pI: 6.9727 |
Length (AA): 2437 |
MW (Da): 277918 |
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 12 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 |
---|---|---|---|---|---|---|---|---|---|
657 | 1543 | 3gjx (A) | 58 | 917 | 12.00 | 0 | 0.91 | 0.440772 | 0.32 |
971 | 1208 | 4hxt (A) | 1 | 241 | 13.00 | 0 | 0.07 | 0.244461 | -0.46 |
1395 | 1465 | 2lo1 (A) | 5 | 70 | 32.00 | 0.000000011 | 1 | 0.480834 | -1.13 |
1396 | 2229 | 3ibv (A) | 27 | 921 | 12.00 | 0 | 0.97 | 0.366024 | 0.5 |
1410 | 1456 | 2dn9 (A) | 18 | 65 | 49.00 | 0.000081 | 1 | 0.660186 | -1.71 |
1410 | 1456 | 4j7z (A) | 16 | 62 | 43.00 | 0.0086 | 1 | 0.652186 | -1.93 |
1908 | 2348 | 3ifq (B) | 146 | 603 | 11.00 | 0 | 0.98 | 0.35876 | -0.58 |
2114 | 2361 | 5aei (A) | 13 | 253 | 7.00 | 0 | 0.17 | 0.269464 | -1.12 |
2140 | 2361 | 4v3r (A) | 12 | 253 | 14.00 | 0.0000000000069 | 0.8 | 0.290796 | -0.91 |
2201 | 2379 | 4rzp (A) | 46 | 219 | 13.00 | 0 | 0.71 | 0.383151 | -1.4 |
2210 | 2382 | 5mfi (A) | 62 | 234 | 12.00 | 0 | 0.99 | 0.397689 | -1.39 |
2239 | 2393 | 4u2x (D) | 335 | 500 | 12.00 | 0.001 | 0.81 | 0.272303 | -0.99 |
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_129678)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT2G26890 | gravitropism defective 2 |
Brugia malayi | Bm1_08070 | DnaJ domain containing protein |
Caenorhabditis elegans | CELE_F18C12.2 | Protein RME-8, isoform A |
Dictyostelium discoideum | DDB_G0286293 | hypothetical protein |
Drosophila melanogaster | Dmel_CG8014 | Receptor mediated endocytosis 8 |
Echinococcus granulosus | EgrG_000345600 | dnaJ subfamily C 3 |
Entamoeba histolytica | EHI_041980 | hypothetical protein, conserved |
Entamoeba histolytica | EHI_188910 | hypothetical protein, conserved |
Entamoeba histolytica | EHI_200560 | hypothetical protein, conserved |
Echinococcus multilocularis | EmuJ_000345600 | dnaJ subfamily C 3 |
Homo sapiens | ENSG00000138246 | DnaJ (Hsp40) homolog, subfamily C, member 13 |
Leishmania braziliensis | LbrM.30.2160 | endosomal trafficking protein RME-8, putative |
Leishmania donovani | LdBPK_302220.1 | endosomal trafficking protein RME-8, putative |
Leishmania infantum | LinJ.30.2220 | endosomal trafficking protein RME-8, putative |
Leishmania major | LmjF.30.2210 | endosomal trafficking protein RME-8, putative |
Leishmania mexicana | LmxM.29.2210 | endosomal trafficking protein RME-8, putative |
Loa Loa (eye worm) | LOAG_05007 | hypothetical protein |
Loa Loa (eye worm) | LOAG_05008 | hypothetical protein |
Mus musculus | ENSMUSG00000032560 | DnaJ (Hsp40) homolog, subfamily C, member 13 |
Oryza sativa | 4349486 | Os10g0575200 |
Schistosoma japonicum | Sjp_0002640 | ko:K09533 DnaJ homolog, subfamily C, member 13, putative |
Schistosoma mansoni | Smp_175760 | endosomal trafficking protein |
Schmidtea mediterranea | mk4.000044.16 | |
Schmidtea mediterranea | mk4.000044.14 | DnaJ homolog subfamily C member 13 |
Schmidtea mediterranea | mk4.000044.12 | DnaJ homolog subfamily C member 13 |
Schmidtea mediterranea | mk4.000044.13 | DnaJ homolog subfamily C member 13 |
Schmidtea mediterranea | mk4.000044.15 | DnaJ homolog subfamily C member 13 |
Trypanosoma brucei gambiense | Tbg972.6.3250 | endosomal trafficking protein RME-8, putative |
Trypanosoma brucei | Tb927.6.3500 | endosomal trafficking protein RME-8, putative |
Trypanosoma congolense | TcIL3000_6_3040 | endosomal trafficking protein RME-8, putative |
Trypanosoma cruzi | TcCLB.511511.10 | endosomal trafficking protein RME-8, putative |
Trypanosoma cruzi | TcCLB.506941.9 | endosomal trafficking protein RME-8, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.6.3500 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.6.3500 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.6.3500 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb927.6.3500 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_F18C12.2 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_F18C12.2 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_F18C12.2 | Caenorhabditis elegans | larval lethal | wormbase |
CELE_F18C12.2 | Caenorhabditis elegans | slow growth | wormbase |
CELE_F18C12.2 | Caenorhabditis elegans | sterile | wormbase |
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 |
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 |
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.