Difference between revisions of "Part:BBa K801999:Design"
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'''Cloning details:'''<br> | '''Cloning details:'''<br> | ||
*Part was designed in RFC10. | *Part was designed in RFC10. | ||
− | *Mutation | + | *Mutation G381A to delete XbaI restriction site |
− | + | *The correctness of part was checked by sequencing. | |
− | + | ||
'''Protein coding:'''<br> | '''Protein coding:'''<br> | ||
− | + | *Green Fluorescent Prtein [Nucleotide 1 to 714]> | |
− | + | *The protein has the amino acid replacements Ser65Thr in order to increased fluorescence, photostability, and to shift the major excitation peak to 488 nm. (see Heim et all., 1995) | |
− | + | *The protein encoded is posttranslationally modified by a cross-link between Ser65 and Gly67 to form the chromophor. | |
− | '''Enzymatic activity:''' | + | '''Enzymatic activity:''' |
− | + | *none | |
− | '''Cytotoxicity:''' | + | '''Cytotoxicity:''' |
− | + | *none | |
===Source=== | ===Source=== | ||
'''Source:''' | '''Source:''' | ||
− | Synthesized<br> | + | *Synthesized<br> |
− | '''Organism:''' | + | '''Organism:''' |
− | + | *Genesequence derived from ''Aequorea victoria'' | |
− | + | *Codonoptimized for ''Escherichia coli'' | |
===References=== | ===References=== |
Revision as of 19:48, 11 September 2012
Test page for standardized BioBrick part descriptions
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]
Keywords:
Abbreviations:
Design Notes
Other versions of this BioBrick:
Cloning details:
Protein coding:
Enzymatic activity:
Cytotoxicity:
Source
Source:
Organism:
References
Literature references:
Seqeuence references:
Structure reference:
Test page for standardized BioBrick part descriptions
Keywords:
fluorescent, reporter
Abbreviations:
- GFP = Green Fluorescent Protein
Design Notes
Other versions of this BioBrick:
- The BioBrick Bba_??? encodes a yellow fluorescent protein (mVenus)derived from GFP.
- The BioBrick Bba_??? encodes GFP in RFC25 for protein fusions.
Cloning details:
- Part was designed in RFC10.
- Mutation G381A to delete XbaI restriction site
- The correctness of part was checked by sequencing.
Protein coding:
- Green Fluorescent Prtein [Nucleotide 1 to 714]>
- The protein has the amino acid replacements Ser65Thr in order to increased fluorescence, photostability, and to shift the major excitation peak to 488 nm. (see Heim et all., 1995)
- The protein encoded is posttranslationally modified by a cross-link between Ser65 and Gly67 to form the chromophor.
Enzymatic activity:
- none
Cytotoxicity:
- none
Source
Source:
- Synthesized
Organism:
- Genesequence derived from Aequorea victoria
- Codonoptimized for Escherichia coli
References
Literature references:
- [http://www.ncbi.nlm.nih.gov/pubmed/20010584 Pubmed: Prasher, 1995: Using GFP to see the light.(Review)]
- [http://www.ncbi.nlm.nih.gov/pubmed/20010584 Pubmed: Prasher, 1995: Using GFP to see the light.(Review)]
Seqeuence references:
- [http://www.ncbi.nlm.nih.gov/nuccore/X83959.1 GeneBank: A.victoria mRNA for green fluorescent protein (ID:gfp1)]
- [http://www.ebi.ac.uk/interpro/IEntry?ac=IPR011584 Interpro: Green fluorescent protein-related ]
- [http://www.uniprot.org/uniprot/P42212 Uniprot: Green fluorescent protein]
- [http://pfam.sanger.ac.uk/family/PF01353 Pfam: Green fluorescent protein]
Structure reference:
- [http://www.rcsb.org/pdb/explore/explore.do?structureId=1EMA PDB: Green Fluorescent Protein from Aequorea victoria]