© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Ophio5|1241 |
| Gene name | |
| Location | scaffold_14:84154..85875 |
| Strand | - |
| Gene length (bp) | 1721 |
| Transcript length (bp) | 1668 |
| Coding sequence length (bp) | 1665 |
| Protein length (aa) | 555 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00443 | UCH | Ubiquitin carboxyl-terminal hydrolase | 2.9E-46 | 110 | 542 |
| PF00240 | ubiquitin | Ubiquitin family | 1.3E-10 | 7 | 75 |
| PF13423 | UCH_1 | Ubiquitin carboxyl-terminal hydrolase | 1.6E-08 | 109 | 516 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q92353|UBP6_SCHPO | Ubiquitin carboxyl-terminal hydrolase 6 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp6 PE=1 SV=2 | 4 | 544 | 2.0E-125 |
| sp|P43593|UBP6_YEAST | Ubiquitin carboxyl-terminal hydrolase 6 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP6 PE=1 SV=1 | 8 | 547 | 4.0E-91 |
| sp|Q84WC6|UBP7_ARATH | Ubiquitin carboxyl-terminal hydrolase 7 OS=Arabidopsis thaliana GN=UBP7 PE=1 SV=1 | 4 | 544 | 2.0E-90 |
| sp|Q949Y0|UBP6_ARATH | Ubiquitin carboxyl-terminal hydrolase 6 OS=Arabidopsis thaliana GN=UBP6 PE=1 SV=1 | 5 | 544 | 1.0E-89 |
| sp|Q9JMA1|UBP14_MOUSE | Ubiquitin carboxyl-terminal hydrolase 14 OS=Mus musculus GN=Usp14 PE=1 SV=3 | 1 | 542 | 2.0E-87 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q92353|UBP6_SCHPO | Ubiquitin carboxyl-terminal hydrolase 6 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp6 PE=1 SV=2 | 4 | 544 | 2.0E-125 |
| sp|P43593|UBP6_YEAST | Ubiquitin carboxyl-terminal hydrolase 6 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=UBP6 PE=1 SV=1 | 8 | 547 | 4.0E-91 |
| sp|Q84WC6|UBP7_ARATH | Ubiquitin carboxyl-terminal hydrolase 7 OS=Arabidopsis thaliana GN=UBP7 PE=1 SV=1 | 4 | 544 | 2.0E-90 |
| sp|Q949Y0|UBP6_ARATH | Ubiquitin carboxyl-terminal hydrolase 6 OS=Arabidopsis thaliana GN=UBP6 PE=1 SV=1 | 5 | 544 | 1.0E-89 |
| sp|Q9JMA1|UBP14_MOUSE | Ubiquitin carboxyl-terminal hydrolase 14 OS=Mus musculus GN=Usp14 PE=1 SV=3 | 1 | 542 | 2.0E-87 |
| sp|P40826|UBP14_RABIT | Ubiquitin carboxyl-terminal hydrolase 14 OS=Oryctolagus cuniculus GN=USP14 PE=1 SV=3 | 28 | 542 | 1.0E-85 |
| sp|P60051|UBP14_PANTR | Ubiquitin carboxyl-terminal hydrolase 14 OS=Pan troglodytes GN=USP14 PE=3 SV=2 | 1 | 542 | 3.0E-85 |
| sp|P54578|UBP14_HUMAN | Ubiquitin carboxyl-terminal hydrolase 14 OS=Homo sapiens GN=USP14 PE=1 SV=3 | 1 | 542 | 3.0E-85 |
| sp|Q0IIF7|UBP14_BOVIN | Ubiquitin carboxyl-terminal hydrolase 14 OS=Bos taurus GN=USP14 PE=2 SV=3 | 1 | 369 | 8.0E-71 |
| sp|Q17361|UBP14_CAEEL | Ubiquitin carboxyl-terminal hydrolase 14 OS=Caenorhabditis elegans GN=usp-14 PE=2 SV=2 | 6 | 544 | 9.0E-70 |
| sp|Q0IIF7|UBP14_BOVIN | Ubiquitin carboxyl-terminal hydrolase 14 OS=Bos taurus GN=USP14 PE=2 SV=3 | 454 | 542 | 7.0E-13 |
| sp|E7F6T8|UBP37_DANRE | Ubiquitin carboxyl-terminal hydrolase 37 OS=Danio rerio GN=usp37 PE=2 SV=1 | 110 | 359 | 2.0E-10 |
| sp|Q9D9M2|UBP12_MOUSE | Ubiquitin carboxyl-terminal hydrolase 12 OS=Mus musculus GN=Usp12 PE=2 SV=2 | 110 | 345 | 3.0E-09 |
| sp|O74442|UBP16_SCHPO | Probable ubiquitin carboxyl-terminal hydrolase 16 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ubp16 PE=1 SV=1 | 85 | 353 | 1.0E-08 |
| sp|A4FUN7|UBP12_DANRE | Ubiquitin carboxyl-terminal hydrolase 12A OS=Danio rerio GN=usp12a PE=2 SV=1 | 110 | 345 | 1.0E-08 |
| sp|A5D9H7|UBP12_BOVIN | Ubiquitin carboxyl-terminal hydrolase 12 OS=Bos taurus GN=USP12 PE=2 SV=1 | 110 | 345 | 2.0E-08 |
| sp|Q9FPS9|UBP15_ARATH | Ubiquitin carboxyl-terminal hydrolase 15 OS=Arabidopsis thaliana GN=UBP15 PE=2 SV=2 | 93 | 350 | 3.0E-08 |
| sp|O75317|UBP12_HUMAN | Ubiquitin carboxyl-terminal hydrolase 12 OS=Homo sapiens GN=USP12 PE=1 SV=2 | 110 | 345 | 3.0E-08 |
| sp|Q4R6D3|UBP50_MACFA | Putative ubiquitin carboxyl-terminal hydrolase 50 OS=Macaca fascicularis GN=USP50 PE=2 SV=1 | 97 | 357 | 5.0E-08 |
| sp|Q6P8X6|UBP50_MOUSE | Putative ubiquitin carboxyl-terminal hydrolase 50 OS=Mus musculus GN=Usp50 PE=2 SV=1 | 110 | 357 | 5.0E-08 |
| sp|P62068|UBP46_HUMAN | Ubiquitin carboxyl-terminal hydrolase 46 OS=Homo sapiens GN=USP46 PE=1 SV=1 | 110 | 345 | 5.0E-08 |
| sp|Q5RBQ4|UBP46_PONAB | Ubiquitin carboxyl-terminal hydrolase 46 OS=Pongo abelii GN=USP46 PE=2 SV=1 | 110 | 345 | 5.0E-08 |
| sp|Q6A4J8|UBP7_MOUSE | Ubiquitin carboxyl-terminal hydrolase 7 OS=Mus musculus GN=Usp7 PE=1 SV=1 | 109 | 350 | 5.0E-08 |
| sp|P62069|UBP46_MOUSE | Ubiquitin carboxyl-terminal hydrolase 46 OS=Mus musculus GN=Usp46 PE=1 SV=1 | 110 | 345 | 5.0E-08 |
| sp|Q5M981|UB12B_XENLA | Ubiquitin carboxyl-terminal hydrolase 12-B OS=Xenopus laevis GN=usp12-b PE=2 SV=2 | 110 | 345 | 6.0E-08 |
| sp|A5WWB0|UBP46_DANRE | Ubiquitin carboxyl-terminal hydrolase 46 OS=Danio rerio GN=usp46 PE=3 SV=2 | 110 | 345 | 7.0E-08 |
| sp|Q86T82|UBP37_HUMAN | Ubiquitin carboxyl-terminal hydrolase 37 OS=Homo sapiens GN=USP37 PE=1 SV=2 | 110 | 356 | 8.0E-08 |
| sp|E2RK09|UBP37_CANLF | Ubiquitin carboxyl-terminal hydrolase 37 OS=Canis lupus familiaris GN=USP37 PE=3 SV=1 | 110 | 356 | 2.0E-07 |
| sp|A3AF13|UBP26_ORYSJ | Ubiquitin carboxyl-terminal hydrolase 26 OS=Oryza sativa subsp. japonica GN=UBP26 PE=3 SV=2 | 107 | 347 | 2.0E-07 |
| sp|Q52KZ6|UB12A_XENLA | Ubiquitin carboxyl-terminal hydrolase 12-A OS=Xenopus laevis GN=usp12-a PE=2 SV=1 | 110 | 345 | 2.0E-07 |
| sp|Q4VSI4|UBP7_RAT | Ubiquitin carboxyl-terminal hydrolase 7 OS=Rattus norvegicus GN=Usp7 PE=1 SV=1 | 109 | 350 | 2.0E-07 |
| sp|Q93009|UBP7_HUMAN | Ubiquitin carboxyl-terminal hydrolase 7 OS=Homo sapiens GN=USP7 PE=1 SV=2 | 109 | 350 | 2.0E-07 |
| sp|F1SRY5|UBP37_PIG | Ubiquitin carboxyl-terminal hydrolase 37 OS=Sus scrofa GN=USP37 PE=3 SV=1 | 110 | 356 | 2.0E-07 |
| sp|A2XDG4|UBP26_ORYSI | Ubiquitin carboxyl-terminal hydrolase 26 OS=Oryza sativa subsp. indica GN=UBP26 PE=3 SV=1 | 107 | 347 | 3.0E-07 |
| sp|F1N5V1|UBP37_BOVIN | Ubiquitin carboxyl-terminal hydrolase 37 OS=Bos taurus GN=USP37 PE=3 SV=1 | 110 | 356 | 3.0E-07 |
| sp|Q6U7I1|UBP7_CHICK | Ubiquitin carboxyl-terminal hydrolase 7 OS=Gallus gallus GN=USP7 PE=2 SV=1 | 109 | 350 | 4.0E-07 |
| sp|E1C213|UBP37_CHICK | Ubiquitin carboxyl-terminal hydrolase 37 OS=Gallus gallus GN=USP37 PE=3 SV=1 | 110 | 359 | 5.0E-07 |
| sp|D3ZJ96|UBP28_RAT | Ubiquitin carboxyl-terminal hydrolase 28 OS=Rattus norvegicus GN=Usp28 PE=2 SV=2 | 102 | 385 | 5.0E-07 |
| sp|Q9SB51|UBP16_ARATH | Ubiquitin carboxyl-terminal hydrolase 16 OS=Arabidopsis thaliana GN=UBP16 PE=1 SV=1 | 103 | 350 | 1.0E-06 |
| sp|Q5I043|UBP28_MOUSE | Ubiquitin carboxyl-terminal hydrolase 28 OS=Mus musculus GN=Usp28 PE=1 SV=1 | 102 | 385 | 2.0E-06 |
| sp|Q9FPS4|UBP23_ARATH | Ubiquitin carboxyl-terminal hydrolase 23 OS=Arabidopsis thaliana GN=UBP23 PE=2 SV=2 | 109 | 350 | 2.0E-06 |
| sp|Q9SCJ9|UBP26_ARATH | Ubiquitin carboxyl-terminal hydrolase 26 OS=Arabidopsis thaliana GN=UBP26 PE=1 SV=3 | 105 | 347 | 5.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0005515 | protein binding | Yes |
| GO:0004843 | cysteine-type deubiquitinase activity | Yes |
| GO:0016579 | protein deubiquitination | Yes |
| GO:0140096 | catalytic activity, acting on a protein | No |
| GO:0043170 | macromolecule metabolic process | No |
| GO:0008150 | biological_process | No |
| GO:1901564 | organonitrogen compound metabolic process | No |
| GO:0044238 | primary metabolic process | No |
| GO:0006508 | proteolysis | No |
| GO:0101005 | deubiquitinase activity | No |
| GO:0043412 | macromolecule modification | No |
| GO:0008152 | metabolic process | No |
| GO:0003674 | molecular_function | No |
| GO:0008233 | peptidase activity | No |
| GO:0071704 | organic substance metabolic process | No |
| GO:0070646 | protein modification by small protein removal | No |
| GO:0005488 | binding | No |
| GO:0016787 | hydrolase activity | No |
| GO:0070647 | protein modification by small protein conjugation or removal | No |
| GO:0019538 | protein metabolic process | No |
| GO:0036211 | protein modification process | No |
| GO:0006807 | nitrogen compound metabolic process | No |
| GO:0019783 | ubiquitin-like protein peptidase activity | No |
| GO:0003824 | catalytic activity | No |
| GO:0008234 | cysteine-type peptidase activity | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 31 | 0.45 |
| Type of sequence | Sequence |
|---|---|
| Locus | Download genbank file of locus
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|1241 MAAVTVVVKHQGKRHDVEVDPASTGEDFKLQLFSLTNVEPARQKILIKGGQLKDEADMGKLGLKAGQVIMMMGTP SSSGGNLVRPKDPIKFVEDMTEAEKAQQLDATPAGLVNLGNTCYLNSTLQTLRSIPELNAALPEYGPTRSSTLAE VDLAHHLSRLYKDMGRTQEAFPPVDFLSALRSAFPQFAERSKSDNGYAQQDAEEAWSQIVQNLKPRVKVKDLAGT DDVLVIDKYMAGQLTSTMECQDPEASKAGEKTVVQKETFYKLSCHIDGTTNHLRNGILAALSEKIEKKSAVLDRE AEYKKTSAISRAPKYLTIHFVRFFWKRQTQKKAKIMRKVTFPQELDVVEFCCDDLKKALIPVRDRVREIRKDEED IERARKRRKKNHEELLADIPGGSGLASSRKDDKTTKAKDAVDGNAGTDETFKTDAEIDAEKDAAVLAAKKELHAM IDPSLRDDDGANQSGLYELRGVVTHQGGSADSGHYTAYVKKSAPVDPKTGKKGEEDGMWWWFNDDKVTEVSVDKI EGLAGGGESHSALILLYKAIPLPTADGTME |
| Coding | >Ophio5|1241 ATGGCGGCAGTCACAGTCGTCGTGAAGCACCAGGGCAAGAGGCACGACGTCGAGGTTGACCCTGCGTCCACGGGC GAGGACTTCAAGCTTCAGCTTTTCAGCCTGACAAACGTCGAGCCGGCGCGGCAAAAGATCCTCATCAAGGGCGGC CAGCTCAAGGATGAGGCCGACATGGGCAAACTGGGGCTCAAGGCCGGCCAAGTCATCATGATGATGGGCACTCCG AGCTCCAGCGGAGGCAACCTCGTCCGCCCAAAGGACCCCATCAAGTTTGTCGAGGACATGACAGAGGCCGAGAAA GCTCAGCAGTTGGACGCCACCCCGGCCGGCCTTGTCAACCTCGGCAACACCTGCTATCTCAACTCGACGCTGCAA ACGCTGCGTTCCATTCCCGAACTCAATGCGGCTTTGCCCGAGTACGGTCCCACCAGGTCGTCGACCCTGGCGGAG GTTGACCTGGCCCATCACCTGTCCCGTCTGTACAAGGACATGGGCCGGACGCAGGAGGCCTTTCCGCCCGTCGAT TTCCTCAGCGCCCTGCGCTCCGCCTTCCCGCAGTTTGCTGAAAGATCCAAATCAGACAATGGTTATGCTCAGCAG GACGCCGAGGAGGCCTGGTCTCAGATCGTCCAGAACCTGAAGCCCAGAGTCAAGGTCAAGGACTTGGCTGGCACC GACGACGTGCTCGTGATTGACAAATACATGGCCGGCCAGCTAACGTCAACGATGGAGTGTCAAGATCCGGAGGCA AGCAAGGCAGGCGAGAAGACCGTGGTCCAAAAGGAAACCTTCTACAAGCTCAGCTGCCATATCGACGGCACGACG AATCACTTGCGGAACGGCATCCTGGCCGCGCTCAGCGAAAAGATTGAAAAGAAATCGGCTGTGCTGGACCGCGAA GCCGAGTACAAGAAGACGTCAGCGATTTCTCGCGCCCCCAAGTATCTGACAATCCATTTTGTGCGCTTCTTTTGG AAGCGTCAGACTCAGAAGAAGGCCAAGATCATGCGCAAGGTGACGTTTCCTCAGGAGCTGGATGTTGTCGAGTTT TGCTGTGACGACCTGAAGAAGGCGTTGATTCCCGTCAGGGACAGGGTGCGCGAAATCCGCAAGGACGAAGAGGAC ATCGAGCGGGCCCGCAAGCGCCGCAAGAAGAACCACGAGGAGCTACTGGCGGACATCCCGGGGGGTTCTGGGCTG GCATCGAGTAGGAAGGACGACAAGACGACCAAAGCCAAGGACGCGGTCGACGGCAACGCGGGCACGGACGAGACG TTCAAGACGGACGCCGAGATCGACGCTGAAAAGGATGCGGCGGTGCTAGCGGCCAAGAAGGAACTGCACGCCATG ATCGACCCGAGTCTTCGGGACGACGACGGCGCCAACCAGTCCGGGCTATACGAACTACGTGGCGTGGTGACGCAC CAGGGCGGCAGCGCCGACAGCGGACACTACACGGCTTACGTCAAGAAGTCGGCGCCGGTGGACCCCAAGACGGGC AAGAAGGGCGAAGAGGATGGCATGTGGTGGTGGTTCAACGATGACAAGGTGACGGAGGTGTCGGTTGACAAGATC GAGGGTTTGGCGGGCGGCGGCGAGTCGCACTCGGCCCTGATTCTGCTCTACAAGGCCATCCCGCTCCCCACGGCG GACGGGACGATGGAG |
| Transcript | >Ophio5|1241 ATGGCGGCAGTCACAGTCGTCGTGAAGCACCAGGGCAAGAGGCACGACGTCGAGGTTGACCCTGCGTCCACGGGC GAGGACTTCAAGCTTCAGCTTTTCAGCCTGACAAACGTCGAGCCGGCGCGGCAAAAGATCCTCATCAAGGGCGGC CAGCTCAAGGATGAGGCCGACATGGGCAAACTGGGGCTCAAGGCCGGCCAAGTCATCATGATGATGGGCACTCCG AGCTCCAGCGGAGGCAACCTCGTCCGCCCAAAGGACCCCATCAAGTTTGTCGAGGACATGACAGAGGCCGAGAAA GCTCAGCAGTTGGACGCCACCCCGGCCGGCCTTGTCAACCTCGGCAACACCTGCTATCTCAACTCGACGCTGCAA ACGCTGCGTTCCATTCCCGAACTCAATGCGGCTTTGCCCGAGTACGGTCCCACCAGGTCGTCGACCCTGGCGGAG GTTGACCTGGCCCATCACCTGTCCCGTCTGTACAAGGACATGGGCCGGACGCAGGAGGCCTTTCCGCCCGTCGAT TTCCTCAGCGCCCTGCGCTCCGCCTTCCCGCAGTTTGCTGAAAGATCCAAATCAGACAATGGTTATGCTCAGCAG GACGCCGAGGAGGCCTGGTCTCAGATCGTCCAGAACCTGAAGCCCAGAGTCAAGGTCAAGGACTTGGCTGGCACC GACGACGTGCTCGTGATTGACAAATACATGGCCGGCCAGCTAACGTCAACGATGGAGTGTCAAGATCCGGAGGCA AGCAAGGCAGGCGAGAAGACCGTGGTCCAAAAGGAAACCTTCTACAAGCTCAGCTGCCATATCGACGGCACGACG AATCACTTGCGGAACGGCATCCTGGCCGCGCTCAGCGAAAAGATTGAAAAGAAATCGGCTGTGCTGGACCGCGAA GCCGAGTACAAGAAGACGTCAGCGATTTCTCGCGCCCCCAAGTATCTGACAATCCATTTTGTGCGCTTCTTTTGG AAGCGTCAGACTCAGAAGAAGGCCAAGATCATGCGCAAGGTGACGTTTCCTCAGGAGCTGGATGTTGTCGAGTTT TGCTGTGACGACCTGAAGAAGGCGTTGATTCCCGTCAGGGACAGGGTGCGCGAAATCCGCAAGGACGAAGAGGAC ATCGAGCGGGCCCGCAAGCGCCGCAAGAAGAACCACGAGGAGCTACTGGCGGACATCCCGGGGGGTTCTGGGCTG GCATCGAGTAGGAAGGACGACAAGACGACCAAAGCCAAGGACGCGGTCGACGGCAACGCGGGCACGGACGAGACG TTCAAGACGGACGCCGAGATCGACGCTGAAAAGGATGCGGCGGTGCTAGCGGCCAAGAAGGAACTGCACGCCATG ATCGACCCGAGTCTTCGGGACGACGACGGCGCCAACCAGTCCGGGCTATACGAACTACGTGGCGTGGTGACGCAC CAGGGCGGCAGCGCCGACAGCGGACACTACACGGCTTACGTCAAGAAGTCGGCGCCGGTGGACCCCAAGACGGGC AAGAAGGGCGAAGAGGATGGCATGTGGTGGTGGTTCAACGATGACAAGGTGACGGAGGTGTCGGTTGACAAGATC GAGGGTTTGGCGGGCGGCGGCGAGTCGCACTCGGCCCTGATTCTGCTCTACAAGGCCATCCCGCTCCCCACGGCG GACGGGACGATGGAGTAG |
| Gene | >Ophio5|1241 ATGGCGGCAGTCACAGGTATACAATCTGATCTTCCGCCCCCGCCCGCCATACCTCTCTGACCTCCGCAGTCGTCG TGAAGCACCAGGGCAAGAGGCACGACGTCGAGGTTGACCCTGCGTCCACGGGCGAGGACTTCAAGCTTCAGCTTT TCAGCCTGACAAACGTCGAGCCGGCGCGGCAAAAGATCCTCATCAAGGGCGGCCAGCTCAAGGATGAGGCCGACA TGGGCAAACTGGGGCTCAAGGCCGGCCAAGTCATCATGATGATGGGCACTCCGAGCTCCAGCGGAGGCAACCTCG TCCGCCCAAAGGACCCCATCAAGTTTGTCGAGGACATGACAGAGGCCGAGAAAGCTCAGCAGTTGGACGCCACCC CGGCCGGCCTTGTCAACCTCGGCAACACCTGCTATCTCAACTCGACGCTGCAAACGCTGCGTTCCATTCCCGAAC TCAATGCGGCTTTGCCCGAGTACGGTCCCACCAGGTCGTCGACCCTGGCGGAGGTTGACCTGGCCCATCACCTGT CCCGTCTGTACAAGGACATGGGCCGGACGCAGGAGGCCTTTCCGCCCGTCGATTTCCTCAGCGCCCTGCGCTCCG CCTTCCCGCAGTTTGCTGAAAGATCCAAATCAGACAATGGTTATGCTCAGCAGGACGCCGAGGAGGCCTGGTCTC AGATCGTCCAGAACCTGAAGCCCAGAGTCAAGGTCAAGGACTTGGCTGGCACCGACGACGTGCTCGTGATTGACA AATACATGGCCGGCCAGCTAACGTCAACGATGGAGTGTCAAGATCCGGAGGCAAGCAAGGCAGGCGAGAAGACCG TGGTCCAAAAGGAAACCTTCTACAAGCTCAGCTGCCATATCGACGGCACGACGAATCACTTGCGGAACGGCATCC TGGCCGCGCTCAGCGAAAAGATTGAAAAGAAATCGGCTGTGCTGGACCGCGAAGCCGAGTACAAGAAGACGTCAG CGATTTCTCGCGCCCCCAAGTATCTGACAATCCATTTTGTGCGCTTCTTTTGGAAGCGTCAGACTCAGAAGAAGG CCAAGATCATGCGCAAGGTGACGTTTCCTCAGGAGCTGGATGTTGTCGAGTTTTGCTGTGACGACCTGAAGAAGG CGTTGATTCCCGTCAGGGACAGGGTGCGCGAAATCCGCAAGGACGAAGAGGACATCGAGCGGGCCCGCAAGCGCC GCAAGAAGAACCACGAGGAGCTACTGGCGGACATCCCGGGGGGTTCTGGGCTGGCATCGAGTAGGAAGGACGACA AGACGACCAAAGCCAAGGACGCGGTCGACGGCAACGCGGGCACGGACGAGACGTTCAAGACGGACGCCGAGATCG ACGCTGAAAAGGATGCGGCGGTGCTAGCGGCCAAGAAGGAACTGCACGCCATGATCGACCCGAGTCTTCGGGACG ACGACGGCGCCAACCAGTCCGGGCTATACGAACTACGTGGCGTGGTGACGCACCAGGGCGGCAGCGCCGACAGCG GACACTACACGGCTTACGTCAAGAAGTCGGCGCCGGTGGACCCCAAGACGGGCAAGAAGGGCGAAGAGGATGGCA TGTGGTGGTGGTTCAACGATGACAAGGTGACGGAGGTGTCGGTTGACAAGATCGAGGGTTTGGCGGGCGGCGGCG AGTCGCACTCGGCCCTGATTCTGCTCTACAAGGCCATCCCGCTCCCCACGGCGGACGGGACGATGGAGTAG |