| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YAL032C | PRP45 | SGDID:S000000030 | sme1 SPBC11G11.06c |
Small nuclear ribonucleoprotein E (snRNP-E) (Sm protein E) (Sm-E) (SmE) |
Schizosaccharomyces pombe | 3jb9_m | Q9USZ3 | 100.00 | 6.50E-96 | 5.00E-100 | 753.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YAL032C | PRP45 | SGDID:S000000030 | PRP19 PSO4 YLL036C |
Pre-mRNA-processing factor 19 (EC 2.3.2.27) (RING-type E3 ubiquitin transferase PRP19) |
2.3.2.27 | Saccharomyces cerevisiae | 5gm6_p | P32523 | 100.00 | 2.00E-106 | 2.00E-110 | 803.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YAL032C | PRP45 | SGDID:S000000030 | SKIP_SNW |
SKIP/SNW domain |
pfam Family | PF02731 | 100.00 | 3.20E-53 | 2.60E-57 | 377.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||||
| YAL032C | PRP45 | SGDID:S000000030 | PRPF19 NMP200 PRP19 SNEV |
Pre-mRNA-processing factor 19 (EC 2.3.2.27) (Nuclear matrix protein 200) (PRP19/PSO4 homolog) (hPso4) (RING-type E3 ubiquitin transferase PRP19) (Senescence evasion factor) |
2.3.2.27 | Homo sapiens | Retinitis Pigmentosa 19,Poikiloderma With Neutropenia |
6id1_r | Q9UMS4 | ENSG00000110107 | PRPF19 | 100.00 | 9.70E-96 | 7.00E-100 | 748.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YAL032C | PRP45 | SGDID:S000000030 | SNRPB COD SNRPB1 |
Small nuclear ribonucleoprotein-associated proteins B and B' (snRNP-B) (Sm protein B/B') (Sm-B/B') (SmB/B') |
Homo sapiens | Burn-Mckeown Syndrome,Spinal Muscular Atrophy,Muscular Atrophy,Lupus Erythematosus,Isolated Pierre Robin Sequence,Cerebrocostomandibular Syndrome,Disease Of Mental Health,Mandibulofacial Dysostosis, Guion-Almeida Type,Otospondylomegaepiphyseal Dysplasia, Autosomal Dominant,Systemic Lupus Erythematosus,Acrofacial Dysostosis 1, Nager Type,Pierre Robin Syndrome |
6qdv_k | P14678 | ENSG00000125835 | SNRPB | 100.00 | 1.50E-68 | 1.20E-72 | 515.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |