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Molecular Biology of the Cell by Bruce Alberts, Alexander Johnson, Julian Lewis, David Morgan, Martin Raff, Keith Roberts, Peter Walter by by Bruce Alberts, Alexander Johnson, Julian Lewis, David Morg

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168 Chapter 3: Proteins

ORIGIN OF REPLICATION

CELL CYCLE REGULATORS

Orc2

METHIONINE SYNTHESIS

Met31

Met32

Erd3

Met4

Swe1

Cks1

Cli1

Cdc28

Cli2

Sic1

Orc1

Orc3

Orc6

Orc5

Cdc5

Orc4

Rpt1

Met28

KINETOCHORE

Okp1

Mit2

Ctf19

Cbf1

Cep3

Cbf2

Mcm21

Mck1

F-box

proteins

YDR131

Das1

Mdm30

Skp2

Hrt3

Me130

YDR306

Dla2

Ufb1 Rcy1

Yak1

YLR224W

Grr1

Cdc4

Cdc34

E2 ubiquitinconjugating

enzyme

Ctfl3

Hrt1

Vma8

Vma4

Tfp1

adaptor

protein 1

Ram2

Ram1

Skp1

Cdc53

Vma2

VACUOLAR H + -ATPase

ASSEMBLY

adaptor

protein 2

scaffold protein

(cullin)

Figure 3–81 A map of some protein–protein interactions of the SCF ubiquitin ligase and other proteins in the yeast

S. cerevisiae. The symbols and/or colors used for the five proteins of the ligase are those in Figure 3–71. Note that 15 different

F-box proteins are shown (purple); those with white lettering (beginning with Y) are known from the genome sequence as

open reading frames. For additional details, see text. (Courtesy of Peter Bowers and David Eisenberg, UCLA-DOE Institute for

Genomics and Proteomics, UCLA.)

MBoC6 m3.82/3.74

vacuolar H + -ATPase assembly (yellow shading) are separate from its function

in the SCF ubiquitin ligase. In fact, only the remaining three functions

of Skp1 illustrated in the diagram—methionine synthesis, cell cycle regulation,

and origin of replication (green shading)—involve ubiquitylation.

3. In cross-species comparisons, those proteins displaying similar patterns of

interactions in the two protein interaction maps are likely to have the same

function in the cell. Thus, as scientists generate more and more highly

detailed maps for multiple organisms, the results will become increasingly

useful for inferring protein function. These map comparisons will be a particularly

powerful tool for deciphering the functions of human proteins,

because a vast amount of direct information about protein function can

be obtained from genetic engineering, mutational, and genetic analyses in

experimental organisms—such as yeast, worms, and flies—that are not feasible

in humans.

What does the future hold? There are likely to be on the order of 10,000 different

proteins in a typical human cell, each of which interacts with 5 to 10 different

partners. Despite the enormous progress made in recent years, we cannot yet

claim to understand even the simplest known cells, such as the small Mycoplasma

bacterium formed from only about 500 gene products (see Figure 1–10). How then

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