Difference between revisions of "Part:BBa K4990013"
Line 19: | Line 19: | ||
REFERENCE | REFERENCE | ||
− | [1]Wilmaerts, D., Bayoumi, M., Dewachter, L., Knapen, W., Mika, J. T., Hofkens, J., Dedecker, P., Maglia, G., Verstraeten, N., & Michiels, J. (2018). The Persistence-Inducing Toxin HokB Forms Dynamic Pores That Cause ATP Leakage. mBio, 9(4), e00744-18. https://doi.org/10.1128/mBio.00744-18 | + | [1] Wilmaerts, D., Bayoumi, M., Dewachter, L., Knapen, W., Mika, J. T., Hofkens, J., Dedecker, P., Maglia, G., Verstraeten, N., & Michiels, J. (2018). The Persistence-Inducing Toxin HokB Forms Dynamic Pores That Cause ATP Leakage. mBio, 9(4), e00744-18. https://doi.org/10.1128/mBio.00744-18 |
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here |
Revision as of 13:22, 12 October 2023
HokB
As HokB belongs to the Hok/Gef family, it is predicted to be a single-span membrane peptide,which is a single-span membrane peptide with a long, negatively charged C-terminal periplasmic tail and a short, positively charged N terminus extending in the cytoplasm. HokB has the ability to selectively insert into the cellular membrane and aggregate to create pores with a diameter of around 0.64nm, which alters the membrane potential, depolarize the membrane, hinder ATP synthesis, decrease the cell's energy ratio, and lead to ATP leakage,[1] ultimately resulting in cell death.
Fig 1.Computational predictions of HokB using the Kyte-Doolittle algorithm and the CBS TMHMM tool.[1]
REFERENCE
[1] Wilmaerts, D., Bayoumi, M., Dewachter, L., Knapen, W., Mika, J. T., Hofkens, J., Dedecker, P., Maglia, G., Verstraeten, N., & Michiels, J. (2018). The Persistence-Inducing Toxin HokB Forms Dynamic Pores That Cause ATP Leakage. mBio, 9(4), e00744-18. https://doi.org/10.1128/mBio.00744-18
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]