© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | OphauB2|2599 |
| Gene name | |
| Location | Contig_183:13552..15796 |
| Strand | + |
| Gene length (bp) | 2244 |
| Transcript length (bp) | 1842 |
| Coding sequence length (bp) | 1842 |
| Protein length (aa) | 614 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00083 | Sugar_tr | Sugar (and other) transporter | 4.5E-22 | 47 | 264 |
| PF00083 | Sugar_tr | Sugar (and other) transporter | 8.8E-14 | 414 | 559 |
| PF07690 | MFS_1 | Major Facilitator Superfamily | 1.9E-18 | 55 | 289 |
| PF07690 | MFS_1 | Major Facilitator Superfamily | 7.4E-09 | 412 | 569 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P25297|PHO84_YEAST | Inorganic phosphate transporter PHO84 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PHO84 PE=1 SV=2 | 25 | 603 | 2.0E-66 |
| 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 | 24 | 518 | 2.0E-63 |
| sp|Q9S735|PHT19_ARATH | Probable inorganic phosphate transporter 1-9 OS=Arabidopsis thaliana GN=PHT1-9 PE=2 SV=1 | 45 | 564 | 2.0E-54 |
| sp|Q01MW8|PHT14_ORYSI | Probable inorganic phosphate transporter 1-4 OS=Oryza sativa subsp. indica GN=PHT1-4 PE=2 SV=2 | 45 | 532 | 1.0E-49 |
| sp|Q8H6H0|PHT16_ORYSJ | Inorganic phosphate transporter 1-6 OS=Oryza sativa subsp. japonica GN=PHT1-6 PE=1 SV=1 | 24 | 535 | 2.0E-49 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P25297|PHO84_YEAST | Inorganic phosphate transporter PHO84 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PHO84 PE=1 SV=2 | 25 | 603 | 2.0E-66 |
| 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 | 24 | 518 | 2.0E-63 |
| sp|Q9S735|PHT19_ARATH | Probable inorganic phosphate transporter 1-9 OS=Arabidopsis thaliana GN=PHT1-9 PE=2 SV=1 | 45 | 564 | 2.0E-54 |
| sp|Q01MW8|PHT14_ORYSI | Probable inorganic phosphate transporter 1-4 OS=Oryza sativa subsp. indica GN=PHT1-4 PE=2 SV=2 | 45 | 532 | 1.0E-49 |
| sp|Q8H6H0|PHT16_ORYSJ | Inorganic phosphate transporter 1-6 OS=Oryza sativa subsp. japonica GN=PHT1-6 PE=1 SV=1 | 24 | 535 | 2.0E-49 |
| sp|Q8H6H2|PHT14_ORYSJ | Probable inorganic phosphate transporter 1-4 OS=Oryza sativa subsp. japonica GN=PHT1-4 PE=2 SV=1 | 45 | 532 | 3.0E-49 |
| sp|Q9SYQ1|PHT18_ARATH | Probable inorganic phosphate transporter 1-8 OS=Arabidopsis thaliana GN=PHT1-8 PE=2 SV=2 | 45 | 564 | 4.0E-49 |
| sp|Q7XRH8|PT113_ORYSJ | Putative inorganic phosphate transporter 1-13 OS=Oryza sativa subsp. japonica GN=PHT1-13 PE=3 SV=2 | 45 | 520 | 1.0E-48 |
| sp|Q96303|PHT14_ARATH | Inorganic phosphate transporter 1-4 OS=Arabidopsis thaliana GN=PHT1-4 PE=1 SV=1 | 22 | 579 | 7.0E-48 |
| sp|Q8GYF4|PHT15_ARATH | Probable inorganic phosphate transporter 1-5 OS=Arabidopsis thaliana GN=PHT1-5 PE=2 SV=2 | 22 | 536 | 9.0E-48 |
| sp|Q8GSD9|PHT12_ORYSJ | Inorganic phosphate transporter 1-2 OS=Oryza sativa subsp. japonica GN=PTH1-2 PE=2 SV=1 | 45 | 530 | 3.0E-47 |
| sp|Q494P0|PHT17_ARATH | Probable inorganic phosphate transporter 1-7 OS=Arabidopsis thaliana GN=PHT1-7 PE=2 SV=2 | 45 | 587 | 9.0E-47 |
| sp|Q7X7V2|PHT15_ORYSJ | Probable inorganic phosphate transporter 1-5 OS=Oryza sativa subsp. japonica GN=PHT1-5 PE=2 SV=2 | 45 | 596 | 3.0E-46 |
| sp|Q94DB8|PT111_ORYSJ | Inorganic phosphate transporter 1-11 OS=Oryza sativa subsp. japonica GN=PHT1-11 PE=2 SV=1 | 38 | 548 | 4.0E-46 |
| sp|Q9P6J9|YHD1_SCHPO | Putative inorganic phosphate transporter C1683.01 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC1683.01 PE=3 SV=1 | 21 | 521 | 3.0E-45 |
| sp|Q9ZWT3|PHT16_ARATH | Probable inorganic phosphate transporter 1-6 OS=Arabidopsis thaliana GN=PHT1-6 PE=1 SV=1 | 45 | 518 | 3.0E-45 |
| sp|Q8VYM2|PHT11_ARATH | Inorganic phosphate transporter 1-1 OS=Arabidopsis thaliana GN=PHT1-1 PE=1 SV=2 | 22 | 532 | 8.0E-45 |
| sp|O42885|YBN1_SCHPO | Putative inorganic phosphate transporter C8E4.01c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC8E4.01c PE=1 SV=2 | 13 | 521 | 1.0E-44 |
| sp|O48639|PHT13_ARATH | Probable inorganic phosphate transporter 1-3 OS=Arabidopsis thaliana GN=PHT1-3 PE=2 SV=1 | 45 | 536 | 3.0E-44 |
| sp|Q8H6G9|PHT17_ORYSJ | Probable inorganic phosphate transporter 1-7 OS=Oryza sativa subsp. japonica GN=PHT1-7 PE=2 SV=1 | 45 | 518 | 7.0E-44 |
| sp|Q8H074|PT112_ORYSJ | Probable inorganic phosphate transporter 1-12 OS=Oryza sativa subsp. japonica GN=PHT1-12 PE=2 SV=1 | 45 | 564 | 3.0E-43 |
| sp|Q8H6G8|PHT18_ORYSJ | Probable inorganic phosphate transporter 1-8 OS=Oryza sativa subsp. japonica GN=PHT1-8 PE=2 SV=1 | 18 | 504 | 2.0E-42 |
| sp|Q7XDZ7|PHT13_ORYSJ | Probable inorganic phosphate transporter 1-3 OS=Oryza sativa subsp. japonica GN=PHT1-3 PE=2 SV=1 | 45 | 518 | 1.0E-41 |
| sp|Q9Y7Q9|YCX2_SCHPO | Probable metabolite transporter C2H8.02 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPCC2H8.02 PE=1 SV=1 | 41 | 578 | 2.0E-41 |
| sp|Q69T94|PT110_ORYSJ | Probable inorganic phosphate transporter 1-10 OS=Oryza sativa subsp. japonica GN=PHT1-10 PE=2 SV=1 | 38 | 587 | 2.0E-41 |
| sp|Q8H6G7|PHT19_ORYSJ | Probable inorganic phosphate transporter 1-9 OS=Oryza sativa subsp. japonica GN=PHT1-9 PE=2 SV=2 | 38 | 597 | 8.0E-40 |
| sp|Q09852|YAEC_SCHPO | Putative inorganic phosphate transporter C23D3.12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC23D3.12 PE=1 SV=1 | 30 | 521 | 9.0E-39 |
| sp|Q96243|PHT12_ARATH | Probable inorganic phosphate transporter 1-2 OS=Arabidopsis thaliana GN=PHT1-2 PE=2 SV=2 | 22 | 504 | 1.0E-37 |
| sp|Q8H6H4|PHT11_ORYSJ | Inorganic phosphate transporter 1-1 OS=Oryza sativa subsp. japonica GN=PHT1-1 PE=2 SV=1 | 45 | 504 | 2.0E-37 |
| sp|P31679|YAAU_ECOLI | Putative metabolite transport protein YaaU OS=Escherichia coli (strain K12) GN=yaaU PE=3 SV=2 | 32 | 279 | 2.0E-10 |
| sp|O94342|YHM9_SCHPO | Probable metabolite transport protein C1271.09 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC1271.09 PE=3 SV=1 | 39 | 267 | 3.0E-09 |
| sp|P38055|YDJE_ECOLI | Inner membrane metabolite transport protein YdjE OS=Escherichia coli (strain K12) GN=ydjE PE=1 SV=2 | 24 | 154 | 3.0E-07 |
| sp|O34691|NAIP_BACSU | Putative niacin/nicotinamide transporter NaiP OS=Bacillus subtilis (strain 168) GN=naiP PE=1 SV=1 | 41 | 202 | 7.0E-07 |
| sp|P25346|GIT1_YEAST | Probable metabolite transport protein GIT1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=GIT1 PE=1 SV=1 | 25 | 208 | 1.0E-06 |
| sp|Q46909|YGCS_ECOLI | Inner membrane metabolite transport protein YgcS OS=Escherichia coli (strain K12) GN=ygcS PE=1 SV=2 | 32 | 194 | 3.0E-06 |
| sp|P71369|Y1104_HAEIN | Putative metabolite transport protein HI_1104 OS=Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) GN=HI_1104 PE=3 SV=1 | 34 | 186 | 3.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0055085 | transmembrane transport | Yes |
| GO:0022857 | transmembrane transporter activity | Yes |
| GO:0016021 | integral component of membrane | Yes |
| GO:0110165 | cellular anatomical entity | No |
| GO:0009987 | cellular process | No |
| GO:0003674 | molecular_function | No |
| GO:0051179 | localization | No |
| GO:0005215 | transporter activity | No |
| GO:0008150 | biological_process | No |
| GO:0031224 | intrinsic component of membrane | No |
| GO:0051234 | establishment of localization | No |
| GO:0005575 | cellular_component | No |
| GO:0006810 | transport | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 11 | 0.5 |
| Domain # | Start | End | Length |
|---|---|---|---|
| 1 | 48 | 70 | 22 |
| 2 | 80 | 102 | 22 |
| 3 | 109 | 131 | 22 |
| 4 | 141 | 163 | 22 |
| 5 | 176 | 198 | 22 |
| 6 | 230 | 252 | 22 |
| 7 | 319 | 341 | 22 |
| 8 | 410 | 432 | 22 |
| 9 | 437 | 459 | 22 |
| 10 | 469 | 491 | 22 |
| 11 | 503 | 525 | 22 |
| 12 | 535 | 557 | 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 | >OphauB2|2599 MPVRRLNRGFLGSDSAALSPQLAQQRRQLRCELDLNSWNMRIWGVAASGFLTDSYNLFSTNVILASVIFVYDANG SPSTALVVNLATLVGSVVGQLLFGFLADWFGRTRLYGIELLLVIISTIGVATTSNGHNDMSFLALFIWWRFVMGI GIGAEYPLSAVITSEWSSTKSRATMLSTVFLMQPIGQALAQLVGLFVLFAFNASKRLQDKRCGLDQAHHAECLEA FDGFWRIVIGSGAIPALLAIIFRFFLYDCGLYSLEVRNKPALALENTQRIYGVPSPPLLASLDSQPLPTGLHVDT PVQFSRQDLHRYLIKEGNWRYLVGASATWFFLDVSFYGLSLDNRRTLSDLWATAHDTPIDESLPCWHSQLPNGQS TVPSWQQRGLPPWQTNLQRPCSTLYDVLVDQAKQYLLTVSLASIAGSICFVVLANRFPRRQWLTASFFVLALVLA VTGAVYYRVNHSPASPVTVVLVAICHFLFNFGANTLTFIIPAEIFPTCYRCTCHGIAAAAGKLGSIVALLVVYAI NQAYDSSTRQGLIFLLFGFVAVFGALFAWAYLPDLERRSPGPPRSLETKTLEEMGEGWQKAQQMGEAFTFRDKCE SVRLRWSSRHSSI* |
| Coding | >OphauB2|2599 ATGCCAGTCCGCCGCCTCAATCGCGGCTTCTTGGGCTCTGACAGCGCTGCCCTGTCGCCTCAACTCGCCCAGCAG CGGCGCCAATTGCGATGTGAGCTCGACCTCAACTCGTGGAACATGCGCATCTGGGGCGTTGCCGCCTCGGGCTTT CTCACAGACTCATACAACCTCTTCTCAACAAACGTCATTCTGGCCTCGGTCATCTTTGTCTACGACGCCAATGGC TCTCCCTCGACTGCCCTGGTGGTCAATCTCGCCACCTTGGTCGGCTCAGTCGTTGGCCAGCTGCTCTTTGGCTTT CTCGCAGACTGGTTCGGCCGCACTCGCCTCTACGGCATCGAGCTGCTCCTCGTCATCATCTCCACCATTGGCGTC GCCACGACTAGCAATGGCCACAACGACATGTCCTTTCTCGCCCTCTTCATCTGGTGGCGCTTCGTCATGGGCATT GGCATTGGCGCCGAGTATCCCCTCAGTGCCGTCATCACCTCGGAGTGGAGCAGTACCAAGTCGCGTGCCACCATG CTCTCAACCGTCTTCCTCATGCAGCCCATTGGCCAGGCCCTCGCCCAGCTTGTCGGCCTCTTTGTTCTCTTTGCC TTCAACGCCTCGAAGCGCCTGCAAGACAAGCGCTGTGGCCTCGACCAGGCCCACCACGCCGAGTGCCTCGAGGCC TTTGATGGCTTCTGGCGCATTGTCATTGGCTCTGGCGCCATTCCTGCCCTGCTGGCCATCATCTTCCGCTTCTTT CTCTACGACTGCGGTCTCTACAGCCTCGAGGTTCGCAACAAGCCTGCCCTCGCCCTTGAAAACACGCAACGCATC TACGGCGTCCCCTCGCCCCCGCTCCTGGCCTCGCTCGATTCGCAGCCCCTGCCTACTGGCCTCCATGTCGACACC CCCGTGCAGTTTTCAAGGCAGGACCTGCATCGCTACTTGATCAAGGAGGGCAACTGGCGCTATCTTGTCGGAGCT TCCGCCACCTGGTTCTTTCTCGACGTCAGCTTCTATGGCCTCTCTCTCGACAATCGCCGCACCTTGTCTGATCTA TGGGCCACGGCACACGACACCCCCATTGACGAGAGCCTGCCCTGCTGGCACTCCCAGCTGCCCAATGGCCAGTCG ACAGTCCCATCCTGGCAGCAGCGTGGACTCCCGCCCTGGCAAACAAACCTGCAGCGCCCCTGCAGCACCCTTTAT GATGTCTTGGTCGACCAGGCCAAGCAGTACCTGCTGACTGTGTCGCTAGCTTCAATTGCCGGCAGCATCTGCTTC GTCGTCCTGGCCAATCGCTTCCCACGCCGTCAGTGGCTGACGGCCTCCTTCTTCGTCTTGGCCCTTGTCTTGGCT GTTACCGGCGCCGTCTATTACCGCGTCAACCATAGTCCGGCCTCGCCCGTTACCGTTGTCTTGGTGGCCATTTGT CACTTCTTGTTCAACTTTGGTGCAAACACCCTCACCTTTATAATACCTGCTGAAATATTCCCCACCTGCTACCGC TGTACCTGCCACGGCATTGCTGCCGCTGCCGGCAAGCTTGGCAGCATCGTCGCCCTGCTTGTCGTCTATGCCATC AACCAGGCTTACGACAGCAGCACTCGCCAGGGCCTCATCTTTCTCCTCTTTGGCTTCGTGGCCGTCTTTGGTGCC CTTTTTGCCTGGGCCTATCTGCCCGATCTCGAGCGCCGCTCCCCGGGCCCCCCGCGCTCTCTCGAGACAAAGACA CTCGAGGAAATGGGTGAAGGCTGGCAAAAGGCTCAACAAATGGGCGAGGCCTTTACCTTTCGCGACAAGTGCGAA TCGGTGCGATTGAGGTGGTCAAGCCGCCATAGCTCCATATAG |
| Transcript | >OphauB2|2599 ATGCCAGTCCGCCGCCTCAATCGCGGCTTCTTGGGCTCTGACAGCGCTGCCCTGTCGCCTCAACTCGCCCAGCAG CGGCGCCAATTGCGATGTGAGCTCGACCTCAACTCGTGGAACATGCGCATCTGGGGCGTTGCCGCCTCGGGCTTT CTCACAGACTCATACAACCTCTTCTCAACAAACGTCATTCTGGCCTCGGTCATCTTTGTCTACGACGCCAATGGC TCTCCCTCGACTGCCCTGGTGGTCAATCTCGCCACCTTGGTCGGCTCAGTCGTTGGCCAGCTGCTCTTTGGCTTT CTCGCAGACTGGTTCGGCCGCACTCGCCTCTACGGCATCGAGCTGCTCCTCGTCATCATCTCCACCATTGGCGTC GCCACGACTAGCAATGGCCACAACGACATGTCCTTTCTCGCCCTCTTCATCTGGTGGCGCTTCGTCATGGGCATT GGCATTGGCGCCGAGTATCCCCTCAGTGCCGTCATCACCTCGGAGTGGAGCAGTACCAAGTCGCGTGCCACCATG CTCTCAACCGTCTTCCTCATGCAGCCCATTGGCCAGGCCCTCGCCCAGCTTGTCGGCCTCTTTGTTCTCTTTGCC TTCAACGCCTCGAAGCGCCTGCAAGACAAGCGCTGTGGCCTCGACCAGGCCCACCACGCCGAGTGCCTCGAGGCC TTTGATGGCTTCTGGCGCATTGTCATTGGCTCTGGCGCCATTCCTGCCCTGCTGGCCATCATCTTCCGCTTCTTT CTCTACGACTGCGGTCTCTACAGCCTCGAGGTTCGCAACAAGCCTGCCCTCGCCCTTGAAAACACGCAACGCATC TACGGCGTCCCCTCGCCCCCGCTCCTGGCCTCGCTCGATTCGCAGCCCCTGCCTACTGGCCTCCATGTCGACACC CCCGTGCAGTTTTCAAGGCAGGACCTGCATCGCTACTTGATCAAGGAGGGCAACTGGCGCTATCTTGTCGGAGCT TCCGCCACCTGGTTCTTTCTCGACGTCAGCTTCTATGGCCTCTCTCTCGACAATCGCCGCACCTTGTCTGATCTA TGGGCCACGGCACACGACACCCCCATTGACGAGAGCCTGCCCTGCTGGCACTCCCAGCTGCCCAATGGCCAGTCG ACAGTCCCATCCTGGCAGCAGCGTGGACTCCCGCCCTGGCAAACAAACCTGCAGCGCCCCTGCAGCACCCTTTAT GATGTCTTGGTCGACCAGGCCAAGCAGTACCTGCTGACTGTGTCGCTAGCTTCAATTGCCGGCAGCATCTGCTTC GTCGTCCTGGCCAATCGCTTCCCACGCCGTCAGTGGCTGACGGCCTCCTTCTTCGTCTTGGCCCTTGTCTTGGCT GTTACCGGCGCCGTCTATTACCGCGTCAACCATAGTCCGGCCTCGCCCGTTACCGTTGTCTTGGTGGCCATTTGT CACTTCTTGTTCAACTTTGGTGCAAACACCCTCACCTTTATAATACCTGCTGAAATATTCCCCACCTGCTACCGC TGTACCTGCCACGGCATTGCTGCCGCTGCCGGCAAGCTTGGCAGCATCGTCGCCCTGCTTGTCGTCTATGCCATC AACCAGGCTTACGACAGCAGCACTCGCCAGGGCCTCATCTTTCTCCTCTTTGGCTTCGTGGCCGTCTTTGGTGCC CTTTTTGCCTGGGCCTATCTGCCCGATCTCGAGCGCCGCTCCCCGGGCCCCCCGCGCTCTCTCGAGACAAAGACA CTCGAGGAAATGGGTGAAGGCTGGCAAAAGGCTCAACAAATGGGCGAGGCCTTTACCTTTCGCGACAAGTGCGAA TCGGTGCGATTGAGGTGGTCAAGCCGCCATAGCTCCATATAG |
| Gene | >OphauB2|2599 ATGCCAGTCCGCCGCCTCAATCGCGGCTTCTTGGGCTCTGACAGCGCTGCCCTGTCGCCTCAACTCGCCCAGGTA TGTATGCCGAGAGCTTTTTTCCCTCTTTCTCTCTTTTCTCTCTCTCTCTCGCTCTCTTTTTTTCCCCCTCCTTCC TGGGATAATCTGACATCTTGTTCTTTTTTTTGCCAAAAAAAAAAACACCACCACCACCACCACCACCACGAAAAC CCATTGCCCAAACAAATAGATGCATCAAAAATGTAAACAAAACACTGGCTAACATGCCCCGTCCAGCAGCGGCGC CAATTGCGATGTGAGCTCGACCTCAACTCGTGGAACATGCGCATCTGGGGCGTTGCCGCCTCGGGCTTTCTCACA GACTCGTTGGTCCTTGTCCCTCCCCTCTGCTCTCCTCCGCCCTCTGGCTAACGGCGGCCAGATACAACCTCTTCT CAACAAACGTCATTCTGGCCTCGGTCATCTTTGTCTACGACGCCAATGGCTCTCCCTCGACTGCCCTGGTGGTCA ATCTCGCCACCTTGGTCGGCTCAGTCGTTGGCCAGCTGCTCTTTGGCTTTCTCGCAGACTGGTTCGGCCGCACTC GCCTCTACGGCATCGAGCTGCTCCTCGTCATCATCTCCACCATTGGCGTCGCCACGACTAGCAATGGCCACAACG ACATGTCCTTTCTCGCCCTCTTCATCTGGTGGCGCTTCGTCATGGGCATTGGTCCGTCTTGGCCCACGCTCTCTG CAACACGCTGTCCTCTGACTGACTGCTCGCTAGGCATTGGCGCCGAGTATCCCCTCAGTGCCGTCATCACCTCGG AGTGGAGCAGTACCAAGTCGCGTGCCACCATGCTCTCAACCGTCTTCCTCATGCAGCCCATTGGCCAGGCCCTCG CCCAGCTTGTCGGCCTCTTTGTTCTCTTTGCCTTCAACGCCTCGAAGCGCCTGCAAGACAAGCGCTGTGGCCTCG ACCAGGCCCACCACGCCGAGTGCCTCGAGGCCTTTGATGGCTTCTGGCGCATTGTCATTGGCTCTGGCGCCATTC CTGCCCTGCTGGCCATCATCTTCCGCTTCTTTCTCTACGACTGCGGTCTCTACAGCCTCGAGGTTCGCAACAAGC CTGCCCTCGCCCTTGAAAACACGCAACGCATCTACGGCGTCCCCTCGCCCCCGCTCCTGGCCTCGCTCGATTCGC AGCCCCTGCCTACTGGCCTCCATGTCGACACCCCCGTGCAGTTTTCAAGGCAGGACCTGCATCGCTACTTGATCA AGGAGGGCAACTGGCGCTATCTTGTCGGAGCTTCCGCCACCTGGTTCTTTCTCGACGTCAGCTTCTATGGCCTCT CTCTCGACAATCGCCGCACCTTGTCTGATCTATGGGCCACGGCACACGACACCCCCATTGACGAGAGCCTGCCCT GCTGGCACTCCCAGCTGCCCAATGGCCAGTCGACAGTCCCATCCTGGCAGCAGCGTGGACTCCCGCCCTGGCAAA CAAACCTGCAGCGCCCCTGCAGCACCCTTTATGATGTCTTGGTCGACCAGGCCAAGCAGTACCTGCTGACTGTGT CGCTAGCTTCAATTGCCGGCAGCATCTGCTTCGTCGTCCTGGCCAATCGCTTCCCACGCCGTCAGTGGCTGACGG CCTCCTTCTTCGTCTTGGCCCTTGTCTTGGCTGTTACCGGCGCCGTCTATTACCGCGTCAACCATAGTCCGGCCT CGCCCGTTACCGTTGTCTTGGTGGCCATTTGTCACTTCTTGTTCAACTTTGGTACGCCACAGCCTGTTTGATCGG CCCTCTGCTTGCCTCCAGCTGACCCTTTAACCATCTACGCCACTAGGTGCAAACACCCTCACCTTTATAATACCT GCTGAAATATTCCCCACCTGCTACCGCTGTACCTGCCACGGCATTGCTGCCGCTGCCGGCAAGCTTGGCAGCATC GTCGCCCTGCTTGTCGTCTATGCCATCAACCAGGCTTACGACAGCAGCACTCGCCAGGGCCTCATCTTTCTCCTC TTTGGCTTCGTGGCCGTCTTTGGTGCCCTTTTTGCCTGGGCCTATCTGCCCGATCTCGAGCGCCGCTCCCCGGGC CCCCCGCGCTCTCTCGAGACAAAGACACTCGAGGAAATGGGTGAAGGCTGGCAAAAGGCTCAACAAATGGGCGAG GCCTTTACCTTTCGCGACAAGTGCGAATCGGTGCGATTGAGGTGGTCAAGCCGCCATAGCTCCATATAG |