Difference between revisions of "Part:BBa K3102012"
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+ | __NOTOC__ | ||
+ | <partinfo>BBa_K3102012 short</partinfo> | ||
+ | TEV protease is the 27 kDa catalytic domain of the Nuclear Inclusion is a (NIa) protein encoded by the tobacco etch virus (TEV). Its sequence specificity is far more stringent than the sequence of factor Xa, thrombin, or enterokinase. TEV protease is a very useful reagent for cleaving fusion proteins. | ||
+ | |||
+ | Consequently, it’s an highly specific cysteine protease that recognizes the amino-acid sequence Glu-Asn-Leu-Tyr-Phe-Gln-(Gly/Ser)(BBa_K3102041) and cleaves between the Gln and Gly/Ser residues. | ||
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+ | |||
+ | <!-- Add more about the biology of this part here | ||
+ | ===Usage and Biology=== | ||
+ | |||
+ | <!-- --> | ||
+ | <span class='h3bb'>Sequence and Features</span> | ||
+ | <partinfo>BBa_K3102012 SequenceAndFeatures</partinfo> | ||
+ | |||
+ | |||
+ | <!-- Uncomment this to enable Functional Parameter display | ||
+ | ===Functional Parameters=== | ||
+ | <partinfo>BBa_K3102012 parameters</partinfo> | ||
+ | <!-- --> |
Latest revision as of 10:53, 16 October 2019
TEV Protease
TEV protease is the 27 kDa catalytic domain of the Nuclear Inclusion is a (NIa) protein encoded by the tobacco etch virus (TEV). Its sequence specificity is far more stringent than the sequence of factor Xa, thrombin, or enterokinase. TEV protease is a very useful reagent for cleaving fusion proteins.
Consequently, it’s an highly specific cysteine protease that recognizes the amino-acid sequence Glu-Asn-Leu-Tyr-Phe-Gln-(Gly/Ser)(BBa_K3102041) and cleaves between the Gln and Gly/Ser residues.
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 492
Illegal NgoMIV site found at 798
Illegal AgeI site found at 153 - 1000COMPATIBLE WITH RFC[1000]