Abstract
During studies of APOBEC3 (A3) anti-human immunodeficiency virus type 1 (anti-HIV-1) mechanisms, we identified a single cysteine at position 320 (C320) that disrupts A3DE activity. This residue is located in the recently identified DNA binding domain in A3G. Replacing C320 with a corresponding tyrosine from A3F (Y307) increased A3DE antiviral activity more than 20-fold. Conversely, replacing A3F Y307 with a cysteine or inserting a similar cysteine into A3B or A3G disrupted the anti-HIV activity of A3. Further investigation uncovered that C320 significantly reduces A3DE catalytic activity.
Cite
CITATION STYLE
Dang, Y., Abudu, A., Son, S., Harjes, E., Spearman, P., Matsuo, H., & Zheng, Y.-H. (2011). Identification of a Single Amino Acid Required for APOBEC3 Antiretroviral Cytidine Deaminase Activity. Journal of Virology, 85(11), 5691–5695. https://doi.org/10.1128/jvi.00243-11
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