Difference between revisions of "Part:BBa K3504001"
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Nsp2 is one of four non structural proteins that together forms the main complex responsible for the synthesis positive-sense viral RNAs, results in the synthesis of both the genomic and subgenomic RNAs, of which the subgenomic RNA is produced in excess of the viral genome. Which allows the virus to self-replicate into millions of copies of the virus.
 
Nsp2 is one of four non structural proteins that together forms the main complex responsible for the synthesis positive-sense viral RNAs, results in the synthesis of both the genomic and subgenomic RNAs, of which the subgenomic RNA is produced in excess of the viral genome. Which allows the virus to self-replicate into millions of copies of the virus.
  
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==Usage==
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===Usage and Biology===
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==Characterization==
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==Improvements==
 
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<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>

Revision as of 17:33, 9 October 2020


nSp2 Protease-Eastern equine encephalitis virus

Part Description

Nsp2 is one of four non structural proteins that together forms the main complex responsible for the synthesis positive-sense viral RNAs, results in the synthesis of both the genomic and subgenomic RNAs, of which the subgenomic RNA is produced in excess of the viral genome. Which allows the virus to self-replicate into millions of copies of the virus.

Usage

Characterization

Improvements

Sequence and Features


Assembly Compatibility:
  • 10
    INCOMPATIBLE WITH RFC[10]
    Illegal EcoRI site found at 487
    Illegal SpeI site found at 435
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal EcoRI site found at 487
    Illegal SpeI site found at 435
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal EcoRI site found at 487
    Illegal BglII site found at 609
    Illegal BamHI site found at 471
    Illegal BamHI site found at 834
  • 23
    INCOMPATIBLE WITH RFC[23]
    Illegal EcoRI site found at 487
    Illegal SpeI site found at 435
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal EcoRI site found at 487
    Illegal SpeI site found at 435
    Illegal NgoMIV site found at 1276
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal BsaI.rc site found at 739
    Illegal BsaI.rc site found at 1386