pI: 7.5206 |
Length (AA): 517 |
MW (Da): 57722 |
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 3 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 |
---|---|---|---|---|---|---|---|---|---|
3 | 129 | 1bxr (A) | 930 | 1054 | 23.00 | 0.0000000000047 | 0.47 | 0.45 | -0.35 |
13 | 517 | 1g8m (A) | 4 | 593 | 37.00 | 0 | 1 | 1.07 | -0.13 |
14 | 517 | 1zcz (A) | 1 | 452 | 44.00 | 0 | 1 | 1.35 | 0.35 |
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_127961)
Species | Accession | Gene Product |
---|---|---|
Arabidopsis thaliana | AT2G35040 | AICARFT/IMPCHase bienzyme family protein |
Candida albicans | CaO19.492 | Bifunctional transforymlase/cyclohydrolase |
Candida albicans | CaO19.8122 | Bifunctional transforymlase/cyclohydrolase |
Dictyostelium discoideum | DDB_G0277087 | AICAR transformylase / IMP cyclohydrolase |
Drosophila melanogaster | Dmel_CG11089 | CG11089 gene product from transcript CG11089-RA |
Escherichia coli | b4006 | fused IMP cyclohydrolase/phosphoribosylaminoimidazolecarboxamide formyltransferase |
Homo sapiens | ENSG00000138363 | 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase |
Mycobacterium leprae | ML0161 | Probable bifunctional purine biosynthesis protein PurH : phosphoribosylaminoimidazolecarboxamide formyltransferase (aicar transf |
Mus musculus | ENSMUSG00000026192 | 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase |
Mycobacterium tuberculosis | Rv0957 | Probable bifunctional purine biosynthesis protein PurH: phosphoribosylaminoimidazolecarboxamide formyltransferase (AICAR transfo |
Mycobacterium ulcerans | MUL_4712 | bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase |
Oryza sativa | 4344931 | Os08g0206600 |
Saccharomyces cerevisiae | YLR028C | bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase ADE16 |
Saccharomyces cerevisiae | YMR120C | bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase ADE17 |
Schmidtea mediterranea | mk4.001379.09 | Bifunctional purine biosynthesis protein PURH |
Schmidtea mediterranea | mk4.001379.10 | Bifunctional purine biosynthesis protein PURH |
Wolbachia endosymbiont of Brugia malayi | Wbm0411 | AICAR transformylase/IMP cyclohydrolase PurH |
Gene/Ortholog | Organism | Phenotype | Source Study |
---|---|---|---|
mtu972 | Mycobacterium tuberculosis | essential | nmpdr |
b4006 | Escherichia coli | non-essential | goodall |
yeastgenome | Systematic deletion of yeast genes | Saccharomyces Genome Database |
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 |
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 |
nmpdr | Genome-scale essentiality datasets from published studies (M. tuberculosis) | National Microbial Pathogen Data Resource |
gerdes | Experimental determination and system-level analysis of essential genes in E. coli MG1655 | Gerdes et al., J Bacteriol. 2003 185:5673-84 |
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.
Species | Known druggable target | Linked compounds | Reference |
---|---|---|---|
Homo sapiens | 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase | Compounds | References |
Mus musculus | 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase | Compounds | References |