Entity Details
| Primary name |
PUS3_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | Q9BZE2 |
| EntryName | PUS3_HUMAN |
| FullName | tRNA pseudouridine(38/39) synthase |
| TaxID | 9606 |
| Evidence | evidence at protein level |
| Length | 481 |
| SequenceStatus | complete |
| DateCreated | 2004-09-27 |
| DateModified | 2021-06-02 |
Subcellular Location
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| Subcellular Location |
| Nucleus |
Domains
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| Domain | Name | Category | Type |
| IPR001406 | Pseudouridine synthase I, TruA | Family | Family |
| IPR020095 | Pseudouridine synthase I, TruA, C-terminal | Family | Homologous superfamily |
| IPR020097 | Pseudouridine synthase I, TruA, alpha/beta domain | Domain | Domain |
| IPR020103 | Pseudouridine synthase, catalytic domain superfamily | Family | Homologous superfamily |
| IPR041707 | Pseudouridine synthase Pus3-like | Family | Family |
Diseases
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| Disease ID | Source | Name | Description |
| 617051 | OMIM | Mental retardation, autosomal recessive 55 (MRT55) | A form of mental retardation, a disorder characterized by significantly below average general intellectual functioning associated with impairments in adaptive behavior and manifested during the developmental period. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
2 interactions