Protein ID | Ophio5|2334 |
Gene name | |
Location | scaffold_199:26813..31611 |
Strand | - |
Gene length (bp) | 4798 |
Transcript length (bp) | 4641 |
Coding sequence length (bp) | 4638 |
Protein length (aa) | 1546 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF16212 | PhoLip_ATPase_C | Phospholipid-translocating P-type ATPase C-terminal | 1.8E-74 | 1104 | 1353 |
PF16209 | PhoLip_ATPase_N | Phospholipid-translocating ATPase N-terminal | 1.2E-18 | 108 | 158 |
PF13246 | Cation_ATPase | Cation transport ATPase (P-type) | 1.2E-12 | 751 | 833 |
PF00702 | Hydrolase | haloacid dehalogenase-like hydrolase | 2.3E-07 | 620 | 986 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|P32660|ATC5_YEAST | Phospholipid-transporting ATPase DNF1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF1 PE=1 SV=2 | 21 | 1374 | 0.0E+00 |
sp|Q12675|ATC4_YEAST | Phospholipid-transporting ATPase DNF2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF2 PE=1 SV=1 | 10 | 1374 | 0.0E+00 |
sp|Q09891|ATCX_SCHPO | Putative phospholipid-transporting ATPase C24B11.12c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC24B11.12c PE=3 SV=1 | 75 | 1361 | 0.0E+00 |
sp|O36028|ATCZ_SCHPO | Putative phospholipid-transporting ATPase C4F10.16c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC4F10.16c PE=3 SV=1 | 48 | 1362 | 0.0E+00 |
sp|Q9XIE6|ALA3_ARATH | Phospholipid-transporting ATPase 3 OS=Arabidopsis thaliana GN=ALA3 PE=1 SV=2 | 350 | 1361 | 0.0E+00 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|P32660|ATC5_YEAST | Phospholipid-transporting ATPase DNF1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF1 PE=1 SV=2 | 21 | 1374 | 0.0E+00 |
sp|Q12675|ATC4_YEAST | Phospholipid-transporting ATPase DNF2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF2 PE=1 SV=1 | 10 | 1374 | 0.0E+00 |
sp|Q09891|ATCX_SCHPO | Putative phospholipid-transporting ATPase C24B11.12c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC24B11.12c PE=3 SV=1 | 75 | 1361 | 0.0E+00 |
sp|O36028|ATCZ_SCHPO | Putative phospholipid-transporting ATPase C4F10.16c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC4F10.16c PE=3 SV=1 | 48 | 1362 | 0.0E+00 |
sp|Q9XIE6|ALA3_ARATH | Phospholipid-transporting ATPase 3 OS=Arabidopsis thaliana GN=ALA3 PE=1 SV=2 | 350 | 1361 | 0.0E+00 |
sp|P98199|AT8B2_MOUSE | Phospholipid-transporting ATPase ID OS=Mus musculus GN=Atp8b2 PE=2 SV=2 | 345 | 1360 | 0.0E+00 |
sp|O43520|AT8B1_HUMAN | Phospholipid-transporting ATPase IC OS=Homo sapiens GN=ATP8B1 PE=1 SV=3 | 343 | 1364 | 0.0E+00 |
sp|P98198|AT8B2_HUMAN | Phospholipid-transporting ATPase ID OS=Homo sapiens GN=ATP8B2 PE=1 SV=2 | 345 | 1360 | 0.0E+00 |
sp|Q9LK90|ALA8_ARATH | Probable phospholipid-transporting ATPase 8 OS=Arabidopsis thaliana GN=ALA8 PE=3 SV=1 | 296 | 1364 | 0.0E+00 |
sp|Q148W0|AT8B1_MOUSE | Phospholipid-transporting ATPase IC OS=Mus musculus GN=Atp8b1 PE=1 SV=2 | 343 | 1364 | 0.0E+00 |
sp|P39524|ATC3_YEAST | Probable phospholipid-transporting ATPase DRS2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DRS2 PE=1 SV=2 | 318 | 1364 | 0.0E+00 |
sp|Q8TF62|AT8B4_HUMAN | Probable phospholipid-transporting ATPase IM OS=Homo sapiens GN=ATP8B4 PE=1 SV=3 | 326 | 1364 | 0.0E+00 |
sp|Q5BL50|AT8B1_XENTR | Phospholipid-transporting ATPase IC OS=Xenopus tropicalis GN=atp8b1 PE=2 SV=1 | 343 | 1357 | 0.0E+00 |
sp|Q9SX33|ALA9_ARATH | Putative phospholipid-transporting ATPase 9 OS=Arabidopsis thaliana GN=ALA9 PE=3 SV=1 | 345 | 1353 | 0.0E+00 |
sp|P70704|AT8A1_MOUSE | Phospholipid-transporting ATPase IA OS=Mus musculus GN=Atp8a1 PE=1 SV=2 | 350 | 1363 | 0.0E+00 |
sp|P98200|AT8A2_MOUSE | Phospholipid-transporting ATPase IB OS=Mus musculus GN=Atp8a2 PE=1 SV=1 | 350 | 1343 | 0.0E+00 |
sp|O94296|YOOC_SCHPO | Probable phospholipid-transporting ATPase C887.12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC887.12 PE=3 SV=1 | 341 | 1370 | 0.0E+00 |
sp|Q9LNQ4|ALA4_ARATH | Probable phospholipid-transporting ATPase 4 OS=Arabidopsis thaliana GN=ALA4 PE=3 SV=2 | 343 | 1361 | 0.0E+00 |
sp|Q9LI83|ALA10_ARATH | Phospholipid-transporting ATPase 10 OS=Arabidopsis thaliana GN=ALA10 PE=3 SV=1 | 345 | 1353 | 0.0E+00 |
sp|Q9SAF5|ALA11_ARATH | Probable phospholipid-transporting ATPase 11 OS=Arabidopsis thaliana GN=ALA11 PE=2 SV=1 | 345 | 1353 | 0.0E+00 |
sp|Q29449|AT8A1_BOVIN | Probable phospholipid-transporting ATPase IA OS=Bos taurus GN=ATP8A1 PE=1 SV=2 | 350 | 1363 | 0.0E+00 |
sp|P57792|ALA12_ARATH | Probable phospholipid-transporting ATPase 12 OS=Arabidopsis thaliana GN=ALA12 PE=2 SV=1 | 350 | 1383 | 0.0E+00 |
sp|Q9SGG3|ALA5_ARATH | Probable phospholipid-transporting ATPase 5 OS=Arabidopsis thaliana GN=ALA5 PE=3 SV=1 | 327 | 1366 | 0.0E+00 |
sp|C7EXK4|AT8A2_BOVIN | Phospholipid-transporting ATPase IB OS=Bos taurus GN=ATP8A2 PE=1 SV=4 | 349 | 1343 | 0.0E+00 |
sp|Q9LVK9|ALA7_ARATH | Probable phospholipid-transporting ATPase 7 OS=Arabidopsis thaliana GN=ALA7 PE=3 SV=3 | 327 | 1361 | 0.0E+00 |
sp|Q9NTI2|AT8A2_HUMAN | Phospholipid-transporting ATPase IB OS=Homo sapiens GN=ATP8A2 PE=1 SV=2 | 350 | 1343 | 0.0E+00 |
sp|Q9SLK6|ALA6_ARATH | Phospholipid-transporting ATPase 6 OS=Arabidopsis thaliana GN=ALA6 PE=1 SV=2 | 327 | 1361 | 0.0E+00 |
sp|A3FIN4|AT8B5_MOUSE | Phospholipid-transporting ATPase FetA OS=Mus musculus GN=Atp8b5 PE=2 SV=1 | 350 | 1357 | 0.0E+00 |
sp|P98204|ALA1_ARATH | Phospholipid-transporting ATPase 1 OS=Arabidopsis thaliana GN=ALA1 PE=2 SV=1 | 326 | 1368 | 0.0E+00 |
sp|Q6UQ17|AT8B3_MOUSE | Phospholipid-transporting ATPase IK OS=Mus musculus GN=Atp8b3 PE=1 SV=1 | 342 | 1307 | 0.0E+00 |
sp|O60423|AT8B3_HUMAN | Phospholipid-transporting ATPase IK OS=Homo sapiens GN=ATP8B3 PE=2 SV=4 | 342 | 1293 | 6.0E-179 |
sp|Q9Y2G3|AT11B_HUMAN | Probable phospholipid-transporting ATPase IF OS=Homo sapiens GN=ATP11B PE=1 SV=2 | 351 | 1339 | 2.0E-173 |
sp|Q9U280|TAT1_CAEEL | Phospholipid-transporting ATPase tat-1 OS=Caenorhabditis elegans GN=tat-1 PE=3 SV=3 | 350 | 1353 | 5.0E-167 |
sp|Q9N0Z4|AT11B_RABIT | Probable phospholipid-transporting ATPase IF (Fragment) OS=Oryctolagus cuniculus GN=ATP11B PE=1 SV=2 | 351 | 1339 | 1.0E-165 |
sp|P98196|AT11A_HUMAN | Probable phospholipid-transporting ATPase IH OS=Homo sapiens GN=ATP11A PE=1 SV=3 | 341 | 1353 | 3.0E-161 |
sp|P98197|AT11A_MOUSE | Probable phospholipid-transporting ATPase IH OS=Mus musculus GN=Atp11a PE=1 SV=1 | 341 | 1353 | 3.0E-159 |
sp|Q8NB49|AT11C_HUMAN | Phospholipid-transporting ATPase IG OS=Homo sapiens GN=ATP11C PE=1 SV=3 | 341 | 1350 | 1.0E-147 |
sp|Q9QZW0|AT11C_MOUSE | Phospholipid-transporting ATPase 11C OS=Mus musculus GN=Atp11c PE=1 SV=2 | 341 | 1350 | 8.0E-142 |
sp|O54827|AT10A_MOUSE | Probable phospholipid-transporting ATPase VA OS=Mus musculus GN=Atp10a PE=1 SV=4 | 706 | 1364 | 3.0E-133 |
sp|Q9Y2Q0|AT8A1_HUMAN | Phospholipid-transporting ATPase IA OS=Homo sapiens GN=ATP8A1 PE=1 SV=1 | 727 | 1363 | 5.0E-133 |
sp|O60312|AT10A_HUMAN | Probable phospholipid-transporting ATPase VA OS=Homo sapiens GN=ATP10A PE=2 SV=2 | 750 | 1361 | 6.0E-133 |
sp|O94823|AT10B_HUMAN | Probable phospholipid-transporting ATPase VB OS=Homo sapiens GN=ATP10B PE=2 SV=2 | 748 | 1348 | 6.0E-132 |
sp|Q9P241|AT10D_HUMAN | Probable phospholipid-transporting ATPase VD OS=Homo sapiens GN=ATP10D PE=2 SV=3 | 740 | 1395 | 7.0E-130 |
sp|Q8K2X1|AT10D_MOUSE | Probable phospholipid-transporting ATPase VD OS=Mus musculus GN=Atp10d PE=2 SV=2 | 740 | 1425 | 3.0E-128 |
sp|Q9GKS6|AT10D_MACFA | Probable phospholipid-transporting ATPase VD (Fragment) OS=Macaca fascicularis GN=ATP10D PE=2 SV=1 | 749 | 1350 | 3.0E-126 |
sp|O70228|ATP9A_MOUSE | Probable phospholipid-transporting ATPase IIA OS=Mus musculus GN=Atp9a PE=1 SV=3 | 352 | 1353 | 1.0E-101 |
sp|O75110|ATP9A_HUMAN | Probable phospholipid-transporting ATPase IIA OS=Homo sapiens GN=ATP9A PE=1 SV=3 | 352 | 1353 | 2.0E-100 |
sp|P98195|ATP9B_MOUSE | Probable phospholipid-transporting ATPase IIB OS=Mus musculus GN=Atp9b PE=1 SV=4 | 353 | 1353 | 4.0E-99 |
sp|F1Q4S1|ATP9B_DANRE | Probable phospholipid-transporting ATPase IIB OS=Danio rerio GN=atp9b PE=3 SV=1 | 353 | 1353 | 2.0E-98 |
sp|D4ABB8|ATP9B_RAT | Probable phospholipid-transporting ATPase IIB OS=Rattus norvegicus GN=Atp9b PE=3 SV=1 | 353 | 1353 | 4.0E-98 |
sp|O43861|ATP9B_HUMAN | Probable phospholipid-transporting ATPase IIB OS=Homo sapiens GN=ATP9B PE=2 SV=4 | 353 | 1353 | 4.0E-97 |
sp|A1A4J6|ATP9B_BOVIN | Probable phospholipid-transporting ATPase IIB OS=Bos taurus GN=ATP9B PE=2 SV=1 | 353 | 1353 | 5.0E-97 |
sp|Q10309|YD56_SCHPO | Putative phospholipid-transporting ATPase C6C3.06c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC6C3.06c PE=3 SV=1 | 351 | 1353 | 3.0E-96 |
sp|P40527|ATC7_YEAST | Probable phospholipid-transporting ATPase NEO1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=NEO1 PE=1 SV=1 | 351 | 1353 | 8.0E-95 |
sp|P98205|ALA2_ARATH | Phospholipid-transporting ATPase 2 OS=Arabidopsis thaliana GN=ALA2 PE=1 SV=1 | 728 | 1367 | 1.0E-92 |
sp|Q9UT43|YFRD_SCHPO | Putative phospholipid-transporting ATPase C821.13c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC821.13c PE=1 SV=2 | 813 | 1363 | 4.0E-77 |
sp|Q12674|ATC8_YEAST | Probable phospholipid-transporting ATPase DNF3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF3 PE=1 SV=1 | 819 | 1374 | 1.0E-72 |
sp|Q9UT43|YFRD_SCHPO | Putative phospholipid-transporting ATPase C821.13c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC821.13c PE=1 SV=2 | 351 | 896 | 3.0E-66 |
sp|Q9P241|AT10D_HUMAN | Probable phospholipid-transporting ATPase VD OS=Homo sapiens GN=ATP10D PE=2 SV=3 | 294 | 647 | 8.0E-63 |
sp|Q9Y2Q0|AT8A1_HUMAN | Phospholipid-transporting ATPase IA OS=Homo sapiens GN=ATP8A1 PE=1 SV=1 | 350 | 650 | 1.0E-62 |
sp|Q8K2X1|AT10D_MOUSE | Probable phospholipid-transporting ATPase VD OS=Mus musculus GN=Atp10d PE=2 SV=2 | 294 | 647 | 5.0E-62 |
sp|O54827|AT10A_MOUSE | Probable phospholipid-transporting ATPase VA OS=Mus musculus GN=Atp10a PE=1 SV=4 | 341 | 649 | 8.0E-59 |
sp|O60312|AT10A_HUMAN | Probable phospholipid-transporting ATPase VA OS=Homo sapiens GN=ATP10A PE=2 SV=2 | 341 | 649 | 8.0E-58 |
sp|O94823|AT10B_HUMAN | Probable phospholipid-transporting ATPase VB OS=Homo sapiens GN=ATP10B PE=2 SV=2 | 331 | 665 | 3.0E-57 |
sp|Q12674|ATC8_YEAST | Probable phospholipid-transporting ATPase DNF3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF3 PE=1 SV=1 | 350 | 647 | 2.0E-45 |
sp|P98205|ALA2_ARATH | Phospholipid-transporting ATPase 2 OS=Arabidopsis thaliana GN=ALA2 PE=1 SV=1 | 351 | 655 | 3.0E-33 |
sp|O54827|AT10A_MOUSE | Probable phospholipid-transporting ATPase VA OS=Mus musculus GN=Atp10a PE=1 SV=4 | 107 | 193 | 2.0E-18 |
sp|Q08853|ATC_PLAFK | Calcium-transporting ATPase OS=Plasmodium falciparum (isolate K1 / Thailand) GN=ATP6 PE=3 SV=1 | 795 | 1186 | 3.0E-18 |
sp|Q8K2X1|AT10D_MOUSE | Probable phospholipid-transporting ATPase VD OS=Mus musculus GN=Atp10d PE=2 SV=2 | 109 | 207 | 7.0E-18 |
sp|Q12674|ATC8_YEAST | Probable phospholipid-transporting ATPase DNF3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF3 PE=1 SV=1 | 728 | 837 | 1.0E-17 |
sp|Q9P241|AT10D_HUMAN | Probable phospholipid-transporting ATPase VD OS=Homo sapiens GN=ATP10D PE=2 SV=3 | 110 | 193 | 4.0E-17 |
sp|O60312|AT10A_HUMAN | Probable phospholipid-transporting ATPase VA OS=Homo sapiens GN=ATP10A PE=2 SV=2 | 108 | 193 | 1.0E-15 |
sp|Q29449|AT8A1_BOVIN | Probable phospholipid-transporting ATPase IA OS=Bos taurus GN=ATP8A1 PE=1 SV=2 | 47 | 228 | 2.0E-14 |
sp|P98196|AT11A_HUMAN | Probable phospholipid-transporting ATPase IH OS=Homo sapiens GN=ATP11A PE=1 SV=3 | 108 | 201 | 2.0E-14 |
sp|P98197|AT11A_MOUSE | Probable phospholipid-transporting ATPase IH OS=Mus musculus GN=Atp11a PE=1 SV=1 | 108 | 201 | 3.0E-14 |
sp|P98204|ALA1_ARATH | Phospholipid-transporting ATPase 1 OS=Arabidopsis thaliana GN=ALA1 PE=2 SV=1 | 55 | 193 | 6.0E-14 |
sp|Q9N0Z4|AT11B_RABIT | Probable phospholipid-transporting ATPase IF (Fragment) OS=Oryctolagus cuniculus GN=ATP11B PE=1 SV=2 | 76 | 197 | 8.0E-14 |
sp|Q5BL50|AT8B1_XENTR | Phospholipid-transporting ATPase IC OS=Xenopus tropicalis GN=atp8b1 PE=2 SV=1 | 110 | 228 | 1.0E-13 |
sp|Q9Y2G3|AT11B_HUMAN | Probable phospholipid-transporting ATPase IF OS=Homo sapiens GN=ATP11B PE=1 SV=2 | 76 | 197 | 1.0E-13 |
sp|O74431|ATC9_SCHPO | Probable cation-transporting ATPase C1672.11c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPCC1672.11c PE=3 SV=1 | 784 | 1104 | 1.0E-13 |
sp|Q8TF62|AT8B4_HUMAN | Probable phospholipid-transporting ATPase IM OS=Homo sapiens GN=ATP8B4 PE=1 SV=3 | 110 | 207 | 8.0E-13 |
sp|P70704|AT8A1_MOUSE | Phospholipid-transporting ATPase IA OS=Mus musculus GN=Atp8a1 PE=1 SV=2 | 47 | 209 | 9.0E-13 |
sp|Q9Y2Q0|AT8A1_HUMAN | Phospholipid-transporting ATPase IA OS=Homo sapiens GN=ATP8A1 PE=1 SV=1 | 47 | 209 | 1.0E-12 |
sp|Q6ATV4|ACA2_ORYSJ | Calcium-transporting ATPase 2, plasma membrane-type OS=Oryza sativa subsp. japonica GN=Os03g0616400 PE=2 SV=1 | 800 | 1180 | 1.0E-12 |
sp|P23634|AT2B4_HUMAN | Plasma membrane calcium-transporting ATPase 4 OS=Homo sapiens GN=ATP2B4 PE=1 SV=2 | 800 | 979 | 1.0E-12 |
sp|O94823|AT10B_HUMAN | Probable phospholipid-transporting ATPase VB OS=Homo sapiens GN=ATP10B PE=2 SV=2 | 110 | 196 | 2.0E-12 |
sp|Q16720|AT2B3_HUMAN | Plasma membrane calcium-transporting ATPase 3 OS=Homo sapiens GN=ATP2B3 PE=1 SV=3 | 788 | 977 | 3.0E-12 |
sp|Q21286|YBF7_CAEEL | Probable cation-transporting ATPase K07E3.7 OS=Caenorhabditis elegans GN=K07E3.7/K07E3.6 PE=3 SV=4 | 707 | 1104 | 3.0E-12 |
sp|Q6Q477|AT2B4_MOUSE | Plasma membrane calcium-transporting ATPase 4 OS=Mus musculus GN=Atp2b4 PE=1 SV=1 | 800 | 979 | 4.0E-12 |
sp|Q64568|AT2B3_RAT | Plasma membrane calcium-transporting ATPase 3 OS=Rattus norvegicus GN=Atp2b3 PE=1 SV=2 | 788 | 977 | 5.0E-12 |
sp|Q9NTI2|AT8A2_HUMAN | Phospholipid-transporting ATPase IB OS=Homo sapiens GN=ATP8A2 PE=1 SV=2 | 76 | 212 | 6.0E-12 |
sp|Q9SX33|ALA9_ARATH | Putative phospholipid-transporting ATPase 9 OS=Arabidopsis thaliana GN=ALA9 PE=3 SV=1 | 88 | 198 | 1.0E-11 |
sp|Q9QZW0|AT11C_MOUSE | Phospholipid-transporting ATPase 11C OS=Mus musculus GN=Atp11c PE=1 SV=2 | 105 | 208 | 1.0E-11 |
sp|Q2QMX9|ACA1_ORYSJ | Calcium-transporting ATPase 1, plasma membrane-type OS=Oryza sativa subsp. japonica GN=Os12g0586600 PE=2 SV=1 | 614 | 958 | 1.0E-11 |
sp|A3FIN4|AT8B5_MOUSE | Phospholipid-transporting ATPase FetA OS=Mus musculus GN=Atp8b5 PE=2 SV=1 | 110 | 207 | 2.0E-11 |
sp|Q8NB49|AT11C_HUMAN | Phospholipid-transporting ATPase IG OS=Homo sapiens GN=ATP11C PE=1 SV=3 | 88 | 208 | 2.0E-11 |
sp|Q9R0K7|AT2B2_MOUSE | Plasma membrane calcium-transporting ATPase 2 OS=Mus musculus GN=Atp2b2 PE=1 SV=2 | 800 | 977 | 2.0E-11 |
sp|P11506|AT2B2_RAT | Plasma membrane calcium-transporting ATPase 2 OS=Rattus norvegicus GN=Atp2b2 PE=1 SV=2 | 800 | 977 | 2.0E-11 |
sp|D3K0R6|AT2B4_BOVIN | Plasma membrane calcium-transporting ATPase 4 OS=Bos taurus GN=ATP2B4 PE=1 SV=2 | 800 | 979 | 4.0E-11 |
sp|Q01814|AT2B2_HUMAN | Plasma membrane calcium-transporting ATPase 2 OS=Homo sapiens GN=ATP2B2 PE=1 SV=2 | 800 | 977 | 6.0E-11 |
sp|C7EXK4|AT8A2_BOVIN | Phospholipid-transporting ATPase IB OS=Bos taurus GN=ATP8A2 PE=1 SV=4 | 87 | 212 | 7.0E-11 |
sp|Q9SLK6|ALA6_ARATH | Phospholipid-transporting ATPase 6 OS=Arabidopsis thaliana GN=ALA6 PE=1 SV=2 | 110 | 198 | 7.0E-11 |
sp|P58165|AT2B2_OREMO | Plasma membrane calcium-transporting ATPase 2 (Fragment) OS=Oreochromis mossambicus GN=atp2b2 PE=2 SV=1 | 785 | 977 | 7.0E-11 |
sp|P57792|ALA12_ARATH | Probable phospholipid-transporting ATPase 12 OS=Arabidopsis thaliana GN=ALA12 PE=2 SV=1 | 108 | 207 | 9.0E-11 |
sp|Q4VNC1|AT134_HUMAN | Probable cation-transporting ATPase 13A4 OS=Homo sapiens GN=ATP13A4 PE=2 SV=3 | 794 | 1104 | 9.0E-11 |
sp|Q9XIE6|ALA3_ARATH | Phospholipid-transporting ATPase 3 OS=Arabidopsis thaliana GN=ALA3 PE=1 SV=2 | 105 | 219 | 1.0E-10 |
sp|Q9LVK9|ALA7_ARATH | Probable phospholipid-transporting ATPase 7 OS=Arabidopsis thaliana GN=ALA7 PE=3 SV=3 | 110 | 198 | 1.0E-10 |
sp|Q9LU41|ACA9_ARATH | Calcium-transporting ATPase 9, plasma membrane-type OS=Arabidopsis thaliana GN=ACA9 PE=2 SV=2 | 756 | 1180 | 1.0E-10 |
sp|P98200|AT8A2_MOUSE | Phospholipid-transporting ATPase IB OS=Mus musculus GN=Atp8a2 PE=1 SV=1 | 76 | 212 | 2.0E-10 |
sp|Q9LNQ4|ALA4_ARATH | Probable phospholipid-transporting ATPase 4 OS=Arabidopsis thaliana GN=ALA4 PE=3 SV=2 | 72 | 207 | 2.0E-10 |
sp|Q9SGG3|ALA5_ARATH | Probable phospholipid-transporting ATPase 5 OS=Arabidopsis thaliana GN=ALA5 PE=3 SV=1 | 75 | 207 | 2.0E-10 |
sp|O94296|YOOC_SCHPO | Probable phospholipid-transporting ATPase C887.12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC887.12 PE=3 SV=1 | 97 | 207 | 3.0E-10 |
sp|Q9NQ11|AT132_HUMAN | Probable cation-transporting ATPase 13A2 OS=Homo sapiens GN=ATP13A2 PE=1 SV=2 | 794 | 1100 | 3.0E-10 |
sp|P98205|ALA2_ARATH | Phospholipid-transporting ATPase 2 OS=Arabidopsis thaliana GN=ALA2 PE=1 SV=1 | 113 | 196 | 4.0E-10 |
sp|P20020|AT2B1_HUMAN | Plasma membrane calcium-transporting ATPase 1 OS=Homo sapiens GN=ATP2B1 PE=1 SV=3 | 800 | 1180 | 4.0E-10 |
sp|Q37145|ACA1_ARATH | Calcium-transporting ATPase 1, chloroplastic OS=Arabidopsis thaliana GN=ACA1 PE=1 SV=3 | 800 | 986 | 5.0E-10 |
sp|P23220|AT2B1_PIG | Plasma membrane calcium-transporting ATPase 1 OS=Sus scrofa GN=ATP2B1 PE=2 SV=1 | 800 | 1180 | 5.0E-10 |
sp|Q9SZR1|ACA10_ARATH | Calcium-transporting ATPase 10, plasma membrane-type OS=Arabidopsis thaliana GN=ACA10 PE=1 SV=2 | 756 | 1180 | 6.0E-10 |
sp|Q6UQ17|AT8B3_MOUSE | Phospholipid-transporting ATPase IK OS=Mus musculus GN=Atp8b3 PE=1 SV=1 | 108 | 207 | 9.0E-10 |
sp|Q9LF79|ACA8_ARATH | Calcium-transporting ATPase 8, plasma membrane-type OS=Arabidopsis thaliana GN=ACA8 PE=1 SV=1 | 794 | 971 | 9.0E-10 |
sp|Q9LK90|ALA8_ARATH | Probable phospholipid-transporting ATPase 8 OS=Arabidopsis thaliana GN=ALA8 PE=3 SV=1 | 113 | 207 | 1.0E-09 |
sp|Q9SAF5|ALA11_ARATH | Probable phospholipid-transporting ATPase 11 OS=Arabidopsis thaliana GN=ALA11 PE=2 SV=1 | 113 | 222 | 1.0E-09 |
sp|O60423|AT8B3_HUMAN | Phospholipid-transporting ATPase IK OS=Homo sapiens GN=ATP8B3 PE=2 SV=4 | 108 | 199 | 1.0E-09 |
sp|Q12674|ATC8_YEAST | Probable phospholipid-transporting ATPase DNF3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF3 PE=1 SV=1 | 103 | 209 | 1.0E-09 |
sp|P11505|AT2B1_RAT | Plasma membrane calcium-transporting ATPase 1 OS=Rattus norvegicus GN=Atp2b1 PE=1 SV=2 | 800 | 1180 | 1.0E-09 |
sp|G5E829|AT2B1_MOUSE | Plasma membrane calcium-transporting ATPase 1 OS=Mus musculus GN=Atp2b1 PE=1 SV=1 | 800 | 1180 | 1.0E-09 |
sp|Q9LI83|ALA10_ARATH | Phospholipid-transporting ATPase 10 OS=Arabidopsis thaliana GN=ALA10 PE=3 SV=1 | 88 | 207 | 2.0E-09 |
sp|Q9U280|TAT1_CAEEL | Phospholipid-transporting ATPase tat-1 OS=Caenorhabditis elegans GN=tat-1 PE=3 SV=3 | 108 | 202 | 3.0E-09 |
sp|P98198|AT8B2_HUMAN | Phospholipid-transporting ATPase ID OS=Homo sapiens GN=ATP8B2 PE=1 SV=2 | 110 | 207 | 7.0E-09 |
sp|Q5XF90|AT134_MOUSE | Probable cation-transporting ATPase 13A4 OS=Mus musculus GN=Atp13a4 PE=2 SV=1 | 731 | 1104 | 7.0E-09 |
sp|Q64542|AT2B4_RAT | Plasma membrane calcium-transporting ATPase 4 OS=Rattus norvegicus GN=Atp2b4 PE=1 SV=1 | 800 | 979 | 9.0E-09 |
sp|P98199|AT8B2_MOUSE | Phospholipid-transporting ATPase ID OS=Mus musculus GN=Atp8b2 PE=2 SV=2 | 110 | 207 | 2.0E-08 |
sp|O70228|ATP9A_MOUSE | Probable phospholipid-transporting ATPase IIA OS=Mus musculus GN=Atp9a PE=1 SV=3 | 104 | 212 | 2.0E-08 |
sp|O75110|ATP9A_HUMAN | Probable phospholipid-transporting ATPase IIA OS=Homo sapiens GN=ATP9A PE=1 SV=3 | 104 | 212 | 2.0E-08 |
sp|Q00804|AT2B1_RABIT | Plasma membrane calcium-transporting ATPase 1 OS=Oryctolagus cuniculus GN=ATP2B1 PE=2 SV=2 | 800 | 979 | 3.0E-08 |
sp|O22218|ACA4_ARATH | Calcium-transporting ATPase 4, plasma membrane-type OS=Arabidopsis thaliana GN=ACA4 PE=1 SV=1 | 780 | 954 | 3.0E-08 |
sp|Q9CFU9|LLCA1_LACLA | Calcium-transporting ATPase 1 OS=Lactococcus lactis subsp. lactis (strain IL1403) GN=yoaB PE=1 SV=1 | 757 | 973 | 4.0E-08 |
sp|Q65X71|ACA6_ORYSJ | Probable calcium-transporting ATPase 6, plasma membrane-type OS=Oryza sativa subsp. japonica GN=Os05g0495600 PE=3 SV=1 | 800 | 958 | 4.0E-08 |
sp|Q5ZKB7|AT134_CHICK | Probable cation-transporting ATPase 13A4 OS=Gallus gallus GN=ATP13A4 PE=2 SV=1 | 794 | 1104 | 4.0E-08 |
sp|P38929|ATC2_YEAST | Calcium-transporting ATPase 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PMC1 PE=1 SV=1 | 353 | 959 | 4.0E-08 |
sp|Q4VNC0|AT135_HUMAN | Probable cation-transporting ATPase 13A5 OS=Homo sapiens GN=ATP13A5 PE=2 SV=1 | 795 | 1104 | 4.0E-08 |
sp|Q9CTG6|AT132_MOUSE | Probable cation-transporting ATPase 13A2 OS=Mus musculus GN=Atp13a2 PE=2 SV=3 | 794 | 1100 | 6.0E-08 |
sp|O64806|ACA7_ARATH | Putative calcium-transporting ATPase 7, plasma membrane-type OS=Arabidopsis thaliana GN=ACA7 PE=3 SV=2 | 614 | 958 | 6.0E-08 |
sp|P39986|ATC6_YEAST | Manganese-transporting ATPase 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=SPF1 PE=1 SV=1 | 764 | 1140 | 8.0E-08 |
sp|O14022|CTA5_SCHPO | Cation-transporting ATPase 5 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=cta5 PE=3 SV=1 | 787 | 1104 | 1.0E-07 |
sp|Q9M2L4|ACA11_ARATH | Putative calcium-transporting ATPase 11, plasma membrane-type OS=Arabidopsis thaliana GN=ACA11 PE=1 SV=1 | 788 | 955 | 3.0E-07 |
sp|F1Q4S1|ATP9B_DANRE | Probable phospholipid-transporting ATPase IIB OS=Danio rerio GN=atp9b PE=3 SV=1 | 104 | 212 | 4.0E-07 |
sp|Q148W0|AT8B1_MOUSE | Phospholipid-transporting ATPase IC OS=Mus musculus GN=Atp8b1 PE=1 SV=2 | 110 | 207 | 9.0E-07 |
sp|Q9LT02|PDR2_ARATH | Probable manganese-transporting ATPase PDR2 OS=Arabidopsis thaliana GN=PDR2 PE=1 SV=1 | 787 | 1095 | 9.0E-07 |
sp|P54678|ATC1_DICDI | Calcium-transporting ATPase PAT1 OS=Dictyostelium discoideum GN=patA PE=2 SV=2 | 800 | 955 | 9.0E-07 |
sp|O43520|AT8B1_HUMAN | Phospholipid-transporting ATPase IC OS=Homo sapiens GN=ATP8B1 PE=1 SV=3 | 110 | 207 | 2.0E-06 |
sp|Q2QY12|ACA4_ORYSJ | Probable calcium-transporting ATPase 4, plasma membrane-type OS=Oryza sativa subsp. japonica GN=Os12g0136900 PE=3 SV=1 | 800 | 958 | 2.0E-06 |
sp|Q2RAS0|ACA5_ORYSJ | Probable calcium-transporting ATPase 5, plasma membrane-type OS=Oryza sativa subsp. japonica GN=Os11g0140400 PE=3 SV=1 | 800 | 958 | 2.0E-06 |
sp|P39524|ATC3_YEAST | Probable phospholipid-transporting ATPase DRS2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DRS2 PE=1 SV=2 | 110 | 209 | 3.0E-06 |
sp|Q9UT43|YFRD_SCHPO | Putative phospholipid-transporting ATPase C821.13c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC821.13c PE=1 SV=2 | 78 | 201 | 5.0E-06 |
sp|Q10309|YD56_SCHPO | Putative phospholipid-transporting ATPase C6C3.06c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC6C3.06c PE=3 SV=1 | 41 | 193 | 9.0E-06 |
SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
---|---|---|
No | 1 - 26 | 0.45 |
Domain # | Start | End | Length |
---|---|---|---|
1 | 140 | 174 | 34 |
2 | 511 | 533 | 22 |
3 | 557 | 579 | 22 |
4 | 1139 | 1156 | 17 |
5 | 1166 | 1188 | 22 |
6 | 1218 | 1240 | 22 |
7 | 1260 | 1277 | 17 |
8 | 1284 | 1306 | 22 |
9 | 1326 | 1344 | 18 |
Expression values
Label | Description | Expression (RPKM) | Confidence interval (low) | Confidence interval (high) |
---|---|---|---|---|
SC16a | Pure fungal culture | 42.90 | 22.33 | 63.46 |
CcL | In ants, during behavior modification | 43.95 | 22.48 | 65.43 |
CcD | In ants, recently dead | 33.97 | 18.15 | 49.79 |
Differential expression
Label1 | Label2 | Q-value | Significant difference |
---|---|---|---|
SC16a | CcL | 0.933098 | no |
SC16a | CcD | 0.349318 | no |
CcL | CcD | 0.292234 | 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|2334 MTTANGSGPGADGNPPKIERPHRTRWATRKMTIKSGRSKRLSLLNRMQQRKRASNEKPSAGDTSEPPLTDRSSED GSDTSSQSEDNGRTLYFNLPLPDDLLSDGHPIQTFPRNKIRTAKYTPLSFVPKNLWFQFHNVANIFFLFLVILGI FPIFGGVNPGLNAVPLIFIIVVTAIKDAVEDYRRTVLDNELNNAPVHRLSHWNNVNVEEGTVSSWRRFKKANTRL FGSMWHAIESLWSQKARTARAERKARKLQEADPEDEVRPSVETTRTRMSVREALSSPFSHESFKSADDDIPMTPV GSPKAVGDLPTLELPDDQDAKRAASLRSMKSDLVNYRRAPEGAKFKKDTWKSIQVGDFVRIYNDDELPADVIILS TSDPDGACYVETKNLDGETNLKVRQALRCGRTLKHARDCERAEFHIQSEPPQPNLYKYNGAIHWKQRVPGCPEDE PANMTEPITIDNLLLRGCNLRNTEWVLGVVIFTGHDTKIMMNAGITPSKRSRIAREMNFNVVCNFGILLIMCLLS GIFNGVAWSKTDASLHFFDFGSIGGSAAMSGFITFWAAIIVFQNLVPISLYITLEIVRTLQAVLIFSDIDMYYAK IDQPCIPKSWNISDDVGQIEYIFSDKTGTLTQNVMEFKKASINGQPYGEAFTEAQAGMQKRLGVDVVAEAARIET EIAEAKVKALAGLRKLYDNPYLHDGSVTFIAPDFVSDLAGLGGPQQQAANEEFMLALSLCHTVIAERSPGDPPSM NFKAQSPDEEALVATARDMGFTVISNNSDGIDLNVLGQDRHYPILNTIEFNSSRKRMSSIVRMPDGQIVLYCKGA DSVIYSRLKRGEQQQLRRQTAEQLEMFAREGLRTLCIARKTLTEKEYEMWKKEHDAAASALENREEKLETVAELI EQDLMLLGGTAIEDRLQDGVPDTIALLGQAGMKLWVLTGDKVETAINIGFSCNLLNNDMELIHLKLDEDETGETS DETFLGTTEKLLEQNLQMFDLVGDDSDLAAARKNHEPPAPTHGLVIDGFTLRWALNDRLRQKFLLLCKQCKSVLC CRVSPAQKAAVVAMVKTGLDVMTLSIGDGANDVAMIQEADVGVGIAGVEGRQAAMSSDYAIAQFRFLQRLMLVHG RWDYRRLAESIANFFYKNVVWTFAIFWFEIFCDFDITYPFDYTYILLFNLIFTSLPVGIMGVLDQDVSDKVSLAV PQLYRRGIERLEWTHSKFWFYMVDGLYQSVMVFFIPYLLFVPAQPVSFSGLGLEDRLRFGAYVAHPAVVTINAYI LINTYRWDWLMLLVVSLSDLSIFFWTGVYSSFVSSGFFFKTAAEVYSEASFWAIFFIVPVICLFPRFAVKSLQKV YWPYDVDIIREQEKMGAFAYLTEGSGSSNRHGSDGGSQKSGSSKKAKHILSGSVDDDLRPIYPPSTATRTTAHNR TQNGSDSTNFSADASLDAAVATGANRLSAEVVPPDRRSDDRVRPSYDRMRPSYDRMRMSMDRVRPSFEASSDFTS AARLQRIESTQNVGFKARLRGLSLTKNAAANSPLSPRSPRSPRTRR |
Coding | >Ophio5|2334 ATGACCACGGCCAATGGCTCCGGGCCTGGCGCCGACGGCAATCCGCCAAAGATTGAGCGCCCCCATCGGACACGC TGGGCCACTCGAAAGATGACCATCAAAAGCGGTCGCTCCAAGCGTCTGTCGCTTCTCAACCGCATGCAACAACGG AAACGCGCATCCAACGAGAAGCCCTCGGCCGGCGACACCTCGGAGCCGCCCCTGACGGACCGCAGTAGCGAAGAC GGTTCTGATACCTCATCTCAATCGGAAGACAACGGCCGCACCCTCTACTTCAATCTGCCTCTTCCCGACGACCTG CTGAGCGACGGCCATCCTATCCAAACTTTTCCCCGGAACAAGATTAGGACCGCAAAGTACACACCGCTCTCTTTC GTGCCCAAGAACCTGTGGTTCCAGTTCCACAATGTGGCCAACATATTTTTCCTTTTCCTCGTCATTCTCGGTATA TTTCCCATTTTCGGCGGCGTCAACCCCGGTCTCAACGCCGTCCCCCTCATCTTCATCATCGTCGTCACCGCAATC AAGGACGCAGTCGAGGATTACCGACGTACCGTTCTCGACAACGAACTCAACAATGCCCCCGTCCACCGATTGTCG CATTGGAACAATGTCAATGTCGAGGAGGGGACCGTCTCGTCCTGGAGGAGGTTTAAAAAGGCCAACACGAGACTG TTTGGCTCCATGTGGCATGCCATCGAGAGTTTGTGGTCCCAAAAGGCCAGGACGGCCAGGGCTGAGCGCAAGGCG CGCAAGCTGCAAGAGGCAGACCCGGAGGACGAGGTTCGCCCATCGGTCGAGACGACACGCACCAGAATGTCGGTC CGTGAGGCTCTCTCCTCGCCCTTCAGCCACGAATCGTTCAAGTCCGCCGATGACGACATCCCCATGACCCCCGTC GGCTCACCCAAAGCCGTCGGCGACCTGCCCACCCTCGAGCTGCCCGACGACCAAGACGCCAAGCGCGCCGCGTCG CTGCGGTCCATGAAGTCCGATCTCGTCAACTACCGCCGCGCTCCGGAGGGGGCAAAGTTCAAAAAGGACACCTGG AAGAGCATCCAGGTCGGCGACTTCGTGCGAATCTACAACGACGACGAGCTGCCCGCCGACGTCATCATCCTGTCC ACCTCGGACCCCGACGGCGCCTGCTACGTCGAGACGAAGAACCTGGACGGTGAGACGAATCTCAAGGTTCGTCAG GCTCTCCGCTGCGGCCGCACCCTCAAGCACGCCCGAGACTGCGAGAGGGCCGAGTTCCACATCCAGAGCGAGCCG CCGCAGCCCAATCTTTACAAGTACAACGGCGCCATCCACTGGAAGCAAAGGGTCCCCGGCTGTCCCGAGGACGAG CCGGCCAACATGACGGAGCCCATCACCATCGACAACCTGCTTCTTCGCGGCTGTAACCTACGCAACACCGAGTGG GTGCTCGGCGTCGTCATCTTCACTGGACACGACACAAAGATCATGATGAACGCCGGCATCACCCCCAGCAAGCGC TCGAGGATCGCCCGCGAGATGAACTTCAACGTCGTTTGTAACTTTGGCATCCTGCTCATCATGTGCCTGCTGTCG GGCATCTTCAACGGCGTCGCTTGGTCCAAGACGGACGCCTCGCTGCATTTTTTCGACTTTGGTTCCATCGGCGGC AGCGCCGCTATGAGCGGCTTCATCACCTTCTGGGCCGCCATCATTGTCTTCCAGAACCTGGTGCCCATCTCCCTC TACATCACGCTCGAGATTGTCCGCACGCTACAGGCCGTTCTCATCTTCAGCGACATCGACATGTACTACGCCAAG ATCGACCAACCGTGCATCCCCAAGTCGTGGAACATCTCCGATGACGTCGGCCAGATCGAATACATCTTTTCCGAC AAGACTGGCACGCTCACGCAGAACGTCATGGAGTTCAAGAAGGCCTCCATCAACGGCCAGCCCTACGGTGAGGCC TTCACGGAGGCGCAGGCTGGTATGCAGAAACGACTCGGCGTCGACGTGGTGGCCGAGGCGGCCAGGATCGAGACC GAGATTGCCGAGGCCAAAGTCAAAGCACTGGCCGGTCTGCGGAAGCTGTACGACAACCCGTACCTTCACGACGGC AGCGTCACCTTCATCGCCCCCGACTTCGTCTCCGACCTGGCGGGCCTAGGCGGGCCCCAGCAGCAGGCGGCTAAC GAGGAGTTTATGCTCGCGCTGTCTCTGTGCCACACGGTCATCGCCGAGAGATCGCCCGGCGACCCACCGAGCATG AACTTCAAGGCGCAGTCGCCCGACGAGGAGGCCCTGGTCGCCACCGCCCGCGACATGGGCTTCACCGTAATCAGC AACAACAGCGACGGCATCGACCTGAACGTACTGGGCCAGGACCGCCACTACCCGATCCTCAATACGATTGAGTTC AACTCGAGCAGGAAGCGGATGAGCTCCATCGTGCGCATGCCCGACGGCCAGATCGTCCTCTACTGCAAGGGCGCC GACTCGGTCATCTACTCGCGCCTCAAGCGGGGCGAGCAGCAGCAGCTGCGGCGCCAGACGGCGGAGCAACTCGAG ATGTTCGCCCGCGAAGGTCTTCGGACGCTCTGCATCGCGCGCAAGACACTGACGGAGAAGGAGTACGAGATGTGG AAGAAGGAGCACGACGCGGCGGCGTCGGCGCTCGAGAACCGCGAGGAGAAATTGGAGACGGTGGCAGAGCTCATC GAGCAGGACCTGATGCTACTGGGCGGCACGGCCATCGAAGATCGCCTGCAGGACGGCGTGCCCGACACCATCGCC CTCCTCGGCCAGGCCGGCATGAAGCTGTGGGTGCTGACGGGCGACAAGGTCGAGACGGCCATCAACATCGGCTTC TCGTGCAATCTGCTCAACAACGACATGGAGCTGATCCACCTCAAGCTCGACGAGGACGAGACGGGCGAGACGAGC GACGAGACGTTCCTGGGCACGACGGAGAAGCTTCTGGAGCAGAACCTGCAGATGTTTGATCTGGTCGGCGACGAC AGCGACCTTGCGGCGGCGAGGAAGAACCACGAGCCGCCGGCGCCGACGCACGGCCTCGTCATCGATGGCTTCACC CTCCGCTGGGCCCTCAACGACCGGCTGCGGCAAAAGTTTCTGCTGCTGTGCAAGCAGTGCAAGTCGGTGCTGTGC TGCCGCGTCAGCCCCGCGCAAAAGGCGGCCGTCGTGGCCATGGTCAAGACGGGGCTGGACGTGATGACGCTGTCG ATTGGCGACGGTGCCAACGACGTGGCCATGATCCAAGAGGCCGACGTGGGCGTCGGTATCGCTGGTGTCGAGGGT CGACAGGCGGCCATGTCGTCCGACTACGCCATTGCCCAGTTCCGCTTCCTGCAGAGGCTGATGCTGGTGCACGGC CGGTGGGACTACCGGCGGCTGGCGGAGAGTATCGCCAACTTCTTCTACAAGAACGTGGTCTGGACCTTTGCCATC TTCTGGTTCGAGATCTTCTGCGACTTCGACATCACCTACCCCTTCGACTACACCTACATTCTCCTGTTCAACCTC ATCTTCACGTCGCTCCCCGTCGGCATCATGGGCGTGCTCGACCAGGACGTCTCGGACAAGGTGTCGCTGGCCGTG CCTCAGCTGTACCGAAGGGGTATCGAACGGCTGGAGTGGACGCACAGCAAGTTTTGGTTTTACATGGTCGACGGC CTCTACCAGTCCGTCATGGTCTTCTTCATCCCATACCTGCTGTTCGTTCCGGCCCAGCCGGTCAGCTTCTCCGGG CTCGGCCTCGAGGATAGGCTTCGGTTCGGCGCCTACGTGGCGCATCCCGCCGTGGTGACGATCAACGCCTACATC CTGATCAACACGTACCGGTGGGATTGGCTGATGCTGCTCGTGGTGAGCCTCAGCGACCTGTCCATCTTCTTCTGG ACGGGCGTCTACTCGTCCTTTGTCTCGTCGGGCTTCTTCTTCAAGACGGCGGCCGAGGTGTACAGCGAGGCCAGC TTCTGGGCCATCTTCTTCATCGTCCCCGTCATCTGCCTCTTCCCGCGCTTCGCCGTCAAGTCGCTGCAGAAGGTC TACTGGCCATACGACGTGGACATTATCCGCGAGCAGGAGAAGATGGGCGCCTTCGCCTACCTGACGGAGGGCAGC GGATCCAGCAACCGGCACGGCAGCGACGGAGGCAGCCAGAAGTCAGGCAGCTCGAAGAAGGCCAAGCACATACTC AGCGGCAGCGTCGACGACGACCTGCGGCCCATCTATCCGCCGTCGACGGCGACGCGGACGACGGCCCACAACCGG ACACAGAACGGCAGCGACTCGACCAACTTTTCGGCCGACGCGTCGCTCGACGCGGCCGTCGCCACGGGCGCTAAT CGGCTATCAGCGGAGGTGGTGCCTCCGGACCGACGGTCGGACGACCGGGTGAGGCCGTCGTACGACCGGATGCGG CCGTCGTACGACCGGATGCGCATGTCAATGGATCGCGTCCGGCCGAGCTTCGAGGCGAGCAGCGATTTCACCTCG GCGGCGCGGCTGCAGCGCATCGAGTCGACGCAAAATGTCGGCTTTAAGGCCAGACTCCGAGGCCTGTCGCTGACC AAGAACGCGGCGGCGAACTCGCCGCTGAGCCCGCGTTCTCCGCGGTCGCCGAGGACGCGGCGC |
Transcript | >Ophio5|2334 ATGACCACGGCCAATGGCTCCGGGCCTGGCGCCGACGGCAATCCGCCAAAGATTGAGCGCCCCCATCGGACACGC TGGGCCACTCGAAAGATGACCATCAAAAGCGGTCGCTCCAAGCGTCTGTCGCTTCTCAACCGCATGCAACAACGG AAACGCGCATCCAACGAGAAGCCCTCGGCCGGCGACACCTCGGAGCCGCCCCTGACGGACCGCAGTAGCGAAGAC GGTTCTGATACCTCATCTCAATCGGAAGACAACGGCCGCACCCTCTACTTCAATCTGCCTCTTCCCGACGACCTG CTGAGCGACGGCCATCCTATCCAAACTTTTCCCCGGAACAAGATTAGGACCGCAAAGTACACACCGCTCTCTTTC GTGCCCAAGAACCTGTGGTTCCAGTTCCACAATGTGGCCAACATATTTTTCCTTTTCCTCGTCATTCTCGGTATA TTTCCCATTTTCGGCGGCGTCAACCCCGGTCTCAACGCCGTCCCCCTCATCTTCATCATCGTCGTCACCGCAATC AAGGACGCAGTCGAGGATTACCGACGTACCGTTCTCGACAACGAACTCAACAATGCCCCCGTCCACCGATTGTCG CATTGGAACAATGTCAATGTCGAGGAGGGGACCGTCTCGTCCTGGAGGAGGTTTAAAAAGGCCAACACGAGACTG TTTGGCTCCATGTGGCATGCCATCGAGAGTTTGTGGTCCCAAAAGGCCAGGACGGCCAGGGCTGAGCGCAAGGCG CGCAAGCTGCAAGAGGCAGACCCGGAGGACGAGGTTCGCCCATCGGTCGAGACGACACGCACCAGAATGTCGGTC CGTGAGGCTCTCTCCTCGCCCTTCAGCCACGAATCGTTCAAGTCCGCCGATGACGACATCCCCATGACCCCCGTC GGCTCACCCAAAGCCGTCGGCGACCTGCCCACCCTCGAGCTGCCCGACGACCAAGACGCCAAGCGCGCCGCGTCG CTGCGGTCCATGAAGTCCGATCTCGTCAACTACCGCCGCGCTCCGGAGGGGGCAAAGTTCAAAAAGGACACCTGG AAGAGCATCCAGGTCGGCGACTTCGTGCGAATCTACAACGACGACGAGCTGCCCGCCGACGTCATCATCCTGTCC ACCTCGGACCCCGACGGCGCCTGCTACGTCGAGACGAAGAACCTGGACGGTGAGACGAATCTCAAGGTTCGTCAG GCTCTCCGCTGCGGCCGCACCCTCAAGCACGCCCGAGACTGCGAGAGGGCCGAGTTCCACATCCAGAGCGAGCCG CCGCAGCCCAATCTTTACAAGTACAACGGCGCCATCCACTGGAAGCAAAGGGTCCCCGGCTGTCCCGAGGACGAG CCGGCCAACATGACGGAGCCCATCACCATCGACAACCTGCTTCTTCGCGGCTGTAACCTACGCAACACCGAGTGG GTGCTCGGCGTCGTCATCTTCACTGGACACGACACAAAGATCATGATGAACGCCGGCATCACCCCCAGCAAGCGC TCGAGGATCGCCCGCGAGATGAACTTCAACGTCGTTTGTAACTTTGGCATCCTGCTCATCATGTGCCTGCTGTCG GGCATCTTCAACGGCGTCGCTTGGTCCAAGACGGACGCCTCGCTGCATTTTTTCGACTTTGGTTCCATCGGCGGC AGCGCCGCTATGAGCGGCTTCATCACCTTCTGGGCCGCCATCATTGTCTTCCAGAACCTGGTGCCCATCTCCCTC TACATCACGCTCGAGATTGTCCGCACGCTACAGGCCGTTCTCATCTTCAGCGACATCGACATGTACTACGCCAAG ATCGACCAACCGTGCATCCCCAAGTCGTGGAACATCTCCGATGACGTCGGCCAGATCGAATACATCTTTTCCGAC AAGACTGGCACGCTCACGCAGAACGTCATGGAGTTCAAGAAGGCCTCCATCAACGGCCAGCCCTACGGTGAGGCC TTCACGGAGGCGCAGGCTGGTATGCAGAAACGACTCGGCGTCGACGTGGTGGCCGAGGCGGCCAGGATCGAGACC GAGATTGCCGAGGCCAAAGTCAAAGCACTGGCCGGTCTGCGGAAGCTGTACGACAACCCGTACCTTCACGACGGC AGCGTCACCTTCATCGCCCCCGACTTCGTCTCCGACCTGGCGGGCCTAGGCGGGCCCCAGCAGCAGGCGGCTAAC GAGGAGTTTATGCTCGCGCTGTCTCTGTGCCACACGGTCATCGCCGAGAGATCGCCCGGCGACCCACCGAGCATG AACTTCAAGGCGCAGTCGCCCGACGAGGAGGCCCTGGTCGCCACCGCCCGCGACATGGGCTTCACCGTAATCAGC AACAACAGCGACGGCATCGACCTGAACGTACTGGGCCAGGACCGCCACTACCCGATCCTCAATACGATTGAGTTC AACTCGAGCAGGAAGCGGATGAGCTCCATCGTGCGCATGCCCGACGGCCAGATCGTCCTCTACTGCAAGGGCGCC GACTCGGTCATCTACTCGCGCCTCAAGCGGGGCGAGCAGCAGCAGCTGCGGCGCCAGACGGCGGAGCAACTCGAG ATGTTCGCCCGCGAAGGTCTTCGGACGCTCTGCATCGCGCGCAAGACACTGACGGAGAAGGAGTACGAGATGTGG AAGAAGGAGCACGACGCGGCGGCGTCGGCGCTCGAGAACCGCGAGGAGAAATTGGAGACGGTGGCAGAGCTCATC GAGCAGGACCTGATGCTACTGGGCGGCACGGCCATCGAAGATCGCCTGCAGGACGGCGTGCCCGACACCATCGCC CTCCTCGGCCAGGCCGGCATGAAGCTGTGGGTGCTGACGGGCGACAAGGTCGAGACGGCCATCAACATCGGCTTC TCGTGCAATCTGCTCAACAACGACATGGAGCTGATCCACCTCAAGCTCGACGAGGACGAGACGGGCGAGACGAGC GACGAGACGTTCCTGGGCACGACGGAGAAGCTTCTGGAGCAGAACCTGCAGATGTTTGATCTGGTCGGCGACGAC AGCGACCTTGCGGCGGCGAGGAAGAACCACGAGCCGCCGGCGCCGACGCACGGCCTCGTCATCGATGGCTTCACC CTCCGCTGGGCCCTCAACGACCGGCTGCGGCAAAAGTTTCTGCTGCTGTGCAAGCAGTGCAAGTCGGTGCTGTGC TGCCGCGTCAGCCCCGCGCAAAAGGCGGCCGTCGTGGCCATGGTCAAGACGGGGCTGGACGTGATGACGCTGTCG ATTGGCGACGGTGCCAACGACGTGGCCATGATCCAAGAGGCCGACGTGGGCGTCGGTATCGCTGGTGTCGAGGGT CGACAGGCGGCCATGTCGTCCGACTACGCCATTGCCCAGTTCCGCTTCCTGCAGAGGCTGATGCTGGTGCACGGC CGGTGGGACTACCGGCGGCTGGCGGAGAGTATCGCCAACTTCTTCTACAAGAACGTGGTCTGGACCTTTGCCATC TTCTGGTTCGAGATCTTCTGCGACTTCGACATCACCTACCCCTTCGACTACACCTACATTCTCCTGTTCAACCTC ATCTTCACGTCGCTCCCCGTCGGCATCATGGGCGTGCTCGACCAGGACGTCTCGGACAAGGTGTCGCTGGCCGTG CCTCAGCTGTACCGAAGGGGTATCGAACGGCTGGAGTGGACGCACAGCAAGTTTTGGTTTTACATGGTCGACGGC CTCTACCAGTCCGTCATGGTCTTCTTCATCCCATACCTGCTGTTCGTTCCGGCCCAGCCGGTCAGCTTCTCCGGG CTCGGCCTCGAGGATAGGCTTCGGTTCGGCGCCTACGTGGCGCATCCCGCCGTGGTGACGATCAACGCCTACATC CTGATCAACACGTACCGGTGGGATTGGCTGATGCTGCTCGTGGTGAGCCTCAGCGACCTGTCCATCTTCTTCTGG ACGGGCGTCTACTCGTCCTTTGTCTCGTCGGGCTTCTTCTTCAAGACGGCGGCCGAGGTGTACAGCGAGGCCAGC TTCTGGGCCATCTTCTTCATCGTCCCCGTCATCTGCCTCTTCCCGCGCTTCGCCGTCAAGTCGCTGCAGAAGGTC TACTGGCCATACGACGTGGACATTATCCGCGAGCAGGAGAAGATGGGCGCCTTCGCCTACCTGACGGAGGGCAGC GGATCCAGCAACCGGCACGGCAGCGACGGAGGCAGCCAGAAGTCAGGCAGCTCGAAGAAGGCCAAGCACATACTC AGCGGCAGCGTCGACGACGACCTGCGGCCCATCTATCCGCCGTCGACGGCGACGCGGACGACGGCCCACAACCGG ACACAGAACGGCAGCGACTCGACCAACTTTTCGGCCGACGCGTCGCTCGACGCGGCCGTCGCCACGGGCGCTAAT CGGCTATCAGCGGAGGTGGTGCCTCCGGACCGACGGTCGGACGACCGGGTGAGGCCGTCGTACGACCGGATGCGG CCGTCGTACGACCGGATGCGCATGTCAATGGATCGCGTCCGGCCGAGCTTCGAGGCGAGCAGCGATTTCACCTCG GCGGCGCGGCTGCAGCGCATCGAGTCGACGCAAAATGTCGGCTTTAAGGCCAGACTCCGAGGCCTGTCGCTGACC AAGAACGCGGCGGCGAACTCGCCGCTGAGCCCGCGTTCTCCGCGGTCGCCGAGGACGCGGCGCTAA |
Gene | >Ophio5|2334 ATGACCACGGCCAATGGCTCCGGGCCTGGCGCCGACGGCAATCCGCCAAAGATTGAGCGCCCCCATCGGACACGC TGGGCCACTCGAAAGATGACCATCAAAAGCGGTCGCTCCAAGCGTCTGTCGCTTCTCAACCGCATGCAACAACGG AAACGCGCATCCAACGAGAAGCCCTCGGCCGGCGACACCTCGGAGCCGCCCCTGACGGACCGCAGTAGCGAAGAC GGTTCTGATACCTCATCTCAATCGGAAGACAACGGCCGCACCCTCTACTTCAATCTGCCTCTTCCCGACGACCTG CTGAGCGACGGCCATCCTATCCAAACTTTTCCCCGGAACAAGATTAGGACCGCAAAGTACACACCGCTCTCTTTC GTGCCCAAGAACCTGTGGTTCCAGTTCCACAATGTGGCCAACATATTTTTCCTTTTCCTCGTCATTCTCGGTGTG AGTAAATCCTTGTCCTCCCCCTGAACCCCTCGCCTCGCCTCGTCTCGTCCCGCACCCATTGCCGTCGGCCGGATC GTTAATCCTCCCCTTTTCCGCAGATATTTCCCATTTTCGGCGGCGTCAACCCCGGTCTCAACGCCGTCCCCCTCA TCTTCATCATCGTCGTCACCGCAATCAAGGACGCAGTCGAGGATTACCGACGTACCGTTCTCGACAACGAACTCA ACAATGCCCCCGTCCACCGATTGTCGCATTGGAACAATGTCAATGTCGAGGAGGGGACCGTCTCGTCCTGGAGGA GGTTTAAAAAGGCCAACACGAGACTGTTTGGCTCCATGTGGCATGCCATCGAGAGTTTGTGGTCCCAAAAGGCCA GGACGGCCAGGGCTGAGCGCAAGGCGCGCAAGCTGCAAGAGGCAGACCCGGAGGACGAGGTTCGCCCATCGGTCG AGACGACACGCACCAGAATGTCGGTCCGTGAGGCTCTCTCCTCGCCCTTCAGCCACGAATCGTTCAAGTCCGCCG ATGACGACATCCCCATGACCCCCGTCGGCTCACCCAAAGCCGTCGGCGACCTGCCCACCCTCGAGCTGCCCGACG ACCAAGACGCCAAGCGCGCCGCGTCGCTGCGGTCCATGAAGTCCGATCTCGTCAACTACCGCCGCGCTCCGGAGG GGGCAAAGTTCAAAAAGGACACCTGGAAGAGCATCCAGGTCGGCGACTTCGTGCGAATCTACAACGACGACGAGC TGCCCGCCGACGTCATCATCCTGTCCACCTCGGACCCCGACGGCGCCTGCTACGTCGAGACGAAGAACCTGGACG GTGAGACGAATCTCAAGGTTCGTCAGGCTCTCCGCTGCGGCCGCACCCTCAAGCACGCCCGAGACTGCGAGAGGG CCGAGTTCCACATCCAGAGCGAGCCGCCGCAGCCCAATCTTTACAAGTACAACGGCGCCATCCACTGGAAGCAAA GGGTCCCCGGCTGTCCCGAGGACGAGCCGGCCAACATGACGGAGCCCATCACCATCGACAACCTGCTTCTTCGCG GCTGTAACCTACGCAACACCGAGTGGGTGCTCGGCGTCGTCATCTTCACTGGACACGACACAAAGATCATGATGA ACGCCGGCATCACCCCCAGCAAGCGCTCGAGGATCGCCCGCGAGATGAACTTCAACGTCGTTTGTAACTTTGGCA TCCTGCTCATCATGTGCCTGCTGTCGGGCATCTTCAACGGCGTCGCTTGGTCCAAGACGGACGCCTCGCTGCATT TTTTCGACTTTGGTTCCATCGGCGGCAGCGCCGCTATGAGCGGCTTCATCACCTTCTGGGCCGCCATCATTGTCT TCCAGAACCTGGTGCCCATCTCCCTCTACATCACGCTCGAGATTGTCCGCACGCTACAGGCCGTTCTCATCTTCA GCGACATCGACATGTACTACGCCAAGATCGACCAACCGTGCATCCCCAAGTCGTGGAACATCTCCGATGACGTCG GCCAGATCGAATACATCTTTTCCGACAAGACTGGCACGCTCACGCAGAACGTCATGGAGTTCAAGAAGGCCTCCA TCAACGGCCAGCCCTACGGTGAGGCCTTCACGGAGGCGCAGGCTGGTATGCAGAAACGACTCGGCGTCGACGTGG TGGCCGAGGCGGCCAGGATCGAGACCGAGATTGCCGAGGCCAAAGTCAAAGCACTGGCCGGTCTGCGGAAGCTGT ACGACAACCCGTACCTTCACGACGGCAGCGTCACCTTCATCGCCCCCGACTTCGTCTCCGACCTGGCGGGCCTAG GCGGGCCCCAGCAGCAGGCGGCTAACGAGGAGTTTATGCTCGCGCTGTCTCTGTGCCACACGGTCATCGCCGAGA GATCGCCCGGCGACCCACCGAGCATGAACTTCAAGGCGCAGTCGCCCGACGAGGAGGCCCTGGTCGCCACCGCCC GCGACATGGGCTTCACCGTAATCAGCAACAACAGCGACGGCATCGACCTGAACGTACTGGGCCAGGACCGCCACT ACCCGATCCTCAATACGATTGAGTTCAACTCGAGCAGGAAGCGGATGAGCTCCATCGTGCGCATGCCCGACGGCC AGATCGTCCTCTACTGCAAGGGCGCCGACTCGGTCATCTACTCGCGCCTCAAGCGGGGCGAGCAGCAGCAGCTGC GGCGCCAGACGGCGGAGCAACTCGAGATGTTCGCCCGCGAAGGTCTTCGGACGCTCTGCATCGCGCGCAAGACAC TGACGGAGAAGGAGTACGAGATGTGGAAGAAGGAGCACGACGCGGCGGCGTCGGCGCTCGAGAACCGCGAGGAGA AATTGGAGACGGTGGCAGAGCTCATCGAGCAGGACCTGATGCTACTGGGCGGCACGGCCATCGAAGATCGCCTGC AGGACGGCGTGCCCGACACCATCGCCCTCCTCGGCCAGGCCGGCATGAAGCTGTGGGTGCTGACGGGCGACAAGG TCGAGACGGCCATCAACATCGGCTTCTCGTGCAATCTGCTCAACAACGACATGGAGCTGATCCACCTCAAGCTCG ACGAGGACGAGACGGGCGAGACGAGCGACGAGACGTTCCTGGGCACGACGGAGAAGCTTCTGGAGCAGAACCTGC AGATGTTTGATCTGGTCGGCGACGACAGCGACCTTGCGGCGGCGAGGAAGAACCACGAGCCGCCGGCGCCGACGC ACGGCCTCGTCATCGATGGCTTCACCCTCCGCTGGGCCCTCAACGACCGGCTGCGGCAAAAGTTTCTGCTGCTGT GCAAGCAGTGCAAGTCGGTGCTGTGCTGCCGCGTCAGCCCCGCGCAAAAGGCGGCCGTCGTGGCCATGGTCAAGA CGGGGCTGGACGTGATGACGCTGTCGATTGGCGACGGTGCCAACGACGTGGCCATGATCCAAGAGGCCGACGTGG GCGTCGGTATCGCTGGTGTCGAGGGTCGACAGGCGGCCATGTCGTCCGACTACGCCATTGCCCAGTTCCGCTTCC TGCAGAGGCTGATGCTGGTGCACGGCCGGTGGGACTACCGGCGGCTGGCGGAGAGTATCGCCAACTTCTTCTACA AGAACGTGGTCTGGACCTTTGCCATCTTCTGGTTCGAGATCTTCTGCGACTTCGACATCACCTACCCCTTCGACT ACACCTACATTCTCCTGTTCAACCTCATCTTCACGTCGCTCCCCGTCGGCATCATGGGCGTGCTCGACCAGGACG TCTCGGACAAGGTGTCGCTGGCCGTGCCTCAGCTGTACCGAAGGGGTATCGAACGGCTGGAGTGGACGCACAGCA AGTTTTGGTGAGTGCAGAGACGGACCCCGATTCTCTAACCTGCGGCGGCTAACGAAAGCACAGGTTTTACATGGT CGACGGCCTCTACCAGTCCGTCATGGTCTTCTTCATCCCATACCTGCTGTTCGTTCCGGCCCAGCCGGTCAGCTT CTCCGGGCTCGGCCTCGAGGATAGGCTTCGGTTCGGCGCCTACGTGGCGCATCCCGCCGTGGTGACGATCAACGC CTACATCCTGATCAACACGTACCGGTGGGATTGGCTGATGCTGCTCGTGGTGAGCCTCAGCGACCTGTCCATCTT CTTCTGGACGGGCGTCTACTCGTCCTTTGTCTCGTCGGGCTTCTTCTTCAAGACGGCGGCCGAGGTGTACAGCGA GGCCAGCTTCTGGGCCATCTTCTTCATCGTCCCCGTCATCTGCCTCTTCCCGCGCTTCGCCGTCAAGTCGCTGCA GAAGGTCTACTGGCCATACGACGTGGACATTATCCGCGAGCAGGAGAAGATGGGCGCCTTCGCCTACCTGACGGA GGGCAGCGGATCCAGCAACCGGCACGGCAGCGACGGAGGCAGCCAGAAGTCAGGCAGCTCGAAGAAGGCCAAGCA CATACTCAGCGGCAGCGTCGACGACGACCTGCGGCCCATCTATCCGCCGTCGACGGCGACGCGGACGACGGCCCA CAACCGGACACAGAACGGCAGCGACTCGACCAACTTTTCGGCCGACGCGTCGCTCGACGCGGCCGTCGCCACGGG CGCTAATCGGCTATCAGCGGAGGTGGTGCCTCCGGACCGACGGTCGGACGACCGGGTGAGGCCGTCGTACGACCG GATGCGGCCGTCGTACGACCGGATGCGCATGTCAATGGATCGCGTCCGGCCGAGCTTCGAGGCGAGCAGCGATTT CACCTCGGCGGCGCGGCTGCAGCGCATCGAGTCGACGCAAAATGTCGGCTTTAAGGCCAGACTCCGAGGCCTGTC GCTGACCAAGAACGCGGCGGCGAACTCGCCGCTGAGCCCGCGTTCTCCGCGGTCGCCGAGGACGCGGCGCTAA |