2010
DOI: 10.1186/1471-2105-11-407
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Predicting β-turns and their types using predicted backbone dihedral angles and secondary structures

Abstract: Backgroundβ-turns are secondary structure elements usually classified as coil. Their prediction is important, because of their role in protein folding and their frequent occurrence in protein chains.ResultsWe have developed a novel method that predicts β-turns and their types using information from multiple sequence alignments, predicted secondary structures and, for the first time, predicted dihedral angles. Our method uses support vector machines, a supervised classification technique, and is trained and tes… Show more

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Cited by 42 publications
(45 citation statements)
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References 58 publications
(84 reference statements)
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“…With increasing temperature, the random coil signal becomes less pronounced, while the β-turn increases, indicating a transition toward a more ordered secondary structur 45,46 . β-turns play an important role in protein folding and stability 47 ; furthermore, they have been previously been associated with the onset of ELP-mediated phase separation 48 . In a β-turn, a tight loop is formed when the carbonyl oxygen of one residue forms a hydrogen bond with the amide proton of an amino acid three residues down the chain.…”
Section: Resultsmentioning
confidence: 99%
“…With increasing temperature, the random coil signal becomes less pronounced, while the β-turn increases, indicating a transition toward a more ordered secondary structur 45,46 . β-turns play an important role in protein folding and stability 47 ; furthermore, they have been previously been associated with the onset of ELP-mediated phase separation 48 . In a β-turn, a tight loop is formed when the carbonyl oxygen of one residue forms a hydrogen bond with the amide proton of an amino acid three residues down the chain.…”
Section: Resultsmentioning
confidence: 99%
“…S-MB might be expected to show higher surfactant activity than MB, because the former peptide may more accurately mimic the leaflet structure containing the N- and C-terminal domains of SP-B (Figure 1). Neural network algorithms also predict that the presence of the N-terminal insertion sequence in S-MB will not influence the ability of PKGG to fold as a β-turn [77,78]. Interestingly, the N-terminal XPXPXPY motif, where X denotes hydrophobic residues, may serve as a lipid insertion sequence to more firmly anchor S-MB to lipid monolayers and bilayers, as has been experimentally observed for the N-terminal SP-B(1–25) peptide [17].…”
Section: Mini-b (Mb) and Super Mini-b (S-mb) Synthetic Peptidesmentioning
confidence: 99%
“…Predicted dihedral angles have been applied successfully for secondary structure prediction [38,39], β-turn prediction [26] and three-dimensional structure of protein fragments [40]. Recently, shape string was successfully used in gamma-turn prediction [41].…”
Section: Methodsmentioning
confidence: 99%