pI: 6.3686 |
Length (AA): 622 |
MW (Da): 70585 |
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 8 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 |
---|---|---|---|---|---|---|---|---|---|
4 | 81 | 1na3 (A) | 2 | 71 | 23.00 | 0.0000000014 | 0.52 | 0.32 | -0.41 |
6 | 183 | 2fo7 (A) | 1 | 134 | 22.00 | 0 | 1 | 0.24 | 0.26 |
451 | 577 | 1na0 (A) | 10 | 119 | 25.00 | 0 | 1 | 0.47 | -0.87 |
2 | 31 | 1w3b (A) | 75 | 104 | 20.00 | 0.1 | 0.16 | 0.259632 | -0.23 |
195 | 563 | 4i1a (B) | 15 | 367 | 13.00 | 0 | 1 | 0.688048 | 0.43 |
338 | 438 | 3vtx (A) | 52 | 176 | 34.00 | 0.22 | 0.71 | 0.351279 | -0.15 |
403 | 529 | 3u3w (A) | 150 | 274 | 14.00 | 0 | 0.55 | 0.42398 | -0.83 |
462 | 532 | 4a1s (B) | 310 | 384 | 13.00 | 0 | 0.28 | 0.308948 | -0.97 |
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 80-100% percentile | amastigotes. | Fernandes MC |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 60-80% percentile | metacyclic. | Fernandes MC |
Fernandes MC | Dual Transcriptome Profiling of Leishmania-Infected Human Macrophages Reveals Distinct Reprogramming Signatures. |
Ortholog group members (OG5_126634)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT3G27960 | tetratricopeptide repeat domain-containing protein |
Arabidopsis thaliana | AT1G27500 | tetratricopeptide repeat domain-containing protein |
Arabidopsis thaliana | AT4G10840 | protein KINESIN LIGHT CHAIN-RELATED 1 |
Babesia bovis | BBOV_IV009180 | hypothetical protein |
Brugia malayi | Bm1_11290 | TPR Domain containing protein |
Dictyostelium discoideum | DDB_G0292714 | hypothetical protein |
Giardia lamblia | GL50803_11177 | Kinesin-like protein |
Leishmania braziliensis | LbrM.34.0680 | hypothetical protein, conserved |
Leishmania donovani | LdBPK_350700.1 | Tetratricopeptide repeat, putative |
Leishmania infantum | LinJ.35.0700 | hypothetical protein, conserved |
Leishmania major | LmjF.35.0690 | hypothetical protein, conserved |
Leishmania mexicana | LmxM.34.0690 | hypothetical protein, conserved |
Loa Loa (eye worm) | LOAG_04261 | TPR Domain containing protein |
Mus musculus | 102634091 | predicted gene, 31757 |
Oryza sativa | 4330477 | Os02g0708400 |
Oryza sativa | 4328037 | Os02g0109800 |
Onchocerca volvulus | OVOC8007 | Tetratricopeptide repeat protein 28 homolog |
Plasmodium berghei | PBANKA_1355400 | tetratricopeptide repeat protein, putative |
Plasmodium falciparum | PF3D7_1342300 | tetratricopeptide repeat protein, putative |
Plasmodium knowlesi | PKNH_1259100 | tetratricopeptide repeat protein, putative |
Plasmodium vivax | PVX_083015 | hsp70 interacting protein, putative |
Plasmodium yoelii | PY01575 | hypothetical protein |
Schmidtea mediterranea | mk4.002060.00 | |
Trypanosoma brucei gambiense | Tbg972.10.4690 | hypothetical protein, conserved |
Trypanosoma brucei | Tb927.10.3770 | predicted TPR repeat protein |
Trypanosoma congolense | TcIL3000_10_3100 | predicted TPR repeat protein |
Trypanosoma cruzi | TcCLB.511001.180 | hypothetical protein, conserved |
Trypanosoma cruzi | TcCLB.509017.40 | hypothetical protein, conserved |
Theileria parva | TP01_0854 | hypothetical protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.10.3770 | Trypanosoma brucei | significant gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.10.3770 | Trypanosoma brucei | significant gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.10.3770 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.10.3770 | Trypanosoma brucei | significant gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
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 |
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.