pI: 9.0525 |
Length (AA): 408 |
MW (Da): 47943 |
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 |
---|---|---|---|---|---|---|---|---|---|
19 | 267 | 2c8m (A) | 1 | 253 | 24.00 | 0 | 1 | 0.72 | -0.98 |
24 | 408 | 1vqz (A) | 3 | 323 | 31.00 | 0 | 1 | 0.99 | -0.02 |
19 | 266 | 2c8m (A) | 1 | 252 | 25.00 | 0 | 1 | 0.786443 | -0.36 |
20 | 408 | 3a7r (A) | 1 | 336 | 33.00 | 0 | 1 | 1.15833 | 0.07 |
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:
Resolution | Method | # Atoms | # Residues | Dep. Date | Pub. Date | Mod. Date |
---|---|---|---|---|---|---|
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 60-80% percentile | sporozoite, early ring, early trophozoite. | PlasmoDB |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Mid 40-60% percentile | intra-erythrocytic - 24 hs, intra-erythrocytic - 48 hs, late ring, late trophozoite, Ring. | Otto TD PlasmoDB Zanghi G |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | intra-erythrocytic - 16 hs, intra-erythrocytic - 32 hs, intra-erythrocytic - 40 hs, early schizont, Oocyst, Male Gametocyte. | Otto TD PlasmoDB Zanghi G Lasonder E |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 0-20% percentile | intra-erythrocytic - 0 hs, intra-erythrocytic - 8 hs, Sporozoite, Female Gametocyte. | Otto TD Zanghi G Lasonder E |
PlasmoDB | Data on upregulation of P. falciparum genes in different life cycle stages, combined from several microarray experiments available in PlasmoDB |
Lasonder E | Integrated transcriptomic and proteomic analyses of P. falciparum gametocytes. Molecular insight into sex-specific processes and translational repression. |
Otto TD | New insights into the blood-stage transcriptome of Plasmodium falciparum using RNA-Seq. |
Zanghi G | A Specific PfEMP1 Is Expressed in P. falciparum Sporozoites and Plays a Role in Hepatocyte Infection. |
Ortholog group members (OG5_127533)
Species | Accession | Gene Product |
---|---|---|
Babesia bovis | BBOV_I003930 | lipoate-protein ligase A, putative |
Brugia malayi | Bm1_20445 | lipoate-protein ligase, mitochondrial precursor, putative |
Candida albicans | CaO19.13012 | similar to S. cerevisiae YJL046W |
Candida albicans | CaO19.5566 | similar to S. cerevisiae YJL046W |
Caenorhabditis elegans | CELE_C45G3.3 | Protein C45G3.3 |
Chlamydia trachomatis | CT_285 | lipoate protein ligase |
Dictyostelium discoideum | DDB_G0287107 | hypothetical protein |
Drosophila melanogaster | Dmel_CG44243 | CG44243 gene product from transcript CG44243-RA |
Escherichia coli | b4386 | lipoate-protein ligase A |
Echinococcus granulosus | EgrG_000833900 | Lipoyltransferase 1 mitochondrial |
Echinococcus multilocularis | EmuJ_000833900 | Lipoyltransferase 1, mitochondrial |
Homo sapiens | ENSG00000144182 | lipoyltransferase 1 |
Leishmania braziliensis | LbrM.07.1130 | lipoate-protein ligase-like,lipoyl ligase, putative,lipoyltransferase, putative,lipoate biosynthesis protein, putative |
Leishmania donovani | LdBPK_071230.1 | lipoate-protein ligase-like |
Leishmania infantum | LinJ.07.1230 | lipoate-protein ligase-like,lipoyl ligase, putative,lipoyltransferase, putative,lipoate biosynthesis protein, putative |
Leishmania major | LmjF.07.1060 | lipoate-protein ligase-like,lipoyl ligase, putative,lipoyltransferase, putative,lipoate biosynthesis protein, putative |
Leishmania mexicana | LmxM.07.1060 | lipoate-protein ligase-like,lipoyl ligase, putative,lipoyltransferase, putative,lipoate biosynthesis protein, putative |
Mus musculus | ENSMUSG00000037216 | lipoyltransferase 1 |
Neospora caninum | NCLIV_035300 | lipoate-protein ligase a, putative |
Onchocerca volvulus | OVOC1932 | Lipoyltransferase 1, mitochondrial homolog |
Plasmodium berghei | PBANKA_1413100 | lipoate-protein ligase 1 |
Plasmodium falciparum | PF3D7_1314600 | lipoate-protein ligase 1 |
Plasmodium knowlesi | PKNH_1415200 | lipoate-protein ligase 1, putative |
Plasmodium vivax | PVX_122550 | lipoate-protein ligase 1, putative |
Plasmodium yoelii | PY00475 | probable lipoate-protein ligase a-related |
Saccharomyces cerevisiae | YJL046W | putative lipoate--protein ligase |
Schistosoma japonicum | Sjp_0057630 | ko:K10105 lipoyltransferase 1, putative |
Schistosoma mansoni | Smp_086960 | lipoate-protein ligase |
Schmidtea mediterranea | mk4.006463.00 | Lipoyltransferase 1, mitochondrial |
Schmidtea mediterranea | mk4.004477.03 | Lipoyltransferase 1, mitochondrial |
Trypanosoma brucei gambiense | Tbg972.8.230 | lipoate-protein ligase, putative,lipoyl ligase, putative,lipoyltransferase, putative,lipoate biosynthesis protein, putative |
Trypanosoma brucei | Tb927.8.630 | lipoyltransferase, putative |
Trypanosoma congolense | TcIL3000_8_110 | lipoyltransferase, putative |
Trypanosoma cruzi | TcCLB.510857.50 | lipoate-protein ligase, putative |
Trypanosoma cruzi | TcCLB.509611.100 | lipoyltransferase, putative |
Toxoplasma gondii | TGME49_271820 | lipoyltransferase and lipoate-protein ligase subfamily protein |
Theileria parva | TP01_1192 | lipoate-protein ligase A, putative |
Trichomonas vaginalis | TVAG_094820 | lipoate-protein ligase, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.8.630 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.8.630 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb927.8.630 | Trypanosoma brucei | significant loss of fitness in procyclic forms | alsford |
Tb927.8.630 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
b4386 | Escherichia coli | non-essential | goodall |
CELE_C45G3.3 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_C45G3.3 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_C45G3.3 | Caenorhabditis elegans | sterile | wormbase |
PBANKA_1413100 | Plasmodium berghei | Essential | plasmo |
TGME49_271820 | Toxoplasma gondii | Probably essential | sidik |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
keio | Systematic single-gene knock-out mutants of E. coli K12 | The Keio Collection |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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 |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
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.