NOTE:
- ProTG4, approximates the sequence of a generic protein from an in silico library of TG4-mapped peptides (7-20 aa).
- ProTG4, may also provide a quantitative measure to identify and thence annotate the canonical form for a generic protein sequence.
- Length ~7-50 amino acids::Library of equivalent length random sequences = 10000
- Length > 50 amino acids::Library of equivalent length random sequences = 100000
- The confidence-of-sequence-identity, is then the weighted average of identical amino acid encompassing fragments from a randomly generated library of equivalent lengths.
- The mapped peptides have been shown to associate with short linear motifs (SLiMS) (p-value < 0.05) and may predispose the protein to misfolding-induced proteostasis.
- Since, the speed of calculation depends on the length of the INPUT sequences,
DO NOT PRESS THE SUBMIT BUTTON MORE THAN ONCE
- For best results (10-20s), please choose fewer (~5- 10) sequences of proteins (>100 amino acids).
- These may be downloaded (Save As) or viewed directly
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Contact information:
Siddhartha Kundu, MD, PhD
Associate Professor,
Department of Biochemistry,
All India Institute of Medical Sciences,
Ansari Nagar, New Delhi - 110029, INDIA
Email:
sidddhartha_kundu@yahoo.co.in
siddhartha_kundu@aiims.edu
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Schema to delineate peptides that correspond to TG4 |
| Algorithm/pipeline of back-end analysis [1] |
| Codon table to identify suitable amino acids for peptide model of TG4 (~PTG4) [1] |
CITATION: [1] Kundu S. Mathematical model of a short translatable G-quadruplex and an assessment of its relevance to misfolding-induced proteostasis. Math Biosc Eng.(2020), 17(3):2470-2493. doi: 10.3934/mbe.2020135 PMID: 32233549 |
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