Background Due to the functional importance of intrinsically disordered proteins or protein regions, prediction of intrinsic protein disorder from amino acid sequence has become an area of active research as witnessed in the 6th experiment on Critical Assessment of Techniques for Protein Structure Prediction (CASP6). Since the initial work by Romero et al. (Identifying disordered regions in proteins from amino acid sequences, IEEE Int. Conf. Neural Netw., 1997), our group has developed several predictors optimized for long disordered regions (>30 residues) with prediction accuracy exceeding 85%. However, these predictors are less successful on short disordered regions (≤30 residues). A probable cause is a length-dependent amino acid compos...
Comparisons were made among four categories of protein flexibility: (1) low-B-factor ordered regions...
Background: Many protein regions and some entire proteins have no definite tertiary structure, exist...
Motivation Intrinsic disorder (ID), i.e.The lack of a unique folded conformation at physiological co...
Abstract Background Due to the functional importance of intrinsically disordered proteins or protein...
Background Our first predictor of protein disorder was published just over a decade ago in the Proc...
BACKGROUND: Intrinsically unstructured or disordered proteins are common and functionally important....
AbstractThe amino acid composition of intrinsically disordered proteins and protein segments charact...
A major challenge in the post-genome era is to determine the function of proteins. The traditional s...
Abstract Motivation: Intrinsically disordered regions are key for the function of num...
AbstractThe recent advances in the prediction of intrinsically disordered proteins and the use of pr...
Intrinsically disordered proteins, defying the traditional protein structure-function paradigm, are ...
AbstractObjectivesA number of published predictors are based on various algorithms and disordered pr...
Background: Intrinsically disordered proteins (IDPs) and regions (IDRs) perform a variety of crucial...
Discovery of intrinsically disordered proteins (IDPs) and protein hybrids that contain both intrinsi...
Many large-scale studies on intrinsically disordered proteins are implicitly based on the structural...
Comparisons were made among four categories of protein flexibility: (1) low-B-factor ordered regions...
Background: Many protein regions and some entire proteins have no definite tertiary structure, exist...
Motivation Intrinsic disorder (ID), i.e.The lack of a unique folded conformation at physiological co...
Abstract Background Due to the functional importance of intrinsically disordered proteins or protein...
Background Our first predictor of protein disorder was published just over a decade ago in the Proc...
BACKGROUND: Intrinsically unstructured or disordered proteins are common and functionally important....
AbstractThe amino acid composition of intrinsically disordered proteins and protein segments charact...
A major challenge in the post-genome era is to determine the function of proteins. The traditional s...
Abstract Motivation: Intrinsically disordered regions are key for the function of num...
AbstractThe recent advances in the prediction of intrinsically disordered proteins and the use of pr...
Intrinsically disordered proteins, defying the traditional protein structure-function paradigm, are ...
AbstractObjectivesA number of published predictors are based on various algorithms and disordered pr...
Background: Intrinsically disordered proteins (IDPs) and regions (IDRs) perform a variety of crucial...
Discovery of intrinsically disordered proteins (IDPs) and protein hybrids that contain both intrinsi...
Many large-scale studies on intrinsically disordered proteins are implicitly based on the structural...
Comparisons were made among four categories of protein flexibility: (1) low-B-factor ordered regions...
Background: Many protein regions and some entire proteins have no definite tertiary structure, exist...
Motivation Intrinsic disorder (ID), i.e.The lack of a unique folded conformation at physiological co...