ConSurf: Using Evolutionary Data to Raise Testable Hypotheses about Protein Function. Issue 3 (15th April 2013)
- Record Type:
- Journal Article
- Title:
- ConSurf: Using Evolutionary Data to Raise Testable Hypotheses about Protein Function. Issue 3 (15th April 2013)
- Main Title:
- ConSurf: Using Evolutionary Data to Raise Testable Hypotheses about Protein Function
- Authors:
- Celniker, Gershon
Nimrod, Guy
Ashkenazy, Haim
Glaser, Fabian
Martz, Eric
Mayrose, Itay
Pupko, Tal
Ben‐Tal, Nir - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Many mutations disappear from the population because they impair protein function and/or stability. Thus, amino acid positions that are essential for proper function evolve more slowly than others, or in other words, the slow evolutionary rate of a position reflects its importance. ConSurf (http://consurf.tau.ac.il), reviewed in this manuscript, exploits this to reveal key amino acid positions that are important for maintaining the native conformation(s) of the protein and its function, be it binding, catalysis, transport, etc. Given the sequence or 3D structure of the query protein as input, a search for similar sequences is conducted and the sequences are aligned. The multiple sequence alignment is subsequently used to calculate the evolutionary rates of each amino acid site, using Bayesian or maximum‐likelihood algorithms. Both algorithms take into account the evolutionary relationships between the sequences, reflected in phylogenetic trees, to alleviate problems due to uneven (biased) sampling in sequence space. This is particularly important when the number of sequences is low. The ConSurf‐DB, a new release of which is presented here, provides precalculated ConSurf conservation analysis of nearly all available structures in the Protein DataBank (PDB). The usefulness of ConSurf for the study of individual proteins and mutations, as well as a range of large‐scale, genome‐wide applications, is<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <p>Many mutations disappear from the population because they impair protein function and/or stability. Thus, amino acid positions that are essential for proper function evolve more slowly than others, or in other words, the slow evolutionary rate of a position reflects its importance. ConSurf (http://consurf.tau.ac.il), reviewed in this manuscript, exploits this to reveal key amino acid positions that are important for maintaining the native conformation(s) of the protein and its function, be it binding, catalysis, transport, etc. Given the sequence or 3D structure of the query protein as input, a search for similar sequences is conducted and the sequences are aligned. The multiple sequence alignment is subsequently used to calculate the evolutionary rates of each amino acid site, using Bayesian or maximum‐likelihood algorithms. Both algorithms take into account the evolutionary relationships between the sequences, reflected in phylogenetic trees, to alleviate problems due to uneven (biased) sampling in sequence space. This is particularly important when the number of sequences is low. The ConSurf‐DB, a new release of which is presented here, provides precalculated ConSurf conservation analysis of nearly all available structures in the Protein DataBank (PDB). The usefulness of ConSurf for the study of individual proteins and mutations, as well as a range of large‐scale, genome‐wide applications, is reviewed.</p> </abstract> … (more)
- Is Part Of:
- Israel journal of chemistry. Volume 53:Issue 3/4(2013)
- Journal:
- Israel journal of chemistry
- Issue:
- Volume 53:Issue 3/4(2013)
- Issue Display:
- Volume 53, Issue 3/4 (2013)
- Year:
- 2013
- Volume:
- 53
- Issue:
- 3/4
- Issue Sort Value:
- 2013-0053-NaN-0000
- Page Start:
- 199
- Page End:
- 206
- Publication Date:
- 2013-04-15
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1869-5868/issues ↗
http://www.sciencefromisrael.com/link.asp?id=300168 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/ijch.201200096 ↗
- Languages:
- English
- ISSNs:
- 0021-2148
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4583.802000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3949.xml