pI: 4.9863 |
Length (AA): 860 |
MW (Da): 97249 |
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 4 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 |
---|---|---|---|---|---|---|---|---|---|
420 | 823 | 4tnd (A) | 82 | 474 | 18.00 | 0 | 1 | 0.523467 | 0.52 |
503 | 857 | 4ian (A) | 676 | 1004 | 32.00 | 0 | 1 | 0.725291 | -0.53 |
626 | 723 | 2h34 (A) | 114 | 211 | 45.00 | 0.017 | 0.86 | 0.380453 | -0.01 |
821 | 857 | 2dyl (A) | 361 | 397 | 30.00 | 0 | 0.29 | 0.316723 | 0.01 |
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_130162)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT3G17750 | protein kinase family protein |
Arabidopsis thaliana | AT1G73460 | putative serine/threonine kinase |
Arabidopsis thaliana | AT1G73450 | putative protein kinase |
Arabidopsis thaliana | AT2G40120 | putative serine/threonine protein kinase |
Babesia bovis | BBOV_III009650 | protein kinase domain containing protein |
Cryptosporidium hominis | Chro.70343 | dual-specificity tyrosine-(Y)-phosphorylation regulated kinase TbPK4 |
Cryptosporidium parvum | cgd7_3050 | protein kinase |
Giardia lamblia | GL50803_17558 | Kinase, CMGC DYRK |
Giardia lamblia | GL50803_137695 | Kinase, CMGC DYRK |
Leishmania braziliensis | LbrM.14.1060 | protein kinase, putative |
Leishmania braziliensis | LbrM.21.1940 | protein kinase, putative |
Leishmania donovani | LdBPK_212010.1 | protein kinase, putative |
Leishmania donovani | LdBPK_141140.1 | protein kinase, putative |
Leishmania infantum | LinJ.14.1140 | protein kinase, putative |
Leishmania infantum | LinJ.21.2010 | protein kinase, putative |
Leishmania major | LmjF.21.1650 | protein kinase, putative |
Leishmania major | LmjF.14.1070 | protein kinase, putative |
Leishmania mexicana | LmxM.14.1070 | protein kinase, putative |
Leishmania mexicana | LmxM.21.1650 | protein kinase, putative |
Neospora caninum | NCLIV_020950 | CMGC kinase, Dyrk family, putative |
Oryza sativa | 4327402 | Os01g0832900 |
Oryza sativa | 4333928 | Os03g0719500 |
Oryza sativa | 4339052 | Os05g0466900 |
Trypanosoma brucei gambiense | Tbg972.10.280 | protein kinase, putative |
Trypanosoma brucei gambiense | Tbg972.7.4330 | protein kinase, putative |
Trypanosoma brucei | Tb927.10.350 | protein kinase PK4, putative |
Trypanosoma brucei | Tb927.7.3880 | Basal body protein |
Trypanosoma congolense | TcIL3000_10_210 | protein kinase, putative |
Trypanosoma cruzi | TcCLB.510519.40 | protein kinase PK4, putative |
Trypanosoma cruzi | TcCLB.506869.60 | protein kinase PK4, putative |
Trypanosoma cruzi | TcCLB.511249.60 | CMGC/DYRK protein kinase, putative |
Toxoplasma gondii | TGME49_204280 | cell-cycle-associated protein kinase DYRK, putative |
Theileria parva | TP04_0880 | protein kinase, putative |
Trichomonas vaginalis | TVAG_000200 | CMGC family protein kinase |
Trichomonas vaginalis | TVAG_396210 | CMGC family protein kinase |
Trichomonas vaginalis | TVAG_048130 | CMGC family protein kinase |
Trichomonas vaginalis | TVAG_238860 | CMGC family protein kinase |
Trichomonas vaginalis | TVAG_362360 | CMGC family protein kinase |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.7.3880 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.7.3880 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.7.3880 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb927.7.3880 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
Tb927.10.350 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.10.350 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.10.350 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.10.350 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
TGME49_204280 | Toxoplasma gondii | Probably essential | sidik |
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 |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
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 |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
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 |
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 | Target | Length | Identity | Alignment span | Linked Drugs | Reference |
---|---|---|---|---|---|---|
Plasmodium falciparum (isolate 3D7) | Cell division control protein 2 homolog | 288 aa | 24.1% | 345 aa | Compounds | References |