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yrdC N6-threonylcarbamoyltransferase domain containing
Summary
- Gene Symbol
-
- YRDC
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Cell membrane
- Cytoplasm
- Disease variant
- Epilepsy
- Intellectual disability
- Mitochondrion
- Phosphoprotein
- Proteomics identification
- Reference proteome
- Transferase
- Transit peptide
- Proteins
| UniProt | Protein Name |
|---|---|
| Q86U90 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| tRNA threonylcarbamoyladenosine modification | ||
| regulation of translational fidelity | ||
| negative regulation of transport |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| cytoplasm | ||
| cytoplasm | ||
| mitochondrion | ||
| mitochondrion | ||
| plasma membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| tRNA binding | ||
| double-stranded RNA binding | ||
| protein binding | ||
| nucleotidyltransferase activity | ||
| L-threonylcarbamoyladenylate synthase |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- YRDC
- Functional Category
-
- C: Energy production and conversion
- J: Translation, ribosomal structure and biogenesis
- O: Posttranslational modification, protein turnover, chaperones
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| double-stranded RNA binding |
| nucleotidyltransferase activity |
| transferase activity |
| InterPro |
|---|
| DHBP synthase RibB-like alpha/beta domain superfamily |
| Threonylcarbamoyl-AMP synthase-like domain |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0080694 | Galloway-Mowat syndrome |
