pI: 9.843 |
Length (AA): 376 |
MW (Da): 43722 |
Paralog Number:
1
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 8 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 | 374 | 1sqg (A) | 5 | 428 | 22.00 | 0 | 1 | 1.08 | -0.55 |
41 | 374 | 1sqg (A) | 97 | 428 | 25.00 | 0 | 1 | 1.23 | -0.68 |
84 | 374 | 1ixk (A) | 3 | 314 | 27.00 | 0 | 1 | 1.04 | -1.29 |
1 | 374 | 2yxl (A) | 82 | 448 | 23.00 | 0 | 1 | 1.15598 | 0.42 |
17 | 374 | 1sqg (A) | 78 | 428 | 25.00 | 0 | 1 | 1.21233 | 0.19 |
96 | 376 | 2frx (A) | 7 | 312 | 23.00 | 0 | 1 | 0.99964 | -0.39 |
97 | 375 | 3m6w (A) | 2 | 300 | 22.00 | 0 | 1 | 1.02422 | -0.63 |
197 | 275 | 2nxc (A) | 118 | 191 | 36.00 | 0.5 | 0.99 | 0.617806 | -0.15 |
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 80-100% percentile | intra-erythrocytic - 40 hs, intra-erythrocytic - 48 hs, merozoite, sporozoite. | Otto TD PlasmoDB |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Upper 60-80% percentile | intra-erythrocytic - 16 hs, intra-erythrocytic - 24 hs, intra-erythrocytic - 32 hs, gametocyte, early ring, early schizont, early trophozoite, late ring, late schizont, late trophozoite, Oocyst, Ring, Sporozoite, Female Gametocyte. | Otto TD PlasmoDB Zanghi G Lasonder E |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Mid 40-60% percentile | intra-erythrocytic - 0 hs, intra-erythrocytic - 8 hs. | Otto TD |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | Male Gametocyte. | Lasonder E |
Zanghi G | A Specific PfEMP1 Is Expressed in P. falciparum Sporozoites and Plays a Role in Hepatocyte Infection. |
Otto TD | New insights into the blood-stage transcriptome of Plasmodium falciparum using RNA-Seq. |
Lasonder E | Integrated transcriptomic and proteomic analyses of P. falciparum gametocytes. Molecular insight into sex-specific processes and translational repression. |
PlasmoDB | Data on upregulation of P. falciparum genes in different life cycle stages, combined from several microarray experiments available in PlasmoDB |
Ortholog group members (OG5_126796)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT4G26600 | S-adenosyl-L-methionine-dependent methyltransferase-like protein |
Arabidopsis thaliana | AT5G55920 | ribosome biogenesis protein OLI2 |
Arabidopsis thaliana | AT3G13180 | NOL1/NOP2/sun family protein / antitermination NusB domain-containing protein |
Babesia bovis | BBOV_II005990 | nucleolar protein-like protein with NOL1/NOP2/sun family putative RNA methylase domain |
Babesia bovis | BBOV_II007520 | sun-family protein, putative |
Brugia malayi | Bm1_29315 | NOL1/NOP2/sun family putative RNA methylase containing protein |
Candida albicans | CaO19.501 | nucleolar protein |
Candida albicans | CaO19.8131 | nucleolar protein |
Caenorhabditis elegans | CELE_W07E6.1 | Protein NOL-1 |
Cryptosporidium hominis | Chro.60375 | nucleolar protein-like |
Cryptosporidium parvum | cgd6_3230 | Nop2p family of SUN/fmu RNA methylase |
Chlamydia trachomatis | CT_553 | RNA methyltransferase |
Dictyostelium discoideum | DDB_G0281685 | NOL1/NOP2/Sun family protein |
Drosophila melanogaster | Dmel_CG8545 | CG8545 gene product from transcript CG8545-RA |
Escherichia coli | b3289 | 16S rRNA m(5)C967 methyltransferase, SAM-dependent |
Escherichia coli | b1835 | 16S rRNA m(5)C1407 methyltransferase, SAM-dependent |
Echinococcus granulosus | EgrG_000218300 | nucleolar protein nol1:nop2 |
Entamoeba histolytica | EHI_198880 | Proliferating-cell nucleolar antigen p120, putative |
Echinococcus multilocularis | EmuJ_000218300 | nucleolar protein nol1:nop2 |
Giardia lamblia | GL50803_16948 | Nucleolar protein NOP2 |
Homo sapiens | ENSG00000111641 | NOP2 nucleolar protein |
Leishmania braziliensis | LbrM.31.0300 | nucleolar protein, putative |
Leishmania donovani | LdBPK_310200.1 | nucleolar protein, putative |
Leishmania infantum | LinJ.31.0200 | nucleolar protein, putative |
Leishmania major | LmjF.31.0190 | nucleolar protein, putative |
Leishmania mexicana | LmxM.30.0190 | nucleolar protein, putative |
Loa Loa (eye worm) | LOAG_09543 | nucleolar protein |
Mus musculus | ENSMUSG00000038279 | NOP2 nucleolar protein |
Mycobacterium tuberculosis | Rv1407 | Probable Fmu protein (sun protein) |
Mycobacterium ulcerans | MUL_1803 | Fmu protein |
Neospora caninum | NCLIV_041000 | Ribosomal RNA small subunit methyltransferase F (RRNA(Cytosine-C)), related |
Neospora caninum | NCLIV_013720 | NOL1/NOP2/sun family domain-containing protein, putative |
Oryza sativa | 4347368 | Os09g0477900 |
Oryza sativa | 4330579 | Os02g0724600 |
Oryza sativa | 4347787 | Os09g0551300 |
Plasmodium berghei | PBANKA_0918800 | rRNA (cytosine-C(5))-methyltransferase, putative |
Plasmodium berghei | PBANKA_1445300 | sun-family protein, putative |
Plasmodium falciparum | PF3D7_1230600 | sun-family protein, putative |
Plasmodium falciparum | PF3D7_1129400 | rRNA (cytosine-C(5))-methyltransferase, putative |
Plasmodium knowlesi | PKNH_1450000 | sun-family protein, putative |
Plasmodium knowlesi | PKNH_0927400 | rRNA (cytosine-C(5))-methyltransferase, putative |
Plasmodium vivax | PVX_124170 | sun-family protein, putative |
Plasmodium vivax | PVX_092085 | proliferating-cell nucleolar antigen p120, putative |
Plasmodium yoelii | PY03774 | RNA methyltransferase, putative |
Plasmodium yoelii | PY05667 | hypothetical protein |
Saccharomyces cerevisiae | YNL061W | Nop2p |
Schistosoma japonicum | Sjp_0025300 | Putative RNA methyltransferase NOL1, putative |
Schistosoma japonicum | Sjp_0025320 | Putative RNA methyltransferase NOL1, putative |
Schistosoma mansoni | Smp_005080.1 | nucleolar protein nol1/nop2 |
Schistosoma mansoni | Smp_005080.2 | nucleolar protein nol1/nop2 |
Schistosoma mansoni | Smp_005080.3 | nucleolar protein nol1/nop2 |
Schmidtea mediterranea | mk4.006816.03 | Putative nucleolar protein nol1/nop2 |
Schmidtea mediterranea | mk4.014144.00 | Putative nucleolar protein nol1/nop2 |
Schmidtea mediterranea | mk4.058797.01 | Putative nucleolar protein nol1/nop2 |
Trypanosoma brucei gambiense | Tbg972.4.3910 | nucleolar protein, putative |
Trypanosoma brucei | Tb927.4.3840 | nucleolar protein, putative |
Trypanosoma congolense | TcIL3000_4_3390 | nucleolar protein, putative |
Trypanosoma cruzi | TcCLB.507583.20 | nucleolar protein, putative |
Trypanosoma cruzi | TcCLB.509951.10 | nucleolar protein, putative |
Toxoplasma gondii | TGME49_213970 | ribosomal RNA small subunit methyltransferase B, putative |
Toxoplasma gondii | TGME49_288530 | NOL1/NOP2/sun family protein |
Theileria parva | TP02_0204 | sun-family protein, putative |
Theileria parva | TP02_0558 | nuclear protein, putative |
Trichomonas vaginalis | TVAG_115490 | ribosomal RNA small subunit methyltransferase B, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
mtu1430 | Mycobacterium tuberculosis | non-essential | nmpdr |
Tb927.4.3840 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb927.4.3840 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.4.3840 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.4.3840 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
b1835 | Escherichia coli | non-essential | goodall |
b3289 | Escherichia coli | non-essential | goodall |
CELE_W07E6.1 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_W07E6.1 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_W07E6.1 | Caenorhabditis elegans | slow growth | wormbase |
YNL061W | Saccharomyces cerevisiae | inviable | yeastgenome |
PBANKA_0918800 | Plasmodium berghei | Essential | plasmo |
PBANKA_1445300 | Plasmodium berghei | Essential | plasmo |
TGME49_213970 | Toxoplasma gondii | Probably essential | sidik |
TGME49_288530 | Toxoplasma gondii | Probably essential | sidik |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
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 |
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 |
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.