NMRAL1
NmrA-like family domain-containing protein 1
Also known as: FLJ25918, HSCARG, NMRL1_HUMAN, SDR48A1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9HBL8
- Gene
- NMRAL1
- Ensembl
- ENSG00000153406
- Chromosome
- 16
- Canonical length
- 299 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes an NADPH sensor protein that preferentially binds to NADPH. The encoded protein also negatively regulates the activity of NF-kappaB in a ubiquitylation-dependent manner. It plays a key role in cellular antiviral response by negatively regulating the interferon response factor 3-mediated expression of interferon beta. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Feb 2015]
Canonical amino-acid sequenceUniProt
299 residues, UniProt reviewed canonical sequence.
>Q9HBL8|NMRAL1
1 MVDKKLVVVF GGTGAQGGSV ARTLLEDGTF KVRVVTRNPR KKAAKELRLQ GAEVVQGDQD
61 DQVIMELALN GAYATFIVTN YWESCSQEQE VKQGKLLADL ARRLGLHYVV YSGLENIKKL
121 TAGRLAAAHF DGKGEVEEYF RDIGVPMTSV RLPCYFENLL SHFLPQKAPD GKSYLLSLPT
181 GDVPMDGMSV SDLGPVVLSL LKMPEKYVGQ NIGLSTCRHT AEEYAALLTK HTRKVVHDAK
241 MTPEDYEKLG FPGARDLANM FRFYALRPDR DIELTLRLNP KALTLDQWLE QHKGDFNLLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against NMRAL1 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)
- 0.24
- Highest tissue expression
- 58 nTPM
Expression across tissuesHPA
Tissue
- liver: 58 nTPM
- basal ganglia: 45 nTPM
- pancreas: 45 nTPM
- spinal cord: 44 nTPM
- stomach: 43 nTPM
- midbrain: 42 nTPM
Single-cell type
- gastric chief cells: 59 nCPM
- extravillous trophoblasts: 59 nCPM
- cytotrophoblasts: 56 nCPM
- epididymal principal cells: 53 nCPM
- migrating cytotrophoblasts: 47 nCPM
- hofbauer cells: 41 nCPM
Immune cell
- gdT-cell: 61 nTPM
- classical monocyte: 59 nTPM
- memory CD8 T-cell: 57 nTPM
- myeloid DC: 54 nTPM
- total PBMC: 54 nTPM
- plasmacytoid DC: 53 nTPM
Brain region
- white matter: 25 nTPM
- medulla oblongata: 24 nTPM
- cerebral cortex: 23 nTPM
- pons: 23 nTPM
- basal ganglia: 23 nTPM
- cerebellum: 21 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)
- 1.33
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.73
- DepMap mean gene effect
- -0.06
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- NAD(P)-binding domain superfamily
- NmrA-like domain
- NmrA-like oxidoreductase
- NmrA-like family
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NMRAL1 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 NMRAL1 as an antibody target. Whether an autoantibody or antibody against NMRAL1 could matter depends on whether native NMRAL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NMRAL1 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 NMRAL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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