© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Ophio5|2692 |
| Gene name | |
| Location | scaffold_218:11898..14826 |
| Strand | + |
| Gene length (bp) | 2928 |
| Transcript length (bp) | 2760 |
| Coding sequence length (bp) | 2757 |
| Protein length (aa) | 919 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00613 | PI3Ka | Phosphoinositide 3-kinase family, accessory domain (PIK domain) | 7.8E-58 | 369 | 542 |
| PF00454 | PI3_PI4_kinase | Phosphatidylinositol 3- and 4-kinase | 1.6E-42 | 661 | 864 |
| PF00792 | PI3K_C2 | Phosphoinositide 3-kinase C2 | 1.3E-32 | 58 | 221 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P22543|VPS34_YEAST | Phosphatidylinositol 3-kinase VPS34 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=VPS34 PE=1 SV=1 | 7 | 919 | 0.0E+00 |
| sp|P42347|PI3K1_SOYBN | Phosphatidylinositol 3-kinase, root isoform OS=Glycine max PE=2 SV=1 | 8 | 918 | 0.0E+00 |
| sp|P42348|PI3K2_SOYBN | Phosphatidylinositol 3-kinase, nodule isoform OS=Glycine max PE=2 SV=1 | 8 | 918 | 0.0E+00 |
| sp|Q5D891|PK3C3_PIG | Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Sus scrofa GN=PIK3C3 PE=2 SV=1 | 5 | 918 | 0.0E+00 |
| sp|P42339|PI3K_ARATH | Phosphatidylinositol 3-kinase VPS34 OS=Arabidopsis thaliana GN=At1g60490 PE=2 SV=2 | 8 | 918 | 0.0E+00 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P22543|VPS34_YEAST | Phosphatidylinositol 3-kinase VPS34 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=VPS34 PE=1 SV=1 | 7 | 919 | 0.0E+00 |
| sp|P42347|PI3K1_SOYBN | Phosphatidylinositol 3-kinase, root isoform OS=Glycine max PE=2 SV=1 | 8 | 918 | 0.0E+00 |
| sp|P42348|PI3K2_SOYBN | Phosphatidylinositol 3-kinase, nodule isoform OS=Glycine max PE=2 SV=1 | 8 | 918 | 0.0E+00 |
| sp|Q5D891|PK3C3_PIG | Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Sus scrofa GN=PIK3C3 PE=2 SV=1 | 5 | 918 | 0.0E+00 |
| sp|P42339|PI3K_ARATH | Phosphatidylinositol 3-kinase VPS34 OS=Arabidopsis thaliana GN=At1g60490 PE=2 SV=2 | 8 | 918 | 0.0E+00 |
| sp|P50520|VPS34_SCHPO | Phosphatidylinositol 3-kinase vps34 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=vps34 PE=2 SV=2 | 347 | 919 | 0.0E+00 |
| sp|Q6AZN6|PK3C3_XENLA | Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Xenopus laevis GN=pik3c3 PE=2 SV=1 | 5 | 918 | 0.0E+00 |
| sp|Q6PF93|PK3C3_MOUSE | Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Mus musculus GN=Pik3c3 PE=1 SV=1 | 335 | 918 | 4.0E-180 |
| sp|O88763|PK3C3_RAT | Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Rattus norvegicus GN=Pik3c3 PE=1 SV=1 | 335 | 918 | 3.0E-179 |
| sp|Q8NEB9|PK3C3_HUMAN | Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Homo sapiens GN=PIK3C3 PE=1 SV=1 | 335 | 918 | 3.0E-179 |
| sp|P54676|PI3K4_DICDI | Phosphatidylinositol 3-kinase VPS34-like OS=Dictyostelium discoideum GN=pikE PE=3 SV=2 | 10 | 919 | 6.0E-178 |
| sp|Q92213|VPS34_CANAX | Phosphatidylinositol 3-kinase VPS34 OS=Candida albicans GN=VPS34 PE=3 SV=1 | 11 | 919 | 8.0E-171 |
| sp|P54675|PI3K3_DICDI | Phosphatidylinositol 3-kinase 3 OS=Dictyostelium discoideum GN=pikC PE=2 SV=2 | 379 | 901 | 2.0E-74 |
| sp|O35904|PK3CD_MOUSE | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform OS=Mus musculus GN=Pik3cd PE=1 SV=2 | 338 | 891 | 2.0E-73 |
| sp|O00329|PK3CD_HUMAN | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform OS=Homo sapiens GN=PIK3CD PE=1 SV=2 | 393 | 891 | 4.0E-73 |
| sp|P54673|PI3K1_DICDI | Phosphatidylinositol 3-kinase 1 OS=Dictyostelium discoideum GN=pikA PE=2 SV=2 | 376 | 916 | 4.0E-72 |
| sp|O02697|PK3CG_PIG | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform OS=Sus scrofa GN=PIK3CG PE=1 SV=2 | 373 | 896 | 6.0E-68 |
| sp|P48736|PK3CG_HUMAN | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform OS=Homo sapiens GN=PIK3CG PE=1 SV=3 | 373 | 896 | 2.0E-67 |
| sp|P54674|PI3K2_DICDI | Phosphatidylinositol 3-kinase 2 OS=Dictyostelium discoideum GN=pikB PE=2 SV=2 | 381 | 915 | 2.0E-67 |
| sp|Q9JHG7|PK3CG_MOUSE | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform OS=Mus musculus GN=Pik3cg PE=1 SV=2 | 373 | 896 | 8.0E-67 |
| sp|O00443|P3C2A_HUMAN | Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha OS=Homo sapiens GN=PIK3C2A PE=1 SV=2 | 393 | 915 | 2.0E-63 |
| sp|Q5RAY1|P3C2A_PONAB | Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha OS=Pongo abelii GN=PIK3C2A PE=2 SV=1 | 393 | 915 | 7.0E-63 |
| sp|Q8BTI9|PK3CB_MOUSE | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform OS=Mus musculus GN=Pik3cb PE=1 SV=2 | 381 | 899 | 2.0E-62 |
| sp|P32871|PK3CA_BOVIN | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform OS=Bos taurus GN=PIK3CA PE=1 SV=1 | 368 | 891 | 2.0E-62 |
| sp|Q61194|P3C2A_MOUSE | Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha OS=Mus musculus GN=Pik3c2a PE=1 SV=2 | 393 | 915 | 4.0E-62 |
| sp|Q9Z1L0|PK3CB_RAT | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform OS=Rattus norvegicus GN=Pik3cb PE=2 SV=1 | 381 | 899 | 4.0E-62 |
| sp|P42336|PK3CA_HUMAN | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform OS=Homo sapiens GN=PIK3CA PE=1 SV=2 | 368 | 891 | 4.0E-62 |
| sp|P42337|PK3CA_MOUSE | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform OS=Mus musculus GN=Pik3ca PE=1 SV=2 | 368 | 891 | 6.0E-62 |
| sp|P42338|PK3CB_HUMAN | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform OS=Homo sapiens GN=PIK3CB PE=1 SV=1 | 381 | 899 | 3.0E-61 |
| sp|O00750|P3C2B_HUMAN | Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit beta OS=Homo sapiens GN=PIK3C2B PE=1 SV=2 | 380 | 915 | 1.0E-56 |
| sp|O70173|P3C2G_RAT | Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit gamma OS=Rattus norvegicus GN=Pik3c2g PE=2 SV=1 | 389 | 915 | 2.0E-55 |
| sp|O70167|P3C2G_MOUSE | Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit gamma OS=Mus musculus GN=Pik3c2g PE=2 SV=1 | 392 | 915 | 3.0E-55 |
| sp|O75747|P3C2G_HUMAN | Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit gamma OS=Homo sapiens GN=PIK3C2G PE=1 SV=3 | 392 | 915 | 3.0E-53 |
| sp|Q94125|AGE1_CAEEL | Phosphatidylinositol 3-kinase age-1 OS=Caenorhabditis elegans GN=age-1 PE=1 SV=6 | 383 | 896 | 8.0E-47 |
| sp|P0C5E7|AGE1_CAEBR | Phosphatidylinositol 3-kinase age-1 OS=Caenorhabditis briggsae GN=age-1 PE=3 SV=1 | 382 | 841 | 1.0E-41 |
| sp|Q8SQY7|STT4_ENCCU | Probable phosphatidylinositol 4-kinase STT4 homolog OS=Encephalitozoon cuniculi (strain GB-M1) GN=STT4 PE=3 SV=2 | 443 | 887 | 4.0E-37 |
| sp|Q8NEB9|PK3C3_HUMAN | Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Homo sapiens GN=PIK3C3 PE=1 SV=1 | 5 | 251 | 1.0E-35 |
| sp|Q6PF93|PK3C3_MOUSE | Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Mus musculus GN=Pik3c3 PE=1 SV=1 | 5 | 251 | 2.0E-35 |
| sp|O88763|PK3C3_RAT | Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Rattus norvegicus GN=Pik3c3 PE=1 SV=1 | 5 | 251 | 6.0E-35 |
| sp|P54677|PI4K_DICDI | Phosphatidylinositol 4-kinase OS=Dictyostelium discoideum GN=pikD PE=3 SV=3 | 661 | 917 | 3.0E-33 |
| sp|Q9SXA1|P4KA1_ARATH | Phosphatidylinositol 4-kinase alpha 1 OS=Arabidopsis thaliana GN=PI4KA1 PE=1 SV=2 | 396 | 887 | 2.0E-30 |
| sp|Q49GP3|PI4KB_DANRE | Phosphatidylinositol 4-kinase beta OS=Danio rerio GN=pi4kb PE=2 SV=2 | 663 | 908 | 1.0E-29 |
| sp|A4IID4|PI4KB_XENTR | Phosphatidylinositol 4-kinase beta OS=Xenopus tropicalis GN=pi4kb PE=2 SV=1 | 663 | 908 | 3.0E-29 |
| sp|O08561|PI4KB_RAT | Phosphatidylinositol 4-kinase beta OS=Rattus norvegicus GN=Pi4kb PE=1 SV=1 | 663 | 908 | 7.0E-29 |
| sp|Q8BKC8|PI4KB_MOUSE | Phosphatidylinositol 4-kinase beta OS=Mus musculus GN=Pi4kb PE=1 SV=2 | 663 | 908 | 7.0E-29 |
| sp|B2KI64|PI4KB_RHIFE | Phosphatidylinositol 4-kinase beta OS=Rhinolophus ferrumequinum GN=PI4KB PE=3 SV=1 | 663 | 908 | 8.0E-29 |
| sp|A9X1A0|PI4KB_PAPAN | Phosphatidylinositol 4-kinase beta OS=Papio anubis GN=PI4KB PE=3 SV=2 | 663 | 908 | 8.0E-29 |
| sp|Q9UBF8|PI4KB_HUMAN | Phosphatidylinositol 4-kinase beta OS=Homo sapiens GN=PI4KB PE=1 SV=1 | 663 | 908 | 8.0E-29 |
| sp|B1MTG7|PI4KB_CALMO | Phosphatidylinositol 4-kinase beta OS=Callicebus moloch GN=PI4KB PE=3 SV=1 | 663 | 908 | 8.0E-29 |
| sp|B0KWC1|PI4KB_CALJA | Phosphatidylinositol 4-kinase beta OS=Callithrix jacchus GN=PI4KB PE=3 SV=1 | 663 | 908 | 9.0E-29 |
| sp|B4UT09|PI4KB_OTOGA | Phosphatidylinositol 4-kinase beta OS=Otolemur garnettii GN=PI4KB PE=3 SV=1 | 663 | 908 | 9.0E-29 |
| sp|B3EX61|PI4KB_SORAR | Phosphatidylinositol 4-kinase beta OS=Sorex araneus GN=PI4KB PE=3 SV=1 | 663 | 908 | 9.0E-29 |
| sp|Q6GN16|PI4KB_XENLA | Phosphatidylinositol 4-kinase beta OS=Xenopus laevis GN=pi4kb PE=2 SV=1 | 663 | 908 | 4.0E-28 |
| sp|O08662|PI4KA_RAT | Phosphatidylinositol 4-kinase alpha OS=Rattus norvegicus GN=Pi4ka PE=1 SV=1 | 428 | 899 | 5.0E-28 |
| sp|O02810|PI4KB_BOVIN | Phosphatidylinositol 4-kinase beta OS=Bos taurus GN=PI4KB PE=1 SV=2 | 663 | 908 | 6.0E-28 |
| sp|Q5UR69|YL615_MIMIV | Putative phosphatidylinositol kinase L615 OS=Acanthamoeba polyphaga mimivirus GN=MIMI_L615 PE=3 SV=1 | 384 | 853 | 8.0E-28 |
| sp|P42356|PI4KA_HUMAN | Phosphatidylinositol 4-kinase alpha OS=Homo sapiens GN=PI4KA PE=1 SV=3 | 428 | 899 | 1.0E-27 |
| sp|O02811|PI4KA_BOVIN | Phosphatidylinositol 4-kinase alpha OS=Bos taurus GN=PI4KA PE=2 SV=1 | 428 | 899 | 3.0E-27 |
| sp|Q9USR3|STT4_SCHPO | Phosphatidylinositol 4-kinase stt4 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=stt4 PE=3 SV=1 | 458 | 896 | 3.0E-27 |
| sp|P37297|STT4_YEAST | Phosphatidylinositol 4-kinase STT4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=STT4 PE=1 SV=1 | 414 | 895 | 9.0E-27 |
| sp|Q9FMJ0|P4KB1_ARATH | Phosphatidylinositol 4-kinase beta 1 OS=Arabidopsis thaliana GN=PI4KB1 PE=1 SV=1 | 663 | 887 | 2.0E-26 |
| sp|Q0WPX9|P4KB2_ARATH | Phosphatidylinositol 4-kinase beta 2 OS=Arabidopsis thaliana GN=PI4KB2 PE=2 SV=1 | 663 | 887 | 2.0E-25 |
| sp|P39104|PIK1_YEAST | Phosphatidylinositol 4-kinase PIK1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PIK1 PE=1 SV=1 | 663 | 917 | 2.0E-25 |
| sp|Q8SR56|VPS34_ENCCU | Probable phosphatidylinositol 3-kinase VPS34 homolog OS=Encephalitozoon cuniculi (strain GB-M1) GN=VPS34 PE=3 SV=2 | 625 | 918 | 4.0E-23 |
| sp|Q9C680|P4KA2_ARATH | Phosphatidylinositol 4-kinase alpha 2 OS=Arabidopsis thaliana GN=PI4KA2 PE=1 SV=1 | 621 | 894 | 5.0E-21 |
| sp|Q9UW20|PIK1_CANAL | Phosphatidylinositol 4-kinase PIK1alpha OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=PIKALPHA PE=3 SV=1 | 663 | 855 | 3.0E-20 |
| sp|Q9UW24|PIK1A_CANAL | Phosphatidylinositol 4-kinase PIK1a OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=PIKA PE=3 SV=1 | 663 | 855 | 2.0E-19 |
| sp|A4QPH2|PI4P2_HUMAN | Putative phosphatidylinositol 4-kinase alpha-like protein P2 OS=Homo sapiens GN=PI4KAP2 PE=5 SV=3 | 664 | 899 | 2.0E-19 |
| sp|Q54ER4|ATR1_DICDI | Probable serine/threonine-protein kinase atr1 OS=Dictyostelium discoideum GN=atr1 PE=3 SV=1 | 619 | 857 | 2.0E-11 |
| sp|Q59LR2|ATR_CANAL | Serine/threonine-protein kinase MEC1 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=MEC1 PE=3 SV=1 | 637 | 888 | 7.0E-10 |
| sp|Q10366|PIK1_SCHPO | Phosphatidylinositol 4-kinase pik1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=pik1 PE=1 SV=1 | 663 | 855 | 1.0E-08 |
| sp|Q75DB8|ATR_ASHGO | Serine/threonine-protein kinase MEC1 OS=Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) GN=MEC1 PE=3 SV=3 | 641 | 857 | 6.0E-07 |
| sp|Q6CT34|ATR_KLULA | Serine/threonine-protein kinase MEC1 OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=MEC1 PE=3 SV=1 | 632 | 825 | 4.0E-06 |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 46 | 0.45 |
Expression values
| Label | Description | Expression (RPKM) | Confidence interval (low) | Confidence interval (high) |
|---|---|---|---|---|
| SC16a | Pure fungal culture | 26.18 | 14.31 | 38.04 |
| CcL | In ants, during behavior modification | 28.31 | 15.24 | 41.38 |
| CcD | In ants, recently dead | 32.34 | 17.53 | 47.14 |
Differential expression
| Label1 | Label2 | Q-value | Significant difference |
|---|---|---|---|
| SC16a | CcL | 0.769539 | no |
| SC16a | CcD | 0.376852 | no |
| CcL | CcD | 0.600483 | no |
| 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 | >Ophio5|2692 MTDYGRMDPFSFAGSKDVDHPVSIRIMNLDGEEPPVKYSTLLDRPDLRHVGSNTSPFSDLYVTVQVWAGSKALTV PVQTAYKSFRSERKWNEWLELPITYKQLPVNARLAITIWDLSPTGGKHALDHSIPFGGTTLPMFDADNQVQKGRQ KCLVHRHRHADGTDNSQTPALLVPRKTPGSRAGKVPCLDKDAEELDRMEKLFKKHEMGEIQRVDWLDQMVFRSFE KRGLQAAKSSMKMLQRQRAVNGDGVEADDDDAQAEDHGRSSPSAFLLNVELPRFDFPVVFADHEYDPPPISSLQP LSASQGSISQRQPQVHFGPGINGLGESSDGFGTRLIKVYDPEVGQRDNPAEAKHRRLFRSSHRHGILDKDLKPNA KVRDELNLIMSYSPTHILSPEETDLVWKFRYHLTRDKRALTKFVKSVNWNDQSEAKQAIQVLGSWTEIDVDDALE LLGPSFDNPAVRSYAVDRLRKADDAELLLYLLQLVQALKYEHISTESDHDGAQDSSLASFLIQRAAANFMLGNYL YWYLMVECDDHSPEQGLDNRNIYRKVAYEFMTQLVRQPDGAENRKTLLRQAELVAIISKIAGEVKVSNESIAKKA DRVKAFLADAKNELVTLDPPLAMPLDPSIKIIGVAADQVTVFKSSLNPIKITFKTTTGSAYPIIFKLGDDLRQDQ LVIQIITLMDQLLRKENLDLKLSPYKILATSTTAGASQFVQSQSLSSIVGKFKTNPALAYLRHHNPDDRQPLGVR QETLDTYIKSCAGYCVITYILGVGDRHLDNLLLAPDGHFFHADFGFILGRDPKPFAPVMKLSKEMVECMGGVQSE HYQRFRQYCFLAYTALRKSSNLILNLFSLMVHANIPDIRLEPDKAVIKVRERFHLELSEEEAIVYFGNVIDGTLT AFAPVVIDKLHEWAQALRA |
| Coding | >Ophio5|2692 ATGACCGACTACGGGAGGATGGACCCCTTCTCCTTTGCGGGGTCCAAGGACGTGGACCATCCCGTCAGCATCCGC ATAATGAACCTGGACGGCGAAGAACCTCCTGTCAAGTACTCGACACTTCTCGACCGGCCTGACCTCCGACATGTC GGTTCAAATACAAGTCCTTTCTCCGATCTCTACGTCACCGTCCAAGTCTGGGCCGGCTCGAAAGCCCTTACTGTA CCTGTACAGACTGCTTACAAGTCGTTTCGATCGGAAAGAAAATGGAACGAGTGGCTCGAGCTTCCCATCACCTAC AAGCAGCTACCGGTCAACGCCCGCCTGGCTATCACAATCTGGGACTTGTCGCCGACCGGAGGCAAGCATGCGCTC GACCATTCCATTCCCTTTGGGGGCACCACCTTGCCCATGTTTGATGCAGACAACCAAGTGCAAAAGGGACGTCAG AAATGCCTCGTGCACAGGCACAGACATGCCGACGGAACCGACAACTCCCAGACGCCAGCCCTGCTCGTGCCGAGA AAGACGCCGGGGTCAAGGGCTGGCAAAGTGCCATGTCTCGACAAGGACGCCGAGGAACTCGATAGAATGGAGAAG CTCTTCAAGAAGCACGAGATGGGGGAGATACAGCGCGTCGACTGGCTGGATCAGATGGTCTTTCGCAGCTTCGAG AAACGTGGACTTCAGGCCGCCAAGTCCTCTATGAAGATGCTCCAGCGCCAGCGCGCTGTCAACGGCGACGGCGTG GAAGCGGACGACGACGACGCCCAAGCTGAAGACCATGGACGCTCCAGCCCGTCTGCCTTTCTTCTCAACGTCGAG CTACCGCGTTTCGACTTTCCCGTCGTCTTTGCAGACCACGAATACGACCCGCCGCCGATATCGTCCCTGCAGCCT CTCTCGGCCTCCCAAGGAAGCATCTCTCAGCGACAGCCCCAAGTTCACTTCGGCCCGGGCATCAACGGCTTAGGG GAAAGCTCCGACGGCTTCGGGACGCGACTCATCAAGGTCTACGACCCCGAGGTGGGTCAGAGGGACAACCCGGCT GAGGCCAAGCACAGAAGACTCTTCCGAAGCTCTCACCGACATGGCATTCTAGATAAAGACCTGAAGCCGAATGCA AAGGTCCGCGACGAACTGAACCTGATCATGTCGTACTCGCCTACGCACATACTATCGCCCGAGGAGACGGACCTG GTCTGGAAGTTTCGCTATCACCTTACTCGTGACAAGAGGGCGTTGACCAAGTTCGTAAAGTCGGTTAACTGGAAT GACCAGAGTGAAGCCAAGCAGGCGATACAGGTCCTCGGGAGCTGGACCGAGATCGACGTGGACGATGCCCTCGAG CTTCTCGGCCCTTCCTTTGACAACCCGGCCGTCCGGTCGTACGCCGTCGATAGGCTGCGCAAGGCCGACGACGCC GAACTGCTACTGTACTTGCTGCAGCTGGTTCAGGCACTCAAGTACGAGCACATCTCGACGGAGTCGGATCATGAC GGCGCGCAGGACTCGTCCCTGGCCAGCTTCCTGATCCAGCGGGCGGCCGCCAACTTCATGCTCGGCAACTATCTG TACTGGTACCTCATGGTGGAATGCGACGACCACAGCCCGGAGCAGGGCCTCGACAACCGCAACATCTACCGCAAG GTTGCGTACGAGTTCATGACGCAGCTTGTCCGGCAGCCGGACGGGGCGGAAAACAGGAAGACCCTACTGCGACAG GCCGAGCTGGTGGCCATCATTTCCAAGATAGCGGGCGAGGTTAAGGTGTCTAACGAGTCCATCGCCAAAAAGGCC GATCGCGTCAAGGCGTTCCTGGCAGATGCCAAGAACGAGCTGGTGACGTTGGATCCGCCGCTTGCGATGCCGTTG GATCCGTCCATCAAGATCATAGGCGTGGCGGCTGACCAGGTGACGGTCTTCAAGTCGTCGCTGAACCCCATCAAA ATCACCTTCAAGACGACGACGGGCAGCGCCTATCCCATCATCTTCAAGTTGGGCGACGACCTGCGACAGGACCAG CTGGTGATACAGATCATCACGCTCATGGACCAGCTGCTGCGCAAAGAGAACCTGGATCTGAAGCTATCGCCGTAC AAGATCCTTGCGACGAGCACGACGGCTGGTGCGTCTCAGTTTGTGCAGTCGCAGAGCCTGTCGAGCATCGTGGGC AAGTTCAAGACCAATCCGGCACTGGCCTACCTGCGTCACCACAACCCGGACGACAGGCAGCCGCTCGGGGTGCGG CAAGAGACGCTCGACACGTACATCAAGTCGTGTGCCGGCTACTGCGTCATCACCTACATCCTCGGCGTCGGCGAC CGTCACCTCGACAACCTGCTCCTCGCGCCGGACGGGCACTTCTTCCACGCCGACTTTGGCTTCATCCTCGGGCGC GATCCCAAGCCGTTTGCGCCGGTGATGAAGCTCTCCAAGGAGATGGTCGAGTGCATGGGCGGCGTCCAGTCGGAG CACTATCAGCGGTTCCGCCAGTACTGCTTCCTCGCCTACACGGCGCTGCGCAAGTCGTCCAACCTCATCCTCAAC CTCTTCAGCCTCATGGTACACGCCAACATTCCCGACATCCGCCTCGAGCCGGACAAGGCCGTCATCAAGGTCCGC GAGCGCTTCCACCTCGAACTTAGCGAGGAGGAGGCCATCGTCTACTTTGGTAACGTCATCGATGGCACCCTGACG GCCTTTGCGCCCGTCGTCATTGACAAGTTGCACGAGTGGGCGCAGGCGTTGCGGGCA |
| Transcript | >Ophio5|2692 ATGACCGACTACGGGAGGATGGACCCCTTCTCCTTTGCGGGGTCCAAGGACGTGGACCATCCCGTCAGCATCCGC ATAATGAACCTGGACGGCGAAGAACCTCCTGTCAAGTACTCGACACTTCTCGACCGGCCTGACCTCCGACATGTC GGTTCAAATACAAGTCCTTTCTCCGATCTCTACGTCACCGTCCAAGTCTGGGCCGGCTCGAAAGCCCTTACTGTA CCTGTACAGACTGCTTACAAGTCGTTTCGATCGGAAAGAAAATGGAACGAGTGGCTCGAGCTTCCCATCACCTAC AAGCAGCTACCGGTCAACGCCCGCCTGGCTATCACAATCTGGGACTTGTCGCCGACCGGAGGCAAGCATGCGCTC GACCATTCCATTCCCTTTGGGGGCACCACCTTGCCCATGTTTGATGCAGACAACCAAGTGCAAAAGGGACGTCAG AAATGCCTCGTGCACAGGCACAGACATGCCGACGGAACCGACAACTCCCAGACGCCAGCCCTGCTCGTGCCGAGA AAGACGCCGGGGTCAAGGGCTGGCAAAGTGCCATGTCTCGACAAGGACGCCGAGGAACTCGATAGAATGGAGAAG CTCTTCAAGAAGCACGAGATGGGGGAGATACAGCGCGTCGACTGGCTGGATCAGATGGTCTTTCGCAGCTTCGAG AAACGTGGACTTCAGGCCGCCAAGTCCTCTATGAAGATGCTCCAGCGCCAGCGCGCTGTCAACGGCGACGGCGTG GAAGCGGACGACGACGACGCCCAAGCTGAAGACCATGGACGCTCCAGCCCGTCTGCCTTTCTTCTCAACGTCGAG CTACCGCGTTTCGACTTTCCCGTCGTCTTTGCAGACCACGAATACGACCCGCCGCCGATATCGTCCCTGCAGCCT CTCTCGGCCTCCCAAGGAAGCATCTCTCAGCGACAGCCCCAAGTTCACTTCGGCCCGGGCATCAACGGCTTAGGG GAAAGCTCCGACGGCTTCGGGACGCGACTCATCAAGGTCTACGACCCCGAGGTGGGTCAGAGGGACAACCCGGCT GAGGCCAAGCACAGAAGACTCTTCCGAAGCTCTCACCGACATGGCATTCTAGATAAAGACCTGAAGCCGAATGCA AAGGTCCGCGACGAACTGAACCTGATCATGTCGTACTCGCCTACGCACATACTATCGCCCGAGGAGACGGACCTG GTCTGGAAGTTTCGCTATCACCTTACTCGTGACAAGAGGGCGTTGACCAAGTTCGTAAAGTCGGTTAACTGGAAT GACCAGAGTGAAGCCAAGCAGGCGATACAGGTCCTCGGGAGCTGGACCGAGATCGACGTGGACGATGCCCTCGAG CTTCTCGGCCCTTCCTTTGACAACCCGGCCGTCCGGTCGTACGCCGTCGATAGGCTGCGCAAGGCCGACGACGCC GAACTGCTACTGTACTTGCTGCAGCTGGTTCAGGCACTCAAGTACGAGCACATCTCGACGGAGTCGGATCATGAC GGCGCGCAGGACTCGTCCCTGGCCAGCTTCCTGATCCAGCGGGCGGCCGCCAACTTCATGCTCGGCAACTATCTG TACTGGTACCTCATGGTGGAATGCGACGACCACAGCCCGGAGCAGGGCCTCGACAACCGCAACATCTACCGCAAG GTTGCGTACGAGTTCATGACGCAGCTTGTCCGGCAGCCGGACGGGGCGGAAAACAGGAAGACCCTACTGCGACAG GCCGAGCTGGTGGCCATCATTTCCAAGATAGCGGGCGAGGTTAAGGTGTCTAACGAGTCCATCGCCAAAAAGGCC GATCGCGTCAAGGCGTTCCTGGCAGATGCCAAGAACGAGCTGGTGACGTTGGATCCGCCGCTTGCGATGCCGTTG GATCCGTCCATCAAGATCATAGGCGTGGCGGCTGACCAGGTGACGGTCTTCAAGTCGTCGCTGAACCCCATCAAA ATCACCTTCAAGACGACGACGGGCAGCGCCTATCCCATCATCTTCAAGTTGGGCGACGACCTGCGACAGGACCAG CTGGTGATACAGATCATCACGCTCATGGACCAGCTGCTGCGCAAAGAGAACCTGGATCTGAAGCTATCGCCGTAC AAGATCCTTGCGACGAGCACGACGGCTGGTGCGTCTCAGTTTGTGCAGTCGCAGAGCCTGTCGAGCATCGTGGGC AAGTTCAAGACCAATCCGGCACTGGCCTACCTGCGTCACCACAACCCGGACGACAGGCAGCCGCTCGGGGTGCGG CAAGAGACGCTCGACACGTACATCAAGTCGTGTGCCGGCTACTGCGTCATCACCTACATCCTCGGCGTCGGCGAC CGTCACCTCGACAACCTGCTCCTCGCGCCGGACGGGCACTTCTTCCACGCCGACTTTGGCTTCATCCTCGGGCGC GATCCCAAGCCGTTTGCGCCGGTGATGAAGCTCTCCAAGGAGATGGTCGAGTGCATGGGCGGCGTCCAGTCGGAG CACTATCAGCGGTTCCGCCAGTACTGCTTCCTCGCCTACACGGCGCTGCGCAAGTCGTCCAACCTCATCCTCAAC CTCTTCAGCCTCATGGTACACGCCAACATTCCCGACATCCGCCTCGAGCCGGACAAGGCCGTCATCAAGGTCCGC GAGCGCTTCCACCTCGAACTTAGCGAGGAGGAGGCCATCGTCTACTTTGGTAACGTCATCGATGGCACCCTGACG GCCTTTGCGCCCGTCGTCATTGACAAGTTGCACGAGTGGGCGCAGGCGTTGCGGGCATGA |
| Gene | >Ophio5|2692 ATGACCGACTACGGGAGGATGGACCCCTTCTCCTTTGCGGGGTCCAAGGACGTGGACCATCCCGTCAGCATCCGC ATGTGAGCCTCTTCCACCCGCCGTCTGCTTGCCCTACTAACGCTCTTCTGTCCGCAGAATGAACCTGGACGGCGA AGAACCTCCTGTCAAGTACTCGACACTTCTCGACCGGCCTGACCTCCGACATGTCGGTTCAAATACAAGGTGGGA GTTGTCCAGGTGCCGCCAGTAGACACGAGAGTTGATGAGCGCTGTGCAGTCCTTTCTCCGATCTCTACGTCACCG TCCAAGTCTGGGCCGGCTCGAAAGCCCTTACTGTACCTGTACAGACTGCTTACAAGTCGTTTCGATCGGAAAGAA AGTATGTCGACACGCCCGCCGTCCCAAGATGAGTCTGCGCATACTGATGCTTGCAAAAGATGGAACGAGTGGCTC GAGCTTCCCATCACCTACAAGCAGCTACCGGTCAACGCCCGCCTGGCTATCACAATCTGGGACTTGTCGCCGACC GGAGGCAAGCATGCGCTCGACCATTCCATTCCCTTTGGGGGCACCACCTTGCCCATGTTTGATGCAGACAACCAA GTGCAAAAGGGACGTCAGAAATGCCTCGTGCACAGGCACAGACATGCCGACGGAACCGACAACTCCCAGACGCCA GCCCTGCTCGTGCCGAGAAAGACGCCGGGGTCAAGGGCTGGCAAAGTGCCATGTCTCGACAAGGACGCCGAGGAA CTCGATAGAATGGAGAAGCTCTTCAAGAAGCACGAGATGGGGGAGATACAGCGCGTCGACTGGCTGGATCAGATG GTCTTTCGCAGCTTCGAGAAACGTGGACTTCAGGCCGCCAAGTCCTCTATGAAGATGCTCCAGCGCCAGCGCGCT GTCAACGGCGACGGCGTGGAAGCGGACGACGACGACGCCCAAGCTGAAGACCATGGACGCTCCAGCCCGTCTGCC TTTCTTCTCAACGTCGAGCTACCGCGTTTCGACTTTCCCGTCGTCTTTGCAGACCACGAATACGACCCGCCGCCG ATATCGTCCCTGCAGCCTCTCTCGGCCTCCCAAGGAAGCATCTCTCAGCGACAGCCCCAAGTTCACTTCGGCCCG GGCATCAACGGCTTAGGGGAAAGCTCCGACGGCTTCGGGACGCGACTCATCAAGGTCTACGACCCCGAGGTGGGT CAGAGGGACAACCCGGCTGAGGCCAAGCACAGAAGACTCTTCCGAAGCTCTCACCGACATGGCATTCTAGATAAA GACCTGAAGCCGAATGCAAAGGTCCGCGACGAACTGAACCTGATCATGTCGTACTCGCCTACGCACATACTATCG CCCGAGGAGACGGACCTGGTCTGGAAGTTTCGCTATCACCTTACTCGTGACAAGAGGGCGTTGACCAAGTTCGTA AAGTCGGTTAACTGGAATGACCAGAGTGAAGCCAAGCAGGCGATACAGGTCCTCGGGAGCTGGACCGAGATCGAC GTGGACGATGCCCTCGAGCTTCTCGGCCCTTCCTTTGACAACCCGGCCGTCCGGTCGTACGCCGTCGATAGGCTG CGCAAGGCCGACGACGCCGAACTGCTACTGTACTTGCTGCAGCTGGTTCAGGCACTCAAGTACGAGCACATCTCG ACGGAGTCGGATCATGACGGCGCGCAGGACTCGTCCCTGGCCAGCTTCCTGATCCAGCGGGCGGCCGCCAACTTC ATGCTCGGCAACTATCTGTACTGGTACCTCATGGTGGAATGCGACGACCACAGCCCGGAGCAGGGCCTCGACAAC CGCAACATCTACCGCAAGGTTGCGTACGAGTTCATGACGCAGCTTGTCCGGCAGCCGGACGGGGCGGAAAACAGG AAGACCCTACTGCGACAGGCCGAGCTGGTGGCCATCATTTCCAAGATAGCGGGCGAGGTTAAGGTGTCTAACGAG TCCATCGCCAAAAAGGCCGATCGCGTCAAGGCGTTCCTGGCAGATGCCAAGAACGAGCTGGTGACGTTGGATCCG CCGCTTGCGATGCCGTTGGATCCGTCCATCAAGATCATAGGCGTGGCGGCTGACCAGGTGACGGTCTTCAAGTCG TCGCTGAACCCCATCAAAATCACCTTCAAGACGACGACGGGCAGCGCCTATCCCATCATCTTCAAGTTGGGCGAC GACCTGCGACAGGACCAGCTGGTGATACAGATCATCACGCTCATGGACCAGCTGCTGCGCAAAGAGAACCTGGAT CTGAAGCTATCGCCGTACAAGATCCTTGCGACGAGCACGACGGCTGGTGCGTCTCAGTTTGTGCAGTCGCAGAGC CTGTCGAGCATCGTGGGCAAGTTCAAGACCAATCCGGCACTGGCCTACCTGCGTCACCACAACCCGGACGACAGG CAGCCGCTCGGGGTGCGGCAAGAGACGCTCGACACGTACATCAAGTCGTGTGCCGGCTACTGCGTCATCACCTAC ATCCTCGGCGTCGGCGACCGTCACCTCGACAACCTGCTCCTCGCGCCGGACGGGCACTTCTTCCACGCCGACTTT GGCTTCATCCTCGGGCGCGATCCCAAGCCGTTTGCGCCGGTGATGAAGCTCTCCAAGGAGATGGTCGAGTGCATG GGCGGCGTCCAGTCGGAGCACTATCAGCGGTTCCGCCAGTACTGCTTCCTCGCCTACACGGCGCTGCGCAAGTCG TCCAACCTCATCCTCAACCTCTTCAGCCTCATGGTACACGCCAACATTCCCGACATCCGCCTCGAGCCGGACAAG GCCGTCATCAAGGTCCGCGAGCGCTTCCACCTCGAACTTAGCGAGGAGGAGGCCATCGTCTACTTTGGTAACGTC ATCGATGGCACCCTGACGGCCTTTGCGCCCGTCGTCATTGACAAGTTGCACGAGTGGGCGCAGGCGTTGCGGGCA TGA |