By Peer Bork
ESI Special Topics,
September 2007
Citing URL - http://www.esi-topics.com/nhp/2007/september-07-PeerBork.html
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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.
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Why
do you think your paper is highly cited?
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“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.”
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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.
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.
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.
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.
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.
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.
Dr. Peer Bork
Senior Group Leader
Head of Unit
Structural and Computational Biology
European Molecular Biology Lab (EMBL)
Heidelberg, Germany
Web
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A Closer Look...
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Below
are images sent in by Peer Bork which correspond with the featured
paper, or current research. |
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Figure 1:

Click for
larger image |
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Figure 1: SMART protein analysis: "Search
results page for a tyrosine kinase, with string
interaction network in a popup." |
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Figure 2:

Click for
larger image |
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Figure 2:
TyrKc
annotation: "Annotation page for TyrKc." |
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ESI Special Topics,
September 2007
Citing URL - http://www.esi-topics.com/nhp/2007/september-07-PeerBork.html
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