© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Ophio5|8439 |
| Gene name | |
| Location | scaffold_94:25917..29125 |
| Strand | - |
| Gene length (bp) | 3208 |
| Transcript length (bp) | 2970 |
| Coding sequence length (bp) | 2967 |
| Protein length (aa) | 989 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00454 | PI3_PI4_kinase | Phosphatidylinositol 3- and 4-kinase | 2.3E-31 | 715 | 928 |
| PF11522 | Pik1 | Yeast phosphatidylinositol-4-OH kinase Pik1 | 6.5E-19 | 109 | 155 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q10366|PIK1_SCHPO | Phosphatidylinositol 4-kinase pik1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=pik1 PE=1 SV=1 | 4 | 989 | 0.0E+00 |
| sp|Q9UW20|PIK1_CANAL | Phosphatidylinositol 4-kinase PIK1alpha OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=PIKALPHA PE=3 SV=1 | 313 | 989 | 6.0E-150 |
| sp|Q9UW24|PIK1A_CANAL | Phosphatidylinositol 4-kinase PIK1a OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=PIKA PE=3 SV=1 | 20 | 989 | 5.0E-147 |
| sp|P39104|PIK1_YEAST | Phosphatidylinositol 4-kinase PIK1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PIK1 PE=1 SV=1 | 571 | 989 | 9.0E-121 |
| sp|B3EX61|PI4KB_SORAR | Phosphatidylinositol 4-kinase beta OS=Sorex araneus GN=PI4KB PE=3 SV=1 | 663 | 988 | 6.0E-74 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q10366|PIK1_SCHPO | Phosphatidylinositol 4-kinase pik1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=pik1 PE=1 SV=1 | 4 | 989 | 0.0E+00 |
| sp|Q9UW20|PIK1_CANAL | Phosphatidylinositol 4-kinase PIK1alpha OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=PIKALPHA PE=3 SV=1 | 313 | 989 | 6.0E-150 |
| sp|Q9UW24|PIK1A_CANAL | Phosphatidylinositol 4-kinase PIK1a OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=PIKA PE=3 SV=1 | 20 | 989 | 5.0E-147 |
| sp|P39104|PIK1_YEAST | Phosphatidylinositol 4-kinase PIK1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PIK1 PE=1 SV=1 | 571 | 989 | 9.0E-121 |
| sp|B3EX61|PI4KB_SORAR | Phosphatidylinositol 4-kinase beta OS=Sorex araneus GN=PI4KB PE=3 SV=1 | 663 | 988 | 6.0E-74 |
| sp|O08561|PI4KB_RAT | Phosphatidylinositol 4-kinase beta OS=Rattus norvegicus GN=Pi4kb PE=1 SV=1 | 663 | 988 | 2.0E-73 |
| sp|Q8BKC8|PI4KB_MOUSE | Phosphatidylinositol 4-kinase beta OS=Mus musculus GN=Pi4kb PE=1 SV=2 | 663 | 988 | 3.0E-73 |
| sp|P54677|PI4K_DICDI | Phosphatidylinositol 4-kinase OS=Dictyostelium discoideum GN=pikD PE=3 SV=3 | 680 | 989 | 3.0E-73 |
| sp|Q49GP3|PI4KB_DANRE | Phosphatidylinositol 4-kinase beta OS=Danio rerio GN=pi4kb PE=2 SV=2 | 663 | 988 | 3.0E-73 |
| sp|A9X1A0|PI4KB_PAPAN | Phosphatidylinositol 4-kinase beta OS=Papio anubis GN=PI4KB PE=3 SV=2 | 663 | 988 | 3.0E-73 |
| sp|B4UT09|PI4KB_OTOGA | Phosphatidylinositol 4-kinase beta OS=Otolemur garnettii GN=PI4KB PE=3 SV=1 | 663 | 988 | 3.0E-73 |
| sp|Q9UBF8|PI4KB_HUMAN | Phosphatidylinositol 4-kinase beta OS=Homo sapiens GN=PI4KB PE=1 SV=1 | 663 | 988 | 4.0E-73 |
| sp|B1MTG7|PI4KB_CALMO | Phosphatidylinositol 4-kinase beta OS=Callicebus moloch GN=PI4KB PE=3 SV=1 | 663 | 988 | 4.0E-73 |
| sp|B0KWC1|PI4KB_CALJA | Phosphatidylinositol 4-kinase beta OS=Callithrix jacchus GN=PI4KB PE=3 SV=1 | 663 | 988 | 4.0E-73 |
| sp|B2KI64|PI4KB_RHIFE | Phosphatidylinositol 4-kinase beta OS=Rhinolophus ferrumequinum GN=PI4KB PE=3 SV=1 | 663 | 988 | 5.0E-73 |
| sp|A4IID4|PI4KB_XENTR | Phosphatidylinositol 4-kinase beta OS=Xenopus tropicalis GN=pi4kb PE=2 SV=1 | 663 | 988 | 5.0E-73 |
| sp|Q6GN16|PI4KB_XENLA | Phosphatidylinositol 4-kinase beta OS=Xenopus laevis GN=pi4kb PE=2 SV=1 | 663 | 988 | 7.0E-73 |
| sp|O02810|PI4KB_BOVIN | Phosphatidylinositol 4-kinase beta OS=Bos taurus GN=PI4KB PE=1 SV=2 | 663 | 988 | 3.0E-72 |
| sp|Q9FMJ0|P4KB1_ARATH | Phosphatidylinositol 4-kinase beta 1 OS=Arabidopsis thaliana GN=PI4KB1 PE=1 SV=1 | 672 | 988 | 1.0E-64 |
| sp|Q0WPX9|P4KB2_ARATH | Phosphatidylinositol 4-kinase beta 2 OS=Arabidopsis thaliana GN=PI4KB2 PE=2 SV=1 | 652 | 988 | 3.0E-63 |
| sp|P37297|STT4_YEAST | Phosphatidylinositol 4-kinase STT4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=STT4 PE=1 SV=1 | 709 | 988 | 4.0E-47 |
| sp|Q9USR3|STT4_SCHPO | Phosphatidylinositol 4-kinase stt4 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=stt4 PE=3 SV=1 | 635 | 988 | 4.0E-46 |
| sp|Q8SQY7|STT4_ENCCU | Probable phosphatidylinositol 4-kinase STT4 homolog OS=Encephalitozoon cuniculi (strain GB-M1) GN=STT4 PE=3 SV=2 | 717 | 988 | 5.0E-43 |
| sp|O08662|PI4KA_RAT | Phosphatidylinositol 4-kinase alpha OS=Rattus norvegicus GN=Pi4ka PE=1 SV=1 | 635 | 988 | 1.0E-38 |
| sp|P42356|PI4KA_HUMAN | Phosphatidylinositol 4-kinase alpha OS=Homo sapiens GN=PI4KA PE=1 SV=3 | 635 | 988 | 3.0E-38 |
| sp|O02811|PI4KA_BOVIN | Phosphatidylinositol 4-kinase alpha OS=Bos taurus GN=PI4KA PE=2 SV=1 | 635 | 988 | 4.0E-38 |
| sp|Q9SXA1|P4KA1_ARATH | Phosphatidylinositol 4-kinase alpha 1 OS=Arabidopsis thaliana GN=PI4KA1 PE=1 SV=2 | 716 | 988 | 4.0E-36 |
| sp|P39104|PIK1_YEAST | Phosphatidylinositol 4-kinase PIK1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PIK1 PE=1 SV=1 | 251 | 451 | 2.0E-34 |
| sp|P54675|PI3K3_DICDI | Phosphatidylinositol 3-kinase 3 OS=Dictyostelium discoideum GN=pikC PE=2 SV=2 | 715 | 977 | 9.0E-34 |
| sp|A4QPH2|PI4P2_HUMAN | Putative phosphatidylinositol 4-kinase alpha-like protein P2 OS=Homo sapiens GN=PI4KAP2 PE=5 SV=3 | 727 | 988 | 3.0E-32 |
| sp|P39104|PIK1_YEAST | Phosphatidylinositol 4-kinase PIK1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PIK1 PE=1 SV=1 | 14 | 275 | 6.0E-32 |
| sp|Q9C680|P4KA2_ARATH | Phosphatidylinositol 4-kinase alpha 2 OS=Arabidopsis thaliana GN=PI4KA2 PE=1 SV=1 | 716 | 988 | 6.0E-30 |
| sp|P54674|PI3K2_DICDI | Phosphatidylinositol 3-kinase 2 OS=Dictyostelium discoideum GN=pikB PE=2 SV=2 | 715 | 963 | 7.0E-29 |
| sp|P54673|PI3K1_DICDI | Phosphatidylinositol 3-kinase 1 OS=Dictyostelium discoideum GN=pikA PE=2 SV=2 | 711 | 983 | 6.0E-28 |
| sp|Q9UW20|PIK1_CANAL | Phosphatidylinositol 4-kinase PIK1alpha OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=PIKALPHA PE=3 SV=1 | 20 | 175 | 2.0E-27 |
| sp|P54676|PI3K4_DICDI | Phosphatidylinositol 3-kinase VPS34-like OS=Dictyostelium discoideum GN=pikE PE=3 SV=2 | 697 | 957 | 2.0E-27 |
| sp|P48736|PK3CG_HUMAN | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform OS=Homo sapiens GN=PIK3CG PE=1 SV=3 | 715 | 924 | 3.0E-26 |
| sp|Q9JHG7|PK3CG_MOUSE | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform OS=Mus musculus GN=Pik3cg PE=1 SV=2 | 715 | 924 | 7.0E-26 |
| sp|P42337|PK3CA_MOUSE | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform OS=Mus musculus GN=Pik3ca PE=1 SV=2 | 716 | 977 | 1.0E-25 |
| sp|P42336|PK3CA_HUMAN | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform OS=Homo sapiens GN=PIK3CA PE=1 SV=2 | 716 | 977 | 1.0E-25 |
| sp|P32871|PK3CA_BOVIN | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform OS=Bos taurus GN=PIK3CA PE=1 SV=1 | 716 | 977 | 1.0E-25 |
| sp|Q61194|P3C2A_MOUSE | Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha OS=Mus musculus GN=Pik3c2a PE=1 SV=2 | 715 | 988 | 4.0E-25 |
| sp|O02697|PK3CG_PIG | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform OS=Sus scrofa GN=PIK3CG PE=1 SV=2 | 715 | 924 | 1.0E-24 |
| sp|O00443|P3C2A_HUMAN | Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha OS=Homo sapiens GN=PIK3C2A PE=1 SV=2 | 715 | 988 | 1.0E-24 |
| sp|P42347|PI3K1_SOYBN | Phosphatidylinositol 3-kinase, root isoform OS=Glycine max PE=2 SV=1 | 715 | 986 | 1.0E-24 |
| sp|Q5RAY1|P3C2A_PONAB | Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha OS=Pongo abelii GN=PIK3C2A PE=2 SV=1 | 715 | 988 | 3.0E-24 |
| sp|P42348|PI3K2_SOYBN | Phosphatidylinositol 3-kinase, nodule isoform OS=Glycine max PE=2 SV=1 | 715 | 986 | 4.0E-24 |
| sp|O70167|P3C2G_MOUSE | Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit gamma OS=Mus musculus GN=Pik3c2g PE=2 SV=1 | 715 | 924 | 5.0E-24 |
| sp|O00750|P3C2B_HUMAN | Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit beta OS=Homo sapiens GN=PIK3C2B PE=1 SV=2 | 715 | 912 | 8.0E-24 |
| sp|O75747|P3C2G_HUMAN | Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit gamma OS=Homo sapiens GN=PIK3C2G PE=1 SV=3 | 715 | 914 | 1.0E-23 |
| sp|P42339|PI3K_ARATH | Phosphatidylinositol 3-kinase VPS34 OS=Arabidopsis thaliana GN=At1g60490 PE=2 SV=2 | 715 | 986 | 1.0E-23 |
| sp|Q8BTI9|PK3CB_MOUSE | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform OS=Mus musculus GN=Pik3cb PE=1 SV=2 | 713 | 924 | 2.0E-23 |
| sp|Q9Z1L0|PK3CB_RAT | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform OS=Rattus norvegicus GN=Pik3cb PE=2 SV=1 | 713 | 924 | 2.0E-23 |
| sp|O70173|P3C2G_RAT | Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit gamma OS=Rattus norvegicus GN=Pik3c2g PE=2 SV=1 | 715 | 914 | 5.0E-23 |
| sp|P22543|VPS34_YEAST | Phosphatidylinositol 3-kinase VPS34 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=VPS34 PE=1 SV=1 | 717 | 957 | 3.0E-22 |
| sp|P50520|VPS34_SCHPO | Phosphatidylinositol 3-kinase vps34 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=vps34 PE=2 SV=2 | 717 | 979 | 5.0E-22 |
| sp|P42338|PK3CB_HUMAN | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoform OS=Homo sapiens GN=PIK3CB PE=1 SV=1 | 713 | 924 | 1.0E-21 |
| sp|Q6AZN6|PK3C3_XENLA | Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Xenopus laevis GN=pik3c3 PE=2 SV=1 | 717 | 983 | 2.0E-21 |
| sp|O35904|PK3CD_MOUSE | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform OS=Mus musculus GN=Pik3cd PE=1 SV=2 | 715 | 931 | 2.0E-21 |
| sp|O00329|PK3CD_HUMAN | Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit delta isoform OS=Homo sapiens GN=PIK3CD PE=1 SV=2 | 715 | 931 | 2.0E-21 |
| sp|Q6PF93|PK3C3_MOUSE | Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Mus musculus GN=Pik3c3 PE=1 SV=1 | 717 | 963 | 6.0E-21 |
| sp|O88763|PK3C3_RAT | Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Rattus norvegicus GN=Pik3c3 PE=1 SV=1 | 717 | 963 | 1.0E-19 |
| sp|Q8NEB9|PK3C3_HUMAN | Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Homo sapiens GN=PIK3C3 PE=1 SV=1 | 717 | 963 | 1.0E-19 |
| sp|Q5D891|PK3C3_PIG | Phosphatidylinositol 3-kinase catalytic subunit type 3 OS=Sus scrofa GN=PIK3C3 PE=2 SV=1 | 717 | 963 | 1.0E-19 |
| sp|Q94125|AGE1_CAEEL | Phosphatidylinositol 3-kinase age-1 OS=Caenorhabditis elegans GN=age-1 PE=1 SV=6 | 714 | 924 | 8.0E-18 |
| sp|P0C5E7|AGE1_CAEBR | Phosphatidylinositol 3-kinase age-1 OS=Caenorhabditis briggsae GN=age-1 PE=3 SV=1 | 714 | 910 | 1.0E-17 |
| sp|Q92213|VPS34_CANAX | Phosphatidylinositol 3-kinase VPS34 OS=Candida albicans GN=VPS34 PE=3 SV=1 | 694 | 957 | 2.0E-16 |
| sp|Q6FRZ9|ATM_CANGA | Serine/threonine-protein kinase TEL1 OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=TEL1 PE=3 SV=1 | 717 | 938 | 4.0E-13 |
| sp|P38110|ATM_YEAST | Serine/threonine-protein kinase TEL1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=TEL1 PE=1 SV=3 | 724 | 927 | 7.0E-13 |
| sp|Q5UR69|YL615_MIMIV | Putative phosphatidylinositol kinase L615 OS=Acanthamoeba polyphaga mimivirus GN=MIMI_L615 PE=3 SV=1 | 764 | 986 | 4.0E-12 |
| sp|Q6CAD2|ATM_YARLI | Serine/threonine-protein kinase TEL1 OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=TEL1 PE=3 SV=1 | 751 | 927 | 6.0E-12 |
| sp|Q4IB89|ATM_GIBZE | Serine/threonine-protein kinase TEL1 OS=Gibberella zeae (strain PH-1 / ATCC MYA-4620 / FGSC 9075 / NRRL 31084) GN=TEL1 PE=3 SV=1 | 718 | 927 | 3.0E-11 |
| sp|Q7RZT9|ATM_NEUCR | Serine/threonine-protein kinase tel1 OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=mus-21 PE=3 SV=2 | 718 | 927 | 1.0E-10 |
| sp|Q54ER4|ATR1_DICDI | Probable serine/threonine-protein kinase atr1 OS=Dictyostelium discoideum GN=atr1 PE=3 SV=1 | 800 | 962 | 2.0E-10 |
| sp|Q2U639|ATM_ASPOR | Serine/threonine-protein kinase tel1 OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=tel1 PE=3 SV=1 | 724 | 938 | 2.0E-10 |
| sp|Q4WVM7|ATM_ASPFU | Serine/threonine-protein kinase tel1 OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=tel1 PE=3 SV=2 | 724 | 927 | 4.0E-10 |
| sp|Q9DE14|ATR_XENLA | Serine/threonine-protein kinase atr OS=Xenopus laevis GN=atr PE=1 SV=2 | 800 | 921 | 4.0E-10 |
| sp|Q9JKK8|ATR_MOUSE | Serine/threonine-protein kinase ATR OS=Mus musculus GN=Atr PE=1 SV=2 | 799 | 927 | 7.0E-10 |
| sp|Q22258|ATR_CAEEL | Serine/threonine-protein kinase ATR OS=Caenorhabditis elegans GN=atl-1 PE=2 SV=2 | 811 | 922 | 9.0E-10 |
| sp|Q13315|ATM_HUMAN | Serine-protein kinase ATM OS=Homo sapiens GN=ATM PE=1 SV=4 | 822 | 927 | 9.0E-10 |
| sp|Q9VK45|TOR_DROME | Target of rapamycin OS=Drosophila melanogaster GN=Tor PE=1 SV=1 | 718 | 918 | 9.0E-10 |
| sp|Q13535|ATR_HUMAN | Serine/threonine-protein kinase ATR OS=Homo sapiens GN=ATR PE=1 SV=3 | 800 | 927 | 9.0E-10 |
| sp|Q6CP76|ATM_KLULA | Serine/threonine-protein kinase TEL1 OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=TEL1 PE=3 SV=1 | 724 | 927 | 1.0E-09 |
| sp|Q5BHE2|ATM_EMENI | Serine/threonine-protein kinase tel1 OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=tel1 PE=3 SV=1 | 724 | 938 | 1.0E-09 |
| sp|Q9M3G7|ATM_ARATH | Serine/threonine-protein kinase ATM OS=Arabidopsis thaliana GN=ATM PE=2 SV=1 | 804 | 927 | 2.0E-09 |
| sp|Q62388|ATM_MOUSE | Serine-protein kinase ATM OS=Mus musculus GN=Atm PE=1 SV=2 | 822 | 927 | 3.0E-09 |
| sp|Q6PQD5|ATM_PIG | Serine-protein kinase ATM OS=Sus scrofa GN=ATM PE=3 SV=2 | 822 | 927 | 3.0E-09 |
| sp|Q5EAK6|ATM_DROME | Serine/threonine-protein kinase ATM OS=Drosophila melanogaster GN=tefu PE=2 SV=1 | 822 | 972 | 3.0E-09 |
| sp|O74630|ATM_SCHPO | Serine/threonine-protein kinase tel1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=tel1 PE=1 SV=1 | 792 | 950 | 4.0E-09 |
| sp|P0CP60|ATM_CRYNJ | Serine/threonine-protein kinase TEL1 OS=Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) GN=TEL1 PE=3 SV=1 | 823 | 927 | 7.0E-09 |
| sp|P0CP61|ATM_CRYNB | Serine/threonine-protein kinase TEL1 OS=Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) GN=TEL1 PE=3 SV=1 | 823 | 927 | 7.0E-09 |
| sp|Q9FR53|TOR_ARATH | Serine/threonine-protein kinase TOR OS=Arabidopsis thaliana GN=TOR PE=1 SV=1 | 697 | 924 | 1.0E-08 |
| sp|P54677|PI4K_DICDI | Phosphatidylinositol 4-kinase OS=Dictyostelium discoideum GN=pikD PE=3 SV=3 | 20 | 122 | 3.0E-08 |
| sp|Q9FMJ0|P4KB1_ARATH | Phosphatidylinositol 4-kinase beta 1 OS=Arabidopsis thaliana GN=PI4KB1 PE=1 SV=1 | 6 | 104 | 3.0E-08 |
| sp|Q0WPX9|P4KB2_ARATH | Phosphatidylinositol 4-kinase beta 2 OS=Arabidopsis thaliana GN=PI4KB2 PE=2 SV=1 | 6 | 104 | 3.0E-08 |
| sp|Q0DJS1|TOR_ORYSJ | Serine/threonine-protein kinase TOR OS=Oryza sativa subsp. japonica GN=TOR PE=2 SV=3 | 697 | 927 | 5.0E-08 |
| sp|Q02099|RAD3_SCHPO | Protein kinase rad3 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=rad3 PE=1 SV=2 | 802 | 927 | 6.0E-08 |
| sp|Q9FKS4|ATR_ARATH | Serine/threonine-protein kinase ATR OS=Arabidopsis thaliana GN=ATR PE=2 SV=2 | 804 | 927 | 9.0E-08 |
| sp|P54677|PI4K_DICDI | Phosphatidylinositol 4-kinase OS=Dictyostelium discoideum GN=pikD PE=3 SV=3 | 320 | 420 | 1.0E-07 |
| sp|Q8BKX6|SMG1_MOUSE | Serine/threonine-protein kinase SMG1 OS=Mus musculus GN=Smg1 PE=1 SV=3 | 822 | 927 | 1.0E-07 |
| sp|Q96Q15|SMG1_HUMAN | Serine/threonine-protein kinase SMG1 OS=Homo sapiens GN=SMG1 PE=1 SV=3 | 822 | 927 | 1.0E-07 |
| sp|Q6FX42|ATR_CANGA | Serine/threonine-protein kinase MEC1 OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=MEC1 PE=3 SV=1 | 799 | 930 | 1.0E-07 |
| sp|Q59LR2|ATR_CANAL | Serine/threonine-protein kinase MEC1 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=MEC1 PE=3 SV=1 | 799 | 927 | 2.0E-07 |
| sp|Q9JLN9|MTOR_MOUSE | Serine/threonine-protein kinase mTOR OS=Mus musculus GN=Mtor PE=1 SV=2 | 811 | 918 | 2.0E-07 |
| sp|P42346|MTOR_RAT | Serine/threonine-protein kinase mTOR OS=Rattus norvegicus GN=Mtor PE=1 SV=1 | 811 | 918 | 2.0E-07 |
| sp|P42345|MTOR_HUMAN | Serine/threonine-protein kinase mTOR OS=Homo sapiens GN=MTOR PE=1 SV=1 | 811 | 918 | 3.0E-07 |
| sp|Q49GP3|PI4KB_DANRE | Phosphatidylinositol 4-kinase beta OS=Danio rerio GN=pi4kb PE=2 SV=2 | 327 | 417 | 2.0E-06 |
| sp|P38111|ATR_YEAST | Serine/threonine-protein kinase MEC1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=MEC1 PE=1 SV=1 | 751 | 930 | 2.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0016773 | phosphotransferase activity, alcohol group as acceptor | Yes |
| GO:0016772 | transferase activity, transferring phosphorus-containing groups | No |
| GO:0003824 | catalytic activity | No |
| GO:0016740 | transferase activity | No |
| GO:0003674 | molecular_function | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 11 | 0.45 |
Expression values
| Label | Description | Expression (RPKM) | Confidence interval (low) | Confidence interval (high) |
|---|---|---|---|---|
| SC16a | Pure fungal culture | 71.49 | 37.17 | 105.81 |
| CcL | In ants, during behavior modification | 85.09 | 40.57 | 129.61 |
| CcD | In ants, recently dead | 71.56 | 37.18 | 105.95 |
Differential expression
| Label1 | Label2 | Q-value | Significant difference |
|---|---|---|---|
| SC16a | CcL | 0.529134 | no |
| SC16a | CcD | 0.996651 | no |
| CcL | CcD | 0.532993 | 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|8439 MSWDLLQRFLESDVFNSNPFLSVSYLSRYADHVGIHHVLCNKLRQFPYEDIEFFLPQLCHLIISVDNESMALEEF LLDLCEESATAALLTFWLFQTYLHDLSPNPQSGPFQTCRRVYNKVQHIVFGLADTARHGKIKENVLPVTVLSSFV LASVALPMIPRWAGPLAVAQARKPQPATDVAPEPSSSPKPIRAQTVSVSTSRSRRAKELRKSTAPDAAGPSDPRP HSSRSLSQAATSTAKRAKTPIGTKRPSALNLESLDARASSASLPLPSPKPTTRPATPVSADMPSADGMLRRHSHH AKASRTADDLTLVQKTRLLRSHYFRSQTQFLTALEGISNRLVIVPKPARMSALRAELALVSRDLPAEVDIPVICP PTLVNGSPGKSRHHRIVRLNPAEATVLNSAEKVPYLLMVEVLRDDFTFDPGTVDNRRLLATLLDGGGRSRRLFDL SSETPRLSPTVARAPEPIVDSVFEPTSGDLGSSPLLKAEDEAPSRYGPPFRQPQAYTHTNQRLSSGATTQTSSTM LEVVSPRTSGGASTSRSSSPSSRRKMTVTLPRNVAAAAPDQPDFSALATHMRTASQMLAQLDATSGKRPKHEVAA IRAKIIASMQSLEEQSFEMEDQGPTFDAIIAKTSGGGGPSDPDLDDDDGDGPLDTAPNASAGRERMENDIKTGGV QRRGDRDDPSAAVFGEAWEAKKERIRKSSPYGWMKNWDLVSVIVKTGADLRQEAFACQLIDVCHRIWVDADVDVW VKLMRILVTGESSGLIETITNGVSLHSLKRSLTLAAADSGQAARQRIATLRDHFLKAFGQPESEPYRAGVDAFKR SLAAYSIISYILQLKDRHNGNVLIDSEGHIIHIDFGFMLSNSPGSVGFEAAPFKLTHEYVDVLGGIGSPDFEDYK RLCKQAFQALRRSADNIIDLVAMMGRDSSMPCFSVGVAHATNSLRQRFQLHLSAVEAEQFVETDLVGKSYGSYYT RLYDTFQYRTQGIY |
| Coding | >Ophio5|8439 ATGTCGTGGGACCTATTGCAAAGATTTCTCGAGTCCGACGTCTTCAATTCGAATCCCTTTCTCTCGGTCTCGTAT CTCTCCCGGTACGCCGACCATGTCGGAATCCACCATGTCCTGTGCAACAAGCTGCGCCAATTTCCCTACGAAGAC ATCGAGTTCTTTCTGCCCCAGCTGTGCCACCTCATAATCAGCGTCGACAATGAGTCCATGGCTCTCGAGGAGTTT TTGTTGGATCTTTGCGAGGAGTCGGCCACGGCCGCCCTGCTGACCTTCTGGCTCTTCCAGACTTACCTACACGAC CTCTCGCCGAATCCCCAGTCGGGCCCCTTTCAGACTTGCAGGCGCGTCTACAACAAAGTCCAGCACATCGTCTTC GGCCTGGCCGACACCGCCCGACACGGCAAGATCAAGGAGAATGTCCTTCCGGTCACCGTCCTCTCCAGCTTCGTC CTCGCTAGCGTCGCGTTGCCCATGATACCGAGATGGGCCGGACCTCTTGCCGTCGCCCAGGCGCGAAAGCCGCAG CCTGCCACCGACGTGGCCCCAGAGCCCAGCTCCAGTCCCAAGCCCATTCGGGCGCAGACCGTGTCAGTTTCCACC TCGAGGTCGAGACGCGCCAAGGAACTGAGGAAGTCGACCGCTCCCGACGCCGCCGGCCCATCGGACCCGCGCCCG CACTCGTCCCGGAGCCTCTCGCAGGCGGCCACGTCGACGGCCAAGAGGGCCAAGACGCCAATCGGCACCAAGCGG CCGTCTGCGCTCAATCTCGAGTCTCTCGACGCCCGGGCCAGCTCCGCATCGCTACCCTTGCCGTCGCCCAAGCCG ACGACGAGACCGGCCACTCCCGTCTCCGCCGACATGCCGTCGGCCGACGGCATGCTCCGGCGGCACTCGCATCAC GCCAAGGCCTCACGGACCGCCGATGACCTGACGCTGGTCCAGAAGACGCGCCTACTGAGGTCCCACTATTTCAGG TCGCAGACGCAGTTTCTGACTGCTCTCGAGGGCATCTCCAACCGGCTTGTCATCGTGCCCAAGCCCGCCCGGATG AGTGCGCTTCGAGCCGAGCTGGCCCTCGTCTCACGAGACCTGCCGGCCGAGGTCGACATCCCCGTCATCTGCCCT CCGACGCTGGTCAACGGGTCACCCGGCAAGAGCCGACACCACAGGATCGTGCGGCTGAACCCGGCCGAGGCCACG GTACTCAACAGCGCCGAAAAGGTGCCCTACCTCTTGATGGTCGAGGTTCTCCGAGACGACTTCACCTTCGACCCA GGTACCGTCGACAACCGACGACTCCTCGCCACCTTGCTCGACGGCGGCGGGAGATCTCGGCGGCTCTTCGACCTA TCGTCGGAGACGCCCAGGTTATCTCCGACGGTTGCGCGGGCCCCCGAGCCCATCGTCGACAGCGTCTTCGAGCCG ACCTCGGGTGACCTGGGCAGCTCGCCTTTGCTCAAGGCCGAGGATGAGGCGCCTAGCAGATACGGGCCCCCTTTC CGGCAGCCTCAGGCTTACACGCATACCAACCAGCGCCTGTCCAGCGGGGCGACGACGCAGACGTCGTCGACGATG CTCGAGGTCGTCAGTCCGCGCACGTCGGGTGGGGCCTCGACGTCTAGGTCGAGCAGCCCCAGCTCCCGGCGCAAA ATGACGGTGACGCTACCCCGGAATGTGGCCGCCGCGGCCCCCGACCAGCCCGACTTCTCGGCCCTGGCGACGCAC ATGAGGACGGCCTCGCAGATGCTAGCGCAGCTCGACGCGACGAGCGGCAAGCGACCTAAGCACGAGGTGGCGGCC ATCAGAGCCAAAATCATCGCGAGCATGCAGAGCCTGGAAGAGCAGAGCTTCGAGATGGAGGACCAGGGCCCAACA TTTGACGCCATCATCGCCAAGACGAGCGGGGGCGGTGGTCCCAGCGACCCAGACCTCGACGACGACGACGGCGAC GGGCCGCTGGACACGGCCCCAAACGCCAGCGCGGGCAGGGAGAGGATGGAGAACGACATCAAGACGGGTGGCGTC CAGCGGCGGGGTGACCGCGACGATCCCAGCGCGGCCGTCTTTGGAGAGGCTTGGGAGGCCAAGAAGGAGCGGATT CGCAAGTCGTCCCCCTACGGCTGGATGAAGAATTGGGACCTGGTCAGCGTCATTGTCAAGACGGGAGCCGACCTG CGGCAGGAGGCCTTTGCTTGTCAGCTCATCGACGTCTGCCACCGGATCTGGGTCGACGCCGACGTCGATGTCTGG GTCAAGCTGATGCGCATCCTGGTGACGGGCGAGTCGTCGGGCCTAATCGAGACCATCACCAACGGCGTCTCGCTC CACTCGCTCAAGCGGAGCCTGACGCTGGCGGCGGCCGACTCGGGCCAGGCGGCGCGACAGCGCATCGCCACGCTG CGCGACCATTTCCTCAAGGCCTTTGGCCAGCCGGAGAGTGAGCCGTACAGAGCCGGCGTCGACGCATTCAAGCGC TCGCTAGCGGCCTACAGCATCATCTCGTACATCCTGCAGCTCAAGGACCGGCACAACGGCAACGTGCTTATCGAC AGCGAGGGCCACATTATTCACATCGACTTTGGCTTTATGCTGTCCAATTCGCCCGGCTCCGTCGGGTTCGAGGCG GCGCCTTTCAAGCTCACGCACGAGTACGTCGACGTGCTGGGCGGCATCGGGTCCCCGGACTTTGAGGACTACAAG AGGCTGTGCAAGCAGGCATTTCAAGCGCTGCGCCGATCGGCGGACAACATCATTGATCTGGTCGCCATGATGGGC CGCGACTCCAGCATGCCGTGCTTCTCGGTGGGCGTAGCTCACGCGACGAACAGCCTCCGACAGCGTTTCCAGCTA CACCTCAGCGCCGTCGAGGCGGAGCAGTTTGTCGAGACGGATCTCGTGGGCAAGTCGTACGGGAGCTACTACACG CGACTGTATGACACGTTCCAGTATCGGACTCAGGGCATCTAC |
| Transcript | >Ophio5|8439 ATGTCGTGGGACCTATTGCAAAGATTTCTCGAGTCCGACGTCTTCAATTCGAATCCCTTTCTCTCGGTCTCGTAT CTCTCCCGGTACGCCGACCATGTCGGAATCCACCATGTCCTGTGCAACAAGCTGCGCCAATTTCCCTACGAAGAC ATCGAGTTCTTTCTGCCCCAGCTGTGCCACCTCATAATCAGCGTCGACAATGAGTCCATGGCTCTCGAGGAGTTT TTGTTGGATCTTTGCGAGGAGTCGGCCACGGCCGCCCTGCTGACCTTCTGGCTCTTCCAGACTTACCTACACGAC CTCTCGCCGAATCCCCAGTCGGGCCCCTTTCAGACTTGCAGGCGCGTCTACAACAAAGTCCAGCACATCGTCTTC GGCCTGGCCGACACCGCCCGACACGGCAAGATCAAGGAGAATGTCCTTCCGGTCACCGTCCTCTCCAGCTTCGTC CTCGCTAGCGTCGCGTTGCCCATGATACCGAGATGGGCCGGACCTCTTGCCGTCGCCCAGGCGCGAAAGCCGCAG CCTGCCACCGACGTGGCCCCAGAGCCCAGCTCCAGTCCCAAGCCCATTCGGGCGCAGACCGTGTCAGTTTCCACC TCGAGGTCGAGACGCGCCAAGGAACTGAGGAAGTCGACCGCTCCCGACGCCGCCGGCCCATCGGACCCGCGCCCG CACTCGTCCCGGAGCCTCTCGCAGGCGGCCACGTCGACGGCCAAGAGGGCCAAGACGCCAATCGGCACCAAGCGG CCGTCTGCGCTCAATCTCGAGTCTCTCGACGCCCGGGCCAGCTCCGCATCGCTACCCTTGCCGTCGCCCAAGCCG ACGACGAGACCGGCCACTCCCGTCTCCGCCGACATGCCGTCGGCCGACGGCATGCTCCGGCGGCACTCGCATCAC GCCAAGGCCTCACGGACCGCCGATGACCTGACGCTGGTCCAGAAGACGCGCCTACTGAGGTCCCACTATTTCAGG TCGCAGACGCAGTTTCTGACTGCTCTCGAGGGCATCTCCAACCGGCTTGTCATCGTGCCCAAGCCCGCCCGGATG AGTGCGCTTCGAGCCGAGCTGGCCCTCGTCTCACGAGACCTGCCGGCCGAGGTCGACATCCCCGTCATCTGCCCT CCGACGCTGGTCAACGGGTCACCCGGCAAGAGCCGACACCACAGGATCGTGCGGCTGAACCCGGCCGAGGCCACG GTACTCAACAGCGCCGAAAAGGTGCCCTACCTCTTGATGGTCGAGGTTCTCCGAGACGACTTCACCTTCGACCCA GGTACCGTCGACAACCGACGACTCCTCGCCACCTTGCTCGACGGCGGCGGGAGATCTCGGCGGCTCTTCGACCTA TCGTCGGAGACGCCCAGGTTATCTCCGACGGTTGCGCGGGCCCCCGAGCCCATCGTCGACAGCGTCTTCGAGCCG ACCTCGGGTGACCTGGGCAGCTCGCCTTTGCTCAAGGCCGAGGATGAGGCGCCTAGCAGATACGGGCCCCCTTTC CGGCAGCCTCAGGCTTACACGCATACCAACCAGCGCCTGTCCAGCGGGGCGACGACGCAGACGTCGTCGACGATG CTCGAGGTCGTCAGTCCGCGCACGTCGGGTGGGGCCTCGACGTCTAGGTCGAGCAGCCCCAGCTCCCGGCGCAAA ATGACGGTGACGCTACCCCGGAATGTGGCCGCCGCGGCCCCCGACCAGCCCGACTTCTCGGCCCTGGCGACGCAC ATGAGGACGGCCTCGCAGATGCTAGCGCAGCTCGACGCGACGAGCGGCAAGCGACCTAAGCACGAGGTGGCGGCC ATCAGAGCCAAAATCATCGCGAGCATGCAGAGCCTGGAAGAGCAGAGCTTCGAGATGGAGGACCAGGGCCCAACA TTTGACGCCATCATCGCCAAGACGAGCGGGGGCGGTGGTCCCAGCGACCCAGACCTCGACGACGACGACGGCGAC GGGCCGCTGGACACGGCCCCAAACGCCAGCGCGGGCAGGGAGAGGATGGAGAACGACATCAAGACGGGTGGCGTC CAGCGGCGGGGTGACCGCGACGATCCCAGCGCGGCCGTCTTTGGAGAGGCTTGGGAGGCCAAGAAGGAGCGGATT CGCAAGTCGTCCCCCTACGGCTGGATGAAGAATTGGGACCTGGTCAGCGTCATTGTCAAGACGGGAGCCGACCTG CGGCAGGAGGCCTTTGCTTGTCAGCTCATCGACGTCTGCCACCGGATCTGGGTCGACGCCGACGTCGATGTCTGG GTCAAGCTGATGCGCATCCTGGTGACGGGCGAGTCGTCGGGCCTAATCGAGACCATCACCAACGGCGTCTCGCTC CACTCGCTCAAGCGGAGCCTGACGCTGGCGGCGGCCGACTCGGGCCAGGCGGCGCGACAGCGCATCGCCACGCTG CGCGACCATTTCCTCAAGGCCTTTGGCCAGCCGGAGAGTGAGCCGTACAGAGCCGGCGTCGACGCATTCAAGCGC TCGCTAGCGGCCTACAGCATCATCTCGTACATCCTGCAGCTCAAGGACCGGCACAACGGCAACGTGCTTATCGAC AGCGAGGGCCACATTATTCACATCGACTTTGGCTTTATGCTGTCCAATTCGCCCGGCTCCGTCGGGTTCGAGGCG GCGCCTTTCAAGCTCACGCACGAGTACGTCGACGTGCTGGGCGGCATCGGGTCCCCGGACTTTGAGGACTACAAG AGGCTGTGCAAGCAGGCATTTCAAGCGCTGCGCCGATCGGCGGACAACATCATTGATCTGGTCGCCATGATGGGC CGCGACTCCAGCATGCCGTGCTTCTCGGTGGGCGTAGCTCACGCGACGAACAGCCTCCGACAGCGTTTCCAGCTA CACCTCAGCGCCGTCGAGGCGGAGCAGTTTGTCGAGACGGATCTCGTGGGCAAGTCGTACGGGAGCTACTACACG CGACTGTATGACACGTTCCAGTATCGGACTCAGGGCATCTACTAG |
| Gene | >Ophio5|8439 ATGTCGTGGGACCTATTGCAAAGATTTCTCGAGTCCGACGTCTTCAATTCGAATCCCTTTCTCTCGGTCTCGTAT CTCTCGTACGTCCTGATTGCCCGCGCCGTTTCCCCCGCCTCCCCCCCCTCCCTCATCTCGTGTCCTCGCTGAAGG CTCGGCAGCCGGTACGCCGACCATGTCGGAATCCACCATGTCCTGTGCAACAAGCTGCGCCAATTTCCCTACGAA GACATCGAGTTCTTTCTGCCCCAGCTGTGCCACCTCATAATCAGCGTCGACAATGAGTCCATGGCTCTCGAGGAG TTTTTGTTGGATCTTTGCGAGGAGTCGGCCACGGCCGCCCTGCTGGTACGGCTTGCATCCCCCCCCCCCCCCTTT TAACAGCATTCACTGCTGACGGCGGCTACAGACCTTCTGGCTCTTCCAGACTTACCTACACGACCTCTCGCCGAA TCCCCAGTCGGGCCCCTTTCAGACTTGCAGGCGCGTCTACAACAAAGTCCAGCACATCGTCTTCGGCCTGGCCGA CACCGCCCGACACGGCAAGATCAAGGAGAATGTCCTTCCGGTCACCGTCCTCTCCAGCTTCGTCCTCGCTAGCGT CGCGTTGCCCATGATACCGAGATGGGCCGGACCTCTTGCCGTCGCCCAGGCGCGAAAGCCGCAGCCTGCCACCGA CGTGGCCCCAGAGCCCAGCTCCAGTCCCAAGCCCATTCGGGCGCAGACCGTGTCAGTTTCCACCTCGAGGTCGAG ACGCGCCAAGGAACTGAGGAAGTCGACCGCTCCCGACGCCGCCGGCCCATCGGACCCGCGCCCGCACTCGTCCCG GAGCCTCTCGCAGGCGGCCACGTCGACGGCCAAGAGGGCCAAGACGCCAATCGGCACCAAGCGGCCGTCTGCGCT CAATCTCGAGTCTCTCGACGCCCGGGCCAGCTCCGCATCGCTACCCTTGCCGTCGCCCAAGCCGACGACGAGACC GGCCACTCCCGTCTCCGCCGACATGCCGTCGGCCGACGGCATGCTCCGGCGGCACTCGCATCACGCCAAGGCCTC ACGGACCGCCGATGACCTGACGCTGGTCCAGAAGACGCGCCTACTGAGGTCCCACTATTTCAGGTCGCAGACGCA GTTTCTGACTGCTCTCGAGGGCATCTCCAACCGGCTTGTCATCGTGCCCAAGCCCGCCCGGATGAGTGCGCTTCG AGCCGAGCTGGCCCTCGTCTCACGAGACCTGCCGGCCGAGGTCGACATCCCCGTCATCTGCCCTCCGACGCTGGT CAACGGGTCACCCGGCAAGAGCCGACACCACAGGATCGTGCGGCTGAACCCGGCCGAGGCCACGGTACTCAACAG CGCCGAAAAGGTGCCCTACCTCTTGATGGTCGAGGTTCTCCGAGACGACTTCACCTTCGACCCAGGTACCGTCGA CAACCGACGACTCCTCGCCACCTTGCTCGACGGCGGCGGGAGATCTCGGCGGCTCTTCGACCTATCGTCGGAGAC GCCCAGGTTATCTCCGACGGTTGCGCGGGCCCCCGAGCCCATCGTCGACAGCGTCTTCGAGCCGACCTCGGGTGA CCTGGGCAGCTCGCCTTTGCTCAAGGCCGAGGATGAGGCGCCTAGCAGATACGGGCCCCCTTTCCGGCAGCCTCA GGCTTACACGCATACCAACCAGCGCCTGTCCAGCGGGGCGACGACGCAGACGTCGTCGACGATGCTCGAGGTCGT CAGTCCGCGCACGTCGGGTGGGGCCTCGACGTCTAGGTCGAGCAGCCCCAGCTCCCGGCGCAAAATGACGGTGAC GCTACCCCGGAATGTGGCCGCCGCGGCCCCCGACCAGCCCGACTTCTCGGCCCTGGCGACGCACATGAGGACGGC CTCGCAGATGCTAGCGCAGCTCGACGCGACGAGCGGCAAGCGACCTAAGCACGAGGTGGCGGCCATCAGAGCCAA AATCATCGCGAGCATGCAGAGCCTGGAAGAGCAGAGCTTCGAGATGGAGGACCAGGGCCCAACATTTGACGCCAT CATCGCCAAGACGAGCGGGGGCGGTGGTCCCAGCGACCCAGACCTCGACGACGACGACGGCGACGGGCCGCTGGA CACGGCCCCAAACGCCAGCGCGGGCAGGGAGAGGATGGAGAACGACATCAAGACGGGTGGCGTCCAGCGGCGGGG TGACCGCGACGATCCCAGCGCGGCCGTCTTTGGAGAGGCTTGGGAGGCCAAGAAGGAGCGGATTCGCAAGTCGTC CCCCTACGGCTGGATGAAGAATTGGGACCTGGTCAGCGTCATTGTCAAGACGGGAGCCGACCTGCGGCAGGAGGC CTTTGCTTGTCAGCTCATCGACGTCTGCCACCGGATCTGGGTCGACGCCGACGTCGATGTCTGGGTCAAGCTGAT GCGCATCCTGGTGACGGGCGAGTCGTCGGGCCTAATCGAGACCATCACCAACGGCGTCTCGCTCCACTCGCTCAA GCGGAGCCTGACGCTGGCGGCGGCCGACTCGGGCCAGGCGGCGCGACAGCGCATCGCCACGCTGCGCGACCATTT CCTCAAGGCCTTTGGCCAGCCGGAGAGTGAGCCGTACAGAGCCGGCGTCGACGCATTCAAGCGCTCGCTAGCGGC CTACAGCATCATCTCGTACATCCTGCAGCTCAAGGACCGGCACAACGGCAACGTGCTTATCGACAGCGAGGGCCA CATTATTCACATCGACTTTGGCTTTATGCTGTCCAATTCGCCCGGCTCCGTCGGGTTCGAGGCGGCGCCTTTCAA GCTCACGCACGAGTACGTCGACGTGCTGGGCGGCATCGGGTCCCCGGACTTTGAGGACTACAAGAGGCTGTGCAA GCAGGCATTTCAAGGTGAGCTGGGAGATGCGTTGGAGAGGAAAGAGGCTAACGGAGAAGCAGCGCTGCGCCGATC GGCGGACAACATCATTGATCTGGTCGCCATGATGGGCCGCGACTCCAGCATGCCGTGCTTCTCGGTGGGCGTAGC TCACGCGACGAACAGCCTCCGACAGCGTTTCCAGCTACACCTCAGCGCCGTCGAGGCGGAGCAGTTTGTCGAGAC GGATCTCGTGGGCAAGTCGTACGGGAGCTACTACACGCGACTGTAAGCCGGCCCCGTCCCCTGTTGCCGCCTGGC GCTGACATGGCTTCGTAGGTATGACACGTTCCAGTATCGGACTCAGGGCATCTACTAG |