pI: 7.419 |
Length (AA): 908 |
MW (Da): 97076 |
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 11 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 |
---|---|---|---|---|---|---|---|---|---|
52 | 243 | 1ltl (A) | 35 | 221 | 19.00 | 0.00000000016 | 0.84 | 0.35 | 0.7 |
203 | 323 | 1qkk (A) | 10 | 134 | 11.00 | 0.000098 | 0 | 0.2 | -0.04 |
315 | 704 | 1hqc (A) | 5 | 307 | 22.00 | 0 | 1 | 0.17 | 0.55 |
321 | 630 | 1g8p (A) | 23 | 347 | 17.00 | 0 | 1 | 0.41 | -0.55 |
5 | 242 | 4pof (A) | 4 | 228 | 17.00 | 0 | 0.64 | 0.352115 | 0.61 |
30 | 110 | 2gqb (A) | 13 | 107 | 30.00 | 0.85 | 0.08 | 0.00480705 | 2.14 |
57 | 620 | 4fdg (B) | 46 | 596 | 27.00 | 0 | 1 | 0.753445 | 1.23 |
128 | 625 | 4r7y (A) | 118 | 1961 | 34.00 | 0 | 1 | 0.795058 | 0.55 |
315 | 618 | 3f8t (A) | 207 | 484 | 35.00 | 0 | 1 | 0.592402 | 0.04 |
353 | 619 | 3f8t (A) | 237 | 485 | 30.00 | 0 | 1 | 0.475353 | 0.34 |
824 | 882 | 2ly1 (A) | 298 | 355 | 33.00 | 0.13 | 0.02 | 0.384578 | -0.06 |
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_130040)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT2G14050 | minichromosome maintenance 9 |
Dictyostelium discoideum | DDB_G0286035 | MCM family protein |
Entamoeba histolytica | EHI_076880 | DNA replication licensing factor, putative |
Echinococcus multilocularis | EmuJ_000016000 | minichromosome maintenance deficient domain |
Echinococcus multilocularis | EmuJ_000016100 | dna replication licensing factor mcm9 |
Echinococcus multilocularis | EmuJ_001037800 | dna replication licensing factor mcm9 |
Echinococcus multilocularis | EmuJ_001037200 | dna replication licensing factor mcm9 |
Echinococcus multilocularis | EmuJ_001037500 | dna replication licensing factor mcm9 |
Homo sapiens | ENSG00000111877 | minichromosome maintenance complex component 9 |
Leishmania braziliensis | LbrM.34.4870 | DNA replication factor, putative |
Leishmania donovani | LdBPK_354970.1 | DNA replication factor, putative |
Leishmania infantum | LinJ.35.4970 | DNA replication factor, putative |
Leishmania major | LmjF.35.4910 | DNA replication factor, putative |
Leishmania mexicana | LmxM.34.4910 | DNA replication factor, putative |
Mus musculus | ENSMUSG00000058298 | minichromosome maintenance complex component 9 |
Oryza sativa | 4340503 | Os06g0218500 |
Schistosoma japonicum | Sjp_0019020 | ko:K10738 minichromosome maintenance protein 9, putative |
Schistosoma mansoni | Smp_151560 | DNA replication licensing factor MCM1 |
Schmidtea mediterranea | mk4.002585.00 | DNA helicase MCM9 |
Trypanosoma brucei gambiense | Tbg972.9.5470 | minichromosome maintenance (MCM) complex subunit, putative |
Trypanosoma brucei | Tb927.9.9600 | DNA replication licensing factor MCM9, putative |
Trypanosoma congolense | TcIL3000_9_3440 | minichromosome maintenance (MCM) complex subunit, putative |
Trypanosoma cruzi | TcCLB.506885.290 | DNA replication licensing factor MCM9, putative |
Trypanosoma cruzi | TcCLB.510729.130 | DNA replication licensing factor MCM9, putative |
Theileria parva | TP04_0509 | hypothetical protein |
Theileria parva | TP04_0510 | DNA replication licensing factor MCM4, putative |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb09.211.1190 | Trypanosoma brucei | significant gain of fitness in bloodstream forms (3 days) | alsford |
Tb09.211.1190 | Trypanosoma brucei | no significant loss or gain of fitness in bloodstream forms (6 days) | alsford |
Tb09.211.1190 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb09.211.1190 | Trypanosoma brucei | significant gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
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 |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
wormbase | C. elegans RNAi experiments | WormBase web site, http://www.wormbase.org, release WS170 |
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 |
shigen | Profiling of E. coli Chromosome (PEC) | National Institute of Genetics, Japan |
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.