Protein fold recognition has been approached by threading an amino aci
d sequence onto a library of folds, calculating a sequence-structure c
ompatibility score, and ranking these scores, Due to imperfections in
the empirically derived pairwise potential functions and the necessari
ly heuristic approach to the sequence-structure alignment problem, the
method benefits from the assessment of threaded models to evaluate th
e most probable structures among the list of possible folds, THREADER
and ANALYST, software tools available through the Internet, facilitate
the alignment and assessment steps of a threading prediction, No proc
ess has been found to be universally reliable for the detection of fol
ds related to the structure of a known input sequence, but several use
ful steps and approaches are discussed.