Literature DB >> 9336476

Sequence walkers: a graphical method to display how binding proteins interact with DNA or RNA sequences.

T D Schneider1.   

Abstract

A graphical method is presented for displaying how binding proteins and other macromolecules interact with individual bases of nucleotide sequences. Characters representing the sequence are either oriented normally and placed above a line indicating favorable contact, or upside-down and placed below the line indicating unfavorable contact. The positive or negative height of each letter shows the contribution of that base to the average sequence conservation of the binding site, as represented by a sequence logo. These sequence 'walkers' can be stepped along raw sequence data to visually search for binding sites. Many walkers, for the same or different proteins, can be simultaneously placed next to a sequence to create a quantitative map of a complex genetic region. One can alter the sequence to quantitatively engineer binding sites. Database anomalies can be visualized by placing a walker at the recorded positions of a binding molecule and by comparing this to locations found by scanning the nearby sequences. The sequence can also be altered to predict whether a change is a polymorphism or a mutation for the recognizer being modeled.

Mesh:

Substances:

Year:  1997        PMID: 9336476      PMCID: PMC147041          DOI: 10.1093/nar/25.21.4408

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


  31 in total

1.  Theory of molecular machines. I. Channel capacity of molecular machines.

Authors:  T D Schneider
Journal:  J Theor Biol       Date:  1991-01-07       Impact factor: 2.691

Review 2.  Dynamic, structural, and regulatory aspects of lambda site-specific recombination.

Authors:  A Landy
Journal:  Annu Rev Biochem       Date:  1989       Impact factor: 23.643

3.  Quantitative analysis of the relationship between nucleotide sequence and functional activity.

Authors:  G D Stormo; T D Schneider; L Gold
Journal:  Nucleic Acids Res       Date:  1986-08-26       Impact factor: 16.971

4.  Efficient excision of phage lambda from the Escherichia coli chromosome requires the Fis protein.

Authors:  C A Ball; R C Johnson
Journal:  J Bacteriol       Date:  1991-07       Impact factor: 3.490

5.  Cellular factors couple recombination with growth phase: characterization of a new component in the lambda site-specific recombination pathway.

Authors:  J F Thompson; L Moitoso de Vargas; C Koch; R Kahmann; A Landy
Journal:  Cell       Date:  1987-09-11       Impact factor: 41.582

6.  Information content of binding sites on nucleotide sequences.

Authors:  T D Schneider; G D Stormo; L Gold; A Ehrenfeucht
Journal:  J Mol Biol       Date:  1986-04-05       Impact factor: 5.469

7.  Nucleotide sequence of bacteriophage lambda DNA.

Authors:  F Sanger; A R Coulson; G F Hong; D F Hill; G B Petersen
Journal:  J Mol Biol       Date:  1982-12-25       Impact factor: 5.469

8.  Computer methods to locate signals in nucleic acid sequences.

Authors:  R Staden
Journal:  Nucleic Acids Res       Date:  1984-01-11       Impact factor: 16.971

9.  A design for computer nucleic-acid-sequence storage, retrieval, and manipulation.

Authors:  T D Schneider; G D Stormo; J S Haemer; L Gold
Journal:  Nucleic Acids Res       Date:  1982-05-11       Impact factor: 16.971

10.  Mutational analysis of a prokaryotic recombinational enhancer element with two functions.

Authors:  P Hübner; W Arber
Journal:  EMBO J       Date:  1989-02       Impact factor: 11.598

View more
  36 in total

1.  Evolution of biological information.

Authors:  T D Schneider
Journal:  Nucleic Acids Res       Date:  2000-07-15       Impact factor: 16.971

2.  Strong minor groove base conservation in sequence logos implies DNA distortion or base flipping during replication and transcription initiation.

Authors:  T D Schneider
Journal:  Nucleic Acids Res       Date:  2001-12-01       Impact factor: 16.971

3.  Molecular flip-flops formed by overlapping Fis sites.

Authors:  Paul N Hengen; Ilya G Lyakhov; Lisa E Stewart; Thomas D Schneider
Journal:  Nucleic Acids Res       Date:  2003-11-15       Impact factor: 16.971

Review 4.  Consensus sequence Zen.

Authors:  Thomas D Schneider
Journal:  Appl Bioinformatics       Date:  2002

5.  Computation-directed identification of OxyR DNA binding sites in Escherichia coli.

Authors:  M Zheng; X Wang; B Doan; K A Lewis; T D Schneider; G Storz
Journal:  J Bacteriol       Date:  2001-08       Impact factor: 3.490

6.  Twenty Years of Delila and Molecular Information Theory: The Altenberg-Austin Workshop in Theoretical Biology Biological Information, Beyond Metaphor: Causality, Explanation, and Unification Altenberg, Austria, 11-14 July 2002.

Authors:  Thomas D Schneider
Journal:  Biol Theory       Date:  2006

7.  TRII: A Probabilistic Scoring of Drosophila melanogaster Translation Initiation Sites.

Authors:  Michael P Weir; Michael D Rice
Journal:  EURASIP J Bioinform Syst Biol       Date:  2010-12-27

8.  The human XPC DNA repair gene: arrangement, splice site information content and influence of a single nucleotide polymorphism in a splice acceptor site on alternative splicing and function.

Authors:  Sikandar G Khan; Vanessa Muniz-Medina; Tala Shahlavi; Carl C Baker; Hiroki Inui; Takahiro Ueda; Steffen Emmert; Thomas D Schneider; Kenneth H Kraemer
Journal:  Nucleic Acids Res       Date:  2002-08-15       Impact factor: 16.971

9.  Phosphate control over nitrogen metabolism in Streptomyces coelicolor: direct and indirect negative control of glnR, glnA, glnII and amtB expression by the response regulator PhoP.

Authors:  Antonio Rodríguez-García; Alberto Sola-Landa; Kristian Apel; Fernando Santos-Beneit; Juan F Martín
Journal:  Nucleic Acids Res       Date:  2009-03-24       Impact factor: 16.971

10.  Two novel FBN1 mutations associated with ectopia lentis and marfanoid habitus in two Chinese families.

Authors:  Liming Zhao; Ting Liang; Jianzhen Xu; Hui Lin; Dandan Li; Yanhua Qi
Journal:  Mol Vis       Date:  2009-04-23       Impact factor: 2.367

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.