pI: 6.2338 |
Length (AA): 602 |
MW (Da): 64951 |
Paralog Number:
0
Signal peptide: N | GPI Anchor: | 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 3 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 |
---|---|---|---|---|---|---|---|---|---|
2 | 597 | 4bju (A) | 1 | 538 | 37.00 | 0 | 1 | 1.30243 | 0.09 |
31 | 596 | 2dka (A) | 24 | 544 | 40.00 | 0 | 1 | 1.2458 | -0.03 |
499 | 602 | 1wjw (A) | 5 | 100 | 52.00 | 0 | 1 | 0.608257 | 0.82 |
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 60-80% percentile | Procyclic, Bloodstream Form. | Siegel TN |
Siegel TN | Genome-wide analysis of mRNA abundance in two life-cycle stages of Trypanosoma brucei and identification of splicing and polyadenylation sites. |
Ortholog group members (OG5_128133)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT5G18070 | phosphoacetylglucosamine mutase |
Babesia bovis | BBOV_III000660 | phosphoglucomutase, putative |
Brugia malayi | Bm1_37950 | Phosphoglucomutase/phosphomannomutase, C-terminal domain containing protein |
Candida albicans | CaO19.12480 | phosphoacetylglucosamine mutase |
Candida albicans | CaO19.5013 | phosphoacetylglucosamine mutase |
Caenorhabditis elegans | CELE_F21D5.1 | Protein F21D5.1 |
Cryptosporidium hominis | Chro.40374 | hypothetical protein |
Cryptosporidium parvum | cgd4_3310 | phosphoacetyl glucosamine mutase |
Drosophila melanogaster | Dmel_CG10627 | nesthocker |
Echinococcus granulosus | EgrG_000613800 | phosphoacetylglucosamine mutase |
Echinococcus multilocularis | EmuJ_000613800 | phosphoacetylglucosamine mutase |
Homo sapiens | ENSG00000013375 | phosphoglucomutase 3 |
Leishmania braziliensis | LbrM.04.0010 | phosphoacetylglucosamine mutase-like gene |
Leishmania donovani | LdBPK_070930.1 | phosphoacetylglucosamine mutase-like protein |
Leishmania infantum | LinJ.07.0930 | phosphoacetylglucosamine mutase-like protein,acetylglucosaminephosphomutase, putative,N-acetylglucosamine-phosphate mutase, puta |
Leishmania major | LmjF.07.0805 | phosphoacetylglucosamine mutase-like protein,acetylglucosaminephosphomutase, putative,N-acetylglucosamine-phosphate mutase, puta |
Leishmania mexicana | LmxM.07.0805 | phosphoacetylglucosamine mutase-like protein,acetylglucosaminephosphomutase, putative,N-acetylglucosamine-phosphate mutase, puta |
Loa Loa (eye worm) | LOAG_03926 | phosphoglucomutase/phosphomannomutase domain-containing protein |
Mus musculus | 109785 | phosphoglucomutase 3 |
Neospora caninum | NCLIV_040500 | GK12616, related |
Oryza sativa | 4342646 | Os07g0195400 |
Onchocerca volvulus | OVOC4292 |
|
Plasmodium berghei | PBANKA_0918200 | phosphoacetylglucosamine mutase, putative |
Plasmodium falciparum | PF3D7_1130000 | phosphoacetylglucosamine mutase, putative |
Plasmodium knowlesi | PKNH_0927900 | phosphoacetylglucosamine mutase, putative |
Plasmodium vivax | PVX_092110 | phosphoacetylglucosamine mutase, putative |
Plasmodium yoelii | PY02130 | phosphoacetylglucosamine mutase |
Saccharomyces cerevisiae | YEL058W | phosphoacetylglucosamine mutase PCM1 |
Schistosoma japonicum | Sjp_0300980 | ko:K01836 phosphoacetylglucosamine mutase [EC5.4.2.3], putative |
Schistosoma mansoni | Smp_157710 | phosphoglucomutase |
Schmidtea mediterranea | mk4.000120.03 | Phosphoacetylglucosamine mutase |
Schmidtea mediterranea | mk4.000120.11 | Phosphoacetylglucosamine mutase |
Schmidtea mediterranea | mk4.000120.10 | Phosphoacetylglucosamine mutase |
Schmidtea mediterranea | mk4.000120.06 | Phosphoacetylglucosamine mutase |
Schmidtea mediterranea | mk4.000120.04 | |
Schmidtea mediterranea | mk4.000120.00 | Phosphoacetylglucosamine mutase |
Schmidtea mediterranea | mk4.000120.05 | Phosphoacetylglucosamine mutase |
Trypanosoma brucei gambiense | Tbg972.8.560 | hypothetical protein, conserved |
Trypanosoma brucei | Tb927.8.980 | phosphoacetylglucosamine mutase |
Trypanosoma congolense | TcIL3000_8_540 | phosphoacetylglucosamine mutase, putative |
Trypanosoma congolense | TcIL3000_0_24070 | phosphoacetylglucosamine mutase, putative |
Trypanosoma cruzi | TcCLB.508569.80 | phosphoacetylglucosamine mutase, putative |
Trypanosoma cruzi | TcCLB.503733.70 | phosphoacetylglucosamine mutase, putative |
Toxoplasma gondii | TGME49_264650 | phosphoacetylglucosamine mutase |
Theileria parva | TP02_0925 | N-acetylglucosamine-phosphate mutase, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.8.980 this record | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.8.980 this record | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.8.980 this record | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.8.980 this record | Trypanosoma brucei | significant gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_F21D5.1 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_F21D5.1 | Caenorhabditis elegans | sterile | wormbase |
YEL058W | Saccharomyces cerevisiae | inviable | yeastgenome |
PBANKA_0918200 | Plasmodium berghei | Slow | plasmo |
TGME49_264650 | Toxoplasma gondii | Probably essential | sidik |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
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 |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
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 |
Affected Entity | Phenotypic quality | Occurs in | Occurs at | Evidence | Observed in | Drugs/Inhibitors |
---|---|---|---|---|---|---|
cell proliferation (GO:0008283) | normal (PATO:0000461) | bloodstream stage trypomastigotes (PLO:0027) | inferred from RNAi experiment (ECO:0000019) | No drug identifiers listed for this gene. | ||
Annotator: | fernan@iib.unsam.edu.ar. | Comment: | normal cell proliferation (no significant loss or gain of fitness) in bloodstream forms (stage 6 days). | References: | 21363968 | |
cell proliferation (GO:0008283) | normal (PATO:0000461) | procyclic (PLO:0034) | inferred from RNAi experiment (ECO:0000019) | No drug identifiers listed for this gene. | ||
Annotator: | fernan@iib.unsam.edu.ar. | Comment: | normal cell proliferation (no significant loss or gain of fitness) in procyclic forms . | References: | 21363968 | |
cell proliferation (GO:0008283) | increased (PATO:0000470) | procyclic (PLO:0034) | inferred from RNAi experiment (ECO:0000019) | No drug identifiers listed for this gene. | ||
Annotator: | fernan@iib.unsam.edu.ar. | Comment: | increased cell proliferation (significant gain of fitness) in differentiation of procyclic to bloodstream forms . | References: | 21363968 |
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.
1 literature reference was collected for this gene.