pI: 6.618 |
Length (AA): 278 |
MW (Da): 29700 |
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 4 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 |
---|---|---|---|---|---|---|---|---|---|
6 | 275 | 3rss (A) | 214 | 488 | 22.00 | 0.000000000099 | 1 | 1.14032 | 0.16 |
6 | 240 | 3rss (A) | 214 | 462 | 31.00 | 0.0000000000066 | 1 | 1.10022 | 0 |
20 | 275 | 3rss (A) | 241 | 488 | 25.00 | 0 | 1 | 1.18386 | -0.27 |
31 | 274 | 3dzv (A) | 9 | 260 | 14.00 | 0 | 1 | 1.0617 | -0.57 |
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_127151)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G19150 | pfkB-like carbohydrate kinase family protein |
Brugia malayi | Bm1_07040 | YjeF-related protein, C-terminus containing protein |
Candida albicans | CaO19.11002 | similar to S. cerevisiae YKL151C |
Candida albicans | CaO19.3508 | similar to S. cerevisiae YKL151C |
Caenorhabditis elegans | CELE_R107.2 | Protein R107.2 |
Cryptosporidium hominis | Chro.70406 | ENSANGP00000015295 |
Cryptosporidium parvum | cgd7_3640 | YjeF family of predicted nucleotide binding proteins |
Dictyostelium discoideum | DDB_G0290799 | uncharacterized protein family, carbohydrate kinase-related |
Drosophila melanogaster | Dmel_CG10424 | CG10424 gene product from transcript CG10424-RA |
Escherichia coli | b4167 | bifunctional NAD(P)H-hydrate repair enzyme |
Echinococcus granulosus | EgrG_000434000 | carbohydrate kinase domain containing protein |
Entamoeba histolytica | EHI_194450 | hypothetical protein, conserved |
Echinococcus multilocularis | EmuJ_000434000 | carbohydrate kinase domain containing protein |
Giardia lamblia | GL50803_4255 | Sugar kinase, putative |
Homo sapiens | ENSG00000213995 | carbohydrate kinase domain containing |
Leishmania braziliensis | LbrM.14.1360 | hypothetical protein, conserved |
Leishmania donovani | LdBPK_141270.1 | Bifunctional NAD(P)H-hydrate repair enzyme |
Leishmania infantum | LinJ.14.1270 | hypothetical protein, conserved |
Leishmania major | LmjF.14.1190 | hypothetical protein, conserved |
Leishmania mexicana | LmxM.14.1190 | hypothetical protein, conserved |
Loa Loa (eye worm) | LOAG_04267 | hypothetical protein |
Mycobacterium leprae | ML0373 | Conserved hypothetical protein |
Mus musculus | ENSMUSG00000031505 | carbohydrate kinase domain containing |
Mycobacterium tuberculosis | Rv3433c | Conserved protein |
Mycobacterium ulcerans | MUL_0877 | transmembrane protein |
Oryza sativa | 4350275 | Os11g0276300 |
Plasmodium berghei | PBANKA_0905100 | ATP-dependent (S)-NAD(P)H-hydrate dehydratase, putative |
Plasmodium falciparum | PF3D7_1143900 | ATP-dependent (S)-NAD(P)H-hydrate dehydratase, putative |
Plasmodium knowlesi | PKNH_0941800 | ATP-dependent (S)-NAD(P)H-hydrate dehydratase, putative |
Plasmodium vivax | PVX_092800 | carbohydrate kinase, putative |
Plasmodium yoelii | PY02608 | YjeF-related protein, C-terminus |
Saccharomyces cerevisiae | YKL151C | NADHX dehydratase |
Schistosoma japonicum | Sjp_0303960 | similar to Uncharacterized protein FLJ10769 homolog precursor, putative |
Schistosoma mansoni | Smp_000470 | hypothetical protein |
Schmidtea mediterranea | mk4.003659.00 | ATP-dependent |
Trypanosoma brucei gambiense | Tbg972.7.4200 | hypothetical protein, conserved |
Trypanosoma brucei | Tb927.7.3770 | Bifunctional NAD(P)H-hydrate repair enzyme |
Trypanosoma congolense | TcIL3000_7_3030 | Bifunctional NAD(P)H-hydrate repair enzyme |
Trypanosoma cruzi | TcCLB.506795.44 | Bifunctional NAD(P)H-hydrate repair enzyme |
Trypanosoma cruzi | TcCLB.509937.20 | Bifunctional NAD(P)H-hydrate repair enzyme |
Toxoplasma gondii | TGME49_258160 | carbohydrate kinase |
Trichomonas vaginalis | TVAG_468220 | conserved hypothetical protein |
Trichomonas vaginalis | TVAG_051000 | conserved hypothetical protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
mtu3494 | Mycobacterium tuberculosis | non-essential | nmpdr |
Tb927.7.3770 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.7.3770 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.7.3770 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.7.3770 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
b4167 | Escherichia coli | non-essential | goodall |
PBANKA_0905100 | Plasmodium berghei | Dispensable | plasmo |
TGME49_258160 | Toxoplasma gondii | Probably non-essential | sidik |
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 |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
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.