© 2022 - Robin Ohm - Utrecht University - The Netherlands
Built with Python Django and Wagtail
| Protein ID | Hirsu2|2118 |
| Gene name | |
| Location | Contig_1494:1360..3850 |
| Strand | - |
| Gene length (bp) | 2490 |
| Transcript length (bp) | 2079 |
| Coding sequence length (bp) | 2079 |
| Protein length (aa) | 693 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF02776 | TPP_enzyme_N | Thiamine pyrophosphate enzyme, N-terminal TPP binding domain | 1.3E-53 | 92 | 253 |
| PF02775 | TPP_enzyme_C | Thiamine pyrophosphate enzyme, C-terminal TPP binding domain | 5.0E-47 | 500 | 646 |
| PF00205 | TPP_enzyme_M | Thiamine pyrophosphate enzyme, central domain | 1.2E-38 | 291 | 435 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P07342|ILVB_YEAST | Acetolactate synthase catalytic subunit, mitochondrial OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ILV2 PE=1 SV=1 | 56 | 691 | 0.0E+00 |
| sp|P36620|ILVB_SCHPO | Acetolactate synthase, mitochondrial OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ilv1 PE=3 SV=2 | 83 | 672 | 0.0E+00 |
| sp|Q5KPJ5|ILVB_CRYNJ | Acetolactate synthase, mitochondrial OS=Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) GN=ILV2 PE=3 SV=1 | 55 | 671 | 0.0E+00 |
| sp|Q6SSJ3|ILVB_CRYNH | Acetolactate synthase, mitochondrial OS=Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) GN=ILV2 PE=3 SV=1 | 55 | 671 | 0.0E+00 |
| sp|P37251|ILVB_BACSU | Acetolactate synthase large subunit OS=Bacillus subtilis (strain 168) GN=ilvB PE=1 SV=4 | 92 | 669 | 1.0E-149 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|P07342|ILVB_YEAST | Acetolactate synthase catalytic subunit, mitochondrial OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ILV2 PE=1 SV=1 | 56 | 691 | 0.0E+00 |
| sp|P36620|ILVB_SCHPO | Acetolactate synthase, mitochondrial OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=ilv1 PE=3 SV=2 | 83 | 672 | 0.0E+00 |
| sp|Q5KPJ5|ILVB_CRYNJ | Acetolactate synthase, mitochondrial OS=Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) GN=ILV2 PE=3 SV=1 | 55 | 671 | 0.0E+00 |
| sp|Q6SSJ3|ILVB_CRYNH | Acetolactate synthase, mitochondrial OS=Cryptococcus neoformans var. grubii serotype A (strain H99 / ATCC 208821 / CBS 10515 / FGSC 9487) GN=ILV2 PE=3 SV=1 | 55 | 671 | 0.0E+00 |
| sp|P37251|ILVB_BACSU | Acetolactate synthase large subunit OS=Bacillus subtilis (strain 168) GN=ilvB PE=1 SV=4 | 92 | 669 | 1.0E-149 |
| sp|P27819|ILVB3_BRANA | Acetolactate synthase 3, chloroplastic OS=Brassica napus PE=3 SV=1 | 22 | 669 | 2.0E-148 |
| sp|P17597|ILVB_ARATH | Acetolactate synthase, chloroplastic OS=Arabidopsis thaliana GN=ALS PE=1 SV=1 | 91 | 669 | 3.0E-148 |
| sp|P27818|ILVB1_BRANA | Acetolactate synthase 1, chloroplastic OS=Brassica napus PE=3 SV=1 | 22 | 669 | 8.0E-148 |
| sp|P09342|ILVB1_TOBAC | Acetolactate synthase 1, chloroplastic OS=Nicotiana tabacum GN=ALS SURA PE=1 SV=1 | 81 | 669 | 2.0E-145 |
| sp|P09114|ILVB2_TOBAC | Acetolactate synthase 2, chloroplastic OS=Nicotiana tabacum GN=ALS SURB PE=1 SV=1 | 91 | 669 | 7.0E-145 |
| sp|Q6K2E8|ILVB1_ORYSJ | Acetolactate synthase 1, chloroplastic OS=Oryza sativa subsp. japonica GN=ALS1 PE=2 SV=1 | 91 | 670 | 1.0E-143 |
| sp|Q57725|ILVB_METJA | Probable acetolactate synthase large subunit OS=Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) GN=ilvB PE=3 SV=1 | 92 | 665 | 1.0E-142 |
| sp|Q9RQ65|ILVI_BUCSC | Acetolactate synthase large subunit OS=Buchnera aphidicola subsp. Schlechtendalia chinensis GN=ilvI PE=3 SV=1 | 92 | 634 | 8.0E-142 |
| sp|Q41768|ILVB1_MAIZE | Acetolactate synthase 1, chloroplastic OS=Zea mays GN=ALS1 PE=3 SV=1 | 91 | 670 | 1.0E-141 |
| sp|P00892|ILVG_ECOLI | Acetolactate synthase isozyme 2 large subunit OS=Escherichia coli (strain K12) GN=ilvG PE=1 SV=3 | 104 | 669 | 2.0E-139 |
| sp|O85293|ILVI_BUCAP | Acetolactate synthase large subunit OS=Buchnera aphidicola subsp. Schizaphis graminum (strain Sg) GN=ilvI PE=3 SV=1 | 92 | 675 | 7.0E-139 |
| sp|P57321|ILVI_BUCAI | Acetolactate synthase large subunit OS=Buchnera aphidicola subsp. Acyrthosiphon pisum (strain APS) GN=ilvI PE=3 SV=1 | 92 | 675 | 1.0E-138 |
| sp|P45261|ILVI_HAEIN | Acetolactate synthase large subunit OS=Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) GN=ilvI PE=3 SV=1 | 92 | 676 | 1.0E-137 |
| sp|P0A623|ILVB_MYCBO | Acetolactate synthase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ilvB PE=3 SV=1 | 105 | 668 | 1.0E-136 |
| sp|P9WG41|ILVB1_MYCTU | Acetolactate synthase large subunit IlvB1 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ilvB1 PE=1 SV=1 | 105 | 668 | 1.0E-136 |
| sp|P9WG40|ILVB1_MYCTO | Acetolactate synthase large subunit IlvB1 OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ilvB1 PE=3 SV=1 | 105 | 668 | 1.0E-136 |
| sp|P00893|ILVI_ECOLI | Acetolactate synthase isozyme 3 large subunit OS=Escherichia coli (strain K12) GN=ilvI PE=1 SV=2 | 92 | 674 | 5.0E-136 |
| sp|Q1XDF6|ILVB_PYRYE | Acetolactate synthase large subunit OS=Pyropia yezoensis GN=ilvB PE=3 SV=1 | 91 | 664 | 6.0E-136 |
| sp|O33112|ILVB_MYCLE | Acetolactate synthase OS=Mycobacterium leprae (strain TN) GN=ilvB PE=3 SV=1 | 106 | 676 | 7.0E-136 |
| sp|Q41769|ILVB2_MAIZE | Acetolactate synthase 2, chloroplastic OS=Zea mays GN=ALS2 PE=3 SV=1 | 91 | 670 | 1.0E-135 |
| sp|Q7U5G1|ILVB_SYNPX | Acetolactate synthase large subunit OS=Synechococcus sp. (strain WH8102) GN=ilvB PE=3 SV=1 | 92 | 664 | 2.0E-135 |
| sp|P14874|ILVB2_BRANA | Acetolactate synthase 2, chloroplastic OS=Brassica napus PE=3 SV=1 | 62 | 670 | 1.0E-134 |
| sp|P08142|ILVB_ECOLI | Acetolactate synthase isozyme 1 large subunit OS=Escherichia coli (strain K12) GN=ilvB PE=1 SV=1 | 92 | 669 | 2.0E-133 |
| sp|P42463|ILVB_CORGL | Acetolactate synthase large subunit OS=Corynebacterium glutamicum (strain ATCC 13032 / DSM 20300 / JCM 1318 / LMG 3730 / NCIMB 10025) GN=ilvB PE=3 SV=1 | 109 | 664 | 5.0E-133 |
| sp|P40811|ILVI_SALTY | Acetolactate synthase isozyme 3 large subunit OS=Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) GN=ilvI PE=3 SV=3 | 92 | 674 | 5.0E-133 |
| sp|P69684|ILVB_PORUM | Acetolactate synthase large subunit OS=Porphyra umbilicalis GN=ilvB PE=3 SV=1 | 84 | 664 | 7.0E-132 |
| sp|P69683|ILVB_PORPU | Acetolactate synthase large subunit OS=Porphyra purpurea GN=ilvB PE=3 SV=1 | 84 | 664 | 7.0E-132 |
| sp|O78518|ILVB_GUITH | Acetolactate synthase large subunit OS=Guillardia theta GN=ilvB PE=3 SV=1 | 101 | 664 | 1.0E-131 |
| sp|Q02137|ILVB_LACLA | Acetolactate synthase large subunit OS=Lactococcus lactis subsp. lactis (strain IL1403) GN=ilvB PE=3 SV=2 | 92 | 662 | 8.0E-131 |
| sp|Q89AP7|ILVI_BUCBP | Acetolactate synthase large subunit OS=Buchnera aphidicola subsp. Baizongia pistaciae (strain Bp) GN=ilvI PE=3 SV=1 | 92 | 628 | 4.0E-130 |
| sp|O19929|ILVB_CYACA | Acetolactate synthase large subunit OS=Cyanidium caldarium GN=ilvB PE=3 SV=1 | 91 | 669 | 5.0E-130 |
| sp|Q59498|ILVB_MYCAV | Acetolactate synthase OS=Mycobacterium avium GN=ilvB PE=3 SV=1 | 105 | 676 | 2.0E-129 |
| sp|Q7XKQ8|ILVB2_ORYSJ | Probable acetolactate synthase 2, chloroplastic OS=Oryza sativa subsp. japonica GN=ALS2 PE=2 SV=2 | 91 | 670 | 2.0E-128 |
| sp|O08353|ILVB_METAO | Probable acetolactate synthase large subunit OS=Methanococcus aeolicus GN=ilvB PE=3 SV=1 | 92 | 686 | 4.0E-127 |
| sp|P27868|ILVB_ARTPT | Acetolactate synthase (Fragment) OS=Arthrospira platensis GN=ilvY PE=3 SV=1 | 103 | 662 | 2.0E-124 |
| sp|P0AEP7|GCL_ECOLI | Glyoxylate carboligase OS=Escherichia coli (strain K12) GN=gcl PE=1 SV=2 | 103 | 677 | 3.0E-70 |
| sp|P0AEP8|GCL_ECO57 | Glyoxylate carboligase OS=Escherichia coli O157:H7 GN=gcl PE=3 SV=2 | 103 | 677 | 3.0E-70 |
| sp|Q93PS3|XSC_DESTI | Sulfoacetaldehyde acetyltransferase OS=Desulfonispora thiosulfatigenes GN=xsc PE=1 SV=1 | 95 | 653 | 3.0E-59 |
| sp|Q04789|ILVX_BACSU | Acetolactate synthase OS=Bacillus subtilis (strain 168) GN=alsS PE=2 SV=3 | 86 | 650 | 2.0E-57 |
| sp|P96591|YDAP_BACSU | Putative thiamine pyrophosphate-containing protein YdaP OS=Bacillus subtilis (strain 168) GN=ydaP PE=2 SV=1 | 91 | 664 | 1.0E-56 |
| sp|Q84H44|XSC_CASDE | Sulfoacetaldehyde acetyltransferase OS=Castellaniella defragrans GN=xsc PE=1 SV=3 | 95 | 659 | 6.0E-50 |
| sp|Q84H41|XSC_ALCXX | Sulfoacetaldehyde acetyltransferase OS=Alcaligenes xylosoxydans xylosoxydans GN=xsc PE=1 SV=3 | 95 | 638 | 5.0E-49 |
| sp|D5AKX8|XSC_RHOCB | Sulfoacetaldehyde acetyltransferase OS=Rhodobacter capsulatus (strain ATCC BAA-309 / NBRC 16581 / SB1003) GN=xsc PE=2 SV=1 | 95 | 603 | 4.0E-46 |
| sp|P27696|ILVB_KLEPN | Acetolactate synthase, catabolic OS=Klebsiella pneumoniae GN=budB PE=1 SV=1 | 93 | 652 | 6.0E-43 |
| sp|Q54970|POXB_STRPN | Pyruvate oxidase OS=Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) GN=spxB PE=3 SV=2 | 105 | 615 | 9.0E-41 |
| sp|Q04524|ILVB_RAOTE | Acetolactate synthase, catabolic OS=Raoultella terrigena GN=budB PE=3 SV=1 | 93 | 652 | 1.0E-38 |
| sp|P07003|POXB_ECOLI | Pyruvate dehydrogenase [ubiquinone] OS=Escherichia coli (strain K12) GN=poxB PE=1 SV=1 | 105 | 657 | 1.0E-37 |
| sp|Q58077|Y663_METJA | Uncharacterized protein MJ0663 OS=Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) GN=MJ0663 PE=3 SV=1 | 93 | 652 | 1.0E-37 |
| sp|Q92UW6|XSC_RHIME | Probable sulfoacetaldehyde acetyltransferase OS=Rhizobium meliloti (strain 1021) GN=xsc PE=3 SV=1 | 95 | 633 | 7.0E-37 |
| sp|P37063|POXB_LACPL | Pyruvate oxidase OS=Lactobacillus plantarum (strain ATCC BAA-793 / NCIMB 8826 / WCFS1) GN=pox5 PE=1 SV=3 | 105 | 654 | 2.0E-36 |
| sp|Q9LF46|HACL_ARATH | 2-hydroxyacyl-CoA lyase OS=Arabidopsis thaliana GN=HACL PE=1 SV=1 | 79 | 581 | 2.0E-35 |
| sp|O06335|ILVB2_MYCTU | Putative acetolactate synthase large subunit IlvB2 OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ilvB2 PE=2 SV=1 | 130 | 584 | 1.0E-32 |
| sp|P0CH62|CHDH_AZOSP | Cyclohexane-1,2-dione hydrolase OS=Azoarcus sp. PE=1 SV=1 | 91 | 651 | 6.0E-32 |
| sp|O05031|Y737_HAEIN | Putative uncharacterized protein HI_0737 OS=Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) GN=HI_0737 PE=5 SV=1 | 92 | 221 | 4.0E-31 |
| sp|Q6NV04|ILVBL_DANRE | Acetolactate synthase-like protein OS=Danio rerio GN=ilvbl PE=2 SV=1 | 91 | 591 | 1.0E-28 |
| sp|A1L0T0|ILVBL_HUMAN | Acetolactate synthase-like protein OS=Homo sapiens GN=ILVBL PE=1 SV=2 | 91 | 581 | 2.0E-28 |
| sp|P20906|MDLC_PSEPU | Benzoylformate decarboxylase OS=Pseudomonas putida GN=mdlC PE=1 SV=2 | 98 | 653 | 1.0E-27 |
| sp|Q0JMH0|HACL_ORYSJ | 2-hydroxyacyl-CoA lyase OS=Oryza sativa subsp. japonica GN=Os01g0505400 PE=3 SV=3 | 108 | 581 | 3.0E-27 |
| sp|Q9LCV9|CEAS_STRCL | N(2)-(2-carboxyethyl)arginine synthase OS=Streptomyces clavuligerus GN=ceaS PE=1 SV=1 | 120 | 646 | 4.0E-27 |
| sp|Q8CHM7|HACL1_RAT | 2-hydroxyacyl-CoA lyase 1 OS=Rattus norvegicus GN=Hacl1 PE=1 SV=1 | 78 | 650 | 1.0E-26 |
| sp|Q9QXE0|HACL1_MOUSE | 2-hydroxyacyl-CoA lyase 1 OS=Mus musculus GN=Hacl1 PE=1 SV=2 | 78 | 652 | 1.0E-26 |
| sp|Q9UJ83|HACL1_HUMAN | 2-hydroxyacyl-CoA lyase 1 OS=Homo sapiens GN=HACL1 PE=1 SV=2 | 92 | 650 | 3.0E-26 |
| sp|A6QQT9|ILVBL_BOVIN | Acetolactate synthase-like protein OS=Bos taurus GN=ILVBL PE=2 SV=2 | 91 | 581 | 9.0E-26 |
| sp|O61856|ILVBL_CAEEL | Acetolactate synthase-like protein OS=Caenorhabditis elegans GN=T26C12.1 PE=3 SV=2 | 91 | 581 | 7.0E-25 |
| sp|Q6DDK5|ILVBL_XENLA | Acetolactate synthase-like protein OS=Xenopus laevis GN=ilvbl PE=2 SV=1 | 93 | 569 | 2.0E-24 |
| sp|Q8Y9Y1|IOLD_LISMO | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) GN=iolD PE=3 SV=1 | 88 | 634 | 5.0E-24 |
| sp|P0AFI0|OXC_ECOLI | Oxalyl-CoA decarboxylase OS=Escherichia coli (strain K12) GN=oxc PE=1 SV=1 | 84 | 581 | 5.0E-24 |
| sp|P0AFI1|OXC_ECO57 | Oxalyl-CoA decarboxylase OS=Escherichia coli O157:H7 GN=oxc PE=3 SV=1 | 84 | 581 | 5.0E-24 |
| sp|Q9HUR2|MDLC_PSEAE | Benzoylformate decarboxylase OS=Pseudomonas aeruginosa (strain ATCC 15692 / PAO1 / 1C / PRS 101 / LMG 12228) GN=mdlC PE=3 SV=1 | 98 | 654 | 1.0E-23 |
| sp|Q92EQ4|IOLD_LISIN | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Listeria innocua serovar 6a (strain CLIP 11262) GN=iolD PE=3 SV=1 | 105 | 634 | 2.0E-23 |
| sp|Q723S8|IOLD_LISMF | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Listeria monocytogenes serotype 4b (strain F2365) GN=iolD PE=3 SV=2 | 88 | 634 | 6.0E-23 |
| sp|P9WG39|ILVG_MYCTU | Acetolactate synthase large subunit IlvG OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=ilvG PE=1 SV=1 | 94 | 653 | 7.0E-23 |
| sp|P9WG38|ILVG_MYCTO | Acetolactate synthase large subunit IlvG OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=ilvG PE=3 SV=1 | 94 | 653 | 7.0E-23 |
| sp|P66947|ILVG_MYCBO | Probable acetolactate synthase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=ilvG PE=3 SV=1 | 94 | 653 | 7.0E-23 |
| sp|Q8BU33|ILVBL_MOUSE | Acetolactate synthase-like protein OS=Mus musculus GN=Ilvbl PE=1 SV=1 | 83 | 581 | 1.0E-22 |
| sp|Q9KAG9|IOLD_BACHD | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Bacillus halodurans (strain ATCC BAA-125 / DSM 18197 / FERM 7344 / JCM 9153 / C-125) GN=iolD PE=3 SV=1 | 98 | 634 | 2.0E-22 |
| sp|Q5WKY8|IOLD_BACSK | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Bacillus clausii (strain KSM-K16) GN=iolD PE=3 SV=1 | 104 | 614 | 3.0E-22 |
| sp|A5YBJ6|IOLD_LACCA | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Lactobacillus casei GN=iolD PE=3 SV=2 | 104 | 625 | 3.0E-22 |
| sp|Q4V1F5|IOLD2_BACCZ | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase 2 OS=Bacillus cereus (strain ZK / E33L) GN=iolD2 PE=3 SV=1 | 104 | 634 | 2.0E-21 |
| sp|Q5KYR0|IOLD_GEOKA | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Geobacillus kaustophilus (strain HTA426) GN=iolD PE=3 SV=1 | 98 | 591 | 8.0E-21 |
| sp|Q54DA9|HACL1_DICDI | Probable 2-hydroxyacyl-CoA lyase 1 OS=Dictyostelium discoideum GN=hacl1 PE=3 SV=1 | 93 | 581 | 2.0E-20 |
| sp|B7JPM3|IOLD_BACC0 | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Bacillus cereus (strain AH820) GN=iolD PE=3 SV=1 | 104 | 591 | 2.0E-20 |
| sp|P42415|IOLD_BACSU | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Bacillus subtilis (strain 168) GN=iolD PE=1 SV=2 | 104 | 646 | 3.0E-20 |
| sp|Q0TUZ2|IOLD_CLOP1 | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Clostridium perfringens (strain ATCC 13124 / DSM 756 / JCM 1290 / NCIMB 6125 / NCTC 8237 / Type A) GN=iolD PE=3 SV=1 | 84 | 591 | 6.0E-20 |
| sp|Q9HUI8|ARUI_PSEAE | Probable 2-ketoarginine decarboxylase AruI OS=Pseudomonas aeruginosa (strain ATCC 15692 / PAO1 / 1C / PRS 101 / LMG 12228) GN=aruI PE=1 SV=1 | 92 | 254 | 6.0E-20 |
| sp|A7ZAH8|IOLD_BACMF | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Bacillus methylotrophicus (strain DSM 23117 / BGSC 10A6 / FZB42) GN=iolD PE=3 SV=1 | 104 | 646 | 5.0E-19 |
| sp|Q65D03|IOLD_BACLD | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Bacillus licheniformis (strain ATCC 14580 / DSM 13 / JCM 2505 / NBRC 12200 / NCIMB 9375 / NRRL NRS-1264 / Gibson 46) GN=iolD PE=3 SV=1 | 104 | 614 | 7.0E-19 |
| sp|B2V4K0|IOLD_CLOBA | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Clostridium botulinum (strain Alaska E43 / Type E3) GN=iolD PE=3 SV=1 | 84 | 614 | 9.0E-19 |
| sp|C1EVJ3|IOLD_BACC3 | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Bacillus cereus (strain 03BB102) GN=iolD PE=3 SV=1 | 104 | 591 | 2.0E-18 |
| sp|A0REB6|IOLD_BACAH | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Bacillus thuringiensis (strain Al Hakam) GN=iolD PE=3 SV=1 | 104 | 591 | 2.0E-18 |
| sp|A4IPB6|IOLD_GEOTN | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Geobacillus thermodenitrificans (strain NG80-2) GN=iolD PE=3 SV=1 | 104 | 591 | 7.0E-18 |
| sp|P10343|YI42_PSEAY | Uncharacterized 42.6 kDa protein in isoamylase 3'region OS=Pseudomonas amyloderamosa PE=4 SV=1 | 95 | 520 | 2.0E-17 |
| sp|P39994|YEC0_YEAST | Putative 2-hydroxyacyl-CoA lyase OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=YEL020C PE=1 SV=1 | 97 | 581 | 1.0E-16 |
| sp|P40149|OXC_OXAFO | Oxalyl-CoA decarboxylase OS=Oxalobacter formigenes GN=oxc PE=1 SV=1 | 132 | 331 | 3.0E-16 |
| sp|Q9P7P6|PDC3_SCHPO | Probable pyruvate decarboxylase C186.09 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC186.09 PE=3 SV=1 | 101 | 651 | 3.0E-16 |
| sp|Q9Y7M1|YGK4_SCHPO | Putative 2-hydroxyacyl-CoA lyase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPBC725.04 PE=3 SV=1 | 92 | 582 | 4.0E-16 |
| sp|P51853|BZNB_PSEFL | Benzaldehyde lyase OS=Pseudomonas fluorescens GN=bznB PE=1 SV=1 | 92 | 593 | 8.0E-14 |
| sp|Q81QB5|IOLD_BACAN | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Bacillus anthracis GN=iolD PE=3 SV=1 | 104 | 389 | 3.0E-13 |
| sp|C3LHY1|IOLD_BACAC | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Bacillus anthracis (strain CDC 684 / NRRL 3495) GN=iolD PE=3 SV=1 | 104 | 389 | 3.0E-13 |
| sp|C3PAZ3|IOLD_BACAA | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Bacillus anthracis (strain A0248) GN=iolD PE=3 SV=1 | 104 | 389 | 3.0E-13 |
| sp|Q6HIK2|IOLD_BACHK | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Bacillus thuringiensis subsp. konkukian (strain 97-27) GN=iolD PE=3 SV=1 | 104 | 389 | 4.0E-13 |
| sp|Q63B73|IOLD1_BACCZ | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase 1 OS=Bacillus cereus (strain ZK / E33L) GN=iolD1 PE=3 SV=1 | 104 | 389 | 5.0E-13 |
| sp|P23234|DCIP_ENTCL | Indole-3-pyruvate decarboxylase OS=Enterobacter cloacae GN=ipdC PE=1 SV=1 | 105 | 651 | 9.0E-13 |
| sp|Q09737|PDC1_SCHPO | Putative pyruvate decarboxylase C13A11.06 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC13A11.06 PE=3 SV=2 | 94 | 629 | 6.0E-11 |
| sp|P9WG37|KDC_MYCTU | Alpha-keto-acid decarboxylase OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=kdc PE=1 SV=1 | 94 | 582 | 6.0E-11 |
| sp|A5U0P1|KDC_MYCTA | Alpha-keto-acid decarboxylase OS=Mycobacterium tuberculosis (strain ATCC 25177 / H37Ra) GN=kdc PE=3 SV=1 | 94 | 582 | 6.0E-11 |
| sp|A1KGY5|KDC_MYCBP | Alpha-keto-acid decarboxylase OS=Mycobacterium bovis (strain BCG / Pasteur 1173P2) GN=kdc PE=3 SV=1 | 94 | 582 | 6.0E-11 |
| sp|Q7U140|KDC_MYCBO | Alpha-keto-acid decarboxylase OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=kdc PE=3 SV=1 | 94 | 582 | 6.0E-11 |
| sp|A1BI74|MEND_CHLPD | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Chlorobium phaeobacteroides (strain DSM 266) GN=menD PE=3 SV=1 | 99 | 615 | 1.0E-10 |
| sp|P9WG36|KDC_MYCTO | Alpha-keto-acid decarboxylase OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=kdc PE=3 SV=1 | 94 | 582 | 2.0E-10 |
| sp|P83779|PDC1_CANAL | Pyruvate decarboxylase OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=PDC11 PE=1 SV=2 | 94 | 582 | 9.0E-10 |
| sp|Q898E8|IOLD_CLOTE | 3D-(3,5/4)-trihydroxycyclohexane-1,2-dione hydrolase OS=Clostridium tetani (strain Massachusetts / E88) GN=iolD PE=3 SV=2 | 98 | 383 | 3.0E-09 |
| sp|B3QL00|MEND_CHLP8 | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Chlorobaculum parvum (strain NCIB 8327) GN=menD PE=3 SV=1 | 84 | 249 | 3.0E-09 |
| sp|P34734|PDC_HANUV | Pyruvate decarboxylase OS=Hanseniaspora uvarum GN=PDC PE=3 SV=1 | 94 | 387 | 4.0E-09 |
| sp|A0PL16|KDC_MYCUA | Alpha-keto-acid decarboxylase OS=Mycobacterium ulcerans (strain Agy99) GN=kdc PE=3 SV=1 | 94 | 582 | 5.0E-09 |
| sp|Q9M039|PDC3_ARATH | Pyruvate decarboxylase 3 OS=Arabidopsis thaliana GN=PDC3 PE=2 SV=1 | 101 | 581 | 7.0E-09 |
| sp|P16467|PDC5_YEAST | Pyruvate decarboxylase isozyme 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PDC5 PE=1 SV=4 | 94 | 581 | 3.0E-08 |
| sp|Q9M040|PDC4_ARATH | Pyruvate decarboxylase 4 OS=Arabidopsis thaliana GN=PDC4 PE=2 SV=1 | 101 | 581 | 4.0E-08 |
| sp|B3EG68|MEND_CHLL2 | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Chlorobium limicola (strain DSM 245 / NBRC 103803) GN=menD PE=3 SV=1 | 138 | 249 | 5.0E-08 |
| sp|B4SET5|MEND_PELPB | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Pelodictyon phaeoclathratiforme (strain DSM 5477 / BU-1) GN=menD PE=3 SV=1 | 84 | 334 | 8.0E-08 |
| sp|Q2LXE3|MEND_SYNAS | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Syntrophus aciditrophicus (strain SB) GN=menD PE=3 SV=2 | 101 | 212 | 2.0E-07 |
| sp|A4SD60|MEND_CHLPM | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Chlorobium phaeovibrioides (strain DSM 265 / 1930) GN=menD PE=3 SV=1 | 99 | 332 | 3.0E-07 |
| sp|P06169|PDC1_YEAST | Pyruvate decarboxylase isozyme 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=PDC1 PE=1 SV=7 | 94 | 582 | 4.0E-07 |
| sp|Q8KBE8|MEND_CHLTE | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Chlorobium tepidum (strain ATCC 49652 / DSM 12025 / NBRC 103806 / TLS) GN=menD PE=3 SV=2 | 99 | 249 | 5.0E-07 |
| sp|Q8E8T4|MEND_SHEON | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Shewanella oneidensis (strain MR-1) GN=menD PE=3 SV=1 | 94 | 378 | 7.0E-07 |
| sp|Q9CBD6|KDC_MYCLE | Alpha-keto-acid decarboxylase OS=Mycobacterium leprae (strain TN) GN=kdc PE=3 SV=1 | 94 | 582 | 7.0E-07 |
| sp|Q9FFT4|PDC2_ARATH | Pyruvate decarboxylase 2 OS=Arabidopsis thaliana GN=PDC2 PE=2 SV=1 | 72 | 581 | 9.0E-07 |
| sp|A6LB35|MEND_PARD8 | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Parabacteroides distasonis (strain ATCC 8503 / DSM 20701 / NCTC 11152) GN=menD PE=3 SV=1 | 100 | 309 | 1.0E-06 |
| sp|A9WB45|MEND_CHLAA | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Chloroflexus aurantiacus (strain ATCC 29366 / DSM 635 / J-10-fl) GN=menD PE=3 SV=1 | 104 | 332 | 1.0E-06 |
| sp|Q6D7W4|MEND_PECAS | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Pectobacterium atrosepticum (strain SCRI 1043 / ATCC BAA-672) GN=menD PE=3 SV=1 | 84 | 201 | 2.0E-06 |
| sp|A3CYZ9|MEND_SHEB5 | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Shewanella baltica (strain OS155 / ATCC BAA-1091) GN=menD PE=3 SV=1 | 94 | 388 | 2.0E-06 |
| sp|A9KU65|MEND_SHEB9 | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Shewanella baltica (strain OS195) GN=menD PE=3 SV=1 | 94 | 388 | 2.0E-06 |
| sp|Q3B612|MEND_CHLL7 | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Chlorobium luteolum (strain DSM 273 / 2530) GN=menD PE=3 SV=1 | 96 | 336 | 2.0E-06 |
| sp|Q6FJA3|PDC1_CANGA | Pyruvate decarboxylase OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=PDC1 PE=3 SV=1 | 94 | 582 | 3.0E-06 |
| sp|C6DBP2|MEND_PECCP | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Pectobacterium carotovorum subsp. carotovorum (strain PC1) GN=menD PE=3 SV=1 | 84 | 201 | 3.0E-06 |
| sp|A4SS26|MEND_AERS4 | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Aeromonas salmonicida (strain A449) GN=menD PE=3 SV=1 | 129 | 391 | 4.0E-06 |
| sp|A6WTY4|MEND_SHEB8 | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Shewanella baltica (strain OS185) GN=menD PE=3 SV=1 | 94 | 388 | 4.0E-06 |
| sp|A1SBA6|MEND_SHEAM | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Shewanella amazonensis (strain ATCC BAA-1098 / SB2B) GN=menD PE=3 SV=1 | 94 | 208 | 5.0E-06 |
| sp|Q87R69|MEND_VIBPA | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Vibrio parahaemolyticus serotype O3:K6 (strain RIMD 2210633) GN=menD PE=3 SV=1 | 85 | 208 | 5.0E-06 |
| sp|Q0HPY8|MEND_SHESR | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Shewanella sp. (strain MR-7) GN=menD PE=3 SV=1 | 94 | 378 | 6.0E-06 |
| sp|A7MZS0|MEND_VIBCB | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Vibrio campbellii (strain ATCC BAA-1116 / BB120) GN=menD PE=3 SV=1 | 84 | 208 | 6.0E-06 |
| sp|P51846|PDC2_TOBAC | Pyruvate decarboxylase 2 OS=Nicotiana tabacum GN=PDC2 PE=2 SV=1 | 101 | 380 | 6.0E-06 |
| sp|A7MHU4|MEND_CROS8 | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Cronobacter sakazakii (strain ATCC BAA-894) GN=menD PE=3 SV=1 | 84 | 201 | 6.0E-06 |
| sp|A0KFN8|MEND_AERHH | 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase OS=Aeromonas hydrophila subsp. hydrophila (strain ATCC 7966 / DSM 30187 / JCM 1027 / KCTC 2358 / NCIMB 9240) GN=menD PE=3 SV=1 | 96 | 244 | 7.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0003824 | catalytic activity | Yes |
| GO:0000287 | magnesium ion binding | Yes |
| GO:0030976 | thiamine pyrophosphate binding | Yes |
| GO:0036094 | small molecule binding | No |
| GO:0043168 | anion binding | No |
| GO:0019842 | vitamin binding | No |
| GO:0097159 | organic cyclic compound binding | No |
| GO:0046872 | metal ion binding | No |
| GO:1901363 | heterocyclic compound binding | No |
| GO:0005488 | binding | No |
| GO:0043167 | ion binding | No |
| GO:1901681 | sulfur compound binding | No |
| GO:0043169 | cation binding | No |
| GO:0003674 | molecular_function | No |
| GO:0050997 | quaternary ammonium group binding | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| No | 1 - 12 | 0.45 |
| 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|2118 MLRNRHATKAFRALGNARPFTSTTQSPASRAAKKAPAAQRRQTTAAAATSAAPQVRPVPSPAFNAQEQDRSHVQP LANAEKSEMDESFIGKSGGEIFHEMMLRQGVKHIFGYAGGAILPVFDAIYNSKHFDFIMPRHEQGAGHMAEGYAR ASGKPGVVLVTSGPGATNVITPIQDALSDGTPLVVFCGQVPTSAIGSDAFQEADVVGISRACTKWNVMVKNIAEL PRRINEAFEIATSGRPGPVLVDLPKDVTAGILRRAIPTETALPSLPSAASQAAMELSRRQLDASLARVADLVNGA RQPVIYAGQGVVLSPGGPELLKQLADKASIPVTTTLLGLGAFDELDGKALHMLGMHGTAYANMAMQEADLIIALG GRFDDRVTGNIAKFAPGAKAAAAEGRGGIVHFEVMPKNINKVVQATEAVEGDVAANLRGLLPRVRPRAMADRAAW FGKIDEWKRRWPLSHYERAGPGGLIKPQSLIEELSRLTADRKQSTYISTGVGQHQMWAAQHFRWRHPRTMITSGG LGTMGFGLPAAIGAKVARPDALVVDIDGDASFNMTMTELATAAQFDIGVKVIVLNNEEQGMVTQWQNLFYEDRYA HTHQVNPDFMKLAESMRVACRRVTDPADVADSLRWLIDTDGPALLEAVTDKKVPVLPMVPAGSALHEFLVYDEET DKKRRELMRQRTCGRHG* |
| Coding | >Hirsu2|2118 ATGCTCCGAAATCGACACGCCACCAAGGCCTTCCGGGCCCTCGGCAACGCCAGGCCCTTCACCTCGACCACCCAG TCGCCCGCCTCCCGAGCAGCCAAGAAGGCCCCGGCCGCACAGAGGCGTCAAACAACGGCCGCTGCCGCCACCTCG GCCGCTCCTCAGGTCCGCCCCGTCCCGAGCCCGGCCTTCAACGCACAAGAACAAGACCGAAGCCATGTCCAGCCG CTGGCCAACGCCGAGAAGAGCGAGATGGACGAATCCTTCATTGGCAAGTCGGGCGGAGAAATCTTTCACGAAATG ATGCTCCGACAGGGCGTTAAGCACATCTTCGGCTATGCCGGCGGAGCCATCCTGCCCGTCTTCGACGCCATCTAC AACTCCAAACACTTCGACTTCATCATGCCCCGCCACGAGCAAGGCGCCGGCCACATGGCCGAGGGCTACGCCAGG GCCTCGGGCAAGCCCGGCGTCGTCCTCGTCACCTCGGGCCCCGGCGCCACCAACGTCATCACCCCGATCCAGGAC GCCCTGTCCGACGGCACGCCGCTCGTCGTCTTCTGCGGCCAGGTCCCGACCTCGGCCATCGGCAGCGACGCCTTC CAGGAGGCCGACGTCGTCGGCATCTCGCGCGCCTGCACCAAGTGGAACGTCATGGTCAAGAACATCGCCGAGCTG CCGCGCCGCATCAACGAGGCCTTCGAGATCGCCACCAGCGGCCGCCCCGGCCCCGTCCTCGTCGACCTGCCCAAG GACGTGACGGCCGGCATCCTGCGCCGCGCCATCCCGACCGAGACGGCCCTGCCGTCGCTGCCCAGCGCCGCCTCC CAGGCCGCCATGGAGCTGAGCCGCAGGCAGCTCGACGCCTCGCTCGCCCGCGTCGCCGACCTCGTCAACGGCGCC CGCCAGCCCGTTATCTACGCCGGCCAGGGCGTCGTCCTCTCCCCCGGCGGGCCCGAGCTGCTCAAGCAGCTGGCC GACAAGGCCTCCATCCCCGTCACCACGACGCTGCTCGGCCTCGGCGCCTTCGACGAGCTCGACGGCAAGGCCCTG CACATGCTCGGCATGCACGGCACCGCCTACGCCAACATGGCGATGCAGGAGGCCGACCTCATCATCGCCCTCGGC GGCCGCTTCGACGACCGCGTCACCGGCAACATCGCCAAGTTCGCGCCCGGCGCCAAGGCCGCCGCCGCCGAGGGC CGCGGCGGCATCGTCCACTTCGAGGTGATGCCCAAGAACATCAACAAGGTGGTGCAGGCGACGGAGGCGGTCGAG GGCGACGTGGCGGCCAACCTGCGCGGCCTGCTGCCGCGCGTCCGGCCGCGCGCCATGGCCGACCGCGCCGCCTGG TTCGGCAAGATCGACGAGTGGAAGCGGCGCTGGCCGCTGTCGCACTACGAGCGGGCCGGGCCCGGCGGCCTCATC AAGCCGCAGTCGCTGATCGAGGAGCTGAGCCGGCTGACGGCGGACCGCAAGCAGTCGACGTACATCTCGACGGGC GTGGGCCAGCACCAGATGTGGGCGGCCCAGCACTTCCGCTGGCGCCACCCGCGCACCATGATCACCTCGGGCGGC CTCGGCACCATGGGCTTCGGCCTGCCGGCCGCCATCGGGGCCAAGGTGGCGCGCCCGGACGCGCTCGTCGTCGAC ATCGACGGCGACGCCTCCTTCAACATGACCATGACGGAGCTGGCGACGGCGGCCCAGTTCGACATCGGCGTCAAG GTCATCGTGCTCAACAACGAGGAGCAGGGCATGGTGACGCAGTGGCAGAACCTCTTCTACGAGGACCGCTACGCC CACACGCACCAGGTCAACCCGGACTTCATGAAGCTGGCCGAGTCGATGCGCGTCGCCTGCCGCCGCGTGACGGAC CCGGCCGACGTCGCCGACAGCCTGCGCTGGCTCATCGACACGGACGGGCCGGCCCTGCTGGAGGCGGTGACGGAC AAGAAGGTGCCGGTGCTGCCCATGGTGCCGGCCGGCTCGGCGCTGCACGAGTTCTTGGTGTACGACGAGGAAACG GACAAGAAGCGGCGCGAGCTGATGCGGCAGAGGACGTGCGGCCGGCACGGGTGA |
| Transcript | >Hirsu2|2118 ATGCTCCGAAATCGACACGCCACCAAGGCCTTCCGGGCCCTCGGCAACGCCAGGCCCTTCACCTCGACCACCCAG TCGCCCGCCTCCCGAGCAGCCAAGAAGGCCCCGGCCGCACAGAGGCGTCAAACAACGGCCGCTGCCGCCACCTCG GCCGCTCCTCAGGTCCGCCCCGTCCCGAGCCCGGCCTTCAACGCACAAGAACAAGACCGAAGCCATGTCCAGCCG CTGGCCAACGCCGAGAAGAGCGAGATGGACGAATCCTTCATTGGCAAGTCGGGCGGAGAAATCTTTCACGAAATG ATGCTCCGACAGGGCGTTAAGCACATCTTCGGCTATGCCGGCGGAGCCATCCTGCCCGTCTTCGACGCCATCTAC AACTCCAAACACTTCGACTTCATCATGCCCCGCCACGAGCAAGGCGCCGGCCACATGGCCGAGGGCTACGCCAGG GCCTCGGGCAAGCCCGGCGTCGTCCTCGTCACCTCGGGCCCCGGCGCCACCAACGTCATCACCCCGATCCAGGAC GCCCTGTCCGACGGCACGCCGCTCGTCGTCTTCTGCGGCCAGGTCCCGACCTCGGCCATCGGCAGCGACGCCTTC CAGGAGGCCGACGTCGTCGGCATCTCGCGCGCCTGCACCAAGTGGAACGTCATGGTCAAGAACATCGCCGAGCTG CCGCGCCGCATCAACGAGGCCTTCGAGATCGCCACCAGCGGCCGCCCCGGCCCCGTCCTCGTCGACCTGCCCAAG GACGTGACGGCCGGCATCCTGCGCCGCGCCATCCCGACCGAGACGGCCCTGCCGTCGCTGCCCAGCGCCGCCTCC CAGGCCGCCATGGAGCTGAGCCGCAGGCAGCTCGACGCCTCGCTCGCCCGCGTCGCCGACCTCGTCAACGGCGCC CGCCAGCCCGTTATCTACGCCGGCCAGGGCGTCGTCCTCTCCCCCGGCGGGCCCGAGCTGCTCAAGCAGCTGGCC GACAAGGCCTCCATCCCCGTCACCACGACGCTGCTCGGCCTCGGCGCCTTCGACGAGCTCGACGGCAAGGCCCTG CACATGCTCGGCATGCACGGCACCGCCTACGCCAACATGGCGATGCAGGAGGCCGACCTCATCATCGCCCTCGGC GGCCGCTTCGACGACCGCGTCACCGGCAACATCGCCAAGTTCGCGCCCGGCGCCAAGGCCGCCGCCGCCGAGGGC CGCGGCGGCATCGTCCACTTCGAGGTGATGCCCAAGAACATCAACAAGGTGGTGCAGGCGACGGAGGCGGTCGAG GGCGACGTGGCGGCCAACCTGCGCGGCCTGCTGCCGCGCGTCCGGCCGCGCGCCATGGCCGACCGCGCCGCCTGG TTCGGCAAGATCGACGAGTGGAAGCGGCGCTGGCCGCTGTCGCACTACGAGCGGGCCGGGCCCGGCGGCCTCATC AAGCCGCAGTCGCTGATCGAGGAGCTGAGCCGGCTGACGGCGGACCGCAAGCAGTCGACGTACATCTCGACGGGC GTGGGCCAGCACCAGATGTGGGCGGCCCAGCACTTCCGCTGGCGCCACCCGCGCACCATGATCACCTCGGGCGGC CTCGGCACCATGGGCTTCGGCCTGCCGGCCGCCATCGGGGCCAAGGTGGCGCGCCCGGACGCGCTCGTCGTCGAC ATCGACGGCGACGCCTCCTTCAACATGACCATGACGGAGCTGGCGACGGCGGCCCAGTTCGACATCGGCGTCAAG GTCATCGTGCTCAACAACGAGGAGCAGGGCATGGTGACGCAGTGGCAGAACCTCTTCTACGAGGACCGCTACGCC CACACGCACCAGGTCAACCCGGACTTCATGAAGCTGGCCGAGTCGATGCGCGTCGCCTGCCGCCGCGTGACGGAC CCGGCCGACGTCGCCGACAGCCTGCGCTGGCTCATCGACACGGACGGGCCGGCCCTGCTGGAGGCGGTGACGGAC AAGAAGGTGCCGGTGCTGCCCATGGTGCCGGCCGGCTCGGCGCTGCACGAGTTCTTGGTGTACGACGAGGAAACG GACAAGAAGCGGCGCGAGCTGATGCGGCAGAGGACGTGCGGCCGGCACGGGTGA |
| Gene | >Hirsu2|2118 ATGCTCCGAAATCGACACGCCACCAAGGCCTTCCGGGCCCTCGGCAACGCCAGGCCCTTCACCTCGACCACCCAG TCGCCCGCCTCCCGAGCAGCCAAGAAGGCCCCGGCCGCACAGAGGCGTCAAACAACGGCCGCTGCCGCCACCTCG GCCGCTCCGTAAGTCGGCCTTGGCCTCCGCCCCCTTTTACCTGCCCGCCCCGGCATCGGCACCTCGTTGAGGGGT CAGGCCAAGAAAAGAAGACCGCAGGGAGGGAGGAAGAACATACGAGTACAAGGCGGAAGAGGATGCGGGACGCAG AGAATCAACCGACAGTCCCACGATACCGCTCCTCCGTACCCTCGCAAGCTGACGGCCCAACCCACAGTCAGGTCC GCCCCGTCCCGAGCCCGGCCTTCAACGCACAAGAACAAGACCGAAGCCATGTCCAGCCGCTGGCCAACGCCGAGA AGAGCGAGATGGACGAATCGTACGCCTCCCCCGTCCCCGATGCTCGACCACCTGCTTGTGTCTGACCATGTCCCA GCTTCATTGGCAAGTCGGGCGGAGAAATCTTTCACGAAATGATGCTCCGACAGGGCGTTAAGCACATCTGTCAGT CGACCACTCCCTTTTCACTCTTTCTCGGCACGCCAACCCAGCTGACATTTTCCTCAGTCGGCTATGCCGGCGGAG CCATCCTGCCCGTCTTCGACGCCATCTACAACTCCAAACACTTCGACTTCATCATGCCCCGCCACGAGCAAGGCG CCGGCCACATGGCCGAGGGCTACGCCAGGGCCTCGGGCAAGCCCGGCGTCGTCCTCGTCACCTCGGGCCCCGGCG CCACCAACGTCATCACCCCGATCCAGGACGCCCTGTCCGACGGCACGCCGCTCGTCGTCTTCTGCGGCCAGGTCC CGACCTCGGCCATCGGCAGCGACGCCTTCCAGGAGGCCGACGTCGTCGGCATCTCGCGCGCCTGCACCAAGTGGA ACGTCATGGTCAAGAACATCGCCGAGCTGCCGCGCCGCATCAACGAGGCCTTCGAGATCGCCACCAGCGGCCGCC CCGGCCCCGTCCTCGTCGACCTGCCCAAGGACGTGACGGCCGGCATCCTGCGCCGCGCCATCCCGACCGAGACGG CCCTGCCGTCGCTGCCCAGCGCCGCCTCCCAGGCCGCCATGGAGCTGAGCCGCAGGCAGCTCGACGCCTCGCTCG CCCGCGTCGCCGACCTCGTCAACGGCGCCCGCCAGCCCGTTATCTACGCCGGCCAGGGCGTCGTCCTCTCCCCCG GCGGGCCCGAGCTGCTCAAGCAGCTGGCCGACAAGGCCTCCATCCCCGTCACCACGACGCTGCTCGGCCTCGGCG CCTTCGACGAGCTCGACGGCAAGGCCCTGCACATGCTCGGCATGCACGGCACCGCCTACGCCAACATGGCGATGC AGGAGGCCGACCTCATCATCGCCCTCGGCGGCCGCTTCGACGACCGCGTCACCGGCAACATCGCCAAGTTCGCGC CCGGCGCCAAGGCCGCCGCCGCCGAGGGCCGCGGCGGCATCGTCCACTTCGAGGTGATGCCCAAGAACATCAACA AGGTGGTGCAGGCGACGGAGGCGGTCGAGGGCGACGTGGCGGCCAACCTGCGCGGCCTGCTGCCGCGCGTCCGGC CGCGCGCCATGGCCGACCGCGCCGCCTGGTTCGGCAAGATCGACGAGTGGAAGCGGCGCTGGCCGCTGTCGCACT ACGAGCGGGCCGGGCCCGGCGGCCTCATCAAGCCGCAGTCGCTGATCGAGGAGCTGAGCCGGCTGACGGCGGACC GCAAGCAGTCGACGTACATCTCGACGGGCGTGGGCCAGCACCAGATGTGGGCGGCCCAGCACTTCCGCTGGCGCC ACCCGCGCACCATGATCACCTCGGGCGGCCTCGGCACCATGGGCTTCGGCCTGCCGGCCGCCATCGGGGCCAAGG TGGCGCGCCCGGACGCGCTCGTCGTCGACATCGACGGCGACGCCTCCTTCAACATGACCATGACGGAGCTGGCGA CGGCGGCCCAGTTCGACATCGGCGTCAAGGTCATCGTGCTCAACAACGAGGAGCAGGGCATGGTGACGCAGTGGC AGAACCTCTTCTACGAGGACCGCTACGCCCACACGCACCAGGTCAACCCGGACTTCATGAAGCTGGCCGAGTCGA TGCGCGTCGCCTGCCGCCGCGTGACGGACCCGGCCGACGTCGCCGACAGCCTGCGCTGGCTCATCGACACGGACG GGCCGGCCCTGCTGGAGGCGGTGACGGACAAGAAGGTGCCGGTGCTGCCCATGGTGCCGGCCGGCTCGGCGCTGC ACGAGTTCTTGGTGTACGACGAGGGTGAGTCTTTTTTTCCCTTTCTGTCGACTCGACGAAGACGAGCGTGAGGAG CTGACGATGGGCGGGCGCGCCCTTGTTGCAGAAACGGACAAGAAGCGGCGCGAGCTGATGCGGCAGAGGACGTGC GGCCGGCACGGGTGA |