© 2023 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Hirsu2|3359 |
| Gene name | |
| Location | Contig_187:17718..19839 |
| Strand | + |
| Gene length (bp) | 2121 |
| Transcript length (bp) | 1833 |
| Coding sequence length (bp) | 1833 |
| Protein length (aa) | 611 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF01699 | Na_Ca_ex | Sodium/calcium exchanger protein | 6.8E-15 | 124 | 277 |
| PF01699 | Na_Ca_ex | Sodium/calcium exchanger protein | 1.0E-16 | 466 | 609 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q99385|VCX1_YEAST | Vacuolar calcium ion transporter OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=VCX1 PE=1 SV=1 | 441 | 610 | 1.0E-31 |
| sp|O59768|VCX1_SCHPO | Vacuolar calcium ion transporter OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=vcx1 PE=3 SV=1 | 434 | 609 | 4.0E-26 |
| sp|Q99385|VCX1_YEAST | Vacuolar calcium ion transporter OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=VCX1 PE=1 SV=1 | 70 | 301 | 7.0E-25 |
| sp|Q75XW3|CAX_APHHA | Ca(2+)/H(+) antiporter OS=Aphanothece halophytica PE=1 SV=1 | 467 | 609 | 9.0E-24 |
| sp|O59768|VCX1_SCHPO | Vacuolar calcium ion transporter OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=vcx1 PE=3 SV=1 | 65 | 260 | 2.0E-23 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q99385|VCX1_YEAST | Vacuolar calcium ion transporter OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=VCX1 PE=1 SV=1 | 441 | 610 | 1.0E-31 |
| sp|O59768|VCX1_SCHPO | Vacuolar calcium ion transporter OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=vcx1 PE=3 SV=1 | 434 | 609 | 4.0E-26 |
| sp|Q99385|VCX1_YEAST | Vacuolar calcium ion transporter OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=VCX1 PE=1 SV=1 | 70 | 301 | 7.0E-25 |
| sp|Q75XW3|CAX_APHHA | Ca(2+)/H(+) antiporter OS=Aphanothece halophytica PE=1 SV=1 | 467 | 609 | 9.0E-24 |
| sp|O59768|VCX1_SCHPO | Vacuolar calcium ion transporter OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=vcx1 PE=3 SV=1 | 65 | 260 | 2.0E-23 |
| sp|Q5KQN0|CAX2_ORYSJ | Vacuolar cation/proton exchanger 2 OS=Oryza sativa subsp. japonica GN=CAX2 PE=2 SV=2 | 466 | 610 | 4.0E-22 |
| sp|Q6K1C4|CAX3_ORYSJ | Vacuolar cation/proton exchanger 3 OS=Oryza sativa subsp. japonica GN=CAX3 PE=2 SV=2 | 466 | 610 | 8.0E-22 |
| sp|Q6YXZ1|CAX4_ORYSJ | Putative vacuolar cation/proton exchanger 4 OS=Oryza sativa subsp. japonica GN=Os02g0138900 PE=3 SV=1 | 439 | 610 | 1.0E-21 |
| sp|Q8L783|CAX5_ARATH | Vacuolar cation/proton exchanger 5 OS=Arabidopsis thaliana GN=CAX5 PE=2 SV=1 | 82 | 281 | 7.0E-21 |
| sp|Q39254|CAX2_ARATH | Vacuolar cation/proton exchanger 2 OS=Arabidopsis thaliana GN=CAX2 PE=1 SV=2 | 439 | 610 | 1.0E-20 |
| sp|Q8L783|CAX5_ARATH | Vacuolar cation/proton exchanger 5 OS=Arabidopsis thaliana GN=CAX5 PE=2 SV=1 | 443 | 610 | 3.0E-20 |
| sp|Q39254|CAX2_ARATH | Vacuolar cation/proton exchanger 2 OS=Arabidopsis thaliana GN=CAX2 PE=1 SV=2 | 97 | 299 | 4.0E-20 |
| sp|Q6K1C4|CAX3_ORYSJ | Vacuolar cation/proton exchanger 3 OS=Oryza sativa subsp. japonica GN=CAX3 PE=2 SV=2 | 48 | 281 | 8.0E-20 |
| sp|Q9LFZ8|CAX6_ARATH | Putative vacuolar cation/proton exchanger 6 OS=Arabidopsis thaliana GN=CAX6 PE=3 SV=3 | 83 | 281 | 1.0E-19 |
| sp|Q9LFZ8|CAX6_ARATH | Putative vacuolar cation/proton exchanger 6 OS=Arabidopsis thaliana GN=CAX6 PE=3 SV=3 | 367 | 610 | 1.0E-18 |
| sp|Q5KQN0|CAX2_ORYSJ | Vacuolar cation/proton exchanger 2 OS=Oryza sativa subsp. japonica GN=CAX2 PE=2 SV=2 | 103 | 281 | 1.0E-18 |
| sp|Q75XW3|CAX_APHHA | Ca(2+)/H(+) antiporter OS=Aphanothece halophytica PE=1 SV=1 | 106 | 281 | 2.0E-18 |
| sp|Q945S5|CAX4_ARATH | Vacuolar cation/proton exchanger 4 OS=Arabidopsis thaliana GN=CAX4 PE=1 SV=2 | 449 | 610 | 2.0E-18 |
| sp|P74072|CAX_SYNY3 | Ca(2+)/H(+) antiporter OS=Synechocystis sp. (strain PCC 6803 / Kazusa) GN=slr1336 PE=1 SV=1 | 470 | 610 | 4.0E-18 |
| sp|Q39253|CAX1_ARATH | Vacuolar cation/proton exchanger 1 OS=Arabidopsis thaliana GN=CAX1 PE=1 SV=3 | 445 | 610 | 4.0E-17 |
| sp|Q769E5|CAX1A_ORYSJ | Vacuolar cation/proton exchanger 1a OS=Oryza sativa subsp. japonica GN=CAX1a PE=1 SV=1 | 466 | 609 | 5.0E-17 |
| sp|Q93Z81|CAX3_ARATH | Vacuolar cation/proton exchanger 3 OS=Arabidopsis thaliana GN=CAX3 PE=1 SV=1 | 467 | 610 | 1.0E-16 |
| sp|P74072|CAX_SYNY3 | Ca(2+)/H(+) antiporter OS=Synechocystis sp. (strain PCC 6803 / Kazusa) GN=slr1336 PE=1 SV=1 | 106 | 281 | 3.0E-16 |
| sp|Q5TKG3|CAX1B_ORYSJ | Vacuolar cation/proton exchanger 1b OS=Oryza sativa subsp. japonica GN=CAX1b PE=2 SV=1 | 126 | 281 | 5.0E-16 |
| sp|Q6YXZ1|CAX4_ORYSJ | Putative vacuolar cation/proton exchanger 4 OS=Oryza sativa subsp. japonica GN=Os02g0138900 PE=3 SV=1 | 126 | 295 | 2.0E-13 |
| sp|Q5TKG3|CAX1B_ORYSJ | Vacuolar cation/proton exchanger 1b OS=Oryza sativa subsp. japonica GN=CAX1b PE=2 SV=1 | 484 | 610 | 2.0E-13 |
| sp|Q769E5|CAX1A_ORYSJ | Vacuolar cation/proton exchanger 1a OS=Oryza sativa subsp. japonica GN=CAX1a PE=1 SV=1 | 55 | 281 | 2.0E-12 |
| sp|Q93Z81|CAX3_ARATH | Vacuolar cation/proton exchanger 3 OS=Arabidopsis thaliana GN=CAX3 PE=1 SV=1 | 96 | 281 | 2.0E-12 |
| sp|Q945S5|CAX4_ARATH | Vacuolar cation/proton exchanger 4 OS=Arabidopsis thaliana GN=CAX4 PE=1 SV=2 | 126 | 278 | 3.0E-12 |
| sp|O34840|CHAA_BACSU | Ca(2+)/H(+) antiporter ChaA OS=Bacillus subtilis (strain 168) GN=chaA PE=1 SV=1 | 457 | 610 | 3.0E-12 |
| sp|Q39253|CAX1_ARATH | Vacuolar cation/proton exchanger 1 OS=Arabidopsis thaliana GN=CAX1 PE=1 SV=3 | 110 | 297 | 4.0E-12 |
| sp|O34840|CHAA_BACSU | Ca(2+)/H(+) antiporter ChaA OS=Bacillus subtilis (strain 168) GN=chaA PE=1 SV=1 | 127 | 289 | 1.0E-10 |
| sp|Q5KTQ9|CAX1C_ORYSJ | Vacuolar cation/proton exchanger 1c OS=Oryza sativa subsp. japonica GN=CAX1c PE=2 SV=1 | 461 | 610 | 4.0E-09 |
| sp|Q9P7B3|YI14_SCHPO | Putative cation exchanger C521.04c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC521.04c PE=1 SV=1 | 83 | 246 | 1.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0016021 | integral component of membrane | Yes |
| GO:0055085 | transmembrane transport | Yes |
| GO:0031224 | intrinsic component of membrane | No |
| GO:0009987 | cellular process | No |
| GO:0110165 | cellular anatomical entity | No |
| GO:0051179 | localization | No |
| GO:0005575 | cellular_component | No |
| GO:0008150 | biological_process | No |
| GO:0051234 | establishment of localization | No |
| GO:0006810 | transport | No |
| Localizations | Signals | Cytoplasm | Nucleus | Extracellular | Cell membrane | Mitochondrion | Plastid | Endoplasmic reticulum | Lysosome vacuole | Golgi apparatus | Peroxisome |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Lysosome/Vacuole | Signal peptide|Transmembrane domain | 0.2 | 0.0951 | 0.1816 | 0.2891 | 0.2034 | 0.0112 | 0.3529 | 0.6975 | 0.4027 | 0.0326 |
| Domain # | Start | End | Length |
|---|---|---|---|
| 1 | 102 | 124 | 22 |
| 2 | 156 | 178 | 22 |
| 3 | 188 | 210 | 22 |
| 4 | 223 | 242 | 19 |
| 5 | 252 | 274 | 22 |
| 6 | 459 | 481 | 22 |
| 7 | 501 | 523 | 22 |
| 8 | 530 | 552 | 22 |
| 9 | 562 | 584 | 22 |
| Orthofinder run ID | 4 |
| Orthogroup | 6101 |
| 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 | >Hirsu2|3359 MSDGGGGGGGGDDDEPPALPPPAQPEPKAGLHTILAFSVKDGIQNTLHPWLSLLARKLKGPSLPPPDDADVLRPL LGLAPACRRSAPSPVARAVLDILCSSWLNTLLIFVPVGVGSYVAGMSPLMTFATNAAAIVPLSALLTDATERVAA YAGDTAGALLNISLGNLVELILFAALAHGHVRIVEASILGSVLVNLLLILGSALLVGSTVNDQPTYNTADAQLLA CLLFVSVFTFLMPTAFDYTFGQEKRSSVISLKLSRISSLLILAIYVLYIMHEIRSRYRGEERARATRDVDVESNL SASNQRQFFAGHPPPPPPLPHFHHSPVPSPRTIRFADEQSALPQGPSAYVAGSRGEMDSLRVPQMHDDYAFDCRG RQRSDGGERRPRANSHQPPMHQRKHSPSLSLRSYHGCLSRDSSVCGNLRAPPRSGLVGLQMLRDGRLDRDPAYVE EEEQTESESLSAVVVSLATLIVTSGLMSVNAELLVDAIDGVTRQTNLSESVIGLIILPIVGNIAEYVTVVAVAAR DKMDLAIAVAVGSSIQIALCVTPLTILAGWILQRDLALTFNFFEMATLMGGVLLANLLILNESSSGLRTTGLKGA LMCACYLIIA* |
| Coding | >Hirsu2|3359 ATGTCCGACGGCGGCGGCGGCGGCGGCGGCGGCGACGACGACGAACCCCCCGCTTTGCCGCCGCCGGCCCAGCCC GAGCCGAAAGCCGGTCTCCATACCATCTTAGCCTTCTCCGTCAAAGACGGCATCCAAAACACCCTGCATCCGTGG CTTTCTCTTCTCGCGAGAAAGCTCAAAGGCCCGTCGCTGCCGCCGCCCGACGACGCCGACGTGCTCCGTCCGCTG CTCGGCCTGGCCCCGGCATGCCGGCGGAGCGCGCCGAGTCCGGTCGCCCGCGCCGTGCTCGACATTCTGTGCTCG TCGTGGCTGAACACGCTCCTGATCTTCGTGCCGGTTGGCGTCGGCAGCTACGTCGCCGGCATGAGCCCGTTGATG ACCTTCGCCACCAATGCCGCCGCCATTGTTCCCCTGTCGGCTCTCCTGACGGACGCAACCGAGAGGGTGGCCGCC TACGCCGGCGACACCGCCGGCGCGCTGCTGAACATCAGCCTGGGGAACCTCGTCGAGCTGATTCTGTTCGCTGCT TTGGCACACGGTCATGTGCGGATAGTGGAAGCCTCCATCCTCGGCTCCGTTCTCGTCAACTTGCTGCTCATTCTC GGCTCGGCCCTCCTTGTGGGCAGCACCGTCAACGACCAGCCGACGTACAACACGGCTGATGCCCAGCTTCTGGCT TGCTTGCTCTTCGTCTCCGTCTTCACGTTTTTGATGCCCACCGCATTCGACTATACCTTTGGCCAAGAGAAGCGA TCGAGTGTGATCAGCTTGAAGCTGAGCAGAATCTCCTCGCTTCTCATCCTGGCCATCTACGTTCTCTACATCATG CACGAGATACGCTCGCGATATCGAGGCGAAGAGCGAGCCAGGGCGACTCGCGATGTCGACGTGGAAAGCAATCTG TCTGCTTCCAACCAGCGGCAGTTCTTTGCTGGTCATCCTCCTCCTCCTCCCCCATTGCCTCACTTTCACCACTCA CCGGTCCCGTCGCCTCGCACCATCCGCTTCGCGGATGAACAGTCGGCTCTGCCCCAGGGGCCATCGGCCTACGTA GCCGGCAGCCGCGGCGAGATGGATTCTCTCCGGGTGCCGCAGATGCACGACGACTATGCGTTCGACTGCCGCGGC CGCCAGCGAAGCGACGGCGGCGAGCGGCGGCCTCGTGCCAACTCGCACCAGCCGCCGATGCACCAGCGCAAGCAC TCCCCGTCGCTGTCGCTGCGCTCCTATCACGGCTGCCTGAGCCGCGACTCCTCCGTCTGCGGCAACCTCCGAGCG CCGCCACGGTCCGGGCTGGTCGGCCTGCAGATGCTGCGCGACGGGCGGCTGGACCGGGATCCGGCCTACGTGGAG GAGGAGGAGCAGACCGAGTCGGAGTCGCTCAGTGCGGTCGTCGTGTCGCTGGCCACGCTCATCGTCACGTCCGGT CTCATGTCCGTCAACGCCGAGCTGCTCGTGGACGCCATCGACGGCGTGACGCGCCAGACCAACCTCTCGGAGTCA GTCATCGGCCTCATCATTCTCCCGATCGTCGGCAACATCGCCGAGTACGTGACGGTTGTGGCTGTCGCCGCGAGA GACAAGATGGACTTGGCCATTGCCGTTGCCGTCGGCTCGTCCATCCAGATCGCCCTCTGCGTCACGCCCCTAACC ATCCTCGCCGGCTGGATCCTGCAGCGAGACCTGGCCCTGACCTTCAATTTCTTCGAGATGGCCACTCTGATGGGC GGCGTGCTGCTCGCAAACCTCCTCATCCTCAACGAATCGAGCAGCGGCCTCAGGACCACCGGCCTGAAGGGCGCG TTGATGTGTGCCTGCTATCTCATCATCGCGTGA |
| Transcript | >Hirsu2|3359 ATGTCCGACGGCGGCGGCGGCGGCGGCGGCGGCGACGACGACGAACCCCCCGCTTTGCCGCCGCCGGCCCAGCCC GAGCCGAAAGCCGGTCTCCATACCATCTTAGCCTTCTCCGTCAAAGACGGCATCCAAAACACCCTGCATCCGTGG CTTTCTCTTCTCGCGAGAAAGCTCAAAGGCCCGTCGCTGCCGCCGCCCGACGACGCCGACGTGCTCCGTCCGCTG CTCGGCCTGGCCCCGGCATGCCGGCGGAGCGCGCCGAGTCCGGTCGCCCGCGCCGTGCTCGACATTCTGTGCTCG TCGTGGCTGAACACGCTCCTGATCTTCGTGCCGGTTGGCGTCGGCAGCTACGTCGCCGGCATGAGCCCGTTGATG ACCTTCGCCACCAATGCCGCCGCCATTGTTCCCCTGTCGGCTCTCCTGACGGACGCAACCGAGAGGGTGGCCGCC TACGCCGGCGACACCGCCGGCGCGCTGCTGAACATCAGCCTGGGGAACCTCGTCGAGCTGATTCTGTTCGCTGCT TTGGCACACGGTCATGTGCGGATAGTGGAAGCCTCCATCCTCGGCTCCGTTCTCGTCAACTTGCTGCTCATTCTC GGCTCGGCCCTCCTTGTGGGCAGCACCGTCAACGACCAGCCGACGTACAACACGGCTGATGCCCAGCTTCTGGCT TGCTTGCTCTTCGTCTCCGTCTTCACGTTTTTGATGCCCACCGCATTCGACTATACCTTTGGCCAAGAGAAGCGA TCGAGTGTGATCAGCTTGAAGCTGAGCAGAATCTCCTCGCTTCTCATCCTGGCCATCTACGTTCTCTACATCATG CACGAGATACGCTCGCGATATCGAGGCGAAGAGCGAGCCAGGGCGACTCGCGATGTCGACGTGGAAAGCAATCTG TCTGCTTCCAACCAGCGGCAGTTCTTTGCTGGTCATCCTCCTCCTCCTCCCCCATTGCCTCACTTTCACCACTCA CCGGTCCCGTCGCCTCGCACCATCCGCTTCGCGGATGAACAGTCGGCTCTGCCCCAGGGGCCATCGGCCTACGTA GCCGGCAGCCGCGGCGAGATGGATTCTCTCCGGGTGCCGCAGATGCACGACGACTATGCGTTCGACTGCCGCGGC CGCCAGCGAAGCGACGGCGGCGAGCGGCGGCCTCGTGCCAACTCGCACCAGCCGCCGATGCACCAGCGCAAGCAC TCCCCGTCGCTGTCGCTGCGCTCCTATCACGGCTGCCTGAGCCGCGACTCCTCCGTCTGCGGCAACCTCCGAGCG CCGCCACGGTCCGGGCTGGTCGGCCTGCAGATGCTGCGCGACGGGCGGCTGGACCGGGATCCGGCCTACGTGGAG GAGGAGGAGCAGACCGAGTCGGAGTCGCTCAGTGCGGTCGTCGTGTCGCTGGCCACGCTCATCGTCACGTCCGGT CTCATGTCCGTCAACGCCGAGCTGCTCGTGGACGCCATCGACGGCGTGACGCGCCAGACCAACCTCTCGGAGTCA GTCATCGGCCTCATCATTCTCCCGATCGTCGGCAACATCGCCGAGTACGTGACGGTTGTGGCTGTCGCCGCGAGA GACAAGATGGACTTGGCCATTGCCGTTGCCGTCGGCTCGTCCATCCAGATCGCCCTCTGCGTCACGCCCCTAACC ATCCTCGCCGGCTGGATCCTGCAGCGAGACCTGGCCCTGACCTTCAATTTCTTCGAGATGGCCACTCTGATGGGC GGCGTGCTGCTCGCAAACCTCCTCATCCTCAACGAATCGAGCAGCGGCCTCAGGACCACCGGCCTGAAGGGCGCG TTGATGTGTGCCTGCTATCTCATCATCGCGTGA |
| Gene | >Hirsu2|3359 ATGTCCGACGGCGGCGGCGGCGGCGGCGGCGGCGACGACGACGAACCCCCCGCTTTGCCGCCGCCGGCCCAGCCC GAGCCGAAAGCCGGTCTCCATACCATCTTAGCCTTCTCCGTCAAAGGTGGGTGTCCTGCTCTGGCCAAAGAGTCT CGTCGTGCCAGCCGCGGCGCCGGCCGGAGAGACCGCCTTGCCTCGCAAAGCTAATGCCGACGGCTCCCGAGCGCG CCAGACGGCATCCAAAACACCCTGCATCCGTGGCTTTCTCTTCTCGCGAGAAAGCTCAAAGGCCCGTCGCTGCCG CCGCCCGACGACGCCGACGTGCTCCGTCCGCTGCTCGGCCTGGCCCCGGCATGCCGGCGGAGCGCGCCGAGTCCG GTCGCCCGCGCCGTGCTCGACATTCTGTGCTCGTCGTGGCTGAACACGCTCCTGATCTTCGTGCCGGTTGGCGTC GGCAGCTACGTCGCCGGCATGAGCCCGTTGATGACCTTCGCCACCAATGCCGCCGCCATTGTTCCCCTGTCGGCT CTCCTGACGGACGCAACCGAGAGGGTGGCCGCCTACGCCGGCGACACCGCCGGCGCGCTGCTGAACATCAGCCTG GGGAACCTCGTCGAGCTGATTCTGTTGTAAGGCGCCCCCCGCCGTCCTTTGCGCTCTTCCGTTTCGCTGCTTTGC TGACGCCCCGGAGCAGCATGTAAGTCGTTGCGTCCCGGAAGCCCGGCAAGGGAGCGCCCTCAACTCACTCTTGCA AGCGCTGCTTTGGCACACGGTCATGTGCGGATAGTGGAAGCCTCCATCCTCGGCTCCGTTCTCGTCAACTTGCTG CTCATTCTCGGCTCGGCCCTCCTTGTGGGCAGCACCGTCAACGACCAGCCGACGTACAACACGGCTGATGCCCAG CTTCTGGCTTGCTTGCTCTTCGTCTCCGTCTTCACGTTTTTGATGCCCGTATGGTGCCTGTCCAGGTCCGAGTTC GCGGCGCGGCGTGCTGACCCCTTGTAGACCGCATTCGACTATACCTTTGGCCAAGAGAAGCGATCGAGTGTGATC AGCTTGAAGCTGAGCAGAATCTCCTCGCTTCTCATCCTGGCCATCTACGTTCTCTACATCATGCACGAGATACGC TCGCGATATCGAGGCGAAGAGCGAGCCAGGGCGACTCGCGATGTCGACGTGGAAAGCAATCTGTCTGCTTCCAAC CAGCGGCAGTTCTTTGCTGGTCATCCTCCTCCTCCTCCCCCATTGCCTCACTTTCACCACTCACCGGTCCCGTCG CCTCGCACCATCCGCTTCGCGGATGAACAGTCGGCTCTGCCCCAGGGGCCATCGGCCTACGTAGCCGGCAGCCGC GGCGAGATGGATTCTCTCCGGGTGCCGCAGATGCACGACGACTATGCGTTCGACTGCCGCGGCCGCCAGCGAAGC GACGGCGGCGAGCGGCGGCCTCGTGCCAACTCGCACCAGCCGCCGATGCACCAGCGCAAGCACTCCCCGTCGCTG TCGCTGCGCTCCTATCACGGCTGCCTGAGCCGCGACTCCTCCGTCTGCGGCAACCTCCGAGCGCCGCCACGGTCC GGGCTGGTCGGCCTGCAGATGCTGCGCGACGGGCGGCTGGACCGGGATCCGGCCTACGTGGAGGAGGAGGAGCAG ACCGAGTCGGAGTCGCTCAGTGCGGTCGTCGTGTCGCTGGCCACGCTCATCGTCACGTCCGGTCTCATGTCCGTC AACGCCGAGCTGCTCGTGGACGCCATCGACGGCGTGACGCGCCAGACCAACCTCTCGGAGTCAGTCATCGGCCTC ATCATTCTCCCGATCGTCGGCAACATCGCCGAGTACGTGACGGTTGTGGCTGTCGCCGCGAGAGACAAGATGGAC TTGGCCATTGCCGTTGCCGTCGGCTCGTCCATCCAGATCGCCCTCTGCGTCACGCCCCTAACCATCCTCGCCGGC TGGATCCTGCAGCGAGACCTGGCCCTGACCTTCAATTTCTTCGAGATGGCCACTCTGATGGGCGGCGTGCTGCTC GCAAACCTCCTCATCCTCAACGAATCGAGCAGCGGCCTCAGGACCACCGGCCTGAAGGGCGCGTTGATGTGTGCC TGCTATCTCATCATCGCGTGA |