| Yeast Systematic Name | Yeast Symbol | SGDID | Analog Name | Analog Description | EC | Organism | Disease | Structure | Uniprot | Human ID | Human Symbol | HHsearch Probability | HHsearch E_value | HHsearch P_value | HHsearch Score | Flag Disease related | Flag Homo sapiens | Flag Mus musculus | Flag Danio rerio | Flag Drosophila melanogaster | Flag Caenorhabditis elegans | Flag Arabidopsis thaliana | Flag Escherichia coli |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YJR117W | STE24 | SGDID:S000003878 | Peptidase_M48_N |
CAAX prenyl protease N-terminal, five membrane helices |
pfam Domain | PF16491 | 99.90 | 7.20E-29 | 5.00E-33 | 215.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||||
| YJR117W | STE24 | SGDID:S000003878 | CAAX prenyl protease (EC 3.4.24.84) |
CAAX prenyl protease (EC 3.4.24.84) |
3.4.24.84 | Saccharomyces mikatae | 4il3_a | M4GGS2 | 100.00 | 2.10E-65 | 1.50E-69 | 510.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YJR117W | STE24 | SGDID:S000003878 | ZMPSTE24 FACE1 STE24 |
CAAX prenyl protease 1 homolog (EC 3.4.24.84) (Farnesylated proteins-converting enzyme 1) (FACE-1) (Prenyl protein-specific endoprotease 1) (Zinc metalloproteinase Ste24 homolog) |
3.4.24.84 | Homo sapiens | Calcinosis,Acroosteolysis,Complete Generalized Lipodystrophy,Acquired Generalized Lipodystrophy,Emery-Dreifuss Muscular Dystrophy,Adiposis Dolorosa,Mandibuloacral Dysplasia With Type B Lipodystrophy,Laminopathy,Skin Atrophy,Osteogenesis Imperfecta, Type Ii,Lipodystrophy, Familial Partial, Type 5,Muscular Dystrophy, Congenital, Lmna-Related,Restrictive Dermopathy, Lethal,Leukodystrophy, Demyelinating, Adult-Onset, Autosomal Dominant,Cardiomyopathy, Dilated, 1a,Reynolds Syndrome,Hutchinson-Gilford Progeria Syndrome,Cardiomyopathy, Dilated, 1h,Arthropathy,Hallermann-Streiff Syndrome,Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant,Charcot-Marie-Tooth Disease, Axonal, Type 2b1,Congenital Generalized Lipodystrophy,Mandibuloacral Dysplasia With Type A Lipodystrophy,Emery-Dreifuss Muscular Dystrophy 3, Autosomal Recessive,Lipodystrophy, Familial Partial, Type 2,Cardiomyopathy, Dilated, With Hypergonadotropic Hypogonadism |
5syt_a | O75844 | ENSG00000084073 | ZMPSTE24 | 100.00 | 3.40E-64 | 2.30E-68 | 498.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |