Protein ID | Hirsu2|11041 |
Gene name | |
Location | Contig_951:2273..4091 |
Strand | + |
Gene length (bp) | 1818 |
Transcript length (bp) | 1761 |
Coding sequence length (bp) | 1761 |
Protein length (aa) | 587 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF01794 | Ferric_reduct | Ferric reductase like transmembrane component | 1.7E-23 | 150 | 268 |
PF08030 | NAD_binding_6 | Ferric reductase NAD binding domain | 5.8E-11 | 437 | 518 |
PF08022 | FAD_binding_8 | FAD-binding domain | 9.2E-06 | 319 | 428 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|P36033|FRE2_YEAST | Ferric/cupric reductase transmembrane component 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE2 PE=1 SV=1 | 87 | 586 | 1.0E-40 |
sp|Q08905|FRE3_YEAST | Ferric reductase transmembrane component 3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE3 PE=1 SV=1 | 79 | 586 | 1.0E-39 |
sp|P53746|FRE4_YEAST | Ferric reductase transmembrane component 4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE4 PE=2 SV=1 | 84 | 586 | 7.0E-32 |
sp|Q08908|FRE5_YEAST | Ferric reductase transmembrane component 5 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE5 PE=2 SV=1 | 93 | 586 | 1.0E-30 |
sp|P78588|FREL_CANAX | Probable ferric reductase transmembrane component OS=Candida albicans GN=CFL1 PE=3 SV=1 | 79 | 568 | 1.0E-27 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|P36033|FRE2_YEAST | Ferric/cupric reductase transmembrane component 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE2 PE=1 SV=1 | 87 | 586 | 1.0E-40 |
sp|Q08905|FRE3_YEAST | Ferric reductase transmembrane component 3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE3 PE=1 SV=1 | 79 | 586 | 1.0E-39 |
sp|P53746|FRE4_YEAST | Ferric reductase transmembrane component 4 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE4 PE=2 SV=1 | 84 | 586 | 7.0E-32 |
sp|Q08908|FRE5_YEAST | Ferric reductase transmembrane component 5 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE5 PE=2 SV=1 | 93 | 586 | 1.0E-30 |
sp|P78588|FREL_CANAX | Probable ferric reductase transmembrane component OS=Candida albicans GN=CFL1 PE=3 SV=1 | 79 | 568 | 1.0E-27 |
sp|Q12473|FRE6_YEAST | Ferric reductase transmembrane component 6 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE6 PE=1 SV=1 | 79 | 586 | 1.0E-27 |
sp|Q5A446|FRE1_CANAL | Ferric/cupric reductase transmembrane component 1 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=CFL1 PE=2 SV=1 | 79 | 568 | 1.0E-27 |
sp|P32791|FRE1_YEAST | Ferric/cupric reductase transmembrane component 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE1 PE=1 SV=1 | 147 | 586 | 2.0E-26 |
sp|O94727|FRP2_SCHPO | Ferric/cupric reductase transmembrane component 2 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=frp2 PE=3 SV=1 | 91 | 569 | 7.0E-12 |
sp|Q9ES45|DUOX2_RAT | Dual oxidase 2 OS=Rattus norvegicus GN=Duox2 PE=2 SV=1 | 146 | 580 | 2.0E-10 |
sp|Q12333|FRE7_YEAST | Ferric/cupric reductase transmembrane component 7 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=FRE7 PE=1 SV=2 | 148 | 530 | 2.0E-10 |
sp|P92949|FRO2_ARATH | Ferric reduction oxidase 2 OS=Arabidopsis thaliana GN=FRO2 PE=1 SV=2 | 148 | 522 | 2.0E-10 |
sp|A6ZN61|FRE7_YEAS7 | Ferric/cupric reductase transmembrane component 7 OS=Saccharomyces cerevisiae (strain YJM789) GN=FRE7 PE=3 SV=1 | 148 | 530 | 7.0E-10 |
sp|Q8HZK2|DUOX2_PIG | Dual oxidase 2 OS=Sus scrofa GN=DUOX2 PE=1 SV=2 | 119 | 580 | 2.0E-09 |
sp|Q8RWS6|FRO6_ARATH | Ferric reduction oxidase 6 OS=Arabidopsis thaliana GN=FRO6 PE=2 SV=1 | 137 | 517 | 2.0E-09 |
sp|F4I4K7|FRO3_ARATH | Ferric reduction oxidase 3, mitochondrial OS=Arabidopsis thaliana GN=FRO3 PE=2 SV=1 | 165 | 514 | 2.0E-08 |
sp|Q3KTM0|FRO7_ARATH | Ferric reduction oxidase 7, chloroplastic OS=Arabidopsis thaliana GN=FRO7 PE=2 SV=1 | 137 | 516 | 3.0E-08 |
sp|C8Z891|AIM14_YEAS8 | Probable metalloreductase AIM14 OS=Saccharomyces cerevisiae (strain Lalvin EC1118 / Prise de mousse) GN=AIM14 PE=3 SV=1 | 184 | 511 | 9.0E-08 |
sp|P53109|AIM14_YEAST | Probable metalloreductase AIM14 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=AIM14 PE=1 SV=1 | 184 | 511 | 1.0E-07 |
sp|Q9FLW2|FRO5_ARATH | Ferric reduction oxidase 5 OS=Arabidopsis thaliana GN=FRO5 PE=2 SV=1 | 37 | 512 | 1.0E-07 |
sp|Q8W110|FRO4_ARATH | Ferric reduction oxidase 4 OS=Arabidopsis thaliana GN=FRO4 PE=2 SV=1 | 166 | 512 | 2.0E-07 |
sp|B3LHL3|AIM14_YEAS1 | Probable metalloreductase AIM14 OS=Saccharomyces cerevisiae (strain RM11-1a) GN=AIM14 PE=3 SV=1 | 184 | 511 | 2.0E-07 |
sp|A6ZU25|AIM14_YEAS7 | Probable metalloreductase AIM14 OS=Saccharomyces cerevisiae (strain YJM789) GN=AIM14 PE=3 SV=1 | 184 | 511 | 2.0E-07 |
sp|C7GPP6|AIM14_YEAS2 | Probable metalloreductase AIM14 OS=Saccharomyces cerevisiae (strain JAY291) GN=AIM14 PE=3 SV=1 | 184 | 491 | 4.0E-07 |
sp|Q9NRD9|DUOX1_HUMAN | Dual oxidase 1 OS=Homo sapiens GN=DUOX1 PE=1 SV=1 | 319 | 579 | 6.0E-07 |
GO Term | Description | Terminal node |
---|---|---|
GO:0016491 | oxidoreductase activity | Yes |
GO:0003674 | molecular_function | No |
GO:0003824 | catalytic activity | No |
SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
---|---|---|
No | 1 - 58 | 0.5 |
Domain # | Start | End | Length |
---|---|---|---|
1 | 27 | 49 | 22 |
2 | 115 | 137 | 22 |
3 | 152 | 174 | 22 |
4 | 187 | 209 | 22 |
5 | 224 | 243 | 19 |
6 | 250 | 272 | 22 |
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 | >Hirsu2|11041 MDPTPSLQIREADGSREEPLNMLFKDVLWWTLGIVALIVLTIRILEILWAKLRQVSAMSQPRDKQGYWRISQWSW MPPLKKHLTYAPLLRKRHNREFRLSSAVNVGTLPSRLHSLLLFLYLASNTAYMFVLDWSVANKFALCAELRGRSG TLSVVNMIPLVILAGRNNPLIPLLKISFDTYNLLHRWIGRVVVAEVIIHTVAWAIPAVAHKGWSAAFGAAVKSVF IGSGFWAAVAMTLLLLLSLSPIRHAFYETFLNTHIILAVVALGGTWIHCSSASLPPLPWAIAVVALWMADRLARV LRLVFTNWSNRGVTDALCEALPGEVTRVTLQLPRYVRIEPGTHAYLRFWGVRPWESHPFSIAWVEYQAANALPTS EKEPLTAVDRKTASTSVSFIIGAQTGMTRLLYDRASKSPAGVRLRAAMEGPYAGHHNLDSYGHVVLFAGSTGITH QISHVRHLLDGYNEGMVATRRLTLVWIIRTYETLEWVRPYMDMILRIPNRKDILRIQVFVTRPQNPRDIVSASST VKMFPGRPNIPLLLVKEVQDQIGAMSVSVCGPGGLADDVRGAVRAVQGDSVIDFIEESFTW* |
Coding | >Hirsu2|11041 ATGGATCCCACCCCGTCACTCCAGATCCGTGAGGCCGATGGCTCTCGGGAAGAGCCCTTGAACATGCTCTTCAAA GATGTCCTCTGGTGGACGCTGGGCATCGTCGCCCTGATTGTTCTGACCATCAGGATCCTGGAGATCCTGTGGGCC AAGCTTCGCCAGGTCTCGGCCATGTCGCAGCCGCGCGACAAGCAGGGCTACTGGAGGATCTCGCAATGGAGCTGG ATGCCGCCCCTCAAGAAGCACCTCACCTACGCCCCGTTGCTGAGGAAGCGCCACAACCGTGAGTTTCGCCTGTCG TCGGCCGTGAATGTCGGCACCCTGCCCTCGCGCCTGCACTCGCTGCTGCTCTTCCTCTACCTCGCCAGCAATACG GCCTACATGTTCGTCCTCGACTGGTCTGTCGCCAACAAGTTCGCCCTCTGCGCCGAGCTGCGCGGCCGCTCCGGC ACCCTCTCCGTCGTCAACATGATCCCCCTCGTCATCCTGGCCGGCCGCAACAACCCCCTGATTCCGCTGCTCAAA ATCAGCTTTGACACGTATAACCTGCTGCATCGCTGGATTGGCCGCGTCGTCGTTGCCGAGGTCATCATCCACACC GTCGCCTGGGCCATCCCGGCCGTCGCCCACAAGGGCTGGTCGGCCGCCTTTGGCGCCGCCGTCAAGAGCGTCTTC ATCGGCTCCGGCTTCTGGGCCGCCGTCGCCATGACGCTCCTGCTCCTGCTCTCCCTCTCCCCCATCCGCCACGCC TTTTACGAGACCTTCCTCAACACGCACATCATCCTGGCCGTCGTCGCCCTCGGCGGCACCTGGATCCACTGCTCC TCGGCCTCGCTCCCGCCCCTGCCCTGGGCCATCGCCGTCGTGGCCCTGTGGATGGCGGACCGGCTCGCCCGCGTC CTCCGCCTCGTCTTCACTAACTGGTCCAACAGGGGTGTGACGGACGCGCTCTGCGAGGCCTTGCCCGGCGAGGTG ACGCGCGTCACGCTGCAGCTCCCGCGCTACGTCCGCATCGAGCCCGGCACGCACGCCTACCTGCGCTTCTGGGGC GTCCGCCCGTGGGAGAGCCACCCCTTCTCCATCGCCTGGGTCGAGTACCAGGCCGCCAACGCGCTGCCCACGTCG GAGAAGGAGCCGCTCACCGCCGTGGACCGTAAAACGGCCTCGACCTCGGTCTCCTTCATCATCGGCGCCCAGACG GGCATGACGCGCCTGCTCTACGACCGCGCCAGCAAGTCGCCCGCCGGCGTCCGGCTGCGGGCCGCCATGGAGGGT CCCTACGCCGGCCACCACAACCTCGACTCGTACGGCCACGTCGTTCTCTTTGCCGGCTCGACGGGCATCACGCAC CAGATTTCGCACGTCCGCCACCTGCTCGACGGCTACAACGAGGGCATGGTGGCGACGCGGAGGCTCACGCTCGTG TGGATCATCCGGACCTACGAGACGCTCGAGTGGGTGCGTCCGTACATGGACATGATCCTGCGGATACCCAACCGC AAGGACATCCTGCGCATCCAGGTCTTCGTCACCCGGCCGCAGAACCCGCGCGACATCGTCAGCGCCAGCTCCACG GTCAAGATGTTCCCCGGACGGCCCAACATTCCGCTGCTCCTGGTCAAGGAGGTGCAGGACCAGATCGGCGCCATG TCGGTGAGCGTGTGCGGGCCCGGCGGCCTGGCCGACGACGTGCGCGGCGCCGTCCGCGCTGTACAGGGCGACTCC GTCATCGACTTCATCGAAGAGAGCTTTACGTGGTGA |
Transcript | >Hirsu2|11041 ATGGATCCCACCCCGTCACTCCAGATCCGTGAGGCCGATGGCTCTCGGGAAGAGCCCTTGAACATGCTCTTCAAA GATGTCCTCTGGTGGACGCTGGGCATCGTCGCCCTGATTGTTCTGACCATCAGGATCCTGGAGATCCTGTGGGCC AAGCTTCGCCAGGTCTCGGCCATGTCGCAGCCGCGCGACAAGCAGGGCTACTGGAGGATCTCGCAATGGAGCTGG ATGCCGCCCCTCAAGAAGCACCTCACCTACGCCCCGTTGCTGAGGAAGCGCCACAACCGTGAGTTTCGCCTGTCG TCGGCCGTGAATGTCGGCACCCTGCCCTCGCGCCTGCACTCGCTGCTGCTCTTCCTCTACCTCGCCAGCAATACG GCCTACATGTTCGTCCTCGACTGGTCTGTCGCCAACAAGTTCGCCCTCTGCGCCGAGCTGCGCGGCCGCTCCGGC ACCCTCTCCGTCGTCAACATGATCCCCCTCGTCATCCTGGCCGGCCGCAACAACCCCCTGATTCCGCTGCTCAAA ATCAGCTTTGACACGTATAACCTGCTGCATCGCTGGATTGGCCGCGTCGTCGTTGCCGAGGTCATCATCCACACC GTCGCCTGGGCCATCCCGGCCGTCGCCCACAAGGGCTGGTCGGCCGCCTTTGGCGCCGCCGTCAAGAGCGTCTTC ATCGGCTCCGGCTTCTGGGCCGCCGTCGCCATGACGCTCCTGCTCCTGCTCTCCCTCTCCCCCATCCGCCACGCC TTTTACGAGACCTTCCTCAACACGCACATCATCCTGGCCGTCGTCGCCCTCGGCGGCACCTGGATCCACTGCTCC TCGGCCTCGCTCCCGCCCCTGCCCTGGGCCATCGCCGTCGTGGCCCTGTGGATGGCGGACCGGCTCGCCCGCGTC CTCCGCCTCGTCTTCACTAACTGGTCCAACAGGGGTGTGACGGACGCGCTCTGCGAGGCCTTGCCCGGCGAGGTG ACGCGCGTCACGCTGCAGCTCCCGCGCTACGTCCGCATCGAGCCCGGCACGCACGCCTACCTGCGCTTCTGGGGC GTCCGCCCGTGGGAGAGCCACCCCTTCTCCATCGCCTGGGTCGAGTACCAGGCCGCCAACGCGCTGCCCACGTCG GAGAAGGAGCCGCTCACCGCCGTGGACCGTAAAACGGCCTCGACCTCGGTCTCCTTCATCATCGGCGCCCAGACG GGCATGACGCGCCTGCTCTACGACCGCGCCAGCAAGTCGCCCGCCGGCGTCCGGCTGCGGGCCGCCATGGAGGGT CCCTACGCCGGCCACCACAACCTCGACTCGTACGGCCACGTCGTTCTCTTTGCCGGCTCGACGGGCATCACGCAC CAGATTTCGCACGTCCGCCACCTGCTCGACGGCTACAACGAGGGCATGGTGGCGACGCGGAGGCTCACGCTCGTG TGGATCATCCGGACCTACGAGACGCTCGAGTGGGTGCGTCCGTACATGGACATGATCCTGCGGATACCCAACCGC AAGGACATCCTGCGCATCCAGGTCTTCGTCACCCGGCCGCAGAACCCGCGCGACATCGTCAGCGCCAGCTCCACG GTCAAGATGTTCCCCGGACGGCCCAACATTCCGCTGCTCCTGGTCAAGGAGGTGCAGGACCAGATCGGCGCCATG TCGGTGAGCGTGTGCGGGCCCGGCGGCCTGGCCGACGACGTGCGCGGCGCCGTCCGCGCTGTACAGGGCGACTCC GTCATCGACTTCATCGAAGAGAGCTTTACGTGGTGA |
Gene | >Hirsu2|11041 ATGGATCCCACCCCGTCACTCCAGATCCGTGAGGCCGATGGCTCTCGGGAAGAGGTACAGCCCAGTTCGACAATT GCCCCGTATTACACGGCGCTAAATGGTGTGAATCAGCCCTTGAACATGCTCTTCAAAGATGTCCTCTGGTGGACG CTGGGCATCGTCGCCCTGATTGTTCTGACCATCAGGATCCTGGAGATCCTGTGGGCCAAGCTTCGCCAGGTCTCG GCCATGTCGCAGCCGCGCGACAAGCAGGGCTACTGGAGGATCTCGCAATGGAGCTGGATGCCGCCCCTCAAGAAG CACCTCACCTACGCCCCGTTGCTGAGGAAGCGCCACAACCGTGAGTTTCGCCTGTCGTCGGCCGTGAATGTCGGC ACCCTGCCCTCGCGCCTGCACTCGCTGCTGCTCTTCCTCTACCTCGCCAGCAATACGGCCTACATGTTCGTCCTC GACTGGTCTGTCGCCAACAAGTTCGCCCTCTGCGCCGAGCTGCGCGGCCGCTCCGGCACCCTCTCCGTCGTCAAC ATGATCCCCCTCGTCATCCTGGCCGGCCGCAACAACCCCCTGATTCCGCTGCTCAAAATCAGCTTTGACACGTAT AACCTGCTGCATCGCTGGATTGGCCGCGTCGTCGTTGCCGAGGTCATCATCCACACCGTCGCCTGGGCCATCCCG GCCGTCGCCCACAAGGGCTGGTCGGCCGCCTTTGGCGCCGCCGTCAAGAGCGTCTTCATCGGCTCCGGCTTCTGG GCCGCCGTCGCCATGACGCTCCTGCTCCTGCTCTCCCTCTCCCCCATCCGCCACGCCTTTTACGAGACCTTCCTC AACACGCACATCATCCTGGCCGTCGTCGCCCTCGGCGGCACCTGGATCCACTGCTCCTCGGCCTCGCTCCCGCCC CTGCCCTGGGCCATCGCCGTCGTGGCCCTGTGGATGGCGGACCGGCTCGCCCGCGTCCTCCGCCTCGTCTTCACT AACTGGTCCAACAGGGGTGTGACGGACGCGCTCTGCGAGGCCTTGCCCGGCGAGGTGACGCGCGTCACGCTGCAG CTCCCGCGCTACGTCCGCATCGAGCCCGGCACGCACGCCTACCTGCGCTTCTGGGGCGTCCGCCCGTGGGAGAGC CACCCCTTCTCCATCGCCTGGGTCGAGTACCAGGCCGCCAACGCGCTGCCCACGTCGGAGAAGGAGCCGCTCACC GCCGTGGACCGTAAAACGGCCTCGACCTCGGTCTCCTTCATCATCGGCGCCCAGACGGGCATGACGCGCCTGCTC TACGACCGCGCCAGCAAGTCGCCCGCCGGCGTCCGGCTGCGGGCCGCCATGGAGGGTCCCTACGCCGGCCACCAC AACCTCGACTCGTACGGCCACGTCGTTCTCTTTGCCGGCTCGACGGGCATCACGCACCAGATTTCGCACGTCCGC CACCTGCTCGACGGCTACAACGAGGGCATGGTGGCGACGCGGAGGCTCACGCTCGTGTGGATCATCCGGACCTAC GAGACGCTCGAGTGGGTGCGTCCGTACATGGACATGATCCTGCGGATACCCAACCGCAAGGACATCCTGCGCATC CAGGTCTTCGTCACCCGGCCGCAGAACCCGCGCGACATCGTCAGCGCCAGCTCCACGGTCAAGATGTTCCCCGGA CGGCCCAACATTCCGCTGCTCCTGGTCAAGGAGGTGCAGGACCAGATCGGCGCCATGTCGGTGAGCGTGTGCGGG CCCGGCGGCCTGGCCGACGACGTGCGCGGCGCCGTCCGCGCTGTACAGGGCGACTCCGTCATCGACTTCATCGAA GAGAGCTTTACGTGGTGA |