RIDA
2-iminobutanoate/2-iminopropanoate deaminase
Also known as: HRSP12, P14.5, PSP, RIDA_HUMAN, UK114
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P52758
- Gene
- RIDA
- Ensembl
- ENSG00000132541
- Chromosome
- 8
- Canonical length
- 137 aa
- Protein class
- Enzymes, Plasma proteins, Predicted intracellular proteins
- Quaternary structure
- Homotrimer
OverviewNCBI Gene
Enables mRNA binding activity. Involved in mRNA catabolic process and mRNA destabilization. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
137 residues, UniProt reviewed canonical sequence.
>P52758|RIDA
1 MSSLIRRVIS TAKAPGAIGP YSQAVLVDRT IYISGQIGMD PSSGQLVSGG VAEEAKQALK
61 NMGEILKAAG CDFTNVVKTT VLLADINDFN TVNEIYKQYF KSNFPARAAY QVAALPKGSR
121 IEIEAVAIQG PLTTASLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RIDA can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.32
- Highest tissue expression
- 1,435 nTPM
Expression across tissuesHPA
Tissue
- liver: 1,435 nTPM
- kidney: 462 nTPM
- basal ganglia: 133 nTPM
- midbrain: 131 nTPM
- amygdala: 108 nTPM
- cerebral cortex: 102 nTPM
Single-cell type
- hepatocytes: 954 nCPM
- cholangiocytes: 194 nCPM
- epididymal efferent duct absorptive cells: 138 nCPM
- parietal cells: 76 nCPM
- esophageal suprabasal cells: 70 nCPM
- proximal tubule cells: 65 nCPM
Immune cell
- T-reg: 14 nTPM
- memory B-cell: 14 nTPM
- naive CD8 T-cell: 13 nTPM
- naive CD4 T-cell: 12 nTPM
- naive B-cell: 12 nTPM
- myeloid DC: 11 nTPM
Brain region
- thalamus: 50 nTPM
- midbrain: 44 nTPM
- basal ganglia: 41 nTPM
- medulla oblongata: 40 nTPM
- cerebellum: 40 nTPM
- hypothalamus: 39 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.98
- gnomAD pLI
- 0.07
- DepMap mean gene effect
- -0.08
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 13% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- lipid metabolic process
- mRNA catabolic process
- mRNA destabilization
- negative regulation of translation
- L-threonine catabolic process to glycine
Molecular functions
- deaminase activity
- mRNA binding
- RNA binding
- 2-iminobutanoate deaminase activity
- 2-iminopropanoate deaminase activity
- RNA endonuclease activity producing 3'-phosphomonoesters, hydrolytic mechanism
Cellular components
Protein domainsUniProt · Pfam · InterPro
- RidA family
- YjgF/YER057c/UK114 family
- RidA, conserved site
- RutC-like superfamily
- Endoribonuclease L-PSP
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RIDA in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads RIDA as an antibody target. Whether an autoantibody or antibody against RIDA could matter depends on whether native RIDA is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RIDA is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label RIDA as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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