motor protein were controlled

by phosphorylation, for example, a protein kinase would

either need to diffuse into position at each step, a much

slower process, or be associated permanently with each

motor protein. One advantage of phosphorylation is that it

requires only a single amino acid on the protein’s surface,

rather than a specific binding site. Phosphates can therefore

be added to many different side chains on the same protein

(as long as protein kinases with the proper specificities

exist), thereby vastly increasing the complexity of regulation

that can be achieved for a single protein.

ANSWER 4–8 In working together in a complex, all three

proteins contribute to the specificity (by binding to the safe

and key directly). They help position one another correctly,

and provide the mechanical bracing that allows them to

perform a task that they could not perform individually

(the key is grasped by two of the proteins, for example).

Moreover, their functions are generally coordinated in time

(for instance, the binding of ATP to one subunit is likely to

require that ATP has already been hydrolyzed to ADP by

another).

ANSWER 4–9 The α helix is right-handed. The three

strands that form the large β sheet are antiparallel. There

are no knots in the polypeptide chain, presumably because

a knot would interfere with the folding of the protein into its

three-dimensional conformation after protein synthesis.

ANSWER 4–10

A. True. Only a few amino acid side chains contribute to the

active site. The rest of the protein is required to maintain

the polypeptide chain in the correct conformation,

provide additional binding sites for regulatory purposes,

and localize the protein in the cell.

B. True. Some enzymes form covalent intermediates with

their substrates (see middle panels of Figure 4−39);

however, in all cases, the enzyme is restored to its

original structure after the reaction.

C. False. β sheets can, in principle, contain any number of

strands because the two strands that form the rims of

the sheet are available for hydrogen-bonding to other

strands. (β sheets in known proteins contain from 2 to 16

strands.)

D. False. It is true that the specificity of an antibody

molecule is exclusively contained in polypeptide loops

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