Literature DB >> 12824310

DSSPcont: Continuous secondary structure assignments for proteins.

Phil Carter1, Claus A F Andersen, Burkhard Rost.   

Abstract

The DSSP program automatically assigns the secondary structure for each residue from the three-dimensional co-ordinates of a protein structure to one of eight states. However, discrete assignments are incomplete in that they cannot capture the continuum of thermal fluctuations. Therefore, DSSPcont (http://cubic.bioc.columbia.edu/services/DSSPcont) introduces a continuous assignment of secondary structure that replaces 'static' by 'dynamic' states. Technically, the continuum results from calculating weighted averages over 10 discrete DSSP assignments with different hydrogen bond thresholds. A DSSPcont assignment for a particular residue is a percentage likelihood of eight secondary structure states, derived from a weighted average of the ten DSSP assignments. The continuous assignments have two important features: (i) they reflect the structural variations due to thermal fluctuations as detected by NMR spectroscopy; and (ii) they reproduce the structural variation between many NMR models from one single model. Therefore, functionally important variation can be extracted from a single X-ray structure using the continuous assignment procedure.

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Year:  2003        PMID: 12824310      PMCID: PMC169032          DOI: 10.1093/nar/gkg626

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  10 in total

1.  The Protein Data Bank.

Authors:  H M Berman; J Westbrook; Z Feng; G Gilliland; T N Bhat; H Weissig; I N Shindyalov; P E Bourne
Journal:  Nucleic Acids Res       Date:  2000-01-01       Impact factor: 16.971

2.  Continuum secondary structure captures protein flexibility.

Authors:  Claus A F Andersen; Arthur G Palmer; Søren Brunak; Burkhard Rost
Journal:  Structure       Date:  2002-02       Impact factor: 5.006

3.  An approach to improving multiple alignments of protein sequences using predicted secondary structure.

Authors:  A J Jennings; C M Edge; M J Sternberg
Journal:  Protein Eng       Date:  2001-04

4.  Configurations of Polypeptide Chains With Favored Orientations Around Single Bonds: Two New Pleated Sheets.

Authors:  L Pauling; R B Corey
Journal:  Proc Natl Acad Sci U S A       Date:  1951-11       Impact factor: 11.205

5.  The structure of proteins; two hydrogen-bonded helical configurations of the polypeptide chain.

Authors:  L PAULING; R B COREY; H R BRANSON
Journal:  Proc Natl Acad Sci U S A       Date:  1951-04       Impact factor: 11.205

6.  Protein folds and families: sequence and structure alignments.

Authors:  L Holm; C Sander
Journal:  Nucleic Acids Res       Date:  1999-01-01       Impact factor: 16.971

7.  Protein fold recognition using sequence-derived predictions.

Authors:  D Fischer; D Eisenberg
Journal:  Protein Sci       Date:  1996-05       Impact factor: 6.725

8.  Protein fold recognition by prediction-based threading.

Authors:  B Rost; R Schneider; C Sander
Journal:  J Mol Biol       Date:  1997-07-18       Impact factor: 5.469

9.  SRS--an indexing and retrieval tool for flat file data libraries.

Authors:  T Etzold; P Argos
Journal:  Comput Appl Biosci       Date:  1993-02

10.  Dictionary of protein secondary structure: pattern recognition of hydrogen-bonded and geometrical features.

Authors:  W Kabsch; C Sander
Journal:  Biopolymers       Date:  1983-12       Impact factor: 2.505

  10 in total
  33 in total

1.  Protein structure prediction using sparse dipolar coupling data.

Authors:  Youxing Qu; Jun-tao Guo; Victor Olman; Ying Xu
Journal:  Nucleic Acids Res       Date:  2004-01-26       Impact factor: 16.971

2.  Protein energetic conformational analysis from NMR chemical shifts (PECAN) and its use in determining secondary structural elements.

Authors:  Hamid R Eghbalnia; Liya Wang; Arash Bahrami; Amir Assadi; John L Markley
Journal:  J Biomol NMR       Date:  2005-05       Impact factor: 2.835

3.  Determination of the folding transition states of barnase by using PhiI-value-restrained simulations validated by double mutant PhiIJ-values.

Authors:  Xavier Salvatella; Christopher M Dobson; Alan R Fersht; Michele Vendruscolo
Journal:  Proc Natl Acad Sci U S A       Date:  2005-08-22       Impact factor: 11.205

4.  Ancient evolutionary origin of diversified variable regions demonstrated by crystal structures of an immune-type receptor in amphioxus.

Authors:  José A Hernández Prada; Robert N Haire; Marc Allaire; Jean Jakoncic; Vivian Stojanoff; John P Cannon; Gary W Litman; David A Ostrov
Journal:  Nat Immunol       Date:  2006-06-25       Impact factor: 25.606

5.  Structural comparison of the two alternative transition states for folding of TI I27.

Authors:  Christian D Geierhaas; Robert B Best; Emanuele Paci; Michele Vendruscolo; Jane Clarke
Journal:  Biophys J       Date:  2006-04-07       Impact factor: 4.033

6.  A PDZ domain recapitulates a unifying mechanism for protein folding.

Authors:  Stefano Gianni; Christian D Geierhaas; Nicoletta Calosci; Per Jemth; Geerten W Vuister; Carlo Travaglini-Allocatelli; Michele Vendruscolo; Maurizio Brunori
Journal:  Proc Natl Acad Sci U S A       Date:  2006-12-19       Impact factor: 11.205

7.  Predicting protein flexibility through the prediction of local structures.

Authors:  Aurélie Bornot; Catherine Etchebest; Alexandre G de Brevern
Journal:  Proteins       Date:  2010-12-06

8.  Orientation preferences of backbone secondary amide functional groups in peptide nucleic acid complexes: quantum chemical calculations reveal an intrinsic preference of cationic D-amino acid-based chiral PNA analogues for the P-form.

Authors:  Christopher M Topham; Jeremy C Smith
Journal:  Biophys J       Date:  2006-10-27       Impact factor: 4.033

9.  Magic-angle spinning solid-state NMR spectroscopy of nanodisc-embedded human CYP3A4.

Authors:  Aleksandra Z Kijac; Ying Li; Stephen G Sligar; Chad M Rienstra
Journal:  Biochemistry       Date:  2007-11-07       Impact factor: 3.162

10.  Hsp70 chaperones and type I PRMTs are sequestered at intranuclear inclusions caused by polyalanine expansions in PABPN1.

Authors:  João Paulo Tavanez; Rocio Bengoechea; Maria T Berciano; Miguel Lafarga; Maria Carmo-Fonseca; Francisco J Enguita
Journal:  PLoS One       Date:  2009-07-29       Impact factor: 3.240

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