Protein ID | Hirsu2|5653 |
Gene name | |
Location | Contig_284:8826..10952 |
Strand | + |
Gene length (bp) | 2126 |
Transcript length (bp) | 1875 |
Coding sequence length (bp) | 1875 |
Protein length (aa) | 625 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF01494 | FAD_binding_3 | FAD binding domain | 6.3E-69 | 23 | 372 |
PF07976 | Phe_hydrox_dim | Phenol hydroxylase, C-terminal dimerisation domain | 2.8E-29 | 406 | 584 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|P15245|PH2M_TRICU | Phenol 2-monooxygenase OS=Trichosporon cutaneum PE=1 SV=3 | 19 | 617 | 1.0E-75 |
sp|Q6SSJ6|MOBA_COMTE | 3-hydroxybenzoate 4-monooxygenase OS=Comamonas testosteroni GN=mobA PE=1 SV=1 | 4 | 617 | 7.0E-69 |
sp|Q58PK7|OTCC_STRRM | Anhydrotetracycline monooxygenase OS=Streptomyces rimosus GN=otcC PE=1 SV=1 | 22 | 383 | 1.0E-27 |
sp|P42535|PCPB_SPHCR | Pentachlorophenol 4-monooxygenase OS=Sphingobium chlorophenolicum GN=pcpB PE=1 SV=4 | 25 | 370 | 4.0E-23 |
sp|O07561|YHJG_BACSU | Uncharacterized aromatic compound monooxygenase YhjG OS=Bacillus subtilis (strain 168) GN=yhjG PE=3 SV=1 | 22 | 420 | 7.0E-23 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|P15245|PH2M_TRICU | Phenol 2-monooxygenase OS=Trichosporon cutaneum PE=1 SV=3 | 19 | 617 | 1.0E-75 |
sp|Q6SSJ6|MOBA_COMTE | 3-hydroxybenzoate 4-monooxygenase OS=Comamonas testosteroni GN=mobA PE=1 SV=1 | 4 | 617 | 7.0E-69 |
sp|Q58PK7|OTCC_STRRM | Anhydrotetracycline monooxygenase OS=Streptomyces rimosus GN=otcC PE=1 SV=1 | 22 | 383 | 1.0E-27 |
sp|P42535|PCPB_SPHCR | Pentachlorophenol 4-monooxygenase OS=Sphingobium chlorophenolicum GN=pcpB PE=1 SV=4 | 25 | 370 | 4.0E-23 |
sp|O07561|YHJG_BACSU | Uncharacterized aromatic compound monooxygenase YhjG OS=Bacillus subtilis (strain 168) GN=yhjG PE=3 SV=1 | 22 | 420 | 7.0E-23 |
sp|Q8KN28|TFDB_DELAC | 2,4-dichlorophenol 6-monooxygenase OS=Delftia acidovorans GN=tfdB PE=1 SV=3 | 24 | 369 | 1.0E-20 |
sp|Q476N1|MHPA_CUPPJ | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Cupriavidus pinatubonensis (strain JMP 134 / LMG 1197) GN=mhpA PE=3 SV=1 | 12 | 380 | 4.0E-20 |
sp|A4T8B6|MHPA_MYCGI | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Mycobacterium gilvum (strain PYR-GCK) GN=mhpA PE=3 SV=1 | 17 | 380 | 2.0E-19 |
sp|A4JPY1|MHPA1_BURVG | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase 1 OS=Burkholderia vietnamiensis (strain G4 / LMG 22486) GN=mhpA1 PE=3 SV=1 | 1 | 380 | 4.0E-19 |
sp|P39888|TCMG_STRGA | Tetracenomycin polyketide synthesis hydroxylase TcmG OS=Streptomyces glaucescens GN=tcmG PE=3 SV=1 | 19 | 370 | 9.0E-19 |
sp|A0R1T4|MHPA_MYCS2 | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Mycobacterium smegmatis (strain ATCC 700084 / mc(2)155) GN=mhpA PE=3 SV=2 | 17 | 380 | 2.0E-18 |
sp|Q13QI0|MHPA_BURXL | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Burkholderia xenovorans (strain LB400) GN=mhpA PE=3 SV=1 | 7 | 380 | 4.0E-18 |
sp|Q54530|DNRF_STREF | Aklavinone 12-hydroxylase RdmE OS=Streptomyces purpurascens GN=rdmE PE=1 SV=1 | 19 | 376 | 1.0E-17 |
sp|Q9S158|MHPA_COMTE | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Comamonas testosteroni GN=mhpA PE=3 SV=1 | 19 | 380 | 1.0E-17 |
sp|B7MPB4|MHPA_ECO81 | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Escherichia coli O81 (strain ED1a) GN=mhpA PE=3 SV=1 | 25 | 371 | 5.0E-17 |
sp|B6HZX3|MHPA_ECOSE | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Escherichia coli (strain SE11) GN=mhpA PE=3 SV=1 | 25 | 371 | 7.0E-17 |
sp|A7ZWZ4|MHPA_ECOHS | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Escherichia coli O9:H4 (strain HS) GN=mhpA PE=3 SV=1 | 25 | 371 | 7.0E-17 |
sp|A7ZI94|MHPA_ECO24 | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Escherichia coli O139:H28 (strain E24377A / ETEC) GN=mhpA PE=3 SV=1 | 25 | 371 | 7.0E-17 |
sp|Q3Z585|MHPA_SHISS | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Shigella sonnei (strain Ss046) GN=mhpA PE=3 SV=1 | 25 | 371 | 7.0E-17 |
sp|B7NK08|MHPA_ECO7I | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Escherichia coli O7:K1 (strain IAI39 / ExPEC) GN=mhpA PE=3 SV=1 | 25 | 371 | 1.0E-16 |
sp|B1LIN2|MHPA_ECOSM | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Escherichia coli (strain SMS-3-5 / SECEC) GN=mhpA PE=3 SV=1 | 25 | 371 | 1.0E-16 |
sp|B7N8Q4|MHPA_ECOLU | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Escherichia coli O17:K52:H18 (strain UMN026 / ExPEC) GN=mhpA PE=3 SV=1 | 25 | 371 | 1.0E-16 |
sp|B7M2Z5|MHPA_ECO8A | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Escherichia coli O8 (strain IAI1) GN=mhpA PE=3 SV=1 | 25 | 371 | 2.0E-16 |
sp|B7L503|MHPA_ECO55 | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Escherichia coli (strain 55989 / EAEC) GN=mhpA PE=3 SV=1 | 25 | 371 | 4.0E-16 |
sp|B1XBJ4|MHPA_ECODH | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Escherichia coli (strain K12 / DH10B) GN=mhpA PE=3 SV=1 | 25 | 371 | 4.0E-16 |
sp|P77397|MHPA_ECOLI | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Escherichia coli (strain K12) GN=mhpA PE=1 SV=1 | 25 | 371 | 4.0E-16 |
sp|A1UJP4|MHPA_MYCSK | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Mycobacterium sp. (strain KMS) GN=mhpA PE=3 SV=1 | 18 | 405 | 4.0E-16 |
sp|Q8X680|MHPA_ECO57 | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Escherichia coli O157:H7 GN=mhpA PE=3 SV=1 | 25 | 371 | 4.0E-16 |
sp|B5Z2Q2|MHPA_ECO5E | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Escherichia coli O157:H7 (strain EC4115 / EHEC) GN=mhpA PE=3 SV=1 | 25 | 371 | 4.0E-16 |
sp|Q1B5E2|MHPA_MYCSS | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Mycobacterium sp. (strain MCS) GN=mhpA PE=3 SV=1 | 18 | 405 | 4.0E-16 |
sp|A3Q339|MHPA_MYCSJ | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Mycobacterium sp. (strain JLS) GN=mhpA PE=3 SV=1 | 24 | 380 | 7.0E-16 |
sp|P27138|TFDB_CUPPJ | 2,4-dichlorophenol 6-monooxygenase OS=Cupriavidus pinatubonensis (strain JMP 134 / LMG 1197) GN=tfdB PE=3 SV=1 | 24 | 369 | 2.0E-15 |
sp|B5XQI9|MHPA_KLEP3 | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Klebsiella pneumoniae (strain 342) GN=mhpA PE=3 SV=1 | 25 | 371 | 2.0E-15 |
sp|Q742Z1|MHPA_MYCPA | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Mycobacterium paratuberculosis (strain ATCC BAA-968 / K-10) GN=mhpA PE=3 SV=1 | 19 | 380 | 3.0E-15 |
sp|P42534|HYDL_STRCO | Putative polyketide hydroxylase OS=Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) GN=SCO5321 PE=3 SV=2 | 13 | 367 | 4.0E-15 |
sp|A4JQH4|MHPA2_BURVG | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase 2 OS=Burkholderia vietnamiensis (strain G4 / LMG 22486) GN=mhpA2 PE=3 SV=1 | 18 | 405 | 4.0E-15 |
sp|A6TAC9|MHPA_KLEP7 | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Klebsiella pneumoniae subsp. pneumoniae (strain ATCC 700721 / MGH 78578) GN=mhpA PE=3 SV=1 | 24 | 371 | 4.0E-15 |
sp|A0KE38|MHPA_BURCH | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Burkholderia cenocepacia (strain HI2424) GN=mhpA PE=3 SV=1 | 18 | 379 | 6.0E-15 |
sp|Q1BGA7|MHPA_BURCA | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Burkholderia cenocepacia (strain AU 1054) GN=mhpA PE=3 SV=1 | 18 | 379 | 6.0E-15 |
sp|A0QB57|MHPA_MYCA1 | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Mycobacterium avium (strain 104) GN=mhpA PE=3 SV=1 | 19 | 380 | 2.0E-14 |
sp|A1TCX2|MHPA_MYCVP | 3-(3-hydroxy-phenyl)propionate/3-hydroxycinnamic acid hydroxylase OS=Mycobacterium vanbaalenii (strain DSM 7251 / PYR-1) GN=mhpA PE=3 SV=1 | 29 | 380 | 9.0E-14 |
sp|Q05355|HYDL_STRHA | Putative polyketide hydroxylase OS=Streptomyces halstedii GN=schC PE=3 SV=1 | 18 | 364 | 1.0E-13 |
sp|P31020|PHEA_PSEUE | Phenol 2-monooxygenase OS=Pseudomonas sp. (strain EST1001) GN=pheA PE=3 SV=1 | 24 | 394 | 1.0E-13 |
sp|P32009|DNRF_STRPE | Aklavinone 12-hydroxylase DnrF OS=Streptomyces peucetius GN=dnrF PE=1 SV=2 | 38 | 384 | 1.0E-10 |
sp|A4XD40|KMO_SALTO | Kynurenine 3-monooxygenase OS=Salinispora tropica (strain ATCC BAA-916 / DSM 44818 / CNB-440) GN=kmo PE=3 SV=1 | 29 | 337 | 8.0E-08 |
sp|Q9U641|CMFB_DICDI | Conditioned medium factor receptor 1 OS=Dictyostelium discoideum GN=cmfB PE=1 SV=1 | 16 | 211 | 2.0E-06 |
GO Term | Description | Terminal node |
---|---|---|
GO:0071949 | FAD binding | Yes |
GO:0036094 | small molecule binding | No |
GO:1901265 | nucleoside phosphate binding | No |
GO:0043168 | anion binding | No |
GO:0000166 | nucleotide binding | No |
GO:0050660 | flavin adenine dinucleotide binding | No |
GO:0097159 | organic cyclic compound binding | No |
GO:1901363 | heterocyclic compound binding | No |
GO:0005488 | binding | No |
GO:0043167 | ion binding | No |
GO:0003674 | molecular_function | No |
SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
---|---|---|
No | 1 - 65 | 0.5 |
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|5653 MDEPYCPEAGLESCPSLDSEERYDVVIVGAGPAGLMLAACLARWGYRIKQVDNRPEPTRAGRADGIQPRYMDMLR SLGLKPAIMSHSPGRIYETAFWSPGAAGHGIVRTGTSASCPASIGARYPFVTCLHQGLIERVFIADLERRGVEVR RPWTVRGFQTGQGTEYPLLVDLARVDGTSSERVRAKYLFSGEGAKSVIRRQLGIPLLHKDPVAFVWAVMDGLMMC TVHSESGSALIIPREEGLVRLYVLIASSEDPDWDRKRSATEDEVKALAGDIFRPYWIQWRRVDWFSIYPIQQAVA DRYTLDQRVFLGGDACHTHSPKAGQGMNTAFLDSVNLAWKMHAVEQGFAHRELLGTYELERRSVAEALIDFDRRY ATLFSQRPAADADGAAGGSDFTRAFKDSCLFVSGHGVRYPPNRLNWSPAHPARSALFRRPGCGAGPTPGQVFVTA DVTRVEDARVVHLEQAVPFNGSFRVLVLAGDPARSSRALRHLADRLSRDGALCGARRGPGGAPSDDDDNPHSLLF TLCTVFTARRADIEIARDVPGALADYRRHVYADDQRGPGVPDGSYPAHGKLGFDADRWGIVVVRPDGHIGCVIRL VEGGGSAEALHQYFSSLSPDGWHS* |
Coding | >Hirsu2|5653 ATGGACGAACCGTACTGCCCCGAGGCGGGCCTCGAGTCGTGTCCGTCTCTAGACAGCGAAGAGCGCTACGATGTT GTCATCGTCGGGGCCGGGCCGGCGGGCCTGATGCTGGCGGCCTGCTTGGCCCGATGGGGCTACCGGATCAAGCAG GTGGACAACCGGCCGGAGCCGACGCGTGCCGGGCGCGCGGACGGCATCCAGCCGCGCTACATGGACATGCTGCGC AGCCTGGGCCTCAAGCCGGCCATCATGTCGCACAGCCCCGGCCGCATCTACGAGACGGCCTTCTGGAGCCCGGGC GCGGCCGGGCACGGCATCGTCCGCACCGGCACGTCGGCCAGCTGTCCGGCCTCCATCGGGGCGCGGTACCCGTTC GTCACCTGCCTCCATCAGGGCCTGATCGAGAGGGTCTTCATCGCCGACCTGGAGCGGAGGGGCGTCGAGGTCCGG CGGCCGTGGACGGTCAGGGGCTTCCAGACGGGCCAGGGGACTGAGTACCCGCTGCTGGTCGACCTGGCCCGCGTC GACGGCACGTCGAGCGAGCGAGTGCGGGCCAAGTATCTCTTCAGCGGCGAGGGGGCCAAGTCTGTCATCAGACGG CAGCTGGGCATCCCGCTCCTCCACAAGGACCCCGTCGCCTTCGTCTGGGCCGTCATGGACGGCCTGATGATGTGT ACCGTCCACAGCGAGAGCGGCTCGGCCCTGATCATACCTCGCGAGGAGGGCCTGGTCCGGCTCTACGTGCTGATT GCCTCGTCGGAAGATCCCGACTGGGACCGTAAGAGGTCGGCGACGGAGGACGAGGTCAAGGCTCTGGCGGGCGAC ATCTTCCGGCCGTACTGGATCCAGTGGCGGCGCGTCGACTGGTTCTCCATCTATCCCATCCAGCAGGCCGTGGCC GACCGCTACACGCTGGACCAGCGGGTGTTTCTGGGAGGCGACGCGTGCCACACACACAGTCCCAAGGCCGGACAG GGCATGAACACGGCCTTCCTCGACTCGGTCAACCTCGCGTGGAAGATGCACGCGGTCGAGCAAGGCTTCGCCCAT CGAGAACTGCTGGGAACGTACGAGCTCGAGCGCCGGTCCGTGGCCGAGGCCCTGATCGACTTCGACCGGCGCTAC GCGACGCTCTTCTCCCAGCGGCCGGCGGCGGACGCCGACGGCGCGGCGGGCGGGTCCGACTTCACAAGGGCCTTC AAGGACTCGTGCCTGTTCGTGAGCGGCCACGGCGTGCGCTACCCGCCCAACCGGCTGAACTGGTCGCCGGCGCAT CCGGCCCGGTCCGCGCTCTTCCGCCGGCCGGGCTGCGGGGCGGGGCCGACGCCGGGCCAGGTCTTCGTCACGGCC GACGTCACGCGGGTCGAGGACGCCCGCGTCGTCCACCTGGAGCAGGCCGTGCCCTTCAACGGCTCGTTCCGCGTC TTAGTCTTGGCCGGCGACCCGGCCCGGAGCTCGCGCGCGCTCCGCCACCTCGCCGACCGCCTGTCGAGAGACGGC GCCCTCTGCGGCGCGCGGCGGGGGCCGGGCGGGGCCCCGTCCGACGACGACGACAACCCGCACAGCCTGCTCTTC ACCCTCTGCACCGTCTTCACCGCCCGGCGGGCCGACATCGAGATCGCGCGCGACGTGCCCGGGGCGCTGGCCGAC TATCGCCGCCACGTCTACGCCGATGACCAACGCGGCCCGGGCGTTCCGGACGGCTCCTATCCGGCCCACGGCAAG CTGGGCTTTGACGCCGACAGATGGGGCATCGTCGTCGTCAGACCGGACGGCCACATCGGCTGCGTCATCCGCCTG GTCGAGGGCGGCGGGAGCGCAGAGGCCCTGCACCAGTACTTCTCGTCCCTGTCCCCCGACGGATGGCACTCGTGA |
Transcript | >Hirsu2|5653 ATGGACGAACCGTACTGCCCCGAGGCGGGCCTCGAGTCGTGTCCGTCTCTAGACAGCGAAGAGCGCTACGATGTT GTCATCGTCGGGGCCGGGCCGGCGGGCCTGATGCTGGCGGCCTGCTTGGCCCGATGGGGCTACCGGATCAAGCAG GTGGACAACCGGCCGGAGCCGACGCGTGCCGGGCGCGCGGACGGCATCCAGCCGCGCTACATGGACATGCTGCGC AGCCTGGGCCTCAAGCCGGCCATCATGTCGCACAGCCCCGGCCGCATCTACGAGACGGCCTTCTGGAGCCCGGGC GCGGCCGGGCACGGCATCGTCCGCACCGGCACGTCGGCCAGCTGTCCGGCCTCCATCGGGGCGCGGTACCCGTTC GTCACCTGCCTCCATCAGGGCCTGATCGAGAGGGTCTTCATCGCCGACCTGGAGCGGAGGGGCGTCGAGGTCCGG CGGCCGTGGACGGTCAGGGGCTTCCAGACGGGCCAGGGGACTGAGTACCCGCTGCTGGTCGACCTGGCCCGCGTC GACGGCACGTCGAGCGAGCGAGTGCGGGCCAAGTATCTCTTCAGCGGCGAGGGGGCCAAGTCTGTCATCAGACGG CAGCTGGGCATCCCGCTCCTCCACAAGGACCCCGTCGCCTTCGTCTGGGCCGTCATGGACGGCCTGATGATGTGT ACCGTCCACAGCGAGAGCGGCTCGGCCCTGATCATACCTCGCGAGGAGGGCCTGGTCCGGCTCTACGTGCTGATT GCCTCGTCGGAAGATCCCGACTGGGACCGTAAGAGGTCGGCGACGGAGGACGAGGTCAAGGCTCTGGCGGGCGAC ATCTTCCGGCCGTACTGGATCCAGTGGCGGCGCGTCGACTGGTTCTCCATCTATCCCATCCAGCAGGCCGTGGCC GACCGCTACACGCTGGACCAGCGGGTGTTTCTGGGAGGCGACGCGTGCCACACACACAGTCCCAAGGCCGGACAG GGCATGAACACGGCCTTCCTCGACTCGGTCAACCTCGCGTGGAAGATGCACGCGGTCGAGCAAGGCTTCGCCCAT CGAGAACTGCTGGGAACGTACGAGCTCGAGCGCCGGTCCGTGGCCGAGGCCCTGATCGACTTCGACCGGCGCTAC GCGACGCTCTTCTCCCAGCGGCCGGCGGCGGACGCCGACGGCGCGGCGGGCGGGTCCGACTTCACAAGGGCCTTC AAGGACTCGTGCCTGTTCGTGAGCGGCCACGGCGTGCGCTACCCGCCCAACCGGCTGAACTGGTCGCCGGCGCAT CCGGCCCGGTCCGCGCTCTTCCGCCGGCCGGGCTGCGGGGCGGGGCCGACGCCGGGCCAGGTCTTCGTCACGGCC GACGTCACGCGGGTCGAGGACGCCCGCGTCGTCCACCTGGAGCAGGCCGTGCCCTTCAACGGCTCGTTCCGCGTC TTAGTCTTGGCCGGCGACCCGGCCCGGAGCTCGCGCGCGCTCCGCCACCTCGCCGACCGCCTGTCGAGAGACGGC GCCCTCTGCGGCGCGCGGCGGGGGCCGGGCGGGGCCCCGTCCGACGACGACGACAACCCGCACAGCCTGCTCTTC ACCCTCTGCACCGTCTTCACCGCCCGGCGGGCCGACATCGAGATCGCGCGCGACGTGCCCGGGGCGCTGGCCGAC TATCGCCGCCACGTCTACGCCGATGACCAACGCGGCCCGGGCGTTCCGGACGGCTCCTATCCGGCCCACGGCAAG CTGGGCTTTGACGCCGACAGATGGGGCATCGTCGTCGTCAGACCGGACGGCCACATCGGCTGCGTCATCCGCCTG GTCGAGGGCGGCGGGAGCGCAGAGGCCCTGCACCAGTACTTCTCGTCCCTGTCCCCCGACGGATGGCACTCGTGA |
Gene | >Hirsu2|5653 ATGGACGAACCGTACTGCCCCGAGGCGGGCCTCGAGTCGTGTCCGTCTCTAGACAGCGAAGAGCGCTACGATGTT GGTAAGTCGAGCCGAGCAGCGAGCGGTACGCGAGGTCTCACTGATGGCCTTCGCAGTCATCGTCGGGGCCGGGCC GGCGGGCCTGATGCTGGCGGCCTGCTTGGCCCGATGGGGCTACCGGATCAAGCAGGTGGACAACCGGCCGGAGCC GACGCGTGCCGGGCGCGCGGACGGCATCCAGCCGCGCTACATGGACATGCTGCGCAGCCTGGGCCTCAAGCCGGC CATCATGTCGCACAGCCCCGGCCGCATCTACGAGACGGCCTTCTGGAGCCCGGGCGCGGCCGGGCACGGCATCGT CCGCACCGGCACGTCGGCCAGCTGTCCGGCCTCCATCGGGGCGCGGTACCCGTTCGTCACCTGCCTCCATCAGGG CCTGATCGAGAGGGTCTTCATCGCCGACCTGGAGCGGAGGGGCGTCGAGGTCCGGCGGCCGTGGACGGTCAGGGG CTTCCAGACGGGCCAGGGGACTGAGTACCCGCTGCTGGTCGACCTGGCCCGCGTCGACGGCACGTCGAGCGAGCG AGTGCGGGCCAAGTATCTCTTCAGCGGCGAGGGGGCCAAGTCTGTCATCAGACGGCAGCTGGGCATCCCGCTCCT CCACAAGGACCCCGTCGCCTTCGTCTGGGCCGTCATGGACGGCCTGGTGACGAGCAACTTCCCCGATATCAAGGC CCGTACGCCCTCAACCGACCCGGACCGGAGCCGGGACTCACGTGCGTGCTGACGCGGCGCAGATGATGTGTACCG TCCACAGCGAGAGCGGCTCGGCCCTGATCATACCTCGCGAGGAGGGCCTGGTCCGGCTCTACGTGCTGATTGCCT CGTCGGAAGATCCCGACTGGGACCGTAAGAGGTCGGCGACGGAGGACGAGGTCAAGGCTCTGGCGGGCGACATCT TCCGGCCGTACTGGATCCAGTGGCGGCGCGTCGACTGGTTCTCCATCTATCCCATCCAGCAGGCCGTGGCCGACC GCTACACGCTGGACCAGCGGGTGTTTCTGGGAGGCGACGCGTGCCACACACACAGTGTAAGCATTGTCTACCTAC CTGCTCGACGGGCGATCCTGTCGCGGGGATCCGTCCCGGACGCCGCCGCCGGGGGCTGACGGGCCGCGCGTTTTC CTTCGGGGCAGCCCAAGGCCGGACAGGGCATGAACACGGCCTTCCTCGACTCGGTCAACCTCGCGTGGAAGATGC ACGCGGTCGAGCAAGGCTTCGCCCATCGAGAACTGCTGGGAACGTACGAGCTCGAGCGCCGGTCCGTGGCCGAGG CCCTGATCGACTTCGACCGGCGCTACGCGACGCTCTTCTCCCAGCGGCCGGCGGCGGACGCCGACGGCGCGGCGG GCGGGTCCGACTTCACAAGGGCCTTCAAGGACTCGTGCCTGTTCGTGAGCGGCCACGGCGTGCGCTACCCGCCCA ACCGGCTGAACTGGTCGCCGGCGCATCCGGCCCGGTCCGCGCTCTTCCGCCGGCCGGGCTGCGGGGCGGGGCCGA CGCCGGGCCAGGTCTTCGTCACGGCCGACGTCACGCGGGTCGAGGACGCCCGCGTCGTCCACCTGGAGCAGGCCG TGCCCTTCAACGGCTCGTTCCGCGTCTTAGTCTTGGCCGGCGACCCGGCCCGGAGCTCGCGCGCGCTCCGCCACC TCGCCGACCGCCTGTCGAGAGACGGCGCCCTCTGCGGCGCGCGGCGGGGGCCGGGCGGGGCCCCGTCCGACGACG ACGACAACCCGCACAGCCTGCTCTTCACCCTCTGCACCGTCTTCACCGCCCGGCGGGCCGACATCGAGATCGCGC GCGACGTGCCCGGGGCGCTGGCCGACTATCGCCGCCACGTCTACGCCGATGACCAACGCGGCCCGGGCGTTCCGG ACGGCTCCTATCCGGCCCACGGCAAGCTGGGCTTTGACGCCGACAGATGGGGCATCGTCGTCGTCAGACCGGACG GCCACATCGGCTGCGTCATCCGCCTGGTCGAGGGCGGCGGGAGCGCAGAGGCCCTGCACCAGTACTTCTCGTCCC TGTCCCCCGACGGATGGCACTCGTGA |