© 2023 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | OphauG2|4876 |
| Gene name | |
| Location | Contig_422:7062..8707 |
| Strand | + |
| Gene length (bp) | 1645 |
| Transcript length (bp) | 1509 |
| Coding sequence length (bp) | 1509 |
| Protein length (aa) | 503 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF03155 | Alg6_Alg8 | ALG6, ALG8 glycosyltransferase family | 1.2E-174 | 17 | 494 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q7RXP5|ALG8_NEUCR | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=alg-8 PE=3 SV=2 | 6 | 502 | 0.0E+00 |
| sp|Q4IJT0|ALG8_GIBZE | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Gibberella zeae (strain PH-1 / ATCC MYA-4620 / FGSC 9075 / NRRL 31084) GN=ALG8 PE=3 SV=1 | 6 | 502 | 0.0E+00 |
| sp|Q5AWM9|ALG8_EMENI | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=alg8 PE=3 SV=1 | 6 | 476 | 0.0E+00 |
| sp|Q1DJR8|ALG8_COCIM | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Coccidioides immitis (strain RS) GN=ALG8 PE=3 SV=1 | 6 | 502 | 0.0E+00 |
| sp|Q2UB20|ALG8_ASPOR | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=alg8 PE=3 SV=1 | 1 | 502 | 0.0E+00 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q7RXP5|ALG8_NEUCR | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=alg-8 PE=3 SV=2 | 6 | 502 | 0.0E+00 |
| sp|Q4IJT0|ALG8_GIBZE | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Gibberella zeae (strain PH-1 / ATCC MYA-4620 / FGSC 9075 / NRRL 31084) GN=ALG8 PE=3 SV=1 | 6 | 502 | 0.0E+00 |
| sp|Q5AWM9|ALG8_EMENI | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=alg8 PE=3 SV=1 | 6 | 476 | 0.0E+00 |
| sp|Q1DJR8|ALG8_COCIM | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Coccidioides immitis (strain RS) GN=ALG8 PE=3 SV=1 | 6 | 502 | 0.0E+00 |
| sp|Q2UB20|ALG8_ASPOR | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=alg8 PE=3 SV=1 | 1 | 502 | 0.0E+00 |
| sp|Q2HA14|ALG8_CHAGB | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) GN=ALG8 PE=3 SV=1 | 6 | 502 | 0.0E+00 |
| sp|Q10479|ALG8_SCHPO | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=alg8 PE=3 SV=1 | 9 | 502 | 3.0E-178 |
| sp|Q5AJD2|ALG8_CANAL | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=ALG8 PE=3 SV=1 | 8 | 502 | 3.0E-151 |
| sp|Q6CJR2|ALG8_KLULA | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=ALG8 PE=3 SV=1 | 12 | 494 | 5.0E-149 |
| sp|P40351|ALG8_YEAST | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ALG8 PE=1 SV=1 | 20 | 492 | 3.0E-146 |
| sp|Q6FKM3|ALG8_CANGA | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=ALG8 PE=3 SV=1 | 25 | 494 | 2.0E-145 |
| sp|Q759R3|ALG8_ASHGO | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) GN=ALG8 PE=3 SV=2 | 14 | 494 | 6.0E-145 |
| sp|Q6BRE5|ALG8_DEBHA | Dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN=ALG8 PE=3 SV=1 | 26 | 502 | 4.0E-143 |
| sp|Q9BVK2|ALG8_HUMAN | Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Homo sapiens GN=ALG8 PE=1 SV=2 | 20 | 492 | 3.0E-110 |
| sp|Q9W3V8|ALG8_DROME | Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Drosophila melanogaster GN=xit PE=2 SV=1 | 15 | 489 | 4.0E-110 |
| sp|O80505|ALG8_ARATH | Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Arabidopsis thaliana GN=At2g44660 PE=2 SV=3 | 15 | 493 | 2.0E-108 |
| sp|Q0P5D9|ALG8_BOVIN | Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Bos taurus GN=ALG8 PE=2 SV=1 | 20 | 493 | 9.0E-107 |
| sp|Q6P8H8|ALG8_MOUSE | Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Mus musculus GN=Alg8 PE=2 SV=2 | 20 | 493 | 1.0E-103 |
| sp|Q554E2|ALG8_DICDI | Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Dictyostelium discoideum GN=alg8 PE=3 SV=1 | 140 | 489 | 2.0E-68 |
| sp|P52887|ALG8_CAEEL | Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Caenorhabditis elegans GN=C08H9.3 PE=3 SV=3 | 18 | 490 | 1.0E-67 |
| sp|Q54QG6|ALG6_DICDI | Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Dictyostelium discoideum GN=alg6 PE=3 SV=1 | 31 | 407 | 2.0E-36 |
| sp|Q802T2|ALG6_CHICK | Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Gallus gallus GN=ALG6 PE=2 SV=1 | 31 | 377 | 2.0E-35 |
| sp|Q9Y672|ALG6_HUMAN | Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Homo sapiens GN=ALG6 PE=1 SV=1 | 31 | 377 | 2.0E-33 |
| sp|Q5NVS8|ALG6_PONAB | Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Pongo abelii GN=ALG6 PE=2 SV=1 | 31 | 377 | 8.0E-33 |
| sp|Q9FF17|ALG6_ARATH | Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Arabidopsis thaliana GN=At5g38460 PE=2 SV=1 | 28 | 403 | 1.0E-30 |
| sp|Q3T1L5|ALG6_RAT | Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Rattus norvegicus GN=Alg6 PE=2 SV=1 | 31 | 377 | 4.0E-30 |
| sp|O43053|ALG6_SCHPO | Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=alg6 PE=3 SV=1 | 31 | 377 | 1.0E-29 |
| sp|Q554E2|ALG8_DICDI | Probable dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Dictyostelium discoideum GN=alg8 PE=3 SV=1 | 14 | 125 | 2.0E-29 |
| sp|Q3TAE8|ALG6_MOUSE | Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Mus musculus GN=Alg6 PE=2 SV=1 | 31 | 377 | 3.0E-29 |
| sp|Q12001|ALG6_YEAST | Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ALG6 PE=1 SV=1 | 31 | 365 | 2.0E-27 |
| sp|Q09226|ALG6_CAEEL | Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Caenorhabditis elegans GN=C08B11.8 PE=3 SV=1 | 31 | 367 | 8.0E-27 |
| sp|Q9VKX7|ALG6_DROME | Probable dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase OS=Drosophila melanogaster GN=gny PE=2 SV=2 | 31 | 373 | 3.0E-23 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0016758 | hexosyltransferase activity | Yes |
| GO:0003674 | molecular_function | No |
| GO:0016740 | transferase activity | No |
| GO:0016757 | glycosyltransferase activity | No |
| GO:0003824 | catalytic activity | No |
| Domain # | Start | End | Length |
|---|---|---|---|
| 1 | 68 | 90 | 22 |
| 2 | 103 | 120 | 17 |
| 3 | 130 | 147 | 17 |
| 4 | 154 | 171 | 17 |
| 5 | 181 | 203 | 22 |
| 6 | 223 | 245 | 22 |
| 7 | 356 | 378 | 22 |
| 8 | 385 | 404 | 19 |
| 9 | 414 | 433 | 19 |
| 10 | 445 | 467 | 22 |
| 11 | 477 | 499 | 22 |
| CAZyme category | E-value | Start | End |
|---|---|---|---|
| GT57 | 9.9E-175 | 17 | 494 |
| Orthofinder run ID | 4 |
| Orthogroup | 4916 |
| Change Orthofinder run |
| Type of sequence | Sequence |
|---|---|
| Locus | Download genbank file of locus
Download genbank file of locus (reverse complement)
The gene with 5 kb flanks (if sufficient flanking sequence is available). For use in cloning design programs. NOTE: features (genes or exons) that are only partially contained within the sequence are completely excluded. |
| Protein | >OphauG2|4876 MADPSYPTLTQCAVVSAAFKVLLFPAYKSTDFEVHRNWLAITYSLPLSEWYFEHTSQWTLDYPPFFAYFEWLLSL VAHLVDPAMVRLYSLNHESWATVCFQRATVLVSDLVLAWALQLFIKSTPLPCRRAAQVAALSVLLSPGLLIIDHI HFQYNGFMYGILILSLVLARCKPTLLLSGLVFAALLCFKHIHLYLAPAYFVFLLRTYCLAPESIFRIRPMNCLKL GAGITAIFAAAFAPFAALGQMPQLLSRLFPFSRGLCHAYWAPNVWALYSMADRILIHVAPRLGLVVKTEALQSVT RGLVGDTAFAVLPEPSPRLCFVLTLLFQALPLGKLMLQPTWDNFIGAVTLCGYASFLFGWHVHEKAVLLVIIPFS LIALRDRRHLSAFRPLAVAGYVSLFPLLFTPAEFPIKTVYTVFWLVLFLMAFDRLAPASNKPRFFLLDRFSTLYI AVSIPLILYTSLLHAVMFGKRYEFLPLMFTSSYSAVGVVGSWVGYMVVYFTS* |
| Coding | >OphauG2|4876 ATGGCCGACCCGTCCTATCCCACGTTGACCCAATGCGCCGTCGTCTCCGCTGCCTTTAAAGTCCTGCTGTTTCCT GCATACAAATCTACCGACTTTGAGGTCCATCGCAACTGGCTGGCCATTACATACAGCCTGCCCCTGTCGGAATGG TACTTTGAGCACACCTCGCAATGGACCCTCGACTATCCTCCCTTTTTTGCCTACTTTGAATGGCTGCTCTCCCTC GTCGCCCACCTCGTCGACCCAGCCATGGTGAGGCTCTACAGCCTCAACCACGAATCCTGGGCCACCGTATGCTTC CAGCGTGCCACCGTGCTCGTGTCCGATCTGGTGCTGGCCTGGGCTCTGCAGCTCTTCATAAAGTCAACCCCGCTG CCTTGTCGCCGTGCCGCTCAGGTGGCCGCCCTGTCGGTGCTCCTGTCACCCGGCCTGCTCATCATTGATCACATT CACTTCCAGTACAACGGCTTCATGTATGGCATTCTCATTCTCTCCCTTGTTCTTGCTCGCTGCAAGCCGACACTG TTGCTCAGCGGCCTTGTCTTTGCTGCCCTGCTATGCTTCAAGCACATCCATCTCTATCTGGCGCCTGCCTACTTT GTCTTTCTGCTGCGCACCTACTGCCTTGCCCCAGAGTCCATCTTTCGCATCAGACCCATGAATTGCCTCAAGTTG GGCGCTGGCATTACTGCCATCTTTGCCGCCGCCTTTGCACCCTTTGCCGCCCTGGGACAGATGCCACAGCTACTC AGCCGTCTCTTTCCCTTTTCCCGTGGCCTATGCCACGCATACTGGGCTCCTAATGTCTGGGCTCTCTATTCAATG GCTGATCGCATCCTGATTCATGTCGCACCTCGCCTTGGTTTAGTCGTCAAGACAGAGGCCCTGCAGAGCGTTACC CGCGGACTTGTCGGCGATACGGCTTTTGCTGTGCTGCCCGAGCCATCTCCCAGGCTGTGCTTTGTCCTGACGCTG CTATTCCAGGCACTGCCTCTAGGCAAGCTGATGCTACAGCCAACATGGGATAACTTTATCGGAGCAGTCACGCTA TGTGGATATGCCTCGTTTCTTTTTGGCTGGCATGTACATGAAAAGGCCGTTTTGCTCGTCATTATCCCCTTTAGT CTCATTGCCCTCAGGGACCGACGACACTTGAGCGCCTTCCGCCCGCTGGCCGTGGCAGGCTACGTGTCCTTATTC CCCCTGCTTTTTACGCCCGCAGAGTTTCCCATCAAGACGGTGTATACAGTGTTTTGGCTCGTCTTATTTCTCATG GCCTTTGACCGGCTGGCCCCAGCGTCCAACAAGCCACGTTTTTTCCTGCTGGACCGCTTCAGCACGCTCTACATT GCCGTGAGCATCCCGCTCATACTCTACACGTCACTGCTTCATGCCGTCATGTTTGGCAAGCGGTACGAGTTTCTG CCCCTCATGTTCACCAGCTCGTACTCGGCAGTAGGAGTTGTCGGTAGCTGGGTAGGATACATGGTTGTTTATTTC ACGTCTTGA |
| Transcript | >OphauG2|4876 ATGGCCGACCCGTCCTATCCCACGTTGACCCAATGCGCCGTCGTCTCCGCTGCCTTTAAAGTCCTGCTGTTTCCT GCATACAAATCTACCGACTTTGAGGTCCATCGCAACTGGCTGGCCATTACATACAGCCTGCCCCTGTCGGAATGG TACTTTGAGCACACCTCGCAATGGACCCTCGACTATCCTCCCTTTTTTGCCTACTTTGAATGGCTGCTCTCCCTC GTCGCCCACCTCGTCGACCCAGCCATGGTGAGGCTCTACAGCCTCAACCACGAATCCTGGGCCACCGTATGCTTC CAGCGTGCCACCGTGCTCGTGTCCGATCTGGTGCTGGCCTGGGCTCTGCAGCTCTTCATAAAGTCAACCCCGCTG CCTTGTCGCCGTGCCGCTCAGGTGGCCGCCCTGTCGGTGCTCCTGTCACCCGGCCTGCTCATCATTGATCACATT CACTTCCAGTACAACGGCTTCATGTATGGCATTCTCATTCTCTCCCTTGTTCTTGCTCGCTGCAAGCCGACACTG TTGCTCAGCGGCCTTGTCTTTGCTGCCCTGCTATGCTTCAAGCACATCCATCTCTATCTGGCGCCTGCCTACTTT GTCTTTCTGCTGCGCACCTACTGCCTTGCCCCAGAGTCCATCTTTCGCATCAGACCCATGAATTGCCTCAAGTTG GGCGCTGGCATTACTGCCATCTTTGCCGCCGCCTTTGCACCCTTTGCCGCCCTGGGACAGATGCCACAGCTACTC AGCCGTCTCTTTCCCTTTTCCCGTGGCCTATGCCACGCATACTGGGCTCCTAATGTCTGGGCTCTCTATTCAATG GCTGATCGCATCCTGATTCATGTCGCACCTCGCCTTGGTTTAGTCGTCAAGACAGAGGCCCTGCAGAGCGTTACC CGCGGACTTGTCGGCGATACGGCTTTTGCTGTGCTGCCCGAGCCATCTCCCAGGCTGTGCTTTGTCCTGACGCTG CTATTCCAGGCACTGCCTCTAGGCAAGCTGATGCTACAGCCAACATGGGATAACTTTATCGGAGCAGTCACGCTA TGTGGATATGCCTCGTTTCTTTTTGGCTGGCATGTACATGAAAAGGCCGTTTTGCTCGTCATTATCCCCTTTAGT CTCATTGCCCTCAGGGACCGACGACACTTGAGCGCCTTCCGCCCGCTGGCCGTGGCAGGCTACGTGTCCTTATTC CCCCTGCTTTTTACGCCCGCAGAGTTTCCCATCAAGACGGTGTATACAGTGTTTTGGCTCGTCTTATTTCTCATG GCCTTTGACCGGCTGGCCCCAGCGTCCAACAAGCCACGTTTTTTCCTGCTGGACCGCTTCAGCACGCTCTACATT GCCGTGAGCATCCCGCTCATACTCTACACGTCACTGCTTCATGCCGTCATGTTTGGCAAGCGGTACGAGTTTCTG CCCCTCATGTTCACCAGCTCGTACTCGGCAGTAGGAGTTGTCGGTAGCTGGGTAGGATACATGGTTGTTTATTTC ACGTCTTGA |
| Gene | >OphauG2|4876 ATGGCCGACCCGTCCTATCCCACGTTGACCCAATGCGCCGTCGTCTCCGCTGCCTTTAAAGTCCTGCTGTTTCCT GCATAGTAAGCCAAGCTCCTATCCTCCTGTCCTTGATTCCTCGGCCCCAGAGATGCCAATCCCACAAACAGCAAA TCTACCGACTTTGAGGTCCATCGCAACTGGCTGGCCATTACATACAGCCTGCCCCTGTCGGAATGGTACTTTGAG CACACCTCGCAATGGACCCTCGACTATCCTCCCTTTTTTGCCTACTTTGAATGGCTGCTCTCCCTCGTCGCCCAC CTCGTCGACCCAGCCATGGTGAGGCTCTACAGCCTCAACCACGAATCCTGGGCCACCGTATGCTTCCAGCGTGCC ACCGTGCTCGTGTCCGATCTGGTGCTGGCCTGGGCTCTGCAGCTCTTCATAAAGTCAACCCCGCTGCCTTGTCGC CGTGCCGCTCAGGTGGCCGCCCTGTCGGTGCTCCTGTCACCCGGCCTGCTCATCATTGATCACATTCACTTCCAG TACAACGGCTTCATGTATGGCATTCTCATTCTCTCCCTTGTTCTTGCTCGCTGCAAGCCGACACTGTTGCTCAGC GGCCTTGTCTTTGCTGCCCTGCTATGCTTCAAGCACATCCATCTCTATCTGGCGCCTGCCTACTTTGTCTTTCTG CTGCGCACCTACTGCCTTGCCCCAGAGTCCATCTTTCGCATCAGACCCATGAATTGCCTCAAGTTGGGCGCTGGC ATTACTGCCATCTTTGCCGCCGCCTTTGCACCCTTTGCCGCCCTGGGACAGATGCCACAGCTACTCAGCCGTCTC TTTCCCTTTTCCCGTGGCCTATGCCACGCATACTGGGCTCCTAATGTCTGGGCTCTCTATTCAATGGCTGATCGC ATCCTGATTCATGGTGAGCCTGTTGTTCGTGATTTTCTCGAGCCTAGTCTTGGAAGCTAATAAATAATACCTGCC CACCACAGTCGCACCTCGCCTTGGTTTAGTCGTCAAGACAGAGGCCCTGCAGAGCGTTACCCGCGGACTTGTCGG CGATACGGCTTTTGCTGTGCTGCCCGAGCCATCTCCCAGGCTGTGCTTTGTCCTGACGCTGCTATTCCAGGCACT GCCTCTAGGCAAGCTGATGCTACAGCCAACATGGGATAACTTTATCGGAGCAGTCACGCTATGTGGATATGCCTC GTTTCTTTTTGGCTGGCATGTACATGAAAAGGCCGTTTTGCTCGTCATTATCCCCTTTAGTCTCATTGCCCTCAG GGACCGACGACACTTGAGCGCCTTCCGCCCGCTGGCCGTGGCAGGCTACGTGTCCTTATTCCCCCTGCTTTTTAC GCCCGCAGAGTTTCCCATCAAGACGGTGTATACAGTGTTTTGGCTCGTCTTATTTCTCATGGCCTTTGACCGGCT GGCCCCAGCGTCCAACAAGCCACGTTTTTTCCTGCTGGACCGCTTCAGCACGCTCTACATTGCCGTGAGCATCCC GCTCATACTCTACACGTCACTGCTTCATGCCGTCATGTTTGGCAAGCGGTACGAGTTTCTGCCCCTCATGTTCAC CAGCTCGTACTCGGCAGTAGGAGTTGTCGGTAGCTGGGTAGGATACATGGTTGTTTATTTCACGTCTTGA |