Structural genomics projects aim to provide an experimental
structure or a good model for every
protein in all completed genomes.
Most of the experimental work will be directed toward proteins whose fold
cannot be readily recognized by simple sequence comparison with proteins
of known structure.
Based on the history of proteins classified in the SCOP
structure database
- only about a quarter of the early structural
genomics targets will have a new fold.
- Among the remaining ones, about half are likely to be evolutionarily
related to proteins of known structure, even though the homology
could not be readily detected by sequence analysis.