Difference between revisions of "Part:BBa K3739002"
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CBM can anchor onto cellulose and GFP can show whether CenA anchor or not. | CBM can anchor onto cellulose and GFP can show whether CenA anchor or not. | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
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+ | =====CBM===== | ||
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+ | Cellulose enzymes have two domains, and the one that helps bind to cellulose is called cellulose binding module (CBM), and therefore it helps our fusion protein bind to cellulose-rich cell wall. Here we choose the CBM of CenA from Cellulomonas fimi, which has been successfully expressed in Escherichia coli. | ||
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+ | =====GFP===== | ||
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+ | Protein tags are peptides genetically fused to the proteins of interest. There are many different kinds of tags developed for different purposes. For labeling experiments, normally the proteins of interest are tagged directly by fluorescent tags. Green fluorescent protein (GFP) make it easier to study protein localization, interactions and dynamics when fusing with other peptides and proteins. | ||
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Latest revision as of 02:13, 22 October 2021
his-GFP-CBM
CBM can anchor onto cellulose and GFP can show whether CenA anchor or not.
Usage and Biology
CBM
Cellulose enzymes have two domains, and the one that helps bind to cellulose is called cellulose binding module (CBM), and therefore it helps our fusion protein bind to cellulose-rich cell wall. Here we choose the CBM of CenA from Cellulomonas fimi, which has been successfully expressed in Escherichia coli.
GFP
Protein tags are peptides genetically fused to the proteins of interest. There are many different kinds of tags developed for different purposes. For labeling experiments, normally the proteins of interest are tagged directly by fluorescent tags. Green fluorescent protein (GFP) make it easier to study protein localization, interactions and dynamics when fusing with other peptides and proteins.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal AgeI site found at 1042
Illegal AgeI site found at 1132 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 73