Difference between revisions of "Part:BBa K801999:Design"
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===Design Notes=== | ===Design Notes=== | ||
− | ''' | + | '''Related BioBrick:''' |
− | <!--* | + | <!--*Other versions:[https://parts.igem.org/wiki/index.php?title=Part:BBa_?????? BBa_??????: Name_of_part] --> |
+ | <!--*Related BioBricks:[https://parts.igem.org/wiki/index.php?title=Part:BBa_?????? BBa_??????: Name_of_part] | ||
'''Cloning details:'''<br> | '''Cloning details:'''<br> | ||
− | <!--* | + | <!--*Designed in RFC10/RFC23/RFC25--> |
<!--*Mutation C889G to delete XbaI restriction site--> | <!--*Mutation C889G to delete XbaI restriction site--> | ||
− | <!--*Truncation upstream/downstream compared to template | + | <!--*Truncation upstream/downstream compared to template, ?explanation?--> |
'''Quality control measures:'''<br> | '''Quality control measures:'''<br> | ||
− | <!--*Test | + | <!--*Test digestion using ?enzyme1? & ?enzyme2?/Not yet performed--> |
<!--*Sequencing using primer ?primer_name?/Not yet sequenced--> | <!--*Sequencing using primer ?primer_name?/Not yet sequenced--> | ||
+ | <!--*Part was partly sequenced/Part was totally sequenced--> | ||
'''Backbone:'''<br> | '''Backbone:'''<br> | ||
Line 57: | Line 59: | ||
'''Source:'''<br> | '''Source:'''<br> | ||
− | <!--* | + | <!--*Commercial system: plasmid name, system name, company name--> |
− | <!--* | + | <!--*Plasmid: p???, provided by ?name_of_person?, ?institute/university?, ?country?--> |
<!--*Preexisting BioBrick ?Bba_number?--> | <!--*Preexisting BioBrick ?Bba_number?--> | ||
<!--*cDNA Clone: ?clone_name?, ?company_name?--> | <!--*cDNA Clone: ?clone_name?, ?company_name?--> | ||
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'''Literature references:'''<br> | '''Literature references:'''<br> | ||
<!--*[http://www.ncbi.nlm.nih.gov/pubmed/?PMID? '''Pubmed:''' ?Author(s)?, ?year?: ?title?]--> | <!--*[http://www.ncbi.nlm.nih.gov/pubmed/?PMID? '''Pubmed:''' ?Author(s)?, ?year?: ?title?]--> | ||
− | |||
− | ''' | + | '''Database references:'''<br> |
<!--*[http://www.ncbi.nlm.nih.gov/nuccore/?accessNr? '''GenBank''': ?title?]--> | <!--*[http://www.ncbi.nlm.nih.gov/nuccore/?accessNr? '''GenBank''': ?title?]--> | ||
<!--*[http://www.ebi.ac.uk/interpro/IEntry?ac=?accessNr? '''Interpro''': ?title?]--> | <!--*[http://www.ebi.ac.uk/interpro/IEntry?ac=?accessNr? '''Interpro''': ?title?]--> | ||
<!--*[http://www.uniprot.org/uniprot/?accessNr? '''Uniprot''': ?title?]--> | <!--*[http://www.uniprot.org/uniprot/?accessNr? '''Uniprot''': ?title?]--> | ||
<!--*[http://pfam.sanger.ac.uk/family/?accessNr? '''Pfam:''' ?title?]--> | <!--*[http://pfam.sanger.ac.uk/family/?accessNr? '''Pfam:''' ?title?]--> | ||
− | + | <!--*[http://www.rcsb.org/pdb/explore/explore.do?structureId=?accessNR? '''PDB:''' ?tile?]--> | |
− | + | <!--*[http://www.brenda-enzymes.info/php/result_flat.php4?ecno=?accessNr? '''Branda:''' ?title?]--> | |
− | <!--*[http://www.rcsb.org/pdb/explore/explore.do?structureId=? | + | |
− | + | ||
Revision as of 01:12, 22 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
Related BioBrick:
Quality control measures:
Backbone:
Protein coding:
Enzymatic activity:
Cytotoxicity:
Safety notes
Intellectual property:
Contact information:
Source
Source:
Organism:
References
Literature references:
Database references:
Test page for standardized BioBrick part descriptions
Keywords:
fluorescent, reporter, chromophore, luminescence, bioluminescence, photoprotein
Used abbreviations:
- GFP = Green Fluorescent Protein
Design Notes
Other versions of this BioBrick:
- The BioBrick BBa_I757008 encodes a yellow fluorescent protein (mVenus) derived from GFP
- The BioBrick BBa_I757008 encodes GFP in RFC25 for protein fusions
Cloning details:
- Part was designed in RFC10
- Mutation G381A to delete XbaI restriction site
- The correctness of the part was checked by sequencing
Protein coding:
- Green Fluorescent Protein [Nucleotide 1 to 714]
- The protein has the amino acid replacements Ser65Thr in order to increase fluorescence, photostability and to shift the major excitation peak to 488 nm. (see Heim et al., 1995)
- The protein encoded is posttranslationally modified by a cross-link between Ser65 and Gly67 to form the chromophore.
Enzymatic activity: none
Cytotoxicity: none
Source
Source:
- Amplified from plasmid: pSB1C3-GFP-generator, provided by Osamu Shimomura, Boston University School of Medicine, USA
Forward Primer:
5'- ATGATGATGATG - 3'
Reverse Primer:
5'- ATGATGATGATG - 3'
Organism:
- Sequence derived from Aequorea victoria
- Codon optimized 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/7854443 Pubmed: Heim, 1995: Improved green fluorescence.(Reference for Chromophore)]
Sequence references:
- [http://www.ncbi.nlm.nih.gov/nuccore/X83959.1 GenBank: 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]