pI: 7.8075 |
Length (AA): 806 |
MW (Da): 89465 |
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 6 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 |
---|---|---|---|---|---|---|---|---|---|
255 | 699 | 1cm8 (A) | 14 | 353 | 25.00 | 0 | 1 | 0.34 | 0.28 |
459 | 655 | 1z57 (A) | 262 | 477 | 30.00 | 0 | 1 | 0.6 | -1.24 |
250 | 674 | 3mi9 (A) | 9 | 334 | 37.00 | 0 | 1 | 0.523395 | 0.76 |
461 | 655 | 4bgq (A) | 111 | 297 | 38.00 | 0 | 1 | 0.657035 | -0.53 |
464 | 572 | 2bdw (A) | 115 | 225 | 32.00 | 0.00000081 | 0.94 | 0.463336 | 0.28 |
467 | 560 | 4bf2 (A) | 785 | 881 | 46.00 | 0 | 0.4 | 0.505725 | 0.23 |
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 | epimastigote, metacyclic. | Smircich P |
Smircich P | Ribosome profiling reveals translation control as a key mechanism generating differential gene expression in Trypanosoma cruzi. |
Ortholog group members (OG5_135486)
Species | Accession | Gene Product |
---|---|---|
Babesia bovis | BBOV_I001950 | protein kinase domain containing protein |
Cryptosporidium hominis | Chro.60177 | cdc2-related protein kinase |
Cryptosporidium parvum | cgd6_1420 | cdc2-related protein kinase, putative |
Leishmania braziliensis | LbrM.27.2100 | protein kinase-like protein |
Leishmania donovani | LdBPK_271860.1 | cdc2-related kinase 9 |
Leishmania infantum | LinJ.27.1860 | protein kinase-like protein |
Leishmania major | LmjF.27.1940 | protein kinase-like protein |
Leishmania mexicana | LmxM.27.1940 | protein kinase-like protein |
Neospora caninum | NCLIV_065460 | CMGC kinase, putative |
Plasmodium berghei | PBANKA_0717300 | cdc2-related protein kinase 3 |
Plasmodium falciparum | PF3D7_0415300 | cdc2-related protein kinase 3 |
Plasmodium knowlesi | PKNH_0506900 | protein kinase, putative |
Plasmodium vivax | PVX_089720 | protein kinase domain containing protein |
Plasmodium yoelii | PY04026 | cdc-2 related kinase 3 |
Trypanosoma brucei gambiense | Tbg.972.2.2560 | protein kinase, putative |
Trypanosoma brucei | Tb927.2.4510 | cdc2-related kinase 9 |
Trypanosoma congolense | TcIL3000_2_850 | cdc2-related kinase 9 |
Trypanosoma cruzi | TcCLB.507209.40 | cdc2-related kinase 9 |
Trypanosoma cruzi | TcCLB.509099.150 | cdc2-related kinase 9 |
Toxoplasma gondii | TGME49_249260 | cell-cycle-associated protein kinase CDK, putative |
Theileria parva | TP03_0140 | cell division cycle 2 protein kinase, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.2.4510 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.2.4510 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.2.4510 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb927.2.4510 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
PBANKA_0717300 | Plasmodium berghei | Essential | plasmo |
TGME49_249260 | Toxoplasma gondii | Essentiality uncertain | sidik |
neb | C. elegans RNAi phenotypes | Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs |
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 |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
keio | Systematic single-gene knock-out mutants of E. coli K12 | The Keio Collection |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
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): 0.4
Species | Target | Length | Identity | Alignment span | Linked Drugs | Reference |
---|---|---|---|---|---|---|
Patiria pectinifera | Cdc2 | 300 aa | 33.2% | 241 aa | Compounds | References |
Rattus norvegicus | Cell division protein kinase 5 | 292 aa | 34.4% | 244 aa | Compounds | References |
Homo sapiens | Cyclin-dependent kinase 1/cyclin B1 | 297 aa | 33.3% | 243 aa | Compounds | References |