pI: 8.1721 |
Length (AA): 266 |
MW (Da): 29829 |
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:
PDB Structures:
Ortholog group members (OG5_134118)
Species | Accession | Gene Product |
---|---|---|
Cryptosporidium hominis | Chro.70196 | similar to protein MGC35182 |
Cryptosporidium parvum | cgd7_1660 | STOP repeat protein involved in microtubule stabilization (possible variant metal binding site at N-terminus) |
Leishmania braziliensis | LbrM.24.2060 | hypothetical protein, conserved |
Leishmania donovani | LdBPK_242060.1 | hypothetical protein, conserved |
Leishmania infantum | LinJ.24.2060 | hypothetical protein, conserved |
Leishmania major | LmjF.24.1980 | hypothetical protein, conserved |
Leishmania mexicana | LmxM.24.1980 | hypothetical protein, conserved |
Neospora caninum | NCLIV_024420 | hypothetical protein |
Plasmodium berghei | PBANKA_0810700 | subpellicular microtubule protein 1, putative |
Plasmodium falciparum | PF3D7_0909500 | subpellicular microtubule protein 1, putative |
Plasmodium knowlesi | PKNH_0707500 | subpellicular microtubule protein 1, putative |
Plasmodium vivax | PVX_135260 | unspecified product |
Plasmodium vivax | PVX_098915 | subpellicular microtubule protein 1, putative |
Plasmodium yoelii | PY03130 | repetitive proline rich protein, putative |
Schistosoma japonicum | Sjp_0036730 | expressed protein |
Schistosoma mansoni | Smp_034680 | hypothetical protein |
Schmidtea mediterranea | mk4.001401.02 | |
Trypanosoma brucei gambiense | Tbg972.8.6300 | hypothetical protein, conserved |
Trypanosoma brucei | Tb927.8.6240 | STOP axonemal protein |
Trypanosoma congolense | TcIL3000_0_45660 | STOP axonemal protein |
Trypanosoma cruzi | TcCLB.511903.190 | STOP axonemal protein, putative |
Trypanosoma cruzi | TcCLB.511065.10 | STOP axonemal protein, putative |
Toxoplasma gondii | TGME49_263520 | microtubule associated protein SPM1 |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.8.6240 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.8.6240 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.8.6240 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.8.6240 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
PBANKA_0810700 | Plasmodium berghei | Dispensable | plasmo |
TGME49_263520 | Toxoplasma gondii | Probably non-essential | sidik |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
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 |
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.