BBa_J34803 1 BBa_J34803 ribosome binding site 2006-10-25T11:00:00Z 2015-08-31T04:08:46Z a Released HQ 2013 a false false _62_ 0 1085 62 In stock false a false Alexandra Choutko BBa_K844000 1 BBa_K844000 10x-Histidine (10x-His) Tag with double stop codon (TAATAA) 2012-10-01T11:00:00Z 2015-05-08T01:13:33Z Constructed through oligonucleotide annealing Released HQ 2013 10x-Histidine tag with double stop codon TAATAA to allow for better extraction of tagged products and protein termination in a single part. false false _1104_ 0 9404 9 In stock true none false Kathleen Miller annotation2206607 1 10x-Histidine Tag range2206607 1 1 30 annotation2206609 1 Stop range2206609 1 34 36 annotation2206608 1 Stop range2206608 1 31 33 BBa_K1988002 1 BBa_K1988002 Pit A: Inorganic P transporter from M. phosphovorus 2016-10-13T11:00:00Z 2016-10-14T05:31:24Z Genetic sequence from 'Deciphering the Genome of Polyphosphate Accumulating Actinobacterium Microlunatus Phosphovorus' by Kawakoshi, et. al. <h1>Pit Homologs</h1> <h2>Overview</h2> <p><b>Name:</b> Inorganic phosphate transporter</p> <p><b>Function: </b> Inorganic phosphate transporters are symporters of divalent metal-chelated phosphate and protons, and thus they require a proton motive force for phosphorus uptake. The electron transport chain is proposed to be the primary source of the proton motive force required for phosphate uptake in the PAO <i>???Ca</i> Accumulibacter phosphatis , and the electron transport chain may also be a source of the proton motive force for phosphate uptake in <i>M. phosphovorus</i>. Once the cell uptakes the phosphate, the phosphate is polymerized by PPK proteins.[1] </p> <p><b>In <i>Microlunatus phosphovorus</i>:</b> Polyphosphate accumulating organisms (PAOs) typically belong to either the Actinobacteria or the Proteobacteria phylum.<i>M. phosphovorus</i>, which has three Pit homologs, is among the species of Actinobacteria with the highest number of Pit genes. While gene expression and activity level of the gene product also contribute to the extent of PAO activity, the theoretical importance of multiple pit genes to PAO activity is supported by the high number of pit genes in the Proteobacteria <i>Candidatus</i> Accumulibacter phosphatis. [1] <i>???Ca</i> Accumulibacter phosphatis is a PAO that is considered crucial to the Enhanced Biological Phosphorus Removal process. [2]</p> <p><b>Location: </b> Membrane [3,4,5]</p> <p><b>Cofactors and Modifications</b> There are currently no known cofactors or modifications of the Pit homologs in <i>M. phosphovorus</i>.</p> <p><b>Images: </b> The three-dimensional structure of all proteins were predicted using the I-TASSER software [3]. All images shown are the models with the highest confidence, which is quantitatively measured with a C-score that typically falls within the range [-5,2], in which 2 represents the highest level of confidence, and -5 represents the lowest level of confidence.</p> <h2>Pit homolog A</h2> <p><b>Locus tag: </b> MLP_00530</p> <p><b>Image</b></p> <p>C-score: -1.69</p> <p><b>Gene length: </b> 1,176 base pairs</p> <p><b>Protein size:</b> 40.2 kDa</p> <p><b>Amino acid sequence: </b>MDWLLISVIA VIALALLFDF TNGFHDAANS VATVVATKAL PARLAPWFSA FFNFSAFFVV GTAVANTVAK VVNHDVEGVA VVFAALVAAI AWNYFTWYVG MPSSSSHAII GGLVGAGLAA GGTGAVNWGV VSKAVLAIVV SPLVAFTIAA VAMLILARIH KQWNLSEDAK AYKGLQLVSA AAVSFGHGAN DAQKTMGIMA AVLAAGGYIG LQADGTFEID WWIPLLAYSA ISIGTVWGGW KIIETMGLRI TKLRASSGLA ANVGAVTAIF GATGLGIPIS TTHAAASSVA GAGVASGKGV NGRVIREMVT AWVVTIPATV IVGFVMFKLT RLPGISAYLV VGAIMAALLT WIVWAMSKAM GADDLAKELP SDAETRQPVA ATRADGHGTG E [4] </p> <p><b>In <i>Microlunatus phosphovorus</i>:</b> Based on phylogenetic analysis, Pit homolog A is most homologous to Pit genes in the phylum Proteobacteria. [1]</p> <p><b>pH Range</b>The pit homologs in <i>M. phosphovorus</i> have yet to be characterized, and so there is no data for the pH range in which the pit homologs function.</p> <p><b>Temperature Range </b> The pit homologs in <i>M. phosphovorus</i> have yet to be characterized, and so there is no data for the pH range in which the Pit homologs function.</p> <h2>Pit homolog B</h2> <p><b>Locus tag:</b> MLP_29830</p> <p><b>Image</b></p> <p>C-score: -1.80 </p> <p><b>Gene length: </b> 1,224 base pairs</p> <p><b>Protein size:</b> 41.8 kDa</p> <p><b>Amino acid sequence: </b> MTEALFILVV VIVTALAFDF TNGFHDTGNA MATSIATGAL KPKAAVALSA ILNLVGAFLS IEVALTVSNK VVSIQDSSGV PIEALMGTPI LTIVFAGLVG GILWNLTTWL LGLPSSSSHA LFGGLIGSAI ASLGLSGVKW DGVITSILIP AFFAPLVAGL VAGIGTWTVY RLVAKIPESR RDAGFRWGQI GSASLVSLAH GTNDAQKTMG VITLALIAYG SWTDTHAIPF WVKAACAFAI AAGTYIGGWR VIRTLGKGLV EIHSPQGMAA ETASAAIILS SSHLGMALST THVATGSILG SGVGKRGAEV RWGVAGRMVV AWVTTLPAAA IVGALCWYLA SVIGGAVGIG VVFAILVAAA AWMFSRSRRT AINPNNVNAE WEGGLAVTEQ QDVAQETAKV PAGAERN [5]</p> <p><b>In <i>Microlunatus phosphovorus</i>:</b> Based on phylogenetic analysis, Pit homolog B is most homologous to Pit genes in the phylum Actinobacteria. [1]</p> <p><b>pH Range</b>The pit homologs in <i>M. phosphovorus</i> have yet to be characterized, and so there is no data for the pH range in which the pit homologs function.</p> <p><b>Temperature Range </b> The pit homologs in <i>M. phosphovorus</i> have yet to be characterized, and so there is no data for the pH range in which the Pit homologs function.</p> <h2>Pit homolog C</h2> <p><b>Locus tag: </b> MLP_51060</p> <p><b>Image</b></p> <p>C-score: -2.18</p> <p><b>Gene length: </b> 1,245 base pairs</p> <p><b>Protein size:</b> 42.2 kDa</p> <p><b>Amino acid sequence: </b>MTVLFVVITV IVVALIFDFT NGFHDSANSM AGPIATGALK PKTAVLIAAV LDVVGACLST EVARTISGGF FDDTLITAPI VLAGLVGAII WNLVTWLLGL PSSSSHALFG GLIGAVIVGA GFASVHYSVV VSKVLLPALV APAVAGIAAA GATALAYRVT RRTPRKYSEK GFKRGQAFTG SLVALAHGTS DGQKTMGVIT LVLIVSGFQA SGTGPHWWVV LAAGLATGLG TYSGGWRIMR TMGKGIVDIE TPQGAAAGAA TTATILASAN LGFGLSTTHV ATGSILGSGL GRRGATVRWS VARRMVTAWV LTLPGAAIVG GLAALLAEHG VVGSIILVSL LAIACVVIWR LSRRNQISHH NVTDSADVAV LSSAAASDTP GEPQLNGSRR SDIAPPAKAE RPKQKKRKKQ RSAA [6]</p> <p><b>In <i>Microlunatus phosphovorus</i>:</b> Based on phylogenetic analysis, Pit homolog C is most homologous to Pit genes in the phylum Actinobacteria. [1]</p> <p><b>pH Range</b>The pit homologs in <i>M. phosphovorus</i> have yet to be characterized, and so there is no data for the pH range in which the pit homologs function.</p> <p><b>Temperature Range </b> The pit homologs in <i>M. phosphovorus</i> have yet to be characterized, and so there is no data for the pH range in which the Pit homologs function.</p> <h2>References</h2> <p>[1] A. Kawakoshi, H. Nakazawa, J. Fukada, M. Sasagawa, Y. Katano, S. Nakamura, A. Hosoyama, H. Sasaki, N. Ichikawa, S. Hanada, Y. Kamagata, K. Nakamura, S. Yamazaki and N. Fujita, "Deciphering the Genome of Polyphosphate Accumulating Actinobacterium <i>Microlunatus phosphovorus</i>", <i>DNA Research</i>, vol. 19, no. 5, pp. 383-394, 2012.<br> [2] Y. Mao, D. Graham, H. Tamaki and T. Zhang, "Dominant and novel clades of <i>Candidatus</i> Accumulibacter phosphatis in 18 globally distributed full-scale wastewater treatment plants",<i>Scientific Reports</i>, vol. 5, p. 11857, 2015.<br> [3] "pit - Phosphate transporter - <i>Microlunatus phosphovorus</i> (strain ATCC 700054 / DSM 10555 / JCM 9379 / NBRC 101784 / NCIMB 13414 / VKM Ac-1990 / NM-1) - pit gene & protein", <i>Uniprot</i>, 2016. [Online]. Available: http://www.uniprot.org/uniprot/F5XGG0. [Accessed: 19- Jul- 2016].<br> [4] "pit - Phosphate transporter - <i>Microlunatus phosphovorus</i> (strain ATCC 700054 / DSM 10555 / JCM 9379 / NBRC 101784 / NCIMB 13414 / VKM Ac-1990 / NM-1) - pit gene & protein", <i>Uniprot</i>, 2016. [Online]. Available: http://www.uniprot.org/uniprot/F5XKC5. [Accessed: 19- Jul- 2016]. <br> [5] "pit - Phosphate transporter - <i>Microlunatus phosphovorus</i> (strain ATCC 700054 / DSM 10555 / JCM 9379 / NBRC 101784 / NCIMB 13414 / VKM Ac-1990 / NM-1) - pit gene & protein", <i>Uniprot</i>, 2016. [Online]. Available: http://www.uniprot.org/uniprot/F5XHB2. [Accessed: 19- Jul- 2016].<br> [6] Yang, R. Yan, A. Roy, D. Xu, J. Poisson and Y. Zhang, "The I-TASSER Suite: protein structure and function prediction", <i>Nature Methods</i>, vol. 12, no. 1, pp. 7-8, 2014.</p> false false _2455_ 26037 26037 9 false Codon optimized for E. coli K-12 using IDT Codon optimizer false Bowman Clark BBa_J23106 1 BBa_J23106 constitutive promoter family member 2006-08-13T11:00:00Z 2015-08-31T04:08:40Z Isolated from library of promoters Released HQ 2013 Later false true _52_ 0 483 95 In stock true N/A true John Anderson BBa_K1988003 1 BBa_K1988003 his-tagged Pit A homologue w/ Anderson Promoter J23106 2016-10-13T11:00:00Z 2016-10-14T05:34:34Z Genetic sequence from 'Deciphering the Genome of Polyphosphate Accumulating Actinobacterium Microlunatus Phosphovorus' by Kawakoshi, et. al. <h1>Pit Homologs</h1> <h2>Overview</h2> <p><b>Name:</b> Inorganic phosphate transporter</p> <p><b>Function: </b> Inorganic phosphate transporters are symporters of divalent metal-chelated phosphate and protons, and thus they require a proton motive force for phosphorus uptake. The electron transport chain is proposed to be the primary source of the proton motive force required for phosphate uptake in the PAO <i>???Ca</i> Accumulibacter phosphatis , and the electron transport chain may also be a source of the proton motive force for phosphate uptake in <i>M. phosphovorus</i>. Once the cell uptakes the phosphate, the phosphate is polymerized by PPK proteins.[1] </p> <p><b>In <i>Microlunatus phosphovorus</i>:</b> Polyphosphate accumulating organisms (PAOs) typically belong to either the Actinobacteria or the Proteobacteria phylum.<i>M. phosphovorus</i>, which has three Pit homologs, is among the species of Actinobacteria with the highest number of Pit genes. While gene expression and activity level of the gene product also contribute to the extent of PAO activity, the theoretical importance of multiple pit genes to PAO activity is supported by the high number of pit genes in the Proteobacteria <i>Candidatus</i> Accumulibacter phosphatis. [1] <i>???Ca</i> Accumulibacter phosphatis is a PAO that is considered crucial to the Enhanced Biological Phosphorus Removal process. [2]</p> <p><b>Location: </b> Membrane [3,4,5]</p> <p><b>Cofactors and Modifications</b> There are currently no known cofactors or modifications of the Pit homologs in <i>M. phosphovorus</i>.</p> <p><b>Images: </b> The three-dimensional structure of all proteins were predicted using the I-TASSER software [3]. All images shown are the models with the highest confidence, which is quantitatively measured with a C-score that typically falls within the range [-5,2], in which 2 represents the highest level of confidence, and -5 represents the lowest level of confidence.</p> <h2>Pit homolog A</h2> <p><b>Locus tag: </b> MLP_00530</p> <p><b>Image</b></p> <p>C-score: -1.69</p> <p><b>Gene length: </b> 1,176 base pairs</p> <p><b>Protein size:</b> 40.2 kDa</p> <p><b>Amino acid sequence: </b>MDWLLISVIA VIALALLFDF TNGFHDAANS VATVVATKAL PARLAPWFSA FFNFSAFFVV GTAVANTVAK VVNHDVEGVA VVFAALVAAI AWNYFTWYVG MPSSSSHAII GGLVGAGLAA GGTGAVNWGV VSKAVLAIVV SPLVAFTIAA VAMLILARIH KQWNLSEDAK AYKGLQLVSA AAVSFGHGAN DAQKTMGIMA AVLAAGGYIG LQADGTFEID WWIPLLAYSA ISIGTVWGGW KIIETMGLRI TKLRASSGLA ANVGAVTAIF GATGLGIPIS TTHAAASSVA GAGVASGKGV NGRVIREMVT AWVVTIPATV IVGFVMFKLT RLPGISAYLV VGAIMAALLT WIVWAMSKAM GADDLAKELP SDAETRQPVA ATRADGHGTG E [4] </p> <p><b>In <i>Microlunatus phosphovorus</i>:</b> Based on phylogenetic analysis, Pit homolog A is most homologous to Pit genes in the phylum Proteobacteria. [1]</p> <p><b>pH Range</b>The pit homologs in <i>M. phosphovorus</i> have yet to be characterized, and so there is no data for the pH range in which the pit homologs function.</p> <p><b>Temperature Range </b> The pit homologs in <i>M. phosphovorus</i> have yet to be characterized, and so there is no data for the pH range in which the Pit homologs function.</p> <h2>Pit homolog B</h2> <p><b>Locus tag:</b> MLP_29830</p> <p><b>Image</b></p> <p>C-score: -1.80 </p> <p><b>Gene length: </b> 1,224 base pairs</p> <p><b>Protein size:</b> 41.8 kDa</p> <p><b>Amino acid sequence: </b> MTEALFILVV VIVTALAFDF TNGFHDTGNA MATSIATGAL KPKAAVALSA ILNLVGAFLS IEVALTVSNK VVSIQDSSGV PIEALMGTPI LTIVFAGLVG GILWNLTTWL LGLPSSSSHA LFGGLIGSAI ASLGLSGVKW DGVITSILIP AFFAPLVAGL VAGIGTWTVY RLVAKIPESR RDAGFRWGQI GSASLVSLAH GTNDAQKTMG VITLALIAYG SWTDTHAIPF WVKAACAFAI AAGTYIGGWR VIRTLGKGLV EIHSPQGMAA ETASAAIILS SSHLGMALST THVATGSILG SGVGKRGAEV RWGVAGRMVV AWVTTLPAAA IVGALCWYLA SVIGGAVGIG VVFAILVAAA AWMFSRSRRT AINPNNVNAE WEGGLAVTEQ QDVAQETAKV PAGAERN [5]</p> <p><b>In <i>Microlunatus phosphovorus</i>:</b> Based on phylogenetic analysis, Pit homolog B is most homologous to Pit genes in the phylum Actinobacteria. [1]</p> <p><b>pH Range</b>The pit homologs in <i>M. phosphovorus</i> have yet to be characterized, and so there is no data for the pH range in which the pit homologs function.</p> <p><b>Temperature Range </b> The pit homologs in <i>M. phosphovorus</i> have yet to be characterized, and so there is no data for the pH range in which the Pit homologs function.</p> <h2>Pit homolog C</h2> <p><b>Locus tag: </b> MLP_51060</p> <p><b>Image</b></p> <p>C-score: -2.18</p> <p><b>Gene length: </b> 1,245 base pairs</p> <p><b>Protein size:</b> 42.2 kDa</p> <p><b>Amino acid sequence: </b>MTVLFVVITV IVVALIFDFT NGFHDSANSM AGPIATGALK PKTAVLIAAV LDVVGACLST EVARTISGGF FDDTLITAPI VLAGLVGAII WNLVTWLLGL PSSSSHALFG GLIGAVIVGA GFASVHYSVV VSKVLLPALV APAVAGIAAA GATALAYRVT RRTPRKYSEK GFKRGQAFTG SLVALAHGTS DGQKTMGVIT LVLIVSGFQA SGTGPHWWVV LAAGLATGLG TYSGGWRIMR TMGKGIVDIE TPQGAAAGAA TTATILASAN LGFGLSTTHV ATGSILGSGL GRRGATVRWS VARRMVTAWV LTLPGAAIVG GLAALLAEHG VVGSIILVSL LAIACVVIWR LSRRNQISHH NVTDSADVAV LSSAAASDTP GEPQLNGSRR SDIAPPAKAE RPKQKKRKKQ RSAA [6]</p> <p><b>In <i>Microlunatus phosphovorus</i>:</b> Based on phylogenetic analysis, Pit homolog C is most homologous to Pit genes in the phylum Actinobacteria. [1]</p> <p><b>pH Range</b>The pit homologs in <i>M. phosphovorus</i> have yet to be characterized, and so there is no data for the pH range in which the pit homologs function.</p> <p><b>Temperature Range </b> The pit homologs in <i>M. phosphovorus</i> have yet to be characterized, and so there is no data for the pH range in which the Pit homologs function.</p> <h2>References</h2> <p>[1] A. Kawakoshi, H. Nakazawa, J. Fukada, M. Sasagawa, Y. Katano, S. Nakamura, A. Hosoyama, H. Sasaki, N. Ichikawa, S. Hanada, Y. Kamagata, K. Nakamura, S. Yamazaki and N. Fujita, "Deciphering the Genome of Polyphosphate Accumulating Actinobacterium <i>Microlunatus phosphovorus</i>", <i>DNA Research</i>, vol. 19, no. 5, pp. 383-394, 2012.<br> [2] Y. Mao, D. Graham, H. Tamaki and T. Zhang, "Dominant and novel clades of <i>Candidatus</i> Accumulibacter phosphatis in 18 globally distributed full-scale wastewater treatment plants",<i>Scientific Reports</i>, vol. 5, p. 11857, 2015.<br> [3] "pit - Phosphate transporter - <i>Microlunatus phosphovorus</i> (strain ATCC 700054 / DSM 10555 / JCM 9379 / NBRC 101784 / NCIMB 13414 / VKM Ac-1990 / NM-1) - pit gene & protein", <i>Uniprot</i>, 2016. [Online]. Available: http://www.uniprot.org/uniprot/F5XGG0. [Accessed: 19- Jul- 2016].<br> [4] "pit - Phosphate transporter - <i>Microlunatus phosphovorus</i> (strain ATCC 700054 / DSM 10555 / JCM 9379 / NBRC 101784 / NCIMB 13414 / VKM Ac-1990 / NM-1) - pit gene & protein", <i>Uniprot</i>, 2016. [Online]. Available: http://www.uniprot.org/uniprot/F5XKC5. [Accessed: 19- Jul- 2016]. <br> [5] "pit - Phosphate transporter - <i>Microlunatus phosphovorus</i> (strain ATCC 700054 / DSM 10555 / JCM 9379 / NBRC 101784 / NCIMB 13414 / VKM Ac-1990 / NM-1) - pit gene & protein", <i>Uniprot</i>, 2016. [Online]. Available: http://www.uniprot.org/uniprot/F5XHB2. [Accessed: 19- Jul- 2016].<br> [6] Yang, R. Yan, A. Roy, D. Xu, J. Poisson and Y. Zhang, "The I-TASSER Suite: protein structure and function prediction", <i>Nature Methods</i>, vol. 12, no. 1, pp. 7-8, 2014.</p> false false _2455_ 26037 26037 9 false Codon optimized for E. coli K-12 using IDT Codon Optimizer false Bowman Clark component2510275 1 BBa_K1988002 component2510274 1 BBa_J34803 component2510279 1 BBa_K844000 component2510273 1 BBa_J23106 annotation2510274 1 BBa_J34803 range2510274 1 44 56 annotation2510273 1 BBa_J23106 range2510273 1 1 35 annotation2510275 1 BBa_K1988002 range2510275 1 63 1235 annotation2510279 1 BBa_K844000 range2510279 1 1244 1279 BBa_J34803_sequence 1 tcacacaggaaag BBa_J23106_sequence 1 tttacggctagctcagtcctaggtatagtgctagc BBa_K844000_sequence 1 catcatcaccatcaccaccatcatcaccattaataa BBa_K1988002_sequence 1 atggattggctgcttatttccgttattgcggttattgcgttggcccttttatttgacttcacgaatggatttcatgatgccgcaaactccgtagcgactgtagtagcaaccaaggctttgcctgctcgcctggccccatggttttccgctttctttaactttagtgctttttttgtggtaggcacggctgttgccaacactgtggcaaaggtagttaaccatgatgttgagggtgtagccgtagtgttcgccgcgttggtagccgccattgcgtggaattatttcacctggtacgtagggatgcccagtagcagctcgcacgctatcattggtgggttggtcggggctggattagcggcaggtggcacaggagcagtgaattggggagttgttagtaaggctgtccttgcaatcgttgtatctcccttggtggcttttacaattgcggcagttgcaatgctgattttggcgcgcattcacaagcagtggaacctttctgaagacgcgaaggcgtataaaggccttcaattggtctctgccgcggcagtgtcctttggacacggtgccaatgacgcacagaagacgatgggaattatggcggctgttctggccgcaggtggatacattgggctgcaagccgacggaacatttgaaattgattggtggattccgctgttagcttactctgcaatctcgattggaactgtatgggggggttggaaaatcattgagactatgggtctgcgtatcaccaaacttcgtgcttccagcgggctggcggccaacgtaggagctgtaaccgcaattttcggtgccacaggactgggcatccccatttccaccactcacgcggcagcatcatcagtagcaggggctggggttgccagcggcaagggagtaaacggacgtgtgattcgtgagatggtaactgcgtgggttgtgacaatccctgcaaccgttatcgtcgggttcgtaatgttcaaattaacccgcctgccgggaatctcagcttaccttgtagtgggcgcaattatggcagccttgttaacttggattgtttgggccatgtccaaagcgatgggggcggacgacttggcgaaagagctgccatccgacgcagaaacgcgccagccagttgcggctacacgcgcagatggacacgggacgggagaa BBa_K1988003_sequence 1 tttacggctagctcagtcctaggtatagtgctagctactagagtcacacaggaaagtactagatggattggctgcttatttccgttattgcggttattgcgttggcccttttatttgacttcacgaatggatttcatgatgccgcaaactccgtagcgactgtagtagcaaccaaggctttgcctgctcgcctggccccatggttttccgctttctttaactttagtgctttttttgtggtaggcacggctgttgccaacactgtggcaaaggtagttaaccatgatgttgagggtgtagccgtagtgttcgccgcgttggtagccgccattgcgtggaattatttcacctggtacgtagggatgcccagtagcagctcgcacgctatcattggtgggttggtcggggctggattagcggcaggtggcacaggagcagtgaattggggagttgttagtaaggctgtccttgcaatcgttgtatctcccttggtggcttttacaattgcggcagttgcaatgctgattttggcgcgcattcacaagcagtggaacctttctgaagacgcgaaggcgtataaaggccttcaattggtctctgccgcggcagtgtcctttggacacggtgccaatgacgcacagaagacgatgggaattatggcggctgttctggccgcaggtggatacattgggctgcaagccgacggaacatttgaaattgattggtggattccgctgttagcttactctgcaatctcgattggaactgtatgggggggttggaaaatcattgagactatgggtctgcgtatcaccaaacttcgtgcttccagcgggctggcggccaacgtaggagctgtaaccgcaattttcggtgccacaggactgggcatccccatttccaccactcacgcggcagcatcatcagtagcaggggctggggttgccagcggcaagggagtaaacggacgtgtgattcgtgagatggtaactgcgtgggttgtgacaatccctgcaaccgttatcgtcgggttcgtaatgttcaaattaacccgcctgccgggaatctcagcttaccttgtagtgggcgcaattatggcagccttgttaacttggattgtttgggccatgtccaaagcgatgggggcggacgacttggcgaaagagctgccatccgacgcagaaacgcgccagccagttgcggctacacgcgcagatggacacgggacgggagaatactagagcatcatcaccatcaccaccatcatcaccattaataa 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