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Structural Models of Receptor Targets in the Low Homology or New Fold Region - The first component of this will be the creation of structural models of proteins whose sequence is known but no structures from experimental techniques, e.g. X-ray crystallography, NMR or cryo-electronmicroscopy, are likely to be available in the near future. Depending on the sequence similarity of the unknown protein with proteins of known structure, either homology modeling methods or fold recognition techniques will be used. For critical proteins which do not appear to have any known structural homologues, new fold protein modeling techniques will be used, although such structures will have a relatively low reliable resolution.
 


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