pI: 5.0154 |
Length (AA): 239 |
MW (Da): 26340 |
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 5 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 |
---|---|---|---|---|---|---|---|---|---|
3 | 230 | 3dup (A) | 31 | 270 | 18.00 | 0 | 1 | 0.853675 | 0.75 |
42 | 218 | 1nqz (A) | 4 | 190 | 25.00 | 0.0000079 | 0.98 | 1.04349 | -0.34 |
43 | 226 | 5t3p (A) | 18 | 210 | 20.00 | 0.000000059 | 0.99 | 1.04377 | -0.24 |
87 | 124 | 1f3y (A) | 31 | 67 | 51.00 | 0.074 | 0.49 | 0.572796 | 1.2 |
97 | 128 | 4kg3 (A) | 129 | 160 | 41.00 | 0.13 | 0.83 | 0.619691 | 0.02 |
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_127325)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G45940 | CoA pyrophosphatase |
Arabidopsis thaliana | AT2G33980 | nudix hydrolase 22 |
Arabidopsis thaliana | AT1G28960 | ppGpp pyrophosphohydrolase |
Brugia malayi | Bm1_26925 | hydrolase, NUDIX family protein |
Candida albicans | CaO19.6591 | similar to S. cerevisiae peroxisomal nudix hydrolase active towards coenzyme A and its derivatives |
Caenorhabditis elegans | CELE_Y87G2A.14 | Protein NDX-8 |
Caenorhabditis elegans | CELE_Y38A8.1 | Protein NDX-3 |
Drosophila melanogaster | Dmel_CG11095 | CG11095 gene product from transcript CG11095-RA |
Escherichia coli | b1813 | putative CoA pyrophosphohydrolase, weak 3-phosphohydroxypyruvate phosphatase |
Homo sapiens | ENSG00000167799 | nudix (nucleoside diphosphate linked moiety X)-type motif 8 |
Homo sapiens | ENSG00000140876 | nudix (nucleoside diphosphate linked moiety X)-type motif 7 |
Leishmania braziliensis | LbrM.35.0380 | NUDIX hydrolase protein, conserved |
Leishmania donovani | LdBPK_360320.1 | Mutt-Nudix-related hydrolase 5, putative |
Leishmania infantum | LinJ.36.0320 | NUDIX hydrolase protein, conserved |
Leishmania major | LmjF.36.0300 | NUDIX hydrolase protein, conserved |
Leishmania mexicana | LmxM.36.0300 | NUDIX hydrolase protein, conserved |
Loa Loa (eye worm) | LOAG_06928 | hydrolase |
Mycobacterium leprae | ML2299c | conserved hypothetical protein |
Mus musculus | ENSMUSG00000024869 | nudix (nucleoside diphosphate linked moiety X)-type motif 8 |
Mus musculus | ENSMUSG00000031767 | nudix (nucleoside diphosphate linked moiety X)-type motif 7 |
Mycobacterium tuberculosis | Rv3672c | Conserved hypothetical protein |
Mycobacterium ulcerans | MUL_4962 | hypothetical protein |
Oryza sativa | 4338090 | Os05g0209400 |
Oryza sativa | 4345421 | Os08g0375900 |
Oryza sativa | 4345423 | Os08g0376200 |
Saccharomyces cerevisiae | YLR151C | Pcd1p |
Schmidtea mediterranea | mk4.003184.05 | Peroxisomal coenzyme A diphosphatase ndx-8 |
Trypanosoma brucei gambiense | Tbg972.10.5700 | NUDIX hydrolase, conserved,predicted MutT/NUDIX family protein, putative |
Trypanosoma brucei | Tb927.10.4680 | Mutt-Nudix-related hydrolase 5, putative |
Trypanosoma congolense | TcIL3000_10_3890 | Mutt-Nudix-related hydrolase 5, putative |
Trypanosoma cruzi | TcCLB.508169.129 | Mutt-Nudix-related hydrolase 5, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
mtu3734 | Mycobacterium tuberculosis | non-essential | nmpdr |
Tb927.10.4680 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.10.4680 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.10.4680 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.10.4680 | Trypanosoma brucei | significant gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
b1813 | Escherichia coli | non-essential | goodall |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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 |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
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 |
neb | C. elegans RNAi phenotypes | Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs |
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.