Protein ID | Hirsu2|6777 |
Gene name | |
Location | Contig_361:7793..9484 |
Strand | + |
Gene length (bp) | 1691 |
Transcript length (bp) | 1500 |
Coding sequence length (bp) | 1500 |
Protein length (aa) | 500 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF00465 | Fe-ADH | Iron-containing alcohol dehydrogenase | 5.2E-104 | 79 | 474 |
PF13685 | Fe-ADH_2 | Iron-containing alcohol dehydrogenase | 1.8E-12 | 83 | 176 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|A6QP15|HOT_BOVIN | Hydroxyacid-oxoacid transhydrogenase, mitochondrial OS=Bos taurus GN=ADHFE1 PE=2 SV=1 | 8 | 498 | 1.0E-165 |
sp|Q4QQW3|HOT_RAT | Hydroxyacid-oxoacid transhydrogenase, mitochondrial OS=Rattus norvegicus GN=Adhfe1 PE=1 SV=1 | 14 | 498 | 4.0E-165 |
sp|Q8R0N6|HOT_MOUSE | Hydroxyacid-oxoacid transhydrogenase, mitochondrial OS=Mus musculus GN=Adhfe1 PE=1 SV=2 | 14 | 498 | 3.0E-164 |
sp|Q08B39|HOT_XENLA | Hydroxyacid-oxoacid transhydrogenase, mitochondrial OS=Xenopus laevis GN=adhfe1 PE=2 SV=1 | 18 | 498 | 8.0E-162 |
sp|Q6P371|HOT_XENTR | Hydroxyacid-oxoacid transhydrogenase, mitochondrial OS=Xenopus tropicalis GN=adhfe1 PE=2 SV=1 | 62 | 498 | 1.0E-161 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|A6QP15|HOT_BOVIN | Hydroxyacid-oxoacid transhydrogenase, mitochondrial OS=Bos taurus GN=ADHFE1 PE=2 SV=1 | 8 | 498 | 1.0E-165 |
sp|Q4QQW3|HOT_RAT | Hydroxyacid-oxoacid transhydrogenase, mitochondrial OS=Rattus norvegicus GN=Adhfe1 PE=1 SV=1 | 14 | 498 | 4.0E-165 |
sp|Q8R0N6|HOT_MOUSE | Hydroxyacid-oxoacid transhydrogenase, mitochondrial OS=Mus musculus GN=Adhfe1 PE=1 SV=2 | 14 | 498 | 3.0E-164 |
sp|Q08B39|HOT_XENLA | Hydroxyacid-oxoacid transhydrogenase, mitochondrial OS=Xenopus laevis GN=adhfe1 PE=2 SV=1 | 18 | 498 | 8.0E-162 |
sp|Q6P371|HOT_XENTR | Hydroxyacid-oxoacid transhydrogenase, mitochondrial OS=Xenopus tropicalis GN=adhfe1 PE=2 SV=1 | 62 | 498 | 1.0E-161 |
sp|Q5RF11|HOT_PONAB | Hydroxyacid-oxoacid transhydrogenase, mitochondrial OS=Pongo abelii GN=ADHFE1 PE=2 SV=1 | 14 | 498 | 1.0E-160 |
sp|Q8IWW8|HOT_HUMAN | Hydroxyacid-oxoacid transhydrogenase, mitochondrial OS=Homo sapiens GN=ADHFE1 PE=1 SV=1 | 18 | 498 | 3.0E-160 |
sp|Q17EN4|HOT_AEDAE | Probable hydroxyacid-oxoacid transhydrogenase, mitochondrial OS=Aedes aegypti GN=AAEL003729 PE=3 SV=1 | 14 | 497 | 2.0E-153 |
sp|Q7Q547|HOT_ANOGA | Probable hydroxyacid-oxoacid transhydrogenase, mitochondrial OS=Anopheles gambiae GN=AGAP006646 PE=3 SV=3 | 14 | 497 | 4.0E-152 |
sp|Q9W265|HOT_DROME | Probable hydroxyacid-oxoacid transhydrogenase, mitochondrial OS=Drosophila melanogaster GN=T3dh PE=2 SV=1 | 60 | 498 | 3.0E-146 |
sp|Q28XT3|HOT_DROPS | Probable hydroxyacid-oxoacid transhydrogenase, mitochondrial OS=Drosophila pseudoobscura pseudoobscura GN=GA17444 PE=3 SV=2 | 60 | 497 | 2.0E-145 |
sp|A8WTJ7|HOT_CAEBR | Probable hydroxyacid-oxoacid transhydrogenase, mitochondrial OS=Caenorhabditis briggsae GN=CBG02769 PE=3 SV=1 | 65 | 497 | 2.0E-137 |
sp|Q9U2M4|HOT_CAEEL | Probable hydroxyacid-oxoacid transhydrogenase, mitochondrial OS=Caenorhabditis elegans GN=Y38F1A.6 PE=3 SV=1 | 65 | 497 | 4.0E-135 |
sp|Q54GJ7|HOT_DICDI | Probable hydroxyacid-oxoacid transhydrogenase, mitochondrial OS=Dictyostelium discoideum GN=adhfe1 PE=3 SV=1 | 69 | 497 | 6.0E-135 |
sp|P31005|MEDH_BACMT | NAD-dependent methanol dehydrogenase OS=Bacillus methanolicus GN=mdh PE=1 SV=3 | 83 | 461 | 7.0E-48 |
sp|A4IP64|ADH1_GEOTN | Long-chain-alcohol dehydrogenase 1 OS=Geobacillus thermodenitrificans (strain NG80-2) GN=adh1 PE=1 SV=1 | 84 | 497 | 2.0E-44 |
sp|P76553|EUTG_ECOLI | Ethanolamine utilization protein EutG OS=Escherichia coli (strain K12) GN=eutG PE=3 SV=2 | 84 | 442 | 4.0E-40 |
sp|P45513|DHAT_CITFR | 1,3-propanediol dehydrogenase OS=Citrobacter freundii GN=dhaT PE=3 SV=1 | 83 | 452 | 4.0E-40 |
sp|Q59477|DHAT_KLEPN | 1,3-propanediol dehydrogenase OS=Klebsiella pneumoniae GN=dhaT PE=1 SV=1 | 83 | 452 | 6.0E-40 |
sp|P71017|GBSB_BACSU | Alcohol dehydrogenase OS=Bacillus subtilis (strain 168) GN=gbsB PE=1 SV=2 | 66 | 441 | 6.0E-37 |
sp|P41795|EUTG_SALTY | Ethanolamine utilization protein EutG OS=Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) GN=eutG PE=3 SV=2 | 84 | 466 | 2.0E-36 |
sp|P0A9S1|FUCO_ECOLI | Lactaldehyde reductase OS=Escherichia coli (strain K12) GN=fucO PE=1 SV=2 | 83 | 466 | 6.0E-35 |
sp|P0A9S2|FUCO_ECO57 | Lactaldehyde reductase OS=Escherichia coli O157:H7 GN=fucO PE=3 SV=2 | 83 | 466 | 6.0E-35 |
sp|P0DJA2|ADH2_ZYMMO | Alcohol dehydrogenase 2 OS=Zymomonas mobilis subsp. mobilis (strain ATCC 31821 / ZM4 / CP4) GN=adhB PE=1 SV=1 | 82 | 496 | 1.0E-34 |
sp|P37686|ADH2_ECOLI | Probable alcohol dehydrogenase OS=Escherichia coli (strain K12) GN=yiaY PE=3 SV=4 | 76 | 497 | 3.0E-34 |
sp|F8DVL8|ADH2_ZYMMA | Alcohol dehydrogenase 2 OS=Zymomonas mobilis subsp. mobilis (strain ATCC 10988 / DSM 424 / LMG 404 / NCIMB 8938 / NRRL B-806 / ZM1) GN=adhB PE=3 SV=1 | 82 | 496 | 6.0E-34 |
sp|Q09669|ADH4_SCHPO | Alcohol dehydrogenase 4 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=adh4 PE=2 SV=1 | 3 | 497 | 1.0E-32 |
sp|P38945|4HDB_CLOK5 | NAD-dependent 4-hydroxybutyrate dehydrogenase OS=Clostridium kluyveri (strain ATCC 8527 / DSM 555 / NCIMB 10680) GN=4hbD PE=3 SV=1 | 140 | 473 | 6.0E-31 |
sp|A6ZTT5|ADH4_YEAS7 | Alcohol dehydrogenase 4 OS=Saccharomyces cerevisiae (strain YJM789) GN=ADH4 PE=3 SV=2 | 83 | 494 | 2.0E-29 |
sp|P10127|ADH4_YEAST | Alcohol dehydrogenase 4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ADH4 PE=1 SV=3 | 83 | 494 | 2.0E-28 |
sp|Q04944|ADHA_CLOAB | NADH-dependent butanol dehydrogenase A OS=Clostridium acetobutylicum (strain ATCC 824 / DSM 792 / JCM 1419 / LMG 5710 / VKM B-1787) GN=bdhA PE=1 SV=2 | 79 | 470 | 3.0E-28 |
sp|Q9F282|ADHA_THEET | Long-chain primary alcohol dehydrogenase AdhA OS=Thermoanaerobacter ethanolicus GN=adhA PE=1 SV=1 | 74 | 497 | 1.0E-26 |
sp|P13604|ADH1_CLOSA | NADPH-dependent butanol dehydrogenase OS=Clostridium saccharobutylicum GN=adh1 PE=3 SV=1 | 81 | 494 | 1.0E-26 |
sp|Q24803|ADH2_ENTHI | Aldehyde-alcohol dehydrogenase 2 OS=Entamoeba histolytica GN=ADH2 PE=1 SV=1 | 102 | 399 | 9.0E-25 |
sp|P0A9Q7|ADHE_ECOLI | Aldehyde-alcohol dehydrogenase OS=Escherichia coli (strain K12) GN=adhE PE=1 SV=2 | 99 | 452 | 5.0E-24 |
sp|P0A9Q8|ADHE_ECO57 | Aldehyde-alcohol dehydrogenase OS=Escherichia coli O157:H7 GN=adhE PE=3 SV=2 | 99 | 452 | 5.0E-24 |
sp|Q9RCG0|MNO_AMYME | Methanol:N,N-dimethyl-4-nitrosoaniline oxidoreductase OS=Amycolatopsis methanolica GN=mno PE=1 SV=1 | 83 | 418 | 6.0E-24 |
sp|O05239|YUGJ_BACSU | Probable NADH-dependent butanol dehydrogenase 1 OS=Bacillus subtilis (strain 168) GN=yugJ PE=3 SV=1 | 79 | 472 | 7.0E-23 |
sp|Q04945|ADHB_CLOAB | NADH-dependent butanol dehydrogenase B OS=Clostridium acetobutylicum (strain ATCC 824 / DSM 792 / JCM 1419 / LMG 5710 / VKM B-1787) GN=bdhB PE=1 SV=1 | 79 | 466 | 3.0E-22 |
sp|C5MRT8|MNO_MYCS8 | Methanol:N,N-dimethyl-4-nitrosoaniline oxidoreductase OS=Mycobacterium sp. (strain DSM 3803 / JC1) PE=1 SV=1 | 83 | 421 | 6.0E-22 |
sp|P33744|ADHE_CLOAB | Aldehyde-alcohol dehydrogenase OS=Clostridium acetobutylicum (strain ATCC 824 / DSM 792 / JCM 1419 / LMG 5710 / VKM B-1787) GN=adhE PE=2 SV=3 | 102 | 407 | 1.0E-21 |
sp|Q53062|MNO_RHOER | Methanol:N,N-dimethyl-4-nitrosoaniline oxidoreductase OS=Rhodococcus erythropolis GN=thcE PE=1 SV=2 | 84 | 421 | 2.0E-20 |
sp|O05240|YUGK_BACSU | Probable NADH-dependent butanol dehydrogenase 2 OS=Bacillus subtilis (strain 168) GN=yugK PE=3 SV=1 | 79 | 463 | 3.0E-19 |
sp|A4ISB9|ADH2_GEOTN | Long-chain-alcohol dehydrogenase 2 OS=Geobacillus thermodenitrificans (strain NG80-2) GN=adh2 PE=1 SV=1 | 79 | 463 | 4.0E-18 |
sp|Q46856|YQHD_ECOLI | Alcohol dehydrogenase YqhD OS=Escherichia coli (strain K12) GN=yqhD PE=1 SV=1 | 100 | 463 | 9.0E-17 |
sp|Q24857|ADH3_ENTHI | Alcohol dehydrogenase 3 OS=Entamoeba histolytica GN=ADH3 PE=2 SV=1 | 134 | 461 | 3.0E-15 |
sp|Q93T12|TFDF_DELAC | Maleylacetate reductase OS=Delftia acidovorans GN=tfdF PE=1 SV=2 | 81 | 400 | 3.0E-15 |
sp|P27101|TCBF_PSESQ | Maleylacetate reductase OS=Pseudomonas sp. (strain P51) GN=tcbF PE=3 SV=1 | 81 | 400 | 3.0E-15 |
sp|P94135|TFDF2_CUPPJ | Maleylacetate reductase 2 OS=Cupriavidus pinatubonensis (strain JMP 134 / LMG 1197) GN=tfdFII PE=1 SV=1 | 81 | 366 | 1.0E-12 |
sp|O30847|CLCE_PSEKB | Maleylacetate reductase OS=Pseudomonas knackmussii (strain DSM 6978 / LMG 23759 / B13) GN=clcE PE=3 SV=1 | 71 | 459 | 5.0E-10 |
sp|O87612|CLCE_PSEAI | Maleylacetate reductase OS=Pseudomonas aeruginosa GN=clcE PE=3 SV=1 | 71 | 459 | 8.0E-10 |
sp|P27137|TFDF1_CUPPJ | Maleylacetate reductase 1 OS=Cupriavidus pinatubonensis (strain JMP 134 / LMG 1197) GN=tfdFI PE=3 SV=1 | 72 | 409 | 8.0E-09 |
sp|O84992|MACA1_RHOOP | Maleylacetate reductase 1 OS=Rhodococcus opacus GN=macA PE=3 SV=1 | 70 | 459 | 9.0E-08 |
GO Term | Description | Terminal node |
---|---|---|
GO:0046872 | metal ion binding | Yes |
GO:0016491 | oxidoreductase activity | Yes |
GO:0055114 | oxidation-reduction process | Yes |
GO:0008152 | metabolic process | No |
GO:0043169 | cation binding | No |
GO:0008150 | biological_process | No |
GO:0043167 | ion binding | No |
GO:0003674 | molecular_function | No |
GO:0003824 | catalytic activity | No |
GO:0005488 | binding | No |
SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
---|---|---|
No | 1 - 11 | 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 | >Hirsu2|6777 MVAPIRVVASPAKRASSLLRTIQYTHPPSCPCHSNPGYHGQSPPALVPRAADAGRRRRYATPVTGKSEQADYAFE MAASSIRFGPGVTREVGMDFKNMGARRVCVVTDSTVDKLDAMRQVREGLTAEGINFDVYSDVRIEPKDSSIKDAI AWVRPKDADAFLAVGGGSVIDTAKLMNLYSAYPDADFLDFVNAPLGKGRPVDKPLKPLIAVPTTAGTGSETTGTA IFDLVAKRAKTGVAHRNLKPTLGICDPINTRTMPAAVKAASGLDVLCHSLESWTAIPYNQRTPRPPNPIMRPAYQ GANPISDVFSLHALRSTIKYLPRAVRDPDDFEAQSQMLLAATLAGIGFGNAGVHLCHGMSYPISGQNPGYKHAGY DVQSPIIPHGVSVAVSAPAVFRFTAASNPERHLQAAEAFGVDTSNVKKESAGEVLAEALTKFLADLGDQPKGLKD LGFGTEHIDALVEGTIPQARVLMLAPGLSKELQAEKEQLRKLYEDAMKH* |
Coding | >Hirsu2|6777 ATGGTTGCCCCCATCCGAGTGGTCGCGAGCCCGGCCAAGCGGGCGTCCAGCCTGCTGCGCACGATCCAGTATACG CACCCGCCGTCGTGCCCCTGCCACTCCAACCCAGGGTACCACGGGCAATCGCCGCCGGCGCTGGTCCCGCGTGCC GCCGACGCCGGCCGCCGCCGGCGCTACGCGACCCCCGTCACCGGCAAGTCGGAGCAGGCCGACTATGCTTTCGAG ATGGCCGCCTCGTCCATCCGCTTCGGCCCGGGCGTCACGCGCGAGGTCGGCATGGACTTCAAGAACATGGGCGCC CGGAGGGTCTGCGTCGTCACCGACTCGACCGTCGACAAGCTCGACGCCATGCGCCAGGTCCGCGAGGGGCTCACG GCCGAGGGCATCAACTTTGACGTCTATTCCGACGTCCGCATAGAGCCCAAGGACAGCTCCATCAAGGACGCCATT GCGTGGGTCAGGCCCAAGGACGCCGACGCCTTCCTCGCCGTCGGTGGCGGCTCCGTCATAGACACGGCCAAGCTC ATGAACCTCTATTCCGCCTACCCGGACGCCGACTTCCTCGACTTTGTCAACGCGCCGCTCGGCAAGGGCCGGCCC GTCGACAAGCCCCTCAAGCCCCTCATCGCCGTCCCCACGACGGCCGGCACCGGCAGCGAGACGACCGGCACGGCC ATCTTCGACCTCGTCGCCAAGCGGGCCAAGACGGGCGTCGCGCACCGGAACCTGAAGCCGACGCTCGGCATCTGC GACCCCATCAACACGAGGACCATGCCGGCCGCCGTCAAGGCCGCCTCGGGCCTCGACGTCCTCTGCCACTCCCTC GAGTCGTGGACCGCCATTCCCTACAATCAGCGGACTCCCAGGCCCCCCAACCCCATCATGCGCCCCGCCTATCAG GGCGCGAACCCCATCTCCGACGTCTTCTCTCTCCACGCCCTCCGCAGCACCATCAAGTATCTGCCCCGTGCCGTG AGGGATCCGGACGACTTTGAGGCCCAGAGCCAGATGCTGCTCGCCGCCACTCTGGCCGGCATCGGCTTCGGCAAC GCGGGCGTGCATCTGTGTCACGGCATGTCCTATCCCATCTCCGGACAGAACCCGGGGTACAAGCATGCGGGCTAT GACGTGCAATCCCCCATCATTCCCCATGGCGTGTCGGTCGCCGTCTCCGCCCCGGCCGTCTTCCGCTTCACGGCG GCCTCGAACCCGGAGCGCCATCTTCAGGCGGCCGAGGCCTTTGGTGTCGACACTTCTAACGTCAAGAAGGAGAGC GCGGGCGAGGTCCTGGCCGAGGCACTGACCAAGTTCCTCGCCGATCTCGGCGACCAGCCAAAGGGGCTGAAGGAC CTGGGATTCGGCACCGAGCATATCGACGCGCTCGTCGAGGGCACCATCCCGCAGGCCCGCGTGCTGATGCTGGCT CCGGGTCTATCGAAGGAGCTCCAGGCCGAGAAGGAACAGCTAAGAAAGCTGTACGAGGATGCCATGAAGCATTGA |
Transcript | >Hirsu2|6777 ATGGTTGCCCCCATCCGAGTGGTCGCGAGCCCGGCCAAGCGGGCGTCCAGCCTGCTGCGCACGATCCAGTATACG CACCCGCCGTCGTGCCCCTGCCACTCCAACCCAGGGTACCACGGGCAATCGCCGCCGGCGCTGGTCCCGCGTGCC GCCGACGCCGGCCGCCGCCGGCGCTACGCGACCCCCGTCACCGGCAAGTCGGAGCAGGCCGACTATGCTTTCGAG ATGGCCGCCTCGTCCATCCGCTTCGGCCCGGGCGTCACGCGCGAGGTCGGCATGGACTTCAAGAACATGGGCGCC CGGAGGGTCTGCGTCGTCACCGACTCGACCGTCGACAAGCTCGACGCCATGCGCCAGGTCCGCGAGGGGCTCACG GCCGAGGGCATCAACTTTGACGTCTATTCCGACGTCCGCATAGAGCCCAAGGACAGCTCCATCAAGGACGCCATT GCGTGGGTCAGGCCCAAGGACGCCGACGCCTTCCTCGCCGTCGGTGGCGGCTCCGTCATAGACACGGCCAAGCTC ATGAACCTCTATTCCGCCTACCCGGACGCCGACTTCCTCGACTTTGTCAACGCGCCGCTCGGCAAGGGCCGGCCC GTCGACAAGCCCCTCAAGCCCCTCATCGCCGTCCCCACGACGGCCGGCACCGGCAGCGAGACGACCGGCACGGCC ATCTTCGACCTCGTCGCCAAGCGGGCCAAGACGGGCGTCGCGCACCGGAACCTGAAGCCGACGCTCGGCATCTGC GACCCCATCAACACGAGGACCATGCCGGCCGCCGTCAAGGCCGCCTCGGGCCTCGACGTCCTCTGCCACTCCCTC GAGTCGTGGACCGCCATTCCCTACAATCAGCGGACTCCCAGGCCCCCCAACCCCATCATGCGCCCCGCCTATCAG GGCGCGAACCCCATCTCCGACGTCTTCTCTCTCCACGCCCTCCGCAGCACCATCAAGTATCTGCCCCGTGCCGTG AGGGATCCGGACGACTTTGAGGCCCAGAGCCAGATGCTGCTCGCCGCCACTCTGGCCGGCATCGGCTTCGGCAAC GCGGGCGTGCATCTGTGTCACGGCATGTCCTATCCCATCTCCGGACAGAACCCGGGGTACAAGCATGCGGGCTAT GACGTGCAATCCCCCATCATTCCCCATGGCGTGTCGGTCGCCGTCTCCGCCCCGGCCGTCTTCCGCTTCACGGCG GCCTCGAACCCGGAGCGCCATCTTCAGGCGGCCGAGGCCTTTGGTGTCGACACTTCTAACGTCAAGAAGGAGAGC GCGGGCGAGGTCCTGGCCGAGGCACTGACCAAGTTCCTCGCCGATCTCGGCGACCAGCCAAAGGGGCTGAAGGAC CTGGGATTCGGCACCGAGCATATCGACGCGCTCGTCGAGGGCACCATCCCGCAGGCCCGCGTGCTGATGCTGGCT CCGGGTCTATCGAAGGAGCTCCAGGCCGAGAAGGAACAGCTAAGAAAGCTGTACGAGGATGCCATGAAGCATTGA |
Gene | >Hirsu2|6777 ATGGTTGCCCCCATCCGAGTGGTCGCGAGCGTGAGTTCCGCAACCGCCACCCCTGATCCTCCAACAACGAGTTGA CCGTCTCCTTCAGCCGGCCAAGCGGGCGTCCAGCCTGCTGCGCACGATCCAGTATACGCACCCGCCGTCGTGCCC CTGCCACTCCAACCCAGGGTACCACGGGCAATCGCCGCCGGCGCTGGTCCCGCGTGCCGCCGACGCCGGCCGCCG CCGGCGCTACGCGACCCCCGTCACCGGCAAGTCGGAGCAGGCCGACTATGCTTTCGAGATGGCCGCCTCGTCCAT CCGCTTCGGCCCGGGCGTCACGCGCGAGGTCGGCATGGACTTCAAGAACATGGGCGCCCGGAGGGTCTGCGTCGT CACCGACTCGACCGTCGACAAGCTCGACGCCATGCGCCAGGTCCGCGAGGGGCTCACGGCCGAGGGCATCAACTT TGACGTCTATTCCGACGTCCGCATAGAGCCCAAGGACAGCTCGTACGTTGGTGCCTCCTGCTCCTCCTCCTACTG CTGCGAGCTGACGCCCGCCCGACTTGCCCCATCTGAAATAATCGCAGCATCAAGGACGCCATTGCGTGGGTCAGG CCCAAGGACGCCGACGCCTTCCTCGCCGTCGGTGGCGGCTCCGTCATAGACACGGCCAAGCTCATGAACCTCTAT TCCGCCTACCCGGACGCCGACTTCCTCGACTTTGTCAACGCGCCGCTCGGCAAGGGCCGGCCCGTCGACAAGCCC CTCAAGCCCCTCATCGCCGTCCCCACGACGGCCGGCACCGGCAGCGAGACGACCGGCACGGCCATCTTCGACCTC GTCGCCAAGCGGGCCAAGACGGGCGTCGCGCACCGGAACCTGAAGCCGACGCTCGGCATCTGCGACCCCATCAAC ACGAGGACCATGCCGGCCGCCGTCAAGGCCGCCTCGGGCCTCGACGTCCTCTGCCACTCCCTCGAGTCGTGGACC GCCATTCCCTACAATCAGCGGACTCCCAGGCCCCCCAACCCCATCATGCGCCCCGCCTATCAGGGCGCGAACCCC ATCTCCGACGTCTTCTCTCTCCACGCCCTCCGCAGCACCATCAAGTATCTGCCCCGTGCCGTGAGGGATCCGGAC GACTTTGAGGCCCAGAGCCAGATGCTGCTCGCCGCCACTCTGGCCGGCATCGGCTTCGGCAACGCGGGCGTGCAT CTGTGTCACGGTACGTCACTGTGCCTCCTCGTGCGGCCTGGACTGACTTTGGATTGCTGGCAGGCATGTCCTATC CCATCTCCGGACAGAACCCGGGGTACAAGCATGCGGGCTATGACGTGCAATCCCCCATCATTCCCCATGGCGTGT CGGTCGCCGTCTCCGCCCCGGCCGTCTTCCGCTTCACGGCGGCCTCGAACCCGGAGCGCCATCTTCAGGCGGCCG AGGCCTTTGGTGTCGACACTTCTAACGTCAAGAAGGAGAGCGCGGGCGAGGTCCTGGCCGAGGCACTGACCAAGT TCCTCGCCGATCTCGGCGACCAGCCAAAGGGGCTGAAGGACCTGGGATTCGGCACCGAGCATATCGACGCGCTCG TCGAGGGCACCATCCCGCAGGCCCGCGTGCTGATGCTGGCTCCGGGTCTATCGAAGGAGCTCCAGGCCGAGAAGG AACAGCTAAGAAAGCTGTACGAGGATGCCATGAAGCATTGA |