Difference between revisions of "Part:BBa K861100"

 
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<partinfo>BBa_K861100 short</partinfo>
 
<partinfo>BBa_K861100 short</partinfo>
  
BcsA is considered to be the catalytic subunit for cellulose biosynthesis from the <i>Escherichia coli str. K-12</i>. The cellulose synthase is located in the cytoplasmic membrane with 8 to 10 predicted transmembrane domains.Besides the high homology to other processive glycosyltransferases, BcsA has been experimentally shown to bind the substrate UDP-glucose.
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BcsA,<a href="https://parts.igem.org/Part:BBa_K861110">BcsB</a>,  <a href="https://parts.igem.org/Part:BBa_K861120">BcsZ</a> and <a href="https://parts.igem.org/Part:BBa_K861130">BcsC</a> are involved in biosynthesis of cellulose in  <i>Escherichia coli</i>. BcsA is considered to be the catalytic subunit for cellulose biosynthesis. The cellulose synthetase is located in the cytoplasmic membrane with 8 to 10 predicted transmembrane domains.Besides the high homology to other processive glycosyltransferases, BcsA has been experimentally shown to bind the substrate UDP-glucose.
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<!-- Add more about the biology of this part here
 
<!-- Add more about the biology of this part here
 
===Usage and Biology===
 
===Usage and Biology===

Latest revision as of 09:39, 22 September 2012

BcsA,cellulose synthetase, catalytic subunit

BcsA,BcsB, BcsZ and BcsC are involved in biosynthesis of cellulose in Escherichia coli. BcsA is considered to be the catalytic subunit for cellulose biosynthesis. The cellulose synthetase is located in the cytoplasmic membrane with 8 to 10 predicted transmembrane domains.Besides the high homology to other processive glycosyltransferases, BcsA has been experimentally shown to bind the substrate UDP-glucose.

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 852
    Illegal BamHI site found at 926
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal AgeI site found at 1534
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 708