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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YPL003W | ULA1 | SGDID:S000005924 | SAE1 AOS1 SUA1 UBLE1A |
SUMO-activating enzyme subunit 1 (Ubiquitin-like 1-activating enzyme E1A) [Cleaved into: SUMO-activating enzyme subunit 1, N-terminally processed] |
Homo sapiens | Adult Dermatomyositis |
1y8q_c | Q9UBE0 | ENSG00000142230 | SAE1 | 99.90 | 2.30E-31 | 1.70E-35 | 260.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL003W | ULA1 | SGDID:S000005924 | UBA1 YKL210W |
Ubiquitin-activating enzyme E1 1 (EC 6.2.1.45) |
6.2.1.45 | Saccharomyces cerevisiae | 3cmm_c | P22515 | 99.90 | 2.70E-28 | 1.90E-32 | 268.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YPL003W | ULA1 | SGDID:S000005924 | ptr3 SPBC1604.21c SPBC211.09 |
Ubiquitin-activating enzyme E1 1 (EC 6.2.1.45) (Poly(A)+ RNA transport protein 3) |
6.2.1.45 | Schizosaccharomyces pombe | 4ii2_a | O94609 | 99.80 | 1.50E-26 | 1.10E-30 | 254.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YPL003W | ULA1 | SGDID:S000005924 | NAE1 APPBP1 HPP1 |
NEDD8-activating enzyme E1 regulatory subunit (Amyloid beta precursor protein-binding protein 1, 59 kDa) (APP-BP1) (Amyloid protein-binding protein 1) (Proto-oncogene protein 1) |
Homo sapiens | Alzheimer Disease |
1tt5_c | Q13564 | ENSG00000159593 | NAE1 | 100.00 | 1.70E-81 | 1.30E-85 | 651.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YPL003W | ULA1 | SGDID:S000005924 | UBA1 A1S9T UBE1 |
Ubiquitin-like modifier-activating enzyme 1 (EC 6.2.1.45) (Protein A1S9) (Ubiquitin-activating enzyme E1) |
6.2.1.45 | Homo sapiens | Congenital Contractures,Spinal Muscular Atrophy,Muscular Atrophy,Wallerian Degeneration,Parkinson Disease, Late-Onset,Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive,Vexas Syndrome,Spinal Muscular Atrophy, X-Linked 2 |
4p22_a | P22314 | ENSG00000130985 | UBA1 | 100.00 | 1.60E-42 | 1.10E-46 | 349.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |