Beginning in mid-February 2008, the 1997-2007 online version of the Science Watch® newsletter, ESI-Topics.com, and in-cites.com, will all be featured together on the redesigned ScienceWatch.com. All previous content from the three sites will be permanently archived, and remain accessible from any existing bookmarks to the archived pages. No new content will be added to this site. Updates and new content (updated biweekly) are available at ScienceWatch.com now.

New Hot Paper Comments

By Peer Bork

ESI Special Topics, September 2007
Citing URL - http://www.esi-topics.com/nhp/2007/september-07-PeerBork.html

A closer look at the work of Peer Bork.Peer Bork answers a few questions about this month's new hot paper in the field of Biology & Biochemistry. The author has also sent along images of their work.


From •>>September 2007 - [late entry]

Field: Biology & Biochemistry
Article Title: SMART 5: domains in the context of genomes and networks
Authors: Letunic, I;Copley, RR;Pils, B;Pinkert, S;Schultz, J;Bork, P
Journal: NUCL ACID RES
Volume: 34
Issue:
Page: :D257-D260
Year: Sp. Iss. SI JAN 1 2006
* European Mol Biol Lab, Meyerhofstr 1, D-69012 Heidelberg, Germany.
* European Mol Biol Lab, D-69012 Heidelberg, Germany.
* Wellcome Trust Ctr Human Genet, Oxford OX3 7BN, England.
* Univ Wurzburg, Biozentrum, D-97074 Wurzburg, Germany.

ST:  Why do you think your paper is highly cited?


“We use SMART daily for many purposes in many very different projects such as genome annotation, domain network analysis, and the identification of binding sites for chemicals, to mention a few.”

SMART (Simple Modular Architecture Research Tool) is a domain search tool that allows the scanning of genes and genomes for many manually curated protein modules which often imply a new functionality for unannotated genes.

Since its first version was published in 1998—"SMART, a simple modular architecture research tool: Identification of signaling domains" with a total of 1,072 citations, according to the ISI Web of KnowledgeSM—there is a constant demand for this functionality, one which might even slightly increase, as sequencing technologies are becoming cheaper.

ST:  Does it describe a new discovery, methodology, or synthesis of knowledge?

The paper describes a new version of our software and resource with a number of new features implemented to make SMART more accessible to scientists from different fields. The new "Genomic" mode in SMART makes it easy to analyze domain architectures in completely sequenced genomes. The network context is now displayed in the results page for more than 350,000 proteins, enabling easy analyses of domain interactions.

ST:  Would you summarize the significance of your paper in layman’s terms?

Function prediction by homology is still a key to annotate genes and genomes, although the first widely used tools, such as fasta and blast, had been already developed in the 80s. (FASTA is an algorithm for rapid comparison and alignment of pairs of protein and DNA sequences developed for database searches. The BLAST algorithm was developed to perform similarity searches faster than FASTA.) SMART provides many manually derived profiles for protein domains, functional units of proteins that can be quickly scanned against large sequence data sets for their annotation. As it is sensitive and accurate, it is one of a few important tools used by a large community of genome researchers and molecular biologists.

ST:  How did you become involved in this research, and were there any particular problems encountered along the way?

I was one of a few researchers who identified many novel protein domains in the 80s and 90s. At that time, a new functional understanding using this domain knowledge was the research goal, but it became clear that, with the growing collection of domains, the identification of already classified domains in novel genes was equally important. Thus a number of domain databases had been established in the mid-90s, among them SMART. Over the years, more domains have been added and the tools have been improved.

ST:  Where do you see your research leading in the future?

We use SMART daily for many purposes in many very different projects such as genome annotation, domain network analysis, and the identification of binding sites for chemicals, to mention a few.

ST:  Are there any social or political implications for your research?

We do basic scientific research and thus, there are only interesting social aspects involving changes within the research field. For example, in the 90th, the domain database developers were sort of competing. They have since learned, over time, to instead join forces and bundle their resources, which is much more beneficial for the scientific community.End

Dr. Peer Bork
Senior Group Leader
Head of Unit
Structural and Computational Biology
European Molecular Biology Lab (EMBL)
Heidelberg, Germany
Web


A Closer Look...

A closer look... Below are images sent in by Peer Bork which correspond with the featured paper, or current research.

Figure 1:

Click for larger image
Click for larger image

Figure 1: SMART protein analysis: "Search results page for a tyrosine kinase, with string interaction network in a popup."
  

Figure 2:

Click for larger image
Click for larger image

Figure 2: TyrKc annotation: "Annotation page for TyrKc."
     

ESI Special Topics, September 2007
Citing URL - http://www.esi-topics.com/nhp/2007/september-07-PeerBork.html

•> Search Special Topics
New Hot Papers Menu || All Topics Menu
New Hot Papers Comments Menu
Help || About || Contact

ScienceWatch.com - Tracking Trends and Perfomance in Basic Research
Go to the new ScienceWatch.com

Write to the Webmaster with questions/comments. Terms of Usage.
The Research Services Group of Thomson Scientific |
(c) 2008 The Thomson Corporation.