Fungal Genomics

at Utrecht University

General Properties

Protein IDOphun1|5648
Gene name
LocationContig_570:1046..5247
Strand+
Gene length (bp)4201
Transcript length (bp)4083
Coding sequence length (bp)4083
Protein length (aa) 1361

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PFAM Domains

PFAM Domain ID Short name Long name E-value Start End
PF16212 PhoLip_ATPase_C Phospholipid-translocating P-type ATPase C-terminal 3.9E-65 1058 1305
PF16209 PhoLip_ATPase_N Phospholipid-translocating ATPase N-terminal 2.0E-22 92 148
PF00702 Hydrolase haloacid dehalogenase-like hydrolase 6.5E-06 859 971
PF13246 Cation_ATPase Cation transport ATPase (P-type) 5.7E-10 604 687
PF00122 E1-E2_ATPase E1-E2 ATPase 4.0E-09 233 442

Swissprot hits

[Show all]
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 57 1349 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=2 208 1344 0.0E+00
sp|O60312|AT10A_HUMAN Probable phospholipid-transporting ATPase VA OS=Homo sapiens GN=ATP10A PE=2 SV=2 90 1221 1.0E-139
sp|P39524|ATC3_YEAST Probable phospholipid-transporting ATPase DRS2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DRS2 PE=1 SV=2 59 688 4.0E-101
sp|Q9LVK9|ALA7_ARATH Probable phospholipid-transporting ATPase 7 OS=Arabidopsis thaliana GN=ALA7 PE=3 SV=3 95 688 3.0E-98
[Show all]
[Show less]
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 57 1349 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=2 208 1344 0.0E+00
sp|O60312|AT10A_HUMAN Probable phospholipid-transporting ATPase VA OS=Homo sapiens GN=ATP10A PE=2 SV=2 90 1221 1.0E-139
sp|P39524|ATC3_YEAST Probable phospholipid-transporting ATPase DRS2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DRS2 PE=1 SV=2 59 688 4.0E-101
sp|Q9LVK9|ALA7_ARATH Probable phospholipid-transporting ATPase 7 OS=Arabidopsis thaliana GN=ALA7 PE=3 SV=3 95 688 3.0E-98
sp|P70704|AT8A1_MOUSE Phospholipid-transporting ATPase IA OS=Mus musculus GN=Atp8a1 PE=1 SV=2 95 696 2.0E-97
sp|Q9Y2Q0|AT8A1_HUMAN Phospholipid-transporting ATPase IA OS=Homo sapiens GN=ATP8A1 PE=1 SV=1 95 696 2.0E-97
sp|P98200|AT8A2_MOUSE Phospholipid-transporting ATPase IB OS=Mus musculus GN=Atp8a2 PE=1 SV=1 95 688 3.0E-95
sp|Q9SLK6|ALA6_ARATH Phospholipid-transporting ATPase 6 OS=Arabidopsis thaliana GN=ALA6 PE=1 SV=2 95 691 4.0E-95
sp|Q9NTI2|AT8A2_HUMAN Phospholipid-transporting ATPase IB OS=Homo sapiens GN=ATP8A2 PE=1 SV=2 98 688 1.0E-94
sp|C7EXK4|AT8A2_BOVIN Phospholipid-transporting ATPase IB OS=Bos taurus GN=ATP8A2 PE=1 SV=4 95 688 3.0E-94
sp|Q29449|AT8A1_BOVIN Probable phospholipid-transporting ATPase IA OS=Bos taurus GN=ATP8A1 PE=1 SV=2 95 696 4.0E-94
sp|P57792|ALA12_ARATH Probable phospholipid-transporting ATPase 12 OS=Arabidopsis thaliana GN=ALA12 PE=2 SV=1 95 688 2.0E-92
sp|Q9LNQ4|ALA4_ARATH Probable phospholipid-transporting ATPase 4 OS=Arabidopsis thaliana GN=ALA4 PE=3 SV=2 83 688 8.0E-92
sp|Q9SGG3|ALA5_ARATH Probable phospholipid-transporting ATPase 5 OS=Arabidopsis thaliana GN=ALA5 PE=3 SV=1 83 688 4.0E-91
sp|O94296|YOOC_SCHPO Probable phospholipid-transporting ATPase C887.12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC887.12 PE=3 SV=1 95 688 1.0E-90
sp|Q9LK90|ALA8_ARATH Probable phospholipid-transporting ATPase 8 OS=Arabidopsis thaliana GN=ALA8 PE=3 SV=1 95 706 7.0E-90
sp|Q9SX33|ALA9_ARATH Putative phospholipid-transporting ATPase 9 OS=Arabidopsis thaliana GN=ALA9 PE=3 SV=1 52 688 7.0E-89
sp|Q148W0|AT8B1_MOUSE Phospholipid-transporting ATPase IC OS=Mus musculus GN=Atp8b1 PE=1 SV=2 95 700 3.0E-88
sp|Q9XIE6|ALA3_ARATH Phospholipid-transporting ATPase 3 OS=Arabidopsis thaliana GN=ALA3 PE=1 SV=2 95 688 6.0E-88
sp|Q9SAF5|ALA11_ARATH Probable phospholipid-transporting ATPase 11 OS=Arabidopsis thaliana GN=ALA11 PE=2 SV=1 95 688 1.0E-87
sp|O43520|AT8B1_HUMAN Phospholipid-transporting ATPase IC OS=Homo sapiens GN=ATP8B1 PE=1 SV=3 95 700 5.0E-87
sp|Q9U280|TAT1_CAEEL Phospholipid-transporting ATPase tat-1 OS=Caenorhabditis elegans GN=tat-1 PE=3 SV=3 758 1222 8.0E-87
sp|O94296|YOOC_SCHPO Probable phospholipid-transporting ATPase C887.12 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC887.12 PE=3 SV=1 752 1295 2.0E-86
sp|Q9LI83|ALA10_ARATH Phospholipid-transporting ATPase 10 OS=Arabidopsis thaliana GN=ALA10 PE=3 SV=1 90 688 3.0E-86
sp|Q9LNQ4|ALA4_ARATH Probable phospholipid-transporting ATPase 4 OS=Arabidopsis thaliana GN=ALA4 PE=3 SV=2 825 1288 5.0E-86
sp|Q9Y2Q0|AT8A1_HUMAN Phospholipid-transporting ATPase IA OS=Homo sapiens GN=ATP8A1 PE=1 SV=1 752 1317 4.0E-85
sp|Q9NTI2|AT8A2_HUMAN Phospholipid-transporting ATPase IB OS=Homo sapiens GN=ATP8A2 PE=1 SV=2 756 1188 4.0E-85
sp|P70704|AT8A1_MOUSE Phospholipid-transporting ATPase IA OS=Mus musculus GN=Atp8a1 PE=1 SV=2 752 1264 5.0E-85
sp|Q29449|AT8A1_BOVIN Probable phospholipid-transporting ATPase IA OS=Bos taurus GN=ATP8A1 PE=1 SV=2 752 1317 2.0E-84
sp|P39524|ATC3_YEAST Probable phospholipid-transporting ATPase DRS2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DRS2 PE=1 SV=2 756 1292 3.0E-84
sp|Q9LVK9|ALA7_ARATH Probable phospholipid-transporting ATPase 7 OS=Arabidopsis thaliana GN=ALA7 PE=3 SV=3 758 1304 3.0E-84
sp|C7EXK4|AT8A2_BOVIN Phospholipid-transporting ATPase IB OS=Bos taurus GN=ATP8A2 PE=1 SV=4 756 1188 6.0E-84
sp|Q9SLK6|ALA6_ARATH Phospholipid-transporting ATPase 6 OS=Arabidopsis thaliana GN=ALA6 PE=1 SV=2 758 1294 2.0E-83
sp|P98200|AT8A2_MOUSE Phospholipid-transporting ATPase IB OS=Mus musculus GN=Atp8a2 PE=1 SV=1 743 1188 3.0E-83
sp|Q6UQ17|AT8B3_MOUSE Phospholipid-transporting ATPase IK OS=Mus musculus GN=Atp8b3 PE=1 SV=1 91 701 6.0E-83
sp|P98198|AT8B2_HUMAN Phospholipid-transporting ATPase ID OS=Homo sapiens GN=ATP8B2 PE=1 SV=2 93 692 9.0E-83
sp|Q5BL50|AT8B1_XENTR Phospholipid-transporting ATPase IC OS=Xenopus tropicalis GN=atp8b1 PE=2 SV=1 95 707 2.0E-82
sp|Q9SGG3|ALA5_ARATH Probable phospholipid-transporting ATPase 5 OS=Arabidopsis thaliana GN=ALA5 PE=3 SV=1 825 1347 1.0E-81
sp|P98199|AT8B2_MOUSE Phospholipid-transporting ATPase ID OS=Mus musculus GN=Atp8b2 PE=2 SV=2 93 688 1.0E-81
sp|Q8TF62|AT8B4_HUMAN Probable phospholipid-transporting ATPase IM OS=Homo sapiens GN=ATP8B4 PE=1 SV=3 93 692 3.0E-81
sp|Q9U280|TAT1_CAEEL Phospholipid-transporting ATPase tat-1 OS=Caenorhabditis elegans GN=tat-1 PE=3 SV=3 67 727 1.0E-80
sp|Q8K2X1|AT10D_MOUSE Probable phospholipid-transporting ATPase VD OS=Mus musculus GN=Atp10d PE=2 SV=2 822 1310 1.0E-80
sp|Q9GKS6|AT10D_MACFA Probable phospholipid-transporting ATPase VD (Fragment) OS=Macaca fascicularis GN=ATP10D PE=2 SV=1 825 1163 2.0E-80
sp|A3FIN4|AT8B5_MOUSE Phospholipid-transporting ATPase FetA OS=Mus musculus GN=Atp8b5 PE=2 SV=1 93 688 6.0E-80
sp|Q9P241|AT10D_HUMAN Probable phospholipid-transporting ATPase VD OS=Homo sapiens GN=ATP10D PE=2 SV=3 825 1310 3.0E-79
sp|Q9XIE6|ALA3_ARATH Phospholipid-transporting ATPase 3 OS=Arabidopsis thaliana GN=ALA3 PE=1 SV=2 759 1295 7.0E-79
sp|O94823|AT10B_HUMAN Probable phospholipid-transporting ATPase VB OS=Homo sapiens GN=ATP10B PE=2 SV=2 818 1267 2.0E-78
sp|P98204|ALA1_ARATH Phospholipid-transporting ATPase 1 OS=Arabidopsis thaliana GN=ALA1 PE=2 SV=1 93 682 3.0E-78
sp|Q9LK90|ALA8_ARATH Probable phospholipid-transporting ATPase 8 OS=Arabidopsis thaliana GN=ALA8 PE=3 SV=1 753 1289 5.0E-78
sp|Q9LI83|ALA10_ARATH Phospholipid-transporting ATPase 10 OS=Arabidopsis thaliana GN=ALA10 PE=3 SV=1 825 1292 5.0E-78
sp|O60423|AT8B3_HUMAN Phospholipid-transporting ATPase IK OS=Homo sapiens GN=ATP8B3 PE=2 SV=4 95 688 1.0E-76
sp|P57792|ALA12_ARATH Probable phospholipid-transporting ATPase 12 OS=Arabidopsis thaliana GN=ALA12 PE=2 SV=1 826 1290 2.0E-76
sp|Q9SAF5|ALA11_ARATH Probable phospholipid-transporting ATPase 11 OS=Arabidopsis thaliana GN=ALA11 PE=2 SV=1 825 1289 5.0E-76
sp|O54827|AT10A_MOUSE Probable phospholipid-transporting ATPase VA OS=Mus musculus GN=Atp10a PE=1 SV=4 759 1287 5.0E-76
sp|Q12675|ATC4_YEAST Phospholipid-transporting ATPase DNF2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF2 PE=1 SV=1 802 1287 9.0E-76
sp|Q5BL50|AT8B1_XENTR Phospholipid-transporting ATPase IC OS=Xenopus tropicalis GN=atp8b1 PE=2 SV=1 756 1304 1.0E-75
sp|P98198|AT8B2_HUMAN Phospholipid-transporting ATPase ID OS=Homo sapiens GN=ATP8B2 PE=1 SV=2 808 1203 5.0E-75
sp|Q8TF62|AT8B4_HUMAN Probable phospholipid-transporting ATPase IM OS=Homo sapiens GN=ATP8B4 PE=1 SV=3 813 1201 5.0E-75
sp|P32660|ATC5_YEAST Phospholipid-transporting ATPase DNF1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF1 PE=1 SV=2 826 1294 3.0E-74
sp|P98204|ALA1_ARATH Phospholipid-transporting ATPase 1 OS=Arabidopsis thaliana GN=ALA1 PE=2 SV=1 826 1336 5.0E-74
sp|Q9Y2G3|AT11B_HUMAN Probable phospholipid-transporting ATPase IF OS=Homo sapiens GN=ATP11B PE=1 SV=2 95 699 6.0E-74
sp|Q9N0Z4|AT11B_RABIT Probable phospholipid-transporting ATPase IF (Fragment) OS=Oryctolagus cuniculus GN=ATP11B PE=1 SV=2 95 699 1.0E-73
sp|P98199|AT8B2_MOUSE Phospholipid-transporting ATPase ID OS=Mus musculus GN=Atp8b2 PE=2 SV=2 818 1203 3.0E-73
sp|Q9SX33|ALA9_ARATH Putative phospholipid-transporting ATPase 9 OS=Arabidopsis thaliana GN=ALA9 PE=3 SV=1 732 1290 2.0E-72
sp|O36028|ATCZ_SCHPO Putative phospholipid-transporting ATPase C4F10.16c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC4F10.16c PE=3 SV=1 816 1304 2.0E-72
sp|Q8NB49|AT11C_HUMAN Phospholipid-transporting ATPase IG OS=Homo sapiens GN=ATP11C PE=1 SV=3 95 711 4.0E-72
sp|Q09891|ATCX_SCHPO Putative phospholipid-transporting ATPase C24B11.12c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC24B11.12c PE=3 SV=1 98 688 6.0E-72
sp|O43520|AT8B1_HUMAN Phospholipid-transporting ATPase IC OS=Homo sapiens GN=ATP8B1 PE=1 SV=3 758 1303 8.0E-72
sp|Q9QZW0|AT11C_MOUSE Phospholipid-transporting ATPase 11C OS=Mus musculus GN=Atp11c PE=1 SV=2 95 711 1.0E-71
sp|A3FIN4|AT8B5_MOUSE Phospholipid-transporting ATPase FetA OS=Mus musculus GN=Atp8b5 PE=2 SV=1 826 1188 3.0E-71
sp|Q148W0|AT8B1_MOUSE Phospholipid-transporting ATPase IC OS=Mus musculus GN=Atp8b1 PE=1 SV=2 758 1303 4.0E-71
sp|Q9Y2G3|AT11B_HUMAN Probable phospholipid-transporting ATPase IF OS=Homo sapiens GN=ATP11B PE=1 SV=2 800 1294 2.0E-70
sp|P98196|AT11A_HUMAN Probable phospholipid-transporting ATPase IH OS=Homo sapiens GN=ATP11A PE=1 SV=3 95 706 2.0E-70
sp|Q09891|ATCX_SCHPO Putative phospholipid-transporting ATPase C24B11.12c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC24B11.12c PE=3 SV=1 825 1224 3.0E-70
sp|P98196|AT11A_HUMAN Probable phospholipid-transporting ATPase IH OS=Homo sapiens GN=ATP11A PE=1 SV=3 831 1230 3.0E-70
sp|P98197|AT11A_MOUSE Probable phospholipid-transporting ATPase IH OS=Mus musculus GN=Atp11a PE=1 SV=1 95 722 3.0E-70
sp|P98205|ALA2_ARATH Phospholipid-transporting ATPase 2 OS=Arabidopsis thaliana GN=ALA2 PE=1 SV=1 760 1290 2.0E-68
sp|O36028|ATCZ_SCHPO Putative phospholipid-transporting ATPase C4F10.16c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC4F10.16c PE=3 SV=1 237 706 5.0E-68
sp|P98197|AT11A_MOUSE Probable phospholipid-transporting ATPase IH OS=Mus musculus GN=Atp11a PE=1 SV=1 831 1288 4.0E-67
sp|Q9N0Z4|AT11B_RABIT Probable phospholipid-transporting ATPase IF (Fragment) OS=Oryctolagus cuniculus GN=ATP11B PE=1 SV=2 800 1294 2.0E-65
sp|Q12675|ATC4_YEAST Phospholipid-transporting ATPase DNF2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF2 PE=1 SV=1 209 688 3.0E-64
sp|P32660|ATC5_YEAST Phospholipid-transporting ATPase DNF1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF1 PE=1 SV=2 232 709 3.0E-64
sp|Q9P241|AT10D_HUMAN Probable phospholipid-transporting ATPase VD OS=Homo sapiens GN=ATP10D PE=2 SV=3 63 524 5.0E-64
sp|Q9QZW0|AT11C_MOUSE Phospholipid-transporting ATPase 11C OS=Mus musculus GN=Atp11c PE=1 SV=2 826 1223 6.0E-63
sp|Q8NB49|AT11C_HUMAN Phospholipid-transporting ATPase IG OS=Homo sapiens GN=ATP11C PE=1 SV=3 826 1308 5.0E-62
sp|Q8K2X1|AT10D_MOUSE Probable phospholipid-transporting ATPase VD OS=Mus musculus GN=Atp10d PE=2 SV=2 73 524 6.0E-62
sp|O54827|AT10A_MOUSE Probable phospholipid-transporting ATPase VA OS=Mus musculus GN=Atp10a PE=1 SV=4 98 575 6.0E-61
sp|O94823|AT10B_HUMAN Probable phospholipid-transporting ATPase VB OS=Homo sapiens GN=ATP10B PE=2 SV=2 95 522 3.0E-60
sp|P98205|ALA2_ARATH Phospholipid-transporting ATPase 2 OS=Arabidopsis thaliana GN=ALA2 PE=1 SV=1 98 715 2.0E-57
sp|F1Q4S1|ATP9B_DANRE Probable phospholipid-transporting ATPase IIB OS=Danio rerio GN=atp9b PE=3 SV=1 829 1189 4.0E-57
sp|P98195|ATP9B_MOUSE Probable phospholipid-transporting ATPase IIB OS=Mus musculus GN=Atp9b PE=1 SV=4 829 1258 3.0E-55
sp|D4ABB8|ATP9B_RAT Probable phospholipid-transporting ATPase IIB OS=Rattus norvegicus GN=Atp9b PE=3 SV=1 829 1189 4.0E-55
sp|O43861|ATP9B_HUMAN Probable phospholipid-transporting ATPase IIB OS=Homo sapiens GN=ATP9B PE=2 SV=4 829 1189 4.0E-54
sp|O70228|ATP9A_MOUSE Probable phospholipid-transporting ATPase IIA OS=Mus musculus GN=Atp9a PE=1 SV=3 829 1189 5.0E-54
sp|O75110|ATP9A_HUMAN Probable phospholipid-transporting ATPase IIA OS=Homo sapiens GN=ATP9A PE=1 SV=3 829 1189 7.0E-54
sp|Q10309|YD56_SCHPO Putative phospholipid-transporting ATPase C6C3.06c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC6C3.06c PE=3 SV=1 95 684 9.0E-54
sp|A1A4J6|ATP9B_BOVIN Probable phospholipid-transporting ATPase IIB OS=Bos taurus GN=ATP9B PE=2 SV=1 829 1189 1.0E-53
sp|Q10309|YD56_SCHPO Putative phospholipid-transporting ATPase C6C3.06c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC6C3.06c PE=3 SV=1 829 1292 5.0E-50
sp|P40527|ATC7_YEAST Probable phospholipid-transporting ATPase NEO1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=NEO1 PE=1 SV=1 829 1183 5.0E-50
sp|P98195|ATP9B_MOUSE Probable phospholipid-transporting ATPase IIB OS=Mus musculus GN=Atp9b PE=1 SV=4 27 729 4.0E-49
sp|O70228|ATP9A_MOUSE Probable phospholipid-transporting ATPase IIA OS=Mus musculus GN=Atp9a PE=1 SV=3 90 684 6.0E-49
sp|D4ABB8|ATP9B_RAT Probable phospholipid-transporting ATPase IIB OS=Rattus norvegicus GN=Atp9b PE=3 SV=1 27 729 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 85 684 9.0E-49
sp|O75110|ATP9A_HUMAN Probable phospholipid-transporting ATPase IIA OS=Homo sapiens GN=ATP9A PE=1 SV=3 90 684 2.0E-48
sp|O43861|ATP9B_HUMAN Probable phospholipid-transporting ATPase IIB OS=Homo sapiens GN=ATP9B PE=2 SV=4 27 686 5.0E-47
sp|A1A4J6|ATP9B_BOVIN Probable phospholipid-transporting ATPase IIB OS=Bos taurus GN=ATP9B PE=2 SV=1 27 681 5.0E-46
sp|F1Q4S1|ATP9B_DANRE Probable phospholipid-transporting ATPase IIB OS=Danio rerio GN=atp9b PE=3 SV=1 27 681 3.0E-45
sp|O60423|AT8B3_HUMAN Phospholipid-transporting ATPase IK OS=Homo sapiens GN=ATP8B3 PE=2 SV=4 827 1248 1.0E-43
sp|Q6UQ17|AT8B3_MOUSE Phospholipid-transporting ATPase IK OS=Mus musculus GN=Atp8b3 PE=1 SV=1 977 1164 1.0E-40
sp|Q9UT43|YFRD_SCHPO Putative phospholipid-transporting ATPase C821.13c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC821.13c PE=1 SV=2 70 191 3.0E-23
sp|Q6UQ17|AT8B3_MOUSE Phospholipid-transporting ATPase IK OS=Mus musculus GN=Atp8b3 PE=1 SV=1 827 946 8.0E-22
sp|O94823|AT10B_HUMAN Probable phospholipid-transporting ATPase VB OS=Homo sapiens GN=ATP10B PE=2 SV=2 593 689 2.0E-11
sp|Q5XF89|AT133_MOUSE Probable cation-transporting ATPase 13A3 OS=Mus musculus GN=Atp13a3 PE=1 SV=1 825 1147 8.0E-10
sp|O36028|ATCZ_SCHPO Putative phospholipid-transporting ATPase C4F10.16c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC4F10.16c PE=3 SV=1 68 226 9.0E-10
sp|O54827|AT10A_MOUSE Probable phospholipid-transporting ATPase VA OS=Mus musculus GN=Atp10a PE=1 SV=4 594 688 1.0E-09
sp|Q9H7F0|AT133_HUMAN Probable cation-transporting ATPase 13A3 OS=Homo sapiens GN=ATP13A3 PE=1 SV=4 827 1147 2.0E-09
sp|Q3TYU2|AT135_MOUSE Probable cation-transporting ATPase 13A5 OS=Mus musculus GN=Atp13a5 PE=2 SV=2 817 1054 2.0E-09
sp|Q5ZKB7|AT134_CHICK Probable cation-transporting ATPase 13A4 OS=Gallus gallus GN=ATP13A4 PE=2 SV=1 860 1054 3.0E-09
sp|Q9GKS6|AT10D_MACFA Probable phospholipid-transporting ATPase VD (Fragment) OS=Macaca fascicularis GN=ATP10D PE=2 SV=1 602 692 4.0E-09
sp|Q4VNC0|AT135_HUMAN Probable cation-transporting ATPase 13A5 OS=Homo sapiens GN=ATP13A5 PE=2 SV=1 817 1054 8.0E-09
sp|Q21286|YBF7_CAEEL Probable cation-transporting ATPase K07E3.7 OS=Caenorhabditis elegans GN=K07E3.7/K07E3.6 PE=3 SV=4 827 1058 1.0E-08
sp|Q9P241|AT10D_HUMAN Probable phospholipid-transporting ATPase VD OS=Homo sapiens GN=ATP10D PE=2 SV=3 602 736 3.0E-08
sp|Q8K2X1|AT10D_MOUSE Probable phospholipid-transporting ATPase VD OS=Mus musculus GN=Atp10d PE=2 SV=2 593 736 6.0E-08
sp|P9WPS5|CTPI_MYCTU Probable cation-transporting ATPase I OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ctpI PE=1 SV=1 814 1135 1.0E-07
sp|Q4VNC1|AT134_HUMAN Probable cation-transporting ATPase 13A4 OS=Homo sapiens GN=ATP13A4 PE=2 SV=3 803 1054 1.0E-07
sp|P9WPS4|CTPI_MYCTO Probable cation-transporting ATPase I OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ctpI PE=3 SV=1 814 1135 1.0E-07
sp|Q12675|ATC4_YEAST Phospholipid-transporting ATPase DNF2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=DNF2 PE=1 SV=1 95 210 2.0E-07
sp|Q5XF90|AT134_MOUSE Probable cation-transporting ATPase 13A4 OS=Mus musculus GN=Atp13a4 PE=2 SV=1 826 1054 2.0E-07
sp|Q92126|ATP4A_XENLA Potassium-transporting ATPase alpha chain 1 OS=Xenopus laevis GN=atp4a PE=2 SV=3 829 1136 9.0E-07
sp|P35317|AT1A_HYDVU Sodium/potassium-transporting ATPase subunit alpha OS=Hydra vulgaris PE=2 SV=1 881 1053 1.0E-06
sp|Q9WV27|AT1A4_MOUSE Sodium/potassium-transporting ATPase subunit alpha-4 OS=Mus musculus GN=Atp1a4 PE=1 SV=3 882 1053 1.0E-06
sp|P17326|AT1A_ARTSF Sodium/potassium-transporting ATPase subunit alpha-A OS=Artemia franciscana PE=2 SV=1 880 1053 2.0E-06
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GO

(None)

SignalP

[Help with interpreting these statistics]
SignalP signal predicted Location
(based on Ymax)
D score
(significance: > 0.45)
No 1 - 42 0.45

Transmembrane Domains

Domain # Start End Length
1 138 160 22
2 381 403 22
3 423 442 19
4 1172 1194 22
5 1204 1226 22
6 1233 1252 19
7 1280 1302 22

Transcription Factor Class

(None)

Expression data

No expression data available for this genome

Sequences

Type of sequenceSequence
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 >Ophun1|5648
MSSASLPEKAPSLLVSSPQRRHLCDDDDDDDDHDTGPRLSMRYRLWTAVKTVYQANVVRLIWRKRHTDASNHGRH
IPLAIEHHRPLVDARRGYAYLSNNVRTSRYTIWDFIPKQLFFQFSRVGNFYFLCVGVPQMIPGLSTTGSFTTILP
LFFFVLLTVAKEGYDDYRRHILDTVENANYATVLGRHDPDIGRAELPPRWRRWNPFRTESTSQPRPAPKDEYLGV
GWVPSRWSQVKVGDVVLLSRDEPVPADLVLLHSDGENGVAYIDTMALDGETSLKTKQVCHALHGCSSIQGIAQCR
ADVVVEDPNPDLFNFQGRVTVSGKTVPLTLSDVVYRGSVLRNTRRAVGLVVNTGEECKVRMNSNQHPHAKRPALE
KIVNKVVFSLAVYVLVLSVGVSMGYVHFRAVYEKHAWFLDGATVPFHQIIIAFIIMFNNVVPLSLYISLEIVKVG
QLLLLNSDMDMYDAETDTPARCNTNTIMENLGQIGYVFSDKTGTLTDNVMKFRKLSVAGTVWLHATDLEESEDHG
KPPTLASRSSLGRRPSSQWRSTGRPDHVQPEVNTAHLMEHMRLRPHSAFSRTARDYLLAVAICHTCLPEIKHGRI
EFQASSPDELALVRAAQELGFGVTQRTSQSITVQVPRPNGQSEKMVFQILDVIEFSSARKRMSVVVRYPDGRISI
ICKGADSVILPRLRLSTLAKQRAHEVRKSAELEREMQRRSEQQEPRNSFGGRRSMTVRRNVEAVADGGAAPVTGW
RSLASRSRSFEVHNLARSSVDRPRTSAVARRGVSLDVSCNQGSTASHLRPQHDRLDFLNDAALHDESEVFSRCFK
HLDDFATEGLRTLVYAQRFVSDSEYRGWKKMYDEATTSLDDRQQMIEQAGELIESGLELVGATAIEDKLQRGVPE
AIDRLRRANIKIWMLTGDKRETAINIAHSARICRLASDLYVLDSDRSPLRAQLSALAEDLQAGSVHSVVVIDGQT
LAAVEKSAELSRRFFDLALLVDSVICCRASPAQKAMLVRAVRSRSRNKHGLTLAIGDGANDLAMIQASHVGVGIS
GKEGLQAARVADYAIGQFRFLQRLLLVHGRWNYVRTAKFVLCTFWKEMFFYLPTAVYQRYSGYSGTSLYQEVSLT
VFNTLFTSLCTICMGIWEQDLGADTVLAVPELYVYGQRGLGLGMAKYLRWMAVAVVEGLAVWYGVWAGYGRVSPS
DDGLYALGTLVFTVGVLWINWKLFILETHYKPSVILASFFLTTMGWFAWLAFLDGVYAPTPSGPYLIRHTLRHTW
GPDPAWWSTLFLVLALVSLIEVAVAILSRRRRRRLLNDTASLAENVEEWDVALWQELEQDPRVRARLRRLARDED
CEDEAGVSSA*
Coding >Ophun1|5648
ATGTCTTCTGCCTCGTTGCCTGAAAAGGCTCCCTCGCTTCTCGTCTCGAGTCCGCAGCGTCGTCACCTCTGTGAC
GATGACGATGACGATGACGACCATGATACCGGTCCCCGTCTGTCGATGCGATACCGCCTCTGGACCGCAGTCAAG
ACCGTCTATCAAGCCAATGTCGTCCGGCTGATATGGCGCAAGAGGCACACGGATGCCTCGAATCACGGTAGACAC
ATTCCTCTCGCCATCGAGCATCACCGTCCGCTCGTCGATGCCCGTCGCGGCTACGCCTATCTTTCCAACAATGTC
CGCACCTCTCGCTATACCATATGGGACTTTATACCCAAGCAACTCTTCTTTCAGTTTTCCCGCGTCGGAAACTTT
TACTTTCTCTGCGTTGGCGTCCCCCAGATGATACCAGGCCTGTCTACAACGGGGTCCTTCACCACCATTCTACCG
CTGTTCTTCTTCGTTCTCCTCACCGTCGCCAAGGAGGGCTACGACGACTATAGACGTCATATCTTGGATACGGTG
GAGAATGCAAACTATGCCACCGTCCTCGGCCGCCATGATCCGGATATCGGCCGCGCCGAATTGCCTCCTCGTTGG
CGACGCTGGAACCCTTTCCGTACCGAGTCCACCAGCCAACCGAGACCGGCTCCCAAGGACGAGTATCTCGGCGTC
GGATGGGTGCCTTCTCGATGGAGTCAGGTCAAGGTCGGCGACGTCGTCTTGTTATCTCGAGATGAGCCCGTGCCC
GCCGACTTGGTTCTTCTACATAGCGATGGCGAGAACGGGGTCGCTTACATCGACACCATGGCCCTAGACGGCGAG
ACTAGCCTCAAGACGAAGCAGGTCTGCCACGCGCTACATGGCTGCAGCTCCATTCAAGGCATCGCCCAATGCCGA
GCAGACGTTGTCGTCGAGGATCCAAACCCAGACCTCTTCAACTTTCAGGGCCGCGTCACCGTCAGCGGCAAGACG
GTGCCCCTGACTCTCAGCGATGTCGTCTACCGGGGCAGCGTGTTGCGAAATACAAGGCGAGCCGTCGGTCTCGTC
GTCAACACGGGCGAAGAGTGCAAGGTCCGGATGAACTCCAACCAGCACCCGCACGCCAAGCGGCCGGCCCTCGAG
AAGATTGTCAACAAGGTAGTCTTTAGCCTTGCCGTCTACGTCCTCGTTCTCTCCGTCGGCGTCTCCATGGGCTAC
GTCCACTTCCGCGCCGTCTATGAGAAGCATGCCTGGTTCCTCGACGGCGCCACAGTCCCGTTCCATCAGATCATC
ATCGCCTTCATCATCATGTTTAACAATGTCGTGCCCCTGTCGCTGTATATATCGCTCGAGATTGTAAAGGTTGGC
CAGCTTCTCCTGCTTAACTCGGACATGGACATGTATGACGCCGAGACAGACACGCCCGCGCGGTGCAACACCAAC
ACCATTATGGAAAACCTCGGTCAGATCGGCTACGTCTTCTCTGACAAGACGGGCACTCTGACGGACAACGTCATG
AAGTTTCGCAAGCTGAGCGTCGCCGGTACCGTCTGGCTTCATGCCACAGACTTGGAGGAGAGCGAGGACCACGGG
AAGCCGCCGACGCTGGCATCTCGCTCGTCGCTGGGTCGGAGACCGTCTTCTCAGTGGCGATCAACGGGCCGACCA
GACCACGTTCAGCCCGAGGTCAACACGGCGCATCTGATGGAGCACATGAGGCTGAGACCGCACTCGGCCTTTTCC
AGGACGGCCAGAGACTACTTGCTGGCCGTAGCCATCTGCCACACATGTCTGCCCGAGATCAAGCACGGGCGGATC
GAGTTCCAGGCGTCTTCTCCCGATGAGCTGGCCCTGGTGAGGGCGGCTCAGGAGCTCGGCTTCGGCGTCACGCAG
CGGACGTCGCAGAGCATAACGGTGCAGGTGCCGCGTCCCAACGGCCAGAGCGAGAAGATGGTGTTTCAGATCCTC
GACGTCATCGAGTTCAGCAGCGCGCGCAAGAGGATGTCGGTCGTGGTTCGGTATCCGGACGGACGCATCTCCATT
ATCTGCAAGGGCGCCGATTCCGTCATCCTGCCTCGGCTGAGGTTGTCGACGCTGGCCAAGCAGAGGGCGCACGAG
GTCCGCAAGAGCGCCGAACTGGAGCGCGAGATGCAGAGACGCAGCGAGCAGCAGGAGCCGCGCAATAGCTTTGGT
GGGAGGCGAAGCATGACGGTGAGGCGCAACGTTGAAGCCGTGGCTGATGGTGGTGCTGCTCCTGTTACAGGCTGG
CGTTCGCTGGCGAGCCGAAGCAGATCCTTTGAGGTTCACAACTTGGCTCGCTCGTCCGTCGACCGACCGCGGACT
TCGGCTGTGGCCCGGAGAGGAGTCTCGCTCGATGTGTCCTGTAACCAAGGCTCGACGGCGTCTCATCTGCGTCCC
CAGCACGACCGCCTCGACTTTCTCAACGATGCTGCCCTGCATGACGAGTCCGAGGTCTTTAGCCGCTGTTTCAAG
CATCTCGACGACTTCGCCACCGAGGGCCTCCGCACTCTCGTCTACGCTCAGAGGTTCGTGTCGGACTCGGAGTAT
CGCGGGTGGAAGAAGATGTATGACGAGGCGACGACGAGCCTCGACGACCGGCAGCAGATGATTGAGCAGGCCGGC
GAGCTGATCGAATCGGGCCTCGAGCTTGTCGGCGCCACGGCCATCGAGGACAAGCTGCAAAGGGGCGTCCCAGAG
GCCATCGACAGGCTTCGGCGGGCCAATATCAAGATCTGGATGCTGACGGGCGACAAGCGGGAAACGGCCATCAAC
ATTGCCCATTCGGCCCGCATCTGTCGGCTGGCGTCGGATCTATACGTGCTCGACTCTGACCGGAGCCCGCTGAGG
GCACAGCTGTCGGCGCTGGCCGAGGATCTACAGGCCGGCTCGGTCCACAGCGTCGTCGTCATCGACGGCCAGACG
CTGGCAGCCGTCGAGAAGTCAGCCGAACTGTCGAGGCGTTTCTTCGACCTGGCCCTGCTCGTCGACTCGGTCATC
TGCTGCCGAGCCTCTCCCGCGCAAAAGGCGATGCTGGTCCGAGCCGTGCGAAGCCGAAGCCGAAACAAGCACGGC
CTGACTCTGGCCATCGGCGACGGCGCAAACGACCTGGCCATGATCCAAGCCAGCCACGTCGGCGTCGGCATCTCG
GGAAAGGAGGGCCTCCAGGCGGCGCGTGTGGCCGATTACGCCATCGGCCAGTTCCGCTTCCTCCAGCGCCTCCTC
CTCGTCCACGGCCGCTGGAACTACGTGCGGACGGCCAAGTTCGTCCTCTGCACCTTTTGGAAGGAGATGTTCTTC
TACCTCCCCACGGCCGTCTACCAGCGCTACAGCGGCTACAGCGGCACCTCGCTCTACCAAGAGGTCAGCCTGACC
GTCTTCAACACGCTCTTCACCAGCCTCTGCACCATCTGCATGGGGATCTGGGAGCAGGACCTCGGCGCCGACACG
GTGCTCGCCGTCCCCGAGCTGTACGTCTACGGCCAGCGCGGGTTGGGTCTCGGCATGGCCAAGTATCTGCGCTGG
ATGGCCGTTGCCGTCGTCGAGGGCCTGGCGGTCTGGTACGGCGTCTGGGCGGGATACGGTCGCGTCTCTCCCTCT
GATGACGGGCTGTACGCGCTGGGGACGCTGGTTTTCACCGTGGGCGTCTTGTGGATCAACTGGAAGCTATTCATC
CTCGAAACCCACTACAAACCATCCGTCATCCTCGCCAGCTTCTTCCTCACAACCATGGGCTGGTTCGCCTGGCTC
GCCTTCCTAGACGGCGTCTACGCCCCGACCCCCTCAGGCCCCTACCTCATCCGCCACACCCTCCGCCATACCTGG
GGCCCCGACCCGGCCTGGTGGTCCACCCTCTTCCTCGTCCTCGCCCTCGTCTCCCTCATCGAGGTGGCCGTCGCC
ATCCTGTCCAGACGACGACGGCGACGCCTCCTCAACGACACGGCATCTCTGGCAGAGAACGTCGAGGAGTGGGAT
GTCGCCCTGTGGCAGGAACTCGAACAGGATCCCCGCGTGCGCGCTAGGCTTCGCCGCCTTGCTCGTGATGAGGAT
TGTGAGGATGAGGCTGGGGTGTCGTCTGCGTGA
Transcript >Ophun1|5648
ATGTCTTCTGCCTCGTTGCCTGAAAAGGCTCCCTCGCTTCTCGTCTCGAGTCCGCAGCGTCGTCACCTCTGTGAC
GATGACGATGACGATGACGACCATGATACCGGTCCCCGTCTGTCGATGCGATACCGCCTCTGGACCGCAGTCAAG
ACCGTCTATCAAGCCAATGTCGTCCGGCTGATATGGCGCAAGAGGCACACGGATGCCTCGAATCACGGTAGACAC
ATTCCTCTCGCCATCGAGCATCACCGTCCGCTCGTCGATGCCCGTCGCGGCTACGCCTATCTTTCCAACAATGTC
CGCACCTCTCGCTATACCATATGGGACTTTATACCCAAGCAACTCTTCTTTCAGTTTTCCCGCGTCGGAAACTTT
TACTTTCTCTGCGTTGGCGTCCCCCAGATGATACCAGGCCTGTCTACAACGGGGTCCTTCACCACCATTCTACCG
CTGTTCTTCTTCGTTCTCCTCACCGTCGCCAAGGAGGGCTACGACGACTATAGACGTCATATCTTGGATACGGTG
GAGAATGCAAACTATGCCACCGTCCTCGGCCGCCATGATCCGGATATCGGCCGCGCCGAATTGCCTCCTCGTTGG
CGACGCTGGAACCCTTTCCGTACCGAGTCCACCAGCCAACCGAGACCGGCTCCCAAGGACGAGTATCTCGGCGTC
GGATGGGTGCCTTCTCGATGGAGTCAGGTCAAGGTCGGCGACGTCGTCTTGTTATCTCGAGATGAGCCCGTGCCC
GCCGACTTGGTTCTTCTACATAGCGATGGCGAGAACGGGGTCGCTTACATCGACACCATGGCCCTAGACGGCGAG
ACTAGCCTCAAGACGAAGCAGGTCTGCCACGCGCTACATGGCTGCAGCTCCATTCAAGGCATCGCCCAATGCCGA
GCAGACGTTGTCGTCGAGGATCCAAACCCAGACCTCTTCAACTTTCAGGGCCGCGTCACCGTCAGCGGCAAGACG
GTGCCCCTGACTCTCAGCGATGTCGTCTACCGGGGCAGCGTGTTGCGAAATACAAGGCGAGCCGTCGGTCTCGTC
GTCAACACGGGCGAAGAGTGCAAGGTCCGGATGAACTCCAACCAGCACCCGCACGCCAAGCGGCCGGCCCTCGAG
AAGATTGTCAACAAGGTAGTCTTTAGCCTTGCCGTCTACGTCCTCGTTCTCTCCGTCGGCGTCTCCATGGGCTAC
GTCCACTTCCGCGCCGTCTATGAGAAGCATGCCTGGTTCCTCGACGGCGCCACAGTCCCGTTCCATCAGATCATC
ATCGCCTTCATCATCATGTTTAACAATGTCGTGCCCCTGTCGCTGTATATATCGCTCGAGATTGTAAAGGTTGGC
CAGCTTCTCCTGCTTAACTCGGACATGGACATGTATGACGCCGAGACAGACACGCCCGCGCGGTGCAACACCAAC
ACCATTATGGAAAACCTCGGTCAGATCGGCTACGTCTTCTCTGACAAGACGGGCACTCTGACGGACAACGTCATG
AAGTTTCGCAAGCTGAGCGTCGCCGGTACCGTCTGGCTTCATGCCACAGACTTGGAGGAGAGCGAGGACCACGGG
AAGCCGCCGACGCTGGCATCTCGCTCGTCGCTGGGTCGGAGACCGTCTTCTCAGTGGCGATCAACGGGCCGACCA
GACCACGTTCAGCCCGAGGTCAACACGGCGCATCTGATGGAGCACATGAGGCTGAGACCGCACTCGGCCTTTTCC
AGGACGGCCAGAGACTACTTGCTGGCCGTAGCCATCTGCCACACATGTCTGCCCGAGATCAAGCACGGGCGGATC
GAGTTCCAGGCGTCTTCTCCCGATGAGCTGGCCCTGGTGAGGGCGGCTCAGGAGCTCGGCTTCGGCGTCACGCAG
CGGACGTCGCAGAGCATAACGGTGCAGGTGCCGCGTCCCAACGGCCAGAGCGAGAAGATGGTGTTTCAGATCCTC
GACGTCATCGAGTTCAGCAGCGCGCGCAAGAGGATGTCGGTCGTGGTTCGGTATCCGGACGGACGCATCTCCATT
ATCTGCAAGGGCGCCGATTCCGTCATCCTGCCTCGGCTGAGGTTGTCGACGCTGGCCAAGCAGAGGGCGCACGAG
GTCCGCAAGAGCGCCGAACTGGAGCGCGAGATGCAGAGACGCAGCGAGCAGCAGGAGCCGCGCAATAGCTTTGGT
GGGAGGCGAAGCATGACGGTGAGGCGCAACGTTGAAGCCGTGGCTGATGGTGGTGCTGCTCCTGTTACAGGCTGG
CGTTCGCTGGCGAGCCGAAGCAGATCCTTTGAGGTTCACAACTTGGCTCGCTCGTCCGTCGACCGACCGCGGACT
TCGGCTGTGGCCCGGAGAGGAGTCTCGCTCGATGTGTCCTGTAACCAAGGCTCGACGGCGTCTCATCTGCGTCCC
CAGCACGACCGCCTCGACTTTCTCAACGATGCTGCCCTGCATGACGAGTCCGAGGTCTTTAGCCGCTGTTTCAAG
CATCTCGACGACTTCGCCACCGAGGGCCTCCGCACTCTCGTCTACGCTCAGAGGTTCGTGTCGGACTCGGAGTAT
CGCGGGTGGAAGAAGATGTATGACGAGGCGACGACGAGCCTCGACGACCGGCAGCAGATGATTGAGCAGGCCGGC
GAGCTGATCGAATCGGGCCTCGAGCTTGTCGGCGCCACGGCCATCGAGGACAAGCTGCAAAGGGGCGTCCCAGAG
GCCATCGACAGGCTTCGGCGGGCCAATATCAAGATCTGGATGCTGACGGGCGACAAGCGGGAAACGGCCATCAAC
ATTGCCCATTCGGCCCGCATCTGTCGGCTGGCGTCGGATCTATACGTGCTCGACTCTGACCGGAGCCCGCTGAGG
GCACAGCTGTCGGCGCTGGCCGAGGATCTACAGGCCGGCTCGGTCCACAGCGTCGTCGTCATCGACGGCCAGACG
CTGGCAGCCGTCGAGAAGTCAGCCGAACTGTCGAGGCGTTTCTTCGACCTGGCCCTGCTCGTCGACTCGGTCATC
TGCTGCCGAGCCTCTCCCGCGCAAAAGGCGATGCTGGTCCGAGCCGTGCGAAGCCGAAGCCGAAACAAGCACGGC
CTGACTCTGGCCATCGGCGACGGCGCAAACGACCTGGCCATGATCCAAGCCAGCCACGTCGGCGTCGGCATCTCG
GGAAAGGAGGGCCTCCAGGCGGCGCGTGTGGCCGATTACGCCATCGGCCAGTTCCGCTTCCTCCAGCGCCTCCTC
CTCGTCCACGGCCGCTGGAACTACGTGCGGACGGCCAAGTTCGTCCTCTGCACCTTTTGGAAGGAGATGTTCTTC
TACCTCCCCACGGCCGTCTACCAGCGCTACAGCGGCTACAGCGGCACCTCGCTCTACCAAGAGGTCAGCCTGACC
GTCTTCAACACGCTCTTCACCAGCCTCTGCACCATCTGCATGGGGATCTGGGAGCAGGACCTCGGCGCCGACACG
GTGCTCGCCGTCCCCGAGCTGTACGTCTACGGCCAGCGCGGGTTGGGTCTCGGCATGGCCAAGTATCTGCGCTGG
ATGGCCGTTGCCGTCGTCGAGGGCCTGGCGGTCTGGTACGGCGTCTGGGCGGGATACGGTCGCGTCTCTCCCTCT
GATGACGGGCTGTACGCGCTGGGGACGCTGGTTTTCACCGTGGGCGTCTTGTGGATCAACTGGAAGCTATTCATC
CTCGAAACCCACTACAAACCATCCGTCATCCTCGCCAGCTTCTTCCTCACAACCATGGGCTGGTTCGCCTGGCTC
GCCTTCCTAGACGGCGTCTACGCCCCGACCCCCTCAGGCCCCTACCTCATCCGCCACACCCTCCGCCATACCTGG
GGCCCCGACCCGGCCTGGTGGTCCACCCTCTTCCTCGTCCTCGCCCTCGTCTCCCTCATCGAGGTGGCCGTCGCC
ATCCTGTCCAGACGACGACGGCGACGCCTCCTCAACGACACGGCATCTCTGGCAGAGAACGTCGAGGAGTGGGAT
GTCGCCCTGTGGCAGGAACTCGAACAGGATCCCCGCGTGCGCGCTAGGCTTCGCCGCCTTGCTCGTGATGAGGAT
TGTGAGGATGAGGCTGGGGTGTCGTCTGCGTGA
Gene >Ophun1|5648
ATGTCTTCTGCCTCGTTGCCTGAAAAGGCTCCCTCGCTTCTCGTCTCGAGTCCGCAGCGTCGTCACCTCTGTGAC
GATGACGATGACGATGACGACCATGATACCGGTCCCCGTCTGTCGATGCGATACCGCCTCTGGACCGCAGTCAAG
ACCGTCTATCAAGCCAATGTCGTCCGGCTGATATGGCGCAAGAGGCACACGGATGCCTCGAATCACGGTAGACAC
ATTCCTCTCGCCATCGAGCATCACCGTCCGCTCGTCGATGCCCGTCGCGGCTACGCCTATCTTTCCAACAATGTC
CGCACCTCTCGCTATACCATATGGGACTTTATACCCAAGCAACTCTTCTTTCAGTTTTCCCGCGTCGGAAACTTT
TACTTTCTCTGCGTTGGCGTCCCCCAGATGGTATGTGAAAATCTCCGTCTCGTAAGTCTTGTCTTGTCCCGTCTC
TTGAGTTGACCGGGCTCCAGATACCAGGCCTGTCTACAACGGGGTCCTTCACCACCATTCTACCGCTGTTCTTCT
TCGTTCTCCTCACCGTCGCCAAGGAGGGCTACGACGACTATAGACGTCATATCTTGGATACGGTGGAGAATGCAA
ACTATGCCACCGTCCTCGGCCGCCATGATCCGGATATCGGCCGCGCCGAATTGCCTCCTCGTTGGCGACGCTGGA
ACCCTTTCCGTACCGAGTCCACCAGCCAACCGAGACCGGCTCCCAAGGACGAGTATCTCGGCGTCGGATGGGTGC
CTTCTCGATGGAGTCAGGTCAAGGTCGGCGACGTCGTCTTGTTATCTCGAGATGAGCCCGTGCCCGCCGACTTGG
TTCTTCTACATAGCGATGGCGAGAACGGGGTCGCTTACATCGACACCATGGCCCTAGACGGCGAGACTAGCCTCA
AGACGAAGCAGGTCTGCCACGCGCTACATGGCTGCAGCTCCATTCAAGGCATCGCCCAATGCCGAGCAGACGTTG
TCGTCGAGGATCCAAACCCAGACCTCTTCAACTTTCAGGGCCGCGTCACCGTCAGCGGCAAGACGGTGCCCCTGA
CTCTCAGCGATGTCGTCTACCGGGGCAGCGTGTTGCGAAATACAAGGCGAGCCGTCGGTCTCGTCGTCAACACGG
GCGAAGAGTGCAAGGTCCGGATGAACTCCAACCAGCACCCGCACGCCAAGCGGCCGGCCCTCGAGAAGATTGTCA
ACAAGGTAGTCTTTAGCCTTGCCGTCTACGTCCTCGTTCTCTCCGTCGGCGTCTCCATGGGCTACGTCCACTTCC
GCGCCGTCTATGAGAAGCATGCCTGGTTCCTCGACGGCGCCACAGTCCCGTTCCATCAGATCATCATCGCCTTCA
TCATCATGTTTAACAATGTCGTGCCCCTGTCGCTGTATATATCGCTCGAGATTGTAAAGGTTGGCCAGCTTCTCC
TGCTTAACTCGGACATGGACATGTATGACGCCGAGACAGACACGCCCGCGCGGTGCAACACCAACACCATTATGG
AAAACCTCGGTCAGATCGGCTACGTCTTCTCTGACAAGACGGGCACTCTGACGGACAACGTCATGAAGTTTCGCA
AGCTGAGCGTCGCCGGTACCGTCTGGCTTCATGCCACAGACTTGGAGGAGAGCGAGGACCACGGGAAGCCGCCGA
CGCTGGCATCTCGCTCGTCGCTGGGTCGGAGACCGTCTTCTCAGTGGCGATCAACGGGCCGACCAGACCACGTTC
AGCCCGAGGTCAACACGGCGCATCTGATGGAGCACATGAGGCTGAGACCGCACTCGGCCTTTTCCAGGACGGCCA
GAGACTACTTGCTGGCCGTAGCCATCTGCCACACATGTCTGCCCGAGATCAAGCACGGGCGGATCGAGTTCCAGG
CGTCTTCTCCCGATGAGCTGGCCCTGGTGAGGGCGGCTCAGGAGCTCGGCTTCGGCGTCACGCAGCGGACGTCGC
AGAGCATAACGGTGCAGGTGCCGCGTCCCAACGGCCAGAGCGAGAAGATGGTGTTTCAGATCCTCGACGTCATCG
AGTTCAGCAGCGCGCGCAAGAGGATGTCGGTCGTGGTTCGGTATCCGGACGGACGCATCTCCATTATCTGCAAGG
GCGCCGATTCCGTCATCCTGCCTCGGCTGAGGTTGTCGACGCTGGCCAAGCAGAGGGCGCACGAGGTCCGCAAGA
GCGCCGAACTGGAGCGCGAGATGCAGAGACGCAGCGAGCAGCAGGAGCCGCGCAATAGCTTTGGTGGGAGGCGAA
GCATGACGGTGAGGCGCAACGTTGAAGCCGTGGCTGATGGTGGTGCTGCTCCTGTTACAGGCTGGCGTTCGCTGG
CGAGCCGAAGCAGATCCTTTGAGGTTCACAACTTGGCTCGCTCGTCCGTCGACCGACCGCGGACTTCGGCTGTGG
CCCGGAGAGGAGTCTCGCTCGATGTGTCCTGTAACCAAGGCTCGACGGCGTCTCATCTGCGTCCCCAGCACGACC
GCCTCGACTTTCTCAACGATGCTGCCCTGCATGACGAGTCCGAGGTCTTTAGCCGCTGTTTCAAGCATCTCGACG
ACTTCGCCACCGAGGGCCTCCGCACTCTCGTCTACGCTCAGAGGTTCGTGTCGGACTCGGAGTATCGCGGGTGGA
AGAAGATGTATGACGAGGCGACGACGAGCCTCGACGACCGGCAGCAGATGATTGAGCAGGCCGGCGAGCTGATCG
AATCGGGCCTCGAGCTTGTCGGCGCCACGGCCATCGAGGACAAGCTGCAAAGGGGCGTCCCAGAGGCCATCGACA
GGCTTCGGCGGGCCAATATCAAGATCTGGATGCTGACGGGCGACAAGCGGGAAACGGCCATCAACATTGCCCATT
CGGCCCGCATCTGTCGGCTGGCGTCGGATCTATACGTGCTCGACTCTGACCGGAGCCCGCTGAGGGCACAGCTGT
CGGCGCTGGCCGAGGATCTACAGGCCGGCTCGGTCCACAGCGTCGTCGTCATCGACGGCCAGACGCTGGCAGCCG
TCGAGAAGTCAGCCGAACTGTCGAGGCGTTTCTTCGACCTGGCCCTGCTCGTCGACTCGGTCATCTGCTGCCGAG
CCTCTCCCGCGCAAAAGGCGATGCTGGTCCGAGCCGTGCGAAGCCGAAGCCGAAACAAGCACGGCCTGACTCTGG
CCATCGGCGACGGCGCAAACGACCTGGCCATGATCCAAGCCAGCCACGTCGGCGTCGGCATCTCGGGAAAGGAGG
GCCTCCAGGCGGCGCGTGTGGCCGATTACGCCATCGGCCAGTTCCGCTTCCTCCAGCGCCTCCTCCTCGTCCACG
GCCGCTGGAACTACGTGCGGACGGCCAAGTTCGTCCTCTGCACCTTTTGGAAGGAGATGTTCTTCTACCTCCCCA
CGGCCGTCTACCAGCGCTACAGCGGCTACAGCGGCACCTCGCTCTACCAAGAGGTCAGCCTGACCGTCTTCAACA
CGCTCTTCACCAGCCTCTGCACCATCTGCATGGGGATCTGGGAGCAGGACCTCGGCGCCGACACGGTGCTCGCCG
TCCCCGAGCTGTACGTCTACGGCCAGCGCGGGTTGGGTCTCGGCATGGCCAAGTATCTGCGCTGGATGGCCGTTG
CCGTCGTCGAGGGCCTGGCGGTCTGGTACGGCGTCTGGGCGGGATACGGTCGCGTCTCTCCCTCTGATGACGGGC
TGTACGCGCTGGGGACGCTGGTTTTCACCGTGGGCGTCTTGTGGATCAACTGGAAGCTATTGTGAGTCGTAATAC
ACCCATAGAAGACACCACCTTACTGACCAACCCTGCAAGCATCCTCGAAACCCACTACAAACCATCCGTCATCCT
CGCCAGCTTCTTCCTCACAACCATGGGCTGGTTCGCCTGGCTCGCCTTCCTAGACGGCGTCTACGCCCCGACCCC
CTCAGGCCCCTACCTCATCCGCCACACCCTCCGCCATACCTGGGGCCCCGACCCGGCCTGGTGGTCCACCCTCTT
CCTCGTCCTCGCCCTCGTCTCCCTCATCGAGGTGGCCGTCGCCATCCTGTCCAGACGACGACGGCGACGCCTCCT
CAACGACACGGCATCTCTGGCAGAGAACGTCGAGGAGTGGGATGTCGCCCTGTGGCAGGAACTCGAACAGGATCC
CCGCGTGCGCGCTAGGCTTCGCCGCCTTGCTCGTGATGAGGATTGTGAGGATGAGGCTGGGGTGTCGTCTGCGTG
A

© 2022 - Robin Ohm - Utrecht University - The Netherlands

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