pI: 6.5663 |
Length (AA): 1234 |
MW (Da): 143753 |
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 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 |
---|---|---|---|---|---|---|---|---|---|
150 | 1231 | 5xh6 (A) | 92 | 1125 | 12.00 | 0 | 1 | 0.583823 | 1.84 |
160 | 944 | 5kk5 (A) | 196 | 1036 | 14.00 | 0 | 1 | 0.396143 | 1.61 |
322 | 514 | 3edu (A) | 1691 | 1888 | 12.00 | 0 | 0.22 | 0.219402 | -1.23 |
503 | 680 | 2wd5 (A) | 499 | 674 | 65.00 | 0 | 1 | 0.968246 | -1.12 |
1048 | 1228 | 1w1w (B) | 181 | 1223 | 44.00 | 0 | 1 | 0.633677 | -0.05 |
1122 | 1207 | 1e69 (A) | 1066 | 1150 | 45.00 | 0.0000013 | 0.66 | 0.514692 | 0.43 |
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_127449)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT3G54670 | structural maintenance of chromosomes 1 |
Babesia bovis | BBOV_IV004610 | structural maintenance of chromosome 1-like protein, putative |
Brugia malayi | Bm1_12960 | SMC family, C-terminal domain containing protein |
Candida albicans | CaO19.11845 | potential SMC chromosomal ATPase similar to S. cerevisiae SMC1 (YFL008W) nuclear cohesin complex ATPase |
Candida albicans | CaO19.4367 | potential SMC chromosomal ATPase similar to S. cerevisiae SMC1 (YFL008W) nuclear cohesin complex ATPase |
Caenorhabditis elegans | CELE_F28B3.7 | Protein HIM-1, isoform B |
Cryptosporidium hominis | Chro.20291 | Xenopus 14s cohesin smc1 subunit |
Cryptosporidium parvum | cgd2_2750 | SMC1 structural maintenance of chromosomes 1 |
Dictyostelium discoideum | DDB_G0291752 | structural maintenance of chromosome protein |
Drosophila melanogaster | Dmel_CG6057 | CG6057 gene product from transcript CG6057-RA |
Echinococcus granulosus | EgrG_000802900 | expressed protein |
Echinococcus granulosus | EgrG_000803000 | structural maintenance of chromosomes protein |
Entamoeba histolytica | EHI_050790 | structural maintenance of chromosomes protein |
Echinococcus multilocularis | EmuJ_000803000 | structural maintenance of chromosomes protein |
Echinococcus multilocularis | EmuJ_000802900 | expressed protein |
Giardia lamblia | GL50803_16188 | SMC1 beta-like protein |
Homo sapiens | ENSG00000077935 | structural maintenance of chromosomes 1B |
Homo sapiens | ENSG00000072501 | structural maintenance of chromosomes 1A |
Leishmania braziliensis | LbrM.34.3440 | structural maintenance of chromosome (SMC) family protein, putative |
Leishmania donovani | LdBPK_353560.1 | structural maintenance of chromosome (SMC) family protein, putative |
Leishmania infantum | LinJ.35.3560 | structural maintenance of chromosome (SMC) family protein, putative |
Leishmania major | LmjF.35.3510 | structural maintenance of chromosome (SMC) family protein, putative |
Leishmania mexicana | LmxM.34.3510 | structural maintenance of chromosome (SMC) family protein, putative |
Loa Loa (eye worm) | LOAG_05552 | hypothetical protein |
Mus musculus | ENSMUSG00000022432 | structural maintenance of chromosomes 1B |
Mus musculus | ENSMUSG00000041133 | structural maintenance of chromosomes 1A |
Neospora caninum | NCLIV_041160 | Xenopus 14s cohesin smc1 subunit, related |
Oryza sativa | 4352932 | Os12g0641500 |
Plasmodium berghei | PBANKA_0917500 | structural maintenance of chromosomes protein 1, putative |
Plasmodium falciparum | PF3D7_1130700 | structural maintenance of chromosomes protein 1, putative |
Plasmodium knowlesi | PKNH_0928800 | structural maintenance of chromosomes protein 1, putative |
Plasmodium vivax | PVX_092140 | structural maintenance of chromosome protein, putative |
Plasmodium yoelii | PY00653 | chromosome segregation protein smc1 |
Saccharomyces cerevisiae | YFL008W | cohesin subunit SMC1 |
Schistosoma japonicum | Sjp_0015150 | ko:K06636 structural maintenance of chromosome 1, putative |
Schistosoma mansoni | Smp_136970 | chondroitin sulfate proteoglycan |
Schmidtea mediterranea | mk4.004021.04 | Structural maintenance of chromosomes protein 1B |
Schmidtea mediterranea | mk4.009253.01 | |
Schmidtea mediterranea | mk4.004021.02 | Structural maintenance of chromosomes protein 1B |
Schmidtea mediterranea | mk4.004021.01 | |
Trypanosoma brucei gambiense | Tbg972.9.7140 | structural maintenance of chromosome 1, putative |
Trypanosoma brucei | Tb927.9.11850 | structural maintenance of chromosome 1, putative |
Trypanosoma congolense | TcIL3000_9_4840 | structural maintenance of chromosome 1, putative |
Trypanosoma cruzi | TcCLB.507011.60 | structural maintenance of chromosome (SMC) family protein, putative |
Trypanosoma cruzi | TcCLB.507005.60 | structural maintenance of chromosome (SMC) family protein, putative |
Toxoplasma gondii | TGME49_288700 | RecF/RecN/SMC N terminal domain-containing protein |
Theileria parva | TP01_0286 | SMC protein, putative |
Trichomonas vaginalis | TVAG_162180 | cohesin subunit Smc1 |
Trichomonas vaginalis | TVAG_266830 | cohesin subunit Smc1 |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
Tb09.211.2970 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (3 days) | alsford |
Tb09.211.2970 | Trypanosoma brucei | significant loss of fitness in bloodstream forms (6 days) | alsford |
Tb09.211.2970 | Trypanosoma brucei | no significant loss or gain of fitness in procyclic forms | alsford |
Tb09.211.2970 | Trypanosoma brucei | no significant loss or gain of fitness in differentiation of procyclic to bloodstream forms | alsford |
CELE_F28B3.7 | Caenorhabditis elegans | embryonic lethal | wormbase |
CELE_F28B3.7 | Caenorhabditis elegans | larval arrest | wormbase |
CELE_F28B3.7 | Caenorhabditis elegans | larval lethal | wormbase |
CELE_F28B3.7 | Caenorhabditis elegans | sterile | wormbase |
YFL008W | Saccharomyces cerevisiae | inviable | yeastgenome |
PBANKA_0917500 | Plasmodium berghei | Essential | plasmo |
TGME49_288700 | Toxoplasma gondii | Probably essential | sidik |
alsford | High-throughput phenotyping using parallel sequencing of RNA interference targets in the African trypanosome | Genome Res 2011, 21:915-924 |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
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 |
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 |
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 |
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.