Protein ID | Ophio5|5222 |
Gene name | |
Location | scaffold_420:14661..18470 |
Strand | + |
Gene length (bp) | 3809 |
Transcript length (bp) | 3753 |
Coding sequence length (bp) | 3750 |
Protein length (aa) | 1250 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF16212 | PhoLip_ATPase_C | Phospholipid-translocating P-type ATPase C-terminal | 1.4E-57 | 1082 | 1249 |
PF16209 | PhoLip_ATPase_N | Phospholipid-translocating ATPase N-terminal | 1.3E-21 | 84 | 140 |
PF00702 | Hydrolase | haloacid dehalogenase-like hydrolase | 1.1E-07 | 480 | 990 |
PF13246 | Cation_ATPase | Cation transport ATPase (P-type) | 1.0E-09 | 625 | 708 |
PF00122 | E1-E2_ATPase | E1-E2 ATPase | 1.5E-09 | 226 | 435 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q12674|ATC8_YEAST | Probable phospholipid-transporting ATPase DNF3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF3 PE=1 SV=1 | 49 | 1248 | 0.0E+00 |
sp|Q9UT43|YFRD_SCHPO | Putative phospholipid-transporting ATPase C821.13c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC821.13c PE=1 SV=2 | 7 | 1250 | 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 | 53 | 709 | 6.0E-97 |
sp|Q9Y2Q0|AT8A1_HUMAN | Phospholipid-transporting ATPase IA OS=Homo sapiens GN=ATP8A1 PE=1 SV=1 | 87 | 709 | 4.0E-92 |
sp|P70704|AT8A1_MOUSE | Phospholipid-transporting ATPase IA OS=Mus musculus GN=Atp8a1 PE=1 SV=2 | 87 | 709 | 1.0E-91 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|Q12674|ATC8_YEAST | Probable phospholipid-transporting ATPase DNF3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF3 PE=1 SV=1 | 49 | 1248 | 0.0E+00 |
sp|Q9UT43|YFRD_SCHPO | Putative phospholipid-transporting ATPase C821.13c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC821.13c PE=1 SV=2 | 7 | 1250 | 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 | 53 | 709 | 6.0E-97 |
sp|Q9Y2Q0|AT8A1_HUMAN | Phospholipid-transporting ATPase IA OS=Homo sapiens GN=ATP8A1 PE=1 SV=1 | 87 | 709 | 4.0E-92 |
sp|P70704|AT8A1_MOUSE | Phospholipid-transporting ATPase IA OS=Mus musculus GN=Atp8a1 PE=1 SV=2 | 87 | 709 | 1.0E-91 |
sp|Q9LVK9|ALA7_ARATH | Probable phospholipid-transporting ATPase 7 OS=Arabidopsis thaliana GN=ALA7 PE=3 SV=3 | 87 | 709 | 4.0E-91 |
sp|C7EXK4|AT8A2_BOVIN | Phospholipid-transporting ATPase IB OS=Bos taurus GN=ATP8A2 PE=1 SV=4 | 85 | 718 | 4.0E-90 |
sp|Q9NTI2|AT8A2_HUMAN | Phospholipid-transporting ATPase IB OS=Homo sapiens GN=ATP8A2 PE=1 SV=2 | 85 | 718 | 2.0E-89 |
sp|Q9SLK6|ALA6_ARATH | Phospholipid-transporting ATPase 6 OS=Arabidopsis thaliana GN=ALA6 PE=1 SV=2 | 87 | 712 | 2.0E-89 |
sp|Q9SX33|ALA9_ARATH | Putative phospholipid-transporting ATPase 9 OS=Arabidopsis thaliana GN=ALA9 PE=3 SV=1 | 41 | 709 | 5.0E-89 |
sp|P98200|AT8A2_MOUSE | Phospholipid-transporting ATPase IB OS=Mus musculus GN=Atp8a2 PE=1 SV=1 | 85 | 718 | 2.0E-88 |
sp|Q9LK90|ALA8_ARATH | Probable phospholipid-transporting ATPase 8 OS=Arabidopsis thaliana GN=ALA8 PE=3 SV=1 | 87 | 709 | 3.0E-88 |
sp|Q9LNQ4|ALA4_ARATH | Probable phospholipid-transporting ATPase 4 OS=Arabidopsis thaliana GN=ALA4 PE=3 SV=2 | 75 | 709 | 5.0E-88 |
sp|Q9SGG3|ALA5_ARATH | Probable phospholipid-transporting ATPase 5 OS=Arabidopsis thaliana GN=ALA5 PE=3 SV=1 | 75 | 709 | 6.0E-88 |
sp|O94296|YOOC_SCHPO | Probable phospholipid-transporting ATPase C887.12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC887.12 PE=3 SV=1 | 15 | 709 | 8.0E-88 |
sp|P57792|ALA12_ARATH | Probable phospholipid-transporting ATPase 12 OS=Arabidopsis thaliana GN=ALA12 PE=2 SV=1 | 87 | 709 | 2.0E-87 |
sp|Q9U280|TAT1_CAEEL | Phospholipid-transporting ATPase tat-1 OS=Caenorhabditis elegans GN=tat-1 PE=3 SV=3 | 775 | 1250 | 1.0E-86 |
sp|Q9LI83|ALA10_ARATH | Phospholipid-transporting ATPase 10 OS=Arabidopsis thaliana GN=ALA10 PE=3 SV=1 | 87 | 709 | 3.0E-86 |
sp|Q9XIE6|ALA3_ARATH | Phospholipid-transporting ATPase 3 OS=Arabidopsis thaliana GN=ALA3 PE=1 SV=2 | 87 | 709 | 4.0E-86 |
sp|Q9SAF5|ALA11_ARATH | Probable phospholipid-transporting ATPase 11 OS=Arabidopsis thaliana GN=ALA11 PE=2 SV=1 | 87 | 709 | 2.0E-85 |
sp|P70704|AT8A1_MOUSE | Phospholipid-transporting ATPase IA OS=Mus musculus GN=Atp8a1 PE=1 SV=2 | 843 | 1243 | 9.0E-85 |
sp|Q29449|AT8A1_BOVIN | Probable phospholipid-transporting ATPase IA OS=Bos taurus GN=ATP8A1 PE=1 SV=2 | 843 | 1243 | 1.0E-84 |
sp|Q9Y2Q0|AT8A1_HUMAN | Phospholipid-transporting ATPase IA OS=Homo sapiens GN=ATP8A1 PE=1 SV=1 | 843 | 1243 | 3.0E-84 |
sp|Q9NTI2|AT8A2_HUMAN | Phospholipid-transporting ATPase IB OS=Homo sapiens GN=ATP8A2 PE=1 SV=2 | 773 | 1212 | 5.0E-84 |
sp|C7EXK4|AT8A2_BOVIN | Phospholipid-transporting ATPase IB OS=Bos taurus GN=ATP8A2 PE=1 SV=4 | 773 | 1212 | 2.0E-83 |
sp|Q5BL50|AT8B1_XENTR | Phospholipid-transporting ATPase IC OS=Xenopus tropicalis GN=atp8b1 PE=2 SV=1 | 73 | 709 | 8.0E-83 |
sp|P39524|ATC3_YEAST | Probable phospholipid-transporting ATPase DRS2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DRS2 PE=1 SV=2 | 844 | 1213 | 9.0E-83 |
sp|Q9LNQ4|ALA4_ARATH | Probable phospholipid-transporting ATPase 4 OS=Arabidopsis thaliana GN=ALA4 PE=3 SV=2 | 844 | 1244 | 3.0E-82 |
sp|Q9SGG3|ALA5_ARATH | Probable phospholipid-transporting ATPase 5 OS=Arabidopsis thaliana GN=ALA5 PE=3 SV=1 | 844 | 1244 | 3.0E-82 |
sp|P98200|AT8A2_MOUSE | Phospholipid-transporting ATPase IB OS=Mus musculus GN=Atp8a2 PE=1 SV=1 | 773 | 1212 | 4.0E-82 |
sp|O94296|YOOC_SCHPO | Probable phospholipid-transporting ATPase C887.12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC887.12 PE=3 SV=1 | 845 | 1200 | 8.0E-82 |
sp|P98198|AT8B2_HUMAN | Phospholipid-transporting ATPase ID OS=Homo sapiens GN=ATP8B2 PE=1 SV=2 | 87 | 713 | 4.0E-80 |
sp|P98199|AT8B2_MOUSE | Phospholipid-transporting ATPase ID OS=Mus musculus GN=Atp8b2 PE=2 SV=2 | 87 | 709 | 2.0E-79 |
sp|Q9LVK9|ALA7_ARATH | Probable phospholipid-transporting ATPase 7 OS=Arabidopsis thaliana GN=ALA7 PE=3 SV=3 | 844 | 1244 | 4.0E-79 |
sp|Q9GKS6|AT10D_MACFA | Probable phospholipid-transporting ATPase VD (Fragment) OS=Macaca fascicularis GN=ATP10D PE=2 SV=1 | 844 | 1187 | 9.0E-79 |
sp|Q6UQ17|AT8B3_MOUSE | Phospholipid-transporting ATPase IK OS=Mus musculus GN=Atp8b3 PE=1 SV=1 | 83 | 710 | 1.0E-78 |
sp|O94823|AT10B_HUMAN | Probable phospholipid-transporting ATPase VB OS=Homo sapiens GN=ATP10B PE=2 SV=2 | 824 | 1245 | 7.0E-78 |
sp|Q9P241|AT10D_HUMAN | Probable phospholipid-transporting ATPase VD OS=Homo sapiens GN=ATP10D PE=2 SV=3 | 844 | 1235 | 8.0E-78 |
sp|Q9XIE6|ALA3_ARATH | Phospholipid-transporting ATPase 3 OS=Arabidopsis thaliana GN=ALA3 PE=1 SV=2 | 845 | 1250 | 9.0E-78 |
sp|Q9SLK6|ALA6_ARATH | Phospholipid-transporting ATPase 6 OS=Arabidopsis thaliana GN=ALA6 PE=1 SV=2 | 844 | 1244 | 2.0E-77 |
sp|Q8K2X1|AT10D_MOUSE | Probable phospholipid-transporting ATPase VD OS=Mus musculus GN=Atp10d PE=2 SV=2 | 841 | 1187 | 2.0E-77 |
sp|O36028|ATCZ_SCHPO | Putative phospholipid-transporting ATPase C4F10.16c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC4F10.16c PE=3 SV=1 | 89 | 709 | 8.0E-77 |
sp|P98204|ALA1_ARATH | Phospholipid-transporting ATPase 1 OS=Arabidopsis thaliana GN=ALA1 PE=2 SV=1 | 81 | 703 | 2.0E-76 |
sp|Q8TF62|AT8B4_HUMAN | Probable phospholipid-transporting ATPase IM OS=Homo sapiens GN=ATP8B4 PE=1 SV=3 | 87 | 709 | 2.0E-76 |
sp|A3FIN4|AT8B5_MOUSE | Phospholipid-transporting ATPase FetA OS=Mus musculus GN=Atp8b5 PE=2 SV=1 | 87 | 716 | 2.0E-76 |
sp|O60423|AT8B3_HUMAN | Phospholipid-transporting ATPase IK OS=Homo sapiens GN=ATP8B3 PE=2 SV=4 | 87 | 709 | 2.0E-75 |
sp|Q9LK90|ALA8_ARATH | Probable phospholipid-transporting ATPase 8 OS=Arabidopsis thaliana GN=ALA8 PE=3 SV=1 | 844 | 1212 | 1.0E-74 |
sp|Q9LI83|ALA10_ARATH | Phospholipid-transporting ATPase 10 OS=Arabidopsis thaliana GN=ALA10 PE=3 SV=1 | 844 | 1249 | 1.0E-74 |
sp|O54827|AT10A_MOUSE | Probable phospholipid-transporting ATPase VA OS=Mus musculus GN=Atp10a PE=1 SV=4 | 845 | 1247 | 1.0E-74 |
sp|P98198|AT8B2_HUMAN | Phospholipid-transporting ATPase ID OS=Homo sapiens GN=ATP8B2 PE=1 SV=2 | 827 | 1242 | 2.0E-74 |
sp|O36028|ATCZ_SCHPO | Putative phospholipid-transporting ATPase C4F10.16c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC4F10.16c PE=3 SV=1 | 835 | 1250 | 3.0E-73 |
sp|Q8TF62|AT8B4_HUMAN | Probable phospholipid-transporting ATPase IM OS=Homo sapiens GN=ATP8B4 PE=1 SV=3 | 845 | 1240 | 3.0E-73 |
sp|P32660|ATC5_YEAST | Phospholipid-transporting ATPase DNF1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF1 PE=1 SV=2 | 845 | 1250 | 4.0E-73 |
sp|P57792|ALA12_ARATH | Probable phospholipid-transporting ATPase 12 OS=Arabidopsis thaliana GN=ALA12 PE=2 SV=1 | 845 | 1212 | 1.0E-72 |
sp|Q9SAF5|ALA11_ARATH | Probable phospholipid-transporting ATPase 11 OS=Arabidopsis thaliana GN=ALA11 PE=2 SV=1 | 845 | 1245 | 1.0E-72 |
sp|O60312|AT10A_HUMAN | Probable phospholipid-transporting ATPase VA OS=Homo sapiens GN=ATP10A PE=2 SV=2 | 845 | 1247 | 2.0E-72 |
sp|Q12675|ATC4_YEAST | Phospholipid-transporting ATPase DNF2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF2 PE=1 SV=1 | 833 | 1218 | 3.0E-72 |
sp|P98199|AT8B2_MOUSE | Phospholipid-transporting ATPase ID OS=Mus musculus GN=Atp8b2 PE=2 SV=2 | 824 | 1242 | 6.0E-72 |
sp|Q9SX33|ALA9_ARATH | Putative phospholipid-transporting ATPase 9 OS=Arabidopsis thaliana GN=ALA9 PE=3 SV=1 | 845 | 1200 | 3.0E-71 |
sp|Q5BL50|AT8B1_XENTR | Phospholipid-transporting ATPase IC OS=Xenopus tropicalis GN=atp8b1 PE=2 SV=1 | 773 | 1218 | 3.0E-71 |
sp|P32660|ATC5_YEAST | Phospholipid-transporting ATPase DNF1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF1 PE=1 SV=2 | 87 | 709 | 3.0E-71 |
sp|A3FIN4|AT8B5_MOUSE | Phospholipid-transporting ATPase FetA OS=Mus musculus GN=Atp8b5 PE=2 SV=1 | 845 | 1229 | 6.0E-70 |
sp|Q9Y2G3|AT11B_HUMAN | Probable phospholipid-transporting ATPase IF OS=Homo sapiens GN=ATP11B PE=1 SV=2 | 87 | 720 | 6.0E-70 |
sp|P98204|ALA1_ARATH | Phospholipid-transporting ATPase 1 OS=Arabidopsis thaliana GN=ALA1 PE=2 SV=1 | 845 | 1212 | 1.0E-69 |
sp|Q9N0Z4|AT11B_RABIT | Probable phospholipid-transporting ATPase IF (Fragment) OS=Oryctolagus cuniculus GN=ATP11B PE=1 SV=2 | 87 | 720 | 3.0E-69 |
sp|Q09891|ATCX_SCHPO | Putative phospholipid-transporting ATPase C24B11.12c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC24B11.12c PE=3 SV=1 | 845 | 1212 | 5.0E-69 |
sp|Q148W0|AT8B1_MOUSE | Phospholipid-transporting ATPase IC OS=Mus musculus GN=Atp8b1 PE=1 SV=2 | 846 | 1197 | 7.0E-69 |
sp|O43520|AT8B1_HUMAN | Phospholipid-transporting ATPase IC OS=Homo sapiens GN=ATP8B1 PE=1 SV=3 | 846 | 1197 | 2.0E-68 |
sp|P98205|ALA2_ARATH | Phospholipid-transporting ATPase 2 OS=Arabidopsis thaliana GN=ALA2 PE=1 SV=1 | 846 | 1246 | 7.0E-68 |
sp|P98196|AT11A_HUMAN | Probable phospholipid-transporting ATPase IH OS=Homo sapiens GN=ATP11A PE=1 SV=3 | 87 | 727 | 1.0E-67 |
sp|Q9Y2G3|AT11B_HUMAN | Probable phospholipid-transporting ATPase IF OS=Homo sapiens GN=ATP11B PE=1 SV=2 | 819 | 1249 | 8.0E-67 |
sp|Q148W0|AT8B1_MOUSE | Phospholipid-transporting ATPase IC OS=Mus musculus GN=Atp8b1 PE=1 SV=2 | 74 | 513 | 8.0E-66 |
sp|Q9P241|AT10D_HUMAN | Probable phospholipid-transporting ATPase VD OS=Homo sapiens GN=ATP10D PE=2 SV=3 | 24 | 507 | 2.0E-65 |
sp|Q8K2X1|AT10D_MOUSE | Probable phospholipid-transporting ATPase VD OS=Mus musculus GN=Atp10d PE=2 SV=2 | 65 | 564 | 4.0E-65 |
sp|Q29449|AT8A1_BOVIN | Probable phospholipid-transporting ATPase IA OS=Bos taurus GN=ATP8A1 PE=1 SV=2 | 87 | 505 | 3.0E-64 |
sp|O43520|AT8B1_HUMAN | Phospholipid-transporting ATPase IC OS=Homo sapiens GN=ATP8B1 PE=1 SV=3 | 74 | 513 | 4.0E-64 |
sp|Q09891|ATCX_SCHPO | Putative phospholipid-transporting ATPase C24B11.12c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC24B11.12c PE=3 SV=1 | 225 | 709 | 2.0E-63 |
sp|P98196|AT11A_HUMAN | Probable phospholipid-transporting ATPase IH OS=Homo sapiens GN=ATP11A PE=1 SV=3 | 850 | 1249 | 3.0E-63 |
sp|O94823|AT10B_HUMAN | Probable phospholipid-transporting ATPase VB OS=Homo sapiens GN=ATP10B PE=2 SV=2 | 87 | 526 | 1.0E-62 |
sp|Q9N0Z4|AT11B_RABIT | Probable phospholipid-transporting ATPase IF (Fragment) OS=Oryctolagus cuniculus GN=ATP11B PE=1 SV=2 | 819 | 1249 | 1.0E-61 |
sp|Q12675|ATC4_YEAST | Phospholipid-transporting ATPase DNF2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF2 PE=1 SV=1 | 201 | 709 | 5.0E-61 |
sp|Q9QZW0|AT11C_MOUSE | Phospholipid-transporting ATPase 11C OS=Mus musculus GN=Atp11c PE=1 SV=2 | 845 | 1249 | 5.0E-61 |
sp|O54827|AT10A_MOUSE | Probable phospholipid-transporting ATPase VA OS=Mus musculus GN=Atp10a PE=1 SV=4 | 90 | 507 | 6.0E-61 |
sp|P98197|AT11A_MOUSE | Probable phospholipid-transporting ATPase IH OS=Mus musculus GN=Atp11a PE=1 SV=1 | 850 | 1249 | 8.0E-61 |
sp|Q8NB49|AT11C_HUMAN | Phospholipid-transporting ATPase IG OS=Homo sapiens GN=ATP11C PE=1 SV=3 | 845 | 1249 | 2.0E-60 |
sp|Q9U280|TAT1_CAEEL | Phospholipid-transporting ATPase tat-1 OS=Caenorhabditis elegans GN=tat-1 PE=3 SV=3 | 60 | 541 | 7.0E-60 |
sp|O60312|AT10A_HUMAN | Probable phospholipid-transporting ATPase VA OS=Homo sapiens GN=ATP10A PE=2 SV=2 | 82 | 507 | 9.0E-59 |
sp|O43861|ATP9B_HUMAN | Probable phospholipid-transporting ATPase IIB OS=Homo sapiens GN=ATP9B PE=2 SV=4 | 790 | 1213 | 6.0E-57 |
sp|F1Q4S1|ATP9B_DANRE | Probable phospholipid-transporting ATPase IIB OS=Danio rerio GN=atp9b PE=3 SV=1 | 848 | 1213 | 1.0E-56 |
sp|A1A4J6|ATP9B_BOVIN | Probable phospholipid-transporting ATPase IIB OS=Bos taurus GN=ATP9B PE=2 SV=1 | 790 | 1213 | 3.0E-56 |
sp|P98195|ATP9B_MOUSE | Probable phospholipid-transporting ATPase IIB OS=Mus musculus GN=Atp9b PE=1 SV=4 | 790 | 1213 | 3.0E-56 |
sp|D4ABB8|ATP9B_RAT | Probable phospholipid-transporting ATPase IIB OS=Rattus norvegicus GN=Atp9b PE=3 SV=1 | 790 | 1213 | 1.0E-55 |
sp|O60423|AT8B3_HUMAN | Phospholipid-transporting ATPase IK OS=Homo sapiens GN=ATP8B3 PE=2 SV=4 | 846 | 1228 | 2.0E-55 |
sp|O70228|ATP9A_MOUSE | Probable phospholipid-transporting ATPase IIA OS=Mus musculus GN=Atp9a PE=1 SV=3 | 848 | 1213 | 2.0E-55 |
sp|O75110|ATP9A_HUMAN | Probable phospholipid-transporting ATPase IIA OS=Homo sapiens GN=ATP9A PE=1 SV=3 | 848 | 1213 | 2.0E-55 |
sp|P98197|AT11A_MOUSE | Probable phospholipid-transporting ATPase IH OS=Mus musculus GN=Atp11a PE=1 SV=1 | 87 | 506 | 9.0E-55 |
sp|Q8NB49|AT11C_HUMAN | Phospholipid-transporting ATPase IG OS=Homo sapiens GN=ATP11C PE=1 SV=3 | 87 | 518 | 9.0E-55 |
sp|Q9QZW0|AT11C_MOUSE | Phospholipid-transporting ATPase 11C OS=Mus musculus GN=Atp11c PE=1 SV=2 | 72 | 518 | 6.0E-54 |
sp|P40527|ATC7_YEAST | Probable phospholipid-transporting ATPase NEO1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=NEO1 PE=1 SV=1 | 848 | 1207 | 5.0E-50 |
sp|Q10309|YD56_SCHPO | Putative phospholipid-transporting ATPase C6C3.06c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC6C3.06c PE=3 SV=1 | 848 | 1210 | 7.0E-49 |
sp|P40527|ATC7_YEAST | Probable phospholipid-transporting ATPase NEO1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=NEO1 PE=1 SV=1 | 62 | 705 | 2.0E-47 |
sp|O70228|ATP9A_MOUSE | Probable phospholipid-transporting ATPase IIA OS=Mus musculus GN=Atp9a PE=1 SV=3 | 82 | 705 | 7.0E-47 |
sp|O75110|ATP9A_HUMAN | Probable phospholipid-transporting ATPase IIA OS=Homo sapiens GN=ATP9A PE=1 SV=3 | 82 | 705 | 2.0E-46 |
sp|P98195|ATP9B_MOUSE | Probable phospholipid-transporting ATPase IIB OS=Mus musculus GN=Atp9b PE=1 SV=4 | 49 | 750 | 7.0E-46 |
sp|D4ABB8|ATP9B_RAT | Probable phospholipid-transporting ATPase IIB OS=Rattus norvegicus GN=Atp9b PE=3 SV=1 | 49 | 750 | 8.0E-46 |
sp|P98205|ALA2_ARATH | Phospholipid-transporting ATPase 2 OS=Arabidopsis thaliana GN=ALA2 PE=1 SV=1 | 90 | 505 | 2.0E-45 |
sp|F1Q4S1|ATP9B_DANRE | Probable phospholipid-transporting ATPase IIB OS=Danio rerio GN=atp9b PE=3 SV=1 | 38 | 702 | 4.0E-45 |
sp|O43861|ATP9B_HUMAN | Probable phospholipid-transporting ATPase IIB OS=Homo sapiens GN=ATP9B PE=2 SV=4 | 38 | 707 | 9.0E-45 |
sp|A1A4J6|ATP9B_BOVIN | Probable phospholipid-transporting ATPase IIB OS=Bos taurus GN=ATP9B PE=2 SV=1 | 49 | 702 | 1.0E-44 |
sp|Q6UQ17|AT8B3_MOUSE | Phospholipid-transporting ATPase IK OS=Mus musculus GN=Atp8b3 PE=1 SV=1 | 996 | 1198 | 3.0E-42 |
sp|Q10309|YD56_SCHPO | Putative phospholipid-transporting ATPase C6C3.06c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC6C3.06c PE=3 SV=1 | 87 | 529 | 4.0E-38 |
sp|Q29449|AT8A1_BOVIN | Probable phospholipid-transporting ATPase IA OS=Bos taurus GN=ATP8A1 PE=1 SV=2 | 601 | 709 | 8.0E-22 |
sp|Q6UQ17|AT8B3_MOUSE | Phospholipid-transporting ATPase IK OS=Mus musculus GN=Atp8b3 PE=1 SV=1 | 846 | 951 | 1.0E-19 |
sp|O43520|AT8B1_HUMAN | Phospholipid-transporting ATPase IC OS=Homo sapiens GN=ATP8B1 PE=1 SV=3 | 600 | 709 | 1.0E-19 |
sp|Q148W0|AT8B1_MOUSE | Phospholipid-transporting ATPase IC OS=Mus musculus GN=Atp8b1 PE=1 SV=2 | 600 | 781 | 3.0E-19 |
sp|Q9U280|TAT1_CAEEL | Phospholipid-transporting ATPase tat-1 OS=Caenorhabditis elegans GN=tat-1 PE=3 SV=3 | 547 | 748 | 1.0E-15 |
sp|Q10309|YD56_SCHPO | Putative phospholipid-transporting ATPase C6C3.06c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC6C3.06c PE=3 SV=1 | 591 | 705 | 9.0E-14 |
sp|Q9QZW0|AT11C_MOUSE | Phospholipid-transporting ATPase 11C OS=Mus musculus GN=Atp11c PE=1 SV=2 | 591 | 732 | 2.0E-12 |
sp|Q8NB49|AT11C_HUMAN | Phospholipid-transporting ATPase IG OS=Homo sapiens GN=ATP11C PE=1 SV=3 | 602 | 732 | 2.0E-11 |
sp|P98205|ALA2_ARATH | Phospholipid-transporting ATPase 2 OS=Arabidopsis thaliana GN=ALA2 PE=1 SV=1 | 602 | 760 | 8.0E-10 |
sp|P98197|AT11A_MOUSE | Probable phospholipid-transporting ATPase IH OS=Mus musculus GN=Atp11a PE=1 SV=1 | 602 | 743 | 9.0E-10 |
sp|O94823|AT10B_HUMAN | Probable phospholipid-transporting ATPase VB OS=Homo sapiens GN=ATP10B PE=2 SV=2 | 614 | 710 | 2.0E-09 |
sp|Q3TYU2|AT135_MOUSE | Probable cation-transporting ATPase 13A5 OS=Mus musculus GN=Atp13a5 PE=2 SV=2 | 889 | 1078 | 3.0E-09 |
sp|Q9GKS6|AT10D_MACFA | Probable phospholipid-transporting ATPase VD (Fragment) OS=Macaca fascicularis GN=ATP10D PE=2 SV=1 | 623 | 713 | 2.0E-08 |
sp|Q09891|ATCX_SCHPO | Putative phospholipid-transporting ATPase C24B11.12c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC24B11.12c PE=3 SV=1 | 90 | 165 | 5.0E-08 |
sp|Q9P241|AT10D_HUMAN | Probable phospholipid-transporting ATPase VD OS=Homo sapiens GN=ATP10D PE=2 SV=3 | 527 | 713 | 1.0E-07 |
sp|Q8K2X1|AT10D_MOUSE | Probable phospholipid-transporting ATPase VD OS=Mus musculus GN=Atp10d PE=2 SV=2 | 614 | 712 | 1.0E-07 |
sp|O54827|AT10A_MOUSE | Probable phospholipid-transporting ATPase VA OS=Mus musculus GN=Atp10a PE=1 SV=4 | 615 | 709 | 1.0E-07 |
sp|P35317|AT1A_HYDVU | Sodium/potassium-transporting ATPase subunit alpha OS=Hydra vulgaris PE=2 SV=1 | 830 | 1077 | 3.0E-07 |
sp|Q5XF90|AT134_MOUSE | Probable cation-transporting ATPase 13A4 OS=Mus musculus GN=Atp13a4 PE=2 SV=1 | 845 | 1078 | 6.0E-07 |
sp|Q9WV27|AT1A4_MOUSE | Sodium/potassium-transporting ATPase subunit alpha-4 OS=Mus musculus GN=Atp1a4 PE=1 SV=3 | 900 | 1077 | 1.0E-06 |
sp|Q4VNC1|AT134_HUMAN | Probable cation-transporting ATPase 13A4 OS=Homo sapiens GN=ATP13A4 PE=2 SV=3 | 845 | 1078 | 2.0E-06 |
sp|Q5ZKB7|AT134_CHICK | Probable cation-transporting ATPase 13A4 OS=Gallus gallus GN=ATP13A4 PE=2 SV=1 | 879 | 1078 | 2.0E-06 |
sp|P19156|ATP4A_PIG | Potassium-transporting ATPase alpha chain 1 OS=Sus scrofa GN=ATP4A PE=1 SV=3 | 853 | 1160 | 2.0E-06 |
sp|O60312|AT10A_HUMAN | Probable phospholipid-transporting ATPase VA OS=Homo sapiens GN=ATP10A PE=2 SV=2 | 621 | 724 | 3.0E-06 |
sp|P50996|ATP4A_CANLF | Potassium-transporting ATPase alpha chain 1 OS=Canis lupus familiaris GN=ATP4A PE=2 SV=3 | 853 | 1160 | 5.0E-06 |
sp|Q92036|AT12A_RHIMB | Potassium-transporting ATPase alpha chain 2 OS=Rhinella marina GN=ATP12A PE=2 SV=1 | 899 | 1131 | 7.0E-06 |
sp|P09626|ATP4A_RAT | Potassium-transporting ATPase alpha chain 1 OS=Rattus norvegicus GN=Atp4a PE=1 SV=3 | 853 | 1160 | 7.0E-06 |
sp|Q64436|ATP4A_MOUSE | Potassium-transporting ATPase alpha chain 1 OS=Mus musculus GN=Atp4a PE=1 SV=3 | 853 | 1160 | 9.0E-06 |
sp|O53114|CTPI_MYCLE | Probable cation-transporting ATPase I OS=Mycobacterium leprae (strain TN) GN=ctpI PE=3 SV=1 | 901 | 1168 | 9.0E-06 |
SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
---|---|---|
No | 1 - 34 | 0.45 |
Domain # | Start | End | Length |
---|---|---|---|
1 | 374 | 396 | 22 |
2 | 417 | 439 | 22 |
3 | 1199 | 1221 | 22 |
4 | 1228 | 1247 | 19 |
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|5222 MSSASLPEKAPAFLVSSPHRPFDDDDPGPRLPLRNRFWAALQSLYQATIVHLILRKKHIDATKHGRHIPLAIDHQ KPLIDTRRGHAYLSNDVRTSRYTIWDFIPKQFFFQFSRVGNFYFLCVGIPQTIPGLSTTGSFTTILPLLFFVLLT VAKEGYDDYRRHLLDKVENANFVTVLGRHDLSVVHARSSRSWRRWVSFRTESTSQPRPSLPKDEYLGVRWVPSRW SHVKVGDVVLLSRDEPVPADLVLLHSDGENGIAYIDTMALDGETSLKTKQVCHALHGCGSIQGIAECRAEFVVED PNPDLFNFNGRVTVRDKTVPLTLSHVVYRGSVVRNTTRAIGLVVNTGEECKVRMNSNQHPRAKRPALEKIVNKVV LTLAIYVLVLSVGVSMGYVHFRADYEKHAWFLDGATVPFHQIIIAFVIMFNNIVPLSLYISLEIVKVGQLLLLNS DVEMYDEETDTPARCNTNTIMENLGQIGYVFSDKTGTLTDNVMRFRKLSVAGTVWLHAMDLEQPETDGPPTPSSL DRHSVRKPTVSKASAIPEDERKTPTLASRSSLGRRPSSQWRSTGRPDLVQPEVNTSDLLEHMRLRPHSAFSRTAR DYLLAVAICHTCLPEVKNGRIEFQASSPDELALVRAAQELGFGVTHRTSQSITLQVSRPSGQSEKMVFQILDVIE FSSTRKRMSIVVRYPDGRTSIVCKGADSVILPRLRLSTLAMQRAHEVRKSADLEREMQRRSEQQEPRNSFGGRRS LTVWRNAEVATDASGGRRSLASRSRSFEVNKMTRSSVDRPRTSVLARRGVSLDVSRNQSTSSTAAHLRPQHDRLD FLNDPAMHDESEVFNRCFRHLDDFATEGLRTLVYAQRFISDSEYRTWKKLYDEATTSLHDRQVMIEAAGELIETS LELVGATAIEDKLQKGVPETIDRLRRANIKIWMVTGDKRETAINIAHSARICRPGSDLYVLDVDRSLLETQLVAL AEDLQAGSVHSVVVIDGQTLAAVEKSAELSRRFFSLAMTVDSVICCRASPAQKAILVRAVRARLGTLKDKDRRGL TLAIGDGANDLAMIQASHVGVGISGKEGLQAARVADYAIAQFRFLQRLLLVHGRWNYVRTAKFILCTFWKEMFFY LPTAIYQRCSGYSGTSLYQEVSLTVFNTLFTSLCTICMGVWEQDLSAETLLAVPELYVYGQRGLGLNMSKYLRWM AVAAVQGLAVWYGVWAGYGIVSPSAHDEGLYALGTLAFTVGVLWINWKLL |
Coding | >Ophio5|5222 ATGTCTTCCGCCTCGTTACCCGAGAAGGCTCCCGCGTTCCTCGTCTCGAGTCCGCATCGTCCCTTCGATGACGAC GACCCCGGCCCTCGTCTGCCTCTGCGAAACCGCTTCTGGGCCGCCCTACAGTCGCTTTACCAGGCTACCATCGTC CATCTGATACTGCGCAAGAAGCACATCGACGCCACCAAGCATGGCAGGCACATTCCACTTGCCATTGACCACCAA AAGCCGCTCATCGACACCCGCCGCGGCCACGCCTATCTTTCCAACGATGTCCGCACCTCTCGCTATACCATATGG GACTTTATACCCAAGCAATTCTTCTTTCAGTTTTCCCGTGTCGGAAACTTTTACTTCCTCTGCGTCGGCATCCCC CAGACGATACCGGGCCTGTCCACGACGGGCTCCTTTACCACCATTTTACCTTTATTGTTCTTCGTCCTCCTCACC GTGGCCAAGGAGGGCTATGATGACTACAGACGGCATCTCTTGGACAAGGTTGAGAATGCAAACTTCGTCACTGTC CTCGGCCGCCATGACCTGAGTGTCGTCCATGCCAGGTCGTCTCGTTCTTGGCGCCGCTGGGTCTCCTTTCGCACC GAATCCACCAGCCAGCCAAGGCCGTCGCTCCCCAAAGATGAGTACCTCGGCGTTCGATGGGTGCCCTCTCGATGG AGTCACGTCAAGGTTGGAGACGTCGTCTTGCTGTCCCGCGACGAACCGGTCCCCGCCGACTTGGTCCTTCTTCAT AGTGATGGCGAGAACGGCATTGCCTACATCGACACCATGGCCTTGGACGGCGAAACCAGTCTCAAGACGAAGCAG GTTTGCCACGCCCTTCACGGATGTGGCTCTATCCAGGGCATTGCCGAATGCCGGGCCGAGTTCGTCGTCGAGGAC CCGAATCCAGACCTTTTCAACTTCAATGGCCGCGTCACCGTCCGGGACAAAACCGTGCCCCTGACCCTCAGCCAT GTCGTCTACCGGGGCAGCGTTGTGCGGAACACGACCCGCGCCATCGGTCTCGTTGTCAACACGGGTGAGGAGTGC AAGGTCCGCATGAACTCCAACCAACACCCGCGTGCGAAGCGGCCGGCCCTCGAGAAGATCGTCAACAAGGTCGTC CTGACCCTGGCAATTTACGTCCTTGTCCTCTCCGTCGGCGTCTCCATGGGCTATGTTCACTTTCGTGCCGACTAC GAGAAGCATGCCTGGTTCCTCGACGGCGCCACAGTCCCGTTTCACCAGATCATCATCGCCTTCGTCATCATGTTC AACAACATTGTACCCCTATCCTTGTATATATCACTGGAAATTGTCAAGGTCGGCCAGCTTCTTCTACTCAACTCT GACGTCGAAATGTACGACGAGGAGACGGACACGCCGGCGCGATGTAATACCAACACCATCATGGAAAACCTCGGC CAAATTGGCTACGTCTTCTCCGACAAGACGGGAACTCTGACGGACAACGTCATGAGGTTCCGCAAGCTCAGCGTC GCCGGCACCGTCTGGCTTCACGCCATGGACCTCGAGCAGCCCGAGACCGACGGGCCTCCGACGCCCTCTTCGCTC GACCGGCATTCGGTTCGGAAGCCGACGGTGAGCAAGGCCTCGGCCATCCCCGAGGACGAACGCAAAACCCCGACG TTGGCATCGCGGTCATCGCTGGGCCGGAGGCCATCGTCACAATGGCGTTCCACCGGTCGCCCAGACCTCGTACAG CCCGAGGTCAACACGTCAGATCTCCTGGAGCACATGAGGCTCCGGCCGCATTCCGCCTTCTCCAGGACAGCCAGA GACTATTTGCTCGCCGTCGCCATCTGCCACACTTGCCTGCCCGAAGTCAAGAACGGAAGGATCGAGTTCCAGGCG TCTTCGCCCGATGAGCTGGCTCTAGTGAGAGCAGCTCAGGAGCTTGGCTTTGGCGTGACCCATCGCACGTCGCAA AGCATAACACTGCAGGTTTCGCGGCCCAGCGGCCAGAGCGAGAAGATGGTTTTCCAGATTCTGGACGTCATCGAG TTTAGCAGCACGCGCAAGAGAATGTCCATTGTCGTTCGCTATCCCGATGGGCGCACATCCATCGTATGCAAAGGC GCCGACTCGGTCATTCTGCCTAGGCTCAGGCTGTCCACTCTGGCGATGCAGAGGGCACACGAGGTCCGGAAGAGT GCCGACCTCGAGCGCGAGATGCAGCGGCGCAGCGAGCAGCAGGAGCCCCGGAACAGCTTTGGCGGGAGGCGAAGC CTGACCGTCTGGCGAAACGCCGAAGTCGCGACTGATGCTAGCGGAGGCCGGCGCTCACTGGCCAGCCGCAGCAGA TCTTTCGAGGTTAACAAGATGACTCGGTCGTCCGTTGACCGACCTCGGACCTCGGTTCTCGCCCGGCGAGGAGTC TCGCTTGACGTGTCTCGAAACCAGTCCACGAGCTCGACGGCCGCTCACTTGCGGCCCCAGCACGATCGTCTGGAC TTTCTCAACGATCCTGCCATGCACGATGAGTCCGAGGTTTTCAACCGGTGCTTCAGGCACCTGGATGACTTCGCC ACAGAAGGTCTCAGGACCCTTGTCTATGCTCAAAGGTTTATCTCGGATTCGGAATACCGCACGTGGAAGAAACTC TACGACGAGGCGACGACGAGCCTTCACGACCGACAGGTAATGATAGAGGCCGCCGGTGAGCTGATTGAGACAAGT CTCGAACTCGTCGGCGCCACCGCCATCGAAGACAAGCTGCAAAAGGGCGTCCCGGAGACTATAGACAGACTGCGA CGGGCCAACATCAAGATCTGGATGGTGACGGGTGATAAGCGTGAGACGGCCATCAATATTGCCCACTCGGCGCGC ATCTGCCGACCGGGATCCGACCTCTACGTCCTGGATGTGGACAGAAGTCTTCTGGAGACGCAGCTCGTGGCCCTG GCCGAGGATTTGCAGGCCGGTTCCGTCCACAGCGTCGTCGTCATCGACGGGCAGACGCTGGCCGCGGTGGAGAAG TCGGCCGAGCTGTCGAGACGCTTCTTCAGCCTGGCCATGACGGTCGACTCCGTAATCTGCTGTCGGGCGTCGCCG GCGCAGAAGGCGATACTGGTCCGGGCCGTGCGCGCGCGCCTGGGTACCCTAAAAGACAAGGACCGGCGCGGGCTT ACGCTGGCCATCGGCGACGGCGCAAATGATCTCGCCATGATCCAGGCCAGCCACGTCGGTGTCGGCATATCCGGA AAGGAGGGCCTCCAGGCGGCGCGCGTGGCCGACTATGCCATCGCCCAGTTCCGCTTCCTACAGCGGCTGCTCCTC GTCCACGGTCGCTGGAACTACGTGCGGACGGCAAAGTTTATCCTTTGCACCTTTTGGAAGGAGATGTTCTTCTAT CTGCCGACGGCCATATACCAGAGATGCAGCGGCTACAGCGGCACCTCGTTGTACCAGGAGGTGAGCCTGACCGTC TTCAACACGCTCTTCACCAGCCTCTGCACCATCTGCATGGGCGTCTGGGAGCAGGACTTGAGCGCCGAGACGCTG CTGGCCGTGCCCGAGCTGTACGTCTACGGCCAACGCGGCCTGGGGCTCAACATGTCCAAGTATCTGCGCTGGATG GCCGTGGCCGCTGTCCAAGGTTTGGCCGTCTGGTACGGCGTCTGGGCCGGATACGGCATCGTCTCGCCGTCGGCT CACGACGAGGGCCTCTACGCGCTGGGGACGCTGGCCTTTACCGTCGGCGTCTTGTGGATCAACTGGAAGCTATTG |
Transcript | >Ophio5|5222 ATGTCTTCCGCCTCGTTACCCGAGAAGGCTCCCGCGTTCCTCGTCTCGAGTCCGCATCGTCCCTTCGATGACGAC GACCCCGGCCCTCGTCTGCCTCTGCGAAACCGCTTCTGGGCCGCCCTACAGTCGCTTTACCAGGCTACCATCGTC CATCTGATACTGCGCAAGAAGCACATCGACGCCACCAAGCATGGCAGGCACATTCCACTTGCCATTGACCACCAA AAGCCGCTCATCGACACCCGCCGCGGCCACGCCTATCTTTCCAACGATGTCCGCACCTCTCGCTATACCATATGG GACTTTATACCCAAGCAATTCTTCTTTCAGTTTTCCCGTGTCGGAAACTTTTACTTCCTCTGCGTCGGCATCCCC CAGACGATACCGGGCCTGTCCACGACGGGCTCCTTTACCACCATTTTACCTTTATTGTTCTTCGTCCTCCTCACC GTGGCCAAGGAGGGCTATGATGACTACAGACGGCATCTCTTGGACAAGGTTGAGAATGCAAACTTCGTCACTGTC CTCGGCCGCCATGACCTGAGTGTCGTCCATGCCAGGTCGTCTCGTTCTTGGCGCCGCTGGGTCTCCTTTCGCACC GAATCCACCAGCCAGCCAAGGCCGTCGCTCCCCAAAGATGAGTACCTCGGCGTTCGATGGGTGCCCTCTCGATGG AGTCACGTCAAGGTTGGAGACGTCGTCTTGCTGTCCCGCGACGAACCGGTCCCCGCCGACTTGGTCCTTCTTCAT AGTGATGGCGAGAACGGCATTGCCTACATCGACACCATGGCCTTGGACGGCGAAACCAGTCTCAAGACGAAGCAG GTTTGCCACGCCCTTCACGGATGTGGCTCTATCCAGGGCATTGCCGAATGCCGGGCCGAGTTCGTCGTCGAGGAC CCGAATCCAGACCTTTTCAACTTCAATGGCCGCGTCACCGTCCGGGACAAAACCGTGCCCCTGACCCTCAGCCAT GTCGTCTACCGGGGCAGCGTTGTGCGGAACACGACCCGCGCCATCGGTCTCGTTGTCAACACGGGTGAGGAGTGC AAGGTCCGCATGAACTCCAACCAACACCCGCGTGCGAAGCGGCCGGCCCTCGAGAAGATCGTCAACAAGGTCGTC CTGACCCTGGCAATTTACGTCCTTGTCCTCTCCGTCGGCGTCTCCATGGGCTATGTTCACTTTCGTGCCGACTAC GAGAAGCATGCCTGGTTCCTCGACGGCGCCACAGTCCCGTTTCACCAGATCATCATCGCCTTCGTCATCATGTTC AACAACATTGTACCCCTATCCTTGTATATATCACTGGAAATTGTCAAGGTCGGCCAGCTTCTTCTACTCAACTCT GACGTCGAAATGTACGACGAGGAGACGGACACGCCGGCGCGATGTAATACCAACACCATCATGGAAAACCTCGGC CAAATTGGCTACGTCTTCTCCGACAAGACGGGAACTCTGACGGACAACGTCATGAGGTTCCGCAAGCTCAGCGTC GCCGGCACCGTCTGGCTTCACGCCATGGACCTCGAGCAGCCCGAGACCGACGGGCCTCCGACGCCCTCTTCGCTC GACCGGCATTCGGTTCGGAAGCCGACGGTGAGCAAGGCCTCGGCCATCCCCGAGGACGAACGCAAAACCCCGACG TTGGCATCGCGGTCATCGCTGGGCCGGAGGCCATCGTCACAATGGCGTTCCACCGGTCGCCCAGACCTCGTACAG CCCGAGGTCAACACGTCAGATCTCCTGGAGCACATGAGGCTCCGGCCGCATTCCGCCTTCTCCAGGACAGCCAGA GACTATTTGCTCGCCGTCGCCATCTGCCACACTTGCCTGCCCGAAGTCAAGAACGGAAGGATCGAGTTCCAGGCG TCTTCGCCCGATGAGCTGGCTCTAGTGAGAGCAGCTCAGGAGCTTGGCTTTGGCGTGACCCATCGCACGTCGCAA AGCATAACACTGCAGGTTTCGCGGCCCAGCGGCCAGAGCGAGAAGATGGTTTTCCAGATTCTGGACGTCATCGAG TTTAGCAGCACGCGCAAGAGAATGTCCATTGTCGTTCGCTATCCCGATGGGCGCACATCCATCGTATGCAAAGGC GCCGACTCGGTCATTCTGCCTAGGCTCAGGCTGTCCACTCTGGCGATGCAGAGGGCACACGAGGTCCGGAAGAGT GCCGACCTCGAGCGCGAGATGCAGCGGCGCAGCGAGCAGCAGGAGCCCCGGAACAGCTTTGGCGGGAGGCGAAGC CTGACCGTCTGGCGAAACGCCGAAGTCGCGACTGATGCTAGCGGAGGCCGGCGCTCACTGGCCAGCCGCAGCAGA TCTTTCGAGGTTAACAAGATGACTCGGTCGTCCGTTGACCGACCTCGGACCTCGGTTCTCGCCCGGCGAGGAGTC TCGCTTGACGTGTCTCGAAACCAGTCCACGAGCTCGACGGCCGCTCACTTGCGGCCCCAGCACGATCGTCTGGAC TTTCTCAACGATCCTGCCATGCACGATGAGTCCGAGGTTTTCAACCGGTGCTTCAGGCACCTGGATGACTTCGCC ACAGAAGGTCTCAGGACCCTTGTCTATGCTCAAAGGTTTATCTCGGATTCGGAATACCGCACGTGGAAGAAACTC TACGACGAGGCGACGACGAGCCTTCACGACCGACAGGTAATGATAGAGGCCGCCGGTGAGCTGATTGAGACAAGT CTCGAACTCGTCGGCGCCACCGCCATCGAAGACAAGCTGCAAAAGGGCGTCCCGGAGACTATAGACAGACTGCGA CGGGCCAACATCAAGATCTGGATGGTGACGGGTGATAAGCGTGAGACGGCCATCAATATTGCCCACTCGGCGCGC ATCTGCCGACCGGGATCCGACCTCTACGTCCTGGATGTGGACAGAAGTCTTCTGGAGACGCAGCTCGTGGCCCTG GCCGAGGATTTGCAGGCCGGTTCCGTCCACAGCGTCGTCGTCATCGACGGGCAGACGCTGGCCGCGGTGGAGAAG TCGGCCGAGCTGTCGAGACGCTTCTTCAGCCTGGCCATGACGGTCGACTCCGTAATCTGCTGTCGGGCGTCGCCG GCGCAGAAGGCGATACTGGTCCGGGCCGTGCGCGCGCGCCTGGGTACCCTAAAAGACAAGGACCGGCGCGGGCTT ACGCTGGCCATCGGCGACGGCGCAAATGATCTCGCCATGATCCAGGCCAGCCACGTCGGTGTCGGCATATCCGGA AAGGAGGGCCTCCAGGCGGCGCGCGTGGCCGACTATGCCATCGCCCAGTTCCGCTTCCTACAGCGGCTGCTCCTC GTCCACGGTCGCTGGAACTACGTGCGGACGGCAAAGTTTATCCTTTGCACCTTTTGGAAGGAGATGTTCTTCTAT CTGCCGACGGCCATATACCAGAGATGCAGCGGCTACAGCGGCACCTCGTTGTACCAGGAGGTGAGCCTGACCGTC TTCAACACGCTCTTCACCAGCCTCTGCACCATCTGCATGGGCGTCTGGGAGCAGGACTTGAGCGCCGAGACGCTG CTGGCCGTGCCCGAGCTGTACGTCTACGGCCAACGCGGCCTGGGGCTCAACATGTCCAAGTATCTGCGCTGGATG GCCGTGGCCGCTGTCCAAGGTTTGGCCGTCTGGTACGGCGTCTGGGCCGGATACGGCATCGTCTCGCCGTCGGCT CACGACGAGGGCCTCTACGCGCTGGGGACGCTGGCCTTTACCGTCGGCGTCTTGTGGATCAACTGGAAGCTATTG TGA |
Gene | >Ophio5|5222 ATGTCTTCCGCCTCGTTACCCGAGAAGGCTCCCGCGTTCCTCGTCTCGAGTCCGCATCGTCCCTTCGATGACGAC GACCCCGGCCCTCGTCTGCCTCTGCGAAACCGCTTCTGGGCCGCCCTACAGTCGCTTTACCAGGCTACCATCGTC CATCTGATACTGCGCAAGAAGCACATCGACGCCACCAAGCATGGCAGGCACATTCCACTTGCCATTGACCACCAA AAGCCGCTCATCGACACCCGCCGCGGCCACGCCTATCTTTCCAACGATGTCCGCACCTCTCGCTATACCATATGG GACTTTATACCCAAGCAATTCTTCTTTCAGTTTTCCCGTGTCGGAAACTTTTACTTCCTCTGCGTCGGCATCCCC CAGACGGTATGTGACACCCCTTACTCTCTTCCCCCTTTCGTCTTGAGCTGACCCAACTTCAGATACCGGGCCTGT CCACGACGGGCTCCTTTACCACCATTTTACCTTTATTGTTCTTCGTCCTCCTCACCGTGGCCAAGGAGGGCTATG ATGACTACAGACGGCATCTCTTGGACAAGGTTGAGAATGCAAACTTCGTCACTGTCCTCGGCCGCCATGACCTGA GTGTCGTCCATGCCAGGTCGTCTCGTTCTTGGCGCCGCTGGGTCTCCTTTCGCACCGAATCCACCAGCCAGCCAA GGCCGTCGCTCCCCAAAGATGAGTACCTCGGCGTTCGATGGGTGCCCTCTCGATGGAGTCACGTCAAGGTTGGAG ACGTCGTCTTGCTGTCCCGCGACGAACCGGTCCCCGCCGACTTGGTCCTTCTTCATAGTGATGGCGAGAACGGCA TTGCCTACATCGACACCATGGCCTTGGACGGCGAAACCAGTCTCAAGACGAAGCAGGTTTGCCACGCCCTTCACG GATGTGGCTCTATCCAGGGCATTGCCGAATGCCGGGCCGAGTTCGTCGTCGAGGACCCGAATCCAGACCTTTTCA ACTTCAATGGCCGCGTCACCGTCCGGGACAAAACCGTGCCCCTGACCCTCAGCCATGTCGTCTACCGGGGCAGCG TTGTGCGGAACACGACCCGCGCCATCGGTCTCGTTGTCAACACGGGTGAGGAGTGCAAGGTCCGCATGAACTCCA ACCAACACCCGCGTGCGAAGCGGCCGGCCCTCGAGAAGATCGTCAACAAGGTCGTCCTGACCCTGGCAATTTACG TCCTTGTCCTCTCCGTCGGCGTCTCCATGGGCTATGTTCACTTTCGTGCCGACTACGAGAAGCATGCCTGGTTCC TCGACGGCGCCACAGTCCCGTTTCACCAGATCATCATCGCCTTCGTCATCATGTTCAACAACATTGTACCCCTAT CCTTGTATATATCACTGGAAATTGTCAAGGTCGGCCAGCTTCTTCTACTCAACTCTGACGTCGAAATGTACGACG AGGAGACGGACACGCCGGCGCGATGTAATACCAACACCATCATGGAAAACCTCGGCCAAATTGGCTACGTCTTCT CCGACAAGACGGGAACTCTGACGGACAACGTCATGAGGTTCCGCAAGCTCAGCGTCGCCGGCACCGTCTGGCTTC ACGCCATGGACCTCGAGCAGCCCGAGACCGACGGGCCTCCGACGCCCTCTTCGCTCGACCGGCATTCGGTTCGGA AGCCGACGGTGAGCAAGGCCTCGGCCATCCCCGAGGACGAACGCAAAACCCCGACGTTGGCATCGCGGTCATCGC TGGGCCGGAGGCCATCGTCACAATGGCGTTCCACCGGTCGCCCAGACCTCGTACAGCCCGAGGTCAACACGTCAG ATCTCCTGGAGCACATGAGGCTCCGGCCGCATTCCGCCTTCTCCAGGACAGCCAGAGACTATTTGCTCGCCGTCG CCATCTGCCACACTTGCCTGCCCGAAGTCAAGAACGGAAGGATCGAGTTCCAGGCGTCTTCGCCCGATGAGCTGG CTCTAGTGAGAGCAGCTCAGGAGCTTGGCTTTGGCGTGACCCATCGCACGTCGCAAAGCATAACACTGCAGGTTT CGCGGCCCAGCGGCCAGAGCGAGAAGATGGTTTTCCAGATTCTGGACGTCATCGAGTTTAGCAGCACGCGCAAGA GAATGTCCATTGTCGTTCGCTATCCCGATGGGCGCACATCCATCGTATGCAAAGGCGCCGACTCGGTCATTCTGC CTAGGCTCAGGCTGTCCACTCTGGCGATGCAGAGGGCACACGAGGTCCGGAAGAGTGCCGACCTCGAGCGCGAGA TGCAGCGGCGCAGCGAGCAGCAGGAGCCCCGGAACAGCTTTGGCGGGAGGCGAAGCCTGACCGTCTGGCGAAACG CCGAAGTCGCGACTGATGCTAGCGGAGGCCGGCGCTCACTGGCCAGCCGCAGCAGATCTTTCGAGGTTAACAAGA TGACTCGGTCGTCCGTTGACCGACCTCGGACCTCGGTTCTCGCCCGGCGAGGAGTCTCGCTTGACGTGTCTCGAA ACCAGTCCACGAGCTCGACGGCCGCTCACTTGCGGCCCCAGCACGATCGTCTGGACTTTCTCAACGATCCTGCCA TGCACGATGAGTCCGAGGTTTTCAACCGGTGCTTCAGGCACCTGGATGACTTCGCCACAGAAGGTCTCAGGACCC TTGTCTATGCTCAAAGGTTTATCTCGGATTCGGAATACCGCACGTGGAAGAAACTCTACGACGAGGCGACGACGA GCCTTCACGACCGACAGGTAATGATAGAGGCCGCCGGTGAGCTGATTGAGACAAGTCTCGAACTCGTCGGCGCCA CCGCCATCGAAGACAAGCTGCAAAAGGGCGTCCCGGAGACTATAGACAGACTGCGACGGGCCAACATCAAGATCT GGATGGTGACGGGTGATAAGCGTGAGACGGCCATCAATATTGCCCACTCGGCGCGCATCTGCCGACCGGGATCCG ACCTCTACGTCCTGGATGTGGACAGAAGTCTTCTGGAGACGCAGCTCGTGGCCCTGGCCGAGGATTTGCAGGCCG GTTCCGTCCACAGCGTCGTCGTCATCGACGGGCAGACGCTGGCCGCGGTGGAGAAGTCGGCCGAGCTGTCGAGAC GCTTCTTCAGCCTGGCCATGACGGTCGACTCCGTAATCTGCTGTCGGGCGTCGCCGGCGCAGAAGGCGATACTGG TCCGGGCCGTGCGCGCGCGCCTGGGTACCCTAAAAGACAAGGACCGGCGCGGGCTTACGCTGGCCATCGGCGACG GCGCAAATGATCTCGCCATGATCCAGGCCAGCCACGTCGGTGTCGGCATATCCGGAAAGGAGGGCCTCCAGGCGG CGCGCGTGGCCGACTATGCCATCGCCCAGTTCCGCTTCCTACAGCGGCTGCTCCTCGTCCACGGTCGCTGGAACT ACGTGCGGACGGCAAAGTTTATCCTTTGCACCTTTTGGAAGGAGATGTTCTTCTATCTGCCGACGGCCATATACC AGAGATGCAGCGGCTACAGCGGCACCTCGTTGTACCAGGAGGTGAGCCTGACCGTCTTCAACACGCTCTTCACCA GCCTCTGCACCATCTGCATGGGCGTCTGGGAGCAGGACTTGAGCGCCGAGACGCTGCTGGCCGTGCCCGAGCTGT ACGTCTACGGCCAACGCGGCCTGGGGCTCAACATGTCCAAGTATCTGCGCTGGATGGCCGTGGCCGCTGTCCAAG GTTTGGCCGTCTGGTACGGCGTCTGGGCCGGATACGGCATCGTCTCGCCGTCGGCTCACGACGAGGGCCTCTACG CGCTGGGGACGCTGGCCTTTACCGTCGGCGTCTTGTGGATCAACTGGAAGCTATTGTGA |