Hepatitis B virus DNA polymerase
| Protein P (DNA polymerase / RNase H) | |||||||
|---|---|---|---|---|---|---|---|
UniProt P03156 | | ||||||
| |||||||
| Protein P | |
|---|---|
| Identifiers | |
| Symbol | ? |
| InterPro | IPR037531 |
Hepatitis B virus DNA polymerase is a hepatitis B viral protein.[1][2] It is a DNA polymerase that can use either DNA or RNA templates and a ribonuclease H that cuts RNA in the duplex. Both functions are supplied by the reverse transcriptase (RT) domain.
Structure
The hepadnaviral P protein is organized into three domains: an N-terminal domain (InterPro: IPR000201) covering the terminal and the spacer, an RT domain related to every other reverse transcriptase domain, and a C-terminal domain (InterPro: IPR001462) regulating the RNase H activity.
Furthermore, hepadnavirus polymerases contain a terminal protein (TP) domain that contains a tyrosine residue that serves as a primer for the synthesis of the (-) DNA strand.[3]
Function
The Hepatitis B virus (HBV) polymerase is a multifunctional enzyme, with both RNA-dependent and DNA-dependent polymerase functions, as well as an RNase H function. It acts on the HBV pre-genomic RNA (pgRNA) to reverse transcribe it to form a new rcDNA molecule within a new capsid. (The pgRNA has another function of being translated into the viral polymerase and core proteins).[3]
HBV core protein dimers are required for packaging of the pgRNA/polymerase complex. Then, after viral polymerase binds to the packaging signal (Hɛ) found at the
Inside the capsid, the pgRNA undergoes reverse transcription, which is initiated by protein priming at the tyrosine residue of the HBV polymerase. Thus, the (-) DNA strand is made.[4] At the same time, the RNA template is degraded by the RNase H activity of the polymerase. A short RNA of about 15–18 nucleotides at the 5′ end of the pgRNA (including the 5′ DR1 sequence) is not degraded and it is used as primer for (+) DNA strand synthesis.[3]
The resulting RC-DNA is partially double stranded. The (-) DNA strand is longer than a genome length, with a covalently bound polymerase and a redundant flap at the 5′ end. However, the (+) DNA strand synthesis is uncompleted by the polymerase, and there is a gap exists down to the
References
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