© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Hirsu2|1188 |
| Gene name | |
| Location | Contig_1252:1144..3332 |
| Strand | - |
| Gene length (bp) | 2188 |
| Transcript length (bp) | 1569 |
| Coding sequence length (bp) | 1569 |
| Protein length (aa) | 523 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00083 | Sugar_tr | Sugar (and other) transporter | 1.1E-17 | 62 | 253 |
| PF00083 | Sugar_tr | Sugar (and other) transporter | 2.7E-12 | 266 | 470 |
| PF07690 | MFS_1 | Major Facilitator Superfamily | 1.2E-12 | 90 | 337 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|O94342|YHM9_SCHPO | Probable metabolite transport protein C1271.09 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC1271.09 PE=3 SV=1 | 8 | 491 | 8.0E-130 |
| sp|P25346|GIT1_YEAST | Probable metabolite transport protein GIT1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=GIT1 PE=1 SV=1 | 14 | 505 | 1.0E-80 |
| sp|Q7XRH8|PT113_ORYSJ | Putative inorganic phosphate transporter 1-13 OS=Oryza sativa subsp. japonica GN=PHT1-13 PE=3 SV=2 | 35 | 434 | 7.0E-27 |
| sp|Q8GYF4|PHT15_ARATH | Probable inorganic phosphate transporter 1-5 OS=Arabidopsis thaliana GN=PHT1-5 PE=2 SV=2 | 59 | 461 | 6.0E-20 |
| sp|Q01MW8|PHT14_ORYSI | Probable inorganic phosphate transporter 1-4 OS=Oryza sativa subsp. indica GN=PHT1-4 PE=2 SV=2 | 60 | 465 | 6.0E-20 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|O94342|YHM9_SCHPO | Probable metabolite transport protein C1271.09 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC1271.09 PE=3 SV=1 | 8 | 491 | 8.0E-130 |
| sp|P25346|GIT1_YEAST | Probable metabolite transport protein GIT1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=GIT1 PE=1 SV=1 | 14 | 505 | 1.0E-80 |
| sp|Q7XRH8|PT113_ORYSJ | Putative inorganic phosphate transporter 1-13 OS=Oryza sativa subsp. japonica GN=PHT1-13 PE=3 SV=2 | 35 | 434 | 7.0E-27 |
| sp|Q8GYF4|PHT15_ARATH | Probable inorganic phosphate transporter 1-5 OS=Arabidopsis thaliana GN=PHT1-5 PE=2 SV=2 | 59 | 461 | 6.0E-20 |
| sp|Q01MW8|PHT14_ORYSI | Probable inorganic phosphate transporter 1-4 OS=Oryza sativa subsp. indica GN=PHT1-4 PE=2 SV=2 | 60 | 465 | 6.0E-20 |
| sp|Q94DB8|PT111_ORYSJ | Inorganic phosphate transporter 1-11 OS=Oryza sativa subsp. japonica GN=PHT1-11 PE=2 SV=1 | 59 | 479 | 7.0E-20 |
| sp|Q8H6H2|PHT14_ORYSJ | Probable inorganic phosphate transporter 1-4 OS=Oryza sativa subsp. japonica GN=PHT1-4 PE=2 SV=1 | 60 | 465 | 7.0E-20 |
| sp|Q8GSD9|PHT12_ORYSJ | Inorganic phosphate transporter 1-2 OS=Oryza sativa subsp. japonica GN=PTH1-2 PE=2 SV=1 | 54 | 432 | 3.0E-19 |
| sp|Q7XDZ7|PHT13_ORYSJ | Probable inorganic phosphate transporter 1-3 OS=Oryza sativa subsp. japonica GN=PHT1-3 PE=2 SV=1 | 54 | 432 | 3.0E-18 |
| sp|Q8VYM2|PHT11_ARATH | Inorganic phosphate transporter 1-1 OS=Arabidopsis thaliana GN=PHT1-1 PE=1 SV=2 | 60 | 458 | 5.0E-18 |
| sp|Q9S735|PHT19_ARATH | Probable inorganic phosphate transporter 1-9 OS=Arabidopsis thaliana GN=PHT1-9 PE=2 SV=1 | 56 | 479 | 2.0E-17 |
| sp|Q7X7V2|PHT15_ORYSJ | Probable inorganic phosphate transporter 1-5 OS=Oryza sativa subsp. japonica GN=PHT1-5 PE=2 SV=2 | 56 | 469 | 2.0E-17 |
| sp|O48639|PHT13_ARATH | Probable inorganic phosphate transporter 1-3 OS=Arabidopsis thaliana GN=PHT1-3 PE=2 SV=1 | 60 | 461 | 4.0E-17 |
| sp|Q8H6H0|PHT16_ORYSJ | Inorganic phosphate transporter 1-6 OS=Oryza sativa subsp. japonica GN=PHT1-6 PE=1 SV=1 | 56 | 460 | 8.0E-17 |
| sp|Q8H074|PT112_ORYSJ | Probable inorganic phosphate transporter 1-12 OS=Oryza sativa subsp. japonica GN=PHT1-12 PE=2 SV=1 | 56 | 448 | 1.0E-16 |
| sp|Q9ZWT3|PHT16_ARATH | Probable inorganic phosphate transporter 1-6 OS=Arabidopsis thaliana GN=PHT1-6 PE=1 SV=1 | 56 | 469 | 2.0E-16 |
| sp|Q494P0|PHT17_ARATH | Probable inorganic phosphate transporter 1-7 OS=Arabidopsis thaliana GN=PHT1-7 PE=2 SV=2 | 56 | 461 | 3.0E-16 |
| sp|Q9P6J9|YHD1_SCHPO | Putative inorganic phosphate transporter C1683.01 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC1683.01 PE=3 SV=1 | 60 | 442 | 7.0E-16 |
| sp|O42885|YBN1_SCHPO | Putative inorganic phosphate transporter C8E4.01c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC8E4.01c PE=1 SV=2 | 32 | 442 | 7.0E-16 |
| sp|Q96303|PHT14_ARATH | Inorganic phosphate transporter 1-4 OS=Arabidopsis thaliana GN=PHT1-4 PE=1 SV=1 | 56 | 461 | 2.0E-15 |
| sp|Q9SYQ1|PHT18_ARATH | Probable inorganic phosphate transporter 1-8 OS=Arabidopsis thaliana GN=PHT1-8 PE=2 SV=2 | 56 | 427 | 2.0E-15 |
| sp|Q8H6H4|PHT11_ORYSJ | Inorganic phosphate transporter 1-1 OS=Oryza sativa subsp. japonica GN=PHT1-1 PE=2 SV=1 | 54 | 408 | 8.0E-15 |
| sp|Q8H6G9|PHT17_ORYSJ | Probable inorganic phosphate transporter 1-7 OS=Oryza sativa subsp. japonica GN=PHT1-7 PE=2 SV=1 | 60 | 448 | 4.0E-14 |
| sp|Q8H6G8|PHT18_ORYSJ | Probable inorganic phosphate transporter 1-8 OS=Oryza sativa subsp. japonica GN=PHT1-8 PE=2 SV=1 | 56 | 408 | 3.0E-13 |
| sp|Q7RVX9|PHO5_NEUCR | Repressible high-affinity phosphate permease OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=pho-5 PE=1 SV=2 | 56 | 509 | 4.0E-12 |
| sp|P25297|PHO84_YEAST | Inorganic phosphate transporter PHO84 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PHO84 PE=1 SV=2 | 5 | 425 | 5.0E-12 |
| sp|Q96243|PHT12_ARATH | Probable inorganic phosphate transporter 1-2 OS=Arabidopsis thaliana GN=PHT1-2 PE=2 SV=2 | 60 | 307 | 9.0E-12 |
| sp|Q69T94|PT110_ORYSJ | Probable inorganic phosphate transporter 1-10 OS=Oryza sativa subsp. japonica GN=PHT1-10 PE=2 SV=1 | 60 | 493 | 1.0E-11 |
| sp|P39352|YJHB_ECOLI | Putative metabolite transport protein YjhB OS=Escherichia coli (strain K12) GN=yjhB PE=1 SV=2 | 56 | 353 | 3.0E-10 |
| sp|Q9Y7Q9|YCX2_SCHPO | Probable metabolite transporter C2H8.02 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPCC2H8.02 PE=1 SV=1 | 60 | 267 | 1.0E-09 |
| sp|Q09852|YAEC_SCHPO | Putative inorganic phosphate transporter C23D3.12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC23D3.12 PE=1 SV=1 | 5 | 266 | 6.0E-09 |
| sp|Q8H6G7|PHT19_ORYSJ | Probable inorganic phosphate transporter 1-9 OS=Oryza sativa subsp. japonica GN=PHT1-9 PE=2 SV=2 | 60 | 430 | 2.0E-08 |
| sp|P31679|YAAU_ECOLI | Putative metabolite transport protein YaaU OS=Escherichia coli (strain K12) GN=yaaU PE=3 SV=2 | 62 | 431 | 2.0E-08 |
| sp|O34691|NAIP_BACSU | Putative niacin/nicotinamide transporter NaiP OS=Bacillus subtilis (strain 168) GN=naiP PE=1 SV=1 | 90 | 478 | 6.0E-08 |
| sp|Q09852|YAEC_SCHPO | Putative inorganic phosphate transporter C23D3.12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC23D3.12 PE=1 SV=1 | 278 | 442 | 1.0E-07 |
| sp|Q5HRH0|PROP_STAEQ | Putative proline/betaine transporter OS=Staphylococcus epidermidis (strain ATCC 35984 / RP62A) GN=proP PE=3 SV=1 | 117 | 345 | 2.0E-06 |
| sp|Q8NXW9|PROP_STAAW | Putative proline/betaine transporter OS=Staphylococcus aureus (strain MW2) GN=proP PE=3 SV=1 | 100 | 384 | 3.0E-06 |
| sp|Q6GBR4|PROP_STAAS | Putative proline/betaine transporter OS=Staphylococcus aureus (strain MSSA476) GN=proP PE=3 SV=1 | 100 | 384 | 3.0E-06 |
| sp|Q7A771|PROP_STAAN | Putative proline/betaine transporter OS=Staphylococcus aureus (strain N315) GN=proP PE=3 SV=1 | 100 | 384 | 5.0E-06 |
| sp|Q99W36|PROP_STAAM | Putative proline/betaine transporter OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=proP PE=3 SV=1 | 100 | 384 | 5.0E-06 |
| sp|Q5HIA2|PROP_STAAC | Putative proline/betaine transporter OS=Staphylococcus aureus (strain COL) GN=proP PE=3 SV=1 | 100 | 384 | 5.0E-06 |
| sp|Q9KWK6|PROP_STAA1 | Putative proline/betaine transporter OS=Staphylococcus aureus (strain Mu3 / ATCC 700698) GN=proP PE=3 SV=3 | 100 | 384 | 5.0E-06 |
| sp|Q6GJ96|PROP_STAAR | Putative proline/betaine transporter OS=Staphylococcus aureus (strain MRSA252) GN=proP PE=3 SV=1 | 100 | 383 | 9.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0016021 | integral component of membrane | Yes |
| GO:0055085 | transmembrane transport | Yes |
| GO:0022857 | transmembrane transporter activity | Yes |
| GO:0031224 | intrinsic component of membrane | No |
| GO:0009987 | cellular process | No |
| GO:0110165 | cellular anatomical entity | No |
| GO:0051179 | localization | No |
| GO:0005215 | transporter activity | No |
| GO:0005575 | cellular_component | No |
| GO:0008150 | biological_process | No |
| GO:0051234 | establishment of localization | No |
| GO:0003674 | molecular_function | No |
| GO:0006810 | transport | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 34 | 0.45 |
| Domain # | Start | End | Length |
|---|---|---|---|
| 1 | 124 | 146 | 22 |
| 2 | 156 | 178 | 22 |
| 3 | 191 | 213 | 22 |
| 4 | 228 | 247 | 19 |
| 5 | 267 | 289 | 22 |
| 6 | 317 | 339 | 22 |
| 7 | 346 | 366 | 20 |
| 8 | 376 | 398 | 22 |
| 9 | 411 | 433 | 22 |
| 10 | 448 | 470 | 22 |
| 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 | >Hirsu2|1188 MFDFRRLVSRSHSSQEQQHENHRERAAENVGDRTSERASVRHTIGSRSFLQTALPVFACGAGLFSDGYINNVIGS VNTVLKLQYGNVYKDSQAAKYVADIAFAGTVVGQLVFGYTSDRWSRSNSLVLSTVILIIFTALATGSYYNGDAVG MFNMLAAWRFFVGIGIGGEYPAGSVGCAESSGELKEGTRNRWFILFTNSMIDWGFVFGAFVPYVVAAAVHNDLSQ YSIIWRTSLGIGIIFPLLLLLMRMRLKEPEEFSKESMKKQTPYLLVLRFYWFRLLCVSVIWFFYDFSTYAFGIYS SSILSGIYGDNAPLTTVFGWNTVVNMFYLPGTMFGAFVSDWIGPKYTLIIGVVLQAVVGYIMAGVYEQISRHVAA FAVVYGIFLTLGELGPGNNLGLLAAKTCATGVRGRYYGIAAAVGKVGAFVGTWVFPYIQASGGKGTVQSAQYPFW VASSLSLLSAVIAFFCIPNIGQDTIAHEDVRFREYLHSKGWDTTLLGLSRDDSNAASYAEDEQTPVKALRSH* |
| Coding | >Hirsu2|1188 ATGTTCGACTTCCGCCGCCTCGTCTCTCGCTCACACTCGTCTCAAGAACAACAGCACGAGAACCATCGCGAGCGC GCCGCCGAGAACGTGGGCGACCGCACAAGCGAGCGCGCCAGCGTGCGACACACCATCGGATCCAGGTCCTTTCTG CAAACCGCCCTGCCCGTCTTTGCCTGCGGCGCTGGCCTCTTTTCCGACGGCTACATCAATAACGTCATCGGCTCC GTCAACACCGTCCTCAAGCTTCAGTATGGCAACGTCTACAAGGACTCGCAGGCCGCCAAGTATGTGGCCGACATT GCCTTTGCCGGCACCGTCGTCGGCCAGCTCGTCTTCGGCTACACCTCCGATCGCTGGTCGCGCTCCAATTCGCTC GTCCTGTCCACCGTCATCCTCATCATCTTCACCGCCCTCGCCACCGGCTCCTACTACAACGGCGATGCTGTCGGC ATGTTCAACATGCTGGCCGCCTGGCGCTTCTTCGTCGGTATCGGCATTGGCGGAGAGTACCCGGCCGGCAGCGTC GGCTGCGCCGAGTCGAGCGGCGAGCTCAAAGAAGGCACCCGCAACCGCTGGTTTATCCTCTTCACCAACAGCATG ATCGACTGGGGCTTCGTCTTTGGCGCCTTCGTCCCCTACGTCGTCGCCGCCGCCGTCCACAACGACCTGAGCCAG TACTCGATCATCTGGCGCACCAGCCTCGGGATCGGCATCATCTTCCCTCTCCTGCTGCTCCTCATGCGCATGCGC CTCAAGGAGCCCGAGGAGTTCTCCAAGGAGTCGATGAAGAAGCAGACGCCATACCTGCTCGTCCTTCGCTTCTAC TGGTTCCGCCTGCTCTGCGTGAGCGTCATCTGGTTCTTTTACGACTTTAGCACCTACGCCTTTGGCATCTACTCA TCCTCCATCCTCAGCGGCATCTACGGCGACAACGCACCCCTGACGACCGTCTTCGGCTGGAACACGGTCGTCAAC ATGTTCTACCTGCCGGGCACCATGTTCGGCGCCTTCGTCAGCGACTGGATCGGCCCCAAGTACACGCTCATCATC GGCGTCGTCCTCCAGGCCGTCGTCGGCTACATCATGGCCGGCGTCTACGAGCAGATCTCGCGCCACGTCGCCGCC TTCGCCGTCGTCTACGGCATCTTCCTCACCCTCGGCGAGCTGGGTCCGGGTAACAACCTGGGCCTGCTGGCGGCC AAGACGTGCGCCACCGGCGTCCGCGGCCGCTACTACGGCATCGCCGCCGCCGTCGGCAAGGTCGGCGCCTTCGTC GGCACCTGGGTCTTCCCCTACATCCAGGCCTCCGGCGGCAAAGGCACGGTCCAGTCGGCCCAGTACCCCTTCTGG GTCGCCTCCAGCCTGTCCCTCCTGTCCGCCGTCATCGCCTTCTTCTGCATCCCCAACATCGGCCAGGACACAATC GCCCACGAAGACGTCCGCTTCCGCGAGTACCTCCATAGCAAGGGCTGGGACACAACTCTGCTCGGCCTTTCCAGG GACGACTCCAACGCAGCCTCGTATGCCGAGGACGAGCAGACGCCCGTCAAGGCGCTGAGAAGCCACTGA |
| Transcript | >Hirsu2|1188 ATGTTCGACTTCCGCCGCCTCGTCTCTCGCTCACACTCGTCTCAAGAACAACAGCACGAGAACCATCGCGAGCGC GCCGCCGAGAACGTGGGCGACCGCACAAGCGAGCGCGCCAGCGTGCGACACACCATCGGATCCAGGTCCTTTCTG CAAACCGCCCTGCCCGTCTTTGCCTGCGGCGCTGGCCTCTTTTCCGACGGCTACATCAATAACGTCATCGGCTCC GTCAACACCGTCCTCAAGCTTCAGTATGGCAACGTCTACAAGGACTCGCAGGCCGCCAAGTATGTGGCCGACATT GCCTTTGCCGGCACCGTCGTCGGCCAGCTCGTCTTCGGCTACACCTCCGATCGCTGGTCGCGCTCCAATTCGCTC GTCCTGTCCACCGTCATCCTCATCATCTTCACCGCCCTCGCCACCGGCTCCTACTACAACGGCGATGCTGTCGGC ATGTTCAACATGCTGGCCGCCTGGCGCTTCTTCGTCGGTATCGGCATTGGCGGAGAGTACCCGGCCGGCAGCGTC GGCTGCGCCGAGTCGAGCGGCGAGCTCAAAGAAGGCACCCGCAACCGCTGGTTTATCCTCTTCACCAACAGCATG ATCGACTGGGGCTTCGTCTTTGGCGCCTTCGTCCCCTACGTCGTCGCCGCCGCCGTCCACAACGACCTGAGCCAG TACTCGATCATCTGGCGCACCAGCCTCGGGATCGGCATCATCTTCCCTCTCCTGCTGCTCCTCATGCGCATGCGC CTCAAGGAGCCCGAGGAGTTCTCCAAGGAGTCGATGAAGAAGCAGACGCCATACCTGCTCGTCCTTCGCTTCTAC TGGTTCCGCCTGCTCTGCGTGAGCGTCATCTGGTTCTTTTACGACTTTAGCACCTACGCCTTTGGCATCTACTCA TCCTCCATCCTCAGCGGCATCTACGGCGACAACGCACCCCTGACGACCGTCTTCGGCTGGAACACGGTCGTCAAC ATGTTCTACCTGCCGGGCACCATGTTCGGCGCCTTCGTCAGCGACTGGATCGGCCCCAAGTACACGCTCATCATC GGCGTCGTCCTCCAGGCCGTCGTCGGCTACATCATGGCCGGCGTCTACGAGCAGATCTCGCGCCACGTCGCCGCC TTCGCCGTCGTCTACGGCATCTTCCTCACCCTCGGCGAGCTGGGTCCGGGTAACAACCTGGGCCTGCTGGCGGCC AAGACGTGCGCCACCGGCGTCCGCGGCCGCTACTACGGCATCGCCGCCGCCGTCGGCAAGGTCGGCGCCTTCGTC GGCACCTGGGTCTTCCCCTACATCCAGGCCTCCGGCGGCAAAGGCACGGTCCAGTCGGCCCAGTACCCCTTCTGG GTCGCCTCCAGCCTGTCCCTCCTGTCCGCCGTCATCGCCTTCTTCTGCATCCCCAACATCGGCCAGGACACAATC GCCCACGAAGACGTCCGCTTCCGCGAGTACCTCCATAGCAAGGGCTGGGACACAACTCTGCTCGGCCTTTCCAGG GACGACTCCAACGCAGCCTCGTATGCCGAGGACGAGCAGACGCCCGTCAAGGCGCTGAGAAGCCACTGA |
| Gene | >Hirsu2|1188 ATGTTCGACTTCCGCCGCCTCGTCTCTCGCTCACACTCGTCTCAAGAACAACAGCACGAGAACCATCGCGAGCGC GCCGCCGAGAACGTGGGCGACCGCACAAGCGAGCGCGCCAGCGTGCGACACACCATCGGATCCAGGTCCTTTCTG CAAACCGCCCTGCCCGTCTTTGCCTGCGGCGCTGGCCTCTTTTCCGACGGCTACATCAATAACGTAAGTCTCGAC ACCAATTGCACAGAATGCAGCAAGTCGCCGCCCAGACGCATCAAGAGAAGACGCCACCAGGGTACGGGGGCGGCG AGACGGAGCCAAGGGACGCAGGCGAGGCCTCAGAAGAGACGGACACTCGGTGAGCCACTGAAAGAAACGAGATGC GAGAGAAAGATAAAAGATGGGGACAAGCAGCGGTTCGCCAAGGAGAGAGACAGGGAGGCGCAGGTCGAGGAGAGG AGTGGCTGAGCGGTCGGGAAGACGAGTCTTGGAACCGTCCGGCAGCTAACAAACCGTCTTCTTCCGCTCTCGCGC CAAAACAAAAATAGGTCATCGGCTCCGTCAACACCGTCCTCAAGCTTCAGTATGGCAACGTCTACAAGGACTCGC AGGCCGCCAAGTATGTGGCCGACATTGCCTTTGCCGGCACCGTCGTCGGCCAGCTCGTCTTCGGCTACACCTCCG ATCGCTGGTCGCGCTCCAATTCGCTCGTCCTGTCCACCGTCATCCTCATCATCTTCACCGCCCTCGCCACCGGCT CCTACTACAACGGCGATGCTGTCGGCATGTTCAACATGCTGGCCGCCTGGCGCTTCTTCGTCGGTATCGGCATTG GCGGTGCGATCGCCTCCCCCGGCCTCTCACCCTGCCAGGAAGGGGCAGGAAAGCTGACGGTCTGGATCCCACAGG AGAGTACCCGGCCGGCAGCGTCGGCTGCGCCGAGTCGAGCGGCGAGCTCAAAGAAGGCACCCGCAACCGCTGGTT TATCCTCTTCACCAACAGCATGATCGACTGGGGCTTCGTCTTTGGCGCCTTCGTCCCCTGTGAGTCCTCCCGCAT GTTCTCCCTTCCACCTTCGACGAATCCCTGCCTCCTCTCCGACGACGAGCCAGTGTCTCTCCCCCCTTTTCTATC TCGGCCGCTTGCAACCCCCTATTCGCTGACGGAGACGGGATTGGAATGAATGCAGACGTCGTCGCCGCCGCCGTC CACAACGACCTGAGCCAGTACTCGATCATCTGGCGCACCAGCCTCGGGATCGGCATCATCTTCCCTCTCCTGCTG CTCCTCATGCGCATGCGCCTCAAGGAGCCCGAGGAGTTCTCCAAGGAGTCGATGAAGAAGCAGACGCCATACCTG CTCGTCCTTCGCTTCTACTGGTTCCGCCTGCTCTGCGTGAGCGTCATCTGGTTCTTTTACGACGTGAGTCTTTCC TCGTACCTGGAAGACAGGGGCATGGCCTTCTAATCGTCGACGTGGATCCGTCGCCCCTCTCCAGTTTAGCACCTA CGCCTTTGGCATCTACTCATCCTCCATCCTCAGCGGCATCTACGGCGACAACGCACCCCTGACGACCGTCTTCGG CTGGAACACGGTCGTCAACATGTTCTACCTGCCGGGCACCATGTTCGGCGCCTTCGTCAGCGACTGGATCGGCCC CAAGTACACGCTCATCATCGGCGTCGTCCTCCAGGCCGTCGTCGGCTACATCATGGCCGGCGTCTACGAGCAGAT CTCGCGCCACGTCGCCGCCTTCGCCGTCGTCTACGGCATCTTCCTCACCCTCGGCGAGCTGGGTCCGGGTAACAA CCTGGGCCTGCTGGCGGCCAAGACGTGCGCCACCGGCGTCCGCGGCCGCTACTACGGCATCGCCGCCGCCGTCGG CAAGGTCGGCGCCTTCGTCGGCACCTGGGTCTTCCCCTACATCCAGGCCTCCGGCGGCAAAGGCACGGTCCAGTC GGCCCAGTACCCCTTCTGGGTCGCCTCCAGCCTGTCCCTCCTGTCCGCCGTCATCGCCTTCTTCTGCATCCCCAA CATCGGCCAGGACACAATCGCCCACGAAGACGTCCGCTTCCGCGAGTACCTCCATAGCAAGGGCTGGGACACAAC TCTGCTCGGCCTTTCCAGGGACGACTCCAACGCAGCCTCGTATGCCGAGGACGAGCAGACGCCCGTCAAGGCGCT GAGAAGCCACTGA |