Difference between revisions of "Part:BBa K2729011"
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==Characterization== | ==Characterization== | ||
The prM protein consists of an N-terminal pr domain followed by the M protein separated by a furin cleavage site.(15) The pr part of the protein consists mainly of β-strands, whereas the M portion consists of a linear structure followed by a mainly α-helical stem region and two transmembrane helices. | The prM protein consists of an N-terminal pr domain followed by the M protein separated by a furin cleavage site.(15) The pr part of the protein consists mainly of β-strands, whereas the M portion consists of a linear structure followed by a mainly α-helical stem region and two transmembrane helices. | ||
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+ | [[File:Tokyotech electrophoresis あはは.png|thumb|left|300px| '''Figure 1:''' '''Result of the Electrophoresis''' ]] | ||
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+ | <br> | ||
+ | As shown in Figure 1, the band of DENV2 prME come around 2,000 bp. | ||
+ | <br style="clear: both" /> | ||
==Sequence and Features== | ==Sequence and Features== |
Revision as of 18:25, 16 October 2018
DENV2 ancC-prM-E (Dengue Virus Serotype II)
Usage and Biology
Flavivirus Capsid (C), prM (precursor Membrane) and Envelope (E) are structural proteins responsible for gathering the viral RNA into a nucleocapsid that forms the core of a mature virus particle.
Characterization
The prM protein consists of an N-terminal pr domain followed by the M protein separated by a furin cleavage site.(15) The pr part of the protein consists mainly of β-strands, whereas the M portion consists of a linear structure followed by a mainly α-helical stem region and two transmembrane helices.
As shown in Figure 1, the band of DENV2 prME come around 2,000 bp.
Sequence and Features
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal XhoI site found at 946
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 1397
Illegal AgeI site found at 1108
Illegal AgeI site found at 1450 - 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI site found at 349