Protein ID | Hirsu2|9738 |
Gene name | |
Location | Contig_73:31775..34715 |
Strand | + |
Gene length (bp) | 2940 |
Transcript length (bp) | 2724 |
Coding sequence length (bp) | 2724 |
Protein length (aa) | 908 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF02867 | Ribonuc_red_lgC | Ribonucleotide reductase, barrel domain | 5.9E-199 | 216 | 739 |
PF00317 | Ribonuc_red_lgN | Ribonucleotide reductase, all-alpha domain | 5.5E-24 | 142 | 212 |
PF03477 | ATP-cone | ATP cone domain | 5.1E-16 | 1 | 89 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|P21524|RIR1_YEAST | Ribonucleoside-diphosphate reductase large chain 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=RNR1 PE=1 SV=2 | 1 | 907 | 0.0E+00 |
sp|Q9UW15|RIR1_NEUCR | Ribonucleoside-diphosphate reductase large chain OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=rnr-1 PE=1 SV=2 | 1 | 907 | 0.0E+00 |
sp|Q7T6Y8|RIR1_MIMIV | Ribonucleoside-diphosphate reductase large subunit OS=Acanthamoeba polyphaga mimivirus GN=RNR1 PE=3 SV=2 | 7 | 769 | 0.0E+00 |
sp|Q8SR37|RIR1_ENCCU | Ribonucleoside-diphosphate reductase large chain OS=Encephalitozoon cuniculi (strain GB-M1) GN=ECU10_0920 PE=3 SV=1 | 9 | 756 | 0.0E+00 |
sp|O15909|RIR1_TRYBB | Ribonucleoside-diphosphate reductase large subunit OS=Trypanosoma brucei brucei GN=RNR1 PE=2 SV=1 | 3 | 759 | 0.0E+00 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|P21524|RIR1_YEAST | Ribonucleoside-diphosphate reductase large chain 1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=RNR1 PE=1 SV=2 | 1 | 907 | 0.0E+00 |
sp|Q9UW15|RIR1_NEUCR | Ribonucleoside-diphosphate reductase large chain OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=rnr-1 PE=1 SV=2 | 1 | 907 | 0.0E+00 |
sp|Q7T6Y8|RIR1_MIMIV | Ribonucleoside-diphosphate reductase large subunit OS=Acanthamoeba polyphaga mimivirus GN=RNR1 PE=3 SV=2 | 7 | 769 | 0.0E+00 |
sp|Q8SR37|RIR1_ENCCU | Ribonucleoside-diphosphate reductase large chain OS=Encephalitozoon cuniculi (strain GB-M1) GN=ECU10_0920 PE=3 SV=1 | 9 | 756 | 0.0E+00 |
sp|O15909|RIR1_TRYBB | Ribonucleoside-diphosphate reductase large subunit OS=Trypanosoma brucei brucei GN=RNR1 PE=2 SV=1 | 3 | 759 | 0.0E+00 |
sp|P50647|RIR1_PLAFG | Ribonucleoside-diphosphate reductase large subunit OS=Plasmodium falciparum (isolate FCR-3 / Gambia) GN=RNR1 PE=3 SV=1 | 1 | 761 | 0.0E+00 |
sp|O61065|RIR1_CRYPV | Ribonucleoside-diphosphate reductase large chain OS=Cryptosporidium parvum GN=RNR1 PE=3 SV=2 | 1 | 759 | 0.0E+00 |
sp|P50648|RIR1_PLAF4 | Ribonucleoside-diphosphate reductase large subunit OS=Plasmodium falciparum (isolate Dd2) GN=RNR1 PE=2 SV=1 | 1 | 761 | 0.0E+00 |
sp|Q54Q71|RIR1_DICDI | Ribonucleoside-diphosphate reductase large subunit OS=Dictyostelium discoideum GN=rnrA PE=3 SV=1 | 1 | 754 | 0.0E+00 |
sp|P32984|RIR1_VAR67 | Ribonucleoside-diphosphate reductase large subunit OS=Variola virus (isolate Human/India/Ind3/1967) GN=I4L PE=2 SV=1 | 1 | 759 | 0.0E+00 |
sp|Q76RD8|RIR1_VACCA | Ribonucleoside-diphosphate reductase large subunit OS=Vaccinia virus (strain Ankara) GN=MVA065L PE=2 SV=1 | 1 | 759 | 0.0E+00 |
sp|P20503|RIR1_VACCC | Ribonucleoside-diphosphate reductase large subunit OS=Vaccinia virus (strain Copenhagen) GN=I4L PE=2 SV=1 | 1 | 759 | 0.0E+00 |
sp|P36602|RIR1_SCHPO | Ribonucleoside-diphosphate reductase large chain OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=cdc22 PE=1 SV=2 | 1 | 798 | 0.0E+00 |
sp|P12848|RIR1_VACCW | Ribonucleoside-diphosphate reductase large subunit OS=Vaccinia virus (strain Western Reserve) GN=VACWR073 PE=1 SV=1 | 1 | 759 | 0.0E+00 |
sp|P21672|RIR3_YEAST | Ribonucleoside-diphosphate reductase large chain 2 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=RNR3 PE=1 SV=4 | 1 | 907 | 0.0E+00 |
sp|P23921|RIR1_HUMAN | Ribonucleoside-diphosphate reductase large subunit OS=Homo sapiens GN=RRM1 PE=1 SV=1 | 1 | 758 | 0.0E+00 |
sp|P07742|RIR1_MOUSE | Ribonucleoside-diphosphate reductase large subunit OS=Mus musculus GN=Rrm1 PE=1 SV=2 | 1 | 758 | 0.0E+00 |
sp|Q5R919|RIR1_PONAB | Ribonucleoside-diphosphate reductase large subunit OS=Pongo abelii GN=RRM1 PE=2 SV=1 | 1 | 758 | 0.0E+00 |
sp|P79732|RIR1_DANRE | Ribonucleoside-diphosphate reductase large subunit OS=Danio rerio GN=rrm1 PE=2 SV=1 | 1 | 768 | 0.0E+00 |
sp|Q03604|RIR1_CAEEL | Ribonucleoside-diphosphate reductase large subunit OS=Caenorhabditis elegans GN=rnr-1 PE=3 SV=1 | 2 | 759 | 0.0E+00 |
sp|Q9SJ20|RIR1_ARATH | Ribonucleoside-diphosphate reductase large subunit OS=Arabidopsis thaliana GN=RNR1 PE=1 SV=1 | 1 | 759 | 0.0E+00 |
sp|P48591|RIR1_DROME | Ribonucleoside-diphosphate reductase large subunit OS=Drosophila melanogaster GN=RnrL PE=1 SV=2 | 1 | 773 | 0.0E+00 |
sp|P42491|RIR1_ASFB7 | Ribonucleoside-diphosphate reductase large subunit OS=African swine fever virus (strain Badajoz 1971 Vero-adapted) GN=Ba71V-045 PE=3 SV=1 | 41 | 739 | 6.0E-170 |
sp|P0C8H8|RIR1_ASFP4 | Ribonucleoside-diphosphate reductase large subunit OS=African swine fever virus (isolate Tick/South Africa/Pretoriuskop Pr4/1996) GN=Pret-057 PE=3 SV=1 | 41 | 739 | 2.0E-169 |
sp|P0C8H7|RIR1_ASFK5 | Ribonucleoside-diphosphate reductase large subunit OS=African swine fever virus (isolate Pig/Kenya/KEN-50/1950) GN=Ken-057 PE=3 SV=1 | 39 | 739 | 2.0E-169 |
sp|P0C8H9|RIR1_ASFWA | Ribonucleoside-diphosphate reductase large subunit OS=African swine fever virus (isolate Warthog/Namibia/Wart80/1980) GN=War-055 PE=3 SV=1 | 41 | 739 | 4.0E-169 |
sp|P26685|RIR1_ASFM2 | Ribonucleoside-diphosphate reductase large subunit OS=African swine fever virus (isolate Tick/Malawi/Lil 20-1/1983) GN=Mal-053 PE=3 SV=1 | 39 | 739 | 2.0E-167 |
sp|O84834|RIR1_CHLTR | Ribonucleoside-diphosphate reductase subunit alpha OS=Chlamydia trachomatis (strain D/UW-3/Cx) GN=nrdA PE=3 SV=2 | 3 | 779 | 3.0E-160 |
sp|Q9PL93|RIR1_CHLMU | Ribonucleoside-diphosphate reductase subunit alpha OS=Chlamydia muridarum (strain MoPn / Nigg) GN=nrdA PE=3 SV=1 | 3 | 779 | 6.0E-160 |
sp|Q9Z6S5|RIR1_CHLPN | Ribonucleoside-diphosphate reductase subunit alpha OS=Chlamydia pneumoniae GN=nrdA PE=3 SV=1 | 3 | 754 | 3.0E-156 |
sp|Q6R7H4|RIR1_OSHVF | Ribonucleoside-diphosphate reductase large subunit OS=Ostreid herpesvirus 1 (isolate France) PE=3 SV=1 | 70 | 741 | 4.0E-147 |
sp|O66503|RIR1_AQUAE | Ribonucleoside-diphosphate reductase subunit alpha OS=Aquifex aeolicus (strain VF5) GN=nrdA PE=3 SV=1 | 1 | 745 | 2.0E-117 |
sp|Q9ZLF9|RIR1_HELPJ | Ribonucleoside-diphosphate reductase subunit alpha OS=Helicobacter pylori (strain J99 / ATCC 700824) GN=nrdA PE=3 SV=1 | 3 | 755 | 1.0E-111 |
sp|P55982|RIR1_HELPY | Ribonucleoside-diphosphate reductase subunit alpha OS=Helicobacter pylori (strain ATCC 700392 / 26695) GN=nrdA PE=3 SV=1 | 3 | 755 | 2.0E-111 |
sp|O83972|RIR1_TREPA | Ribonucleoside-diphosphate reductase subunit alpha OS=Treponema pallidum (strain Nichols) GN=nrdA PE=3 SV=1 | 128 | 744 | 3.0E-97 |
sp|P74240|RIR1_SYNY3 | Ribonucleoside-diphosphate reductase subunit alpha OS=Synechocystis sp. (strain PCC 6803 / Kazusa) GN=nrdA PE=3 SV=1 | 3 | 642 | 1.0E-87 |
sp|P37426|RIR1_SALTY | Ribonucleoside-diphosphate reductase 1 subunit alpha OS=Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) GN=nrdA PE=3 SV=1 | 1 | 750 | 7.0E-85 |
sp|P89462|RIR1_HHV2H | Ribonucleoside-diphosphate reductase large subunit OS=Human herpesvirus 2 (strain HG52) GN=UL39 PE=3 SV=1 | 121 | 754 | 4.0E-82 |
sp|P00452|RIR1_ECOLI | Ribonucleoside-diphosphate reductase 1 subunit alpha OS=Escherichia coli (strain K12) GN=nrdA PE=1 SV=2 | 1 | 750 | 2.0E-81 |
sp|P50642|RIR1_EHV4 | Ribonucleoside-diphosphate reductase large subunit OS=Equine herpesvirus 4 (strain 1942) PE=3 SV=1 | 152 | 745 | 2.0E-81 |
sp|P50643|RIR1_SUHVK | Ribonucleoside-diphosphate reductase large subunit OS=Suid herpesvirus 1 (strain Kaplan) GN=RR1 PE=3 SV=1 | 190 | 752 | 3.0E-81 |
sp|P09853|RIR1_HHV23 | Ribonucleoside-diphosphate reductase large subunit OS=Human herpesvirus 2 (strain 333) PE=3 SV=2 | 121 | 754 | 8.0E-81 |
sp|P50646|RIR1_BHV1C | Ribonucleoside-diphosphate reductase large subunit OS=Bovine herpesvirus 1.1 (strain Cooper) GN=UL39 PE=3 SV=1 | 152 | 752 | 5.0E-80 |
sp|P08543|RIR1_HHV11 | Ribonucleoside-diphosphate reductase large subunit OS=Human herpesvirus 1 (strain 17) GN=UL39 PE=3 SV=2 | 121 | 745 | 1.0E-79 |
sp|P57276|RIR1_BUCAI | Ribonucleoside-diphosphate reductase subunit alpha OS=Buchnera aphidicola subsp. Acyrthosiphon pisum (strain APS) GN=nrdA PE=3 SV=1 | 1 | 743 | 2.0E-78 |
sp|P43754|RIR1_HAEIN | Ribonucleoside-diphosphate reductase subunit alpha OS=Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) GN=nrdA PE=3 SV=1 | 1 | 754 | 6.0E-78 |
sp|P28846|RIR1_EHV1B | Ribonucleoside-diphosphate reductase large subunit OS=Equine herpesvirus 1 (strain Ab4p) GN=21 PE=3 SV=1 | 152 | 745 | 2.0E-77 |
sp|Q77MS1|RIR1_GAHVM | Ribonucleoside-diphosphate reductase large subunit OS=Gallid herpesvirus 2 (strain Chicken/Md5/ATCC VR-987) GN=MDV052 PE=3 SV=1 | 193 | 756 | 5.0E-77 |
sp|Q8K9W3|RIR1_BUCAP | Ribonucleoside-diphosphate reductase subunit alpha OS=Buchnera aphidicola subsp. Schizaphis graminum (strain Sg) GN=nrdA PE=3 SV=1 | 1 | 746 | 4.0E-76 |
sp|Q89AS4|RIR1_BUCBP | Ribonucleoside-diphosphate reductase subunit alpha OS=Buchnera aphidicola subsp. Baizongia pistaciae (strain Bp) GN=nrdA PE=3 SV=1 | 1 | 766 | 5.0E-75 |
sp|Q6UDJ2|RIR1_PSHV1 | Ribonucleoside-diphosphate reductase large subunit OS=Psittacid herpesvirus 1 (isolate Amazon parrot/-/97-0001/1997) GN=UL39 PE=3 SV=1 | 202 | 745 | 6.0E-75 |
sp|P09248|RIR1_VZVD | Ribonucleoside-diphosphate reductase large subunit OS=Varicella-zoster virus (strain Dumas) GN=ORF19 PE=3 SV=1 | 152 | 745 | 2.0E-70 |
sp|Q4JQV6|RIR1_VZVO | Ribonucleoside-diphosphate reductase large subunit OS=Varicella-zoster virus (strain Oka vaccine) GN=ORF19 PE=3 SV=1 | 152 | 745 | 2.0E-70 |
sp|P32282|RIR1_BPT4 | Ribonucleoside-diphosphate reductase subunit alpha OS=Enterobacteria phage T4 GN=NRDA PE=3 SV=1 | 22 | 754 | 3.0E-69 |
sp|Q6GZT8|RIR1_FRG3G | Putative ribonucleoside-diphosphate reductase large subunit OS=Frog virus 3 (isolate Goorha) GN=FV3-038R PE=3 SV=1 | 197 | 745 | 2.0E-61 |
sp|Q2HR67|RIR1_HHV8P | Ribonucleoside-diphosphate reductase OS=Human herpesvirus 8 type P (isolate GK18) GN=ORF61 PE=3 SV=1 | 137 | 743 | 9.0E-60 |
sp|Q9HI70|NDRZ_THEAC | Vitamin B12-dependent ribonucleoside-diphosphate reductase OS=Thermoplasma acidophilum (strain ATCC 25905 / DSM 1728 / JCM 9062 / NBRC 15155 / AMRC-C165) GN=Ta1475 PE=1 SV=2 | 192 | 714 | 3.0E-58 |
sp|Q01037|RIR1_SHV21 | Ribonucleoside-diphosphate reductase large subunit OS=Saimiriine herpesvirus 2 (strain 11) GN=61 PE=3 SV=1 | 190 | 751 | 3.0E-58 |
sp|Q66663|RIR1_EHV2 | Ribonucleoside-diphosphate reductase large subunit OS=Equine herpesvirus 2 (strain 86/87) GN=61 PE=3 SV=1 | 190 | 743 | 5.0E-58 |
sp|P9WH77|NRDZ_MYCTU | Vitamin B12-dependent ribonucleoside-diphosphate reductase OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=nrdZ PE=1 SV=2 | 96 | 763 | 2.0E-56 |
sp|P9WH76|NRDZ_MYCTO | Vitamin B12-dependent ribonucleoside-diphosphate reductase OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=nrdZ PE=2 SV=1 | 96 | 739 | 4.0E-56 |
sp|P0CG99|RIR1A_MYCS2 | Ribonucleoside-diphosphate reductase subunit alpha 1 OS=Mycobacterium smegmatis (strain ATCC 700084 / mc(2)155) GN=nrdE1 PE=1 SV=1 | 104 | 746 | 2.0E-54 |
sp|P0CH00|RIR1B_MYCS2 | Ribonucleoside-diphosphate reductase subunit alpha 2 OS=Mycobacterium smegmatis (strain ATCC 700084 / mc(2)155) GN=nrdE2 PE=1 SV=1 | 104 | 746 | 2.0E-54 |
sp|O36411|RIR1_ALHV1 | Ribonucleoside-diphosphate reductase large subunit OS=Alcelaphine herpesvirus 1 (strain C500) GN=61 PE=3 SV=1 | 183 | 779 | 3.0E-52 |
sp|P50620|RIR1_BACSU | Ribonucleoside-diphosphate reductase subunit alpha OS=Bacillus subtilis (strain 168) GN=nrdE PE=3 SV=1 | 162 | 743 | 2.0E-51 |
sp|P9WH75|RIR1_MYCTU | Ribonucleoside-diphosphate reductase subunit alpha OS=Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) GN=nrdE PE=1 SV=1 | 128 | 746 | 2.0E-50 |
sp|P9WH74|RIR1_MYCTO | Ribonucleoside-diphosphate reductase subunit alpha OS=Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) GN=nrdE PE=3 SV=1 | 128 | 746 | 2.0E-50 |
sp|P0A5W9|RIR1_MYCBO | Ribonucleoside-diphosphate reductase subunit alpha OS=Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) GN=nrdE PE=1 SV=1 | 128 | 746 | 2.0E-50 |
sp|P03190|RIR1_EBVB9 | Ribonucleoside-diphosphate reductase large subunit OS=Epstein-Barr virus (strain B95-8) GN=BORF2 PE=3 SV=1 | 70 | 746 | 8.0E-49 |
sp|P0C702|RIR1_EBVA8 | Ribonucleoside-diphosphate reductase large subunit OS=Epstein-Barr virus (strain AG876) GN=BORF2 PE=3 SV=1 | 70 | 746 | 8.0E-49 |
sp|Q3KSU5|RIR1_EBVG | Ribonucleoside-diphosphate reductase large subunit OS=Epstein-Barr virus (strain GD1) GN=BORF2 PE=3 SV=1 | 72 | 746 | 1.0E-48 |
sp|P78027|RIR1_MYCPN | Ribonucleoside-diphosphate reductase subunit alpha OS=Mycoplasma pneumoniae (strain ATCC 29342 / M129) GN=nrdE PE=3 SV=1 | 90 | 743 | 2.0E-48 |
sp|P39452|RIR3_ECOLI | Ribonucleoside-diphosphate reductase 2 subunit alpha OS=Escherichia coli (strain K12) GN=nrdE PE=2 SV=3 | 141 | 746 | 7.0E-48 |
sp|Q9CBQ0|RIR1_MYCLE | Ribonucleoside-diphosphate reductase subunit alpha OS=Mycobacterium leprae (strain TN) GN=nrdE PE=3 SV=2 | 128 | 746 | 6.0E-47 |
sp|P47473|RIR1_MYCGE | Ribonucleoside-diphosphate reductase subunit alpha OS=Mycoplasma genitalium (strain ATCC 33530 / G-37 / NCTC 10195) GN=nrdE PE=3 SV=1 | 90 | 743 | 7.0E-47 |
sp|Q08698|RIR3_SALTY | Ribonucleoside-diphosphate reductase 2 subunit alpha OS=Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) GN=nrdE PE=1 SV=2 | 141 | 746 | 9.0E-47 |
sp|Q196Z5|RIR1_IIV3 | Ribonucleoside-diphosphate reductase large subunit OS=Invertebrate iridescent virus 3 GN=IIV3-065R PE=3 SV=1 | 139 | 743 | 4.0E-46 |
sp|Q6MNP6|NRDJ_BDEBA | Vitamin B12-dependent ribonucleotide reductase OS=Bdellovibrio bacteriovorus (strain ATCC 15356 / DSM 50701 / NCIB 9529 / HD100) GN=nrdJ PE=3 SV=1 | 211 | 751 | 1.0E-34 |
sp|O64173|NRDEB_BPSPB | Ribonucleoside-diphosphate reductase nrdEB subunit alpha OS=Bacillus phage SPbeta GN=bnrdE PE=3 SV=1 | 67 | 429 | 8.0E-34 |
sp|O31875|NRDEB_BACSU | Ribonucleoside-diphosphate reductase NrdEB subunit alpha OS=Bacillus subtilis (strain 168) GN=nrdEB PE=3 SV=2 | 67 | 429 | 8.0E-34 |
sp|E7FHX6|NDRZ_PYRFU | Vitamin B12-dependent ribonucleoside-diphosphate reductase OS=Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1) GN=rnr PE=1 SV=1 | 440 | 713 | 8.0E-34 |
sp|O54196|NRDJ_STRC2 | Vitamin B12-dependent ribonucleotide reductase OS=Streptomyces clavuligerus (strain ATCC 27064 / DSM 738 / JCM 4710 / NBRC 13307 / NCIMB 12785 / NRRL 3585 / VKM Ac-602) GN=nrdJ PE=2 SV=2 | 196 | 787 | 4.0E-33 |
sp|Q82KE2|NRDJ_STRAW | Vitamin B12-dependent ribonucleotide reductase OS=Streptomyces avermitilis (strain ATCC 31267 / DSM 46492 / JCM 5070 / NBRC 14893 / NCIMB 12804 / NRRL 8165 / MA-4680) GN=nrdJ PE=3 SV=1 | 196 | 787 | 2.0E-32 |
sp|O69981|NRDJ_STRCO | Vitamin B12-dependent ribonucleotide reductase OS=Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) GN=nrdJ PE=2 SV=1 | 196 | 774 | 3.0E-31 |
sp|O55716|RIR1_IIV6 | Ribonucleoside-diphosphate reductase large subunit OS=Invertebrate iridescent virus 6 GN=IIV6-085L PE=3 SV=1 | 429 | 764 | 3.0E-30 |
sp|Q7UI46|NRDJ_RHOBA | Vitamin B12-dependent ribonucleotide reductase OS=Rhodopirellula baltica (strain DSM 10527 / NCIMB 13988 / SH1) GN=nrdJ PE=3 SV=1 | 214 | 774 | 2.0E-29 |
sp|O55716|RIR1_IIV6 | Ribonucleoside-diphosphate reductase large subunit OS=Invertebrate iridescent virus 6 GN=IIV6-085L PE=3 SV=1 | 132 | 429 | 7.0E-20 |
sp|Q72S00|NRDJ_LEPIC | Vitamin B12-dependent ribonucleotide reductase OS=Leptospira interrogans serogroup Icterohaemorrhagiae serovar copenhageni (strain Fiocruz L1-130) GN=nrdJ PE=3 SV=2 | 214 | 557 | 6.0E-19 |
sp|Q8F3P1|NRDJ_LEPIN | Vitamin B12-dependent ribonucleotide reductase OS=Leptospira interrogans serogroup Icterohaemorrhagiae serovar Lai (strain 56601) GN=nrdJ PE=3 SV=2 | 214 | 557 | 6.0E-19 |
sp|Q06A28|RIR1_MUHVS | Viral inhibitor of RIP activation OS=Murid herpesvirus 1 (strain Smith) GN=M45 PE=1 SV=1 | 299 | 626 | 1.0E-15 |
sp|Q8UEM4|NRDJ_AGRFC | Vitamin B12-dependent ribonucleotide reductase OS=Agrobacterium fabrum (strain C58 / ATCC 33970) GN=nrdJ PE=3 SV=1 | 334 | 679 | 8.0E-14 |
sp|P50641|RIR1_HHV7J | Ribonucleoside-diphosphate reductase large subunit-like protein U28 OS=Human herpesvirus 7 (strain JI) GN=U28 PE=3 SV=1 | 286 | 738 | 3.0E-13 |
sp|Q9QJ39|RIR1_HHV6Z | Ribonucleoside-diphosphate reductase large subunit-like protein U28 OS=Human herpesvirus 6B (strain Z29) GN=U28 PE=3 SV=1 | 297 | 738 | 3.0E-12 |
sp|P52343|RIR1_HHV6U | Ribonucleoside-diphosphate reductase large subunit-like protein U28 OS=Human herpesvirus 6A (strain Uganda-1102) GN=U28 PE=1 SV=1 | 297 | 738 | 4.0E-12 |
sp|Q89MB9|NRDJ_BRADU | Vitamin B12-dependent ribonucleotide reductase OS=Bradyrhizobium diazoefficiens (strain JCM 10833 / IAM 13628 / NBRC 14792 / USDA 110) GN=nrdJ PE=3 SV=1 | 334 | 675 | 1.0E-11 |
sp|Q9XD73|NRDJ_STRCT | Vitamin B12-dependent ribonucleotide reductase (Fragment) OS=Streptomyces cattleya GN=nrdJ PE=3 SV=1 | 444 | 774 | 4.0E-07 |
sp|E7FHX6|NDRZ_PYRFU | Vitamin B12-dependent ribonucleoside-diphosphate reductase OS=Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1) GN=rnr PE=1 SV=1 | 96 | 247 | 2.0E-06 |
GO Term | Description | Terminal node |
---|---|---|
GO:0006260 | DNA replication | Yes |
GO:0004748 | ribonucleoside-diphosphate reductase activity, thioredoxin disulfide as acceptor | Yes |
GO:0005524 | ATP binding | Yes |
GO:0034641 | cellular nitrogen compound metabolic process | No |
GO:1901265 | nucleoside phosphate binding | No |
GO:1901360 | organic cyclic compound metabolic process | No |
GO:0008152 | metabolic process | No |
GO:0097159 | organic cyclic compound binding | No |
GO:0009987 | cellular process | No |
GO:0044260 | cellular macromolecule metabolic process | No |
GO:1901363 | heterocyclic compound binding | No |
GO:0006139 | nucleobase-containing compound metabolic process | No |
GO:0030554 | adenyl nucleotide binding | No |
GO:0036094 | small molecule binding | No |
GO:0071704 | organic substance metabolic process | No |
GO:0003824 | catalytic activity | No |
GO:0061731 | ribonucleoside-diphosphate reductase activity | No |
GO:0005488 | binding | No |
GO:0032555 | purine ribonucleotide binding | No |
GO:0008150 | biological_process | No |
GO:0046483 | heterocycle metabolic process | No |
GO:0000166 | nucleotide binding | No |
GO:0016725 | oxidoreductase activity, acting on CH or CH2 groups | No |
GO:0097367 | carbohydrate derivative binding | No |
GO:0090304 | nucleic acid metabolic process | No |
GO:0043170 | macromolecule metabolic process | No |
GO:0044237 | cellular metabolic process | No |
GO:0006725 | cellular aromatic compound metabolic process | No |
GO:0003674 | molecular_function | No |
GO:0032553 | ribonucleotide binding | No |
GO:0043168 | anion binding | No |
GO:0017076 | purine nucleotide binding | No |
GO:0032559 | adenyl ribonucleotide binding | No |
GO:0044238 | primary metabolic process | No |
GO:0016728 | oxidoreductase activity, acting on CH or CH2 groups, disulfide as acceptor | No |
GO:0043167 | ion binding | No |
GO:0035639 | purine ribonucleoside triphosphate binding | No |
GO:0006807 | nitrogen compound metabolic process | No |
GO:0006259 | DNA metabolic process | No |
GO:0016491 | oxidoreductase activity | No |
SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
---|---|---|
No | 1 - 18 | 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|9738 MYVRKRDGRQERVQFDKITARVSRLCYGLDTEHVDPVAITQKVISGVYGGVTTIQLDDLAAETAAYMTVTHPDYA ILAARIAVSNLHKQTKKQWSAVVSDLYHYVNPKNGKASPMISQETYECVMRHKEELDSAIVYDRDFNYQYFGFKT LERSYLLKLEGKIVERPQHMIMRVAVGIWGNNIERVIETYNLMSSKFFTHASPTLFNAGTPQCQLSSCFLVDMKE DSIEGIYDTLKTCAMISKMAGGIGLNVHRIRATGSYIAGTNGTSNGVIPMLRVFNNTARYVDQGGNKRPGAFAIY LEPWHADVFEFLDLRKNHGKEEVRARDLFLALWIPDLFMKRVEKNGDWTLMCPNECPGLADCYGEEFEALYEKYE REGRGRKTIRAQKLWYSILEAQTETGNPFMLYKDHCNRKSNQKNLGTIRSSNLCTEIIEYCAPDEVAVCNLASMA LPAYVDYNEGCYDFKKLHEVTQVVVRNLNKIIDVNHYPVPEARNSNMRHRPIGVGVQGLADAFLALRMPFESPEA RELNKQIFETIYHAALTASMELAKEQGPYSSFKGSPASEGILQFDMWNVKPSDLWEWETLREQIKEHGIRNSLLL APMPTASTSQILGNNECFEPYTSNIYQRRVLAGEFQVVNPWLLKDLVDMGLWSDAMKNRIIAEGGSIQNIPNIPA DIKALYKTVWEISQRQVVQMAADRGAFIDQSQSLNIHMKDPSMGKITSMHFAGWKMGLKTGMYYLRTQAAAAPIQ FTVDQQALKVADTNTGRERMPKKRTAPAGTSYMSSPSAVPRAPPVKEETGRSMSSNGMPTPSTTPPRGPEGEAKA RVVASPSKTATMKADVADGDSPKVLPTEPTEKLPLGEAGSERASGQAEDRDENSEERERDIYSDAVLACSIENPE SCVMCSG* |
Coding | >Hirsu2|9738 ATGTATGTCAGGAAGCGCGATGGACGCCAGGAGCGCGTCCAGTTCGACAAGATCACGGCCCGCGTGTCCCGTCTG TGTTACGGCCTCGACACGGAGCACGTTGACCCCGTCGCCATCACTCAAAAGGTCATCTCTGGCGTCTACGGCGGT GTGACCACAATCCAGCTCGATGATCTGGCTGCCGAGACCGCTGCGTACATGACCGTTACGCACCCCGACTATGCC ATTCTGGCGGCCCGCATCGCCGTCTCCAACCTGCACAAGCAGACCAAGAAGCAGTGGTCGGCCGTGGTCAGCGAC CTGTACCACTACGTCAACCCCAAGAATGGCAAGGCGTCGCCCATGATCTCACAGGAGACGTACGAGTGCGTGATG AGACACAAGGAAGAGCTGGACTCGGCCATAGTCTACGACCGGGACTTCAATTACCAGTACTTCGGCTTCAAGACG TTGGAGCGCTCATACCTGCTCAAGCTCGAGGGCAAGATCGTCGAGCGCCCACAACACATGATCATGCGTGTCGCC GTCGGCATCTGGGGAAACAACATCGAGCGCGTCATCGAGACGTACAATCTCATGTCCAGCAAGTTCTTCACCCAC GCCTCCCCCACACTCTTCAATGCGGGTACGCCTCAGTGCCAGCTGTCTTCGTGCTTCCTCGTCGACATGAAGGAG GACAGCATCGAGGGCATCTACGACACGCTCAAGACGTGCGCCATGATCTCCAAGATGGCGGGCGGCATCGGCCTG AACGTCCACCGCATCCGCGCCACGGGCTCCTACATCGCCGGCACCAACGGCACGTCCAACGGCGTCATCCCCATG CTGCGCGTCTTCAACAACACAGCCCGCTATGTCGACCAGGGCGGCAACAAGCGGCCCGGCGCCTTCGCCATCTAC CTGGAGCCGTGGCACGCCGACGTCTTTGAGTTCCTGGATCTCCGCAAGAACCACGGCAAGGAGGAGGTTCGTGCT CGCGACCTGTTCCTGGCTTTGTGGATCCCAGACCTGTTCATGAAGCGGGTGGAGAAGAACGGCGACTGGACCCTC ATGTGCCCCAACGAATGCCCGGGCCTGGCAGACTGCTATGGCGAAGAGTTCGAGGCTCTGTACGAGAAGTACGAG CGCGAGGGCCGCGGACGCAAGACGATTCGGGCCCAGAAGCTGTGGTACTCGATCCTGGAGGCTCAGACGGAGACG GGCAACCCGTTCATGCTCTACAAGGATCACTGCAACCGCAAGAGCAACCAGAAGAACCTGGGCACGATCCGCAGC TCGAACCTGTGCACCGAGATCATCGAGTACTGCGCGCCGGACGAGGTGGCCGTGTGCAACCTGGCGTCGATGGCG CTGCCCGCCTACGTCGACTACAACGAGGGCTGCTACGACTTCAAGAAGCTCCACGAGGTGACGCAGGTGGTGGTG CGCAACCTGAATAAGATCATCGACGTCAACCACTACCCCGTGCCGGAGGCGCGCAACAGCAACATGCGCCACCGG CCGATCGGCGTGGGCGTGCAGGGCCTGGCCGACGCCTTCCTGGCGCTGCGCATGCCCTTTGAGTCGCCCGAGGCG CGCGAGCTGAACAAGCAAATCTTCGAGACCATCTACCACGCCGCCCTCACGGCCTCGATGGAGCTGGCCAAGGAG CAGGGCCCCTACTCGTCCTTCAAGGGCTCGCCCGCGTCCGAGGGCATCCTCCAATTCGACATGTGGAACGTCAAG CCGTCGGACCTATGGGAGTGGGAGACGCTGCGGGAGCAGATCAAGGAGCACGGGATCCGCAACAGCCTGCTGCTG GCGCCGATGCCGACGGCCAGCACGTCGCAGATCCTGGGCAACAACGAGTGCTTCGAGCCGTACACGTCCAACATC TACCAGCGGCGCGTGCTGGCGGGCGAGTTCCAGGTGGTCAACCCGTGGCTGCTCAAGGACCTGGTCGACATGGGC CTCTGGTCGGACGCGATGAAGAACCGGATCATCGCGGAGGGCGGGTCGATCCAGAACATCCCCAACATCCCGGCC GACATCAAGGCGCTCTACAAGACGGTGTGGGAGATTTCGCAGAGGCAGGTGGTGCAGATGGCGGCGGACCGCGGC GCCTTCATCGACCAGTCGCAGTCGCTCAACATTCACATGAAGGACCCGTCGATGGGCAAGATCACCAGCATGCAC TTCGCGGGCTGGAAGATGGGCCTGAAGACGGGCATGTACTACCTGCGGACGCAGGCGGCGGCGGCGCCGATCCAG TTCACGGTGGACCAGCAGGCGCTGAAGGTGGCCGACACCAACACGGGCCGGGAGCGGATGCCGAAGAAGCGGACG GCGCCGGCGGGCACGAGCTACATGTCGTCTCCGTCGGCGGTGCCGCGGGCACCGCCGGTCAAGGAGGAGACGGGC CGGTCGATGAGCTCGAACGGGATGCCGACGCCGAGCACGACGCCGCCGCGGGGCCCCGAAGGCGAGGCCAAGGCG CGGGTGGTGGCGTCGCCGAGCAAGACGGCGACGATGAAGGCGGACGTGGCGGACGGCGACAGCCCCAAGGTGCTG CCAACGGAGCCGACGGAGAAGTTGCCGCTGGGCGAGGCCGGCAGCGAGCGGGCGAGCGGGCAGGCAGAGGACAGG GACGAGAACAGCGAGGAGCGCGAGCGAGACATTTACTCGGACGCGGTGTTGGCATGCAGCATCGAGAACCCAGAA TCGTGCGTCATGTGCAGTGGCTAA |
Transcript | >Hirsu2|9738 ATGTATGTCAGGAAGCGCGATGGACGCCAGGAGCGCGTCCAGTTCGACAAGATCACGGCCCGCGTGTCCCGTCTG TGTTACGGCCTCGACACGGAGCACGTTGACCCCGTCGCCATCACTCAAAAGGTCATCTCTGGCGTCTACGGCGGT GTGACCACAATCCAGCTCGATGATCTGGCTGCCGAGACCGCTGCGTACATGACCGTTACGCACCCCGACTATGCC ATTCTGGCGGCCCGCATCGCCGTCTCCAACCTGCACAAGCAGACCAAGAAGCAGTGGTCGGCCGTGGTCAGCGAC CTGTACCACTACGTCAACCCCAAGAATGGCAAGGCGTCGCCCATGATCTCACAGGAGACGTACGAGTGCGTGATG AGACACAAGGAAGAGCTGGACTCGGCCATAGTCTACGACCGGGACTTCAATTACCAGTACTTCGGCTTCAAGACG TTGGAGCGCTCATACCTGCTCAAGCTCGAGGGCAAGATCGTCGAGCGCCCACAACACATGATCATGCGTGTCGCC GTCGGCATCTGGGGAAACAACATCGAGCGCGTCATCGAGACGTACAATCTCATGTCCAGCAAGTTCTTCACCCAC GCCTCCCCCACACTCTTCAATGCGGGTACGCCTCAGTGCCAGCTGTCTTCGTGCTTCCTCGTCGACATGAAGGAG GACAGCATCGAGGGCATCTACGACACGCTCAAGACGTGCGCCATGATCTCCAAGATGGCGGGCGGCATCGGCCTG AACGTCCACCGCATCCGCGCCACGGGCTCCTACATCGCCGGCACCAACGGCACGTCCAACGGCGTCATCCCCATG CTGCGCGTCTTCAACAACACAGCCCGCTATGTCGACCAGGGCGGCAACAAGCGGCCCGGCGCCTTCGCCATCTAC CTGGAGCCGTGGCACGCCGACGTCTTTGAGTTCCTGGATCTCCGCAAGAACCACGGCAAGGAGGAGGTTCGTGCT CGCGACCTGTTCCTGGCTTTGTGGATCCCAGACCTGTTCATGAAGCGGGTGGAGAAGAACGGCGACTGGACCCTC ATGTGCCCCAACGAATGCCCGGGCCTGGCAGACTGCTATGGCGAAGAGTTCGAGGCTCTGTACGAGAAGTACGAG CGCGAGGGCCGCGGACGCAAGACGATTCGGGCCCAGAAGCTGTGGTACTCGATCCTGGAGGCTCAGACGGAGACG GGCAACCCGTTCATGCTCTACAAGGATCACTGCAACCGCAAGAGCAACCAGAAGAACCTGGGCACGATCCGCAGC TCGAACCTGTGCACCGAGATCATCGAGTACTGCGCGCCGGACGAGGTGGCCGTGTGCAACCTGGCGTCGATGGCG CTGCCCGCCTACGTCGACTACAACGAGGGCTGCTACGACTTCAAGAAGCTCCACGAGGTGACGCAGGTGGTGGTG CGCAACCTGAATAAGATCATCGACGTCAACCACTACCCCGTGCCGGAGGCGCGCAACAGCAACATGCGCCACCGG CCGATCGGCGTGGGCGTGCAGGGCCTGGCCGACGCCTTCCTGGCGCTGCGCATGCCCTTTGAGTCGCCCGAGGCG CGCGAGCTGAACAAGCAAATCTTCGAGACCATCTACCACGCCGCCCTCACGGCCTCGATGGAGCTGGCCAAGGAG CAGGGCCCCTACTCGTCCTTCAAGGGCTCGCCCGCGTCCGAGGGCATCCTCCAATTCGACATGTGGAACGTCAAG CCGTCGGACCTATGGGAGTGGGAGACGCTGCGGGAGCAGATCAAGGAGCACGGGATCCGCAACAGCCTGCTGCTG GCGCCGATGCCGACGGCCAGCACGTCGCAGATCCTGGGCAACAACGAGTGCTTCGAGCCGTACACGTCCAACATC TACCAGCGGCGCGTGCTGGCGGGCGAGTTCCAGGTGGTCAACCCGTGGCTGCTCAAGGACCTGGTCGACATGGGC CTCTGGTCGGACGCGATGAAGAACCGGATCATCGCGGAGGGCGGGTCGATCCAGAACATCCCCAACATCCCGGCC GACATCAAGGCGCTCTACAAGACGGTGTGGGAGATTTCGCAGAGGCAGGTGGTGCAGATGGCGGCGGACCGCGGC GCCTTCATCGACCAGTCGCAGTCGCTCAACATTCACATGAAGGACCCGTCGATGGGCAAGATCACCAGCATGCAC TTCGCGGGCTGGAAGATGGGCCTGAAGACGGGCATGTACTACCTGCGGACGCAGGCGGCGGCGGCGCCGATCCAG TTCACGGTGGACCAGCAGGCGCTGAAGGTGGCCGACACCAACACGGGCCGGGAGCGGATGCCGAAGAAGCGGACG GCGCCGGCGGGCACGAGCTACATGTCGTCTCCGTCGGCGGTGCCGCGGGCACCGCCGGTCAAGGAGGAGACGGGC CGGTCGATGAGCTCGAACGGGATGCCGACGCCGAGCACGACGCCGCCGCGGGGCCCCGAAGGCGAGGCCAAGGCG CGGGTGGTGGCGTCGCCGAGCAAGACGGCGACGATGAAGGCGGACGTGGCGGACGGCGACAGCCCCAAGGTGCTG CCAACGGAGCCGACGGAGAAGTTGCCGCTGGGCGAGGCCGGCAGCGAGCGGGCGAGCGGGCAGGCAGAGGACAGG GACGAGAACAGCGAGGAGCGCGAGCGAGACATTTACTCGGACGCGGTGTTGGCATGCAGCATCGAGAACCCAGAA TCGTGCGTCATGTGCAGTGGCTAA |
Gene | >Hirsu2|9738 ATGTATGTCAGGAAGCGCGGTATGTACATTTTCCTCATCTCTCTGCTCAAGATGAGCGGTAGAGGGAGATGGGTT GGCTAATGCGTGTCGCCGTCAGATGGACGCCAGGAGCGCGTCCAGTTCGACAAGATCACGGCCCGCGTGTCCCGT CTGTGTTACGGCCTCGACACGGAGCACGTTGACCCCGTCGCCATCACTCAAAAGGTCATCTCTGGCGTCTACGGC GGTGTGACCACAATCCAGCTCGATGATCTGGTGAGTAGAGCCTCCGGACCCAGCCATGGTATGCCACGACTAACA GGTACGACCGTCGCCAGGCTGCCGAGACCGCTGCGTACATGACCGTTACGCACCCCGACTATGCCATTCTGGCGG CCCGCATCGCCGTCTCCAACCTGCACAAGCAGACCAAGAAGCAGTGGTCGGCCGTGGTCAGCGACCTGTACCACT ACGTCAACCCCAAGAATGGCAAGGCGTCGCCCATGATCTCACAGGAGACGTACGAGTGCGTGATGAGACACAAGG AAGAGCTGGACTCGGCCATAGTCTACGACCGGGACTTCAATTACCAGTACTTCGGCTTCAAGACGTTGGAGCGCT CATACCTGCTCAAGCTCGAGGGCAAGATCGTCGAGCGCCCACAACACATGATCATGCGTGTCGCCGTCGGCATCT GGGGAAACAACATCGAGCGCGTCATCGAGACGTACAATCTCATGTCCAGCAAGTTCTTCACCCACGCCTCCCCCA CACTCTTCAATGCGGGTACGCCTCAGTGCCAGCTGTCTTCGTGCTTCCTCGTCGACATGAAGGAGGACAGCATCG AGGGCATCTACGACACGCTCAAGACGTGCGCCATGATCTCCAAGATGGCGGGCGGCATCGGCCTGAACGTCCACC GCATCCGCGCCACGGGCTCCTACATCGCCGGCACCAACGGCACGTCCAACGGCGTCATCCCCATGCTGCGCGTCT TCAACAACACAGCCCGCTATGTCGACCAGGGCGGCAACAAGCGGCCCGGCGCCTTCGCCATCTACCTGGAGCCGT GGCACGCCGACGTCTTTGAGTTCCTGGATCTCCGCAAGAACCACGGCAAGGAGGAGGTTCGTGCTCGCGACCTGT TCCTGGCTTTGTGGATCCCAGACCTGTTCATGAAGCGGGTGGAGAAGAACGGCGACTGGACCCTCATGTGCCCCA ACGAATGCCCGGGCCTGGCAGACTGCTATGGCGAAGAGTTCGAGGCTCTGTACGAGAAGTACGAGCGCGAGGGCC GCGGACGCAAGACGATTCGGGCCCAGAAGCTGTGGTACTCGATCCTGGAGGCTCAGACGGAGACGGGCAACCCGT TCATGCTCTACAAGGATCACTGCAACCGCAAGAGCAACCAGAAGAACCTGGGCACGATCCGCAGCTCGAACCTGT GCACCGAGATCATCGAGTACTGCGCGCCGGACGAGGTGGCCGTGTGCAACCTGGCGTCGATGGCGCTGCCCGCCT ACGTCGACTACAACGAGGGCTGCTACGACTTCAAGAAGCTCCACGAGGTGACGCAGGTGGTGGTGCGCAACCTGA ATAAGATCATCGACGTCAACCACTACCCCGTGCCGGAGGCGCGCAACAGCAACATGCGCCACCGGCCGATCGGCG TGGGCGTGCAGGGCCTGGCCGACGCCTTCCTGGCGCTGCGCATGCCCTTTGAGTCGCCCGAGGCGCGCGAGCTGA ACAAGCAAATCTTCGAGACCATCTACCACGCCGCCCTCACGGCCTCGATGGAGCTGGCCAAGGAGCAGGGCCCCT ACTCGTCCTTCAAGGGCTCGCCCGCGTCCGAGGGCATCCTCCAATTCGACATGTGGAACGTCAAGCCGTCGGACC TATGGGAGTGGGAGACGCTGCGGGAGCAGATCAAGGAGCACGGGATCCGCAACAGCCTGCTGCTGGCGCCGATGC CGACGGCCAGCACGTCGCAGATCCTGGGCAACAACGAGTGCTTCGAGCCGTACACGTCCAACATCTACCAGCGGC GCGTGCTGGCGGGCGAGTTCCAGGTGGTCAACCCGTGGCTGCTCAAGGACCTGGTCGACATGGGCCTCTGGTCGG ACGCGATGAAGAACCGGATCATCGCGGAGGGCGGGTCGATCCAGAACATCCCCAACATCCCGGCCGACATCAAGG CGCTCTACAAGACGGTGTGGGAGATTTCGCAGAGGCAGGTGGTGCAGATGGCGGCGGACCGCGGCGCCTTCATCG ACCAGTCGCAGTCGCTCAACATTCACATGAAGGACCCGTCGATGGGCAAGATCACCAGCATGCACTTCGCGGGCT GGAAGATGGGCCTGAAGACGGGCATGTACTACCTGCGGACGCAGGCGGCGGCGGCGCCGATCCAGTTCACGGTGG ACCAGCAGGCGCTGAAGGTGGCCGACACCAACACGGGCCGGGAGCGGATGCCGAAGAAGCGGACGGCGCCGGCGG GCACGAGCTACATGTCGTCTCCGTCGGCGGTGCCGCGGGCACCGCCGGTCAAGGAGGAGACGGGCCGGTCGATGA GCTCGAACGGGATGCCGACGCCGAGCACGACGCCGCCGCGGGGCCCCGAAGGCGAGGCCAAGGCGCGGGTGGTGG CGTCGCCGAGCAAGACGGCGACGATGAAGGCGGACGTGGCGGACGGCGACAGCCCCAAGGTGCTGCCAACGGAGC CGACGGAGAAGTTGCCGCTGGGCGAGGCCGGCAGCGAGCGGGCGAGCGGGCAGGCAGAGGACAGGGACGAGAACA GCGAGGAGCGCGAGCGAGACATTTACTCGGACGCGGTGTTGGCATGTAAGCGCCGACCTCCCCTTCTCTTTTTAC TCTCATCCAAGGACGATAACTGACGGGACGTCTCCCCTTCCAACAGGCAGCATCGAGAACCCAGAATCGTGCGTC ATGTGCAGTGGCTAA |