| Acc# | Gene | Locus | DB | Organism | Product | Score | E-value | Identities | Positives | Gaps |
|---|---|---|---|---|---|---|---|---|---|---|
| Q9HFZ3 | RBT2 | TrEMBL | Candida albicans (Yeast) | Repressed by TUP1 protein 2. | 84.7 | 3e-15 | 100/471 (21%) | 194/471 (41%) | 20/471 (4%) | |
| Q08908 | FRE5 | FRE5_YEAST | SP | Saccharomyces cerevisiae (Baker's yeast) | Ferric reductase transmembrane component 5 precursor (EC 1.16.1.7) (Ferric-chelate reductase 5). | 75.1 | 3e-12 | 106/474 (22%) | 192/474 (40%) | 24/474 (5%) |
| Q8J268 | FREA | TrEMBL | Emericella nidulans (Aspergillus nidulans) | Metalloreductase. | 73.6 | 8e-12 | 97/515 (18%) | 205/515 (39%) | 33/515 (6%) | |
| Q04800 | FRP1 | FRP1_SCHPO | SP | Schizosaccharomyces pombe (Fission yeast) | Ferric reductase transmembrane component (EC 1.16.1.7) (Ferric-chelate reductase). | 71.6 | 3e-11 | 58/263 (22%) | 104/263 (39%) | 29/263 (11%) |
| Q9LTA0 | TrEMBL | Arabidopsis thaliana (Mouse-ear cress) | FRO2-like protein, NADPH oxidase-like. | 70.1 | 8e-11 | 76/378 (20%) | 154/378 (40%) | 6/378 (1%) | ||
| O94727 | SPBC947.05C | TrEMBL | Schizosaccharomyces pombe (Fission yeast) | Ferric reductase transmembrane component. | 69.7 | 1e-10 | 100/490 (20%) | 188/490 (38%) | 34/490 (6%) | |
| Q9LT99 | TrEMBL | Arabidopsis thaliana (Mouse-ear cress) | FRO1-like protein, NADPH oxidase-like. | 68.9 | 2e-10 | 75/365 (20%) | 150/365 (41%) | 18/365 (4%) | ||
| Q9FLW2 | TrEMBL | Arabidopsis thaliana (Mouse-ear cress) | FRO2 homolog. | 68.6 | 2e-10 | 63/260 (24%) | 100/260 (38%) | 7/260 (2%) | ||
| Q8RWS6 | AT5G49730 | TrEMBL | Arabidopsis thaliana (Mouse-ear cress) | Putative FRO2, NADPH oxidase. | 67.0 | 7e-10 | 77/383 (20%) | 153/383 (39%) | 11/383 (2%) | |
| Q12473 | FRE6 | FRE6_YEAST | SP | Saccharomyces cerevisiae (Baker's yeast) | Ferric reductase transmembrane component 6 precursor (EC 1.16.1.7) (Ferric-chelate reductase 6). | 67.0 | 7e-10 | 83/402 (20%) | 157/402 (39%) | 33/402 (8%) |
| Q9FLW3 | TrEMBL | Arabidopsis thaliana (Mouse-ear cress) | FRO2 homolog. | 65.9 | 2e-09 | 61/260 (23%) | 98/260 (37%) | 7/260 (2%) | ||
| Q8W110 | TrEMBL | Arabidopsis thaliana (Mouse-ear cress) | AT5g23980/MZF18_14. | 65.9 | 2e-09 | 61/260 (23%) | 98/260 (37%) | 7/260 (2%) | ||
| P53746 | FRE4 | FRE4_YEAST | SP | Saccharomyces cerevisiae (Baker's yeast) | Ferric reductase transmembrane component 4 precursor (EC 1.16.1.7) (Ferric-chelate reductase 4). | 63.5 | 8e-09 | 103/500 (20%) | 204/500 (40%) | 25/500 (5%) |
| Q9Y861 | CFL1 | TrEMBL | Candida albicans (Yeast) | Ferric reductase. | 61.6 | 3e-08 | 71/358 (19%) | 130/358 (36%) | 6/358 (1%) | |
| Q08905 | FRE3 | FRE3_YEAST | SP | Saccharomyces cerevisiae (Baker's yeast) | Ferric reductase transmembrane component 3 precursor (EC 1.16.1.7) (Ferric-chelate reductase 3). | 61.6 | 3e-08 | 53/251 (21%) | 113/251 (45%) | 7/251 (2%) |
| P78588 | CFL1 | FREL_CANAL | SP | Candida albicans (Yeast) | Probable ferric reductase transmembrane component (EC 1.16.1.7) (Ferric-chelate reductase). | 61.2 | 4e-08 | 71/358 (19%) | 131/358 (36%) | 6/358 (1%) |
| P32791 | FRE1 | FRE1_YEAST | SP | Saccharomyces cerevisiae (Baker's yeast) | Ferric reductase transmembrane component 1 precursor (EC 1.16.1.7) (Ferric-chelate reductase 1). | 60.5 | 7e-08 | 86/430 (20%) | 163/430 (37%) | 24/430 (5%) |
| P36033 | FRE2 | FRE2_YEAST | SP | Saccharomyces cerevisiae (Baker's yeast) | Ferric reductase transmembrane component 2 precursor (EC 1.16.1.7) (Ferric-chelate reductase 2). | 60.5 | 7e-08 | 54/257 (21%) | 113/257 (43%) | 13/257 (5%) |
| Q12209 | YLR047C | TrEMBL | Saccharomyces cerevisiae (Baker's yeast) | Chromosome XII reading frame ORF YLR047C. | 60.1 | 9e-08 | 82/372 (22%) | 139/372 (37%) | 16/372 (4%) | |
| Q9FGS9 | TrEMBL | Arabidopsis thaliana (Mouse-ear cress) | FRO1 and FRO2-like protein. | 59.7 | 1e-07 | 87/402 (21%) | 168/402 (41%) | 11/402 (2%) | ||
| Q8VY13 | AT5G50160 | TrEMBL | Arabidopsis thaliana (Mouse-ear cress) | Putative FRO1 and FRO2. | 59.7 | 1e-07 | 87/402 (21%) | 168/402 (41%) | 11/402 (2%) | |
| Q9LMM2 | F22L4.13 | TrEMBL | Arabidopsis thaliana (Mouse-ear cress) | F22L4.13 protein. | 59.3 | 1e-07 | 60/272 (22%) | 114/272 (41%) | 9/272 (3%) | |
| P92950 | FRO1 | TrEMBL | Arabidopsis thaliana (Mouse-ear cress) | FRO1 protein. | 59.3 | 1e-07 | 60/272 (22%) | 114/272 (41%) | 9/272 (3%) | |
| Q9LMM3 | F22L4.12 | TrEMBL | Arabidopsis thaliana (Mouse-ear cress) | F22L4.12 protein. | 58.2 | 3e-07 | 68/331 (20%) | 129/331 (38%) | 8/331 (2%) | |
| P92949 | FRO2 | TrEMBL | Arabidopsis thaliana (Mouse-ear cress) | FRO2 protein. | 58.2 | 3e-07 | 68/331 (20%) | 129/331 (38%) | 8/331 (2%) | |
| Q94EK6 | FRO1 | TrEMBL | Pisum sativum (Garden pea) | Ferric-chelate reductase. | 57.4 | 6e-07 | 58/258 (22%) | 102/258 (39%) | 7/258 (2%) | |
| Q86GL4 | TrEMBL | Dictyostelium discoideum (Slime mold) | Superoxide-generating NADPH oxidase flavocytochrome isoform B. | 55.1 | 3e-06 | 90/418 (21%) | 173/418 (41%) | 19/418 (4%) | ||
| O23122 | F19G10.4 | TrEMBL | Arabidopsis thaliana (Mouse-ear cress) | F19G10.4 protein. | 51.6 | 3e-05 | 68/307 (22%) | 121/307 (39%) | 9/307 (2%) | |
| Q12333 | FRE7 | FRE7_YEAST | SP | Saccharomyces cerevisiae (Baker's yeast) | Ferric reductase transmembrane component 7 (EC 1.16.1.7) (Ferric-chelate reductase 7). | 50.1 | 9e-05 | 80/414 (19%) | 155/414 (37%) | 21/414 (5%) |
Scores for sequence family classification (score includes all domains): Model Description Score E-value N -------- ----------- ----- ------- --- Ferric_reduct Ferric reductase like transmembrane com 53.9 3.6e-12 1 Parsed for domains: Model Domain seq-f seq-t hmm-f hmm-t score E-value -------- ------- ----- ----- ----- ----- ----- ------- Ferric_reduct 1/1 75 589 .. 1 684 [] 53.9 3.6e-12
CDS Sequence
ATGGACGAAG AACTTCAGAA GCATTTAGAA ATTTCAAGAA ACACCAAGTA CCAGTGGATT GCGTGCATTT TCAGTTTAGT TATATTTCTT GCCAACGGCA TTGTTTTTTA CTGGATTCCT AGACTTCTTA GAGATAAACG ATTTGTCAAA ACAAACAGAT TCAAACCGTA TTTTGCTTTC GTTGACATTT GGCAAACCAT TAATACCCCG TTCTCAATTA AAGTCGGAAA GAAAACCCAC TACTTCAAAC CCAGTCTACT TGCCTTAGGT GCATGTTTCA TTTTATTAAA TGGCAAGCTA TGCTACATTG AGACCGACGA TTTGGACTAC AAACCCCGCA TATTTATAAT TGGGAAACGA TGTGCTAGAA TTGCTTTGGG TCAGATGCCA GCAATGTTTT TATCAGTTAC CAAAGGTGAT TTCATTACCG CCCTTACAGG CTTGACATAC GAACGTGCGG CATTCTTCCA TGCCTGGTTT GCTACATTAA TGTTCCTGAT GATGACAGCA CATGTGGGGA TAATCGGGTT TTATTGGGCT CATCCAAATT ACGACATTGC TCCTAAATAT CCAAAAAACG TTTATGGAAT TATCGGCTAT GCGTGTTTTG TGTTTTTGGT ATTTGGCAAT GTGGCCTTGA TTAGACGTTA TGCGTTTGAG TTTTTGATGG TAAACCACCG GGTCCATTCA TTCATTATGT TGTTGATGGC TTTCTTACAC AATGACAGAG CCAAAGCCAT GGTCATCCTT GCTATCCATT TGCTTGTGTT GGACAAAGTG CTTGGCAGAA TCTACGGTAT CGTACACTCT TTAAAATCTC CAACAAAAGG GTTGTCAGAA TTTGAGATAC TCGACGATGA GACTTTGCGT GTCAGTATCC CCGTGAAAAC ATCAAAGACT GATCCAACAC CTTGGTACAG ATTATTTCTA TTCAAATATG GAACTTGGTT AGCTGGCCTG CATGTTTACT TAAATGTAAG AAAAGTCGAT TTCTTCCAAC ACCATCCCTT TGCAGTTGCA AGTTTACCTG AATCTGGTAA AATTACTTTG GTTATCAAAA AGAGAAACGG GTTTACAAAG AAATTGTACG ACAAGGTCAA AACAATGCGC GACGAACAAC TCGACAGCGA AACTTCCGAA ACCGACCCCA ACATTGTTAA ATTAAAAGCT GCTTTCCGTG GTCCATCACT GGGTAAATTC CAACCATTAA TCACATTTGA CTCAGTGGCA TTTCTCGCCC AAGATTATGG CGCATCATTT GTATTGCCAC TTTGCTTGGA CTTGTTGCAG ACTATTGAAA AAAAGGAAGT GGCTAAAAAC TATTTGGGCC GACCAGCTCA CCCTTATTTG AAAGTGTATT GGTCAGTAAA GAGGTTAAAC AATATCTACT GGTATGAAGA TTTGGTTAGA AAATTATTGC CATTCATCAA TTCAGGGAAA CTTACCATGA ATGTGTTTGT ACAAGAAAGT GTTGAACTCG AAGCTACTAA ACTGGTGTCA ACTAAAAAGT TGGATATTGT CTCTGTCACC AGCGACCCCC TGTCAATTAC AAACTCAGAA ATAAAGTTTA TCTATGAAGA ACCAATGGAG GTATCACAAG TCATTCAATC ACACATTTCC AGTATGCATT TCCCAGAGGA AAAAGCGTTC AAGTCGCTTG CTATAATGAG TTGCGGAAAT GACAACTTTG GAAGCCAAGT AGAAAGCGAG TCACAAAAGT ACAGATGGGT TAAAGATGCA CCAAATATTT ATTTCTATAA CGAGTCGTAC GAAACATAG
AA Sequence
MDEELQKHLE ISRNTKYQWI ACIFSLVIFL ANGIVFYWIP RLLRDKRFVK TNRFKPYFAF VDIWQTINTP FSIKVGKKTH YFKPSLLALG ACFILLNGKL CYIETDDLDY KPRIFIIGKR CARIALGQMP AMFLSVTKGD FITALTGLTY ERAAFFHAWF ATLMFLMMTA HVGIIGFYWA HPNYDIAPKY PKNVYGIIGY ACFVFLVFGN VALIRRYAFE FLMVNHRVHS FIMLLMAFLH NDRAKAMVIL AIHLLVLDKV LGRIYGIVHS LKSPTKGLSE FEILDDETLR VSIPVKTSKT DPTPWYRLFL FKYGTWLAGL HVYLNVRKVD FFQHHPFAVA SLPESGKITL VIKKRNGFTK KLYDKVKTMR DEQLDSETSE TDPNIVKLKA AFRGPSLGKF QPLITFDSVA FLAQDYGASF VLPLCLDLLQ TIEKKEVAKN YLGRPAHPYL KVYWSVKRLN NIYWYEDLVR KLLPFINSGK LTMNVFVQES VELEATKLVS TKKLDIVSVT SDPLSITNSE IKFIYEEPME VSQVIQSHIS SMHFPEEKAF KSLAIMSCGN DNFGSQVESE SQKYRWVKDA PNIYFYNESY ET*