© 2023 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | OphauB2|4163 |
| Gene name | |
| Location | Contig_273:54..1988 |
| Strand | - |
| Gene length (bp) | 1934 |
| Transcript length (bp) | 1863 |
| Coding sequence length (bp) | 1863 |
| Protein length (aa) | 621 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00141 | peroxidase | Peroxidase | 1.3E-22 | 58 | 246 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|D4AUF4|WSCD2_ARTBC | WSC domain-containing protein ARB_07870 OS=Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) GN=ARB_07870 PE=1 SV=1 | 1 | 529 | 3.0E-134 |
| sp|Q7XZP5|APX5_ARATH | L-ascorbate peroxidase 5, peroxisomal OS=Arabidopsis thaliana GN=APX5 PE=1 SV=2 | 60 | 236 | 2.0E-16 |
| sp|Q6ZJJ1|APX4_ORYSJ | Probable L-ascorbate peroxidase 4 OS=Oryza sativa subsp. japonica GN=APX4 PE=2 SV=1 | 67 | 240 | 3.0E-13 |
| sp|Q8GY91|APX6_ARATH | Putative L-ascorbate peroxidase 6 OS=Arabidopsis thaliana GN=APX6 PE=2 SV=1 | 62 | 193 | 4.0E-13 |
| sp|Q1PER6|APX2_ARATH | L-ascorbate peroxidase 2, cytosolic OS=Arabidopsis thaliana GN=APX2 PE=2 SV=3 | 43 | 240 | 2.0E-12 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|D4AUF4|WSCD2_ARTBC | WSC domain-containing protein ARB_07870 OS=Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) GN=ARB_07870 PE=1 SV=1 | 1 | 529 | 3.0E-134 |
| sp|Q7XZP5|APX5_ARATH | L-ascorbate peroxidase 5, peroxisomal OS=Arabidopsis thaliana GN=APX5 PE=1 SV=2 | 60 | 236 | 2.0E-16 |
| sp|Q6ZJJ1|APX4_ORYSJ | Probable L-ascorbate peroxidase 4 OS=Oryza sativa subsp. japonica GN=APX4 PE=2 SV=1 | 67 | 240 | 3.0E-13 |
| sp|Q8GY91|APX6_ARATH | Putative L-ascorbate peroxidase 6 OS=Arabidopsis thaliana GN=APX6 PE=2 SV=1 | 62 | 193 | 4.0E-13 |
| sp|Q1PER6|APX2_ARATH | L-ascorbate peroxidase 2, cytosolic OS=Arabidopsis thaliana GN=APX2 PE=2 SV=3 | 43 | 240 | 2.0E-12 |
| sp|A4R606|CCPR2_MAGO7 | Putative heme-binding peroxidase OS=Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) GN=MGG_10368 PE=3 SV=1 | 67 | 247 | 1.0E-10 |
| sp|P48534|APX1_PEA | L-ascorbate peroxidase, cytosolic OS=Pisum sativum GN=APX1 PE=1 SV=2 | 67 | 247 | 1.0E-10 |
| sp|Q42564|APX3_ARATH | L-ascorbate peroxidase 3, peroxisomal OS=Arabidopsis thaliana GN=APX3 PE=1 SV=1 | 67 | 240 | 4.0E-10 |
| sp|Q7SDV9|CCPR_NEUCR | Cytochrome c peroxidase, mitochondrial OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=ccp-1 PE=3 SV=1 | 67 | 308 | 9.0E-10 |
| sp|Q05431|APX1_ARATH | L-ascorbate peroxidase 1, cytosolic OS=Arabidopsis thaliana GN=APX1 PE=1 SV=2 | 67 | 240 | 1.0E-09 |
| sp|Q10N21|APX1_ORYSJ | L-ascorbate peroxidase 1, cytosolic OS=Oryza sativa subsp. japonica GN=APX1 PE=1 SV=1 | 67 | 247 | 2.0E-09 |
| sp|A2XFC7|APX1_ORYSI | L-ascorbate peroxidase 1, cytosolic OS=Oryza sativa subsp. indica GN=APX1 PE=2 SV=1 | 67 | 247 | 2.0E-09 |
| sp|A4QVH4|CCPR_MAGO7 | Cytochrome c peroxidase, mitochondrial OS=Magnaporthe oryzae (strain 70-15 / ATCC MYA-4617 / FGSC 8958) GN=CCP1 PE=3 SV=1 | 67 | 254 | 7.0E-09 |
| sp|P0C0V3|CCPR_EMENI | Cytochrome c peroxidase, mitochondrial OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=ccp1 PE=3 SV=1 | 67 | 304 | 1.0E-08 |
| sp|Q9FE01|APX2_ORYSJ | L-ascorbate peroxidase 2, cytosolic OS=Oryza sativa subsp. japonica GN=APX2 PE=1 SV=1 | 67 | 247 | 2.0E-08 |
| sp|P0CP54|CCPR_CRYNJ | Cytochrome c peroxidase, mitochondrial OS=Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) GN=CCP1 PE=3 SV=1 | 67 | 291 | 5.0E-08 |
| sp|P0CP55|CCPR_CRYNB | Cytochrome c peroxidase, mitochondrial OS=Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) GN=CCP1 PE=3 SV=1 | 67 | 291 | 5.0E-08 |
| sp|Q4PBY6|CCPR_USTMA | Cytochrome c peroxidase, mitochondrial OS=Ustilago maydis (strain 521 / FGSC 9021) GN=CCP1 PE=3 SV=1 | 67 | 198 | 6.0E-08 |
| sp|Q5B1Z0|CCPR2_EMENI | Putative heme-binding peroxidase OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=AN5440 PE=3 SV=1 | 67 | 198 | 1.0E-07 |
| sp|Q4WLG9|CCPR2_ASPFU | Putative heme-binding peroxidase OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=AFUA_6G13570 PE=3 SV=1 | 67 | 199 | 1.0E-07 |
| sp|Q7XJ02|APX7_ORYSJ | Probable L-ascorbate peroxidase 7, chloroplastic OS=Oryza sativa subsp. japonica GN=APX7 PE=2 SV=1 | 67 | 257 | 1.0E-07 |
| sp|O23474|PER40_ARATH | Peroxidase 40 OS=Arabidopsis thaliana GN=PER40 PE=2 SV=2 | 63 | 235 | 1.0E-07 |
| sp|Q69SV0|APX8_ORYSJ | Probable L-ascorbate peroxidase 8, chloroplastic OS=Oryza sativa subsp. japonica GN=APX8 PE=2 SV=2 | 67 | 257 | 2.0E-07 |
| sp|Q6C0Z6|CCPR_YARLI | Cytochrome c peroxidase, mitochondrial OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=CCP1 PE=3 SV=1 | 67 | 237 | 3.0E-07 |
| sp|Q42593|APXT_ARATH | L-ascorbate peroxidase T, chloroplastic OS=Arabidopsis thaliana GN=APXT PE=2 SV=2 | 67 | 198 | 3.0E-07 |
| sp|Q4PD66|CCPR2_USTMA | Putative heme-binding peroxidase OS=Ustilago maydis (strain 521 / FGSC 9021) GN=CCP2 PE=3 SV=1 | 67 | 250 | 1.0E-06 |
| sp|P0C0L1|APX6_ORYSJ | Probable L-ascorbate peroxidase 6, chloroplastic OS=Oryza sativa subsp. japonica GN=APX6 PE=2 SV=1 | 67 | 257 | 2.0E-06 |
| sp|P19136|PEM4_PHACH | Manganese peroxidase H4 OS=Phanerochaete chrysosporium PE=1 SV=1 | 61 | 239 | 9.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0004601 | peroxidase activity | Yes |
| GO:0006979 | response to oxidative stress | Yes |
| GO:0020037 | heme binding | Yes |
| GO:0003824 | catalytic activity | No |
| GO:0046906 | tetrapyrrole binding | No |
| GO:0003674 | molecular_function | No |
| GO:0050896 | response to stimulus | No |
| GO:0005488 | binding | No |
| GO:0008150 | biological_process | No |
| GO:0016209 | antioxidant activity | No |
| GO:0006950 | response to stress | No |
| GO:1901363 | heterocyclic compound binding | No |
| GO:0016491 | oxidoreductase activity | No |
| GO:0016684 | oxidoreductase activity, acting on peroxide as acceptor | No |
| GO:0097159 | organic cyclic compound binding | No |
| SignalP signal predicted | Location | Score |
|---|---|---|
| Yes | 1 - 18 | 0.999721 |
| CAZyme category | E-value | Start | End |
|---|---|---|---|
| AA2 | 2.8E-27 | 60 | 246 |
| Orthofinder run ID | 4 |
| Orthogroup | 2086 |
| Change Orthofinder run |
| Type of sequence | Sequence |
|---|---|
| Locus | Download genbank file of locus
Download genbank file of locus (reverse complement)
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 | >OphauB2|4163 MRSLSALLALGLAGSALADPTWPSDVDELEEIMYQLTSFRARKFADTVSPCSSEASGPGRHNAAEWLRTAFHDMS TANSFFHLGGLDASLQYELENGENTGPGHKTTLQFMSPYVSPRCSLSDLVAMGVYMSVRSCGGPAVPIRAGRKDA TQKGPAGVPQPQNSVFTFKQQFQRMGFTNEEMIQVTACGHTLGGVHKDEFPELMPAAGVKNGEAPSDETPTVFDN KVVTEYLAGKTQNPLVVGPSAKINKNSDSKVFDSDGNKTLQAMADAEQFNAVCQKVLQKMIDVVPPGVTLTDPIE PYMVKPVNLQLTLVNGGRELALSGYIRVRTTELARESIKNITLTYKGRSGSSQCASSSCTVTSTIQGVGRGFDDS FAFFPISTRIPASSGISSFIVTINKADGTRETHDNNGEAYPLHDDVVFQAPQSCVRGSSGSLTVVAAVRNEAAAQ GAKANVWYRVPQTNSPVPQLKKTTIDLVKGQCVGQYTLFSADYKIEGGLAYQSYVDVMAGDKSDAFKSVAGLGGT CGVFEGAVSCQDVERQLSRRGVEAKVFERQVNATTSTAPVTTAPPPTTSTTAPVPTATRAPPSHRPAVGGYKLVS CWTEGNNCICLLGHRVWARV* |
| Coding | >OphauB2|4163 ATGCGATCCCTTTCGGCCTTGCTGGCCCTAGGTCTCGCCGGCTCAGCACTGGCAGACCCAACATGGCCTTCGGAC GTGGATGAGCTCGAGGAAATCATGTACCAGCTGACGTCGTTTCGGGCGCGCAAGTTTGCCGATACAGTGAGCCCC TGCTCTAGCGAGGCTTCGGGCCCGGGGCGGCACAACGCGGCCGAGTGGCTGCGGACTGCCTTTCACGACATGTCG ACGGCCAACTCATTCTTCCACCTTGGCGGCCTCGACGCCTCGCTGCAGTACGAGCTGGAGAATGGCGAGAACACG GGGCCCGGCCACAAGACGACGCTGCAGTTCATGTCGCCGTATGTCTCGCCGCGCTGCAGTCTTTCTGACCTGGTG GCCATGGGCGTCTACATGTCTGTCCGCTCGTGTGGCGGCCCAGCCGTTCCCATTCGCGCGGGCAGAAAGGACGCC ACGCAAAAGGGGCCGGCCGGAGTCCCGCAGCCGCAAAACTCCGTCTTTACCTTTAAGCAGCAGTTTCAGCGCATG GGGTTTACCAATGAAGAGATGATCCAGGTGACGGCCTGTGGCCACACCCTCGGCGGCGTCCACAAGGACGAGTTT CCTGAGCTGATGCCTGCAGCCGGCGTCAAGAATGGAGAGGCGCCATCTGACGAGACGCCCACCGTCTTTGACAAC AAGGTGGTGACGGAGTATCTTGCCGGCAAGACGCAGAATCCTCTGGTCGTGGGTCCCTCGGCCAAGATTAACAAG AACTCGGACTCAAAGGTCTTTGACTCTGACGGCAACAAGACGCTGCAGGCCATGGCAGACGCCGAGCAGTTCAAT GCCGTGTGCCAAAAGGTGCTGCAAAAAATGATTGACGTGGTGCCGCCCGGCGTCACGCTGACGGATCCCATTGAG CCCTACATGGTCAAGCCAGTCAACCTGCAGCTAACATTGGTCAATGGAGGCCGCGAGCTGGCACTGAGTGGATAC ATTCGCGTCAGGACGACTGAATTGGCGCGCGAGAGCATCAAGAACATCACGTTGACGTACAAGGGCCGCTCTGGC TCATCCCAGTGCGCCTCAAGCTCGTGCACAGTGACGAGTACCATTCAAGGCGTTGGACGCGGCTTTGACGACAGC TTTGCCTTTTTCCCAATCTCAACAAGGATTCCCGCCTCATCGGGCATCTCGTCCTTTATCGTCACCATCAACAAG GCCGACGGCACAAGAGAGACGCACGACAACAATGGCGAGGCATACCCCTTGCACGACGACGTGGTCTTCCAGGCA CCGCAAAGCTGTGTGCGAGGGTCCAGCGGCTCGCTGACCGTTGTGGCGGCTGTGCGCAACGAGGCAGCGGCGCAG GGAGCCAAGGCCAATGTCTGGTATCGGGTGCCCCAGACCAACAGCCCCGTGCCGCAACTCAAGAAGACGACGATT GACCTGGTCAAGGGCCAGTGCGTTGGCCAGTACACGCTGTTTAGCGCAGACTACAAGATTGAGGGCGGACTGGCC TATCAGTCATATGTCGATGTCATGGCTGGTGACAAGTCGGATGCCTTTAAGAGCGTTGCTGGTCTTGGCGGCACC TGCGGCGTCTTTGAGGGCGCAGTCAGCTGTCAAGATGTCGAGCGGCAGCTCTCGCGCAGAGGCGTCGAGGCCAAG GTGTTTGAGCGCCAGGTTAATGCCACGACAAGCACTGCTCCCGTGACAACGGCGCCGCCCCCAACAACTAGCACG ACTGCTCCTGTGCCCACGGCCACTCGGGCTCCTCCAAGTCACCGCCCAGCCGTTGGCGGGTACAAGCTGGTGTCG TGCTGGACAGAGGGCAACAATTGCATATGTCTATTGGGGCACCGAGTATGGGCGCGAGTGTAA |
| Transcript | >OphauB2|4163 ATGCGATCCCTTTCGGCCTTGCTGGCCCTAGGTCTCGCCGGCTCAGCACTGGCAGACCCAACATGGCCTTCGGAC GTGGATGAGCTCGAGGAAATCATGTACCAGCTGACGTCGTTTCGGGCGCGCAAGTTTGCCGATACAGTGAGCCCC TGCTCTAGCGAGGCTTCGGGCCCGGGGCGGCACAACGCGGCCGAGTGGCTGCGGACTGCCTTTCACGACATGTCG ACGGCCAACTCATTCTTCCACCTTGGCGGCCTCGACGCCTCGCTGCAGTACGAGCTGGAGAATGGCGAGAACACG GGGCCCGGCCACAAGACGACGCTGCAGTTCATGTCGCCGTATGTCTCGCCGCGCTGCAGTCTTTCTGACCTGGTG GCCATGGGCGTCTACATGTCTGTCCGCTCGTGTGGCGGCCCAGCCGTTCCCATTCGCGCGGGCAGAAAGGACGCC ACGCAAAAGGGGCCGGCCGGAGTCCCGCAGCCGCAAAACTCCGTCTTTACCTTTAAGCAGCAGTTTCAGCGCATG GGGTTTACCAATGAAGAGATGATCCAGGTGACGGCCTGTGGCCACACCCTCGGCGGCGTCCACAAGGACGAGTTT CCTGAGCTGATGCCTGCAGCCGGCGTCAAGAATGGAGAGGCGCCATCTGACGAGACGCCCACCGTCTTTGACAAC AAGGTGGTGACGGAGTATCTTGCCGGCAAGACGCAGAATCCTCTGGTCGTGGGTCCCTCGGCCAAGATTAACAAG AACTCGGACTCAAAGGTCTTTGACTCTGACGGCAACAAGACGCTGCAGGCCATGGCAGACGCCGAGCAGTTCAAT GCCGTGTGCCAAAAGGTGCTGCAAAAAATGATTGACGTGGTGCCGCCCGGCGTCACGCTGACGGATCCCATTGAG CCCTACATGGTCAAGCCAGTCAACCTGCAGCTAACATTGGTCAATGGAGGCCGCGAGCTGGCACTGAGTGGATAC ATTCGCGTCAGGACGACTGAATTGGCGCGCGAGAGCATCAAGAACATCACGTTGACGTACAAGGGCCGCTCTGGC TCATCCCAGTGCGCCTCAAGCTCGTGCACAGTGACGAGTACCATTCAAGGCGTTGGACGCGGCTTTGACGACAGC TTTGCCTTTTTCCCAATCTCAACAAGGATTCCCGCCTCATCGGGCATCTCGTCCTTTATCGTCACCATCAACAAG GCCGACGGCACAAGAGAGACGCACGACAACAATGGCGAGGCATACCCCTTGCACGACGACGTGGTCTTCCAGGCA CCGCAAAGCTGTGTGCGAGGGTCCAGCGGCTCGCTGACCGTTGTGGCGGCTGTGCGCAACGAGGCAGCGGCGCAG GGAGCCAAGGCCAATGTCTGGTATCGGGTGCCCCAGACCAACAGCCCCGTGCCGCAACTCAAGAAGACGACGATT GACCTGGTCAAGGGCCAGTGCGTTGGCCAGTACACGCTGTTTAGCGCAGACTACAAGATTGAGGGCGGACTGGCC TATCAGTCATATGTCGATGTCATGGCTGGTGACAAGTCGGATGCCTTTAAGAGCGTTGCTGGTCTTGGCGGCACC TGCGGCGTCTTTGAGGGCGCAGTCAGCTGTCAAGATGTCGAGCGGCAGCTCTCGCGCAGAGGCGTCGAGGCCAAG GTGTTTGAGCGCCAGGTTAATGCCACGACAAGCACTGCTCCCGTGACAACGGCGCCGCCCCCAACAACTAGCACG ACTGCTCCTGTGCCCACGGCCACTCGGGCTCCTCCAAGTCACCGCCCAGCCGTTGGCGGGTACAAGCTGGTGTCG TGCTGGACAGAGGGCAACAATTGCATATGTCTATTGGGGCACCGAGTATGGGCGCGAGTGTAA |
| Gene | >OphauB2|4163 ATGCGATCCCTTTCGGCCTTGCTGGCCCTAGGTCTCGCCGGCTCAGCACTGGCAGACCCAACATGGCCTTCGGAC GTGGATGAGCTCGAGGAAATCATGTACCAGCTGACGTCGTTTCGGGCGCGCAAGTTTGCCGATACAGTGAGCCCC TGCTCTAGCGAGGCTTCGGGCCCGGGGCGGCACAACGCGGCCGAGTGGCTGCGGACTGCCTTTCACGACATGTCG ACGGCCAACTCATTCTTCCACCTTGGCGGCCTCGACGCCTCGCTGCAGTACGAGCTGGAGAATGGCGAGAACACG GGGCCCGGCCACAAGACGACGCTGCAGTTCATGTCGCCGTATGTCTCGCCGCGCTGCAGTCTTTCTGACCTGGTG GCCATGGGCGTCTACATGTCTGTCCGCTCGTGTGGCGGCCCAGCCGTTCCCATTCGCGCGGGCAGAAAGGACGCC ACGCAAAAGGGGCCGGCCGGAGTCCCGCAGCCGCAAAACTCCGTCTTTACCTTTAAGCAGCAGTTTCAGCGCATG GGGTTTACCAATGAAGAGATGATCCAGGTGACGGCCTGTGGCCACACCCTCGGCGGCGTCCACAAGGACGAGTTT CCTGAGCTGATGCCTGCAGCCGGCGTCAAGAATGGAGAGGCGCCATCTGACGAGACGCCCACCGTCTTTGACAAC AAGGTGGTGACGGAGTATCTTGCCGGCAAGACGCAGAATCCTCTGGTCGTGGGTCCCTCGGCCAAGATTAACAAG AACTCGGACTCAAAGGTCTTTGACTCTGACGGCAACAAGACGCTGCAGGCCATGGCAGACGCCGAGCAGTTCAAT GCCGTGTGCCAAAAGGTGCTGCAAAAAATGATTGACGTGGTGCCGCCCGGCGTCACGCTGACGGATCCCATTGAG CCCTACATGGTCAAGCCAGTCAACCTGCAGCTAACATTGGTCAATGGAGGCCGCGAGCTGGCACTGAGTGGATAC ATTCGCGTCAGGACGACTGAATTGGCGCGCGAGAGCATCAAGAACATCACGTTGACGTACAAGGGCCGCTCTGGC TCATCCCAGTGCGCCTCAAGCTCGTGCACAGTGACGAGTACCATTCAAGGCGTTGGACGCGGCTTTGACGACAGC TTTGCCTTTTTCCCAATCTCAACAAGGATTCCCGCCTCATCGGGCATCTCGTCCTTTATCGTCACCATCAACAAG GCCGACGGCACAAGAGAGACGCACGACAACAATGGCGAGGCATACCCCTTGCACGACGACGTGGTCTTCCAGGCA CCGCAAAGCTGTGTGCGAGGGTCCAGCGGCTCGCTGACCGTTGTGGCGGCTGTGCGCAACGAGGCAGCGGCGCAG GGAGCCAAGGCCAATGTCTGGTATCGGGTGCCCCAGACCAACAGCCCCGTGCCGCAACTCAAGAAGACGACGATT GACCTGGTCAAGGGCCAGTGCGTTGGCCAGTACACGCTGTTTAGCGCAGACTACAAGATTGAGGGCGGACTGGCC TATCAGTCATATGTCGATGTCATGGCTGGTGACAAGTCGGATGCCTTTAAGAGCGTTGCTGGTCTTGGCGGCACC TGCGGCGTCTTTGAGGGCGCAGTCAGCTGTCAAGATGTCGAGCGGCAGCTCTCGCGCAGAGGCGTCGAGGCCAAG GTGTTTGAGCGCCAGGTTAATGCCACGACAAGCACTGCTCCCGTGACAACGGCGCCGCCCCCAACAACTAGCACG ACTGCTCCTGTGCCCACGGCCACTCGGGCTCCTCCAAGTCACCGCCCAGCCGTTGGCGGGTACAAGCTGGTGTCG TGCTGGACAGAGGGCAACAATGTGCGTGCGCTCAATGGCATCTCGTTTGCCAATGACACCATGACGCTGGAAAAG TGCATGAATTACTGCAGTGCATATGTCTATTGGGGCACCGAGTATGGGCGCGAGTGTAA |