Theoretical models: Difference between revisions
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Empirically-determined templates with adequate sequence identity are available for less than half of all protein sequences. One of the major goals of [[structural genomics]] is to increase the sequence diversity of the available empirically-determined structures that can be used as templates for homology modeling. | Empirically-determined templates with adequate sequence identity are available for less than half of all protein sequences. One of the major goals of [[structural genomics]] is to increase the sequence diversity of the available empirically-determined structures that can be used as templates for homology modeling. | ||
A number of free servers have libraries of homology models generated in advance for protein sequences, and many will create homology models for a submitted protein sequence. For more, please see | |||
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[[Homology modeling servers]]. | |||
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When no suitable template exists, the [http://targetdb.pdb.org Structural Genomics Target Database] should be searched with your sequence. In some cases, a sequence-similar protein has already been crystallized and diffracted, but the model may not have been completed, or the completed model may not yet have been deposited in the [[PDB]]. In such cases, it may be worthwhile to contact the team that has made the most progress on a closely related sequence. | When no suitable template exists, the [http://targetdb.pdb.org Structural Genomics Target Database] should be searched with your sequence. In some cases, a sequence-similar protein has already been crystallized and diffracted, but the model may not have been completed, or the completed model may not yet have been deposited in the [[PDB]]. In such cases, it may be worthwhile to contact the team that has made the most progress on a closely related sequence. | ||
See also the list of resources at [[User:Wayne Decatur/Homology Modeling]]. | See also the list of resources at [[User:Wayne Decatur/Homology Modeling]]. | ||