© 2022 - Robin Ohm - Utrecht University - The Netherlands
Built with Python Django and Wagtail
| Protein ID | Ophio5|6518 |
| Gene name | |
| Location | scaffold_574:9109..11925 |
| Strand | + |
| Gene length (bp) | 2816 |
| Transcript length (bp) | 2763 |
| Coding sequence length (bp) | 2760 |
| Protein length (aa) | 920 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF01055 | Glyco_hydro_31 | Glycosyl hydrolases family 31 | 3.5E-156 | 239 | 796 |
| PF16863 | NtCtMGAM_N | N-terminal barrel of NtMGAM and CtMGAM, maltase-glucoamylase | 1.5E-38 | 35 | 147 |
| PF13802 | Gal_mutarotas_2 | Galactose mutarotase-like | 3.4E-16 | 149 | 212 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q2UQV7|AGDC_ASPOR | Probable alpha/beta-glucosidase agdC OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=agdC PE=3 SV=1 | 21 | 894 | 0.0E+00 |
| sp|B8MZ41|AGDC_ASPFN | Probable alpha/beta-glucosidase agdC OS=Aspergillus flavus (strain ATCC 200026 / FGSC A1120 / NRRL 3357 / JCM 12722 / SRRC 167) GN=agdC PE=3 SV=1 | 21 | 894 | 0.0E+00 |
| sp|Q0CMA7|AGDC_ASPTN | Probable alpha/beta-glucosidase agdC OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=agdC PE=3 SV=1 | 15 | 880 | 0.0E+00 |
| sp|Q4WRH9|AGDC_ASPFU | Probable alpha/beta-glucosidase agdC OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=agdC PE=3 SV=1 | 21 | 880 | 0.0E+00 |
| sp|B0XNL6|AGDC_ASPFC | Probable alpha/beta-glucosidase agdC OS=Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) GN=agdC PE=3 SV=1 | 21 | 880 | 0.0E+00 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q2UQV7|AGDC_ASPOR | Probable alpha/beta-glucosidase agdC OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=agdC PE=3 SV=1 | 21 | 894 | 0.0E+00 |
| sp|B8MZ41|AGDC_ASPFN | Probable alpha/beta-glucosidase agdC OS=Aspergillus flavus (strain ATCC 200026 / FGSC A1120 / NRRL 3357 / JCM 12722 / SRRC 167) GN=agdC PE=3 SV=1 | 21 | 894 | 0.0E+00 |
| sp|Q0CMA7|AGDC_ASPTN | Probable alpha/beta-glucosidase agdC OS=Aspergillus terreus (strain NIH 2624 / FGSC A1156) GN=agdC PE=3 SV=1 | 15 | 880 | 0.0E+00 |
| sp|Q4WRH9|AGDC_ASPFU | Probable alpha/beta-glucosidase agdC OS=Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) GN=agdC PE=3 SV=1 | 21 | 880 | 0.0E+00 |
| sp|B0XNL6|AGDC_ASPFC | Probable alpha/beta-glucosidase agdC OS=Neosartorya fumigata (strain CEA10 / CBS 144.89 / FGSC A1163) GN=agdC PE=3 SV=1 | 21 | 880 | 0.0E+00 |
| sp|A1D1E6|AGDC_NEOFI | Probable alpha/beta-glucosidase agdC OS=Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / FGSC A1164 / NRRL 181) GN=agdC PE=3 SV=1 | 21 | 880 | 0.0E+00 |
| sp|A1CNK4|AGDC_ASPCL | Probable alpha/beta-glucosidase agdC OS=Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1) GN=agdC PE=3 SV=1 | 1 | 919 | 0.0E+00 |
| sp|Q5AWI5|AGDC_EMENI | Alpha/beta-glucosidase agdC OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=agdC PE=2 SV=2 | 18 | 880 | 0.0E+00 |
| sp|D4B0X3|AGD1_ARTBC | Probable alpha/beta-glucosidase ARB_02101 OS=Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) GN=ARB_02101 PE=1 SV=1 | 9 | 901 | 0.0E+00 |
| sp|Q9C0Y4|AGLU_SCHPO | Alpha-glucosidase OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=agl1 PE=1 SV=2 | 21 | 917 | 0.0E+00 |
| sp|O74254|AMYG_CANAL | Glucoamylase 1 OS=Candida albicans (strain SC5314 / ATCC MYA-2876) GN=GAM1 PE=1 SV=2 | 20 | 886 | 5.0E-177 |
| sp|Q92442|AGLU_MUCJA | Alpha-glucosidase OS=Mucor javanicus PE=1 SV=1 | 28 | 839 | 7.0E-173 |
| sp|Q9URX4|YFZB_SCHPO | Uncharacterized family 31 glucosidase C1039.11c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC1039.11c PE=3 SV=1 | 19 | 909 | 3.0E-171 |
| sp|Q09901|YAJ1_SCHPO | Uncharacterized family 31 glucosidase C30D11.01c OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=SPAC30D11.01c PE=3 SV=2 | 14 | 914 | 5.0E-169 |
| sp|P56526|AGLU_ASPNG | Alpha-glucosidase OS=Aspergillus niger GN=aglA PE=1 SV=1 | 14 | 907 | 3.0E-168 |
| sp|Q12558|AGLU_ASPOR | Alpha-glucosidase OS=Aspergillus oryzae (strain ATCC 42149 / RIB 40) GN=agdA PE=2 SV=1 | 14 | 920 | 8.0E-167 |
| sp|P22861|AMYG_SCHOC | Glucoamylase 1 OS=Schwanniomyces occidentalis GN=GAM1 PE=1 SV=1 | 9 | 896 | 2.0E-162 |
| sp|Q9S7Y7|XYL1_ARATH | Alpha-xylosidase 1 OS=Arabidopsis thaliana GN=XYL1 PE=1 SV=1 | 33 | 836 | 2.0E-137 |
| sp|P29064|AGLU_CANTS | Alpha-glucosidase OS=Candida tsukubaensis PE=1 SV=1 | 21 | 847 | 7.0E-137 |
| sp|Q653V7|AGLU_ORYSJ | Probable alpha-glucosidase Os06g0675700 OS=Oryza sativa subsp. japonica GN=Os06g0675700 PE=1 SV=1 | 53 | 435 | 3.0E-98 |
| sp|O04893|AGLU_SPIOL | Alpha-glucosidase OS=Spinacia oleracea PE=1 SV=1 | 22 | 430 | 5.0E-90 |
| sp|O04931|AGLU_BETVU | Alpha-glucosidase OS=Beta vulgaris PE=1 SV=1 | 32 | 430 | 1.0E-88 |
| sp|Q43763|AGLU_HORVU | Alpha-glucosidase OS=Hordeum vulgare PE=2 SV=1 | 53 | 435 | 9.0E-88 |
| sp|P70699|LYAG_MOUSE | Lysosomal alpha-glucosidase OS=Mus musculus GN=Gaa PE=1 SV=2 | 24 | 423 | 3.0E-79 |
| sp|F4J6T7|XYL2_ARATH | Putative alpha-xylosidase 2 OS=Arabidopsis thaliana GN=XYL2 PE=5 SV=1 | 43 | 424 | 4.0E-78 |
| sp|P10253|LYAG_HUMAN | Lysosomal alpha-glucosidase OS=Homo sapiens GN=GAA PE=1 SV=4 | 50 | 423 | 6.0E-77 |
| sp|Q6P7A9|LYAG_RAT | Lysosomal alpha-glucosidase OS=Rattus norvegicus GN=Gaa PE=2 SV=1 | 24 | 423 | 1.0E-76 |
| sp|Q5R7A9|LYAG_PONAB | Lysosomal alpha-glucosidase OS=Pongo abelii GN=GAA PE=2 SV=1 | 50 | 423 | 1.0E-75 |
| sp|Q9MYM4|LYAG_BOVIN | Lysosomal alpha-glucosidase OS=Bos taurus GN=GAA PE=2 SV=1 | 50 | 423 | 3.0E-74 |
| sp|Q653V7|AGLU_ORYSJ | Probable alpha-glucosidase Os06g0675700 OS=Oryza sativa subsp. japonica GN=Os06g0675700 PE=1 SV=1 | 517 | 837 | 7.0E-69 |
| sp|O62653|SUIS_SUNMU | Sucrase-isomaltase, intestinal OS=Suncus murinus GN=SI PE=2 SV=3 | 22 | 423 | 5.0E-66 |
| sp|Q43763|AGLU_HORVU | Alpha-glucosidase OS=Hordeum vulgare PE=2 SV=1 | 532 | 852 | 7.0E-66 |
| sp|P07768|SUIS_RABIT | Sucrase-isomaltase, intestinal OS=Oryctolagus cuniculus GN=SI PE=1 SV=3 | 22 | 423 | 1.0E-65 |
| sp|O43451|MGA_HUMAN | Maltase-glucoamylase, intestinal OS=Homo sapiens GN=MGAM PE=1 SV=5 | 22 | 423 | 6.0E-65 |
| sp|O04893|AGLU_SPIOL | Alpha-glucosidase OS=Spinacia oleracea PE=1 SV=1 | 538 | 838 | 1.0E-62 |
| sp|P23739|SUIS_RAT | Sucrase-isomaltase, intestinal OS=Rattus norvegicus GN=Si PE=1 SV=5 | 22 | 423 | 1.0E-60 |
| sp|P14410|SUIS_HUMAN | Sucrase-isomaltase, intestinal OS=Homo sapiens GN=SI PE=1 SV=6 | 22 | 423 | 2.0E-59 |
| sp|Q2M2H8|MGAL_HUMAN | Probable maltase-glucoamylase 2 OS=Homo sapiens GN=MGAM2 PE=2 SV=3 | 23 | 425 | 7.0E-58 |
| sp|Q6P7A9|LYAG_RAT | Lysosomal alpha-glucosidase OS=Rattus norvegicus GN=Gaa PE=2 SV=1 | 504 | 885 | 3.0E-57 |
| sp|P23739|SUIS_RAT | Sucrase-isomaltase, intestinal OS=Rattus norvegicus GN=Si PE=1 SV=5 | 24 | 450 | 3.0E-57 |
| sp|P70699|LYAG_MOUSE | Lysosomal alpha-glucosidase OS=Mus musculus GN=Gaa PE=1 SV=2 | 536 | 885 | 4.0E-57 |
| sp|Q2M2H8|MGAL_HUMAN | Probable maltase-glucoamylase 2 OS=Homo sapiens GN=MGAM2 PE=2 SV=3 | 19 | 423 | 6.0E-57 |
| sp|O04931|AGLU_BETVU | Alpha-glucosidase OS=Beta vulgaris PE=1 SV=1 | 517 | 892 | 8.0E-57 |
| sp|P07768|SUIS_RABIT | Sucrase-isomaltase, intestinal OS=Oryctolagus cuniculus GN=SI PE=1 SV=3 | 24 | 423 | 1.0E-56 |
| sp|O43451|MGA_HUMAN | Maltase-glucoamylase, intestinal OS=Homo sapiens GN=MGAM PE=1 SV=5 | 9 | 423 | 1.0E-56 |
| sp|O43451|MGA_HUMAN | Maltase-glucoamylase, intestinal OS=Homo sapiens GN=MGAM PE=1 SV=5 | 556 | 899 | 2.0E-56 |
| sp|P07768|SUIS_RABIT | Sucrase-isomaltase, intestinal OS=Oryctolagus cuniculus GN=SI PE=1 SV=3 | 504 | 880 | 5.0E-56 |
| sp|P14410|SUIS_HUMAN | Sucrase-isomaltase, intestinal OS=Homo sapiens GN=SI PE=1 SV=6 | 550 | 919 | 6.0E-56 |
| sp|Q9MYM4|LYAG_BOVIN | Lysosomal alpha-glucosidase OS=Bos taurus GN=GAA PE=2 SV=1 | 504 | 886 | 2.0E-55 |
| sp|P14410|SUIS_HUMAN | Sucrase-isomaltase, intestinal OS=Homo sapiens GN=SI PE=1 SV=6 | 22 | 423 | 2.0E-55 |
| sp|P23739|SUIS_RAT | Sucrase-isomaltase, intestinal OS=Rattus norvegicus GN=Si PE=1 SV=5 | 556 | 880 | 7.0E-55 |
| sp|P07768|SUIS_RABIT | Sucrase-isomaltase, intestinal OS=Oryctolagus cuniculus GN=SI PE=1 SV=3 | 537 | 839 | 3.0E-54 |
| sp|Q5R7A9|LYAG_PONAB | Lysosomal alpha-glucosidase OS=Pongo abelii GN=GAA PE=2 SV=1 | 504 | 886 | 3.0E-53 |
| sp|P10253|LYAG_HUMAN | Lysosomal alpha-glucosidase OS=Homo sapiens GN=GAA PE=1 SV=4 | 549 | 886 | 6.0E-53 |
| sp|Q2M2H8|MGAL_HUMAN | Probable maltase-glucoamylase 2 OS=Homo sapiens GN=MGAM2 PE=2 SV=3 | 541 | 907 | 1.0E-52 |
| sp|O43451|MGA_HUMAN | Maltase-glucoamylase, intestinal OS=Homo sapiens GN=MGAM PE=1 SV=5 | 508 | 889 | 2.0E-52 |
| sp|P14410|SUIS_HUMAN | Sucrase-isomaltase, intestinal OS=Homo sapiens GN=SI PE=1 SV=6 | 537 | 912 | 2.0E-52 |
| sp|O62653|SUIS_SUNMU | Sucrase-isomaltase, intestinal OS=Suncus murinus GN=SI PE=2 SV=3 | 37 | 423 | 4.0E-51 |
| sp|O62653|SUIS_SUNMU | Sucrase-isomaltase, intestinal OS=Suncus murinus GN=SI PE=2 SV=3 | 537 | 850 | 2.0E-49 |
| sp|Q2M2H8|MGAL_HUMAN | Probable maltase-glucoamylase 2 OS=Homo sapiens GN=MGAM2 PE=2 SV=3 | 556 | 839 | 1.0E-48 |
| sp|F4J6T7|XYL2_ARATH | Putative alpha-xylosidase 2 OS=Arabidopsis thaliana GN=XYL2 PE=5 SV=1 | 535 | 836 | 6.0E-48 |
| sp|O62653|SUIS_SUNMU | Sucrase-isomaltase, intestinal OS=Suncus murinus GN=SI PE=2 SV=3 | 504 | 884 | 9.0E-46 |
| sp|Q8BHN3|GANAB_MOUSE | Neutral alpha-glucosidase AB OS=Mus musculus GN=Ganab PE=1 SV=1 | 542 | 911 | 1.0E-43 |
| sp|Q8BVW0|GANC_MOUSE | Neutral alpha-glucosidase C OS=Mus musculus GN=Ganc PE=1 SV=2 | 542 | 887 | 2.0E-43 |
| sp|Q9US55|GLU2A_SCHPO | Glucosidase 2 subunit alpha OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=gls2 PE=3 SV=1 | 542 | 917 | 2.0E-42 |
| sp|Q14697|GANAB_HUMAN | Neutral alpha-glucosidase AB OS=Homo sapiens GN=GANAB PE=1 SV=3 | 542 | 909 | 2.0E-42 |
| sp|B9F676|GLU2A_ORYSJ | Probable glucan 1,3-alpha-glucosidase OS=Oryza sativa subsp. japonica GN=Os03g0216600 PE=3 SV=1 | 517 | 911 | 7.0E-42 |
| sp|P79403|GANAB_PIG | Neutral alpha-glucosidase AB OS=Sus scrofa GN=GANAB PE=1 SV=1 | 542 | 911 | 2.0E-41 |
| sp|Q9F234|AGL2_BACTQ | Alpha-glucosidase 2 OS=Bacillus thermoamyloliquefaciens PE=3 SV=1 | 150 | 422 | 2.0E-41 |
| sp|Q8TET4|GANC_HUMAN | Neutral alpha-glucosidase C OS=Homo sapiens GN=GANC PE=2 SV=3 | 540 | 898 | 3.0E-41 |
| sp|Q4R4N7|GANAB_MACFA | Neutral alpha-glucosidase AB OS=Macaca fascicularis GN=GANAB PE=2 SV=1 | 542 | 909 | 5.0E-41 |
| sp|Q94502|GANAB_DICDI | Neutral alpha-glucosidase AB OS=Dictyostelium discoideum GN=modA PE=3 SV=1 | 542 | 887 | 1.0E-40 |
| sp|Q9BE70|GANC_MACFA | Neutral alpha-glucosidase C (Fragment) OS=Macaca fascicularis GN=GANC PE=2 SV=2 | 540 | 898 | 9.0E-40 |
| sp|Q9FN05|PSL5_ARATH | Probable glucan 1,3-alpha-glucosidase OS=Arabidopsis thaliana GN=PSL5 PE=1 SV=1 | 542 | 891 | 5.0E-39 |
| sp|P23739|SUIS_RAT | Sucrase-isomaltase, intestinal OS=Rattus norvegicus GN=Si PE=1 SV=5 | 553 | 860 | 2.0E-38 |
| sp|O00906|AGLU_TETPY | Lysosomal acid alpha-glucosidase OS=Tetrahymena pyriformis PE=1 SV=1 | 556 | 826 | 4.0E-38 |
| sp|P38138|GLU2A_YEAST | Glucosidase 2 subunit alpha OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ROT2 PE=1 SV=1 | 542 | 837 | 1.0E-37 |
| sp|O00906|AGLU_TETPY | Lysosomal acid alpha-glucosidase OS=Tetrahymena pyriformis PE=1 SV=1 | 67 | 423 | 3.0E-37 |
| sp|Q8BVW0|GANC_MOUSE | Neutral alpha-glucosidase C OS=Mus musculus GN=Ganc PE=1 SV=2 | 150 | 422 | 2.0E-34 |
| sp|Q8BHN3|GANAB_MOUSE | Neutral alpha-glucosidase AB OS=Mus musculus GN=Ganab PE=1 SV=1 | 119 | 422 | 1.0E-33 |
| sp|P79403|GANAB_PIG | Neutral alpha-glucosidase AB OS=Sus scrofa GN=GANAB PE=1 SV=1 | 119 | 422 | 1.0E-33 |
| sp|Q9F234|AGL2_BACTQ | Alpha-glucosidase 2 OS=Bacillus thermoamyloliquefaciens PE=3 SV=1 | 518 | 838 | 2.0E-33 |
| sp|Q8TET4|GANC_HUMAN | Neutral alpha-glucosidase C OS=Homo sapiens GN=GANC PE=2 SV=3 | 150 | 422 | 2.0E-33 |
| sp|Q9BE70|GANC_MACFA | Neutral alpha-glucosidase C (Fragment) OS=Macaca fascicularis GN=GANC PE=2 SV=2 | 150 | 422 | 4.0E-33 |
| sp|Q14697|GANAB_HUMAN | Neutral alpha-glucosidase AB OS=Homo sapiens GN=GANAB PE=1 SV=3 | 119 | 422 | 3.0E-31 |
| sp|Q4R4N7|GANAB_MACFA | Neutral alpha-glucosidase AB OS=Macaca fascicularis GN=GANAB PE=2 SV=1 | 119 | 422 | 3.0E-31 |
| sp|B9F676|GLU2A_ORYSJ | Probable glucan 1,3-alpha-glucosidase OS=Oryza sativa subsp. japonica GN=Os03g0216600 PE=3 SV=1 | 12 | 422 | 9.0E-31 |
| sp|Q9FN05|PSL5_ARATH | Probable glucan 1,3-alpha-glucosidase OS=Arabidopsis thaliana GN=PSL5 PE=1 SV=1 | 137 | 422 | 4.0E-29 |
| sp|D0KQM8|AGLU_SULS9 | Alpha-glucosidase OS=Sulfolobus solfataricus (strain 98/2) GN=malA PE=1 SV=1 | 110 | 423 | 3.0E-28 |
| sp|P0CD66|AGLU_SULSO | Alpha-glucosidase OS=Sulfolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) GN=malA PE=1 SV=1 | 110 | 423 | 3.0E-28 |
| sp|Q94502|GANAB_DICDI | Neutral alpha-glucosidase AB OS=Dictyostelium discoideum GN=modA PE=3 SV=1 | 150 | 422 | 8.0E-27 |
| sp|B3PEE6|OL4AG_CELJU | Oligosaccharide 4-alpha-D-glucosyltransferase OS=Cellvibrio japonicus (strain Ueda107) GN=agd31B PE=1 SV=1 | 558 | 858 | 5.0E-26 |
| sp|Q9US55|GLU2A_SCHPO | Glucosidase 2 subunit alpha OS=Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN=gls2 PE=3 SV=1 | 151 | 422 | 4.0E-25 |
| sp|P38138|GLU2A_YEAST | Glucosidase 2 subunit alpha OS=Saccharomyces cerevisiae (strain ATCC 204508 / S288c) GN=ROT2 PE=1 SV=1 | 151 | 422 | 7.0E-24 |
| sp|D0KQM8|AGLU_SULS9 | Alpha-glucosidase OS=Sulfolobus solfataricus (strain 98/2) GN=malA PE=1 SV=1 | 540 | 797 | 7.0E-20 |
| sp|P0CD66|AGLU_SULSO | Alpha-glucosidase OS=Sulfolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) GN=malA PE=1 SV=1 | 540 | 797 | 7.0E-20 |
| sp|Q5AW25|AGDD_EMENI | Alpha-xylosidase OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=agdD PE=1 SV=1 | 529 | 797 | 4.0E-17 |
| sp|Q9P999|XYLS_SULSO | Alpha-xylosidase OS=Sulfolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) GN=xylS PE=1 SV=1 | 556 | 835 | 1.0E-15 |
| sp|P31434|XYLS_ECOLI | Alpha-xylosidase OS=Escherichia coli (strain K12) GN=yicI PE=1 SV=2 | 93 | 422 | 4.0E-14 |
| sp|A7LXT0|GH31A_BACO1 | Alpha-xylosidase BoGH31A OS=Bacteroides ovatus (strain ATCC 8483 / DSM 1896 / JCM 5824 / NCTC 11153) GN=BACOVA_02646 PE=1 SV=1 | 560 | 835 | 9.0E-13 |
| sp|P32138|YIHQ_ECOLI | Alpha-glucosidase YihQ OS=Escherichia coli (strain K12) GN=yihQ PE=1 SV=3 | 545 | 758 | 3.0E-11 |
| sp|P31434|XYLS_ECOLI | Alpha-xylosidase OS=Escherichia coli (strain K12) GN=yicI PE=1 SV=2 | 543 | 796 | 3.0E-10 |
| sp|Q01336|YCR2_ESCVU | Uncharacterized family 31 glucosidase ORF2 (Fragment) OS=Escherichia vulneris PE=3 SV=1 | 194 | 422 | 4.0E-10 |
| sp|Q9P999|XYLS_SULSO | Alpha-xylosidase OS=Sulfolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) GN=xylS PE=1 SV=1 | 151 | 425 | 2.0E-08 |
| sp|Q5AW25|AGDD_EMENI | Alpha-xylosidase OS=Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN=agdD PE=1 SV=1 | 151 | 420 | 5.0E-07 |
| sp|A7LXT0|GH31A_BACO1 | Alpha-xylosidase BoGH31A OS=Bacteroides ovatus (strain ATCC 8483 / DSM 1896 / JCM 5824 / NCTC 11153) GN=BACOVA_02646 PE=1 SV=1 | 170 | 426 | 3.0E-06 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0004553 | hydrolase activity, hydrolyzing O-glycosyl compounds | Yes |
| GO:0005975 | carbohydrate metabolic process | Yes |
| GO:0016787 | hydrolase activity | No |
| GO:0071704 | organic substance metabolic process | No |
| GO:0044238 | primary metabolic process | No |
| GO:0003824 | catalytic activity | No |
| GO:0008150 | biological_process | No |
| GO:0003674 | molecular_function | No |
| GO:0008152 | metabolic process | No |
| GO:0016798 | hydrolase activity, acting on glycosyl bonds | No |
| SignalP signal predicted | Location (based on Ymax) |
D score (significance: > 0.45) |
|---|---|---|
| Yes | 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 | >Ophio5|6518 MRLWSPFFLFATAAAHGLDACHGYEASHVLHTDSGLTASLRLVGEPCNVYGTDLDDLTLQVTHETDDRLHVKIQD RANQVYQVPESVFPRPGGRSSARSSKLKFKYITSPFSFQVLRAGSNEVLFDSSAASLVFQSQYLRLRTALPKDPY LYGLGEHSDPLRLKTSNYIRTLWNADSYGVSGDTNLYGSHPFYLEQRQTGSHGVFLLNSNGMDVIINSTHDGEQY LEYNTLGGVLDFWFFSGPSPIAVAQQYGQVTGLPAMQPYWGLGFHQCRYGYRDAYDVAEVVHNYSLAKIPLETMW TDIDYMDRRRTFTLDPERFPLGMMRQLVSHLHDHDQRYVVMVDPAVAYQDYPPLRQGVEDDVFLRRDNGSLWLGV VWPGVTVFPDWFASKAQEYWNGQFDSFFNASEGVDIDALWIDMNEPSNTMCPWPCDKPYESAKGMPPPPPPVRQP PRPLPGWPCDFQPQGTCKSERAGAHGMEAAMVPLTVLTPDTEGAPVPRPVGTLGDAKGLPDRNFLYPKYAIHNKM ASHDSWNSDRGGLSNRTVHTDVHHQNGLVMYDTHNLFGSMMSSASREAMLARRPDKRPLIITRSTYAGAGSKVGH WLGDNKSTWDMYRNSIRSMLAFTALFQFSMVGADVCGFGGDTTEELCARWASLGAFATFYRNHNVEGTLSQEFYR WESVTDSARKAIAIRYRLLDYMYTAMRASSADGRPAIQPVFYLYPHDRSTWPLELQYFYGPALLVAPVTEQGATS VRVYLPDDVFYDWYSHKPILGEAAEHTFVNQDMTAIPLLIRGGNVLPARLHSTMTTTELRRQEFELLVALDAQGE ATGELYLDDGEAIDPTHDHTLVSFHYSHRERLLSARGVFDCPGTAPRVVKVTVLGAGQRPKAGIREHGSADGSSM YSESHEVDLRLDGSRTVHVG |
| Coding | >Ophio5|6518 ATGAGGCTCTGGAGTCCATTCTTCTTGTTCGCCACCGCGGCCGCCCACGGTCTTGATGCCTGCCACGGCTACGAG GCTTCCCATGTGCTGCATACAGACAGCGGCTTGACGGCCAGTCTGAGGCTCGTGGGTGAACCTTGCAACGTGTAC GGCACCGACCTGGATGACCTCACCCTCCAAGTCACGCATGAGACAGACGACCGCCTTCACGTCAAGATCCAAGAC CGCGCCAATCAGGTCTACCAGGTTCCCGAGTCCGTCTTCCCGCGTCCAGGTGGCCGCAGCTCTGCGCGTAGTAGC AAGCTCAAGTTCAAGTACATCACGTCGCCATTTTCCTTCCAGGTCCTCCGTGCCGGCTCCAATGAGGTGCTCTTT GACTCGTCGGCAGCATCACTCGTGTTCCAGTCACAGTACCTGCGCTTGCGAACCGCCCTCCCTAAGGATCCGTAT CTGTACGGGCTCGGGGAGCATTCAGATCCGTTGCGGCTGAAGACCAGTAACTATATCCGGACCCTGTGGAACGCC GACAGCTACGGCGTGTCCGGCGACACCAACTTGTACGGATCTCACCCCTTTTATCTCGAGCAGCGCCAGACGGGC TCCCATGGCGTCTTCCTGCTCAACTCCAACGGCATGGACGTCATCATCAACTCGACGCACGATGGAGAGCAGTAC CTTGAGTACAACACCCTCGGCGGCGTCCTGGACTTTTGGTTCTTCTCCGGCCCGAGCCCCATCGCCGTCGCCCAG CAGTACGGCCAGGTGACGGGCTTGCCTGCCATGCAGCCGTACTGGGGGCTGGGCTTTCACCAGTGCCGCTATGGC TACCGCGATGCCTATGACGTGGCCGAGGTGGTGCACAACTACAGCCTGGCCAAGATTCCGCTCGAGACCATGTGG ACCGACATCGACTACATGGACCGTCGGCGCACCTTTACCCTCGACCCCGAACGTTTCCCCCTCGGCATGATGCGG CAGCTCGTCTCTCACTTGCATGACCATGACCAGCGCTACGTCGTCATGGTCGATCCGGCCGTGGCCTACCAGGAC TACCCTCCGCTGCGGCAGGGCGTCGAGGACGATGTCTTTCTTCGGCGCGACAACGGCTCTCTGTGGCTGGGCGTC GTGTGGCCCGGCGTGACCGTGTTCCCGGACTGGTTTGCCAGCAAGGCGCAGGAATACTGGAACGGCCAGTTCGAC TCCTTCTTCAACGCCTCCGAGGGCGTTGACATTGACGCTCTTTGGATCGACATGAATGAGCCGAGCAACACCATG TGCCCCTGGCCTTGCGACAAGCCGTATGAGTCGGCCAAGGGGATGCCTCCGCCGCCTCCTCCGGTGCGTCAGCCG CCGCGGCCGCTGCCTGGCTGGCCGTGTGACTTCCAGCCGCAGGGCACGTGCAAGTCCGAGAGGGCCGGAGCGCAC GGGATGGAGGCGGCCATGGTGCCGTTGACGGTACTGACGCCGGACACTGAAGGCGCTCCGGTGCCACGCCCTGTC GGTACTCTCGGCGACGCCAAAGGCCTCCCCGATCGGAACTTTCTGTATCCAAAATACGCCATTCACAACAAGATG GCCTCGCACGACTCGTGGAACTCGGACCGCGGTGGCCTCTCGAACCGCACCGTCCACACCGACGTTCACCACCAG AACGGGCTCGTCATGTACGATACTCACAACCTGTTTGGGTCCATGATGTCGTCGGCATCGCGAGAAGCCATGCTG GCGCGCCGGCCGGACAAGCGCCCGCTCATCATCACGCGCAGCACCTATGCCGGCGCAGGGTCCAAGGTCGGCCAC TGGCTGGGCGACAACAAGTCGACCTGGGACATGTACCGCAACTCGATCCGCTCCATGCTGGCCTTTACCGCCCTC TTCCAGTTCTCCATGGTGGGCGCCGATGTGTGCGGCTTCGGCGGCGATACGACCGAGGAGCTGTGCGCCCGATGG GCATCGCTAGGCGCCTTTGCCACCTTTTACCGCAACCACAACGTGGAGGGGACGCTATCGCAAGAGTTCTATCGC TGGGAGAGCGTCACAGACAGCGCTCGCAAGGCCATTGCCATCCGCTACCGCCTGCTCGACTACATGTACACGGCC ATGCGCGCCTCCAGCGCCGACGGCCGGCCCGCCATCCAGCCCGTCTTCTACCTCTACCCGCACGACCGGAGCACC TGGCCGCTCGAGCTGCAGTACTTTTACGGCCCGGCCCTTCTGGTGGCGCCCGTGACGGAGCAGGGCGCGACGAGC GTACGCGTCTACCTCCCGGACGACGTCTTCTACGACTGGTACTCGCACAAGCCCATCCTCGGGGAGGCCGCCGAG CACACGTTTGTCAACCAGGACATGACGGCTATCCCTCTCCTCATCCGCGGCGGAAACGTCCTCCCCGCGCGTCTT CACTCGACCATGACGACGACGGAGCTGCGCCGCCAAGAGTTTGAGCTACTCGTCGCCCTCGACGCCCAAGGCGAG GCGACGGGAGAGCTATACCTCGACGACGGGGAGGCCATCGATCCGACACATGATCACACTCTCGTGTCTTTTCAC TATAGCCACCGCGAGCGCCTCCTCTCGGCCCGTGGCGTCTTCGACTGTCCCGGCACCGCGCCCCGTGTCGTCAAG GTCACCGTCTTGGGCGCCGGCCAGCGGCCCAAGGCGGGCATTCGTGAACATGGTAGCGCCGACGGGTCGAGCATG TATAGCGAGAGCCATGAGGTTGATTTGCGGCTGGATGGGTCGCGTACCGTTCACGTAGGT |
| Transcript | >Ophio5|6518 ATGAGGCTCTGGAGTCCATTCTTCTTGTTCGCCACCGCGGCCGCCCACGGTCTTGATGCCTGCCACGGCTACGAG GCTTCCCATGTGCTGCATACAGACAGCGGCTTGACGGCCAGTCTGAGGCTCGTGGGTGAACCTTGCAACGTGTAC GGCACCGACCTGGATGACCTCACCCTCCAAGTCACGCATGAGACAGACGACCGCCTTCACGTCAAGATCCAAGAC CGCGCCAATCAGGTCTACCAGGTTCCCGAGTCCGTCTTCCCGCGTCCAGGTGGCCGCAGCTCTGCGCGTAGTAGC AAGCTCAAGTTCAAGTACATCACGTCGCCATTTTCCTTCCAGGTCCTCCGTGCCGGCTCCAATGAGGTGCTCTTT GACTCGTCGGCAGCATCACTCGTGTTCCAGTCACAGTACCTGCGCTTGCGAACCGCCCTCCCTAAGGATCCGTAT CTGTACGGGCTCGGGGAGCATTCAGATCCGTTGCGGCTGAAGACCAGTAACTATATCCGGACCCTGTGGAACGCC GACAGCTACGGCGTGTCCGGCGACACCAACTTGTACGGATCTCACCCCTTTTATCTCGAGCAGCGCCAGACGGGC TCCCATGGCGTCTTCCTGCTCAACTCCAACGGCATGGACGTCATCATCAACTCGACGCACGATGGAGAGCAGTAC CTTGAGTACAACACCCTCGGCGGCGTCCTGGACTTTTGGTTCTTCTCCGGCCCGAGCCCCATCGCCGTCGCCCAG CAGTACGGCCAGGTGACGGGCTTGCCTGCCATGCAGCCGTACTGGGGGCTGGGCTTTCACCAGTGCCGCTATGGC TACCGCGATGCCTATGACGTGGCCGAGGTGGTGCACAACTACAGCCTGGCCAAGATTCCGCTCGAGACCATGTGG ACCGACATCGACTACATGGACCGTCGGCGCACCTTTACCCTCGACCCCGAACGTTTCCCCCTCGGCATGATGCGG CAGCTCGTCTCTCACTTGCATGACCATGACCAGCGCTACGTCGTCATGGTCGATCCGGCCGTGGCCTACCAGGAC TACCCTCCGCTGCGGCAGGGCGTCGAGGACGATGTCTTTCTTCGGCGCGACAACGGCTCTCTGTGGCTGGGCGTC GTGTGGCCCGGCGTGACCGTGTTCCCGGACTGGTTTGCCAGCAAGGCGCAGGAATACTGGAACGGCCAGTTCGAC TCCTTCTTCAACGCCTCCGAGGGCGTTGACATTGACGCTCTTTGGATCGACATGAATGAGCCGAGCAACACCATG TGCCCCTGGCCTTGCGACAAGCCGTATGAGTCGGCCAAGGGGATGCCTCCGCCGCCTCCTCCGGTGCGTCAGCCG CCGCGGCCGCTGCCTGGCTGGCCGTGTGACTTCCAGCCGCAGGGCACGTGCAAGTCCGAGAGGGCCGGAGCGCAC GGGATGGAGGCGGCCATGGTGCCGTTGACGGTACTGACGCCGGACACTGAAGGCGCTCCGGTGCCACGCCCTGTC GGTACTCTCGGCGACGCCAAAGGCCTCCCCGATCGGAACTTTCTGTATCCAAAATACGCCATTCACAACAAGATG GCCTCGCACGACTCGTGGAACTCGGACCGCGGTGGCCTCTCGAACCGCACCGTCCACACCGACGTTCACCACCAG AACGGGCTCGTCATGTACGATACTCACAACCTGTTTGGGTCCATGATGTCGTCGGCATCGCGAGAAGCCATGCTG GCGCGCCGGCCGGACAAGCGCCCGCTCATCATCACGCGCAGCACCTATGCCGGCGCAGGGTCCAAGGTCGGCCAC TGGCTGGGCGACAACAAGTCGACCTGGGACATGTACCGCAACTCGATCCGCTCCATGCTGGCCTTTACCGCCCTC TTCCAGTTCTCCATGGTGGGCGCCGATGTGTGCGGCTTCGGCGGCGATACGACCGAGGAGCTGTGCGCCCGATGG GCATCGCTAGGCGCCTTTGCCACCTTTTACCGCAACCACAACGTGGAGGGGACGCTATCGCAAGAGTTCTATCGC TGGGAGAGCGTCACAGACAGCGCTCGCAAGGCCATTGCCATCCGCTACCGCCTGCTCGACTACATGTACACGGCC ATGCGCGCCTCCAGCGCCGACGGCCGGCCCGCCATCCAGCCCGTCTTCTACCTCTACCCGCACGACCGGAGCACC TGGCCGCTCGAGCTGCAGTACTTTTACGGCCCGGCCCTTCTGGTGGCGCCCGTGACGGAGCAGGGCGCGACGAGC GTACGCGTCTACCTCCCGGACGACGTCTTCTACGACTGGTACTCGCACAAGCCCATCCTCGGGGAGGCCGCCGAG CACACGTTTGTCAACCAGGACATGACGGCTATCCCTCTCCTCATCCGCGGCGGAAACGTCCTCCCCGCGCGTCTT CACTCGACCATGACGACGACGGAGCTGCGCCGCCAAGAGTTTGAGCTACTCGTCGCCCTCGACGCCCAAGGCGAG GCGACGGGAGAGCTATACCTCGACGACGGGGAGGCCATCGATCCGACACATGATCACACTCTCGTGTCTTTTCAC TATAGCCACCGCGAGCGCCTCCTCTCGGCCCGTGGCGTCTTCGACTGTCCCGGCACCGCGCCCCGTGTCGTCAAG GTCACCGTCTTGGGCGCCGGCCAGCGGCCCAAGGCGGGCATTCGTGAACATGGTAGCGCCGACGGGTCGAGCATG TATAGCGAGAGCCATGAGGTTGATTTGCGGCTGGATGGGTCGCGTACCGTTCACGTAGGTTGA |
| Gene | >Ophio5|6518 ATGAGGCTCTGGAGTCCATTCTTCTTGTTCGCCACCGCGGCCGCCCACGGTCTTGATGCCTGCCACGGCTACGAG GCTTCCCATGTGCTGCATACAGACAGCGGCTTGACGGCCAGTCTGAGGCTCGTGGGTGAACCTTGCAACGTGTAC GGCACCGACCTGGATGACCTCACCCTCCAAGTCACGCATGAGACAGGTGTGTAACTTGTGATGAGCTCAGAGTTC CGTACATGGCTGACGGCTCATCAGACGACCGCCTTCACGTCAAGATCCAAGACCGCGCCAATCAGGTCTACCAGG TTCCCGAGTCCGTCTTCCCGCGTCCAGGTGGCCGCAGCTCTGCGCGTAGTAGCAAGCTCAAGTTCAAGTACATCA CGTCGCCATTTTCCTTCCAGGTCCTCCGTGCCGGCTCCAATGAGGTGCTCTTTGACTCGTCGGCAGCATCACTCG TGTTCCAGTCACAGTACCTGCGCTTGCGAACCGCCCTCCCTAAGGATCCGTATCTGTACGGGCTCGGGGAGCATT CAGATCCGTTGCGGCTGAAGACCAGTAACTATATCCGGACCCTGTGGAACGCCGACAGCTACGGCGTGTCCGGCG ACACCAACTTGTACGGATCTCACCCCTTTTATCTCGAGCAGCGCCAGACGGGCTCCCATGGCGTCTTCCTGCTCA ACTCCAACGGCATGGACGTCATCATCAACTCGACGCACGATGGAGAGCAGTACCTTGAGTACAACACCCTCGGCG GCGTCCTGGACTTTTGGTTCTTCTCCGGCCCGAGCCCCATCGCCGTCGCCCAGCAGTACGGCCAGGTGACGGGCT TGCCTGCCATGCAGCCGTACTGGGGGCTGGGCTTTCACCAGTGCCGCTATGGCTACCGCGATGCCTATGACGTGG CCGAGGTGGTGCACAACTACAGCCTGGCCAAGATTCCGCTCGAGACCATGTGGACCGACATCGACTACATGGACC GTCGGCGCACCTTTACCCTCGACCCCGAACGTTTCCCCCTCGGCATGATGCGGCAGCTCGTCTCTCACTTGCATG ACCATGACCAGCGCTACGTCGTCATGGTCGATCCGGCCGTGGCCTACCAGGACTACCCTCCGCTGCGGCAGGGCG TCGAGGACGATGTCTTTCTTCGGCGCGACAACGGCTCTCTGTGGCTGGGCGTCGTGTGGCCCGGCGTGACCGTGT TCCCGGACTGGTTTGCCAGCAAGGCGCAGGAATACTGGAACGGCCAGTTCGACTCCTTCTTCAACGCCTCCGAGG GCGTTGACATTGACGCTCTTTGGATCGACATGAATGAGCCGAGCAACACCATGTGCCCCTGGCCTTGCGACAAGC CGTATGAGTCGGCCAAGGGGATGCCTCCGCCGCCTCCTCCGGTGCGTCAGCCGCCGCGGCCGCTGCCTGGCTGGC CGTGTGACTTCCAGCCGCAGGGCACGTGCAAGTCCGAGAGGGCCGGAGCGCACGGGATGGAGGCGGCCATGGTGC CGTTGACGGTACTGACGCCGGACACTGAAGGCGCTCCGGTGCCACGCCCTGTCGGTACTCTCGGCGACGCCAAAG GCCTCCCCGATCGGAACTTTCTGTATCCAAAATACGCCATTCACAACAAGATGGCCTCGCACGACTCGTGGAACT CGGACCGCGGTGGCCTCTCGAACCGCACCGTCCACACCGACGTTCACCACCAGAACGGGCTCGTCATGTACGATA CTCACAACCTGTTTGGGTCCATGATGTCGTCGGCATCGCGAGAAGCCATGCTGGCGCGCCGGCCGGACAAGCGCC CGCTCATCATCACGCGCAGCACCTATGCCGGCGCAGGGTCCAAGGTCGGCCACTGGCTGGGCGACAACAAGTCGA CCTGGGACATGTACCGCAACTCGATCCGCTCCATGCTGGCCTTTACCGCCCTCTTCCAGTTCTCCATGGTGGGCG CCGATGTGTGCGGCTTCGGCGGCGATACGACCGAGGAGCTGTGCGCCCGATGGGCATCGCTAGGCGCCTTTGCCA CCTTTTACCGCAACCACAACGTGGAGGGGACGCTATCGCAAGAGTTCTATCGCTGGGAGAGCGTCACAGACAGCG CTCGCAAGGCCATTGCCATCCGCTACCGCCTGCTCGACTACATGTACACGGCCATGCGCGCCTCCAGCGCCGACG GCCGGCCCGCCATCCAGCCCGTCTTCTACCTCTACCCGCACGACCGGAGCACCTGGCCGCTCGAGCTGCAGTACT TTTACGGCCCGGCCCTTCTGGTGGCGCCCGTGACGGAGCAGGGCGCGACGAGCGTACGCGTCTACCTCCCGGACG ACGTCTTCTACGACTGGTACTCGCACAAGCCCATCCTCGGGGAGGCCGCCGAGCACACGTTTGTCAACCAGGACA TGACGGCTATCCCTCTCCTCATCCGCGGCGGAAACGTCCTCCCCGCGCGTCTTCACTCGACCATGACGACGACGG AGCTGCGCCGCCAAGAGTTTGAGCTACTCGTCGCCCTCGACGCCCAAGGCGAGGCGACGGGAGAGCTATACCTCG ACGACGGGGAGGCCATCGATCCGACACATGATCACACTCTCGTGTCTTTTCACTATAGCCACCGCGAGCGCCTCC TCTCGGCCCGTGGCGTCTTCGACTGTCCCGGCACCGCGCCCCGTGTCGTCAAGGTCACCGTCTTGGGCGCCGGCC AGCGGCCCAAGGCGGGCATTCGTGAACATGGTAGCGCCGACGGGTCGAGCATGTATAGCGAGAGCCATGAGGTTG ATTTGCGGCTGGATGGGTCGCGTACCGTTCACGTAGGTTGA |