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About PPRESearch
PPRESearch is the first web program to search for PPRE elements
online in the promoter region of any gene of interest.PPRESearch
is developed very carefully, taking into consideration all the
important parameters that are required for PPAR binding for
better accuracy in searching
the PPREs. The special features
which make PPRESearch unique and accurate in PPRE prediction are
as follows. PPRESearch searches for the
PPRE repeats from the
PPRE database. PPREs in the database are collected from the
literature and which were shown to be experimentally validated
through in vitro or in vivo binding assays. The
PPRE isoform specificity, binding efficiency, pubmed id and
their experimental validation assay
type (in vitro or
in vivo) for each PPRE as reported in the literatures are
also included in the database and are displayed in output,
PPRESearch allows
the user to set threshold binding efficiency
when searching for PPRE elements in a gene. In addition user
could also search for PPREs with few mismatches
from their PPRE
consensus. For better user experience and understanding the
PPRESearch displays the predicted promoter gene region with the
mismatch
nucleotide bases from its consensus in bold letters and
outputs the start position of the gene promoter region. The
information on PPRE isoform specificity
and its corresponding
binding strength helps to user to understand the PPAR isoform
that can bind to it and preferences of PPARs. By this way
PPRESearch
implicates the preferential binding of PPARs to PPRE
repeats.
Studies have
reported that the binding strength of PPAR to DNA
varies based on their matches from their flanking consensus (C(A/G)(A/G)A(A/T)CT).
PPREs having greater than 4 matches from their consensus of 7
nucleotides have better binding strength to PPARs. PPRESearch
searches for 5’ flanking
sequence of the predicted PPRE element
and displays the 5’ flanking sequence and its total number of
matches from its consensus. PPRESearch also allows
the user to
set threshold flanking count when predicting PPRE. Other studies
have also reported that PPARs can bind to the DR2 PPRE repeats.
In PPRESearch
the user can search for both DR1 and DR2 type PPRE
repeats. This is one of the special features in PPRESearch
program where other transcription factor binding
programs only
predicts DR1 repeats.
Thus using the above mentioned PPRESearch features provide the
good user flexibility which further helps to widen and narrow
their search for
better prediction of PPRE, making PPRESearch a
promising tool for the researches in PPRE prediction.
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