Difference between revisions of "Lecture 09"
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[[Image:L09_s007.jpg|frame|none|Lecture 09, Slide 007<br> | [[Image:L09_s007.jpg|frame|none|Lecture 09, Slide 007<br> | ||
+ | The "Accessible Surface" depends on the probe radius. For solvent accessible surfaces a probe radius of 1.4A is commonly used since this approximates the radius of a water-molecule. | ||
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Revision as of 00:35, 27 November 2006
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Structure Analysis
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Lecture 09, Slide 005
Rotamers are low-energy conformations of side-chain dihedral angles. Only a small number of rotamer states and combinations are significantly populated in natural proteins. This tremendously simplifies protein structure modelling and prediction problems. However it also guides analysis, e.g. in enzyme active sites the rotamers often exist in strained, rare conformations.
Rotamers are low-energy conformations of side-chain dihedral angles. Only a small number of rotamer states and combinations are significantly populated in natural proteins. This tremendously simplifies protein structure modelling and prediction problems. However it also guides analysis, e.g. in enzyme active sites the rotamers often exist in strained, rare conformations.