pI: 7.3689 |
Length (AA): 438 |
MW (Da): 47520 |
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 6 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 |
---|---|---|---|---|---|---|---|---|---|
31 | 242 | 1jbk (A) | 157 | 351 | 13.00 | 0 | 0.43 | 0.21 | -0.06 |
48 | 374 | 1in4 (A) | 19 | 324 | 19.00 | 0 | 1 | 0.84 | 0.19 |
3 | 351 | 4fdg (B) | 254 | 594 | 37.00 | 0.000000013 | 1 | 1.1057 | 0.9 |
3 | 357 | 4r7y (A) | 254 | 1963 | 33.00 | 0.000000000019 | 1 | 1.1884 | -0.19 |
26 | 352 | 3f8t (A) | 187 | 485 | 28.00 | 0 | 1 | 0.905675 | -0.05 |
30 | 350 | 4r7z (A) | 264 | 956 | 33.00 | 0 | 1 | 1.08208 | -0.17 |
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_129017)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT3G09660 | minichromosome maintenance 8 |
Dictyostelium discoideum | DDB_G0283009 | MCM family protein |
Drosophila melanogaster | Dmel_CG31293 | recombination-defective |
Echinococcus granulosus | EgrG_000772700 | dna replication licensing factor mcm8 |
Entamoeba histolytica | EHI_140670 | DNA replication licensing factor, putative |
Echinococcus multilocularis | EmuJ_000772700 | dna replication licensing factor mcm8 |
Homo sapiens | ENSG00000125885 | minichromosome maintenance complex component 8 |
Leishmania braziliensis | LbrM.05.0320 | DNA replication licensing factor, putative,minichromosome maintenance protein-like protein |
Leishmania donovani | LdBPK_050330.1 | DNA replication licensing factor, putative |
Leishmania infantum | LinJ.05.0330 | DNA replication licensing factor, putative,minichromosome maintenance protein-like protein |
Leishmania major | LmjF.05.0330 | DNA replication licensing factor, putative,minichromosome maintenance protein-like protein |
Leishmania mexicana | LmxM.05.0330 | DNA replication licensing factor, putative,minichromosome maintenance protein-like protein |
Mus musculus | ENSMUSG00000027353 | minichromosome maintenance deficient 8 (S. cerevisiae) |
Neospora caninum | NCLIV_058290 | DNA replication licensing factor, putative |
Oryza sativa | 4339038 | Os05g0464100 |
Plasmodium berghei | PBANKA_0609800 | DNA helicase MCM8, putative |
Plasmodium falciparum | PF3D7_1211300 | DNA helicase MCM8, putative |
Plasmodium knowlesi | PKNH_1311400 | DNA helicase MCM8, putative |
Plasmodium vivax | PVX_084595 | DNA replication licensing factor MCM8, putative |
Plasmodium yoelii | PY02431 | MCM2/3/5 family |
Schistosoma japonicum | Sjp_0046030 | Conserved hypothetical protein |
Schistosoma japonicum | Sjp_0046020 | expressed protein |
Schistosoma japonicum | Sjp_0098620 | DNA replication licensing factor MCM8, putative |
Schistosoma japonicum | Sjp_0119450 | hypothetical protein |
Schistosoma japonicum | Sjp_0079950 | ko:K10737 minichromosome maintenance protein 8, putative |
Schistosoma japonicum | Sjp_0099600 | hypothetical protein |
Schistosoma mansoni | Smp_169450 | DNA replication licensing factor MCM8 |
Schmidtea mediterranea | mk4.000367.10 | DNA replication licensing factor MCM8, putative |
Schmidtea mediterranea | mk4.000367.11 | DNA replication licensing factor REC |
Trypanosoma brucei gambiense | Tbg972.10.12700 | minichromosome maintenance (MCM) complex subunit, putative,minichromosome maintenance protein-like protein |
Trypanosoma brucei | Tb927.10.10410 | DNA replication licensing factor MCM8, putative |
Trypanosoma brucei | Tb11.v5.0535 | minichromosome maintenance (MCM) complex subunit, putative |
Trypanosoma congolense | TcIL3000_10_8890 | DNA replication licensing factor MCM8, putative |
Trypanosoma cruzi | TcCLB.503425.29 | DNA replication licensing factor MCM8, putative |
Trypanosoma cruzi | TcCLB.503555.10 | DNA replication licensing factor MCM8, putative |
Toxoplasma gondii | TGME49_315600 | MCM2/3/5 family protein |
Theileria parva | TP01_0666 | DNA replication licensing factor MCM4, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb927.10.10410 | Trypanosoma brucei | significant gain of fitness in bloodstream forms (3 days) | alsford |
Tb927.10.10410 | Trypanosoma brucei | significant gain of fitness in bloodstream forms (6 days) | alsford |
Tb927.10.10410 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb927.10.10410 | Trypanosoma brucei | significant gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
TGME49_315600 | Toxoplasma gondii | Probably non-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.