© 2023 - Robin Ohm - Utrecht University - The Netherlands
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| Protein ID | Hirsu2|3784 |
| Gene name | |
| Location | Contig_2006:1050..3161 |
| Strand | - |
| Gene length (bp) | 2111 |
| Transcript length (bp) | 1473 |
| Coding sequence length (bp) | 1473 |
| Protein length (aa) | 491 |
| PFAM Domain ID | Short name | Long name | E-value | Start | End |
|---|---|---|---|---|---|
| PF00232 | Glyco_hydro_1 | Glycosyl hydrolase family 1 | 2.0E-139 | 6 | 476 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q25BW4|BGL1B_PHACH | Beta-glucosidase 1B OS=Phanerochaete chrysosporium GN=BGL1B PE=1 SV=1 | 7 | 472 | 2.0E-164 |
| sp|Q25BW5|BGL1A_PHACH | Beta-glucosidase 1A OS=Phanerochaete chrysosporium GN=BGL1A PE=1 SV=1 | 3 | 476 | 1.0E-154 |
| sp|Q8L7J2|BGL06_ORYSJ | Beta-glucosidase 6 OS=Oryza sativa subsp. japonica GN=BGLU6 PE=1 SV=1 | 3 | 474 | 2.0E-131 |
| sp|Q339X2|BGL34_ORYSJ | Beta-glucosidase 34 OS=Oryza sativa subsp. japonica GN=BGLU34 PE=2 SV=1 | 3 | 476 | 1.0E-129 |
| sp|Q9FLU8|BGL32_ARATH | Beta-glucosidase 32 OS=Arabidopsis thaliana GN=BGLU32 PE=2 SV=2 | 6 | 479 | 2.0E-129 |
| Swissprot ID | Swissprot Description | Start | End | E-value |
|---|---|---|---|---|
| sp|Q25BW4|BGL1B_PHACH | Beta-glucosidase 1B OS=Phanerochaete chrysosporium GN=BGL1B PE=1 SV=1 | 7 | 472 | 2.0E-164 |
| sp|Q25BW5|BGL1A_PHACH | Beta-glucosidase 1A OS=Phanerochaete chrysosporium GN=BGL1A PE=1 SV=1 | 3 | 476 | 1.0E-154 |
| sp|Q8L7J2|BGL06_ORYSJ | Beta-glucosidase 6 OS=Oryza sativa subsp. japonica GN=BGLU6 PE=1 SV=1 | 3 | 474 | 2.0E-131 |
| sp|Q339X2|BGL34_ORYSJ | Beta-glucosidase 34 OS=Oryza sativa subsp. japonica GN=BGLU34 PE=2 SV=1 | 3 | 476 | 1.0E-129 |
| sp|Q9FLU8|BGL32_ARATH | Beta-glucosidase 32 OS=Arabidopsis thaliana GN=BGLU32 PE=2 SV=2 | 6 | 479 | 2.0E-129 |
| sp|Q9FZE0|BGL40_ARATH | Beta-glucosidase 40 OS=Arabidopsis thaliana GN=BGLU40 PE=2 SV=1 | 3 | 467 | 2.0E-128 |
| sp|Q0DA21|BGL25_ORYSJ | Beta-glucosidase 25 OS=Oryza sativa subsp. japonica GN=BGLU25 PE=2 SV=2 | 3 | 480 | 3.0E-128 |
| sp|Q9SPP9|RG1_RAUSE | Raucaffricine-O-beta-D-glucosidase OS=Rauvolfia serpentina GN=RG PE=1 SV=1 | 3 | 490 | 7.0E-128 |
| sp|Q9FLU9|BGL31_ARATH | Beta-glucosidase 31 OS=Arabidopsis thaliana GN=BGLU31 PE=2 SV=1 | 6 | 479 | 1.0E-125 |
| sp|Q5Z9Z0|BGL24_ORYSJ | Beta-glucosidase 24 OS=Oryza sativa subsp. japonica GN=BGLU24 PE=2 SV=1 | 7 | 474 | 2.0E-125 |
| sp|Q9FIW4|BGL42_ARATH | Beta-glucosidase 42 OS=Arabidopsis thaliana GN=BGLU42 PE=2 SV=1 | 7 | 481 | 6.0E-124 |
| sp|Q9M1C9|BGL30_ARATH | Beta-glucosidase 30 OS=Arabidopsis thaliana GN=BGLU30 PE=2 SV=1 | 6 | 476 | 2.0E-123 |
| sp|O64882|BGL17_ARATH | Beta-glucosidase 17 OS=Arabidopsis thaliana GN=BGLU17 PE=2 SV=1 | 6 | 483 | 2.0E-123 |
| sp|Q8GXT2|BGL29_ARATH | Beta-glucosidase 29 OS=Arabidopsis thaliana GN=BGLU29 PE=2 SV=2 | 6 | 489 | 3.0E-123 |
| sp|Q7XKV5|BGL11_ORYSJ | Beta-glucosidase 11 OS=Oryza sativa subsp. japonica GN=BGLU11 PE=3 SV=2 | 3 | 481 | 1.0E-120 |
| sp|Q42707|F26G_CHESP | Furostanol glycoside 26-O-beta-glucosidase OS=Cheilocostus speciosus GN=F26G PE=1 SV=1 | 6 | 474 | 5.0E-120 |
| sp|Q9FIU7|BGL41_ARATH | Putative beta-glucosidase 41 OS=Arabidopsis thaliana GN=BGLU41 PE=3 SV=2 | 3 | 474 | 9.0E-119 |
| sp|Q7XPY7|BGL14_ORYSJ | Probable inactive beta-glucosidase 14 OS=Oryza sativa subsp. japonica GN=BGLU14 PE=2 SV=2 | 7 | 475 | 3.0E-118 |
| sp|A2SY66|VICHY_VICSN | Vicianin hydrolase (Fragment) OS=Vicia sativa subsp. nigra PE=1 SV=1 | 3 | 476 | 4.0E-118 |
| sp|Q7XKV4|BGL12_ORYSJ | Beta-glucosidase 12 OS=Oryza sativa subsp. japonica GN=BGLU12 PE=1 SV=2 | 3 | 476 | 1.0E-117 |
| sp|Q7F9K4|BGL10_ORYSJ | Beta-glucosidase 10 OS=Oryza sativa subsp. japonica GN=BGLU10 PE=2 SV=1 | 3 | 474 | 2.0E-117 |
| sp|Q9LV33|BGL44_ARATH | Beta-glucosidase 44 OS=Arabidopsis thaliana GN=BGLU44 PE=2 SV=1 | 3 | 474 | 2.0E-117 |
| sp|B8AVF0|BGL12_ORYSI | Beta-glucosidase 12 OS=Oryza sativa subsp. indica GN=BGLU12 PE=3 SV=1 | 3 | 476 | 3.0E-117 |
| sp|Q4V3B3|BGL28_ARATH | Beta-glucosidase 28 OS=Arabidopsis thaliana GN=BGLU28 PE=2 SV=1 | 7 | 474 | 1.0E-116 |
| sp|Q5N863|BGL04_ORYSJ | Beta-glucosidase 4 OS=Oryza sativa subsp. japonica GN=BGLU4 PE=2 SV=1 | 7 | 474 | 2.0E-116 |
| sp|Q9LU02|BGL13_ARATH | Beta-glucosidase 13 OS=Arabidopsis thaliana GN=BGLU13 PE=2 SV=1 | 7 | 478 | 3.0E-116 |
| sp|Q75I93|BGL07_ORYSJ | Beta-glucosidase 7 OS=Oryza sativa subsp. japonica GN=BGLU7 PE=1 SV=1 | 3 | 474 | 4.0E-116 |
| sp|Q9M1D0|BGL16_ARATH | Beta-glucosidase 16 OS=Arabidopsis thaliana GN=BGLU16 PE=2 SV=1 | 7 | 479 | 2.0E-115 |
| sp|Q84YK7|BGL27_ORYSJ | Beta-glucosidase 27 OS=Oryza sativa subsp. japonica GN=BGLU27 PE=2 SV=1 | 6 | 474 | 6.0E-115 |
| sp|Q75W17|FURH_VIBFR | Furcatin hydrolase OS=Viburnum furcatum PE=1 SV=1 | 6 | 476 | 6.0E-115 |
| sp|O64879|BGL15_ARATH | Beta-glucosidase 15 OS=Arabidopsis thaliana GN=BGLU15 PE=1 SV=1 | 7 | 478 | 1.0E-114 |
| sp|Q75I94|BGL08_ORYSJ | Beta-glucosidase 8 OS=Oryza sativa subsp. japonica GN=BGLU8 PE=1 SV=1 | 3 | 474 | 5.0E-114 |
| sp|Q9ZT64|CBG_PINCO | Coniferin beta-glucosidase OS=Pinus contorta PE=1 SV=1 | 7 | 474 | 2.0E-113 |
| sp|O80690|BGL46_ARATH | Beta-glucosidase 46 OS=Arabidopsis thaliana GN=BGLU46 PE=1 SV=2 | 7 | 481 | 5.0E-113 |
| sp|Q0J0N4|BGL30_ORYSJ | Beta-glucosidase 30 OS=Oryza sativa subsp. japonica GN=BGLU30 PE=2 SV=1 | 6 | 474 | 5.0E-113 |
| sp|Q5QMT0|BGL01_ORYSJ | Beta-glucosidase 1 OS=Oryza sativa subsp. japonica GN=BGLU1 PE=2 SV=1 | 3 | 478 | 2.0E-112 |
| sp|Q9LV34|BGL43_ARATH | Beta-glucosidase 43 OS=Arabidopsis thaliana GN=BGLU43 PE=2 SV=2 | 3 | 478 | 3.0E-112 |
| sp|Q9FH03|BGL12_ARATH | Beta-glucosidase 12 OS=Arabidopsis thaliana GN=BGLU12 PE=2 SV=1 | 7 | 467 | 5.0E-112 |
| sp|Q7XSK0|BGL18_ORYSJ | Beta-glucosidase 18 OS=Oryza sativa subsp. japonica GN=BGLU18 PE=3 SV=2 | 7 | 474 | 9.0E-112 |
| sp|A3RF67|BAGBG_DALNI | Isoflavonoid 7-O-beta-apiosyl-glucoside beta-glycosidase OS=Dalbergia nigrescens PE=1 SV=1 | 6 | 489 | 3.0E-111 |
| sp|Q7XKV2|BGL13_ORYSJ | Beta-glucosidase 13 OS=Oryza sativa subsp. japonica GN=BGLU13 PE=2 SV=2 | 3 | 476 | 5.0E-111 |
| sp|A3BMZ5|BGL26_ORYSJ | Beta-glucosidase 26 OS=Oryza sativa subsp. japonica GN=BGLU26 PE=1 SV=1 | 3 | 478 | 1.0E-110 |
| sp|Q9M1D1|BGL27_ARATH | Beta-glucosidase 27 OS=Arabidopsis thaliana GN=BGLU27 PE=2 SV=2 | 7 | 474 | 2.0E-110 |
| sp|Q9C8Y9|BGL22_ARATH | Beta-glucosidase 22 OS=Arabidopsis thaliana GN=BGLU22 PE=1 SV=1 | 3 | 481 | 3.0E-110 |
| sp|D5MTF8|HGL1D_WHEAT | 4-hydroxy-7-methoxy-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-2-yl glucoside beta-D-glucosidase 1d, chloroplastic OS=Triticum aestivum GN=GLU1D PE=1 SV=1 | 10 | 467 | 1.0E-109 |
| sp|Q9C525|BGL21_ARATH | Beta-glucosidase 21 OS=Arabidopsis thaliana GN=BGLU21 PE=1 SV=1 | 3 | 484 | 1.0E-109 |
| sp|Q8GVD0|BGLC_OLEEU | Beta-glucosidase OS=Olea europaea GN=GLU PE=1 SV=1 | 7 | 489 | 1.0E-109 |
| sp|Q8GU20|SG1_RAUSE | Strictosidine-O-beta-D-glucosidase OS=Rauvolfia serpentina GN=SGR1 PE=1 SV=1 | 7 | 475 | 2.0E-109 |
| sp|Q9ZP27|AVCO2_AVESA | Avenacosidase 2 OS=Avena sativa GN=P60B PE=1 SV=1 | 7 | 471 | 1.0E-108 |
| sp|Q9SR37|BGL23_ARATH | Beta-glucosidase 23 OS=Arabidopsis thaliana GN=BGLU23 PE=1 SV=1 | 3 | 484 | 2.0E-108 |
| sp|O64883|BGL26_ARATH | Beta-glucosidase 26, peroxisomal OS=Arabidopsis thaliana GN=BGLU26 PE=1 SV=1 | 6 | 490 | 2.0E-108 |
| sp|Q9FYS3|HGGL_SECCE | 4-hydroxy-7-methoxy-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-2-yl glucoside beta-D-glucosidase, chloroplastic OS=Secale cereale PE=1 SV=1 | 10 | 467 | 1.0E-107 |
| sp|Q2QSR8|BGL38_ORYSJ | Beta-glucosidase 38 OS=Oryza sativa subsp. japonica GN=BGLU38 PE=2 SV=2 | 3 | 474 | 2.0E-107 |
| sp|Q1XH04|HGL1C_WHEAT | 4-hydroxy-7-methoxy-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-2-yl glucoside beta-D-glucosidase 1c, chloroplastic OS=Triticum aestivum GN=GLU1C PE=1 SV=1 | 10 | 467 | 2.0E-107 |
| sp|Q7EXZ4|BGL28_ORYSJ | Beta-glucosidase 28 OS=Oryza sativa subsp. japonica GN=BGLU28 PE=2 SV=1 | 6 | 467 | 6.0E-107 |
| sp|Q38786|AVCO1_AVESA | Avenacosidase 1 OS=Avena sativa GN=P60A PE=1 SV=1 | 7 | 471 | 9.0E-107 |
| sp|O80689|BGL45_ARATH | Beta-glucosidase 45 OS=Arabidopsis thaliana GN=BGLU45 PE=1 SV=1 | 7 | 476 | 1.0E-106 |
| sp|Q1XH05|HGL1B_WHEAT | 4-hydroxy-7-methoxy-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-2-yl glucoside beta-D-glucosidase 1b, chloroplastic OS=Triticum aestivum GN=GLU1B PE=1 SV=1 | 10 | 467 | 1.0E-106 |
| sp|P26204|BGLS_TRIRP | Non-cyanogenic beta-glucosidase OS=Trifolium repens PE=1 SV=1 | 3 | 455 | 3.0E-106 |
| sp|Q9SLA0|BGL14_ARATH | Beta-glucosidase 14 OS=Arabidopsis thaliana GN=BGLU14 PE=3 SV=2 | 7 | 478 | 7.0E-106 |
| sp|Q7XSK2|BGL16_ORYSJ | Beta-glucosidase 16 OS=Oryza sativa subsp. japonica GN=BGLU16 PE=3 SV=2 | 7 | 476 | 8.0E-106 |
| sp|P37702|BGL38_ARATH | Myrosinase 1 OS=Arabidopsis thaliana GN=TGG1 PE=1 SV=1 | 11 | 459 | 1.0E-105 |
| sp|Q1XIR9|HGL1A_WHEAT | 4-hydroxy-7-methoxy-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-2-yl glucoside beta-D-glucosidase 1a, chloroplastic OS=Triticum aestivum GN=GLU1A PE=1 SV=1 | 10 | 467 | 1.0E-105 |
| sp|Q9LKR7|BGL24_ARATH | Beta-glucosidase 24 OS=Arabidopsis thaliana GN=BGLU24 PE=2 SV=2 | 3 | 476 | 2.0E-105 |
| sp|Q41761|HGGL2_MAIZE | 4-hydroxy-7-methoxy-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-2-yl glucoside beta-D-glucosidase 2, chloroplastic OS=Zea mays GN=GLU2 PE=1 SV=1 | 7 | 481 | 4.0E-105 |
| sp|P29736|MYRA_SINAL | Myrosinase MA1 OS=Sinapis alba PE=1 SV=2 | 14 | 467 | 2.0E-104 |
| sp|Q9LIF9|BGL19_ARATH | Beta-glucosidase 19 OS=Arabidopsis thaliana GN=BGLU19 PE=2 SV=1 | 3 | 481 | 2.0E-104 |
| sp|Q9C5C2|BGL37_ARATH | Myrosinase 2 OS=Arabidopsis thaliana GN=TGG2 PE=1 SV=1 | 9 | 474 | 3.0E-104 |
| sp|P29092|MYR3_SINAL | Myrosinase MB3 OS=Sinapis alba PE=1 SV=1 | 3 | 466 | 9.0E-104 |
| sp|Q00326|MYRO_BRANA | Myrosinase OS=Brassica napus PE=2 SV=1 | 3 | 467 | 1.0E-102 |
| sp|P49235|HGGL1_MAIZE | 4-hydroxy-7-methoxy-3-oxo-3,4-dihydro-2H-1,4-benzoxazin-2-yl glucoside beta-D-glucosidase 1, chloroplastic OS=Zea mays GN=GLU1 PE=1 SV=1 | 7 | 481 | 8.0E-101 |
| sp|B7F7K7|BGL31_ORYSJ | Beta-glucosidase 31 OS=Oryza sativa subsp. japonica GN=BGLU31 PE=2 SV=1 | 7 | 462 | 2.0E-100 |
| sp|Q84WV2|BGL20_ARATH | Beta-glucosidase 20 OS=Arabidopsis thaliana GN=BGLU20 PE=2 SV=1 | 3 | 467 | 2.0E-100 |
| sp|Q8K1F9|LCTL_MOUSE | Lactase-like protein OS=Mus musculus GN=Lctl PE=2 SV=1 | 6 | 475 | 5.0E-100 |
| sp|Q9SE50|BGL18_ARATH | Beta-D-glucopyranosyl abscisate beta-glucosidase OS=Arabidopsis thaliana GN=BGLU18 PE=1 SV=2 | 3 | 467 | 7.0E-100 |
| sp|A3C053|BGL29_ORYSJ | Beta-glucosidase 29 OS=Oryza sativa subsp. japonica GN=BGLU29 PE=2 SV=2 | 6 | 478 | 1.0E-99 |
| sp|Q9SVS1|BGL47_ARATH | Beta-glucosidase 47 OS=Arabidopsis thaliana GN=BGLU47 PE=3 SV=2 | 7 | 483 | 1.0E-99 |
| sp|Q6UWM7|LCTL_HUMAN | Lactase-like protein OS=Homo sapiens GN=LCTL PE=1 SV=2 | 6 | 474 | 4.0E-99 |
| sp|Q0J0G2|BGL32_ORYSJ | Beta-glucosidase 32 OS=Oryza sativa subsp. japonica GN=BGLU32 PE=2 SV=2 | 7 | 462 | 1.0E-98 |
| sp|O48779|BGL33_ARATH | Beta-glucosidase 33 OS=Arabidopsis thaliana GN=BGLU33 PE=2 SV=1 | 7 | 480 | 3.0E-97 |
| sp|O82772|BGL25_ARATH | Probable inactive beta-glucosidase 25 OS=Arabidopsis thaliana GN=BGLU25 PE=2 SV=1 | 6 | 476 | 5.0E-97 |
| sp|P97265|GBA3_CAVPO | Cytosolic beta-glucosidase OS=Cavia porcellus GN=Gba3 PE=1 SV=1 | 6 | 477 | 5.0E-97 |
| sp|Q8GRX1|BGL34_ARATH | Myrosinase 4 OS=Arabidopsis thaliana GN=TGG4 PE=1 SV=1 | 3 | 476 | 5.0E-97 |
| sp|Q3ECS3|BGL35_ARATH | Myrosinase 5 OS=Arabidopsis thaliana GN=TGG5 PE=1 SV=1 | 3 | 476 | 5.0E-97 |
| sp|P09849|LPH_RABIT | Lactase-phlorizin hydrolase OS=Oryctolagus cuniculus GN=LCT PE=1 SV=1 | 7 | 467 | 6.0E-96 |
| sp|P09848|LPH_HUMAN | Lactase-phlorizin hydrolase OS=Homo sapiens GN=LCT PE=1 SV=3 | 7 | 467 | 9.0E-96 |
| sp|Q02401|LPH_RAT | Lactase-phlorizin hydrolase OS=Rattus norvegicus GN=Lct PE=2 SV=2 | 7 | 467 | 4.0E-95 |
| sp|B3H5Q1|BGL11_ARATH | Beta-glucosidase 11 OS=Arabidopsis thaliana GN=BGLU11 PE=2 SV=2 | 7 | 467 | 1.0E-94 |
| sp|Q93ZI4|BGL10_ARATH | Beta-glucosidase 10 OS=Arabidopsis thaliana GN=BGLU10 PE=2 SV=1 | 7 | 467 | 1.0E-94 |
| sp|Q8RZL1|BGL03_ORYSJ | Beta-glucosidase 3 OS=Oryza sativa subsp. japonica GN=BGLU3 PE=2 SV=2 | 7 | 482 | 3.0E-94 |
| sp|Q53NF0|BGL35_ORYSJ | Putative beta-glucosidase 35 OS=Oryza sativa subsp. japonica GN=BGLU35 PE=3 SV=2 | 3 | 477 | 3.0E-93 |
| sp|Q5RF65|GBA3_PONAB | Cytosolic beta-glucosidase OS=Pongo abelii GN=GBA3 PE=2 SV=1 | 6 | 467 | 5.0E-93 |
| sp|Q95X01|MYRO1_BREBR | Myrosinase 1 OS=Brevicoryne brassicae PE=1 SV=1 | 7 | 465 | 6.0E-93 |
| sp|P09848|LPH_HUMAN | Lactase-phlorizin hydrolase OS=Homo sapiens GN=LCT PE=1 SV=3 | 10 | 487 | 2.0E-92 |
| sp|Q02401|LPH_RAT | Lactase-phlorizin hydrolase OS=Rattus norvegicus GN=Lct PE=2 SV=2 | 10 | 487 | 2.0E-92 |
| sp|Q03506|BGLA_BACCI | Beta-glucosidase OS=Bacillus circulans GN=bglA PE=1 SV=3 | 3 | 466 | 2.0E-92 |
| sp|Q08638|BGLA_THEMA | Beta-glucosidase A OS=Thermotoga maritima (strain ATCC 43589 / MSB8 / DSM 3109 / JCM 10099) GN=bglA PE=1 SV=1 | 7 | 466 | 2.0E-92 |
| sp|P09849|LPH_RABIT | Lactase-phlorizin hydrolase OS=Oryctolagus cuniculus GN=LCT PE=1 SV=1 | 10 | 487 | 3.0E-91 |
| sp|Q9H227|GBA3_HUMAN | Cytosolic beta-glucosidase OS=Homo sapiens GN=GBA3 PE=1 SV=2 | 6 | 467 | 3.0E-91 |
| sp|Q9STP4|BGL09_ARATH | Beta-glucosidase 9 OS=Arabidopsis thaliana GN=BGLU9 PE=2 SV=2 | 3 | 467 | 3.0E-91 |
| sp|B9K7M5|BGLA_THENN | 1,4-beta-D-glucan glucohydrolase OS=Thermotoga neapolitana (strain ATCC 49049 / DSM 4359 / NS-E) GN=gghA PE=1 SV=2 | 7 | 474 | 4.0E-91 |
| sp|P09849|LPH_RABIT | Lactase-phlorizin hydrolase OS=Oryctolagus cuniculus GN=LCT PE=1 SV=1 | 4 | 484 | 1.0E-90 |
| sp|P0C946|BGLA_THENE | 1,4-beta-D-glucan glucohydrolase (Fragment) OS=Thermotoga neapolitana GN=bglA PE=3 SV=1 | 7 | 462 | 3.0E-90 |
| sp|B7F8N7|BGL02_ORYSJ | Beta-glucosidase 2 OS=Oryza sativa subsp. japonica GN=BGLU2 PE=2 SV=1 | 7 | 456 | 2.0E-89 |
| sp|P22505|BGLB_PAEPO | Beta-glucosidase B OS=Paenibacillus polymyxa GN=bglB PE=1 SV=1 | 7 | 477 | 2.0E-89 |
| sp|Q0J0G1|BGL33_ORYSJ | Probable inactive beta-glucosidase 33 OS=Oryza sativa subsp. japonica GN=BGLU33 PE=2 SV=2 | 7 | 462 | 3.0E-89 |
| sp|Q60DX8|BGL22_ORYSJ | Beta-glucosidase 22 OS=Oryza sativa subsp. japonica GN=BGLU22 PE=2 SV=1 | 7 | 484 | 1.0E-88 |
| sp|O65458|BGL03_ARATH | Beta-glucosidase 3 OS=Arabidopsis thaliana GN=BGLU3 PE=3 SV=2 | 7 | 467 | 1.0E-87 |
| sp|Q9ZUI3|BGL04_ARATH | Beta-glucosidase 4 OS=Arabidopsis thaliana GN=BGLU4 PE=2 SV=2 | 3 | 481 | 6.0E-87 |
| sp|P10482|BGLS_CALSA | Beta-glucosidase A OS=Caldicellulosiruptor saccharolyticus GN=bglA PE=3 SV=1 | 6 | 477 | 4.0E-86 |
| sp|E3W9M3|AA7GT_DELGR | Cyanidin 3-O-glucoside 7-O-glucosyltransferase (acyl-glucose) OS=Delphinium grandiflorum GN=AA7GT PE=1 SV=1 | 7 | 478 | 4.0E-86 |
| sp|P09848|LPH_HUMAN | Lactase-phlorizin hydrolase OS=Homo sapiens GN=LCT PE=1 SV=3 | 4 | 480 | 3.0E-85 |
| sp|P12614|BGLS_AGRSA | Beta-glucosidase OS=Agrobacterium sp. (strain ATCC 21400) GN=abg PE=3 SV=1 | 7 | 466 | 4.0E-85 |
| sp|Q3ECW8|BGL01_ARATH | Beta-glucosidase 1 OS=Arabidopsis thaliana GN=BGLU1 PE=2 SV=2 | 3 | 467 | 1.0E-84 |
| sp|Q8RXN9|BGL05_ARATH | Putative beta-glucosidase 5 OS=Arabidopsis thaliana GN=BGLU5 PE=5 SV=2 | 3 | 467 | 2.0E-84 |
| sp|Q5JK35|BGL05_ORYSJ | Beta-glucosidase 5 OS=Oryza sativa subsp. japonica GN=BGLU5 PE=2 SV=1 | 7 | 471 | 2.0E-84 |
| sp|P26205|BGLT_TRIRP | Cyanogenic beta-glucosidase (Fragment) OS=Trifolium repens GN=LI PE=1 SV=1 | 11 | 385 | 2.0E-84 |
| sp|Q02401|LPH_RAT | Lactase-phlorizin hydrolase OS=Rattus norvegicus GN=Lct PE=2 SV=2 | 4 | 481 | 6.0E-84 |
| sp|P26208|BGLA_CLOTH | Beta-glucosidase A OS=Clostridium thermocellum (strain ATCC 27405 / DSM 1237 / NBRC 103400 / NCIMB 10682 / NRRL B-4536 / VPI 7372) GN=bglA PE=3 SV=1 | 3 | 474 | 7.0E-84 |
| sp|Q67XN2|BGL08_ARATH | Beta-glucosidase 8 OS=Arabidopsis thaliana GN=BGLU8 PE=2 SV=1 | 7 | 467 | 2.0E-83 |
| sp|Q60DY1|BGL21_ORYSJ | Beta-glucosidase 21 OS=Oryza sativa subsp. japonica GN=BGLU21 PE=2 SV=2 | 7 | 485 | 3.0E-83 |
| sp|B9FHH2|BGL20_ORYSJ | Beta-glucosidase 20 OS=Oryza sativa subsp. japonica GN=BGLU20 PE=2 SV=1 | 7 | 483 | 1.0E-82 |
| sp|Q0DIT2|BGL19_ORYSJ | Beta-glucosidase 19 OS=Oryza sativa subsp. japonica GN=BGLU19 PE=2 SV=1 | 7 | 483 | 2.0E-81 |
| sp|P22073|BGLA_PAEPO | Beta-glucosidase A OS=Paenibacillus polymyxa GN=bglA PE=1 SV=1 | 7 | 477 | 1.0E-80 |
| sp|Q9C8K1|BGL36_ARATH | Putative myrosinase 6 OS=Arabidopsis thaliana GN=TGG6 PE=5 SV=2 | 10 | 476 | 7.0E-79 |
| sp|Q86Z14|KLOTB_HUMAN | Beta-klotho OS=Homo sapiens GN=KLB PE=1 SV=1 | 6 | 476 | 1.0E-77 |
| sp|Q9LZJ1|BGL07_ARATH | Beta-glucosidase 7 OS=Arabidopsis thaliana GN=BGLU7 PE=2 SV=2 | 7 | 467 | 3.0E-77 |
| sp|Q682B4|BGL06_ARATH | Putative beta-glucosidase 6 OS=Arabidopsis thaliana GN=BGLU6 PE=5 SV=1 | 7 | 317 | 3.0E-77 |
| sp|Q6L597|BGL23_ORYSJ | Putative beta-glucosidase 23 OS=Oryza sativa subsp. japonica GN=BGLU23 PE=5 SV=2 | 23 | 483 | 2.0E-74 |
| sp|P42403|BGLC_BACSU | Aryl-phospho-beta-D-glucosidase BglC OS=Bacillus subtilis (strain 168) GN=bglC PE=1 SV=1 | 6 | 466 | 7.0E-74 |
| sp|E3W9M2|AA5GT_DIACA | Cyanidin 3-O-glucoside 5-O-glucosyltransferase (acyl-glucose) OS=Dianthus caryophyllus GN=AA5GT PE=1 SV=1 | 7 | 466 | 1.0E-73 |
| sp|Q99N32|KLOTB_MOUSE | Beta-klotho OS=Mus musculus GN=Klb PE=1 SV=1 | 6 | 476 | 1.0E-73 |
| sp|Q8S3J3|HIUH_SOYBN | Hydroxyisourate hydrolase OS=Glycine max GN=HIUH PE=1 SV=1 | 3 | 464 | 1.0E-72 |
| sp|O35082|KLOT_MOUSE | Klotho OS=Mus musculus GN=Kl PE=1 SV=2 | 6 | 476 | 2.0E-71 |
| sp|Q8WP17|KLOT_MACFA | Klotho OS=Macaca fascicularis GN=KL PE=2 SV=1 | 4 | 487 | 4.0E-71 |
| sp|Q97EZ2|LACG_CLOAB | 6-phospho-beta-galactosidase OS=Clostridium acetobutylicum (strain ATCC 824 / DSM 792 / JCM 1419 / LMG 5710 / VKM B-1787) GN=lacG PE=3 SV=1 | 10 | 480 | 7.0E-70 |
| sp|Q3E8E5|BGL39_ARATH | Putative myrosinase 3 OS=Arabidopsis thaliana GN=TGG3 PE=5 SV=1 | 30 | 440 | 2.0E-69 |
| sp|P94248|BGLFU_BIFBR | Bifunctional beta-D-glucosidase/beta-D-fucosidase OS=Bifidobacterium breve PE=1 SV=1 | 7 | 478 | 2.0E-69 |
| sp|Q9UEF7|KLOT_HUMAN | Klotho OS=Homo sapiens GN=KL PE=1 SV=2 | 4 | 487 | 7.0E-69 |
| sp|Q9Z2Y9|KLOT_RAT | Klotho OS=Rattus norvegicus GN=Kl PE=1 SV=1 | 6 | 474 | 1.0E-68 |
| sp|Q7XSK1|BGL17_ORYSJ | Putative beta-glucosidase 17 OS=Oryza sativa subsp. japonica GN=BGLU17 PE=5 SV=3 | 7 | 275 | 4.0E-58 |
| sp|O05508|GMUD_BACSU | 6-phospho-beta-glucosidase GmuD OS=Bacillus subtilis (strain 168) GN=gmuD PE=1 SV=1 | 3 | 480 | 2.0E-56 |
| sp|Q29ZJ1|LACG_LACRH | 6-phospho-beta-galactosidase OS=Lactobacillus rhamnosus GN=lacG PE=3 SV=1 | 7 | 473 | 4.0E-56 |
| sp|Q59437|BGLA_ENTAG | Beta-glucosidase A OS=Enterobacter agglomerans GN=bglA PE=3 SV=1 | 7 | 467 | 4.0E-54 |
| sp|Q9EV38|LACG_STRGC | 6-phospho-beta-galactosidase OS=Streptococcus gordonii (strain Challis / ATCC 35105 / CH1 / DL1 / V288) GN=lacG PE=3 SV=2 | 6 | 481 | 4.0E-54 |
| sp|P14696|LACG_LACCA | 6-phospho-beta-galactosidase OS=Lactobacillus casei GN=lacG PE=3 SV=1 | 7 | 467 | 7.0E-54 |
| sp|P50977|LACG_LACAI | 6-phospho-beta-galactosidase OS=Lactobacillus acidophilus GN=lacG PE=3 SV=1 | 6 | 481 | 2.0E-53 |
| sp|B3W7I3|LACG_LACCB | 6-phospho-beta-galactosidase OS=Lactobacillus casei (strain BL23) GN=lacG PE=3 SV=1 | 7 | 467 | 2.0E-53 |
| sp|A3CPH0|LACG_STRSV | 6-phospho-beta-galactosidase OS=Streptococcus sanguinis (strain SK36) GN=lacG PE=3 SV=1 | 6 | 481 | 2.0E-53 |
| sp|C7N8L9|LACG_LEPBD | 6-phospho-beta-galactosidase OS=Leptotrichia buccalis (strain ATCC 14201 / DSM 1135 / JCM 12969 / NCTC 10249 / C-1013-b) GN=lacG PE=1 SV=1 | 7 | 478 | 7.0E-53 |
| sp|Q8E4S2|LACG_STRA3 | 6-phospho-beta-galactosidase OS=Streptococcus agalactiae serotype III (strain NEM316) GN=lacG PE=3 SV=1 | 6 | 467 | 2.0E-52 |
| sp|P11546|LACG_LACLL | 6-phospho-beta-galactosidase OS=Lactococcus lactis subsp. lactis GN=lacG PE=1 SV=2 | 6 | 481 | 2.0E-52 |
| sp|B7ECS8|BGL09_ORYSJ | Putative beta-glucosidase 9 OS=Oryza sativa subsp. japonica GN=BGLU9 PE=5 SV=2 | 3 | 228 | 1.0E-51 |
| sp|Q5X9Y7|LACG_STRP6 | 6-phospho-beta-galactosidase OS=Streptococcus pyogenes serotype M6 (strain ATCC BAA-946 / MGAS10394) GN=lacG PE=3 SV=1 | 6 | 481 | 4.0E-51 |
| sp|Q4L868|LACG_STAHJ | 6-phospho-beta-galactosidase OS=Staphylococcus haemolyticus (strain JCSC1435) GN=lacG PE=3 SV=1 | 7 | 481 | 5.0E-51 |
| sp|P0DB41|LACG_STRPQ | 6-phospho-beta-galactosidase OS=Streptococcus pyogenes serotype M3 (strain SSI-1) GN=lacG PE=3 SV=1 | 6 | 481 | 5.0E-51 |
| sp|P0DB40|LACG_STRP3 | 6-phospho-beta-galactosidase OS=Streptococcus pyogenes serotype M3 (strain ATCC BAA-595 / MGAS315) GN=lacG PE=3 SV=1 | 6 | 481 | 5.0E-51 |
| sp|Q1JK01|LACG_STRPC | 6-phospho-beta-galactosidase OS=Streptococcus pyogenes serotype M12 (strain MGAS9429) GN=lacG PE=3 SV=1 | 6 | 481 | 5.0E-51 |
| sp|Q1J9V2|LACG_STRPB | 6-phospho-beta-galactosidase OS=Streptococcus pyogenes serotype M12 (strain MGAS2096) GN=lacG PE=3 SV=1 | 6 | 481 | 5.0E-51 |
| sp|Q97SA9|LACG1_STRPN | 6-phospho-beta-galactosidase 1 OS=Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) GN=lacG1 PE=3 SV=1 | 6 | 471 | 6.0E-51 |
| sp|Q1JEZ3|LACG_STRPD | 6-phospho-beta-galactosidase OS=Streptococcus pyogenes serotype M2 (strain MGAS10270) GN=lacG PE=3 SV=1 | 6 | 481 | 7.0E-51 |
| sp|A2RGE8|LACG_STRPG | 6-phospho-beta-galactosidase OS=Streptococcus pyogenes serotype M5 (strain Manfredo) GN=lacG PE=3 SV=1 | 6 | 481 | 2.0E-50 |
| sp|P50978|LACG_STRMU | 6-phospho-beta-galactosidase OS=Streptococcus mutans serotype c (strain ATCC 700610 / UA159) GN=lacG PE=3 SV=2 | 6 | 480 | 2.0E-50 |
| sp|Q48RC8|LACG_STRPM | 6-phospho-beta-galactosidase OS=Streptococcus pyogenes serotype M28 (strain MGAS6180) GN=lacG PE=3 SV=1 | 6 | 481 | 2.0E-50 |
| sp|B9DU98|LACG_STRU0 | 6-phospho-beta-galactosidase OS=Streptococcus uberis (strain ATCC BAA-854 / 0140J) GN=lacG PE=3 SV=1 | 6 | 480 | 3.0E-50 |
| sp|Q8NZE1|LACG_STRP8 | 6-phospho-beta-galactosidase OS=Streptococcus pyogenes serotype M18 (strain MGAS8232) GN=lacG PE=3 SV=1 | 6 | 481 | 3.0E-50 |
| sp|Q99Y18|LACG_STRP1 | 6-phospho-beta-galactosidase OS=Streptococcus pyogenes serotype M1 GN=lacG PE=3 SV=1 | 6 | 481 | 3.0E-50 |
| sp|Q8DQZ1|LACG1_STRR6 | 6-phospho-beta-galactosidase 1 OS=Streptococcus pneumoniae (strain ATCC BAA-255 / R6) GN=lacG1 PE=3 SV=1 | 6 | 471 | 7.0E-50 |
| sp|Q8DPP6|LACG2_STRR6 | 6-phospho-beta-galactosidase 2 OS=Streptococcus pneumoniae (strain ATCC BAA-255 / R6) GN=lacG2 PE=3 SV=1 | 6 | 480 | 1.0E-49 |
| sp|B8ZQ59|LACG_STRPJ | 6-phospho-beta-galactosidase OS=Streptococcus pneumoniae (strain ATCC 700669 / Spain 23F-1) GN=lacG PE=3 SV=1 | 6 | 480 | 2.0E-49 |
| sp|Q97QL9|LACG2_STRPN | 6-phospho-beta-galactosidase 2 OS=Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) GN=lacG2 PE=3 SV=1 | 6 | 480 | 2.0E-49 |
| sp|Q1J4Q7|LACG_STRPF | 6-phospho-beta-galactosidase OS=Streptococcus pyogenes serotype M4 (strain MGAS10750) GN=lacG PE=3 SV=2 | 6 | 481 | 3.0E-49 |
| sp|P67769|LACG_STAAW | 6-phospho-beta-galactosidase OS=Staphylococcus aureus (strain MW2) GN=lacG PE=3 SV=1 | 6 | 481 | 4.0E-49 |
| sp|Q6G7C5|LACG_STAAS | 6-phospho-beta-galactosidase OS=Staphylococcus aureus (strain MSSA476) GN=lacG PE=3 SV=1 | 6 | 481 | 4.0E-49 |
| sp|P67768|LACG_STAAN | 6-phospho-beta-galactosidase OS=Staphylococcus aureus (strain N315) GN=lacG PE=1 SV=1 | 6 | 481 | 4.0E-49 |
| sp|P67767|LACG_STAAM | 6-phospho-beta-galactosidase OS=Staphylococcus aureus (strain Mu50 / ATCC 700699) GN=lacG PE=3 SV=1 | 6 | 481 | 4.0E-49 |
| sp|Q2YYJ9|LACG_STAAB | 6-phospho-beta-galactosidase OS=Staphylococcus aureus (strain bovine RF122 / ET3-1) GN=lacG PE=3 SV=1 | 6 | 481 | 4.0E-49 |
| sp|A5IUX8|LACG_STAA9 | 6-phospho-beta-galactosidase OS=Staphylococcus aureus (strain JH9) GN=lacG PE=3 SV=1 | 6 | 481 | 4.0E-49 |
| sp|A6U3R9|LACG_STAA2 | 6-phospho-beta-galactosidase OS=Staphylococcus aureus (strain JH1) GN=lacG PE=3 SV=1 | 6 | 481 | 4.0E-49 |
| sp|A7X569|LACG_STAA1 | 6-phospho-beta-galactosidase OS=Staphylococcus aureus (strain Mu3 / ATCC 700698) GN=lacG PE=3 SV=1 | 6 | 481 | 4.0E-49 |
| sp|Q6GEP0|LACG_STAAR | 6-phospho-beta-galactosidase OS=Staphylococcus aureus (strain MRSA252) GN=lacG PE=3 SV=1 | 6 | 481 | 5.0E-49 |
| sp|P38645|BGLB_THEBI | Thermostable beta-glucosidase B OS=Thermobispora bispora GN=bglB PE=1 SV=1 | 6 | 188 | 7.0E-49 |
| sp|Q8CNF8|LACG_STAES | 6-phospho-beta-galactosidase OS=Staphylococcus epidermidis (strain ATCC 12228) GN=lacG PE=3 SV=1 | 7 | 481 | 8.0E-49 |
| sp|Q5HM41|LACG_STAEQ | 6-phospho-beta-galactosidase OS=Staphylococcus epidermidis (strain ATCC 35984 / RP62A) GN=lacG PE=3 SV=1 | 7 | 481 | 8.0E-49 |
| sp|P11175|LACG_STAAU | 6-phospho-beta-galactosidase OS=Staphylococcus aureus GN=lacG PE=3 SV=1 | 6 | 481 | 2.0E-48 |
| sp|A8YYF6|LACG_STAAT | 6-phospho-beta-galactosidase OS=Staphylococcus aureus (strain USA300 / TCH1516) GN=lacG PE=3 SV=1 | 6 | 481 | 2.0E-48 |
| sp|A6QJ33|LACG_STAAE | 6-phospho-beta-galactosidase OS=Staphylococcus aureus (strain Newman) GN=lacG PE=3 SV=1 | 6 | 481 | 2.0E-48 |
| sp|Q2G2D5|LACG_STAA8 | 6-phospho-beta-galactosidase OS=Staphylococcus aureus (strain NCTC 8325) GN=lacG PE=3 SV=1 | 6 | 481 | 2.0E-48 |
| sp|Q2FEU3|LACG_STAA3 | 6-phospho-beta-galactosidase OS=Staphylococcus aureus (strain USA300) GN=lacG PE=3 SV=1 | 6 | 481 | 2.0E-48 |
| sp|C1CEE7|LACG_STRZJ | 6-phospho-beta-galactosidase OS=Streptococcus pneumoniae (strain JJA) GN=lacG PE=3 SV=1 | 6 | 480 | 5.0E-48 |
| sp|Q5HE16|LACG_STAAC | 6-phospho-beta-galactosidase OS=Staphylococcus aureus (strain COL) GN=lacG PE=3 SV=1 | 6 | 481 | 5.0E-48 |
| sp|B4U1G6|LACG_STREM | 6-phospho-beta-galactosidase OS=Streptococcus equi subsp. zooepidemicus (strain MGCS10565) GN=lacG PE=3 SV=1 | 7 | 477 | 2.0E-47 |
| sp|C0MDS5|LACG_STRS7 | 6-phospho-beta-galactosidase OS=Streptococcus equi subsp. zooepidemicus (strain H70) GN=lacG PE=3 SV=1 | 7 | 477 | 3.0E-47 |
| sp|P26206|ARBB_DICCH | 6-phospho-beta-glucosidase OS=Dickeya chrysanthemi GN=arbB PE=3 SV=1 | 7 | 475 | 4.0E-47 |
| sp|P42973|BGLA_BACSU | Aryl-phospho-beta-D-glucosidase BglA OS=Bacillus subtilis (strain 168) GN=bglA PE=1 SV=1 | 7 | 455 | 5.0E-47 |
| sp|Q86Z14|KLOTB_HUMAN | Beta-klotho OS=Homo sapiens GN=KLB PE=1 SV=1 | 4 | 490 | 1.0E-46 |
| sp|P11988|BGLB_ECOLI | 6-phospho-beta-glucosidase BglB OS=Escherichia coli (strain K12) GN=bglB PE=1 SV=2 | 6 | 466 | 5.0E-46 |
| sp|Q46130|ABGA_CLOLO | 6-phospho-beta-glucosidase OS=Clostridium longisporum GN=abgA PE=3 SV=1 | 1 | 475 | 5.0E-46 |
| sp|Q48409|CASB_KLEOX | Phospho-cellobiase OS=Klebsiella oxytoca GN=casB PE=3 SV=1 | 6 | 479 | 8.0E-46 |
| sp|Q99N32|KLOTB_MOUSE | Beta-klotho OS=Mus musculus GN=Klb PE=1 SV=1 | 7 | 469 | 1.0E-45 |
| sp|Q8WP17|KLOT_MACFA | Klotho OS=Macaca fascicularis GN=KL PE=2 SV=1 | 6 | 451 | 3.0E-45 |
| sp|Q46829|BGLA_ECOLI | 6-phospho-beta-glucosidase BglA OS=Escherichia coli (strain K12) GN=bglA PE=1 SV=2 | 6 | 475 | 5.0E-45 |
| sp|Q9UEF7|KLOT_HUMAN | Klotho OS=Homo sapiens GN=KL PE=1 SV=2 | 6 | 451 | 2.0E-44 |
| sp|P40740|BGLH_BACSU | Aryl-phospho-beta-D-glucosidase BglH OS=Bacillus subtilis (strain 168) GN=bglH PE=1 SV=2 | 3 | 475 | 4.0E-43 |
| sp|Q9Z2Y9|KLOT_RAT | Klotho OS=Rattus norvegicus GN=Kl PE=1 SV=1 | 6 | 474 | 2.0E-41 |
| sp|O35082|KLOT_MOUSE | Klotho OS=Mus musculus GN=Kl PE=1 SV=2 | 6 | 474 | 7.0E-41 |
| sp|P24240|ASCB_ECOLI | 6-phospho-beta-glucosidase AscB OS=Escherichia coli (strain K12) GN=ascB PE=3 SV=2 | 6 | 475 | 3.0E-36 |
| sp|O52629|BGAL_PYRWO | Beta-galactosidase OS=Pyrococcus woesei PE=1 SV=1 | 7 | 487 | 2.0E-31 |
| sp|Q9FMD8|BGL02_ARATH | Putative beta-glucosidase 2 OS=Arabidopsis thaliana GN=BGLU2 PE=5 SV=2 | 144 | 432 | 7.0E-31 |
| sp|P29737|MYR1_SINAL | Myrosinase MB1 (Fragment) OS=Sinapis alba PE=1 SV=1 | 263 | 466 | 1.0E-29 |
| sp|P29738|MYR2_SINAL | Myrosinase MB2 (Fragment) OS=Sinapis alba PE=1 SV=1 | 263 | 467 | 1.0E-27 |
| sp|Q7XPY5|BGL15_ORYSJ | Putative beta-glucosidase 15 OS=Oryza sativa subsp. japonica GN=BGLU15 PE=5 SV=2 | 269 | 475 | 4.0E-25 |
| sp|P14288|BGAL_SULAC | Beta-galactosidase OS=Sulfolobus acidocaldarius (strain ATCC 33909 / DSM 639 / JCM 8929 / NBRC 15157 / NCIMB 11770) GN=bgaS PE=1 SV=2 | 6 | 473 | 2.0E-22 |
| sp|Q93Y07|SFR2_ARATH | Beta-glucosidase-like SFR2, chloroplastic OS=Arabidopsis thaliana GN=SFR2 PE=1 SV=1 | 63 | 483 | 4.0E-20 |
| sp|Q8L6H7|SFR2_ORYSJ | Beta-glucosidase-like SFR2, chloroplastic OS=Oryza sativa subsp. japonica GN=SFR2 PE=2 SV=1 | 63 | 483 | 5.0E-19 |
| sp|P22498|BGAL_SULSO | Beta-galactosidase OS=Sulfolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) GN=lacS PE=1 SV=2 | 6 | 473 | 2.0E-18 |
| sp|P50388|BGAL_SULSH | Beta-galactosidase OS=Sulfolobus shibatae GN=bglY PE=3 SV=1 | 6 | 485 | 3.0E-18 |
| sp|P38645|BGLB_THEBI | Thermostable beta-glucosidase B OS=Thermobispora bispora GN=bglB PE=1 SV=1 | 376 | 481 | 1.0E-10 |
| GO Term | Description | Terminal node |
|---|---|---|
| GO:0004553 | hydrolase activity, hydrolyzing O-glycosyl compounds | Yes |
| GO:0005975 | carbohydrate metabolic process | Yes |
| GO:0016798 | hydrolase activity, acting on glycosyl bonds | No |
| GO:0071704 | organic substance metabolic process | No |
| GO:0008152 | metabolic process | No |
| GO:0003824 | catalytic activity | No |
| GO:0044238 | primary metabolic process | No |
| GO:0008150 | biological_process | No |
| GO:0016787 | hydrolase activity | No |
| GO:0003674 | molecular_function | No |
| Localizations | Signals | Cytoplasm | Nucleus | Extracellular | Cell membrane | Mitochondrion | Plastid | Endoplasmic reticulum | Lysosome vacuole | Golgi apparatus | Peroxisome |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Cytoplasm | 0.7496 | 0.3861 | 0.2346 | 0.0767 | 0.3957 | 0.0458 | 0.0915 | 0.1537 | 0.1043 | 0.0354 |
| CAZyme category | E-value | Start | End |
|---|---|---|---|
| GH1 | 8.3E-154 | 6 | 477 |
| Orthofinder run ID | 4 |
| Orthogroup | 542 |
| Change Orthofinder run |
| Type of sequence | Sequence |
|---|---|
| Locus | Download genbank file of locus
Download genbank file of locus (reverse complement)
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|3784 MGSQPALPADFEWGFATAAYQIEGAVAEDGRGPSIWDTFCHLEPSRTKGANGDVACDHYHRFEADLDLLSRYGAT VYRFSLSWSRLIPLGGRADPVNEAGLRFYDGLIDGLVRRGIAPWVTLYHWDLPQALHDRYGGWLDVDEAQRDFER YARLCFARYGDRVRNWITINEPWIQAVFGYSTGGNAPGRSSTNPLCAEGDSATEPWIVGKALILSHARAVVAYNQ DFRPAQGGRIGISLNGDYYEPWDGADSRDCEAAERRMQFQIGWFANPIFLQSDYPPCMRAQLGDRLPRFDAAELA LLRAAETDFYGMNYYTAQFARHRAGPPPATDYTGNVDERQHDRAGAPVGEASGVGWLRACPGQFRKHLARVHRLY GKPIYVTENGCPCPGEDAMTRDEAVDDHFRIRYFASHLDALCRAVREDGVPVQGYFAWALLDNLEWSDGYGPRFG VTFTDYKTLERTPKKSALLLRHMLAERQGIKLDAEDEQAS* |
| Coding | >Hirsu2|3784 ATGGGCAGCCAGCCAGCGCTGCCGGCCGACTTCGAATGGGGCTTCGCCACGGCGGCCTACCAGATCGAGGGCGCC GTGGCCGAAGACGGGCGCGGGCCGTCCATCTGGGACACCTTCTGCCACCTGGAGCCGTCGCGGACCAAGGGCGCC AACGGCGACGTCGCCTGCGATCACTACCACCGCTTCGAGGCCGACCTCGACCTGCTCAGCCGCTACGGCGCCACC GTCTACCGCTTCTCGCTCTCCTGGTCGCGTCTGATCCCGCTCGGCGGCCGCGCCGACCCGGTCAACGAGGCCGGC CTGCGCTTCTACGACGGCCTCATCGACGGCCTCGTCCGCCGCGGCATCGCCCCCTGGGTCACCCTCTACCACTGG GACCTGCCGCAGGCGCTGCACGACCGCTACGGCGGCTGGCTCGACGTCGACGAGGCCCAGCGCGACTTTGAACGT TACGCCCGCCTGTGCTTTGCCCGTTATGGTGACCGCGTTCGCAACTGGATCACCATCAACGAGCCGTGGATCCAG GCCGTCTTTGGCTACAGCACCGGCGGCAACGCCCCGGGACGGAGCAGCACCAACCCCCTGTGCGCCGAGGGCGAC AGCGCGACCGAGCCGTGGATCGTCGGCAAGGCCCTCATCCTCAGCCACGCGCGCGCCGTCGTCGCCTACAACCAG GACTTCCGCCCGGCCCAGGGCGGCCGCATCGGCATCTCCCTCAACGGCGACTACTACGAGCCGTGGGACGGCGCC GACAGCCGTGACTGCGAGGCGGCCGAGCGACGGATGCAGTTCCAGATCGGCTGGTTTGCCAATCCCATCTTCCTC CAGAGCGACTACCCGCCCTGCATGCGGGCCCAGCTCGGCGACCGGCTCCCGCGCTTCGACGCGGCCGAGCTGGCG CTGCTGCGGGCCGCCGAGACGGACTTCTACGGCATGAACTACTACACGGCGCAGTTCGCCCGCCACCGGGCCGGG CCGCCGCCCGCGACCGACTACACCGGCAACGTCGACGAGCGGCAGCACGACCGCGCCGGCGCGCCCGTCGGCGAA GCCAGCGGCGTCGGCTGGCTGCGCGCCTGCCCCGGCCAGTTCCGCAAGCACCTGGCCCGCGTCCACCGGCTGTAC GGCAAGCCCATCTACGTGACGGAGAACGGCTGCCCGTGCCCCGGCGAGGACGCCATGACGCGCGACGAGGCCGTC GACGACCATTTCCGCATCCGCTACTTCGCCTCTCACCTCGACGCCCTCTGCCGCGCTGTCCGCGAGGACGGCGTC CCGGTCCAGGGCTACTTTGCCTGGGCCCTGCTGGACAACCTAGAGTGGTCGGACGGGTACGGCCCACGCTTCGGC GTCACCTTCACAGACTACAAGACACTGGAACGGACGCCCAAGAAATCGGCCCTGCTGCTGAGGCACATGCTCGCC GAGAGGCAGGGGATCAAGCTTGACGCCGAGGACGAGCAAGCGTCGTGA |
| Transcript | >Hirsu2|3784 ATGGGCAGCCAGCCAGCGCTGCCGGCCGACTTCGAATGGGGCTTCGCCACGGCGGCCTACCAGATCGAGGGCGCC GTGGCCGAAGACGGGCGCGGGCCGTCCATCTGGGACACCTTCTGCCACCTGGAGCCGTCGCGGACCAAGGGCGCC AACGGCGACGTCGCCTGCGATCACTACCACCGCTTCGAGGCCGACCTCGACCTGCTCAGCCGCTACGGCGCCACC GTCTACCGCTTCTCGCTCTCCTGGTCGCGTCTGATCCCGCTCGGCGGCCGCGCCGACCCGGTCAACGAGGCCGGC CTGCGCTTCTACGACGGCCTCATCGACGGCCTCGTCCGCCGCGGCATCGCCCCCTGGGTCACCCTCTACCACTGG GACCTGCCGCAGGCGCTGCACGACCGCTACGGCGGCTGGCTCGACGTCGACGAGGCCCAGCGCGACTTTGAACGT TACGCCCGCCTGTGCTTTGCCCGTTATGGTGACCGCGTTCGCAACTGGATCACCATCAACGAGCCGTGGATCCAG GCCGTCTTTGGCTACAGCACCGGCGGCAACGCCCCGGGACGGAGCAGCACCAACCCCCTGTGCGCCGAGGGCGAC AGCGCGACCGAGCCGTGGATCGTCGGCAAGGCCCTCATCCTCAGCCACGCGCGCGCCGTCGTCGCCTACAACCAG GACTTCCGCCCGGCCCAGGGCGGCCGCATCGGCATCTCCCTCAACGGCGACTACTACGAGCCGTGGGACGGCGCC GACAGCCGTGACTGCGAGGCGGCCGAGCGACGGATGCAGTTCCAGATCGGCTGGTTTGCCAATCCCATCTTCCTC CAGAGCGACTACCCGCCCTGCATGCGGGCCCAGCTCGGCGACCGGCTCCCGCGCTTCGACGCGGCCGAGCTGGCG CTGCTGCGGGCCGCCGAGACGGACTTCTACGGCATGAACTACTACACGGCGCAGTTCGCCCGCCACCGGGCCGGG CCGCCGCCCGCGACCGACTACACCGGCAACGTCGACGAGCGGCAGCACGACCGCGCCGGCGCGCCCGTCGGCGAA GCCAGCGGCGTCGGCTGGCTGCGCGCCTGCCCCGGCCAGTTCCGCAAGCACCTGGCCCGCGTCCACCGGCTGTAC GGCAAGCCCATCTACGTGACGGAGAACGGCTGCCCGTGCCCCGGCGAGGACGCCATGACGCGCGACGAGGCCGTC GACGACCATTTCCGCATCCGCTACTTCGCCTCTCACCTCGACGCCCTCTGCCGCGCTGTCCGCGAGGACGGCGTC CCGGTCCAGGGCTACTTTGCCTGGGCCCTGCTGGACAACCTAGAGTGGTCGGACGGGTACGGCCCACGCTTCGGC GTCACCTTCACAGACTACAAGACACTGGAACGGACGCCCAAGAAATCGGCCCTGCTGCTGAGGCACATGCTCGCC GAGAGGCAGGGGATCAAGCTTGACGCCGAGGACGAGCAAGCGTCGTGA |
| Gene | >Hirsu2|3784 ATGGGCAGCCAGCCAGCGCTGCCGGCCGACTTCGAATGGGGCTTCGCCACGGCGGCCTACCAGATCGAGGGCGCC GTGGCCGAAGACGGGCGCGGGCCGTCCATCTGGGACACCTTCTGCCACCTGGAGCCGTCGCGGACCAAGGGCGCC AACGGCGACGTCGCCTGCGATCACTACCACCGCTTCGAGGCCGACCTCGACCTGCTCAGCCGCTACGGCGCCACC GTCTACCGCTTCTCGCTCTCCTGGTCGCGTCTGATCCCGCTCGGCGGCCGCGCCGACCCGGTCAACGAGGCCGGC CTGCGCTTCTACGACGGCCTCATCGACGGCCTCGTCCGCCGCGGCATCGCCCCCTGGGTCACCCTCTACCACTGG GACCTGCCGCAGGCGCTGCACGACCGCTACGGCGGCTGGCTCGACGTCGACGAGGCCCAGCGCGACTTTGAACGT TACGCCCGCCTGTGCTTTGCCCGTTATGGTGACCGCGTTCGCAACTGGATCACCATCAACGAGCCGTGGATCCAG GCCGTCTTTGTGAGTCGTCGACCCCTTTTCCTCCCCTGCGCGCTTGAGAAGCGGGACTCCAAAGAGGGGCGTGGC CGAGGGAGAGAGAGGTGGAGAGAGAGAGAGACATAGAGAAAAAGAGAGAGAGAGAGAGACAGAGAGAGAGAGAGA GAGAGACAGAGAGAGAGAGAGAGAGAGCGAGAGAGAGAGGGAGAGAAAGAGAGAGAGAGAGAGAAAGAGAGAGAG AGAAAGACAAGAGACAGGAACAGAGACAAAGAGACATACGTATCGTGGACTGGCGTCTGACCACTTCAACGACCG GCCCGGCGTCGGATCGGGCGAGGACAAAAGGGCTACAGCACCGGCGGCAACGCCCCGGGACGGAGCAGCACCAAC CCCCTGTGCGCCGAGGGCGACAGCGCGACCGAGCCGTGGATCGTCGGCAAGGCCCTCATCCTCAGCCACGCGCGC GCCGTCGTCGCCTACAACCAGGACTTCCGCCCGGCCCAGGGCGGCCGCATCGGCATCTCCCTCAACGGCGACTAC TACGAGCCGTGGGACGGCGCCGACAGCCGTGACTGCGAGGCGGCCGAGCGACGGATGCAGTTCCAGATCGGCTGG TTTGCCAATCCCATCTTGTGAGTGGCCTTGGCCAGACACAGACTTGTCCCTCTCCCCCGGCCATCCATCCATCCA CCCTGTCGACTGACCGGCTGGCCTCCTCCCCTGACTTCTTCTTCTTCACTCTTCCCCGTCCGCACCCTGCAGCCT CCAGAGCGACTACCCGCCCTGCATGCGGGCCCAGCTCGGCGACCGGCTCCCGCGCTTCGACGCGGCCGAGCTGGC GCTGCTGCGGGCCGCCGAGACGGACTTCTACGGCATGAACTACTACACGGCGCAGTTCGCCCGCCACCGGGCCGG GCCGCCGCCCGCGACCGACTACACCGGCAACGTCGACGAGCGGCAGCACGACCGCGCCGGCGCGCCCGTCGGCGA AGCCAGCGGCGTCGGCTGGCTGCGCGCCTGCCCCGGCCAGTTCCGCAAGCACCTGGCCCGCGTCCACCGGCTGTA CGGCAAGCCCATCTACGTGACGGAGAACGGCTGCCCGTGCCCCGGCGAGGACGCCATGACGCGCGACGAGGCCGT CGACGACCATTTCCGCATCCGCTACTTCGCCTCTCACCTCGACGCCCTCTGCCGCGCTGTCCGCGAGGACGGCGT CCCGGTCCAGGGCTACTTTGCCTGGGCCCTGCTGGACAACCTAGGTAAGGAGGGGGGCGAAACCTCACGATCCAT CTTTTTCGCGGCTTGTGCATCTCAAGCTCACCAGTACGGGCCCGCTCGTTTGTGGACGGGGTATTGACAAAATAC AGAGTGGTCGGACGGGTACGGCCCACGCTTCGGCGTCACCTTCACAGACTACAAGACACTGGAACGGACGCCCAA GAAATCGGCCCTGCTGCTGAGGCACATGCTCGCCGAGAGGCAGGGGATCAAGGTGGGCCGCACGGCGACCGACTG GCCCCTTGTTCCCGTGGCGTGTCAAGAAACTAATGTACAGCTTTCGGGCCCAGCAGCTTGACGCCGAGGACGAGC AAGCGTCGTGA |