pI: 7.342 |
Length (AA): 650 |
MW (Da): 70567 |
Paralog Number:
0
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 7 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 |
---|---|---|---|---|---|---|---|---|---|
25 | 348 | 1u5q (A) | 28 | 316 | 15.00 | 0 | 1 | 0.64 | -0.57 |
188 | 595 | 1b3u (A) | 70 | 483 | 13.00 | 0.000068 | 0.08 | 0.69 | -0.41 |
24 | 321 | 2vwi (D) | 16 | 298 | 15.00 | 0 | 1 | 0.350862 | 0.68 |
109 | 264 | 1sl0 (A) | 216 | 380 | 32.00 | 0.88 | 0.39 | 0.1727 | 2.27 |
432 | 591 | 4g3a (A) | 50 | 206 | 14.00 | 0 | 0.46 | 0.435254 | -0.59 |
586 | 638 | 4k35 (A) | 13 | 60 | 23.00 | 0 | 0.04 | 0.196638 | -0.05 |
586 | 638 | 2kpy (A) | 54 | 106 | 42.00 | 0.0014 | 0.02 | 0.362238 | 0.62 |
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 |
---|---|---|---|
Mid 40-60% percentile | amastigotes, metacyclic. | Fernandes MC |
Fernandes MC | Dual Transcriptome Profiling of Leishmania-Infected Human Macrophages Reveals Distinct Reprogramming Signatures. |
Ortholog group members (OG5_129163)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT1G71410 | putative protein kinase |
Arabidopsis thaliana | AT1G22870 | protein kinase family protein |
Brugia malayi | Bm1_03320 | Protein kinase domain containing protein |
Candida albicans | CaO19.765 | similar to C terminus of S. cerevisiae SCY1 (YGL083W) suppressor of GTPase mutant |
Candida albicans | CaO19.764 | similar to N terminus of S.cereviisae SCY1 (YGL083W) suppressor of GTPase mutant |
Candida albicans | CaO19.8384 | similar to N terminus of S.cereviisae SCY1 (YGL083W) suppressor of GTPase mutant |
Candida albicans | CaO19.8385 | similar to C terminus of S.cereviisae SCY1 (YGL083W) suppressor of GTPase mutant |
Caenorhabditis elegans | CELE_ZC581.9 | Protein ZC581.9 |
Dictyostelium discoideum | DDB_G0270808 | SCY1 family protein kinase |
Drosophila melanogaster | Dmel_CG1951 | CG1951 gene product from transcript CG1951-RA |
Echinococcus granulosus | EgrG_001185650 | scy1 protein 2 |
Echinococcus multilocularis | EmuJ_001185650 | scy1 protein 2 |
Homo sapiens | ENSG00000136021 | SCY1-like 2 (S. cerevisiae) |
Leishmania braziliensis | LbrM.35.0210 | hypothetical protein, unknown function |
Leishmania donovani | LdBPK_360150.1 | hypothetical protein, unknown function |
Leishmania infantum | LinJ.36.0150 | hypothetical protein, unknown function |
Leishmania major | LmjF.36.0140 | hypothetical protein, unknown function |
Leishmania mexicana | LmxM.36.0140 | hypothetical protein, unknown function |
Loa Loa (eye worm) | LOAG_07792 | SCY1 protein kinase |
Loa Loa (eye worm) | LOAG_05285 | hypothetical protein |
Loa Loa (eye worm) | LOAG_06308 | SCY1 protein kinase |
Mus musculus | ENSMUSG00000069539 | SCY1-like 2 (S. cerevisiae) |
Neospora caninum | NCLIV_005990 | DEHA2D02640p, related |
Oryza sativa | 4326650 | Os01g0616100 |
Saccharomyces cerevisiae | YGL083W | Scy1p |
Schistosoma japonicum | Sjp_0100510 | SCY1-like protein 2, putative |
Schistosoma mansoni | Smp_126740 | protein kinase |
Schmidtea mediterranea | mk4.000982.12 | SCY1-like protein 2 |
Schmidtea mediterranea | mk4.000982.14 | SCY1-like protein 2 |
Schmidtea mediterranea | mk4.000982.13 | |
Schmidtea mediterranea | mk4.010605.00 | |
Toxoplasma gondii | TGME49_222960 | SCY kinase-related protein (incomplete catalytic triad) |
Trichomonas vaginalis | TVAG_024740 | serine-threonine protein kinase, putative |
Trichomonas vaginalis | TVAG_477100 | TKL family protein kinase |
Trichomonas vaginalis | TVAG_052050 | TKL family protein kinase |
Trichomonas vaginalis | TVAG_295330 | conserved hypothetical protein |
Trichomonas vaginalis | TVAG_179950 | serine-threonine protein kinase, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
CELE_ZC581.9 | Caenorhabditis elegans | larval arrest | wormbase |
TGME49_222960 | Toxoplasma gondii | Essentiality uncertain | sidik |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
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 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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.