Protein ID | Ophio5|1368 |
Gene name | |
Location | scaffold_146:24236..26947 |
Strand | - |
Gene length (bp) | 2711 |
Transcript length (bp) | 2526 |
Coding sequence length (bp) | 2523 |
Protein length (aa) | 841 |
PFAM Domain ID | Short name | Long name | E-value | Start | End |
---|---|---|---|---|---|
PF13307 | Helicase_C_2 | Helicase C-terminal domain | 1.1E-59 | 631 | 812 |
PF06733 | DEAD_2 | DEAD_2 | 1.2E-47 | 208 | 393 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|A1D8E4|CHL1_NEOFI | ATP-dependent DNA helicase chl1 OS=Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN=chl1 PE=3 SV=1 | 15 | 841 | 0.0E+00 |
sp|A7UXD4|CHL1_NEUCR | ATP-dependent DNA helicase chl1 OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=chl1 PE=3 SV=2 | 40 | 841 | 0.0E+00 |
sp|A3LN13|CHL1_PICST | ATP-dependent DNA helicase CHL1 OS=Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) GN=CHL1 PE=3 SV=2 | 16 | 812 | 0.0E+00 |
sp|A6ZWN8|CHL1_YEAS7 | ATP-dependent DNA helicase CHL1 OS=Saccharomyces cerevisiae (strain YJM789) GN=CHL1 PE=3 SV=1 | 16 | 841 | 0.0E+00 |
sp|P22516|CHL1_YEAST | ATP-dependent DNA helicase CHL1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=CHL1 PE=1 SV=1 | 16 | 841 | 0.0E+00 |
Swissprot ID | Swissprot Description | Start | End | E-value |
---|---|---|---|---|
sp|A1D8E4|CHL1_NEOFI | ATP-dependent DNA helicase chl1 OS=Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN=chl1 PE=3 SV=1 | 15 | 841 | 0.0E+00 |
sp|A7UXD4|CHL1_NEUCR | ATP-dependent DNA helicase chl1 OS=Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) GN=chl1 PE=3 SV=2 | 40 | 841 | 0.0E+00 |
sp|A3LN13|CHL1_PICST | ATP-dependent DNA helicase CHL1 OS=Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) GN=CHL1 PE=3 SV=2 | 16 | 812 | 0.0E+00 |
sp|A6ZWN8|CHL1_YEAS7 | ATP-dependent DNA helicase CHL1 OS=Saccharomyces cerevisiae (strain YJM789) GN=CHL1 PE=3 SV=1 | 16 | 841 | 0.0E+00 |
sp|P22516|CHL1_YEAST | ATP-dependent DNA helicase CHL1 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=CHL1 PE=1 SV=1 | 16 | 841 | 0.0E+00 |
sp|Q5AD67|CHL1_CANAL | ATP-dependent DNA helicase CHL1 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=CHL1 PE=3 SV=1 | 15 | 839 | 0.0E+00 |
sp|Q6CAX3|CHL1_YARLI | ATP-dependent DNA helicase CHL1 OS=Yarrowia lipolytica (strain CLIB 122 / E 150) GN=CHL1 PE=3 SV=1 | 15 | 838 | 0.0E+00 |
sp|Q6BZD9|CHL1_DEBHA | ATP-dependent DNA helicase CHL1 OS=Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / JCM 1990 / NBRC 0083 / IGC 2968) GN=CHL1 PE=3 SV=2 | 16 | 812 | 0.0E+00 |
sp|O14147|CHL1_SCHPO | ATP-dependent DNA helicase chl1 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=chl1 PE=3 SV=1 | 15 | 841 | 0.0E+00 |
sp|Q6FKT4|CHL1_CANGA | ATP-dependent DNA helicase CHL1 OS=Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) GN=CHL1 PE=3 SV=1 | 13 | 838 | 0.0E+00 |
sp|Q2U587|CHL1_ASPOR | ATP-dependent DNA helicase chl1 OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=chl1 PE=3 SV=1 | 170 | 838 | 0.0E+00 |
sp|Q750G3|CHL1_ASHGO | ATP-dependent DNA helicase CHL1 OS=Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) GN=CHL1 PE=3 SV=1 | 15 | 841 | 0.0E+00 |
sp|A2QY22|CHL1_ASPNC | ATP-dependent DNA helicase chl1 OS=Aspergillus niger (strain CBS 513.88 / FGSC A1513) GN=chl1 PE=3 SV=1 | 11 | 838 | 0.0E+00 |
sp|A7ERG1|CHL1_SCLS1 | ATP-dependent DNA helicase CHL1 OS=Sclerotinia sclerotiorum (strain ATCC 18683 / 1980 / Ss-1) GN=CHL1 PE=3 SV=1 | 1 | 841 | 0.0E+00 |
sp|Q1E5T3|CHL1_COCIM | ATP-dependent DNA helicase CHL1 OS=Coccidioides immitis (strain RS) GN=CHL1 PE=3 SV=1 | 16 | 812 | 0.0E+00 |
sp|Q4WWE9|CHL1_ASPFU | ATP-dependent DNA helicase chl1 OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=chl1 PE=3 SV=1 | 102 | 841 | 0.0E+00 |
sp|Q6CIF0|CHL1_KLULA | ATP-dependent DNA helicase CHL1 OS=Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) GN=CHL1 PE=3 SV=1 | 15 | 818 | 0.0E+00 |
sp|A1CJ34|CHL1_ASPCL | ATP-dependent DNA helicase chl1 OS=Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1) GN=chl1 PE=3 SV=1 | 194 | 812 | 0.0E+00 |
sp|A5DNW6|CHL1_PICGU | ATP-dependent DNA helicase CHL1 OS=Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) GN=CHL1 PE=3 SV=2 | 14 | 813 | 0.0E+00 |
sp|A7TTL0|CHL1_VANPO | ATP-dependent DNA helicase CHL1 OS=Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294) GN=CHL1 PE=3 SV=1 | 14 | 812 | 1.0E-180 |
sp|A5DUW8|CHL1_LODEL | ATP-dependent DNA helicase CHL1 OS=Lodderomyces elongisporus (strain ATCC 11503 / CBS 2605 / JCM 1781 / NBRC 1676 / NRRL YB-4239) GN=CHL1 PE=3 SV=1 | 15 | 812 | 1.0E-174 |
sp|A8MPP1|D11L8_HUMAN | Putative ATP-dependent RNA helicase DDX11-like protein 8 OS=Homo sapiens GN=DDX11L8 PE=1 SV=1 | 13 | 813 | 2.0E-167 |
sp|Q6AXC6|DDX11_MOUSE | Probable ATP-dependent DNA helicase DDX11 OS=Mus musculus GN=Ddx11 PE=1 SV=1 | 25 | 812 | 2.0E-154 |
sp|Q92771|DDX12_HUMAN | Putative ATP-dependent RNA helicase DDX12 OS=Homo sapiens GN=DDX12P PE=5 SV=3 | 26 | 838 | 1.0E-153 |
sp|Q96FC9|DDX11_HUMAN | Probable ATP-dependent DNA helicase DDX11 OS=Homo sapiens GN=DDX11 PE=1 SV=1 | 13 | 750 | 1.0E-138 |
sp|Q21489|CHL1_CAEEL | ATP-dependent DNA helicase chl-1 OS=Caenorhabditis elegans GN=chl-1 PE=3 SV=2 | 15 | 811 | 5.0E-116 |
sp|Q5SXJ3|FANCJ_MOUSE | Fanconi anemia group J protein homolog OS=Mus musculus GN=Brip1 PE=2 SV=1 | 14 | 812 | 2.0E-72 |
sp|Q3YK19|FANCJ_CHICK | Fanconi anemia group J protein homolog OS=Gallus gallus GN=BRIP1 PE=2 SV=1 | 190 | 812 | 3.0E-70 |
sp|A4K436|RTEL1_BOVIN | Regulator of telomere elongation helicase 1 OS=Bos taurus GN=RTEL1 PE=2 SV=1 | 205 | 839 | 2.0E-67 |
sp|Q9BX63|FANCJ_HUMAN | Fanconi anemia group J protein OS=Homo sapiens GN=BRIP1 PE=1 SV=1 | 205 | 812 | 1.0E-66 |
sp|P0C928|RTEL1_DANRE | Regulator of telomere elongation helicase 1 OS=Danio rerio GN=rtel1 PE=3 SV=1 | 205 | 839 | 2.0E-65 |
sp|Q0VGM9|RTEL1_MOUSE | Regulator of telomere elongation helicase 1 OS=Mus musculus GN=Rtel1 PE=1 SV=2 | 205 | 839 | 3.0E-64 |
sp|Q5RJZ1|RTEL1_RAT | Regulator of telomere elongation helicase 1 OS=Rattus norvegicus GN=Rtel1 PE=2 SV=2 | 205 | 839 | 9.0E-64 |
sp|Q6H1L8|RTEL1_MUSSP | Regulator of telomere elongation helicase 1 OS=Mus spretus GN=Rtel1 PE=2 SV=1 | 205 | 812 | 5.0E-63 |
sp|Q9NZ71|RTEL1_HUMAN | Regulator of telomere elongation helicase 1 OS=Homo sapiens GN=RTEL1 PE=1 SV=2 | 205 | 839 | 5.0E-62 |
sp|B3MSG8|RTEL1_DROAN | Regulator of telomere elongation helicase 1 homolog OS=Drosophila ananassae GN=GF20802 PE=3 SV=1 | 205 | 840 | 4.0E-59 |
sp|Q60452|ERCC2_CRIGR | TFIIH basal transcription factor complex helicase XPD subunit OS=Cricetulus griseus GN=ERCC2 PE=1 SV=1 | 196 | 812 | 1.0E-56 |
sp|O08811|ERCC2_MOUSE | TFIIH basal transcription factor complex helicase XPD subunit OS=Mus musculus GN=Ercc2 PE=1 SV=2 | 196 | 812 | 6.0E-56 |
sp|P18074|ERCC2_HUMAN | TFIIH basal transcription factor complex helicase XPD subunit OS=Homo sapiens GN=ERCC2 PE=1 SV=1 | 196 | 812 | 6.0E-56 |
sp|Q55G81|ERCC2_DICDI | TFIIH basal transcription factor complex helicase repD subunit OS=Dictyostelium discoideum GN=repD PE=2 SV=1 | 198 | 811 | 4.0E-55 |
sp|A6QLJ0|ERCC2_BOVIN | TFIIH basal transcription factor complex helicase XPD subunit OS=Bos taurus GN=ERCC2 PE=2 SV=1 | 196 | 812 | 3.0E-54 |
sp|P26659|RAD15_SCHPO | DNA repair helicase rad15 OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=rad15 PE=1 SV=2 | 196 | 812 | 6.0E-51 |
sp|P06839|RAD3_YEAST | DNA repair helicase RAD3 OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=RAD3 PE=1 SV=1 | 202 | 820 | 3.0E-48 |
sp|Q8W4M7|ERCC2_ARATH | DNA repair helicase UVH6 OS=Arabidopsis thaliana GN=UVH6 PE=1 SV=1 | 200 | 811 | 6.0E-45 |
sp|B4GU19|RTEL1_DROPE | Regulator of telomere elongation helicase 1 homolog OS=Drosophila persimilis GN=GL14463 PE=3 SV=1 | 525 | 839 | 3.0E-43 |
sp|Q29FS3|RTEL1_DROPS | Regulator of telomere elongation helicase 1 homolog OS=Drosophila pseudoobscura pseudoobscura GN=GA17940 PE=3 SV=2 | 525 | 839 | 3.0E-43 |
sp|B4NDG5|RTEL1_DROWI | Regulator of telomere elongation helicase 1 homolog OS=Drosophila willistoni GN=GK24923 PE=3 SV=1 | 534 | 839 | 3.0E-43 |
sp|B4L1Z2|RTEL1_DROMO | Regulator of telomere elongation helicase 1 homolog OS=Drosophila mojavensis GN=GI15901 PE=3 SV=1 | 534 | 839 | 4.0E-42 |
sp|B4I0K4|RTEL1_DROSE | Regulator of telomere elongation helicase 1 homolog OS=Drosophila sechellia GN=GM12432 PE=3 SV=1 | 525 | 840 | 4.0E-42 |
sp|B4M891|RTEL1_DROVI | Regulator of telomere elongation helicase 1 homolog OS=Drosophila virilis GN=GJ16649 PE=3 SV=1 | 534 | 839 | 4.0E-42 |
sp|B4PZB4|RTEL1_DROYA | Regulator of telomere elongation helicase 1 homolog OS=Drosophila yakuba GN=GE16425 PE=3 SV=1 | 525 | 840 | 1.0E-41 |
sp|B3NSW1|RTEL1_DROER | Regulator of telomere elongation helicase 1 homolog OS=Drosophila erecta GN=GG18780 PE=3 SV=1 | 525 | 840 | 2.0E-41 |
sp|Q9W484|RTEL1_DROME | Regulator of telomere elongation helicase 1 homolog OS=Drosophila melanogaster GN=CG4078 PE=1 SV=1 | 525 | 840 | 2.0E-41 |
sp|B4JNS2|RTEL1_DROGR | Regulator of telomere elongation helicase 1 homolog OS=Drosophila grimshawi GN=GH24089 PE=3 SV=1 | 534 | 839 | 6.0E-41 |
sp|Q16X92|RTEL1_AEDAE | Regulator of telomere elongation helicase 1 homolog OS=Aedes aegypti GN=AAEL008960 PE=3 SV=1 | 534 | 840 | 8.0E-41 |
sp|B0W9F4|RTEL1_CULQU | Regulator of telomere elongation helicase 1 homolog OS=Culex quinquefasciatus GN=CPIJ003765 PE=3 SV=1 | 534 | 840 | 2.0E-39 |
sp|Q7QEI1|RTEL1_ANOGA | Regulator of telomere elongation helicase 1 homolog OS=Anopheles gambiae GN=AGAP000634 PE=3 SV=5 | 534 | 839 | 5.0E-38 |
sp|Q5RE34|RTEL1_PONAB | Regulator of telomere elongation helicase 1 OS=Pongo abelii GN=RTEL1 PE=2 SV=1 | 534 | 839 | 3.0E-36 |
sp|A8WS58|RTEL1_CAEBR | Regulator of telomere elongation helicase 1 homolog OS=Caenorhabditis briggsae GN=rtel-1 PE=3 SV=1 | 552 | 813 | 1.0E-29 |
sp|Q93575|RTEL1_CAEEL | Regulator of telomere elongation helicase 1 homolog OS=Caenorhabditis elegans GN=rtel-1 PE=3 SV=3 | 552 | 841 | 3.0E-24 |
sp|B4PZB4|RTEL1_DROYA | Regulator of telomere elongation helicase 1 homolog OS=Drosophila yakuba GN=GE16425 PE=3 SV=1 | 205 | 396 | 9.0E-23 |
sp|B3NSW1|RTEL1_DROER | Regulator of telomere elongation helicase 1 homolog OS=Drosophila erecta GN=GG18780 PE=3 SV=1 | 205 | 396 | 1.0E-22 |
sp|Q9W484|RTEL1_DROME | Regulator of telomere elongation helicase 1 homolog OS=Drosophila melanogaster GN=CG4078 PE=1 SV=1 | 205 | 396 | 1.0E-22 |
sp|Q7QEI1|RTEL1_ANOGA | Regulator of telomere elongation helicase 1 homolog OS=Anopheles gambiae GN=AGAP000634 PE=3 SV=5 | 196 | 393 | 4.0E-22 |
sp|B4L1Z2|RTEL1_DROMO | Regulator of telomere elongation helicase 1 homolog OS=Drosophila mojavensis GN=GI15901 PE=3 SV=1 | 205 | 396 | 4.0E-22 |
sp|B4M891|RTEL1_DROVI | Regulator of telomere elongation helicase 1 homolog OS=Drosophila virilis GN=GJ16649 PE=3 SV=1 | 205 | 396 | 4.0E-22 |
sp|Q9HM14|XPD_THEAC | ATP-dependent DNA helicase Ta0057 OS=Thermoplasma acidophilum (strain ATCC 25905 / DSM 1728 / JCM 9062 / NBRC 15155 / AMRC-C165) GN=Ta0057 PE=1 SV=1 | 203 | 821 | 8.0E-22 |
sp|B4JNS2|RTEL1_DROGR | Regulator of telomere elongation helicase 1 homolog OS=Drosophila grimshawi GN=GH24089 PE=3 SV=1 | 205 | 393 | 2.0E-21 |
sp|B4NDG5|RTEL1_DROWI | Regulator of telomere elongation helicase 1 homolog OS=Drosophila willistoni GN=GK24923 PE=3 SV=1 | 205 | 393 | 3.0E-21 |
sp|Q29FS3|RTEL1_DROPS | Regulator of telomere elongation helicase 1 homolog OS=Drosophila pseudoobscura pseudoobscura GN=GA17940 PE=3 SV=2 | 205 | 396 | 5.0E-21 |
sp|Q5RE34|RTEL1_PONAB | Regulator of telomere elongation helicase 1 OS=Pongo abelii GN=RTEL1 PE=2 SV=1 | 205 | 376 | 5.0E-21 |
sp|B4GU19|RTEL1_DROPE | Regulator of telomere elongation helicase 1 homolog OS=Drosophila persimilis GN=GL14463 PE=3 SV=1 | 205 | 396 | 5.0E-21 |
sp|Q93575|RTEL1_CAEEL | Regulator of telomere elongation helicase 1 homolog OS=Caenorhabditis elegans GN=rtel-1 PE=3 SV=3 | 206 | 401 | 7.0E-18 |
sp|Q16X92|RTEL1_AEDAE | Regulator of telomere elongation helicase 1 homolog OS=Aedes aegypti GN=AAEL008960 PE=3 SV=1 | 167 | 376 | 7.0E-18 |
sp|B0W9F4|RTEL1_CULQU | Regulator of telomere elongation helicase 1 homolog OS=Culex quinquefasciatus GN=CPIJ003765 PE=3 SV=1 | 191 | 393 | 7.0E-18 |
sp|A8WS58|RTEL1_CAEBR | Regulator of telomere elongation helicase 1 homolog OS=Caenorhabditis briggsae GN=rtel-1 PE=3 SV=1 | 185 | 401 | 1.0E-17 |
sp|B4I0K4|RTEL1_DROSE | Regulator of telomere elongation helicase 1 homolog OS=Drosophila sechellia GN=GM12432 PE=3 SV=1 | 205 | 393 | 2.0E-13 |
sp|B3MSG8|RTEL1_DROAN | Regulator of telomere elongation helicase 1 homolog OS=Drosophila ananassae GN=GF20802 PE=3 SV=1 | 11 | 80 | 9.0E-11 |
sp|B3NSW1|RTEL1_DROER | Regulator of telomere elongation helicase 1 homolog OS=Drosophila erecta GN=GG18780 PE=3 SV=1 | 11 | 86 | 1.0E-10 |
sp|B4PZB4|RTEL1_DROYA | Regulator of telomere elongation helicase 1 homolog OS=Drosophila yakuba GN=GE16425 PE=3 SV=1 | 11 | 86 | 1.0E-10 |
sp|B4M891|RTEL1_DROVI | Regulator of telomere elongation helicase 1 homolog OS=Drosophila virilis GN=GJ16649 PE=3 SV=1 | 11 | 75 | 2.0E-10 |
sp|Q29FS3|RTEL1_DROPS | Regulator of telomere elongation helicase 1 homolog OS=Drosophila pseudoobscura pseudoobscura GN=GA17940 PE=3 SV=2 | 11 | 80 | 2.0E-10 |
sp|B4GU19|RTEL1_DROPE | Regulator of telomere elongation helicase 1 homolog OS=Drosophila persimilis GN=GL14463 PE=3 SV=1 | 11 | 80 | 2.0E-10 |
sp|Q9W484|RTEL1_DROME | Regulator of telomere elongation helicase 1 homolog OS=Drosophila melanogaster GN=CG4078 PE=1 SV=1 | 11 | 86 | 4.0E-10 |
sp|B4L1Z2|RTEL1_DROMO | Regulator of telomere elongation helicase 1 homolog OS=Drosophila mojavensis GN=GI15901 PE=3 SV=1 | 11 | 75 | 4.0E-10 |
sp|B4NDG5|RTEL1_DROWI | Regulator of telomere elongation helicase 1 homolog OS=Drosophila willistoni GN=GK24923 PE=3 SV=1 | 11 | 75 | 4.0E-10 |
sp|B4I0K4|RTEL1_DROSE | Regulator of telomere elongation helicase 1 homolog OS=Drosophila sechellia GN=GM12432 PE=3 SV=1 | 11 | 75 | 6.0E-10 |
sp|Q7QEI1|RTEL1_ANOGA | Regulator of telomere elongation helicase 1 homolog OS=Anopheles gambiae GN=AGAP000634 PE=3 SV=5 | 11 | 93 | 2.0E-09 |
sp|B4JNS2|RTEL1_DROGR | Regulator of telomere elongation helicase 1 homolog OS=Drosophila grimshawi GN=GH24089 PE=3 SV=1 | 11 | 75 | 8.0E-09 |
sp|B0W9F4|RTEL1_CULQU | Regulator of telomere elongation helicase 1 homolog OS=Culex quinquefasciatus GN=CPIJ003765 PE=3 SV=1 | 11 | 75 | 1.0E-08 |
sp|Q16X92|RTEL1_AEDAE | Regulator of telomere elongation helicase 1 homolog OS=Aedes aegypti GN=AAEL008960 PE=3 SV=1 | 10 | 75 | 1.0E-08 |
sp|P0C928|RTEL1_DANRE | Regulator of telomere elongation helicase 1 OS=Danio rerio GN=rtel1 PE=3 SV=1 | 11 | 71 | 1.0E-07 |
GO Term | Description | Terminal node |
---|---|---|
GO:0003678 | DNA helicase activity | Yes |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | Yes |
GO:0004386 | helicase activity | Yes |
GO:0005524 | ATP binding | Yes |
GO:0003676 | nucleic acid binding | Yes |
GO:0006139 | nucleobase-containing compound metabolic process | Yes |
GO:0003677 | DNA binding | Yes |
GO:0032555 | purine ribonucleotide binding | No |
GO:1901360 | organic cyclic compound metabolic process | No |
GO:0003674 | molecular_function | No |
GO:0044237 | cellular metabolic process | No |
GO:0008152 | metabolic process | No |
GO:0043167 | ion binding | No |
GO:0140097 | catalytic activity, acting on DNA | No |
GO:0016817 | hydrolase activity, acting on acid anhydrides | No |
GO:0046483 | heterocycle metabolic process | No |
GO:0044238 | primary metabolic process | No |
GO:0140657 | ATP-dependent activity | No |
GO:0043168 | anion binding | No |
GO:0006725 | cellular aromatic compound metabolic process | No |
GO:0008150 | biological_process | No |
GO:0097159 | organic cyclic compound binding | No |
GO:0140640 | catalytic activity, acting on a nucleic acid | No |
GO:1901265 | nucleoside phosphate binding | No |
GO:0035639 | purine ribonucleoside triphosphate binding | No |
GO:0034641 | cellular nitrogen compound metabolic process | No |
GO:0003824 | catalytic activity | No |
GO:0006807 | nitrogen compound metabolic process | No |
GO:0008094 | ATP-dependent activity, acting on DNA | No |
GO:0032559 | adenyl ribonucleotide binding | No |
GO:0036094 | small molecule binding | No |
GO:0071704 | organic substance metabolic process | No |
GO:0097367 | carbohydrate derivative binding | No |
GO:0000166 | nucleotide binding | No |
GO:0032553 | ribonucleotide binding | No |
GO:1901363 | heterocyclic compound binding | No |
GO:0017076 | purine nucleotide binding | No |
GO:0030554 | adenyl nucleotide binding | No |
GO:0016787 | hydrolase activity | No |
GO:0009987 | cellular process | No |
GO:0005488 | binding | No |
SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
---|---|---|
No | 1 - 34 | 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 | >Ophio5|1368 MEAVDDAARHLEALDFHHPYTPYHVQEQLMKTVYQVLETGNGQVGILESPTGTGKSLSLICASLTWLRNYKSREQ DAALEAAGAAYRDEPPWLVEQLMRRKREELAQRWEERENRLEAARQKEKAAEERSRKRKRRDDAAAPRPDAEEDD AEWLLDDRRETAGVGSGDALSGLSKESRELLEGLGLGGPKKMRDDQEEMPGEEIKIYYTSRTHSQLSQFIAELRR PSFPSSLPASIAEERGMTSERVKLLPLSSRQRLCINPSVARLGSTQAINDRCAELQQAKSGKKCAYMPSEELRSQ THQFRDAALAALPDIEDLHRLGKSLAVCPYYASRTALPAAEMVTLPYPLLLQKKAREALGIKLEGSVVIIDEAHN IMDAVSSVHAAEVKLSELRRARGMLAVYVKRFGKRLRGENRINVGRLGRVIDGLTEWMETAQSFKEEAGIVAPSE LTRPKGIDLLDMFGLIQYIQESRMAYKIEGYAAQVVAGEKPGLRPSSTPVLHSLVSFLAALTNTSDEGRFFYRKT GSSSPDMQVSYLLLSPTHAFSSIVASARAVILAGGTMSPFDDYRNHLFPKLAASKLTTLSCGHVVPAENLCVWTL EGTRPGAMPFDFSFQRRGDGELMRQLGLAMVNLCSVVPDGVVVFFPSYGYLEEVVRAWQPGIWERLQARKSVFQE TRGCSGDDVLQQYSEAILNAETKRGALLLSVVGGKMSEGINFSDRLGRCVVMVGMPYPNSASPEWKAKMEYIEAT ATSSGADAKQAAREFYDNACMRAVNQSIGRAIRHRGDFAAIVLADRRYASVRIRARLPAWIRGEKGTEDAAKAGG MLSGLMGALGQFFRGR |
Coding | >Ophio5|1368 ATGGAAGCCGTCGATGATGCCGCCCGCCACCTGGAAGCCCTCGACTTTCACCATCCATATACGCCCTACCATGTC CAGGAGCAGCTCATGAAGACGGTCTATCAGGTACTGGAAACTGGAAATGGGCAGGTTGGCATTCTAGAGAGCCCC ACAGGCACGGGGAAATCGCTGTCCCTAATCTGCGCGTCGTTGACGTGGCTTCGCAACTACAAATCCAGAGAGCAG GACGCGGCGCTGGAAGCCGCGGGCGCCGCCTATCGAGACGAGCCGCCTTGGTTGGTCGAGCAGCTGATGCGTCGC AAAAGGGAAGAGCTCGCGCAGAGGTGGGAGGAGAGGGAGAACCGGCTGGAGGCCGCCAGACAGAAAGAGAAGGCC GCGGAGGAGCGGTCGAGGAAGCGGAAGCGTAGGGACGATGCTGCTGCGCCGCGTCCCGACGCAGAGGAAGACGAC GCAGAGTGGCTCCTCGACGACCGCCGAGAGACCGCCGGCGTCGGCTCTGGGGATGCGCTCTCGGGCTTGAGCAAG GAGTCTCGAGAATTGCTGGAGGGCCTCGGCCTTGGCGGACCCAAGAAAATGCGTGACGACCAGGAGGAGATGCCG GGAGAGGAAATCAAGATCTACTACACGTCGAGAACGCACTCGCAGCTGTCGCAATTCATCGCCGAGCTGCGCCGT CCCTCGTTTCCTTCCTCGCTGCCCGCTTCCATAGCAGAGGAGAGAGGGATGACGTCGGAAAGGGTAAAGCTGCTA CCTTTGTCGTCCCGTCAGCGGCTCTGCATCAACCCGTCCGTGGCCCGACTTGGCTCGACGCAAGCCATCAATGAT CGTTGCGCCGAGCTGCAGCAGGCCAAGTCCGGCAAGAAATGCGCCTACATGCCGAGCGAGGAACTGCGCAGCCAG ACTCACCAGTTCCGCGACGCCGCTCTGGCCGCGCTGCCGGACATTGAAGACCTGCACCGGCTGGGCAAGTCGCTG GCCGTGTGCCCTTATTACGCGTCCCGCACTGCGCTGCCGGCGGCTGAAATGGTGACGCTGCCGTATCCGCTGCTA CTGCAGAAGAAGGCGCGCGAGGCGCTGGGCATCAAGCTGGAGGGCAGTGTGGTGATTATCGACGAGGCGCACAAC ATCATGGATGCCGTGTCTAGCGTGCACGCGGCCGAGGTGAAGCTGAGTGAGCTCCGTAGGGCGAGGGGCATGCTG GCCGTCTATGTCAAGCGGTTCGGGAAGAGGCTCAGGGGCGAGAATCGAATCAACGTCGGGAGGCTGGGTCGCGTC ATCGACGGCTTGACGGAGTGGATGGAGACCGCTCAGAGCTTCAAGGAAGAGGCCGGTATCGTGGCCCCGAGCGAG CTGACGCGGCCCAAGGGCATCGACCTACTCGACATGTTTGGGCTGATTCAGTACATACAAGAGTCGAGGATGGCT TACAAGATCGAGGGCTATGCCGCTCAAGTCGTGGCGGGCGAGAAGCCAGGGCTGAGGCCGAGCTCGACGCCTGTG CTACACTCGCTGGTCTCCTTCCTGGCAGCCCTCACCAACACCAGCGACGAAGGCCGCTTCTTCTACCGAAAGACA GGCAGCAGCTCGCCCGACATGCAGGTGTCATACCTGCTGCTATCGCCGACGCACGCCTTCTCGTCCATTGTGGCC AGCGCCCGAGCGGTGATTCTGGCAGGGGGCACCATGTCGCCCTTTGACGACTACCGAAACCATCTGTTCCCGAAG CTCGCGGCGTCTAAATTGACGACGCTCAGCTGCGGCCACGTCGTGCCGGCAGAGAACCTGTGCGTATGGACGCTC GAGGGGACGAGGCCGGGCGCTATGCCTTTCGACTTCAGCTTCCAGCGCCGCGGCGATGGAGAACTCATGAGGCAG CTGGGACTCGCCATGGTCAATCTGTGTTCCGTCGTACCCGACGGCGTCGTCGTCTTCTTCCCGAGCTACGGCTAC CTGGAGGAGGTGGTACGCGCATGGCAGCCGGGGATCTGGGAGCGTCTCCAGGCACGCAAGTCCGTCTTCCAGGAG ACGAGGGGCTGTTCCGGCGACGACGTGCTGCAGCAGTACTCTGAAGCCATCCTCAACGCCGAAACCAAGCGGGGT GCCCTCTTGCTCAGCGTCGTGGGCGGCAAGATGTCCGAAGGCATCAACTTCTCCGACCGGCTCGGACGGTGTGTC GTCATGGTCGGCATGCCGTACCCTAACTCTGCTTCACCGGAGTGGAAGGCCAAGATGGAATACATCGAGGCCACG GCCACCAGCTCCGGAGCGGACGCGAAGCAGGCAGCACGCGAATTCTACGACAACGCCTGCATGCGGGCCGTCAAC CAGAGCATCGGACGGGCAATCCGGCACCGTGGCGACTTCGCGGCTATCGTCCTGGCGGACCGACGCTACGCCTCC GTCCGGATCCGGGCTCGGTTGCCGGCGTGGATCCGTGGCGAGAAGGGGACCGAAGATGCGGCCAAGGCTGGTGGT ATGCTGAGTGGCTTGATGGGGGCTTTGGGGCAGTTCTTCCGCGGACGA |
Transcript | >Ophio5|1368 ATGGAAGCCGTCGATGATGCCGCCCGCCACCTGGAAGCCCTCGACTTTCACCATCCATATACGCCCTACCATGTC CAGGAGCAGCTCATGAAGACGGTCTATCAGGTACTGGAAACTGGAAATGGGCAGGTTGGCATTCTAGAGAGCCCC ACAGGCACGGGGAAATCGCTGTCCCTAATCTGCGCGTCGTTGACGTGGCTTCGCAACTACAAATCCAGAGAGCAG GACGCGGCGCTGGAAGCCGCGGGCGCCGCCTATCGAGACGAGCCGCCTTGGTTGGTCGAGCAGCTGATGCGTCGC AAAAGGGAAGAGCTCGCGCAGAGGTGGGAGGAGAGGGAGAACCGGCTGGAGGCCGCCAGACAGAAAGAGAAGGCC GCGGAGGAGCGGTCGAGGAAGCGGAAGCGTAGGGACGATGCTGCTGCGCCGCGTCCCGACGCAGAGGAAGACGAC GCAGAGTGGCTCCTCGACGACCGCCGAGAGACCGCCGGCGTCGGCTCTGGGGATGCGCTCTCGGGCTTGAGCAAG GAGTCTCGAGAATTGCTGGAGGGCCTCGGCCTTGGCGGACCCAAGAAAATGCGTGACGACCAGGAGGAGATGCCG GGAGAGGAAATCAAGATCTACTACACGTCGAGAACGCACTCGCAGCTGTCGCAATTCATCGCCGAGCTGCGCCGT CCCTCGTTTCCTTCCTCGCTGCCCGCTTCCATAGCAGAGGAGAGAGGGATGACGTCGGAAAGGGTAAAGCTGCTA CCTTTGTCGTCCCGTCAGCGGCTCTGCATCAACCCGTCCGTGGCCCGACTTGGCTCGACGCAAGCCATCAATGAT CGTTGCGCCGAGCTGCAGCAGGCCAAGTCCGGCAAGAAATGCGCCTACATGCCGAGCGAGGAACTGCGCAGCCAG ACTCACCAGTTCCGCGACGCCGCTCTGGCCGCGCTGCCGGACATTGAAGACCTGCACCGGCTGGGCAAGTCGCTG GCCGTGTGCCCTTATTACGCGTCCCGCACTGCGCTGCCGGCGGCTGAAATGGTGACGCTGCCGTATCCGCTGCTA CTGCAGAAGAAGGCGCGCGAGGCGCTGGGCATCAAGCTGGAGGGCAGTGTGGTGATTATCGACGAGGCGCACAAC ATCATGGATGCCGTGTCTAGCGTGCACGCGGCCGAGGTGAAGCTGAGTGAGCTCCGTAGGGCGAGGGGCATGCTG GCCGTCTATGTCAAGCGGTTCGGGAAGAGGCTCAGGGGCGAGAATCGAATCAACGTCGGGAGGCTGGGTCGCGTC ATCGACGGCTTGACGGAGTGGATGGAGACCGCTCAGAGCTTCAAGGAAGAGGCCGGTATCGTGGCCCCGAGCGAG CTGACGCGGCCCAAGGGCATCGACCTACTCGACATGTTTGGGCTGATTCAGTACATACAAGAGTCGAGGATGGCT TACAAGATCGAGGGCTATGCCGCTCAAGTCGTGGCGGGCGAGAAGCCAGGGCTGAGGCCGAGCTCGACGCCTGTG CTACACTCGCTGGTCTCCTTCCTGGCAGCCCTCACCAACACCAGCGACGAAGGCCGCTTCTTCTACCGAAAGACA GGCAGCAGCTCGCCCGACATGCAGGTGTCATACCTGCTGCTATCGCCGACGCACGCCTTCTCGTCCATTGTGGCC AGCGCCCGAGCGGTGATTCTGGCAGGGGGCACCATGTCGCCCTTTGACGACTACCGAAACCATCTGTTCCCGAAG CTCGCGGCGTCTAAATTGACGACGCTCAGCTGCGGCCACGTCGTGCCGGCAGAGAACCTGTGCGTATGGACGCTC GAGGGGACGAGGCCGGGCGCTATGCCTTTCGACTTCAGCTTCCAGCGCCGCGGCGATGGAGAACTCATGAGGCAG CTGGGACTCGCCATGGTCAATCTGTGTTCCGTCGTACCCGACGGCGTCGTCGTCTTCTTCCCGAGCTACGGCTAC CTGGAGGAGGTGGTACGCGCATGGCAGCCGGGGATCTGGGAGCGTCTCCAGGCACGCAAGTCCGTCTTCCAGGAG ACGAGGGGCTGTTCCGGCGACGACGTGCTGCAGCAGTACTCTGAAGCCATCCTCAACGCCGAAACCAAGCGGGGT GCCCTCTTGCTCAGCGTCGTGGGCGGCAAGATGTCCGAAGGCATCAACTTCTCCGACCGGCTCGGACGGTGTGTC GTCATGGTCGGCATGCCGTACCCTAACTCTGCTTCACCGGAGTGGAAGGCCAAGATGGAATACATCGAGGCCACG GCCACCAGCTCCGGAGCGGACGCGAAGCAGGCAGCACGCGAATTCTACGACAACGCCTGCATGCGGGCCGTCAAC CAGAGCATCGGACGGGCAATCCGGCACCGTGGCGACTTCGCGGCTATCGTCCTGGCGGACCGACGCTACGCCTCC GTCCGGATCCGGGCTCGGTTGCCGGCGTGGATCCGTGGCGAGAAGGGGACCGAAGATGCGGCCAAGGCTGGTGGT ATGCTGAGTGGCTTGATGGGGGCTTTGGGGCAGTTCTTCCGCGGACGATGA |
Gene | >Ophio5|1368 ATGGAAGCCGTCGATGATGCCGCCCGCCACCTGGAAGCCCTCGACTTTCACCATCCATATACGCCCTACCATGTC CAGGAGCAGCTCATGAAGACGGTCTATCAGGTACTGGAAACTGGAAATGGGCAGGTTGGCATTCTAGAGAGCCCC ACAGGCACGGTACATCTCGGCTCGCTTCTCGTCTGGCATTTGTCGCGTCTGCGAGCTGACTGACCGGTCGTCTCA GGGGAAATCGCTGTCCCTAATCTGCGCGTCGTTGACGTGGCTTCGCAACTACAAATCCAGAGAGCAGGACGCGGC GCTGGAAGCCGCGGGCGCCGCCTATCGAGACGAGCCGCCTTGGTTGGTCGAGCAGCTGATGCGTCGCAAAAGGGA AGAGCTCGCGCAGAGGTGGGAGGAGAGGGAGAACCGGCTGGAGGCCGCCAGACAGAAAGAGAAGGCCGCGGAGGA GCGGTCGAGGAAGCGGAAGCGTAGGGACGATGCTGCTGCGCCGCGTCCCGACGCAGAGGAAGACGACGCAGAGTG GCTCCTCGACGACCGCCGAGAGACCGCCGGCGTCGGCTCTGGGGATGCGCTCTCGGGCTTGAGCAAGGAGTCTCG AGAATTGCTGGAGGGCCTCGGCCTTGGCGGACCCAAGAAAATGCGTGACGACCAGGAGGAGATGCCGGGAGAGGA AATCAAGGTGCGAGGCGCAAAGCGAGCCATCGAAGCGCATGAGAGAGGAGATAGTGACGTCGGTAGATCTACTAC ACGTCGAGAACGCACTCGCAGCTGTCGCAATTCATCGCCGAGCTGCGCCGTCCCTCGTTTCCTTCCTCGCTGCCC GCTTCCATAGCAGAGGAGAGAGGGATGACGTCGGAAAGGGTAAAGCTGCTACCTTTGTCGTCCCGTCAGCGGCTC TGCATCAACCCGTCCGTGGCCCGACTTGGCTCGACGCAAGCCATCAATGATCGTTGCGCCGAGCTGCAGCAGGCC AAGTCCGGCAAGAAATGCGCCTACATGCCGAGCGAGGAACTGCGCAGCCAGACTCACCAGTTCCGCGACGCCGCT CTGGCCGCGCTGCCGGACATTGAAGACCTGCACCGGCTGGGCAAGTCGCTGGCCGTGTGCCCTTATTACGCGTCC CGCACTGCGCTGCCGGCGGCTGAAATGGTGACGCTGCCGTATCCGCTGCTACTGCAGAAGAAGGCGCGCGAGGCG CTGGGCATCAAGCTGGAGGGCAGTGTGGTGATTATCGACGAGGCGCACAACATCATGGATGCCGTGTCTAGCGTG CACGCGGCCGAGGTGAAGCTGAGTGAGCTCCGTAGGGCGAGGGGCATGCTGGCCGTCTATGTCAAGCGGTTCGGG AAGAGGCTCAGGGGCGAGAATCGAATCAACGTCGGGAGGCTGGGTCGCGTCATCGACGGCTTGACGGAGTGGATG GAGACCGCTCAGAGCTTCAAGGTAGGGCAGAGCTGTTCCACGGTCAAGGATAAGGCGTCGAACTGACTTGTCGGG CGCAGGAAGAGGCCGGTATCGTGGCCCCGAGCGAGCTGACGCGGCCCAAGGGCATCGACCTACTCGACATGTTTG GGCTGATTCAGTACATACAAGAGTCGAGGATGGCTTACAAGATCGAGGGCTATGCCGCTCAAGTCGTGGCGGGCG AGAAGCCAGGGCTGAGGCCGAGCTCGACGCCTGTGCTACACTCGCTGGTCTCCTTCCTGGCAGCCCTCACCAACA CCAGCGACGAAGGCCGCTTCTTCTACCGAAAGACAGGCAGCAGCTCGCCCGACATGCAGGTGTCATACCTGCTGC TATCGCCGACGCACGCCTTCTCGTCCATTGTGGCCAGCGCCCGAGCGGTGATTCTGGCAGGGGGCACCATGTCGC CCTTTGACGACTACCGAAACCATCTGTTCCCGAAGCTCGCGGCGTCTAAATTGACGACGCTCAGCTGCGGCCACG TCGTGCCGGCAGAGAACCTGTGCGTATGGACGCTCGAGGGGACGAGGCCGGGCGCTATGCCTTTCGACTTCAGCT TCCAGCGCCGCGGCGATGGAGAACTCATGAGGCAGCTGGGACTCGCCATGGTCAATCTGTGTTCCGTCGTACCCG ACGGCGTCGTCGTCTTCTTCCCGAGCTACGGCTACCTGGAGGAGGTGGTACGCGCATGGCAGCCGGGGATCTGGG AGCGTCTCCAGGCACGCAAGTCCGTCTTCCAGGAGACGAGGGGCTGTTCCGGCGACGACGTGCTGCAGCAGTACT CTGAAGCCATCCTCAACGCCGAAACCAAGCGGGGTGCCCTCTTGCTCAGCGTCGTGGGCGGCAAGATGTCCGAAG GCATCAACTTCTCCGACCGGCTCGGACGGTGTGTCGTCATGGTCGGCATGCCGTACCCTAACTCTGCTTCACCGG AGTGGAAGGCCAAGATGGAATACATCGAGGCCACGGCCACCAGCTCCGGAGCGGACGCGAAGCAGGCAGCACGCG AATTCTACGACAACGCCTGCATGCGGGCCGTCAACCAGAGCATCGGACGGGCAATCCGGCACCGTGGCGACTTCG CGGCTATCGTCCTGGCGGACCGACGCTACGCCTCCGTCCGGATCCGGGCTCGGTTGCCGGCGTGGATCCGTGGCG AGAAGGGGACCGAAGATGCGGCCAAGGCTGGTGGTATGCTGAGTGGCTTGATGGGGGCTTTGGGGCAGTTCTTCC GCGGACGATGA |