| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YLR186W | EMG1 | SGDID:S000004176 | nep1 AF_0734 |
Ribosomal RNA small subunit methyltransferase Nep1 (EC 2.1.1.-) (16S rRNA (pseudouridine-N1-)-methyltransferase Nep1) |
2.1.1.- | Archaeoglobus fulgidus | 3o7b_a | O29524 | 100.00 | 1.50E-56 | 1.10E-60 | 385.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YLR186W | EMG1 | SGDID:S000004176 | EMG1 NEP1 YLR186W L9470.5 |
Ribosomal RNA small subunit methyltransferase NEP1 (EC 2.1.1.260) (18S rRNA (pseudouridine(1189)-N1)-methyltransferase) (18S rRNA Psi1189 methyltransferase) (Essential for mitotic growth protein 1) (Nucleolar essential protein 1) |
2.1.1.260 | Saccharomyces cerevisiae | 3oii_a | Q06287 | 100.00 | 6.50E-74 | 4.80E-78 | 497.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YLR186W | EMG1 | SGDID:S000004176 | nep1 MJ0557 |
Ribosomal RNA small subunit methyltransferase Nep1 (EC 2.1.1.-) (16S rRNA (pseudouridine-N1-)-methyltransferase Nep1) (16S rRNA Psi914 methyltransferase) |
2.1.1.- | Methanocaldococcus jannaschii | 3bbd_b | Q57977 | 100.00 | 8.60E-56 | 6.50E-60 | 373.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YLR186W | EMG1 | SGDID:S000004176 | EMG1 C2F |
Ribosomal RNA small subunit methyltransferase NEP1 (EC 2.1.1.-) (18S rRNA (pseudouridine(1248)-N1)-methyltransferase) (18S rRNA Psi1248 methyltransferase) (Nucleolar protein EMG1 homolog) (Protein C2f) (Ribosome biogenesis protein NEP1) |
2.1.1.- | Homo sapiens | Brown-Sequard Syndrome,Deafness, Autosomal Recessive 9,Atypical Polypoid Adenomyoma,Dyskeratosis Congenita,Diamond-Blackfan Anemia,Schopf-Schulz-Passarge Syndrome,Microcephaly,Cardiomyopathy, Familial Restrictive, 1,Treacher Collins Syndrome 1,Bowen-Conradi Syndrome,Shwachman-Diamond Syndrome 1 |
5fai_a | Q92979 | ENSG00000126749 | EMG1 | 100.00 | 1.80E-59 | 1.30E-63 | 402.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |