Difference between revisions of "Part:BBa K1442033"
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<partinfo>BBa_K1442033 short</partinfo> | <partinfo>BBa_K1442033 short</partinfo> | ||
− | + | Each unique RNA dependent RNA polymerase (RdRP) initiates de novo replication of a RNA strand by interacting with RdRP-specific RNA sequences, henceforth called RdRP/RNA promoters. Please refer to Section: RdRP function for further details. The RdRP chosen for our project is taken from the Hepatitis C virus (HCV). The C2 RNA promoter was identified as such by Heinz, Kao (2000) , along with a number of other sequences. All of them possess a few common characteristics: an initiation cytidylate at the 3’ end, where the replication starts; and a stable secondary structure- single stranded tail and a stem of various length. Replication stops at the 5’ end. | |
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+ | == Usage == | ||
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+ | Used as an RNA promoter to direct replication by RdRP. | ||
+ | |||
+ | |||
+ | == Mathematical Modelling == | ||
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Revision as of 01:17, 16 October 2014
C2 3
Each unique RNA dependent RNA polymerase (RdRP) initiates de novo replication of a RNA strand by interacting with RdRP-specific RNA sequences, henceforth called RdRP/RNA promoters. Please refer to Section: RdRP function for further details. The RdRP chosen for our project is taken from the Hepatitis C virus (HCV). The C2 RNA promoter was identified as such by Heinz, Kao (2000) , along with a number of other sequences. All of them possess a few common characteristics: an initiation cytidylate at the 3’ end, where the replication starts; and a stable secondary structure- single stranded tail and a stem of various length. Replication stops at the 5’ end.
Usage
Used as an RNA promoter to direct replication by RdRP.
Mathematical Modelling
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 38
Illegal NgoMIV site found at 67 - 1000COMPATIBLE WITH RFC[1000]