| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YJR129C | EFM3 | SGDID:S000003890 | Methyltransf_16 |
Lysine methyltransferase |
pfam Family | PF10294 | 97.30 | 1.80E-07 | 2.60E-11 | 67.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||||
| YJR129C | EFM3 | SGDID:S000003890 | CMQ451C |
CMQ451C |
Cyanidioschyzon merolae | 3bzb_b | D0VWS8 | 97.70 | 1.20E-08 | 1.60E-12 | 82.40 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YJR129C | EFM3 | SGDID:S000003890 | CAMKMT C2orf34 CLNMT |
Calmodulin-lysine N-methyltransferase (CLNMT) (CaM KMT) (EC 2.1.1.60) |
2.1.1.60 | Homo sapiens | Cystinuria,2p21 Microdeletion Syndrome Without Cystinuria,Meier-Gorlin Syndrome 1,Hypotonia,Myasthenic Syndrome, Congenital, 22,Hypotonia-Cystinuria Syndrome |
4pwy_a | Q7Z624 | ENSG00000143919 | CAMKMT | 98.70 | 2.60E-12 | 3.30E-16 | 105.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YJR129C | EFM3 | SGDID:S000003890 | VCPKMT C14orf138 METTL21D |
Protein-lysine methyltransferase METTL21D (EC 2.1.1.-) (Methyltransferase-like protein 21D) (VCP lysine methyltransferase) (VCP-KMT) (Valosin-containing protein lysine methyltransferase) |
2.1.1.- | Homo sapiens | Pontocerebellar Hypoplasia, Type 2a,Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia |
4lg1_c | Q9H867 | ENSG00000100483 | VCPKMT | 98.20 | 3.50E-10 | 4.40E-14 | 90.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |