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computer modeling in molecular biology.pdf

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2 Modell<strong>in</strong>n Prote<strong>in</strong> Structures 21the core was counted, and the root-mean-square deviation of the ma<strong>in</strong> cha<strong>in</strong> atomsof the core was calculated. (The po<strong>in</strong>ts correspond<strong>in</strong>g to 100% residue identity areprote<strong>in</strong>s for which the structure was determ<strong>in</strong>ed <strong>in</strong> two or more crystal environments,and the deviations show that crystal pack<strong>in</strong>g forces can modify slightly the conformationof the prote<strong>in</strong>s.) Figure 2-6 shows the changes <strong>in</strong> the fraction of residues <strong>in</strong>'? 2.4-c0cm>2m:3c 1.2-mc2 0 0.6-80.0 1I I I I 100 80 60 40 20 0Percent residue identityFigure 2-5. The relationship between the divergence of the am<strong>in</strong>o-acid sequence of the coreof related prote<strong>in</strong>s and the divergence of the ma<strong>in</strong> cha<strong>in</strong> conformation of the core.c%o I 80 ' 60 I 40 I 2bSequence identity ("YO)' 0 'Figure 2-6. The relationship between the divergence of the am<strong>in</strong>o-acid sequence of the coreof related prote<strong>in</strong>s and the relative size of the core.

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