Difference between revisions of "Part:BBa K3394003:Design"
(→References) |
(→Source) |
||
| Line 13: | Line 13: | ||
===Source=== | ===Source=== | ||
| − | + | GenBank: HQ657205.1 (NCBI) | |
===References=== | ===References=== | ||
Lu, P., & Feng, M. G. (2008). Bifunctional enhancement of a β-glucanase-xylanase fusion enzyme by optimization of peptide linkers. Applied microbiology and biotechnology, 79(4), 579-587. | Lu, P., & Feng, M. G. (2008). Bifunctional enhancement of a β-glucanase-xylanase fusion enzyme by optimization of peptide linkers. Applied microbiology and biotechnology, 79(4), 579-587. | ||
Latest revision as of 11:48, 22 October 2020
Glycine-serine (GS) linker
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
We decided to include GS linker in our design to keep the catalytic domain of endo5a separate from the cellulose-binding domain (CBD).
Source
GenBank: HQ657205.1 (NCBI)
References
Lu, P., & Feng, M. G. (2008). Bifunctional enhancement of a β-glucanase-xylanase fusion enzyme by optimization of peptide linkers. Applied microbiology and biotechnology, 79(4), 579-587.