© 2022 - Robin Ohm - Utrecht University - The Netherlands
Built with Python Django and Wagtail
| Protein ID | OphauG2|3564 |
| Gene name | |
| Location | Contig_274:10969..12972 |
| Strand | + |
| Gene length (bp) | 2003 |
| Transcript length (bp) | 1518 |
| Coding sequence length (bp) | 1518 |
| Protein length (aa) | 506 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00083 | Sugar_tr | Sugar (and other) transporter | 1.0E-17 | 48 | 239 |
| PF00083 | Sugar_tr | Sugar (and other) transporter | 1.5E-14 | 257 | 452 |
| PF07690 | MFS_1 | Major Facilitator Superfamily | 3.8E-12 | 51 | 309 |
| PF07690 | MFS_1 | Major Facilitator Superfamily | 1.5E-10 | 301 | 461 |
| 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 | 38 | 464 | 8.0E-127 |
| sp|P25346|GIT1_YEAST | Probable metabolite transport protein GIT1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=GIT1 PE=1 SV=1 | 13 | 488 | 9.0E-84 |
| sp|Q94DB8|PT111_ORYSJ | Inorganic phosphate transporter 1-11 OS=Oryza sativa subsp. japonica GN=PHT1-11 PE=2 SV=1 | 43 | 461 | 2.0E-23 |
| sp|Q7XRH8|PT113_ORYSJ | Putative inorganic phosphate transporter 1-13 OS=Oryza sativa subsp. japonica GN=PHT1-13 PE=3 SV=2 | 38 | 416 | 3.0E-19 |
| sp|Q8H6H0|PHT16_ORYSJ | Inorganic phosphate transporter 1-6 OS=Oryza sativa subsp. japonica GN=PHT1-6 PE=1 SV=1 | 40 | 442 | 2.0E-18 |
| 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 | 38 | 464 | 8.0E-127 |
| sp|P25346|GIT1_YEAST | Probable metabolite transport protein GIT1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=GIT1 PE=1 SV=1 | 13 | 488 | 9.0E-84 |
| sp|Q94DB8|PT111_ORYSJ | Inorganic phosphate transporter 1-11 OS=Oryza sativa subsp. japonica GN=PHT1-11 PE=2 SV=1 | 43 | 461 | 2.0E-23 |
| sp|Q7XRH8|PT113_ORYSJ | Putative inorganic phosphate transporter 1-13 OS=Oryza sativa subsp. japonica GN=PHT1-13 PE=3 SV=2 | 38 | 416 | 3.0E-19 |
| sp|Q8H6H0|PHT16_ORYSJ | Inorganic phosphate transporter 1-6 OS=Oryza sativa subsp. japonica GN=PHT1-6 PE=1 SV=1 | 40 | 442 | 2.0E-18 |
| sp|Q8GYF4|PHT15_ARATH | Probable inorganic phosphate transporter 1-5 OS=Arabidopsis thaliana GN=PHT1-5 PE=2 SV=2 | 1 | 488 | 3.0E-18 |
| sp|Q8H074|PT112_ORYSJ | Probable inorganic phosphate transporter 1-12 OS=Oryza sativa subsp. japonica GN=PHT1-12 PE=2 SV=1 | 40 | 430 | 3.0E-18 |
| sp|Q9SYQ1|PHT18_ARATH | Probable inorganic phosphate transporter 1-8 OS=Arabidopsis thaliana GN=PHT1-8 PE=2 SV=2 | 40 | 478 | 4.0E-18 |
| sp|Q8H6H2|PHT14_ORYSJ | Probable inorganic phosphate transporter 1-4 OS=Oryza sativa subsp. japonica GN=PHT1-4 PE=2 SV=1 | 44 | 491 | 4.0E-18 |
| sp|Q7XDZ7|PHT13_ORYSJ | Probable inorganic phosphate transporter 1-3 OS=Oryza sativa subsp. japonica GN=PHT1-3 PE=2 SV=1 | 38 | 414 | 8.0E-18 |
| sp|Q01MW8|PHT14_ORYSI | Probable inorganic phosphate transporter 1-4 OS=Oryza sativa subsp. indica GN=PHT1-4 PE=2 SV=2 | 44 | 491 | 8.0E-18 |
| sp|Q8VYM2|PHT11_ARATH | Inorganic phosphate transporter 1-1 OS=Arabidopsis thaliana GN=PHT1-1 PE=1 SV=2 | 43 | 440 | 1.0E-17 |
| sp|Q9S735|PHT19_ARATH | Probable inorganic phosphate transporter 1-9 OS=Arabidopsis thaliana GN=PHT1-9 PE=2 SV=1 | 40 | 461 | 2.0E-17 |
| sp|Q9ZWT3|PHT16_ARATH | Probable inorganic phosphate transporter 1-6 OS=Arabidopsis thaliana GN=PHT1-6 PE=1 SV=1 | 37 | 424 | 2.0E-17 |
| sp|Q494P0|PHT17_ARATH | Probable inorganic phosphate transporter 1-7 OS=Arabidopsis thaliana GN=PHT1-7 PE=2 SV=2 | 40 | 440 | 3.0E-17 |
| sp|O48639|PHT13_ARATH | Probable inorganic phosphate transporter 1-3 OS=Arabidopsis thaliana GN=PHT1-3 PE=2 SV=1 | 44 | 440 | 7.0E-17 |
| sp|Q96303|PHT14_ARATH | Inorganic phosphate transporter 1-4 OS=Arabidopsis thaliana GN=PHT1-4 PE=1 SV=1 | 40 | 430 | 1.0E-16 |
| sp|Q8GSD9|PHT12_ORYSJ | Inorganic phosphate transporter 1-2 OS=Oryza sativa subsp. japonica GN=PTH1-2 PE=2 SV=1 | 38 | 414 | 4.0E-16 |
| sp|Q8H6G9|PHT17_ORYSJ | Probable inorganic phosphate transporter 1-7 OS=Oryza sativa subsp. japonica GN=PHT1-7 PE=2 SV=1 | 43 | 461 | 1.0E-15 |
| sp|Q7X7V2|PHT15_ORYSJ | Probable inorganic phosphate transporter 1-5 OS=Oryza sativa subsp. japonica GN=PHT1-5 PE=2 SV=2 | 40 | 471 | 1.0E-15 |
| sp|Q69T94|PT110_ORYSJ | Probable inorganic phosphate transporter 1-10 OS=Oryza sativa subsp. japonica GN=PHT1-10 PE=2 SV=1 | 44 | 476 | 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 | 16 | 383 | 2.0E-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 | 37 | 491 | 1.0E-12 |
| sp|Q8H6G7|PHT19_ORYSJ | Probable inorganic phosphate transporter 1-9 OS=Oryza sativa subsp. japonica GN=PHT1-9 PE=2 SV=2 | 44 | 504 | 3.0E-12 |
| sp|O42885|YBN1_SCHPO | Putative inorganic phosphate transporter C8E4.01c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC8E4.01c PE=1 SV=2 | 44 | 424 | 1.0E-11 |
| sp|Q8H6H4|PHT11_ORYSJ | Inorganic phosphate transporter 1-1 OS=Oryza sativa subsp. japonica GN=PHT1-1 PE=2 SV=1 | 38 | 390 | 2.0E-11 |
| sp|Q96243|PHT12_ARATH | Probable inorganic phosphate transporter 1-2 OS=Arabidopsis thaliana GN=PHT1-2 PE=2 SV=2 | 44 | 390 | 2.0E-10 |
| sp|P39352|YJHB_ECOLI | Putative metabolite transport protein YjhB OS=Escherichia coli (strain K12) GN=yjhB PE=1 SV=2 | 20 | 339 | 3.0E-09 |
| sp|Q9Y7Q9|YCX2_SCHPO | Probable metabolite transporter C2H8.02 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPCC2H8.02 PE=1 SV=1 | 44 | 249 | 4.0E-08 |
| sp|O34691|NAIP_BACSU | Putative niacin/nicotinamide transporter NaiP OS=Bacillus subtilis (strain 168) GN=naiP PE=1 SV=1 | 74 | 411 | 6.0E-08 |
| sp|Q6GBR4|PROP_STAAS | Putative proline/betaine transporter OS=Staphylococcus aureus (strain MSSA476) GN=proP PE=3 SV=1 | 84 | 370 | 1.0E-07 |
| sp|Q8NXW9|PROP_STAAW | Putative proline/betaine transporter OS=Staphylococcus aureus (strain MW2) GN=proP PE=3 SV=1 | 84 | 370 | 1.0E-07 |
| sp|Q7A771|PROP_STAAN | Putative proline/betaine transporter OS=Staphylococcus aureus (strain N315) GN=proP PE=3 SV=1 | 84 | 370 | 2.0E-07 |
| sp|Q99W36|PROP_STAAM | Putative proline/betaine transporter OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=proP PE=3 SV=1 | 84 | 370 | 2.0E-07 |
| sp|Q5HIA2|PROP_STAAC | Putative proline/betaine transporter OS=Staphylococcus aureus (strain COL) GN=proP PE=3 SV=1 | 84 | 370 | 2.0E-07 |
| sp|Q9KWK6|PROP_STAA1 | Putative proline/betaine transporter OS=Staphylococcus aureus (strain Mu3 / ATCC 700698) GN=proP PE=3 SV=3 | 84 | 370 | 2.0E-07 |
| sp|Q09852|YAEC_SCHPO | Putative inorganic phosphate transporter C23D3.12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC23D3.12 PE=1 SV=1 | 260 | 462 | 3.0E-07 |
| sp|Q6GJ96|PROP_STAAR | Putative proline/betaine transporter OS=Staphylococcus aureus (strain MRSA252) GN=proP PE=3 SV=1 | 84 | 370 | 6.0E-07 |
| sp|Q9P6J9|YHD1_SCHPO | Putative inorganic phosphate transporter C1683.01 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC1683.01 PE=3 SV=1 | 16 | 241 | 1.0E-06 |
| sp|P25297|PHO84_YEAST | Inorganic phosphate transporter PHO84 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PHO84 PE=1 SV=2 | 35 | 504 | 3.0E-06 |
| sp|Q9P6J9|YHD1_SCHPO | Putative inorganic phosphate transporter C1683.01 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC1683.01 PE=3 SV=1 | 260 | 424 | 4.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0022857 | transmembrane transporter activity | Yes |
| GO:0016021 | integral component of membrane | Yes |
| GO:0055085 | transmembrane transport | Yes |
| GO:0051234 | establishment of localization | No |
| GO:0003674 | molecular_function | No |
| GO:0005215 | transporter activity | No |
| GO:0051179 | localization | No |
| GO:0006810 | transport | No |
| GO:0009987 | cellular process | No |
| GO:0031224 | intrinsic component of membrane | No |
| GO:0008150 | biological_process | No |
| GO:0005575 | cellular_component | No |
| GO:0110165 | cellular anatomical entity | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 11 | 0.5 |
| Domain # | Start | End | Length |
|---|---|---|---|
| 1 | 77 | 99 | 22 |
| 2 | 109 | 128 | 19 |
| 3 | 178 | 200 | 22 |
| 4 | 210 | 229 | 19 |
| 5 | 256 | 278 | 22 |
| 6 | 298 | 320 | 22 |
| 7 | 329 | 348 | 19 |
| 8 | 358 | 380 | 22 |
| 9 | 393 | 415 | 22 |
| 10 | 430 | 452 | 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 | >OphauG2|3564 MSTWGRRLLRRWSPTEEESHHQTAPPPASSKPFFQTVLPVFACGAGLFSDGYINNVIGSVNTVLRLQYGSQYTSS RAARYVADIAFAGTVIGQLVFGFASDRWSRSNSLVLSTVILIVFTALAAGSYFRGDTVAMFDMLAAWRFFVGIGI GGEYPAGSVGCAESSGEMKTGTRNRWFILFTNSMIDVGFVFGAFIPYVIAAAASNRHYDTIWRTSLAIGVLFPIV LLLIRMRLKEPQEFARESMRRKTPYLLVLRFYWFRLFCVSLIWFLYDFSIYAFGIYSSSILSGLYGDDAPLTTIF GWNTVINVFYLPGTLLGAWVSDKLGPRNTLIIGVCAQAIVGYIMAAVYAHISTRIALFAVIYGLFLSLGELGPGN NIGLLAAKTCATGVRGRYYGISAAIGKIGAFVGTLVFPYIQAAGGKDTVESAQYPFWVASSLCLLSAAVAFFFVP NVGQDTISREDVRFREYLEAQGWDTSQLGLSKNDSRDISYAQQELQIDQLSHKAR* |
| Coding | >OphauG2|3564 ATGTCGACCTGGGGCCGCCGCCTGCTACGACGCTGGTCGCCCACCGAGGAGGAATCGCATCACCAAACCGCGCCG CCGCCGGCGTCCTCGAAACCCTTTTTCCAAACCGTGCTGCCCGTGTTTGCCTGCGGCGCTGGCCTCTTCTCTGAC GGCTACATCAACAATGTCATTGGCTCCGTCAACACGGTATTGCGGCTTCAATATGGGAGCCAGTACACGTCGTCG CGCGCCGCTCGCTATGTCGCCGACATTGCCTTTGCCGGCACCGTCATAGGCCAGCTCGTCTTTGGCTTTGCGTCG GATCGCTGGTCGCGGTCAAACTCGCTCGTCCTCTCCACCGTCATCCTCATAGTCTTTACCGCGCTGGCAGCCGGC TCTTATTTCCGCGGCGACACTGTGGCCATGTTTGACATGCTGGCTGCGTGGCGCTTTTTTGTCGGCATTGGCATT GGCGGCGAGTATCCCGCTGGCAGCGTCGGCTGCGCAGAATCGAGCGGCGAAATGAAGACCGGCACCCGCAACCGC TGGTTCATCCTCTTTACAAACAGCATGATTGACGTGGGTTTCGTCTTTGGCGCCTTCATCCCCTACGTCATTGCC GCCGCCGCCAGTAATCGCCACTACGACACCATTTGGCGCACCAGCCTGGCCATTGGCGTCCTTTTCCCAATTGTC CTCTTGCTCATCCGCATGCGCCTCAAGGAACCCCAAGAATTCGCCCGCGAGTCGATGCGCCGCAAGACGCCCTAT CTCCTCGTTTTGCGCTTCTACTGGTTCCGTCTGTTTTGCGTCAGCCTCATTTGGTTTCTCTACGACTTTAGCATC TACGCCTTTGGCATCTACTCGTCGTCGATTCTTAGCGGTCTCTATGGCGACGACGCCCCCCTCACCACAATCTTT GGCTGGAACACCGTCATCAACGTCTTCTACCTCCCTGGGACCCTCCTCGGCGCCTGGGTCAGCGACAAGTTGGGG CCCAGAAACACCCTCATCATCGGCGTCTGCGCCCAGGCCATTGTTGGCTACATCATGGCCGCCGTGTACGCTCAT ATCTCGACGCGAATCGCTCTCTTTGCCGTCATCTATGGCCTCTTTCTCTCCCTCGGCGAACTAGGCCCAGGCAAC AATATTGGTCTCTTGGCTGCAAAGACTTGCGCCACCGGCGTCCGAGGCCGCTACTATGGCATTTCAGCCGCCATT GGAAAGATTGGCGCCTTTGTCGGCACTCTCGTCTTCCCCTATATTCAGGCTGCCGGAGGCAAAGACACAGTCGAG TCGGCGCAGTATCCCTTTTGGGTCGCCTCCAGTCTCTGCCTTCTCTCTGCTGCCGTTGCCTTCTTCTTTGTGCCA AACGTTGGCCAGGATACCATTTCTCGAGAAGACGTGCGCTTTCGTGAATACCTCGAGGCTCAGGGCTGGGACACG TCTCAGCTGGGTCTCTCAAAAAACGACTCCCGTGACATTTCCTATGCTCAACAAGAGCTGCAGATTGATCAATTG TCGCACAAGGCTAGATAG |
| Transcript | >OphauG2|3564 ATGTCGACCTGGGGCCGCCGCCTGCTACGACGCTGGTCGCCCACCGAGGAGGAATCGCATCACCAAACCGCGCCG CCGCCGGCGTCCTCGAAACCCTTTTTCCAAACCGTGCTGCCCGTGTTTGCCTGCGGCGCTGGCCTCTTCTCTGAC GGCTACATCAACAATGTCATTGGCTCCGTCAACACGGTATTGCGGCTTCAATATGGGAGCCAGTACACGTCGTCG CGCGCCGCTCGCTATGTCGCCGACATTGCCTTTGCCGGCACCGTCATAGGCCAGCTCGTCTTTGGCTTTGCGTCG GATCGCTGGTCGCGGTCAAACTCGCTCGTCCTCTCCACCGTCATCCTCATAGTCTTTACCGCGCTGGCAGCCGGC TCTTATTTCCGCGGCGACACTGTGGCCATGTTTGACATGCTGGCTGCGTGGCGCTTTTTTGTCGGCATTGGCATT GGCGGCGAGTATCCCGCTGGCAGCGTCGGCTGCGCAGAATCGAGCGGCGAAATGAAGACCGGCACCCGCAACCGC TGGTTCATCCTCTTTACAAACAGCATGATTGACGTGGGTTTCGTCTTTGGCGCCTTCATCCCCTACGTCATTGCC GCCGCCGCCAGTAATCGCCACTACGACACCATTTGGCGCACCAGCCTGGCCATTGGCGTCCTTTTCCCAATTGTC CTCTTGCTCATCCGCATGCGCCTCAAGGAACCCCAAGAATTCGCCCGCGAGTCGATGCGCCGCAAGACGCCCTAT CTCCTCGTTTTGCGCTTCTACTGGTTCCGTCTGTTTTGCGTCAGCCTCATTTGGTTTCTCTACGACTTTAGCATC TACGCCTTTGGCATCTACTCGTCGTCGATTCTTAGCGGTCTCTATGGCGACGACGCCCCCCTCACCACAATCTTT GGCTGGAACACCGTCATCAACGTCTTCTACCTCCCTGGGACCCTCCTCGGCGCCTGGGTCAGCGACAAGTTGGGG CCCAGAAACACCCTCATCATCGGCGTCTGCGCCCAGGCCATTGTTGGCTACATCATGGCCGCCGTGTACGCTCAT ATCTCGACGCGAATCGCTCTCTTTGCCGTCATCTATGGCCTCTTTCTCTCCCTCGGCGAACTAGGCCCAGGCAAC AATATTGGTCTCTTGGCTGCAAAGACTTGCGCCACCGGCGTCCGAGGCCGCTACTATGGCATTTCAGCCGCCATT GGAAAGATTGGCGCCTTTGTCGGCACTCTCGTCTTCCCCTATATTCAGGCTGCCGGAGGCAAAGACACAGTCGAG TCGGCGCAGTATCCCTTTTGGGTCGCCTCCAGTCTCTGCCTTCTCTCTGCTGCCGTTGCCTTCTTCTTTGTGCCA AACGTTGGCCAGGATACCATTTCTCGAGAAGACGTGCGCTTTCGTGAATACCTCGAGGCTCAGGGCTGGGACACG TCTCAGCTGGGTCTCTCAAAAAACGACTCCCGTGACATTTCCTATGCTCAACAAGAGCTGCAGATTGATCAATTG TCGCACAAGGCTAGATAG |
| Gene | >OphauG2|3564 ATGTCGACCTGGGGCCGCCGCCTGCTACGACGCTGGTCGCCCACCGAGGAGGAATCGCATCACCAAACCGCGCCG CCGCCGGCGTCCTCGAAACCCTTTTTCCAAACCGTGCTGCCCGTGTTTGCCTGCGGCGCTGGCCTCTTCTCTGAC GGCTACATCAACAATGCAAGTTTACCGACTCGTGGCCTCGTGAAACCACAGACTTACATTCTTGTCCACCTTTTC CTCAGGTCATTGGCTCCGTCAACACGGTATTGCGGCTTCAATATGGGAGCCAGTACACGTCGTCGCGCGCCGCTC GCTATGTCGCCGACATTGCCTTTGCCGGCACCGTCATAGGCCAGCTCGTCTTTGGCTTTGCGTCGGATCGCTGGT CGCGGTCAAACTCGCTCGTCCTCTCCACCGTCATCCTCATAGTCTTTACCGCGCTGGCAGCCGGCTCTTATTTCC GCGGCGACACTGTGGCCATGTTTGACATGCTGGCTGCGTGGCGCTTTTTTGTCGGCATTGGCATTGGCGGTGAGC TCGATTTTTTTTTTATAAATGTATAAAACAGACCGACACACACCCTTTGACTACAAGACGACAACACCTTTGACT GCGAGACACCTTCAAGACACCTTTGACTGCAAGACACCTTGGACTGCAATACAGATAAAAGAGTGCTAACATCAA CCCCTCACAGGCGAGTATCCCGCTGGCAGCGTCGGCTGCGCAGAATCGAGCGGCGAAATGAAGACCGGCACCCGC AACCGCTGGTTCATCCTCTTTACAAACAGCATGATTGACGTGGGTTTCGTCTTTGGCGCCTTCATCCCCTGTACG TCTTTTTTTTTTCCCCTCCGCCTCTCTCTCCTCGAGCCACAAAGAGTCGCATTCTGCTCTTGAAGCGTCAACAAG AAATATACTCCCAGACGCTAGAACAAAATTCTCACACACATTTTTCTTCTTTCTTCTAGACGTCATTGCCGCCGC CGCCAGTAATCGCCACTACGACACCATTTGGCGCACCAGCCTGGCCATTGGCGTCCTTTTCCCAATTGTCCTCTT GCTCATCCGCATGCGCCTCAAGGAACCCCAAGAATTCGCCCGCGAGTCGATGCGCCGCAAGACGCCCTATCTCCT CGTTTTGCGCTTCTACTGGTTCCGTCTGTTTTGCGTCAGCCTCATTTGGTTTCTCTACGACGTGAGTCTTTTCTT CTTTTTCTCTCTTTTTTTCCCTTTTTTTCCTTCTTTTTTTCCTTTTTTTCCTTTTCTTCTTCTTCTTTTTCTTCT TAAAAAAGCCACTCACGTCTCGACAGTTTAGCATCTACGCCTTTGGCATCTACTCGTCGTCGATTCTTAGCGGTC TCTATGGCGACGACGCCCCCCTCACCACAATCTTTGGCTGGAACACCGTCATCAACGTCTTCTACCTCCCTGGGA CCCTCCTCGGCGCCTGGGTCAGCGACAAGTTGGGGCCCAGAAACACCCTCATCATCGGCGTCTGCGCCCAGGCCA TTGTTGGCTACATCATGGCCGCCGTGTACGCTCATATCTCGACGCGAATCGCTCTCTTTGCCGTCATCTATGGCC TCTTTCTCTCCCTCGGCGAACTAGGCCCAGGCAACAATATTGGTCTCTTGGCTGCAAAGACTTGCGCCACCGGCG TCCGAGGCCGCTACTATGGCATTTCAGCCGCCATTGGAAAGATTGGCGCCTTTGTCGGCACTCTCGTCTTCCCCT ATATTCAGGCTGCCGGAGGCAAAGACACAGTCGAGTCGGCGCAGTATCCCTTTTGGGTCGCCTCCAGTCTCTGCC TTCTCTCTGCTGCCGTTGCCTTCTTCTTTGTGCCAAACGTTGGCCAGGATACCATTTCTCGAGAAGACGTGCGCT TTCGTGAATACCTCGAGGCTCAGGGCTGGGACACGTCTCAGCTGGGTCTCTCAAAAAACGACTCCCGTGACATTT CCTATGCTCAACAAGAGCTGCAGATTGATCAATTGTCGCACAAGGCTAGATAG |