pI: 6.1051 |
Length (AA): 1707 |
MW (Da): 188848 |
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 10 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 |
---|---|---|---|---|---|---|---|---|---|
1056 | 1438 | 2bis (A) | 1 | 425 | 32.00 | 0 | 1 | 0.5 | -0.31 |
1268 | 1406 | 2f9f (A) | 16 | 152 | 31.00 | 0.0000000084 | 1 | 0.6 | -1.64 |
562 | 1161 | 4bzy (A) | 45 | 599 | 32.00 | 0 | 1 | 0.575394 | 0.28 |
759 | 919 | 2wsk (A) | 153 | 336 | 28.00 | 0.0023 | 1 | 0.372118 | -0.47 |
872 | 938 | 3o0w (A) | 27 | 84 | 45.00 | 0.35 | 0.08 | 0.12105 | 1.77 |
960 | 1438 | 3s28 (A) | 213 | 766 | 15.00 | 0 | 0.91 | 0.0915093 | 0.92 |
1055 | 1440 | 3c48 (A) | 0 | 404 | 26.00 | 0 | 1 | 0.583028 | -0.51 |
1209 | 1438 | 4hln (A) | 334 | 601 | 33.00 | 0.00000000014 | 1 | 0.370539 | -0.25 |
1268 | 1406 | 2f9f (A) | 16 | 152 | 31.00 | 0.000000017 | 1 | 0.545229 | -1.13 |
1271 | 1438 | 4x7r (A) | 324 | 491 | 26.00 | 0.0000037 | 1 | 0.507218 | -0.78 |
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:
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 60-80% percentile | VEG Tachyzoite. | Gregory |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Mid 40-60% percentile | ME49 Tachyzoite, ME49 merozoite, ME49 Oocyst, ME49 Bradyzoite. | Gregory Hehl AB Fritz HM Sibley/Greg |
Gregory | ToxoDB |
Sibley/Greg | ToxoDB |
Hehl AB | Asexual expansion of Toxoplasma gondii merozoites is distinct from tachyzoites and entails expression of non-overlapping gene families to attach, invade, and replicate within feline enterocytes. |
Fritz HM | Transcriptomic analysis of toxoplasma development reveals many novel functions and structures specific to sporozoites and oocysts. |
Ortholog group members (OG5_127579)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT2G36390 | 1,4-alpha-glucan branching enzyme 2-1 |
Arabidopsis thaliana | AT5G03650 | 1,4-alpha-glucan branching enzyme |
Brugia malayi | Bm1_02775 | 1,4-alpha-glucan branching enzyme |
Candida albicans | CaO19.13067 | likely glycogen branching enzyme |
Candida albicans | CaO19.5622 | likely glycogen branching enzyme |
Caenorhabditis elegans | CELE_T04A8.7 | Protein T04A8.7, isoform B |
Cryptosporidium hominis | Chro.60381 | 1,4-alpha-glucan branching enzyme |
Cryptosporidium parvum | cgd6_3280 | glycogen branching enzyme (1,4-alpha-glucan branching enzyme) |
Chlamydia trachomatis | CT_866 | 1,4-alpha-glucan branching enzyme |
Dictyostelium discoideum | DDB_G0274105 | 1,4-alpha-glucan branching enzyme |
Drosophila melanogaster | Dmel_CG33138 | 1,4-Alpha-Glucan Branching Enzyme |
Escherichia coli | b3432 | 1,4-alpha-glucan branching enzyme |
Echinococcus granulosus | EgrG_000239850 | glucan 14 alpha branching enzyme 1 |
Entamoeba histolytica | EHI_106090 | 1,4-alpha-glucan branching enzyme, putative |
Entamoeba histolytica | EHI_038160 | 1,4-alpha-glucan branching enzyme, putative |
Echinococcus multilocularis | EmuJ_000239850 | glucan (1,4 alpha), branching enzyme 1 |
Giardia lamblia | GL50803_15823 | 1,4-alpha-glucan branching enzyme |
Homo sapiens | ENSG00000114480 | glucan (1,4-alpha-), branching enzyme 1 |
Loa Loa (eye worm) | LOAG_06995 | hypothetical protein |
Mus musculus | ENSMUSG00000022707 | glucan (1,4-alpha-), branching enzyme 1 |
Mycobacterium tuberculosis | Rv1326c | 1,4-alpha-glucan branching enzyme GlgB (glycogen branching enzyme) |
Mycobacterium ulcerans | MUL_3936 | glycogen branching protein |
Neospora caninum | NCLIV_058980 | 1,4-alpha-glucan branching enzyme, putative |
Neospora caninum | NCLIV_004200 | hypothetical protein |
Oryza sativa | 4329532 | Os02g0528200 |
Oryza sativa | 4342117 | Os06g0726400 |
Saccharomyces cerevisiae | YEL011W | 1,4-alpha-glucan branching enzyme |
Schistosoma japonicum | Sjp_0065120 | ko:K00700 1,4-alpha-glucan branching enzyme [EC2.4.1.18], putative |
Schistosoma mansoni | Smp_094880 | starch branching enzyme II |
Schmidtea mediterranea | mk4.001372.07 | 1,4-alpha-glucan-branching enzyme |
Schmidtea mediterranea | mk4.001372.05 | |
Schmidtea mediterranea | mk4.001372.06 | |
Schmidtea mediterranea | mk4.001372.08 | 1,4-alpha-glucan-branching enzyme |
Schmidtea mediterranea | mk4.011524.03 | 1,4-alpha-glucan-branching enzyme |
Schmidtea mediterranea | mk4.005975.02 | 1,4-alpha-glucan-branching enzyme |
Toxoplasma gondii | TGME49_209960 | glycosyltransferase |
Toxoplasma gondii | TGME49_316520 | 1,4-alpha-glucan-branching enzyme |
Trichomonas vaginalis | TVAG_453180 | amylase, putative |
Trichomonas vaginalis | TVAG_276310 | starch branching enzyme II, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
mtu1349 | Mycobacterium tuberculosis | essential | nmpdr |
b3432 | Escherichia coli | non-essential | goodall |
CELE_T04A8.7 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_T04A8.7 | Caenorhabditis elegans | slow growth | wormbase |
TGME49_316520 | Toxoplasma gondii | Essentiality uncertain | sidik |
TGME49_209960 this record | Toxoplasma gondii | Essentiality uncertain | sidik |
TGME49_316520 | Toxoplasma gondii | Probably non-essential | sidik |
TGME49_209960 this record | Toxoplasma gondii | Probably non-essential | sidik |
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 |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
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 |
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.
Druggability index (range: 0 to 1): 0.1
Species | Target | Length | Identity | Alignment span | Linked Drugs | Reference |
---|---|---|---|---|---|---|
Mycobacterium tuberculosis | Glycosyltransferase MshA | 480 aa | 29.2% | 415 aa | Compounds | References |
Mycobacterium leprae | GLYCOSYLTRANSFERASE MSHA | 428 aa | 28.6% | 378 aa | Compounds | References |