© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | OphauG2|7114 |
| Gene name | |
| Location | Contig_8:5192..6917 |
| Strand | - |
| Gene length (bp) | 1725 |
| Transcript length (bp) | 1650 |
| Coding sequence length (bp) | 1650 |
| Protein length (aa) | 550 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00251 | Glyco_hydro_32N | Glycosyl hydrolases family 32 N-terminal domain | 3.5E-75 | 46 | 357 |
| PF08244 | Glyco_hydro_32C | Glycosyl hydrolases family 32 C terminal | 2.0E-06 | 423 | 510 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|A5DHM6|INUE_PICGU | Extracellular exo-inulinase OS=Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) GN=PGUG_02777 PE=1 SV=2 | 42 | 520 | 1.0E-86 |
| sp|A8W7I5|INUE_PICGM | Extracellular exo-inulinase inuE OS=Meyerozyma guilliermondii PE=1 SV=3 | 42 | 520 | 7.0E-86 |
| sp|Q6BJW6|INV_DEBHA | Invertase OS=Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN=INV PE=3 SV=2 | 42 | 503 | 2.0E-82 |
| sp|P00724|INV2_YEAST | Invertase 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=SUC2 PE=1 SV=1 | 42 | 516 | 1.0E-81 |
| sp|P10594|INV1_YEASX | Invertase 1 OS=Saccharomyces cerevisiae GN=SUC1 PE=1 SV=1 | 42 | 516 | 1.0E-81 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|A5DHM6|INUE_PICGU | Extracellular exo-inulinase OS=Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) GN=PGUG_02777 PE=1 SV=2 | 42 | 520 | 1.0E-86 |
| sp|A8W7I5|INUE_PICGM | Extracellular exo-inulinase inuE OS=Meyerozyma guilliermondii PE=1 SV=3 | 42 | 520 | 7.0E-86 |
| sp|Q6BJW6|INV_DEBHA | Invertase OS=Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN=INV PE=3 SV=2 | 42 | 503 | 2.0E-82 |
| sp|P00724|INV2_YEAST | Invertase 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=SUC2 PE=1 SV=1 | 42 | 516 | 1.0E-81 |
| sp|P10594|INV1_YEASX | Invertase 1 OS=Saccharomyces cerevisiae GN=SUC1 PE=1 SV=1 | 42 | 516 | 1.0E-81 |
| sp|P28999|INU1_KLUMA | Inulinase OS=Kluyveromyces marxianus GN=INU1 PE=1 SV=1 | 42 | 500 | 2.0E-81 |
| sp|P10596|INV4_YEASX | Invertase 4 OS=Saccharomyces cerevisiae GN=SUC4 PE=3 SV=1 | 42 | 516 | 6.0E-81 |
| sp|P40912|INV1_WICAO | Invertase OS=Wickerhamomyces anomalus GN=INV1 PE=3 SV=1 | 33 | 523 | 2.0E-79 |
| sp|O59852|INV1_SCHPO | Invertase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=inv1 PE=1 SV=1 | 37 | 534 | 3.0E-76 |
| sp|O42878|INVX_SCHPO | Putative invertase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC8E11.01c PE=3 SV=3 | 40 | 502 | 1.0E-75 |
| sp|P24133|INV_SCHOC | Invertase OS=Schwanniomyces occidentalis GN=INV PE=1 SV=1 | 42 | 500 | 2.0E-75 |
| sp|Q9Y746|INV_KLULA | Invertase OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=INV1 PE=3 SV=1 | 42 | 500 | 4.0E-71 |
| sp|P05656|SACC_BACSU | Levanase OS=Bacillus subtilis (strain 168) GN=sacC PE=1 SV=1 | 37 | 491 | 3.0E-64 |
| sp|A2R0E0|INUE_ASPNC | Extracellular exo-inulinase inuE OS=Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN=inuE PE=2 SV=1 | 9 | 534 | 3.0E-62 |
| sp|Q76HP6|INUE_ASPNG | Extracellular exo-inulinase inuE OS=Aspergillus niger GN=inuE PE=1 SV=1 | 9 | 534 | 1.0E-61 |
| sp|E1ABX2|INUE_ASPFI | Extracellular exo-inulinase inuE OS=Aspergillus ficuum GN=exoI PE=1 SV=1 | 9 | 534 | 1.0E-61 |
| sp|Q96TU3|INUE_ASPAW | Extracellular exo-inulinase inuE OS=Aspergillus awamori GN=inuE PE=1 SV=1 | 34 | 534 | 6.0E-58 |
| sp|O94220|INU2_ASPFI | Extracellular endo-inulinase inu2 OS=Aspergillus ficuum GN=inu2 PE=1 SV=1 | 41 | 447 | 3.0E-43 |
| sp|O74641|INUA_ASPNG | Extracellular endo-inulinase inuA OS=Aspergillus niger GN=inuA PE=1 SV=1 | 41 | 447 | 9.0E-43 |
| sp|A5ABL2|INUA_ASPNC | Extracellular endo-inulinase inuA OS=Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN=inuA PE=1 SV=1 | 41 | 447 | 6.0E-42 |
| sp|O07003|LEVB_BACSU | Levanbiose-producing levanase OS=Bacillus subtilis (strain 168) GN=levB PE=1 SV=1 | 41 | 388 | 4.0E-41 |
| sp|O31411|SACC_BACL7 | Levanase (Fragment) OS=Bacillus sp. (strain L7) PE=1 SV=2 | 37 | 541 | 4.0E-41 |
| sp|O74642|INUB_ASPNG | Extracellular endo-inulinase inuB OS=Aspergillus niger GN=inuB PE=1 SV=1 | 41 | 353 | 7.0E-41 |
| sp|O33833|BFRA_THEMA | Beta-fructosidase OS=Thermotoga maritima (strain ATCC 43589 / MSB8 / DSM 3109 / JCM 10099) GN=bfrA PE=1 SV=1 | 41 | 381 | 1.0E-38 |
| sp|P94469|LEVB_GEOSE | Levanbiose-producing levanase (Fragment) OS=Geobacillus stearothermophilus GN=levB PE=1 SV=2 | 65 | 388 | 2.0E-38 |
| sp|Q03174|FRUA_STRMU | Fructan beta-fructosidase OS=Streptococcus mutans serotype c (strain ATCC 700610 / UA159) GN=fruA PE=2 SV=2 | 37 | 499 | 4.0E-30 |
| sp|F8DVG5|SCR_ZYMMA | Sucrose-6-phosphate hydrolase OS=Zymomonas mobilis subsp. mobilis (strain ATCC 10988 / DSM 424 / LMG 404 / NCIMB 8938 / NRRL B-806 / ZM1) GN=sacA PE=3 SV=1 | 43 | 393 | 1.0E-28 |
| sp|P0DJA7|SCR_ZYMMO | Sucrose-6-phosphate hydrolase OS=Zymomonas mobilis subsp. mobilis (strain ATCC 31821 / ZM4 / CP4) GN=sacA PE=1 SV=1 | 43 | 393 | 2.0E-28 |
| sp|P40714|CSCA_ECOLX | Sucrose-6-phosphate hydrolase OS=Escherichia coli GN=cscA PE=3 SV=1 | 41 | 514 | 4.0E-27 |
| sp|P16553|RAFD_ECOLX | Raffinose invertase OS=Escherichia coli GN=rafD PE=3 SV=1 | 43 | 514 | 6.0E-27 |
| sp|P07819|SCRB_BACSU | Sucrose-6-phosphate hydrolase OS=Bacillus subtilis (strain 168) GN=sacA PE=3 SV=2 | 40 | 516 | 1.0E-26 |
| sp|P27217|SCRB_KLEPN | Sucrose-6-phosphate hydrolase OS=Klebsiella pneumoniae GN=scrB PE=1 SV=3 | 43 | 504 | 5.0E-25 |
| sp|A1STJ9|SCRB_PSYIN | Probable sucrose-6-phosphate hydrolase OS=Psychromonas ingrahamii (strain 37) GN=Ping_0974 PE=3 SV=1 | 41 | 349 | 5.0E-24 |
| sp|P37075|SCRB_SALTM | Sucrose-6-phosphate hydrolase OS=Salmonella typhimurium GN=scrB PE=3 SV=1 | 43 | 491 | 8.0E-24 |
| sp|P13394|SCRB_VIBAL | Sucrose-6-phosphate hydrolase OS=Vibrio alginolyticus GN=scrB PE=2 SV=1 | 43 | 500 | 5.0E-20 |
| sp|Q43857|INVA_VICFA | Acid beta-fructofuranosidase OS=Vicia faba GN=VCINV PE=2 SV=1 | 42 | 534 | 9.0E-20 |
| sp|Q70XE6|6FEH_BETVU | Fructan 6-exohydrolase OS=Beta vulgaris GN=6-FEH PE=1 SV=1 | 29 | 362 | 4.0E-19 |
| sp|P49174|INVA_MAIZE | Beta-fructofuranosidase, cell wall isozyme OS=Zea mays PE=2 SV=1 | 42 | 382 | 5.0E-19 |
| sp|A5EZZ8|SCRB_VIBC3 | Probable sucrose-6-phosphate hydrolase OS=Vibrio cholerae serotype O1 (strain ATCC 39541 / Classical Ogawa 395 / O395) GN=cscA PE=3 SV=1 | 38 | 239 | 1.0E-18 |
| sp|Q56660|SCRB_VIBCL | Probable sucrose-6-phosphate hydrolase OS=Vibrio cholerae PE=3 SV=1 | 38 | 239 | 2.0E-18 |
| sp|Q67XZ3|INV3_ARATH | Beta-fructofuranosidase, insoluble isoenzyme CWINV3 OS=Arabidopsis thaliana GN=CWINV3 PE=1 SV=2 | 36 | 351 | 2.0E-18 |
| sp|Q9KLT6|SCRB_VIBCH | Probable sucrose-6-phosphate hydrolase OS=Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) GN=VC_A0655 PE=3 SV=1 | 38 | 239 | 6.0E-18 |
| sp|Q43866|INV1_ARATH | Beta-fructofuranosidase, insoluble isoenzyme CWINV1 OS=Arabidopsis thaliana GN=CWINV1 PE=1 SV=1 | 40 | 382 | 1.0E-17 |
| sp|Q04937|SCRB_LACLL | Sucrose-6-phosphate hydrolase OS=Lactococcus lactis subsp. lactis GN=scrB PE=1 SV=1 | 30 | 491 | 2.0E-17 |
| sp|O24509|INVA_PHAVU | Acid beta-fructofuranosidase OS=Phaseolus vulgaris PE=2 SV=1 | 42 | 534 | 3.0E-17 |
| sp|P80065|INVB_DAUCA | Beta-fructofuranosidase, soluble isoenzyme I OS=Daucus carota GN=INV*DC4 PE=1 SV=2 | 42 | 349 | 5.0E-17 |
| sp|Q39041|INVA4_ARATH | Acid beta-fructofuranosidase 4, vacuolar OS=Arabidopsis thaliana GN=BFRUCT4 PE=2 SV=2 | 42 | 357 | 7.0E-17 |
| sp|P29001|INVA_VIGRR | Acid beta-fructofuranosidase OS=Vigna radiata var. radiata GN=INVA PE=1 SV=1 | 42 | 534 | 9.0E-17 |
| sp|P43471|SCRB_PEDPE | Sucrose-6-phosphate hydrolase OS=Pediococcus pentosaceus GN=scrB PE=3 SV=2 | 31 | 537 | 1.0E-15 |
| sp|P93761|INV1_CAPAN | Acid beta-fructofuranosidase AIV-18 OS=Capsicum annuum PE=2 SV=1 | 42 | 353 | 4.0E-15 |
| sp|Q9LIB9|INV5_ARATH | Beta-fructofuranosidase, insoluble isoenzyme CWINV5 OS=Arabidopsis thaliana GN=CWINV5 PE=2 SV=2 | 3 | 351 | 2.0E-14 |
| sp|Q0JDC6|INV3_ORYSJ | Beta-fructofuranosidase, insoluble isoenzyme 3 OS=Oryza sativa subsp. japonica GN=CIN3 PE=2 SV=1 | 30 | 351 | 3.0E-14 |
| sp|Q01IS8|INV3_ORYSI | Beta-fructofuranosidase, insoluble isoenzyme 3 OS=Oryza sativa subsp. indica GN=CIN3 PE=2 SV=2 | 30 | 351 | 3.0E-14 |
| sp|Q43348|INVA3_ARATH | Acid beta-fructofuranosidase 3, vacuolar OS=Arabidopsis thaliana GN=BFRUCT3 PE=2 SV=1 | 42 | 369 | 5.0E-14 |
| sp|P26792|INV1_DAUCA | Beta-fructofuranosidase, insoluble isoenzyme 1 OS=Daucus carota GN=INV1 PE=1 SV=1 | 30 | 351 | 5.0E-14 |
| sp|P49175|INV1_MAIZE | Beta-fructofuranosidase 1 OS=Zea mays GN=IVR1 PE=3 SV=1 | 42 | 357 | 8.0E-14 |
| sp|Q2UXF7|6FEH_WHEAT | Fructan 6-exohydrolase OS=Triticum aestivum GN=6-FEH PE=1 SV=1 | 2 | 351 | 1.0E-13 |
| sp|Q39693|INV3_DAUCA | Beta-fructofuranosidase, insoluble isoenzyme 3 OS=Daucus carota GN=INV3 PE=3 SV=1 | 30 | 351 | 1.0E-13 |
| sp|P29000|INVA_SOLLC | Acid beta-fructofuranosidase OS=Solanum lycopersicum GN=TIV1 PE=2 SV=1 | 42 | 349 | 1.0E-13 |
| sp|Q43089|INV1_PEA | Beta-fructofuranosidase, cell wall isozyme OS=Pisum sativum GN=BFRUCT1 PE=2 SV=1 | 40 | 351 | 3.0E-13 |
| sp|B6DZD0|1FEH_TRIUA | Fructan 1-exohydrolase OS=Triticum urartu GN=1-FEH PE=3 SV=1 | 41 | 351 | 5.0E-13 |
| sp|Q9FSV7|SST_FESAR | Sucrose:sucrose 1-fructosyltransferase OS=Festuca arundinacea GN=1-SST PE=1 SV=1 | 42 | 353 | 1.0E-12 |
| sp|Q84PN8|1FEH1_WHEAT | Fructan 1-exohydrolase w1 OS=Triticum aestivum GN=1-FEHw1 PE=1 SV=1 | 41 | 367 | 2.0E-12 |
| sp|P13522|SCRB_STRMU | Sucrose-6-phosphate hydrolase OS=Streptococcus mutans serotype c (strain ATCC 700610 / UA159) GN=scrB PE=3 SV=3 | 40 | 513 | 3.0E-12 |
| sp|Q5JJV0|INV4_ORYSJ | Beta-fructofuranosidase, insoluble isoenzyme 4 OS=Oryza sativa subsp. japonica GN=CIN4 PE=2 SV=1 | 41 | 491 | 3.0E-12 |
| sp|Q1PEF8|INV2_ARATH | Beta-fructofuranosidase, insoluble isoenzyme CWINV2 OS=Arabidopsis thaliana GN=CWINV2 PE=2 SV=1 | 41 | 248 | 4.0E-12 |
| sp|Q5FC15|GFT_ASPOF | 6(G)-fructosyltransferase OS=Asparagus officinalis GN=FT1 PE=1 SV=1 | 42 | 509 | 5.0E-12 |
| sp|B6DZD1|1FEH_AEGSP | Fructan 1-exohydrolase OS=Aegilops speltoides GN=1-FEH PE=3 SV=1 | 41 | 351 | 7.0E-12 |
| sp|B6DZD2|1FEH_AEGTA | Fructan 1-exohydrolase OS=Aegilops tauschii GN=1-FEH PE=3 SV=1 | 41 | 351 | 2.0E-11 |
| sp|Q84LA1|1FEH2_WHEAT | Fructan 1-exohydrolase w2 OS=Triticum aestivum GN=1-FEHw2 PE=1 SV=1 | 41 | 351 | 2.0E-11 |
| sp|Q39692|INV2_DAUCA | Beta-fructofuranosidase, insoluble isoenzyme 2 OS=Daucus carota GN=INV2 PE=3 SV=1 | 30 | 453 | 2.0E-11 |
| sp|Q56UD0|INV6_ORYSJ | Beta-fructofuranosidase, insoluble isoenzyme 6 OS=Oryza sativa subsp. japonica GN=CIN6 PE=2 SV=1 | 42 | 515 | 2.0E-11 |
| sp|B6DXP5|1FEH_LEYCH | Fructan 1-exohydrolase OS=Leymus chinensis GN=1-FEH PE=2 SV=1 | 41 | 367 | 2.0E-11 |
| sp|Q0E0P0|INV1_ORYSJ | Beta-fructofuranosidase, insoluble isoenzyme 1 OS=Oryza sativa subsp. japonica GN=CIN1 PE=2 SV=1 | 42 | 351 | 5.0E-11 |
| sp|Q05936|SCRB_STAXY | Sucrose-6-phosphate hydrolase OS=Staphylococcus xylosus GN=scrB PE=3 SV=1 | 41 | 347 | 5.0E-11 |
| sp|B6DZC8|1FEH3_WHEAT | Fructan 1-exohydrolase w3 OS=Triticum aestivum GN=1-FEHw3 PE=1 SV=1 | 41 | 351 | 7.0E-11 |
| sp|Q8W413|INV4_ARATH | Beta-fructofuranosidase, insoluble isoenzyme CWINV4 OS=Arabidopsis thaliana GN=CWINV4 PE=2 SV=1 | 41 | 351 | 8.0E-11 |
| sp|A2X5P7|INV1_ORYSI | Beta-fructofuranosidase, insoluble isoenzyme 1 OS=Oryza sativa subsp. indica GN=CIN1 PE=2 SV=2 | 42 | 382 | 1.0E-10 |
| sp|Q0JDC5|INV2_ORYSJ | Beta-fructofuranosidase, insoluble isoenzyme 2 OS=Oryza sativa subsp. japonica GN=CIN2 PE=1 SV=1 | 38 | 351 | 2.0E-10 |
| sp|Q01IS7|INV2_ORYSI | Beta-fructofuranosidase, insoluble isoenzyme 2 OS=Oryza sativa subsp. indica GN=CIN2 PE=2 SV=2 | 38 | 351 | 3.0E-10 |
| sp|Q70AT7|1FEH_HORVU | Fructan 1-exohydrolase OS=Hordeum vulgare GN=1-FEH PE=2 SV=1 | 41 | 352 | 3.0E-10 |
| sp|D2IGW7|1FEH_BROPI | Fructan 1-exohydrolase OS=Bromus pictus GN=1-FEHa PE=1 SV=1 | 41 | 351 | 3.0E-10 |
| sp|Q8W4S6|INV6_ARATH | Beta-fructofuranosidase, insoluble isoenzyme CWINV6 OS=Arabidopsis thaliana GN=CWINV6 PE=2 SV=1 | 42 | 349 | 4.0E-10 |
| sp|P92916|GFT_ALLCE | Bifunctional 6(G)-fructosyltransferase/2,1-fructan:2,1-fructan 1-fructosyltransferase OS=Allium cepa PE=1 SV=1 | 42 | 357 | 7.0E-09 |
| sp|Q56UD1|INV5_ORYSJ | Beta-fructofuranosidase, insoluble isoenzyme 5 OS=Oryza sativa subsp. japonica GN=CIN5 PE=2 SV=3 | 42 | 244 | 7.0E-08 |
| sp|P07635|INV7_YEASX | Invertase 7 (Fragments) OS=Saccharomyces cerevisiae GN=SUC7 PE=3 SV=1 | 42 | 104 | 4.0E-07 |
| sp|P10597|INV5_YEASX | Invertase 5 (Fragment) OS=Saccharomyces cerevisiae GN=SUC5 PE=3 SV=1 | 42 | 82 | 1.0E-06 |
| sp|P10595|INV3_YEASX | Invertase 3 (Fragment) OS=Saccharomyces cerevisiae GN=SUC3 PE=3 SV=1 | 42 | 82 | 1.0E-06 |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| Yes | 1 - 20 | 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 | >OphauG2|7114 MMLACLVTVALCLAELVSCRLYGPHTVGHESIIADDYDGPYRPQLHFSPPYGFMNDPNGLFRDANGTWHLYYQLD PTGLTAGNQHWGHATSLDLYHWVNQPIAIYPPAKDVYVFSGSVVVDPENTSGFFPDQDNGVVAIYTLAPYNPDGS PGPQVQAISISHDGGYTFTPYEGNPVIPGTSPHFRDPKVIRHEGKWVMAVAYPVDFAIGIFVSSNLIDWEPTSNF TDPGIKGAQWECPNLIPISYTDETGVILGDTWLMLVSINPGAPLGGSITYYVPGSFDGRRFKPLDSAARLSDFGK DNYAGQFFYGLSEYESPVSIAWASNWQYAQDVPTDKEGWRSAMSLPRQMHLVKTADNDWKLAAEPYDLTPVRGEL LVQSSRLRNEFVSLNFEHLSSNAVYWEANLTDIPREGLPPMAVFHVSFQSRDTAERLSFEYSLADGIFSMDRGGL RGFKHAEFTNKFWYRSPARGGEWSMKGIIDRSVAEVFLNNGLDSATMTFYAQQPLTRMAIGSAHVSEEEVCVSAS VTGLRSGWKGAEGRRPNELEPIDC* |
| Coding | >OphauG2|7114 ATGATGCTGGCTTGCCTTGTTACCGTTGCTCTCTGCCTTGCCGAGTTGGTCTCATGCAGACTTTACGGCCCCCAC ACTGTCGGCCATGAGTCCATCATTGCCGACGACTACGACGGCCCCTATCGGCCTCAGCTTCACTTCTCGCCCCCT TATGGCTTCATGAACGATCCCAACGGGCTCTTTCGTGACGCTAATGGCACCTGGCATCTATACTATCAGCTTGAC CCCACAGGCCTGACAGCAGGAAATCAGCATTGGGGCCATGCCACTTCTCTCGATCTCTACCACTGGGTCAACCAG CCTATCGCCATCTACCCTCCTGCCAAGGACGTCTATGTATTTTCTGGTAGTGTCGTTGTAGACCCTGAAAACACT TCTGGCTTCTTCCCCGACCAGGACAACGGCGTCGTGGCCATATATACTCTGGCCCCCTATAACCCTGACGGCAGC CCAGGTCCCCAAGTACAGGCCATTTCCATTTCCCATGATGGCGGATACACCTTTACTCCGTACGAGGGCAACCCC GTTATCCCTGGCACGTCGCCTCACTTTCGTGACCCCAAGGTGATTCGCCATGAGGGGAAATGGGTAATGGCCGTG GCATATCCCGTTGACTTTGCCATTGGCATCTTTGTTTCATCAAATCTCATTGACTGGGAGCCAACCAGCAACTTT ACCGACCCAGGAATCAAGGGCGCCCAGTGGGAGTGTCCCAATCTGATTCCCATTTCCTATACCGATGAGACGGGA GTGATACTTGGCGACACGTGGCTCATGCTTGTCTCCATCAATCCCGGGGCGCCTTTGGGTGGATCCATCACGTAT TACGTTCCAGGCTCATTTGACGGGCGTCGCTTCAAGCCCCTGGACTCGGCTGCGAGACTGTCCGATTTTGGCAAA GATAATTACGCTGGTCAGTTCTTCTACGGTCTTTCTGAGTACGAGAGCCCCGTCTCAATAGCCTGGGCCTCCAAC TGGCAGTACGCGCAAGACGTTCCCACCGATAAAGAAGGGTGGAGAAGCGCAATGAGCCTACCGCGACAGATGCAC TTGGTCAAGACGGCGGACAATGACTGGAAGTTGGCGGCAGAACCGTATGACCTCACACCGGTCAGGGGAGAGCTT CTGGTGCAAAGCTCAAGGCTCCGTAATGAGTTTGTGTCGTTGAATTTCGAGCATCTGTCTTCCAATGCCGTGTAC TGGGAAGCAAACCTTACGGACATTCCTCGCGAGGGCTTGCCACCCATGGCCGTCTTCCACGTCAGTTTTCAGAGT CGTGACACGGCAGAACGGCTCAGCTTCGAATACTCGTTGGCAGATGGCATCTTTTCCATGGACCGCGGGGGCCTG CGGGGCTTTAAACACGCGGAATTCACCAACAAGTTTTGGTATCGGAGCCCTGCGCGCGGGGGCGAATGGAGCATG AAGGGCATTATTGACCGGTCCGTTGCAGAGGTGTTTCTCAACAATGGGCTTGACAGCGCCACCATGACGTTTTAC GCGCAGCAGCCGCTGACACGCATGGCGATTGGGAGTGCTCATGTGAGCGAGGAGGAGGTGTGCGTCAGCGCAAGC GTAACAGGCTTGCGCAGCGGGTGGAAAGGAGCTGAAGGGCGGCGGCCGAATGAGCTTGAGCCTATTGATTGCTAG |
| Transcript | >OphauG2|7114 ATGATGCTGGCTTGCCTTGTTACCGTTGCTCTCTGCCTTGCCGAGTTGGTCTCATGCAGACTTTACGGCCCCCAC ACTGTCGGCCATGAGTCCATCATTGCCGACGACTACGACGGCCCCTATCGGCCTCAGCTTCACTTCTCGCCCCCT TATGGCTTCATGAACGATCCCAACGGGCTCTTTCGTGACGCTAATGGCACCTGGCATCTATACTATCAGCTTGAC CCCACAGGCCTGACAGCAGGAAATCAGCATTGGGGCCATGCCACTTCTCTCGATCTCTACCACTGGGTCAACCAG CCTATCGCCATCTACCCTCCTGCCAAGGACGTCTATGTATTTTCTGGTAGTGTCGTTGTAGACCCTGAAAACACT TCTGGCTTCTTCCCCGACCAGGACAACGGCGTCGTGGCCATATATACTCTGGCCCCCTATAACCCTGACGGCAGC CCAGGTCCCCAAGTACAGGCCATTTCCATTTCCCATGATGGCGGATACACCTTTACTCCGTACGAGGGCAACCCC GTTATCCCTGGCACGTCGCCTCACTTTCGTGACCCCAAGGTGATTCGCCATGAGGGGAAATGGGTAATGGCCGTG GCATATCCCGTTGACTTTGCCATTGGCATCTTTGTTTCATCAAATCTCATTGACTGGGAGCCAACCAGCAACTTT ACCGACCCAGGAATCAAGGGCGCCCAGTGGGAGTGTCCCAATCTGATTCCCATTTCCTATACCGATGAGACGGGA GTGATACTTGGCGACACGTGGCTCATGCTTGTCTCCATCAATCCCGGGGCGCCTTTGGGTGGATCCATCACGTAT TACGTTCCAGGCTCATTTGACGGGCGTCGCTTCAAGCCCCTGGACTCGGCTGCGAGACTGTCCGATTTTGGCAAA GATAATTACGCTGGTCAGTTCTTCTACGGTCTTTCTGAGTACGAGAGCCCCGTCTCAATAGCCTGGGCCTCCAAC TGGCAGTACGCGCAAGACGTTCCCACCGATAAAGAAGGGTGGAGAAGCGCAATGAGCCTACCGCGACAGATGCAC TTGGTCAAGACGGCGGACAATGACTGGAAGTTGGCGGCAGAACCGTATGACCTCACACCGGTCAGGGGAGAGCTT CTGGTGCAAAGCTCAAGGCTCCGTAATGAGTTTGTGTCGTTGAATTTCGAGCATCTGTCTTCCAATGCCGTGTAC TGGGAAGCAAACCTTACGGACATTCCTCGCGAGGGCTTGCCACCCATGGCCGTCTTCCACGTCAGTTTTCAGAGT CGTGACACGGCAGAACGGCTCAGCTTCGAATACTCGTTGGCAGATGGCATCTTTTCCATGGACCGCGGGGGCCTG CGGGGCTTTAAACACGCGGAATTCACCAACAAGTTTTGGTATCGGAGCCCTGCGCGCGGGGGCGAATGGAGCATG AAGGGCATTATTGACCGGTCCGTTGCAGAGGTGTTTCTCAACAATGGGCTTGACAGCGCCACCATGACGTTTTAC GCGCAGCAGCCGCTGACACGCATGGCGATTGGGAGTGCTCATGTGAGCGAGGAGGAGGTGTGCGTCAGCGCAAGC GTAACAGGCTTGCGCAGCGGGTGGAAAGGAGCTGAAGGGCGGCGGCCGAATGAGCTTGAGCCTATTGATTGCTAG |
| Gene | >OphauG2|7114 ATGATGCTGGCTTGCCTTGTTACCGTTGCTCTCTGCCTTGCCGAGTTGGTCTCATGCAGACTTTACGGCCCCCAC ACTGTCGGCCATGAGTCCATCATTGCCGACGACTACGACGGCCCCTATCGGCCTCAGCTTCACTTCTCGCCCCCT TATGGCTTCATGAACGATCCCAACGGGCTCTTTCGTGACGCTAATGGCACCTGGCATCTATACTATCAGCTTGAC CCCACAGGCCTGACAGCAGGAAATCAGCATTGGGGCCATGCCACTTCTCTCGATCTCTACCACTGGGTCAACCAG CCTATCGCCATCTACCCTCCTGCCAAGGACGTCTATGTATTTTCTGGTAGTGTCGTTGTAGACCCTGAAAACACT TCTGGCTTCTTCCCCGACCAGGACAACGGCGTCGTGGCCATATATGTAGGCACCATGTTCTTCATGCCTTGATCA TGAACAAGCCCCTGGTCATCTGGCAATGGCTAACTCTGGACGCAGACTCTGGCCCCCTATAACCCTGACGGCAGC CCAGGTCCCCAAGTACAGGCCATTTCCATTTCCCATGATGGCGGATACACCTTTACTCCGTACGAGGGCAACCCC GTTATCCCTGGCACGTCGCCTCACTTTCGTGACCCCAAGGTGATTCGCCATGAGGGGAAATGGGTAATGGCCGTG GCATATCCCGTTGACTTTGCCATTGGCATCTTTGTTTCATCAAATCTCATTGACTGGGAGCCAACCAGCAACTTT ACCGACCCAGGAATCAAGGGCGCCCAGTGGGAGTGTCCCAATCTGATTCCCATTTCCTATACCGATGAGACGGGA GTGATACTTGGCGACACGTGGCTCATGCTTGTCTCCATCAATCCCGGGGCGCCTTTGGGTGGATCCATCACGTAT TACGTTCCAGGCTCATTTGACGGGCGTCGCTTCAAGCCCCTGGACTCGGCTGCGAGACTGTCCGATTTTGGCAAA GATAATTACGCTGGTCAGTTCTTCTACGGTCTTTCTGAGTACGAGAGCCCCGTCTCAATAGCCTGGGCCTCCAAC TGGCAGTACGCGCAAGACGTTCCCACCGATAAAGAAGGGTGGAGAAGCGCAATGAGCCTACCGCGACAGATGCAC TTGGTCAAGACGGCGGACAATGACTGGAAGTTGGCGGCAGAACCGTATGACCTCACACCGGTCAGGGGAGAGCTT CTGGTGCAAAGCTCAAGGCTCCGTAATGAGTTTGTGTCGTTGAATTTCGAGCATCTGTCTTCCAATGCCGTGTAC TGGGAAGCAAACCTTACGGACATTCCTCGCGAGGGCTTGCCACCCATGGCCGTCTTCCACGTCAGTTTTCAGAGT CGTGACACGGCAGAACGGCTCAGCTTCGAATACTCGTTGGCAGATGGCATCTTTTCCATGGACCGCGGGGGCCTG CGGGGCTTTAAACACGCGGAATTCACCAACAAGTTTTGGTATCGGAGCCCTGCGCGCGGGGGCGAATGGAGCATG AAGGGCATTATTGACCGGTCCGTTGCAGAGGTGTTTCTCAACAATGGGCTTGACAGCGCCACCATGACGTTTTAC GCGCAGCAGCCGCTGACACGCATGGCGATTGGGAGTGCTCATGTGAGCGAGGAGGAGGTGTGCGTCAGCGCAAGC GTAACAGGCTTGCGCAGCGGGTGGAAAGGAGCTGAAGGGCGGCGGCCGAATGAGCTTGAGCCTATTGATTGCTAG |