Part:BBa_K3102042:Design
Cellulose Acetate degradation (CAE, EG1, Tev, HlyA)
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 2958
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 124
Illegal NgoMIV site found at 1234
Illegal NgoMIV site found at 4120
Illegal NgoMIV site found at 4426
Illegal AgeI site found at 254
Illegal AgeI site found at 341
Illegal AgeI site found at 479
Illegal AgeI site found at 662
Illegal AgeI site found at 710
Illegal AgeI site found at 878
Illegal AgeI site found at 1091 - 1000COMPATIBLE WITH RFC[1000]
Design Notes
none
Source
CAE, Neisseria Sicca, sequence found through genebank : https://www.ncbi.nlm.nih.gov/protein/BAJ21448.1
EG1, Neisseria Sicca, sequence found through genebank https://www.ncbi.nlm.nih.gov/protein/BAJ21449.1
TEV protease, Tobacco etch virus, sequence found through Uniprot https://www.uniprot.org/uniprot/Q0GDU8
Promoter (BBa_I719005), RBS (BBa_B0034) and Terminator (BBa_B0015) are from the iGEM Registry.
References
Moriyoshi K, Ohmoto T, Ohe T, Sakai K. Role of Endo-1,4-β-glucanases from Neisseria sicca SB in synergistic degradation of cellulose acetate. Biosci Biotechnol Biochem. 2003;67(2):250–7.
Phan, J., Zdanov, A., Evdokimov, A. G., Tropea, J. E., Peters, H. P. K., Kapust, R. B., Li, M., Wlodawer, A., and Waugh, D. S. (2002). Structural basis for the substrate specificity of tobacco etch virus protease. J. Biol. Chem. 277: 50564-50572.