© 2022 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | OphauG2|6285 |
| Gene name | |
| Location | Contig_633:9111..10988 |
| Strand | - |
| Gene length (bp) | 1877 |
| Transcript length (bp) | 1638 |
| Coding sequence length (bp) | 1638 |
| Protein length (aa) | 546 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF03169 | OPT | OPT oligopeptide transporter protein | 1.4E-110 | 16 | 544 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P53134|YGL4_YEAST | Putative oligopeptide transporter YGL114W OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=YGL114W PE=1 SV=1 | 14 | 544 | 7.0E-130 |
| sp|Q6R3K6|YSL6_ARATH | Probable metal-nicotianamine transporter YSL6 OS=Arabidopsis thaliana GN=YSL6 PE=2 SV=2 | 13 | 545 | 8.0E-19 |
| sp|Q7XRV1|YSL5_ORYSJ | Probable metal-nicotianamine transporter YSL5 OS=Oryza sativa subsp. japonica GN=YSL5 PE=2 SV=3 | 13 | 545 | 3.0E-17 |
| sp|Q6R3K8|YSL4_ARATH | Probable metal-nicotianamine transporter YSL4 OS=Arabidopsis thaliana GN=YSL4 PE=2 SV=1 | 1 | 545 | 3.0E-16 |
| sp|Q6R3K9|YSL2_ARATH | Metal-nicotianamine transporter YSL2 OS=Arabidopsis thaliana GN=YSL2 PE=1 SV=1 | 262 | 543 | 5.0E-16 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P53134|YGL4_YEAST | Putative oligopeptide transporter YGL114W OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=YGL114W PE=1 SV=1 | 14 | 544 | 7.0E-130 |
| sp|Q6R3K6|YSL6_ARATH | Probable metal-nicotianamine transporter YSL6 OS=Arabidopsis thaliana GN=YSL6 PE=2 SV=2 | 13 | 545 | 8.0E-19 |
| sp|Q7XRV1|YSL5_ORYSJ | Probable metal-nicotianamine transporter YSL5 OS=Oryza sativa subsp. japonica GN=YSL5 PE=2 SV=3 | 13 | 545 | 3.0E-17 |
| sp|Q6R3K8|YSL4_ARATH | Probable metal-nicotianamine transporter YSL4 OS=Arabidopsis thaliana GN=YSL4 PE=2 SV=1 | 1 | 545 | 3.0E-16 |
| sp|Q6R3K9|YSL2_ARATH | Metal-nicotianamine transporter YSL2 OS=Arabidopsis thaliana GN=YSL2 PE=1 SV=1 | 262 | 543 | 5.0E-16 |
| sp|Q0E4J6|YSL8_ORYSJ | Probable metal-nicotianamine transporter YSL8 OS=Oryza sativa subsp. japonica GN=YSL8 PE=2 SV=1 | 13 | 543 | 1.0E-15 |
| sp|Q6H3Z6|YSL2_ORYSJ | Metal-nicotianamine transporter YSL2 OS=Oryza sativa subsp. japonica GN=YSL2 PE=2 SV=2 | 237 | 543 | 3.0E-15 |
| sp|Q6H7J6|YSL14_ORYSJ | Probable metal-nicotianamine transporter YSL14 OS=Oryza sativa subsp. japonica GN=YSL14 PE=2 SV=1 | 262 | 543 | 6.0E-15 |
| sp|Q5JQD7|YSL12_ORYSJ | Probable metal-nicotianamine transporter YSL12 OS=Oryza sativa subsp. japonica GN=YSL12 PE=2 SV=2 | 262 | 543 | 2.0E-14 |
| sp|Q7XRV2|YSL6_ORYSJ | Probable metal-nicotianamine transporter YSL6 OS=Oryza sativa subsp. japonica GN=YSL6 PE=2 SV=1 | 283 | 545 | 7.0E-14 |
| sp|Q2EF88|YSL3_ARATH | Metal-nicotianamine transporter YSL3 OS=Arabidopsis thaliana GN=YSL3 PE=2 SV=1 | 264 | 543 | 9.0E-14 |
| sp|Q7XN54|YSL16_ORYSJ | Probable metal-nicotianamine transporter YSL16 OS=Oryza sativa subsp. japonica GN=YSL16 PE=2 SV=2 | 233 | 543 | 2.0E-13 |
| sp|Q6H3Z3|YSL15_ORYSJ | Iron-phytosiderophore transporter YSL15 OS=Oryza sativa subsp. japonica GN=YSL15 PE=2 SV=1 | 264 | 543 | 3.0E-13 |
| sp|Q7X660|YSL11_ORYSJ | Probable metal-nicotianamine transporter YSL11 OS=Oryza sativa subsp. japonica GN=YSL11 PE=2 SV=1 | 262 | 543 | 5.0E-13 |
| sp|Q9SHY2|YSL7_ARATH | Probable metal-nicotianamine transporter YSL7 OS=Arabidopsis thaliana GN=YSL7 PE=2 SV=1 | 264 | 543 | 2.0E-12 |
| sp|Q941V3|YSL18_ORYSJ | Probable metal-nicotianamine transporter YSL18 OS=Oryza sativa subsp. japonica GN=YSL18 PE=2 SV=1 | 264 | 543 | 3.0E-11 |
| sp|Q7XKF4|YSL13_ORYSJ | Probable metal-nicotianamine transporter YSL13 OS=Oryza sativa subsp. japonica GN=YSL13 PE=2 SV=2 | 283 | 543 | 9.0E-11 |
| sp|Q6R3L0|YSL1_ARATH | Metal-nicotianamine transporter YSL1 OS=Arabidopsis thaliana GN=YSL1 PE=2 SV=2 | 264 | 543 | 1.0E-10 |
| sp|Q9AY27|YS1_MAIZE | Iron-phytosiderophore transporter yellow stripe 1 OS=Zea mays GN=YS1 PE=2 SV=1 | 264 | 543 | 2.0E-10 |
| sp|Q7XUJ2|YSL9_ORYSJ | Probable metal-nicotianamine transporter YSL9 OS=Oryza sativa subsp. japonica GN=YSL9 PE=2 SV=2 | 262 | 545 | 1.0E-09 |
| sp|Q6AVD0|YSL3_ORYSJ | Probable metal-nicotianamine transporter YSL3 OS=Oryza sativa subsp. japonica GN=YSL3 PE=2 SV=2 | 262 | 540 | 3.0E-09 |
| sp|Q0J932|YSL10_ORYSJ | Probable metal-nicotianamine transporter YSL10 OS=Oryza sativa subsp. japonica GN=YSL10 PE=2 SV=2 | 283 | 543 | 1.0E-08 |
| sp|Q941V3|YSL18_ORYSJ | Probable metal-nicotianamine transporter YSL18 OS=Oryza sativa subsp. japonica GN=YSL18 PE=2 SV=1 | 17 | 190 | 5.0E-08 |
| sp|Q7XUJ2|YSL9_ORYSJ | Probable metal-nicotianamine transporter YSL9 OS=Oryza sativa subsp. japonica GN=YSL9 PE=2 SV=2 | 13 | 165 | 1.0E-07 |
| sp|Q6R3K4|YSL8_ARATH | Probable metal-nicotianamine transporter YSL8 OS=Arabidopsis thaliana GN=YSL8 PE=1 SV=2 | 262 | 543 | 4.0E-07 |
| sp|Q9LUN2|YSL5_ARATH | Probable metal-nicotianamine transporter YSL5 OS=Arabidopsis thaliana GN=YSL5 PE=1 SV=1 | 262 | 543 | 4.0E-07 |
| sp|Q6ZCX1|YSL17_ORYSJ | Probable metal-nicotianamine transporter YSL17 OS=Oryza sativa subsp. japonica GN=YSL17 PE=2 SV=1 | 17 | 176 | 5.0E-07 |
| sp|Q688S6|YSL4_ORYSJ | Probable metal-nicotianamine transporter YSL4 OS=Oryza sativa subsp. japonica GN=YSL4 PE=2 SV=1 | 278 | 543 | 1.0E-06 |
| sp|Q6ZGM7|YSL7_ORYSJ | Probable metal-nicotianamine transporter YSL7 OS=Oryza sativa subsp. japonica GN=YSL7 PE=2 SV=1 | 262 | 543 | 1.0E-06 |
| sp|Q6R3K9|YSL2_ARATH | Metal-nicotianamine transporter YSL2 OS=Arabidopsis thaliana GN=YSL2 PE=1 SV=1 | 13 | 176 | 2.0E-06 |
| sp|Q2EF88|YSL3_ARATH | Metal-nicotianamine transporter YSL3 OS=Arabidopsis thaliana GN=YSL3 PE=2 SV=1 | 13 | 165 | 4.0E-06 |
| sp|Q6R3L0|YSL1_ARATH | Metal-nicotianamine transporter YSL1 OS=Arabidopsis thaliana GN=YSL1 PE=2 SV=2 | 14 | 179 | 6.0E-06 |
| sp|Q6ZGM7|YSL7_ORYSJ | Probable metal-nicotianamine transporter YSL7 OS=Oryza sativa subsp. japonica GN=YSL7 PE=2 SV=1 | 17 | 177 | 8.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0035673 | oligopeptide transmembrane transporter activity | Yes |
| GO:0003674 | molecular_function | No |
| GO:0005215 | transporter activity | No |
| GO:0042887 | amide transmembrane transporter activity | No |
| GO:0022857 | transmembrane transporter activity | No |
| GO:1904680 | peptide transmembrane transporter activity | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 67 | 0.5 |
| Domain # | Start | End | Length |
|---|---|---|---|
| 1 | 21 | 40 | 19 |
| 2 | 44 | 63 | 19 |
| 3 | 76 | 98 | 22 |
| 4 | 118 | 140 | 22 |
| 5 | 241 | 263 | 22 |
| 6 | 336 | 358 | 22 |
| 7 | 409 | 427 | 18 |
| 8 | 431 | 453 | 22 |
| 9 | 474 | 496 | 22 |
| 10 | 521 | 543 | 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 | >OphauG2|6285 MTPERDTLHLDRQRHFTARSVVAGLGVGTVICAANVYFGLQTGWVSIMSMPASLMGFGLFRLLRPHLQFPFSPVE NVLLQSVACGMAIMPLGCGLVGVMPAMEYLLTSDEQGPLAMSMTQLMVWSIGLCYFGVVFAVPLRRQVIIRERLR FPSGFSTAILISVLHGQIKPGTQQERDGLEAAARGGFASLALQPEREAGREPDNEPVHESVHEPRRHIEHEPLLS SESGHQHQDSWSNMRLLLLCFATSGLFTLCTYFIPVLRQLPVFGSVAANTWLWTLNPSPAYIGQGIIMGTETTLH MTVGALVGWAILSPWAKMQGWAPGPVDDWERGSKGWILWVSLAIMLVDAVVSLGYIALRPVWRAVVLYFTPSTHG YSRVGFATNQAQSDANTDLDKDDAPPEQRISDRVVIVGLVLSVLLCIVTVRLVFEALVPLYATVTAVLMALVLSI MGVRALGETDLNPVSGISKLAQLFFALIIPQSNPASVLINLVAGAIGALQAGDLMQDLKTGHLLGAAPRAQFWGQ IIGASFGAIVSALLYRLYTT* |
| Coding | >OphauG2|6285 ATGACGCCCGAGAGGGATACACTACACTTGGACCGCCAGCGCCACTTCACGGCGCGCAGTGTTGTGGCAGGTCTC GGCGTCGGGACCGTCATCTGCGCTGCCAATGTCTACTTTGGCCTGCAGACGGGCTGGGTTTCCATCATGTCCATG CCTGCCAGCCTCATGGGCTTCGGCCTGTTCCGCCTGCTGCGCCCGCACCTACAGTTCCCGTTTAGCCCGGTGGAA AACGTGCTGCTGCAGAGCGTTGCCTGTGGCATGGCCATTATGCCTCTGGGCTGCGGCCTGGTTGGAGTGATGCCA GCCATGGAGTATCTCTTGACGAGCGATGAGCAAGGCCCGCTGGCCATGAGCATGACGCAGCTCATGGTGTGGTCC ATTGGCCTGTGCTATTTCGGAGTCGTCTTTGCCGTGCCACTTCGGCGCCAGGTGATTATTCGAGAGCGCCTGAGG TTCCCCAGCGGCTTCAGTACTGCTATTTTGATTTCCGTCCTGCACGGCCAGATTAAGCCGGGGACGCAACAGGAG CGAGATGGTCTAGAGGCAGCGGCACGAGGGGGGTTTGCCAGTCTGGCTCTGCAGCCAGAGCGCGAGGCAGGGCGC GAGCCAGACAACGAGCCAGTTCACGAGTCAGTCCACGAGCCGCGACGTCACATAGAACACGAGCCGCTACTTTCC TCCGAATCTGGCCACCAACACCAAGACTCGTGGTCCAACATGCGTCTCCTCCTGCTTTGCTTTGCCACCTCGGGC CTCTTCACCCTTTGCACCTACTTTATTCCCGTTCTGCGCCAGCTGCCCGTCTTTGGCTCCGTCGCCGCAAACACT TGGCTCTGGACCCTGAATCCGAGCCCGGCGTACATTGGCCAAGGCATCATCATGGGGACCGAGACGACGCTTCAC ATGACTGTGGGCGCCCTTGTCGGCTGGGCCATTCTCAGCCCTTGGGCCAAGATGCAGGGCTGGGCGCCGGGGCCC GTGGACGACTGGGAGCGCGGCAGCAAGGGCTGGATTCTCTGGGTCTCTTTGGCCATAATGCTTGTTGATGCCGTC GTCAGCCTCGGGTACATTGCCCTACGCCCCGTCTGGCGCGCTGTCGTCTTGTATTTCACGCCATCCACCCACGGC TACTCGCGCGTTGGGTTTGCCACGAATCAGGCGCAGTCAGATGCAAATACCGACTTGGACAAGGATGATGCGCCT CCGGAGCAGCGCATTAGTGACCGCGTCGTCATTGTCGGCCTCGTCTTGTCCGTCTTGCTCTGCATTGTCACGGTG CGTCTCGTCTTTGAAGCCTTGGTACCTCTGTATGCCACCGTTACCGCCGTCTTAATGGCACTTGTTCTCAGCATC ATGGGGGTCCGCGCGCTGGGAGAGACGGACCTCAACCCCGTCTCAGGCATCAGCAAGCTGGCCCAGCTCTTCTTT GCTCTCATCATTCCTCAGTCGAACCCTGCCAGCGTTCTCATCAATCTTGTTGCCGGCGCCATTGGGGCGCTCCAA GCGGGAGATCTCATGCAAGACCTTAAGACGGGTCATTTACTCGGTGCCGCGCCACGAGCGCAGTTCTGGGGCCAG ATTATCGGAGCAAGCTTTGGGGCTATCGTCAGTGCGCTTCTCTACCGCCTATACACCACGTAA |
| Transcript | >OphauG2|6285 ATGACGCCCGAGAGGGATACACTACACTTGGACCGCCAGCGCCACTTCACGGCGCGCAGTGTTGTGGCAGGTCTC GGCGTCGGGACCGTCATCTGCGCTGCCAATGTCTACTTTGGCCTGCAGACGGGCTGGGTTTCCATCATGTCCATG CCTGCCAGCCTCATGGGCTTCGGCCTGTTCCGCCTGCTGCGCCCGCACCTACAGTTCCCGTTTAGCCCGGTGGAA AACGTGCTGCTGCAGAGCGTTGCCTGTGGCATGGCCATTATGCCTCTGGGCTGCGGCCTGGTTGGAGTGATGCCA GCCATGGAGTATCTCTTGACGAGCGATGAGCAAGGCCCGCTGGCCATGAGCATGACGCAGCTCATGGTGTGGTCC ATTGGCCTGTGCTATTTCGGAGTCGTCTTTGCCGTGCCACTTCGGCGCCAGGTGATTATTCGAGAGCGCCTGAGG TTCCCCAGCGGCTTCAGTACTGCTATTTTGATTTCCGTCCTGCACGGCCAGATTAAGCCGGGGACGCAACAGGAG CGAGATGGTCTAGAGGCAGCGGCACGAGGGGGGTTTGCCAGTCTGGCTCTGCAGCCAGAGCGCGAGGCAGGGCGC GAGCCAGACAACGAGCCAGTTCACGAGTCAGTCCACGAGCCGCGACGTCACATAGAACACGAGCCGCTACTTTCC TCCGAATCTGGCCACCAACACCAAGACTCGTGGTCCAACATGCGTCTCCTCCTGCTTTGCTTTGCCACCTCGGGC CTCTTCACCCTTTGCACCTACTTTATTCCCGTTCTGCGCCAGCTGCCCGTCTTTGGCTCCGTCGCCGCAAACACT TGGCTCTGGACCCTGAATCCGAGCCCGGCGTACATTGGCCAAGGCATCATCATGGGGACCGAGACGACGCTTCAC ATGACTGTGGGCGCCCTTGTCGGCTGGGCCATTCTCAGCCCTTGGGCCAAGATGCAGGGCTGGGCGCCGGGGCCC GTGGACGACTGGGAGCGCGGCAGCAAGGGCTGGATTCTCTGGGTCTCTTTGGCCATAATGCTTGTTGATGCCGTC GTCAGCCTCGGGTACATTGCCCTACGCCCCGTCTGGCGCGCTGTCGTCTTGTATTTCACGCCATCCACCCACGGC TACTCGCGCGTTGGGTTTGCCACGAATCAGGCGCAGTCAGATGCAAATACCGACTTGGACAAGGATGATGCGCCT CCGGAGCAGCGCATTAGTGACCGCGTCGTCATTGTCGGCCTCGTCTTGTCCGTCTTGCTCTGCATTGTCACGGTG CGTCTCGTCTTTGAAGCCTTGGTACCTCTGTATGCCACCGTTACCGCCGTCTTAATGGCACTTGTTCTCAGCATC ATGGGGGTCCGCGCGCTGGGAGAGACGGACCTCAACCCCGTCTCAGGCATCAGCAAGCTGGCCCAGCTCTTCTTT GCTCTCATCATTCCTCAGTCGAACCCTGCCAGCGTTCTCATCAATCTTGTTGCCGGCGCCATTGGGGCGCTCCAA GCGGGAGATCTCATGCAAGACCTTAAGACGGGTCATTTACTCGGTGCCGCGCCACGAGCGCAGTTCTGGGGCCAG ATTATCGGAGCAAGCTTTGGGGCTATCGTCAGTGCGCTTCTCTACCGCCTATACACCACGTAA |
| Gene | >OphauG2|6285 ATGACGCCCGAGAGGGATACACTACACTTGGACCGCCAGCGCCACTTCACGGCGCGCAGTGTTGTGGCAGGTCTC GGCGTCGGGACCGTCATCTGCGCTGCCAATGTCTACTTTGGCCTGCAGACGGGCTGGGTTTCCATCATGTCCATG CCTGCCAGCCTCATGGGCTTCGGCCTGTTCCGCCTGCTGCGCCCGCACCTACAGTTCCCGTTTAGCCCGGTGGAA AACGTGCTGCTGCAGAGCGTTGCCTGTGGCATGGCCATTATGCCTCTGGGCTGCGGCCTGGTTGGAGTGGTGAGT CTGGTGGGGAGACAAACTTGGCAGAGCGACTCTGAGCTGACCAGCCCAGATGCCAGCCATGGAGTATCTCTTGAC GAGCGATGAGCAAGGCCCGCTGGCCATGAGCATGACGCAGCTCATGGTGTGGTCCATTGGCCTGTGCTATTTCGG AGTCGTCTTTGCCGTGCCACTGTGAGGACAAGCAAGAGTTGGGCCCAAGACGACGCGAGACCTGCACCCGCTAAC TGCAAGGCCAGTCGGCGCCAGGTGATTATTCGAGAGCGCCTGAGGTTCCCCAGCGGCTTCAGTACTGCTATTTTG ATTTCCGTCCTGCACGGCCAGATTAAGCCGGGGACGCAACAGGAGCGAGATGGTCTAGAGGCAGCGGCACGAGGG GGGTTTGCCAGTCTGGCTCTGCAGCCAGAGCGCGAGGCAGGGCGCGAGCCAGACAACGAGCCAGTTCACGAGTCA GTCCACGAGCCGCGACGTCACATAGAACACGAGCCGCTACTTTCCTCCGAATCTGGCCACCAACACCAAGACTCG TGGTCCAACATGCGTCTCCTCCTGCTTTGCTTTGCCACCTCGGGCCTCTTCACCCTTTGCACCTACTTTATTCCC GTTCTGCGCCAGCTGCCCGTCTTTGGCTCCGTCGCCGCAAACACTTGGCTCTGGACCCTGAATCCGAGCCCGGCG TACATTGGCCAAGGCATCATCATGGGGACCGAGACGACGCTTCACATGACTGTGGGCGCCCTTGTCGGCTGGGCC ATTCTCAGCCCTTGGGCCAAGATGCAGGGCTGGGCGCCGGGGCCCGTGGACGACTGGGAGCGCGGCAGCAAGGGC TGGATTCTCTGGGTCTCTTTGGCCATAATGCTTGTTGATGCCGTCGTCAGCCTCGGGTACATTGCCCTACGCCCC GTCTGGCGCGCTGTCGTCTTGTATTTCACGCCATCCACCCACGGCTACTCGCGCGTTGGGTTTGCCACGAATCAG GCGCAGTCAGATGCAAATACCGACTTGGACAAGGATGATGCGCCTCCGGAGCAGCGCATTAGTGACCGCGTCGTC ATTGTCGGCCTCGTCTTGTCCGTCTTGCTCTGCATTGTCACGGTGCGTCTCGTCTTTGAAGCCTTGGTACCTCTG TATGCCACCGTTACCGCCGTCTTAATGGCACTTGTTCTCAGCATCATGGGGGTCCGCGCGCTGGGAGAGACGGAC CTCAACCCCGTCTCAGGCATCAGCAAGCTGGCCCAGCTCTTCTTTGCTCTCATCATTCCTCAGTCGAACCCTGCC AGCGTTCTCATCAATCTTGTTGCCGGCGCCATTGTAAGACCAAGTCCAATCTACTCTGGTCAAGACGTGATGCTA ACGAGGAGCGTCCCAGTCTGAAGCTGTTGGTGGCATCCGGATGCCCTCTCTTTGTTCTCCTCTGCTAACCTCAAC AGGGGGCGCTCCAAGCGGGAGATCTCATGCAAGACCTTAAGACGGGTCATTTACTCGGTGCCGCGCCACGAGCGC AGTTCTGGGGCCAGATTATCGGAGCAAGCTTTGGGGCTATCGTCAGTGCGCTTCTCTACCGCCTATACACCACGT AA |