pI: 8.5114 |
Length (AA): 997 |
MW (Da): 112273 |
Paralog Number:
1
Signal peptide: N | GPI Anchor: N | Predicted trans-membrane segments: 0
Targets have been classified into druggability groups (DG) according to their druggability score in network driven prioritizations. DGs range from 1 to 5; the higher the group number, the higher the chance of the target to be druggable
Modbase 3D models:
There are 2 models calculated for this protein. More info on
these models, including the
models themselves is available at:
Modbase
Target Beg | Target End | Template | Template Beg | Template End | Identity | Evalue | Model Score | MPQS | zDope |
---|---|---|---|---|---|---|---|---|---|
96 | 986 | 5fjs (A) | 59 | 799 | 34.00 | 0 | 1 | 0.991481 | 0.38 |
108 | 987 | 5fjs (A) | 72 | 800 | 38.00 | 0 | 1 | 1.01695 | 0.18 |
Help me make sense of these data.
A more detailed description of these scores is available at the Modbase Model Evaluation Help Pages, and in the papers referenced therein.
PDB Structures:
Ortholog group members (OG5_130651)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT1G33700 | Beta-glucosidase, GBA2 type protein |
Arabidopsis thaliana | AT4G10060 | beta-glucosidase, GBA2 type family protein |
Arabidopsis thaliana | AT5G49900 | Beta-glucosidase, GBA2 type family protein |
Arabidopsis thaliana | AT3G24180 | Beta-glucosidase, GBA2 type family protein |
Caenorhabditis elegans | CELE_R08F11.1 | Protein R08F11.1 |
Caenorhabditis elegans | CELE_Y105E8A.10 | Protein HPO-13, isoform C |
Dictyostelium discoideum | DDB_G0292446 | hypothetical protein |
Drosophila melanogaster | Dmel_CG33090 | CG33090 gene product from transcript CG33090-RE |
Echinococcus granulosus | EgrG_000876700 | non lysosomal glucosylceramidase |
Echinococcus granulosus | EgrG_000822700 | bile acid beta glucosidase |
Echinococcus multilocularis | EmuJ_000822700 | bile acid beta glucosidase |
Echinococcus multilocularis | EmuJ_000876700 | non lysosomal glucosylceramidase |
Homo sapiens | ENSG00000070610 | glucosidase, beta (bile acid) 2 |
Loa Loa (eye worm) | LOAG_09338 | hypothetical protein |
Mus musculus | ENSMUSG00000028467 | glucosidase beta 2 |
Oryza sativa | 4348876 | Os10g0473400 |
Oryza sativa | 4350171 | Os11g0242100 |
Oryza sativa | 9268048 | Os07g0444000 |
Oryza sativa | 4344485 | Os08g0111200 |
Schistosoma japonicum | Sjp_0046440 | Non-lysosomal glucosylceramidase, putative |
Schistosoma japonicum | Sjp_0312230 | Non-lysosomal glucosylceramidase, putative |
Schistosoma japonicum | Sjp_0046460 | Non-lysosomal glucosylceramidase, putative |
Schistosoma mansoni | Smp_155750.1 | bile acid beta-glucosidase-related |
Schistosoma mansoni | Smp_155750.2 | bile acid beta-glucosidase-related |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
CELE_R08F11.1 | Caenorhabditis elegans | embryonic lethal | wormbase |
neb | C. elegans RNAi phenotypes | Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs |
keio | Systematic single-gene knock-out mutants of E. coli K12 | The Keio Collection |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
In TDR Targets, information about phenotypes that are caused by drugs, or by genetic manipulation of cells (e.g. gene knockouts or knockdowns) is manually curated from the literature. These descriptions help to describe the potential of the target for drug development. If no information is available for this gene or if the information is incomplete, this may mean that i) the papers containing this information either appeared after the curation effort for this organism was carried out or they were inadvertently missed by curators; or that ii) the curation effort for this organism has not yet started.
In any case, if you have information about papers containing relevant validation data for this target, please contact us.
Species | Known druggable target | Linked compounds | Reference |
---|---|---|---|
Mus musculus | glucosidase beta 2 | Compounds | References |
Homo sapiens | glucosidase, beta (bile acid) 2 | Compounds | References |