RPL7
Large ribosomal subunit protein uL30
Also known as: humL7-1, L7, RL7_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P18124
- Gene
- RPL7
- Ensembl
- ENSG00000147604
- Chromosome
- 8
- Canonical length
- 248 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins, Ribosomal proteins
- Subcellular location
- Nucleoli,Endoplasmic reticulum,Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L30P family of ribosomal proteins. It contains an N-terminal basic region-leucine zipper (BZIP)-like domain and the RNP consensus submotif RNP2. In vitro the BZIP-like domain mediates homodimerization and stable binding to DNA and RNA, with a preference for 28S rRNA and mRNA. The protein can inhibit cell-free translation of mRNAs, suggesting that it plays a regulatory role in the translation apparatus. It is located in the cytoplasm. The protein has been shown to be an autoantigen in patients with systemic autoimmune diseases, such as systemic lupus erythematosus. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
248 residues, UniProt reviewed canonical sequence.
>P18124|RPL7
1 MEGVEEKKKE VPAVPETLKK KRRNFAELKI KRLRKKFAQK MLRKARRKLI YEKAKHYHKE
61 YRQMYRTEIR MARMARKAGN FYVPAEPKLA FVIRIRGING VSPKVRKVLQ LLRLRQIFNG
121 TFVKLNKASI NMLRIVEPYI AWGYPNLKSV NELIYKRGYG KINKKRIALT DNALIARSLG
181 KYGIICMEDL IHEIYTVGKR FKEANNFLWP FKLSSPRGGM KKKTTHFVEG GDAGNREDQI
241 NRLIRRMNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RPL7 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)
- 0.35
- Highest tissue expression
- 3,912 nTPM
Expression across tissuesHPA
Tissue
- ovary: 3,912 nTPM
- breast: 3,082 nTPM
- pancreas: 2,954 nTPM
- bone marrow: 2,894 nTPM
- skin: 2,733 nTPM
- tonsil: 2,495 nTPM
Single-cell type
- decidual stromal cells: 8,937 nCPM
- extravillous trophoblasts: 5,955 nCPM
- ovarian stromal cells: 5,906 nCPM
- epididymal basal cells: 5,577 nCPM
- esophageal suprabasal cells: 5,419 nCPM
- esophageal basal cells: 5,173 nCPM
Immune cell
- total PBMC: 26,935 nTPM
- naive CD4 T-cell: 17,646 nTPM
- memory B-cell: 14,400 nTPM
- MAIT T-cell: 12,657 nTPM
- naive CD8 T-cell: 12,475 nTPM
- naive B-cell: 12,256 nTPM
Brain region
- spinal cord: 614 nTPM
- white matter: 562 nTPM
- basal ganglia: 530 nTPM
- medulla oblongata: 507 nTPM
- hypothalamus: 496 nTPM
- thalamus: 474 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)
- 0.18
- gnomAD pLI
- 1
- gnomAD missense Z
- 1.15
- DepMap mean gene effect
- -1.58
- DepMap dependency class
- pan
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 11% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cytoplasmic translation
- maturation of LSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA)
- ribosomal large subunit biogenesis
- rRNA processing
- translation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Large ribosomal subunit protein uL30, eukaryota
- Large ribosomal subunit protein uL30, N-terminal, eukaryota
- Large ribosomal subunit protein uL30-like, ferredoxin-like fold domain
- Large ribosomal subunit protein uL30, conserved site
- Large ribosomal subunit protein uL30, eukaryota/archaea
- Large ribosomal subunit protein uL30, ferredoxin-like fold domain superfamily
- Large ribosomal subunit protein uL30
- Ribosomal protein L30p/L7e
- Ribosomal L30 N-terminal domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RPL7 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 RPL7 as an antibody target. Whether an autoantibody or antibody against RPL7 could matter depends on whether native RPL7 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RPL7 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.
Source-annotated serology context
The source annotations explicitly mention antibody, autoantibody, autoantigen, or autoimmune context. This is biological context, not study-specific reactivity.
- The protein has been shown to be an autoantigen in patients with systemic autoimmune diseases, such as systemic lupus erythematosus.
Loading the interactive Seroatlas protein explorer...