pI: 7.1942 |
Length (AA): 380 |
MW (Da): 42384 |
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 2 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 |
---|---|---|---|---|---|---|---|---|---|
87 | 366 | 4k6j (A) | 669 | 950 | 11.00 | 0 | 0 | 0.803742 | -0.11 |
139 | 249 | 3u1c (A) | 5 | 92 | 34.00 | 0.14 | 0.06 | 0.302205 | 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:
Ortholog group members (OG5_128667)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT1G67370 | asynaptic 1 |
Babesia bovis | BBOV_II002160 | HORMA domain containing protein |
Brugia malayi | Bm1_43185 | Em:AC002378.1 |
Candida albicans | CaO19.10816 | DNA-binding protein, involved in meiosis |
Candida albicans | CaO19.3306 | DNA-binding protein, involved in meiosis |
Caenorhabditis elegans | CELE_ZK381.1 | Protein HIM-3 |
Cryptosporidium hominis | Chro.50207 | essential protein for meiotic synapsis |
Cryptosporidium parvum | cgd5_1750 | conserved protein with N-terminal HORMA domain |
Echinococcus granulosus | EgrG_000163900 | HORMA domain containing protein 2 |
Echinococcus multilocularis | EmuJ_000163900 | HORMA domain containing protein 2 |
Giardia lamblia | GL50803_4084 | Hop1 |
Homo sapiens | ENSG00000176635 | HORMA domain containing 2 |
Homo sapiens | ENSG00000143452 | HORMA domain containing 1 |
Leishmania braziliensis | LbrM.35.1240 | hypothetical protein, conserved |
Leishmania donovani | LdBPK_361170.1 | HORMA domain containing protein, putative |
Leishmania infantum | LinJ.36.1170 | hypothetical protein, conserved |
Leishmania major | LmjF.36.1110 | hypothetical protein, conserved |
Leishmania mexicana | LmxM.36.1110 | hypothetical protein, conserved |
Loa Loa (eye worm) | LOAG_01638 | hypothetical protein |
Loa Loa (eye worm) | LOAG_10393 | hypothetical protein |
Mus musculus | ENSMUSG00000020419 | HORMA domain containing 2 |
Mus musculus | ENSMUSG00000028109 | HORMA domain containing 1 |
Oryza sativa | 4347514 | Os09g0506800 |
Onchocerca volvulus | OVOC1489 |
|
Onchocerca volvulus | OVOC10490 |
|
Plasmodium berghei | PBANKA_1407900 | HORMA domain protein, putative |
Plasmodium falciparum | PF3D7_1309400 | HORMA domain protein, putative |
Plasmodium knowlesi | PKNH_1409800 | HORMA domain protein, putative |
Plasmodium vivax | PVX_122300 | HORMA domain protein, putative |
Plasmodium yoelii | PY02325 | HORMA domain, putative |
Saccharomyces cerevisiae | YIL072W | Hop1p |
Schistosoma japonicum | Sjp_0036110 | HORMA domain-containing protein 2, putative |
Schistosoma japonicum | Sjp_0312300 | expressed protein |
Schistosoma mansoni | Smp_169930 | hypothetical protein |
Schmidtea mediterranea | mk4.001053.00 | |
Trypanosoma brucei gambiense | Tbg972.10.6680 | hypothetical protein, conserved,predicted HORMA domain protein |
Trypanosoma brucei | Tb927.10.5490 | predicted HORMA domain protein |
Trypanosoma congolense | TcIL3000_10_4620 | predicted HORMA domain protein |
Trypanosoma cruzi | TcCLB.503611.50 | hypothetical protein, conserved |
Trypanosoma cruzi | TcCLB.506679.260 | hypothetical protein, conserved |
Toxoplasma gondii | TGME49_291860 | HORMA domain-containing protein |
Theileria parva | TP04_0349 | hypothetical protein |
Trichomonas vaginalis | TVAG_230730 | synaptonemal complex axial element Hop1 |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.10.5490 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.10.5490 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.10.5490 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.10.5490 | Trypanosoma brucei | significant loss of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_ZK381.1 | Caenorhabditis elegans | embryonic arrest | wormbase |
CELE_ZK381.1 | Caenorhabditis elegans | embryonic lethal | wormbase |
PBANKA_1407900 | Plasmodium berghei | Dispensable | plasmo |
TGME49_291860 | Toxoplasma gondii | Probably non-essential | sidik |
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 |
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 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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 |
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.