BBa_I11030 1 BBa_I11030 integrase from E. coli phage P22 2004-09-02T11:00:00Z 2015-08-31T04:07:30Z Nuc Acid Res, 2001; 29(11):2205-2216 P22 Integrase with LVA tag false false _2_ 0 102 7 It's complicated false false mschomp annotation1126751 1 LVA range1126751 1 1162 1194 annotation2214028 1 Help:Barcodes range2214028 1 1201 1225 annotation1126718 1 Integrase p22 range1126718 1 1 1161 annotation1126806 1 stop range1126806 1 1195 1200 BBa_B0034 1 BBa_B0034 RBS (Elowitz 1999) -- defines RBS efficiency 2003-01-31T12:00:00Z 2015-08-31T04:07:20Z Released HQ 2013 RBS based on Elowitz repressilator. false true _1_ 0 24 7 In stock false Varies from -6 to +1 region from original sequence to accomodate BioBricks suffix. <p>No secondary structures are formed in the given RBS region. Users should check for secondary structures induced in the RBS by upstream and downstream elements in the +50 to -50 region, as such structures will greatly affect the strength of the RBS. Contact info for this part: <a href="mailto:(bchow@media.mit.edu)">Brian Chow</a> true Vinay S Mahajan, Voichita D. Marinescu, Brian Chow, Alexander D Wissner-Gross and Peter Carr IAP, 2003. annotation23325 1 conserved range23325 1 5 8 BBa_K200021 1 BBa_K200021 pLacI+RBS 2009-10-14T11:00:00Z 2015-05-08T01:11:21Z Both parts from the Registry Promoter for the LacI gene ligated to a RBS false false _298_ 0 5155 9 It's complicated false N/A false Royah Vaezi component2041370 1 BBa_R0011 component2041376 1 BBa_B0034 annotation2041370 1 BBa_R0011 range2041370 1 1 54 annotation2041376 1 BBa_B0034 range2041376 1 64 75 BBa_K318013 1 BBa_K318013 T + pLac + RBS + Int (P22) + T 2010-07-12T11:00:00Z 2015-05-08T01:11:57Z Biobricks This composite part is an inducible P22 Int integrase generator which acts on the P22 attB and attP recombination sites. It is composed of the following biobricks: BBa_B1006, BBa_K200021, BBa_I11030, BBa_B1006. false false _438_ 0 4845 9 Not in stock false To minimize potential transcription due to upstream promoter activity, a terminator was placed upstream of the pLac promoter. A terminator was placed downstream of the Int encoding sequence to end transcription after the recombinase is produced. Note that to fully repress the pLac promoter, overproduction of the lacI repressor protein is necessary. false Nathaniel Pantalone, Justin Vrana component2257266 1 BBa_B1006 component2257284 1 BBa_B1006 component2257274 1 BBa_K200021 component2257279 1 BBa_I11030 annotation2257279 1 BBa_I11030 range2257279 1 129 1353 annotation2257284 1 BBa_B1006 range2257284 1 1362 1400 annotation2257266 1 BBa_B1006 range2257266 1 1 39 annotation2257274 1 BBa_K200021 range2257274 1 48 122 BBa_R0011 1 lacI+pL Promoter (lacI regulated, lambda pL hybrid) 2003-01-31T12:00:00Z 2015-05-08T01:14:14Z represillator of Elowitz and Leibler (2000) Released HQ 2013 Inverting regulatory region controlled by LacI (<bb_part>BBa_C0010</bb_part>, <bb_part>BBa_C0011</bb_part>, etc.) <p> The PLlac 0-1 promoter is a hybrid regulatory region consisting of the promoter P(L) of phage lambda with the cI binding sites replaced with lacO1. The hybrid design allows for strong promotion that can nevertheless be tightly repressed by LacI, the Lac inhibitor (i.e. repressor) (<bb_part>BBa_C0010</bb_part>) ([LUTZ97]). The activity of the promoter can be regulated over a >600-fold range by IPTG in E.Coli DH5-alpha-Z1 (same paper reference). false true _1_ 0 24 7 In stock false <P> <P>hybrid promoter design to create strong promoter that is, at the same time, highly repressible. note that the upstream operator installed in this hybrid is slightly different than the one in the original source (Lutz and Bujard, 1997). the most upstream operator region is slightly truncated in the represillator version, so that both operators in the hybrid are the same sequence. see references for details. also, the sequence has been truncated after the transcriptional start site.<P>LacI binds to this regulator. This part is incompatible with species containing active LacI coding regions. Lactose and IPTG disable the operation of LacI and increase transcription. This part is incompatible with environments containing lactose or lactose analogs. true Neelaksh Varshney, Grace Kenney, Daniel Shen, Samantha Sutton annotation2002 1 -10 range2002 1 43 48 annotation2001 1 lac O1 range2001 1 26 42 annotation2000 1 -35 range2000 1 20 25 annotation7064 1 BBa_R0011 range7064 1 1 54 annotation1999 1 lac O1 range1999 1 3 19 BBa_B1006 1 BBa_B1006 Terminator (artificial, large, %T~>90) 2006-08-30T11:00:00Z 2015-08-31T04:07:21Z modified E. coli thr terminator, replaced all A-T pairs in stem with C-G pairs Released HQ 2013 Artificial terminator, estimated %T~>90% *8bp stem, 6nt loop *Bidirectional, estimated reverse %T~>90% false true _41_ 0 745 41 In stock false Bidirectional, with the reverse estimated to be less effective than the forward. Has a polyA tail of 9 residues. true Haiyao Huang annotation1898431 1 PolyA range1898431 1 1 9 annotation1898430 1 PolyA range1898430 1 32 39 annotation1898428 1 B1006 range1898428 1 1 39 annotation1898429 1 modified thr terminator range1898429 1 10 31 BBa_B0034_sequence 1 aaagaggagaaa BBa_B1006_sequence 1 aaaaaaaaaccccgcccctgacagggcggggtttttttt BBa_K200021_sequence 1 aattgtgagcggataacaattgacattgtgagcggataacaagatactgagcacatactagagaaagaggagaaa BBa_R0011_sequence 1 aattgtgagcggataacaattgacattgtgagcggataacaagatactgagcaca BBa_I11030_sequence 1 atgtcactattccgcagaggtgaaacctggtacgccagtttcacattgccgaacggcaaaagatttaagcagtctcttgggacaaaggacaaaaggcaggccacagagcttcatgacaagctgaaggcagaagcatggagggtaagtaaattaggagagacgcctgacatgacttttgagggggcctgtgtcaggtggttagaggagaaggcgcataagaagtcgctggatgatgacaagagtcggataggattctggctccagcattttgcaggaatgcagttgaaggatattaccgagacgaagatttactccgccatccagaagataactaatcggcggcatgaggaaaactggaagttaatggatgaagcatgcaggaagaatgggaagcagcctccggtattcaagcctaagccggcagcagtagctacaaaagcaactcacctttcattcattaaggcactcctccgggctgctgaacgcgaatggaagatgctggataaggctccgatcatcaaagttcctcagccgaaaaataagcgtatccgctggcttgagcctcacgaggcaaaaaggttgattgatgaatgccaggaaccgctaaagtcagtcgtagagtttgcgctttctactggcttaaggcggtctaacattatcaatctggagtggcagcagatagacatgcaacgaaaggtggcatggatacacccggaacaaagcaagtctaatcatgccattggagtggcgctgaatgataccgcttgccgggtgctgaaaaagcaaatcggcaatcatcacaaatgggtgttcgtctacaaggaaagcagcaccaaaccagacggaactaaatcacctgtagtgaggaagatgcgctatgacgctaatactgcatggagggcagcattaaaacgagcgggcattgaagacttccgttttcatgacctgaggcacacgtgggcaagttggttagttcaggctggcgttccgatttcggtattgcaggaaatgggtggctgggagtctatcgaaatggttcgccgatatgctcatctggcaccaaatcacctgactgaacatgctcgacaaattgactcgatttttggtacttctgtcccaaatatgtcccacagtaaaaataaggaaggcacgaataatacggcagcaaacgacgaaaactacgctttagtagcttaataaccctgatagtgctagtgtagatccc BBa_K318013_sequence 1 aaaaaaaaaccccgcccctgacagggcggggtttttttttactagagaattgtgagcggataacaattgacattgtgagcggataacaagatactgagcacatactagagaaagaggagaaatactagatgtcactattccgcagaggtgaaacctggtacgccagtttcacattgccgaacggcaaaagatttaagcagtctcttgggacaaaggacaaaaggcaggccacagagcttcatgacaagctgaaggcagaagcatggagggtaagtaaattaggagagacgcctgacatgacttttgagggggcctgtgtcaggtggttagaggagaaggcgcataagaagtcgctggatgatgacaagagtcggataggattctggctccagcattttgcaggaatgcagttgaaggatattaccgagacgaagatttactccgccatccagaagataactaatcggcggcatgaggaaaactggaagttaatggatgaagcatgcaggaagaatgggaagcagcctccggtattcaagcctaagccggcagcagtagctacaaaagcaactcacctttcattcattaaggcactcctccgggctgctgaacgcgaatggaagatgctggataaggctccgatcatcaaagttcctcagccgaaaaataagcgtatccgctggcttgagcctcacgaggcaaaaaggttgattgatgaatgccaggaaccgctaaagtcagtcgtagagtttgcgctttctactggcttaaggcggtctaacattatcaatctggagtggcagcagatagacatgcaacgaaaggtggcatggatacacccggaacaaagcaagtctaatcatgccattggagtggcgctgaatgataccgcttgccgggtgctgaaaaagcaaatcggcaatcatcacaaatgggtgttcgtctacaaggaaagcagcaccaaaccagacggaactaaatcacctgtagtgaggaagatgcgctatgacgctaatactgcatggagggcagcattaaaacgagcgggcattgaagacttccgttttcatgacctgaggcacacgtgggcaagttggttagttcaggctggcgttccgatttcggtattgcaggaaatgggtggctgggagtctatcgaaatggttcgccgatatgctcatctggcaccaaatcacctgactgaacatgctcgacaaattgactcgatttttggtacttctgtcccaaatatgtcccacagtaaaaataaggaaggcacgaataatacggcagcaaacgacgaaaactacgctttagtagcttaataaccctgatagtgctagtgtagatccctactagagaaaaaaaaaccccgcccctgacagggcggggtttttttt igem2sbol 1 iGEM to SBOL conversion Conversion of the iGEM parts registry to SBOL2.1 James Alastair McLaughlin Chris J. Myers 2017-03-06T15:00:00.000Z