| Acc# | Gene | Locus | DB | Organism | Product | Score | E-value | Identities | Positives | Gaps |
|---|---|---|---|---|---|---|---|---|---|---|
| Q12333 | FRE7 | FRE7_YEAST | SP | Saccharomyces cerevisiae (Baker's yeast) | Ferric reductase transmembrane component 7 (EC 1.16.1.7) (Ferric-chelate reductase 7). | 301 | 2e-80 | 187/613 (30%) | 303/613 (49%) | 47/613 (7%) |
| Q8J268 | FREA | TrEMBL | Emericella nidulans (Aspergillus nidulans) | Metalloreductase. | 105 | 1e-21 | 106/477 (22%) | 188/477 (39%) | 41/477 (8%) | |
| P78588 | CFL1 | FREL_CANAL | SP | Candida albicans (Yeast) | Probable ferric reductase transmembrane component (EC 1.16.1.7) (Ferric-chelate reductase). | 94.0 | 5e-18 | 81/335 (24%) | 137/335 (40%) | 5/335 (1%) |
| Q9Y861 | CFL1 | TrEMBL | Candida albicans (Yeast) | Ferric reductase. | 94.0 | 5e-18 | 81/335 (24%) | 136/335 (40%) | 5/335 (1%) | |
| 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). | 93.2 | 9e-18 | 99/417 (23%) | 172/417 (41%) | 15/417 (3%) |
| 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). | 91.3 | 3e-17 | 83/341 (24%) | 136/341 (39%) | 18/341 (5%) |
| Q9HFZ3 | RBT2 | TrEMBL | Candida albicans (Yeast) | Repressed by TUP1 protein 2. | 84.7 | 3e-15 | 84/335 (25%) | 133/335 (39%) | 4/335 (1%) | |
| 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). | 84.3 | 4e-15 | 79/358 (22%) | 154/358 (43%) | 10/358 (2%) |
| 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). | 80.5 | 6e-14 | 68/278 (24%) | 121/278 (43%) | 11/278 (3%) |
| 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). | 79.7 | 1e-13 | 65/270 (24%) | 122/270 (45%) | 3/270 (1%) |
| 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). | 77.8 | 4e-13 | 76/345 (22%) | 146/345 (42%) | 4/345 (1%) |
| Q9FLW2 | TrEMBL | Arabidopsis thaliana (Mouse-ear cress) | FRO2 homolog. | 53.5 | 8e-06 | 63/280 (22%) | 107/280 (38%) | 8/280 (2%) | ||
| Q9FLW3 | TrEMBL | Arabidopsis thaliana (Mouse-ear cress) | FRO2 homolog. | 53.1 | 1e-05 | 60/277 (21%) | 103/277 (37%) | 5/277 (1%) | ||
| Q8W110 | TrEMBL | Arabidopsis thaliana (Mouse-ear cress) | AT5g23980/MZF18_14. | 53.1 | 1e-05 | 60/277 (21%) | 103/277 (37%) | 5/277 (1%) | ||
| Q9FGS9 | TrEMBL | Arabidopsis thaliana (Mouse-ear cress) | FRO1 and FRO2-like protein. | 52.4 | 2e-05 | 74/345 (21%) | 124/345 (35%) | 26/345 (7%) | ||
| Q8VY13 | AT5G50160 | TrEMBL | Arabidopsis thaliana (Mouse-ear cress) | Putative FRO1 and FRO2. | 52.4 | 2e-05 | 74/345 (21%) | 124/345 (35%) | 26/345 (7%) | |
| Q9XYS3 | TrEMBL | Dictyostelium discoideum (Slime mold) | Superoxide-generating NADPH oxidase flavocytochrome. | 51.2 | 4e-05 | 50/246 (20%) | 96/246 (39%) | 19/246 (7%) |
Scores for sequence family classification (score includes all domains): Model Description Score E-value N -------- ----------- ----- ------- --- Ferric_reduct Ferric reductase like transmembrane c 263.5 2.7e-75 1 NAD_binding_1 Oxidoreductase NAD-binding domain -16.8 0.069 1 LysE LysE type translocator -73.4 7.2 1 PsaL Photosystem I reaction centre subunit -112.7 5.6 1 ER_lumen_recept ER lumen protein retaining receptor -159.0 4.4 1 Parsed for domains: Model Domain seq-f seq-t hmm-f hmm-t score E-value -------- ------- ----- ----- ----- ----- ----- ------- PsaL 1/1 103 204 .. 1 159 [] -112.7 5.6 ER_lumen_recept 1/1 157 277 .. 1 210 [] -159.0 4.4 LysE 1/1 160 359 .. 1 201 [] -73.4 7.2 NAD_binding_1 1/1 419 529 .. 1 133 [] -16.8 0.069 Ferric_reduct 1/1 104 584 .. 1 684 [] 263.5 2.7e-75
CDS Sequence
ATGATGAAAA GAGGTGTGTC GTATAATGGA TTGGATTGTC TTGCAGATGC GTCCAGTGAT GCCTACATGA AGTACAAGCA CCAGCTGCAG GCCGAAATTC CATGGGTCTC TCAGACAAAG TATGCAAAGT ACACTGTTTA CTTTGGAATA GCCACGATTT TTGTGGCATT CGTTAAGCAA ATATACTACA AATACCGAGA TTATACATAT AGATCCAAGC AGTCCTCCAA CTTTGGAACC TCACTCATTG ATATATGGAT ATCATATTGT CGCTATTACG GATATAAACA ATTACCAACA TGGTTAACAT ACTTTTCAAT ACCAGGATCA GTGGGTTCAG CACTGTACAT GTTCTTATCG TCGCTTTACA TGTTGTGCTA TTGCCTTGTA CCGCATTTCT GGTATAGAGG ATGTGCTGGT TTTGGCTCAT CGCCGTTAGC TGTACGCGCT GGTCTTATGG CGACGGCACT AACCCCATTT ATTTATGTTT TGGCAGGCAA ATCAAATGCT ATCACTTTAT TGACTGGTAT CAGTTATGAA AAACTAAACA CTTTCCATCA ATATACTGGT GTTGCTTGTT TCATATTATC AGTCATTCAC GTGGTCCCAT TTATTTATCA GGACTTGGCT GAAGGCGGAA GCAGTAATTT GAAGATGAAT TTCAAAGACA GTTTTGAGTA CTATAGTGGT ATACCGCCAT TAATTCTATT GGGTCTTTTG TGTATTCTCT CGAAATCGTA CATCAGAAAA GTGGTATATG AATTGTTTCT ACATGCCCAT TGGATGATGG GTATTGCTTA TTTTGGGACA TTAATTTGGC ATATAAACAA AGAGTTAGGT GCGGATGACT ACATGTGGGG TGCATTAGCT TTTTGGGCCA CTCAAATTAT TTACAGGATC TTGATGAAAA CAGCATTCAA GCCAAACGCA ATGTTTTTAA GATCAAGACA AGCACAATTG GAAAAACTAG GCAGCGATGG GGTATATCAA GTCGTAATTG GAAATACCAC TGGTGTTAAT TGGAAACCTG GCCAACATTG TTATCTTAGA TTTGCTGGTG TTAGAATACT TGACAGCCAT CCTTTTTCAA TTGCATCCGT TGATGAAGAA GATAAAACTG CCATGAAGTT TATCATCAAA GCACAGAAAG GATTAACACG CAAGATTTAT CAGGAATTGG ATAAGCTGAT AACTTCTAAT AAAAATGTTT ATGTGGATGG TCCATACGGA GGCACATTTA GAGATCCAAG GTCATTTAAA AGAGTGGTTT TGTTGGCAAC CGGCACTGGA GTCACTGCCA CTTTGCCATT TTTGACGTAT TTAGCAAAAA CTGATTCGAT AGTTAAACGA GTTTCATTTA TTTGGATTGT GCGCCTGCAA GAAGATATAC ACTGGGTCAA AAGTGAATTG CAAGAGTGTC AAAAATTAGG TGGGAGTAAA ATAGATATAC ATATCCATGT TGCTGCTAAG AAATCGATAT ATACCAAAGG TGATTTTGAA AAGGAGATCG AAAGCGAAGA AACTAACTTG AATGAAGAAG ACTGGTTAAT TGATTATGGT AAACCATCGG TGACAAGTAT TCTAAAACTG ATGGCAGGTA GCTTAGCTGC TCGTAATATG ATAGTTTGTT CAGGAAGCGA TTCTTTGAAA AGAGAGGTGA GCAGTATCGT TTCTGAACTC CAATCGTTGG TGTTTAACAA TGACTTGGTC AGATCCAACG TTGAAGAAAT ATATTTGCAC ACTGAGTCTT TTGGATGGTA A
AA Sequence
MMKRGVSYNG LDCLADASSD AYMKYKHQLQ AEIPWVSQTK YAKYTVYFGI ATIFVAFVKQ IYYKYRDYTY RSKQSSNFGT SLIDIWISYC RYYGYKQLPT WLTYFSIPGS VGSALYMFLS SLYMLCYCLV PHFWYRGCAG FGSSPLAVRA GLMATALTPF IYVLAGKSNA ITLLTGISYE KLNTFHQYTG VACFILSVIH VVPFIYQDLA EGGSSNLKMN FKDSFEYYSG IPPLILLGLL CILSKSYIRK VVYELFLHAH WMMGIAYFGT LIWHINKELG ADDYMWGALA FWATQIIYRI LMKTAFKPNA MFLRSRQAQL EKLGSDGVYQ VVIGNTTGVN WKPGQHCYLR FAGVRILDSH PFSIASVDEE DKTAMKFIIK AQKGLTRKIY QELDKLITSN KNVYVDGPYG GTFRDPRSFK RVVLLATGTG VTATLPFLTY LAKTDSIVKR VSFIWIVRLQ EDIHWVKSEL QECQKLGGSK IDIHIHVAAK KSIYTKGDFE KEIESEETNL NEEDWLIDYG KPSVTSILKL MAGSLAARNM IVCSGSDSLK REVSSIVSEL QSLVFNNDLV RSNVEEIYLH TESFGW*