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ABSTRACT: Unlabelled
Multiple sequence alignments become biologically meaningful only if conserved and functionally important residues and secondary structural elements preserved can be identified at equivalent positions. This is particularly important for transmembrane proteins like G-protein coupled receptors (GPCRs) with seven transmembrane helices. TM-MOTIF is a software package and an effective alignment viewer to identify and display conserved motifs and amino acid substitutions (AAS) at each position of the aligned set of homologous sequences of GPCRs. The key feature of the package is to display the predicted membrane topology for seven transmembrane helices in seven colours (VIBGYOR colouring scheme) and to map the identified motifs on its respective helices /loop regions. It is an interactive package which provides options to the user to submit query or pre-aligned set of GPCR sequences to align with a reference sequence, like rhodopsin, whose structure has been solved experimentally. It also provides the possibility to identify the nearest homologue from the available inbuilt GPCR or Olfactory Receptor cluster dataset whose association is already known for its receptor type.Availability
The database is available for free at mini@ncbs.res.in.
SUBMITTER: Nagarathnam B
PROVIDER: S-EPMC3218415 | biostudies-literature | 2011
REPOSITORIES: biostudies-literature
Nagarathnam Balasubramanian B Sankar Kannan K Dharnidharka Varadhan V Balakrishnan Veluchamy V Archunan Govindaraju G Sowdhamini Ramanathan R
Bioinformation 20111031 5
<h4>Unlabelled</h4>Multiple sequence alignments become biologically meaningful only if conserved and functionally important residues and secondary structural elements preserved can be identified at equivalent positions. This is particularly important for transmembrane proteins like G-protein coupled receptors (GPCRs) with seven transmembrane helices. TM-MOTIF is a software package and an effective alignment viewer to identify and display conserved motifs and amino acid substitutions (AAS) at eac ...[more]