Difference between revisions of "Part:BBa K4165156"
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The amino acid sequence of the MM2 peptide is LTPHKHHKHLHA. Its charge is +2.5, hydrophobicity is 33 %, molecular weight is 1455.67 Da. MM2 can reduce tau aggregates of full-length tau but not PHF* or PHF (VQIINK and VQIVYK respectively). | The amino acid sequence of the MM2 peptide is LTPHKHHKHLHA. Its charge is +2.5, hydrophobicity is 33 %, molecular weight is 1455.67 Da. MM2 can reduce tau aggregates of full-length tau but not PHF* or PHF (VQIINK and VQIVYK respectively). | ||
+ | <span class='h3bb'> <p style=" font-weight: bold; font-size:17px;"> Sequence and Features</p> </span> | ||
+ | <partinfo>BBa_K4165156 SequenceAndFeatures</partinfo> | ||
===Dry Lab=== | ===Dry Lab=== | ||
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===References=== | ===References=== | ||
1. Malhis, M. (2021). Selection and characterization of D-enantiomeric peptides for the investigation of options for therapy and diagnosis of Alzheimer's disease . University of Bayreuth (Germany). | 1. Malhis, M. (2021). Selection and characterization of D-enantiomeric peptides for the investigation of options for therapy and diagnosis of Alzheimer's disease . University of Bayreuth (Germany). |
Revision as of 17:22, 10 October 2022
MM2 Peptide
Tau binding peptide targeting the PHF seed of Tau
Usage and Biology
The amino acid sequence of the MM2 peptide is LTPHKHHKHLHA. Its charge is +2.5, hydrophobicity is 33 %, molecular weight is 1455.67 Da. MM2 can reduce tau aggregates of full-length tau but not PHF* or PHF (VQIINK and VQIVYK respectively).
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Dry Lab
Modeling
MM2 is modeled by AlphaFold2, ITASSER and TrRosetta, best model obtained from TrRosetta.
Figure 1.: Predicted 3D structure of Synthetic peptide MM2.
Table 1: Quality assessment parameters of MM2 model.
References
1. Malhis, M. (2021). Selection and characterization of D-enantiomeric peptides for the investigation of options for therapy and diagnosis of Alzheimer's disease . University of Bayreuth (Germany).