© 2023 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Ophio5|6532 |
| Gene name | |
| Location | scaffold_578:4827..7155 |
| Strand | + |
| Gene length (bp) | 2328 |
| Transcript length (bp) | 2271 |
| Coding sequence length (bp) | 2268 |
| Protein length (aa) | 756 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00172 | Zn_clus | Fungal Zn(2)-Cys(6) binuclear cluster domain | 8.2E-08 | 96 | 133 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P10563|QUTA_EMENI | Quinic acid utilization activator OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=qutA PE=3 SV=2 | 84 | 140 | 2.0E-07 |
| sp|G4MZJ4|XLNR_MAGO7 | Xylanolytic transcriptional activator xlnR homolog OS=Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) GN=xlr1 PE=3 SV=1 | 81 | 139 | 1.0E-06 |
| sp|Q0CV52|XLNR_ASPTN | Xylanolytic transcriptional activator xlnR OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=xlnR PE=3 SV=2 | 83 | 139 | 1.0E-06 |
| sp|Q2UD93|XLNR_ASPOR | Xylanolytic transcriptional activator xlnR OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=xlnR PE=1 SV=2 | 89 | 139 | 1.0E-06 |
| sp|B8N6M6|XLNR_ASPFN | Xylanolytic transcriptional activator xlnR OS=Aspergillus flavus (strain ATCC 200026 / FGSC A1120 / NRRL 3357 / JCM 12722 / SRRC 167) GN=xlnR PE=3 SV=1 | 89 | 139 | 1.0E-06 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P10563|QUTA_EMENI | Quinic acid utilization activator OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=qutA PE=3 SV=2 | 84 | 140 | 2.0E-07 |
| sp|G4MZJ4|XLNR_MAGO7 | Xylanolytic transcriptional activator xlnR homolog OS=Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) GN=xlr1 PE=3 SV=1 | 81 | 139 | 1.0E-06 |
| sp|Q0CV52|XLNR_ASPTN | Xylanolytic transcriptional activator xlnR OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=xlnR PE=3 SV=2 | 83 | 139 | 1.0E-06 |
| sp|Q2UD93|XLNR_ASPOR | Xylanolytic transcriptional activator xlnR OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=xlnR PE=1 SV=2 | 89 | 139 | 1.0E-06 |
| sp|B8N6M6|XLNR_ASPFN | Xylanolytic transcriptional activator xlnR OS=Aspergillus flavus (strain ATCC 200026 / FGSC A1120 / NRRL 3357 / JCM 12722 / SRRC 167) GN=xlnR PE=3 SV=1 | 89 | 139 | 1.0E-06 |
| sp|Q5AVS0|XLNR_EMENI | Xylanolytic transcriptional activator xlnR OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=xlnR PE=2 SV=2 | 89 | 139 | 2.0E-06 |
| sp|A1DIC0|XLNR_NEOFI | Xylanolytic transcriptional activator xlnR OS=Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN=xlnR PE=3 SV=2 | 89 | 139 | 2.0E-06 |
| sp|B0XUL1|XLNR_ASPFC | Xylanolytic transcriptional activator xlnR OS=Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) GN=xlnR PE=3 SV=1 | 89 | 139 | 2.0E-06 |
| sp|Q96WP8|XLNR_ASPKA | Xylanolytic transcriptional activator xlnR OS=Aspergillus kawachii GN=xlnR PE=3 SV=2 | 89 | 139 | 2.0E-06 |
| sp|O42804|XLNR_ASPNG | Xylanolytic transcriptional activator xlnR OS=Aspergillus niger GN=xlnR PE=1 SV=2 | 89 | 139 | 2.0E-06 |
| sp|A2R5W7|XLNR_ASPNC | Xylanolytic transcriptional activator xlnR OS=Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN=xlnR PE=3 SV=2 | 89 | 139 | 2.0E-06 |
| sp|A2QJX5|ARAR_ASPNC | Arabinanolytic transcriptional activator araR OS=Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN=araR PE=3 SV=1 | 70 | 205 | 4.0E-06 |
| sp|Q4WZV6|XLNR_ASPFU | Xylanolytic transcriptional activator xlnR OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=xlnR PE=3 SV=1 | 89 | 139 | 6.0E-06 |
| sp|A1C7P9|XLNR_ASPCL | Xylanolytic transcriptional activator xlnR OS=Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1) GN=xlnR PE=3 SV=2 | 89 | 139 | 8.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0006355 | regulation of transcription, DNA-templated | Yes |
| GO:0008270 | zinc ion binding | Yes |
| GO:0000981 | DNA-binding transcription factor activity, RNA polymerase II-specific | Yes |
| GO:0008150 | biological_process | No |
| GO:0051252 | regulation of RNA metabolic process | No |
| GO:0060255 | regulation of macromolecule metabolic process | No |
| GO:0019222 | regulation of metabolic process | No |
| GO:0050794 | regulation of cellular process | No |
| GO:0140110 | transcription regulator activity | No |
| GO:0031323 | regulation of cellular metabolic process | No |
| GO:0065007 | biological regulation | No |
| GO:0046872 | metal ion binding | No |
| GO:0010468 | regulation of gene expression | No |
| GO:0043167 | ion binding | No |
| GO:0043169 | cation binding | No |
| GO:0003674 | molecular_function | No |
| GO:0019219 | regulation of nucleobase-containing compound metabolic process | No |
| GO:0051171 | regulation of nitrogen compound metabolic process | No |
| GO:0005488 | binding | No |
| GO:0080090 | regulation of primary metabolic process | No |
| GO:0009889 | regulation of biosynthetic process | No |
| GO:0050789 | regulation of biological process | No |
| GO:0003700 | DNA-binding transcription factor activity | No |
| GO:1903506 | regulation of nucleic acid-templated transcription | No |
| GO:2001141 | regulation of RNA biosynthetic process | No |
| GO:0046914 | transition metal ion binding | No |
| GO:0010556 | regulation of macromolecule biosynthetic process | No |
| GO:0031326 | regulation of cellular biosynthetic process | No |
| Localizations | Signals | Cytoplasm | Nucleus | Extracellular | Cell membrane | Mitochondrion | Plastid | Endoplasmic reticulum | Lysosome vacuole | Golgi apparatus | Peroxisome |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Nucleus | Nuclear localization signal | 0.3318 | 0.8309 | 0.1053 | 0.0162 | 0.0631 | 0.0029 | 0.0861 | 0.0537 | 0.0272 | 0.0021 |
| Transcription Factor Class (based on PFAM domains) |
|---|
| Fungal Specific TF |
| Orthofinder run ID | 4 |
| Orthogroup | 3184 |
| 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 | >Ophio5|6532 MASREQTPSPSQQVAYASNGLEMLQAASDAAQAIDNPQALHDAVAAVEAVSGPDLGSLASAEPAPSPTTSASASL PLVPGAVRDPTINPKLTRLRRACDMCSMRKVKCDDSSIPCRPCRELGVDCTYERETKRRGPPNKHAEAAKAAKRA RVELAVPVTAATPAAVPISAAPSSSAAASPSPHNAAKTLVSISADAAVDADALAPLPVLEHLVDDFFTYVHPLAP FPHEPTFRQSFANREDRTRPEFLGLLASMVAALVASFPRSAREHLKAQHGPQLFPRPVAMVDRCRDVALLTRGSR WVLKQPKTLDDAATSYFLGLASAYVGQWNASRHFLAETLTLMRELGFARPKHPGDLPTFGNDAYSDDPLPFNHVK DQIGKRIFWCLLLGVRSFSQLGASHTPTDLVIAPSTPSLPYPAYPDNVDDICVLANQVIHQPEGSVTLLTGFRFA IDIYTTMNGVVSLELAYGMSTLPWADQRLLLRDGLVAAKSIVDNLPPELQLGGQLTAAEDDDDDDAGLQYVPPAW PNPQPAHDVRALIKAQPLRRRQLQLEIQRANIFVSQLATRSYFVELYFTLRDVHLSESQAEGTTATESTAAAAAA AAAGAASSDEEKALQDADDKEMLDLMTQERDLLVQNLLTIISSLSQRNMEPNGGALISKLRRVALSLLHEAPERK GEFAIKADEALAQLVESLSKLDSWSSSSSSSSSSSSSSDQSLMMTAEDEHVELRAWAELRDFQLRFVADAGFADL LGGVHG |
| Coding | >Ophio5|6532 ATGGCGAGCCGCGAACAGACGCCATCGCCATCGCAGCAAGTCGCCTACGCCAGCAACGGGCTGGAGATGCTCCAG GCCGCCAGCGATGCTGCCCAGGCCATCGATAACCCGCAGGCTCTTCACGATGCCGTCGCCGCTGTCGAGGCCGTA TCCGGTCCGGACCTCGGATCGTTGGCTTCGGCCGAGCCTGCTCCGTCACCGACGACTTCTGCTTCGGCATCGCTG CCTCTCGTTCCCGGCGCCGTTCGTGATCCGACCATTAACCCGAAGCTGACACGTCTTCGCCGTGCTTGCGACATG TGCAGTATGCGCAAGGTCAAATGCGACGACTCCAGTATCCCCTGTCGTCCATGCCGCGAACTCGGTGTCGATTGC ACCTACGAGCGCGAGACGAAACGTCGCGGTCCGCCCAACAAGCACGCTGAAGCTGCCAAGGCGGCCAAACGCGCC CGCGTCGAGCTCGCCGTCCCCGTTACGGCTGCCACTCCCGCTGCTGTTCCCATCTCGGCCGCTCCGTCTTCATCA GCTGCCGCCTCACCATCGCCGCACAACGCGGCCAAGACTCTGGTCAGCATCTCGGCCGATGCCGCCGTCGACGCA GACGCCCTCGCTCCCCTCCCTGTCCTCGAGCATCTGGTCGACGACTTCTTCACCTACGTCCATCCTCTCGCCCCC TTCCCCCACGAGCCTACCTTTCGCCAGTCCTTTGCCAACCGCGAGGACCGCACGCGTCCCGAATTCCTCGGCCTG CTCGCTTCCATGGTAGCAGCCCTGGTGGCATCCTTTCCGCGGAGCGCCCGCGAGCACCTCAAGGCCCAGCACGGC CCGCAGCTCTTCCCGCGACCCGTCGCCATGGTCGATCGCTGCCGTGATGTCGCCCTTTTGACGCGCGGCAGCCGC TGGGTGCTCAAGCAGCCCAAGACGCTGGACGACGCTGCCACGAGCTACTTCCTCGGCCTCGCCTCTGCCTACGTC GGCCAATGGAACGCATCGCGCCATTTCCTGGCCGAGACGCTGACGCTGATGCGGGAGCTGGGTTTCGCCCGTCCC AAGCACCCGGGCGATCTTCCGACGTTTGGAAACGACGCCTACTCGGACGACCCGCTCCCCTTTAACCACGTCAAG GACCAGATTGGGAAGCGCATATTTTGGTGTCTGCTGCTGGGTGTCCGCTCCTTTTCCCAGCTCGGCGCGTCCCAT ACGCCGACCGATCTCGTCATCGCCCCGTCGACGCCCAGTCTTCCCTACCCGGCCTACCCTGACAACGTCGACGAC ATTTGCGTCTTGGCCAACCAAGTCATCCACCAGCCCGAGGGCAGCGTCACCCTCCTCACGGGCTTCCGCTTCGCA ATCGACATCTACACTACTATGAACGGCGTCGTCAGCCTCGAACTGGCTTACGGAATGAGCACCCTCCCCTGGGCA GATCAGCGGCTGCTGCTTCGTGACGGCCTCGTCGCCGCAAAGAGCATCGTCGACAACCTCCCTCCGGAACTCCAG CTCGGCGGCCAGCTCACGGCCGCTGAAGACGACGACGACGACGACGCCGGCCTCCAGTACGTGCCTCCGGCCTGG CCCAACCCGCAGCCAGCGCACGACGTCCGGGCTCTCATCAAGGCTCAACCCCTCCGCCGTCGCCAGCTCCAGCTC GAGATCCAAAGGGCCAACATCTTCGTCTCCCAACTCGCGACGCGCTCCTACTTTGTCGAGCTATACTTTACCCTA CGGGACGTCCACCTCAGCGAATCCCAAGCCGAGGGCACAACAGCAACGGAATCGACAGCAGCAGCAGCAGCAGCA GCAGCAGCAGGAGCAGCATCATCAGACGAAGAGAAAGCCCTCCAAGACGCCGACGACAAGGAAATGCTAGACCTC ATGACGCAAGAACGAGACCTCCTGGTGCAAAACCTCCTCACCATCATCAGCTCACTGTCACAACGAAACATGGAA CCCAACGGCGGAGCGCTCATCAGCAAACTCCGTCGAGTAGCCCTGTCCCTCTTACACGAGGCGCCGGAACGGAAA GGCGAATTCGCCATCAAGGCGGACGAGGCGCTCGCGCAGCTGGTGGAGTCGTTGAGCAAGTTGGATAGCTGGTCA TCATCATCGTCATCGTCGTCGTCGTCGTCGTCGTCGTCGGATCAGTCGCTCATGATGACGGCCGAGGACGAGCAC GTCGAGTTGAGGGCCTGGGCCGAGTTGAGGGATTTCCAGCTTCGCTTTGTGGCGGATGCTGGCTTTGCGGATTTG CTGGGCGGAGTCCATGGT |
| Transcript | >Ophio5|6532 ATGGCGAGCCGCGAACAGACGCCATCGCCATCGCAGCAAGTCGCCTACGCCAGCAACGGGCTGGAGATGCTCCAG GCCGCCAGCGATGCTGCCCAGGCCATCGATAACCCGCAGGCTCTTCACGATGCCGTCGCCGCTGTCGAGGCCGTA TCCGGTCCGGACCTCGGATCGTTGGCTTCGGCCGAGCCTGCTCCGTCACCGACGACTTCTGCTTCGGCATCGCTG CCTCTCGTTCCCGGCGCCGTTCGTGATCCGACCATTAACCCGAAGCTGACACGTCTTCGCCGTGCTTGCGACATG TGCAGTATGCGCAAGGTCAAATGCGACGACTCCAGTATCCCCTGTCGTCCATGCCGCGAACTCGGTGTCGATTGC ACCTACGAGCGCGAGACGAAACGTCGCGGTCCGCCCAACAAGCACGCTGAAGCTGCCAAGGCGGCCAAACGCGCC CGCGTCGAGCTCGCCGTCCCCGTTACGGCTGCCACTCCCGCTGCTGTTCCCATCTCGGCCGCTCCGTCTTCATCA GCTGCCGCCTCACCATCGCCGCACAACGCGGCCAAGACTCTGGTCAGCATCTCGGCCGATGCCGCCGTCGACGCA GACGCCCTCGCTCCCCTCCCTGTCCTCGAGCATCTGGTCGACGACTTCTTCACCTACGTCCATCCTCTCGCCCCC TTCCCCCACGAGCCTACCTTTCGCCAGTCCTTTGCCAACCGCGAGGACCGCACGCGTCCCGAATTCCTCGGCCTG CTCGCTTCCATGGTAGCAGCCCTGGTGGCATCCTTTCCGCGGAGCGCCCGCGAGCACCTCAAGGCCCAGCACGGC CCGCAGCTCTTCCCGCGACCCGTCGCCATGGTCGATCGCTGCCGTGATGTCGCCCTTTTGACGCGCGGCAGCCGC TGGGTGCTCAAGCAGCCCAAGACGCTGGACGACGCTGCCACGAGCTACTTCCTCGGCCTCGCCTCTGCCTACGTC GGCCAATGGAACGCATCGCGCCATTTCCTGGCCGAGACGCTGACGCTGATGCGGGAGCTGGGTTTCGCCCGTCCC AAGCACCCGGGCGATCTTCCGACGTTTGGAAACGACGCCTACTCGGACGACCCGCTCCCCTTTAACCACGTCAAG GACCAGATTGGGAAGCGCATATTTTGGTGTCTGCTGCTGGGTGTCCGCTCCTTTTCCCAGCTCGGCGCGTCCCAT ACGCCGACCGATCTCGTCATCGCCCCGTCGACGCCCAGTCTTCCCTACCCGGCCTACCCTGACAACGTCGACGAC ATTTGCGTCTTGGCCAACCAAGTCATCCACCAGCCCGAGGGCAGCGTCACCCTCCTCACGGGCTTCCGCTTCGCA ATCGACATCTACACTACTATGAACGGCGTCGTCAGCCTCGAACTGGCTTACGGAATGAGCACCCTCCCCTGGGCA GATCAGCGGCTGCTGCTTCGTGACGGCCTCGTCGCCGCAAAGAGCATCGTCGACAACCTCCCTCCGGAACTCCAG CTCGGCGGCCAGCTCACGGCCGCTGAAGACGACGACGACGACGACGCCGGCCTCCAGTACGTGCCTCCGGCCTGG CCCAACCCGCAGCCAGCGCACGACGTCCGGGCTCTCATCAAGGCTCAACCCCTCCGCCGTCGCCAGCTCCAGCTC GAGATCCAAAGGGCCAACATCTTCGTCTCCCAACTCGCGACGCGCTCCTACTTTGTCGAGCTATACTTTACCCTA CGGGACGTCCACCTCAGCGAATCCCAAGCCGAGGGCACAACAGCAACGGAATCGACAGCAGCAGCAGCAGCAGCA GCAGCAGCAGGAGCAGCATCATCAGACGAAGAGAAAGCCCTCCAAGACGCCGACGACAAGGAAATGCTAGACCTC ATGACGCAAGAACGAGACCTCCTGGTGCAAAACCTCCTCACCATCATCAGCTCACTGTCACAACGAAACATGGAA CCCAACGGCGGAGCGCTCATCAGCAAACTCCGTCGAGTAGCCCTGTCCCTCTTACACGAGGCGCCGGAACGGAAA GGCGAATTCGCCATCAAGGCGGACGAGGCGCTCGCGCAGCTGGTGGAGTCGTTGAGCAAGTTGGATAGCTGGTCA TCATCATCGTCATCGTCGTCGTCGTCGTCGTCGTCGTCGGATCAGTCGCTCATGATGACGGCCGAGGACGAGCAC GTCGAGTTGAGGGCCTGGGCCGAGTTGAGGGATTTCCAGCTTCGCTTTGTGGCGGATGCTGGCTTTGCGGATTTG CTGGGCGGAGTCCATGGTTGA |
| Gene | >Ophio5|6532 ATGGCGAGCCGCGAACAGACGCCATCGCCATCGCAGCAAGTCGCCTACGCCAGCAACGGGCTGGAGATGCTCCAG GCCGCCAGCGATGCTGCCCAGGCCATCGATAACCCGCAGGCTCTTCACGATGCCGTCGCCGCTGTCGAGGCCGTA TCCGGTCCGGACCTCGGATCGTTGGCTTCGGCCGAGCCTGCTCCGTCACCGACGACTTCTGCTTCGGCATCGCTG CCTCTCGTTCCCGGCGCCGTTCGTGATCCGACCATTAACCCGAAGCTGACACGTCTTCGCCGTGCTTGCGACATG TGCAGTATGCGCAAGGTCAAATGCGACGACTCCAGTATCCCCTGTCGTCCATGCCGCGAACTCGGTGTCGATTGC ACCTACGAGCGCGAGACGAAACGTCGCGGTCCGCCCAACAAGCACGCTGAAGCTGCCAAGGCGGCCAAACGCGCC CGCGTCGAGCTCGCCGTCCCCGTTACGGCTGCCACTCCCGCTGCTGTTCCCATCTCGGCCGCTCCGTCTTCATCA GCTGCCGCCTCACCATCGCCGCACAACGCGGCCAAGACTCTGGTCAGCATCTCGGCCGATGCCGCCGTCGACGCA GACGCCCTCGCTCCCCTCCCTGTCCTCGAGCATCTGGTCGACGACTTCTTCACCTACGTCCATCCTCTCGCCCCC TTCCCCCACGAGCCTACCTTTCGCCAGTCCTTTGCCAACCGCGAGGACCGCACGCGTCCCGAATTCCTCGGCCTG CTCGCTTCCATGGTAGCAGCCCTGGTGGCATCCTTTCCGCGGAGCGCCCGCGAGCACCTCAAGGCCCAGCACGGC CCGCAGCTCTTCCCGCGACCCGTCGCCATGGTCGATCGCTGCCGTGATGTCGCCCTTTTGACGCGCGGCAGCCGC TGGGTGCTCAAGCAGCCCAAGACGCTGGACGACGCTGCCACGAGCTACTTCCTCGGCCTCGCCTCTGCCTACGTC GGCCAATGGAACGCATCGCGCCATTTCCTGGCCGAGACGCTGACGCTGATGCGGGAGCTGGGTTTCGCCCGTCCC AAGCACCCGGGCGATCTTCCGACGTTTGGAAACGACGCCTACTCGGACGACCCGCTCCCCTTTAACCACGTCAAG GACCAGATTGGGAAGCGCATATTTTGGTGTCTGCTGCTGGGTGTCCGGTGGGACTTTTCTGTCCCCAACTTGGCG GATCTCATGTCTGACGTGGTTGATGGCAGCTCCTTTTCCCAGCTCGGCGCGTCCCATACGCCGACCGATCTCGTC ATCGCCCCGTCGACGCCCAGTCTTCCCTACCCGGCCTACCCTGACAACGTCGACGACATTTGCGTCTTGGCCAAC CAAGTCATCCACCAGCCCGAGGGCAGCGTCACCCTCCTCACGGGCTTCCGCTTCGCAATCGACATCTACACTACT ATGAACGGCGTCGTCAGCCTCGAACTGGCTTACGGAATGAGCACCCTCCCCTGGGCAGATCAGCGGCTGCTGCTT CGTGACGGCCTCGTCGCCGCAAAGAGCATCGTCGACAACCTCCCTCCGGAACTCCAGCTCGGCGGCCAGCTCACG GCCGCTGAAGACGACGACGACGACGACGCCGGCCTCCAGTACGTGCCTCCGGCCTGGCCCAACCCGCAGCCAGCG CACGACGTCCGGGCTCTCATCAAGGCTCAACCCCTCCGCCGTCGCCAGCTCCAGCTCGAGATCCAAAGGGCCAAC ATCTTCGTCTCCCAACTCGCGACGCGCTCCTACTTTGTCGAGCTATACTTTACCCTACGGGACGTCCACCTCAGC GAATCCCAAGCCGAGGGCACAACAGCAACGGAATCGACAGCAGCAGCAGCAGCAGCAGCAGCAGCAGGAGCAGCA TCATCAGACGAAGAGAAAGCCCTCCAAGACGCCGACGACAAGGAAATGCTAGACCTCATGACGCAAGAACGAGAC CTCCTGGTGCAAAACCTCCTCACCATCATCAGCTCACTGTCACAACGAAACATGGAACCCAACGGCGGAGCGCTC ATCAGCAAACTCCGTCGAGTAGCCCTGTCCCTCTTACACGAGGCGCCGGAACGGAAAGGCGAATTCGCCATCAAG GCGGACGAGGCGCTCGCGCAGCTGGTGGAGTCGTTGAGCAAGTTGGATAGCTGGTCATCATCATCGTCATCGTCG TCGTCGTCGTCGTCGTCGTCGGATCAGTCGCTCATGATGACGGCCGAGGACGAGCACGTCGAGTTGAGGGCCTGG GCCGAGTTGAGGGATTTCCAGCTTCGCTTTGTGGCGGATGCTGGCTTTGCGGATTTGCTGGGCGGAGTCCATGGT TGA |