pI: 5.2205 |
Length (AA): 1370 |
MW (Da): 143805 |
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 10 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 |
---|---|---|---|---|---|---|---|---|---|
4 | 470 | 1b63 (A) | 3 | 324 | 36.00 | 0 | 1 | 0.2 | 0.89 |
18 | 217 | 1h7s (A) | 29 | 209 | 34.00 | 0 | 1 | 0.37 | -0.02 |
2 | 445 | 4p7a (A) | 6 | 322 | 46.00 | 0 | 1 | 0.196188 | 1.06 |
12 | 482 | 3h4l (A) | 43 | 393 | 23.00 | 0 | 1 | 0.0823956 | 1.18 |
221 | 256 | 3bog (C) | 3 | 76 | 42.00 | 0.47 | 0.02 | 0.402377 | 0.24 |
382 | 451 | 1bkn (A) | 234 | 320 | 26.00 | 0 | 0.52 | 0.332695 | -0.32 |
582 | 808 | 5cwp (A) | 3 | 229 | 15.00 | 0.011 | 0.06 | 0.326193 | -0.29 |
918 | 1365 | 3rbn (A) | 21 | 284 | 23.00 | 0 | 0.74 | -0.343493 | 1.8 |
1112 | 1316 | 3mje (A) | 125 | 324 | 29.00 | 0.86 | 0.12 | 0.206735 | 1.23 |
1187 | 1321 | 4ke2 (A) | 34 | 172 | 19.00 | 0 | 0.23 | 0.28714 | -0.39 |
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 |
---|---|---|---|
Mid 40-60% percentile | amastigotes. | Fernandes MC |
Upregulation Percent | Ranking | Stage | Dataset |
---|---|---|---|
Lower 20-40% percentile | metacyclic. | Fernandes MC |
Fernandes MC | Dual Transcriptome Profiling of Leishmania-Infected Human Macrophages Reveals Distinct Reprogramming Signatures. |
Ortholog group members (OG5_127201)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT4G09140 | DNA mismatch repair protein MLH1 |
Babesia bovis | BBOV_IV010910 | DNA mismatch repair protein, putative |
Brugia malayi | Bm1_19980 | DNA mismatch repair protein MutL containing protein |
Candida albicans | CaO19.11638 | mismatch repair protein |
Candida albicans | CaO19.4162 | mismatch repair protein |
Caenorhabditis elegans | CELE_T28A8.7 | Protein MLH-1 |
Cryptosporidium hominis | Chro.50122 | hypothetical protein |
Cryptosporidium parvum | cgd5_2560 | MutL family ATpase |
Chlamydia trachomatis | CT_575 | DNA mismatch repair protein MutL |
Dictyostelium discoideum | DDB_G0287393 | MutL DNA mismatch repair protein |
Drosophila melanogaster | Dmel_CG11482 | CG11482 gene product from transcript CG11482-RB |
Escherichia coli | b4170 | methyl-directed mismatch repair protein |
Echinococcus granulosus | EgrG_000761100 | DNA mismatch repair protein Mlh1 |
Entamoeba histolytica | EHI_129950 | DNA mismatch repair protein MLH1, putative |
Echinococcus multilocularis | EmuJ_000761100 | DNA mismatch repair protein Mlh1 |
Giardia lamblia | GL50803_16149 | Mlh1-like protein |
Homo sapiens | ENSG00000076242 | mutL homolog 1 |
Leishmania braziliensis | LbrM.24.1460 | mismatch repair protein, putative |
Leishmania donovani | LdBPK_241460.1 | mismatch repair protein, putative |
Leishmania infantum | LinJ.24.1460 | mismatch repair protein, putative |
Leishmania major | LmjF.24.1420 | mismatch repair protein, putative |
Leishmania mexicana | LmxM.24.1420 | mismatch repair protein, putative |
Loa Loa (eye worm) | LOAG_07794 | hypothetical protein |
Mus musculus | ENSMUSG00000032498 | mutL homolog 1 (E. coli) |
Neospora caninum | NCLIV_039530 | DNA mismatch repair protein, putative |
Oryza sativa | 4325393 | Os01g0958900 |
Plasmodium berghei | PBANKA_0930200 | DNA mismatch repair protein MLH, putative |
Plasmodium falciparum | PF3D7_1117800 | DNA mismatch repair protein MLH |
Plasmodium knowlesi | PKNH_0915500 | DNA mismatch repair protein MLH, putative |
Plasmodium vivax | PVX_091525 | DNA mismatch repair protein MLH, putative |
Plasmodium yoelii | PY05214 | hMLH1 gene product-related |
Saccharomyces cerevisiae | YMR167W | mismatch repair ATPase MLH1 |
Schistosoma japonicum | Sjp_0066040 | ko:K08734 DNA mismatch repair protein MLH1, putative |
Schistosoma japonicum | Sjp_0106760 | ko:K08734 DNA mismatch repair protein MLH1, putative |
Schistosoma japonicum | Sjp_0123060 | IPR002099,DNA mismatch repair protein;IPR011186,DNA mismatch repair protein Mlh1;IPR013507,DNA mismatch repair protein, C-termin |
Schistosoma mansoni | Smp_009550 | DNA mismatch repair protein MLH1 |
Schmidtea mediterranea | mk4.004482.04 | |
Schmidtea mediterranea | mk4.021716.00 | Mlh1 |
Schmidtea mediterranea | mk4.004482.05 | DNA mismatch repair protein Mlh1 |
Trypanosoma brucei gambiense | Tbg972.8.7030 | mismatch repair protein MLH1, putative |
Trypanosoma brucei | Tb927.8.6840 | mismatch repair protein MLH1 |
Trypanosoma congolense | TcIL3000_8_6750 | mismatch repair protein MLH1, putative |
Trypanosoma cruzi | TcCLB.507991.60 | mismatch repair protein MLH1, putative |
Trypanosoma cruzi | TcCLB.504035.140 | mismatch repair protein MLH1, putative |
Toxoplasma gondii | TGME49_266390 | DNA mismatch repair protein, C-terminal domain-containing protein |
Treponema pallidum | TP0303 | DNA mismatch repair protein (mutL) |
Theileria parva | TP01_0756 | DNA mismatch repair protein MLH1, putative |
Trichomonas vaginalis | TVAG_226330 | mismatch repair protein Mlh1B (mutL homolog) |
Trichomonas vaginalis | TVAG_364540 | mismatch repair protein Mlh1C (mutL homolog) |
Trichomonas vaginalis | TVAG_302400 | mismatch repair protein Mlh1A (mutL homolog) |
Wolbachia endosymbiont of Brugia malayi | Wbm0396 | DNA mismatch repair protein |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.8.6840 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.8.6840 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.8.6840 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.8.6840 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
b4170 | Escherichia coli | non-essential | goodall |
CELE_T28A8.7 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_T28A8.7 | Caenorhabditis elegans | sterile | wormbase |
PBANKA_0930200 | Plasmodium berghei | Essential | plasmo |
TGME49_266390 | Toxoplasma gondii | Essentiality uncertain | sidik |
blattner | Systematic mutagenesis of the E. coli (MG1655) genome | J Bacteriol 2004, 186:4921-4930 |
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 |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
keio | Systematic single-gene knock-out mutants of E. coli K12 | The Keio Collection |
neb | C. elegans RNAi phenotypes | Data obtained from Wormbase WS150, curated by K. Chaudary and T. Carlow, New England Biolabs |
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 |
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.