| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YPR089W | YPR089W | SGDID:S000006293 | DIL |
DIL domain |
pfam Repeat | PF01843 | 99.60 | 1.00E-20 | 1.10E-24 | 165.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||||
| YPR089W | YPR089W | SGDID:S000006293 | MYO2 CDC66 YOR326W O6167 |
Myosin-2 (Cell division control protein 66) (Class V unconventional myosin MYO2) (Type V myosin heavy chain MYO2) (Myosin V MYO2) |
Saccharomyces cerevisiae | 2f6h_x | P19524 | 100.00 | 4.20E-40 | 4.30E-44 | 354.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YPR089W | YPR089W | SGDID:S000006293 | MYO4 SHE1 YAL029C FUN22 |
Myosin-4 (SWI5-dependent HO expression protein 1) |
Saccharomyces cerevisiae | 3mmi_a | P32492 | 100.00 | 6.70E-37 | 6.80E-41 | 327.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YPR089W | YPR089W | SGDID:S000006293 | MYO5C |
Unconventional myosin-Vc |
Homo sapiens | Griscelli Syndrome, Type 1,Diarrhea 2, With Microvillus Atrophy,Congenital Diarrhea,Griscelli Syndrome |
4l8t_a | Q9NQX4 | ENSG00000128833 | MYO5C | 100.00 | 3.00E-48 | 3.10E-52 | 420.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YPR089W | YPR089W | SGDID:S000006293 | MYO5A MYH12 |
Unconventional myosin-Va (Dilute myosin heavy chain, non-muscle) (Myosin heavy chain 12) (Myosin-12) (Myoxin) |
Homo sapiens | Griscelli Syndrome, Type 1,Chediak-Higashi Syndrome,Seizure Disorder,Pathologic Nystagmus,Giant Axonal Neuropathy 2,Dystonia,Albinism, Oculocutaneous, Type V,Griscelli Syndrome, Type 3,Microphthalmia,Piebald Trait,Cardiomyopathy, Dilated, 1p,Hermansky-Pudlak Syndrome,Bardet-Biedl Syndrome 2,Usher Syndrome,Acrocephalopolydactylous Dysplasia,Griscelli Syndrome, Type 2,Diarrhea 2, With Microvillus Atrophy,Congenital Diarrhea,Griscelli Syndrome |
4lli_b | Q9Y4I1 | ENSG00000197535 | MYO5A | 100.00 | 3.40E-46 | 3.60E-50 | 396.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |