RIMKLB
Beta-citrylglutamate synthase B
Also known as: FAM80B, KIAA1238, NAAGS, NAAGS-I, RIMKB_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9ULI2
- Gene
- RIMKLB
- Ensembl
- ENSG00000166532
- Chromosome
- 12
- Canonical length
- 386 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Centriolar satellite
OverviewNCBI Gene
Predicted to enable N-acetyl-L-aspartate-L-glutamate ligase activity and citrate-L-glutamate ligase activity. Predicted to be involved in glutamine family amino acid metabolic process. Predicted to be located in cytosol. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
386 residues, UniProt reviewed canonical sequence.
>Q9ULI2|RIMKLB
1 MCSSVAAKLW FLTDRRIRED YPQKEILRAL KAKCCEEELD FRAVVMDEVV LTIEQGNLGL
61 RINGELITAY PQVVVVRVPT PWVQSDSDIT VLRHLEKMGC RLMNRPQAIL NCVNKFWTFQ
121 ELAGHGVPLP DTFSYGGHEN FAKMIDEAEV LEFPMVVKNT RGHRGKAVFL ARDKHHLADL
181 SHLIRHEAPY LFQKYVKESH GRDVRVIVVG GRVVGTMLRC STDGRMQSNC SLGGVGMMCS
241 LSEQGKQLAI QVSNILGMDV CGIDLLMKDD GSFCVCEANA NVGFIAFDKA CNLDVAGIIA
301 DYAASLLPSG RLTRRMSLLS VVSTASETSE PELGPPASTA VDNMSASSSS VDSDPESTER
361 ELLTKLPGGL FNMNQLLANE IKLLVDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RIMKLB 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
- 60 nTPM
Expression across tissuesHPA
Tissue
- blood vessel: 60 nTPM
- endometrium: 38 nTPM
- fallopian tube: 32 nTPM
- testis: 30 nTPM
- cerebellum: 29 nTPM
- cervix: 29 nTPM
Single-cell type
- endometrial glandular cells: 5,303 nCPM
- endometrial luminal cells: 1,415 nCPM
- late spermatids: 543 nCPM
- syncytiotrophoblasts: 398 nCPM
- alveolar cells type 2: 347 nCPM
- early spermatids: 258 nCPM
Immune cell
- basophil: 2.1 nTPM
- naive CD4 T-cell: 1.4 nTPM
- memory CD8 T-cell: 1.3 nTPM
- naive B-cell: 1.3 nTPM
- classical monocyte: 1.2 nTPM
- NK-cell: 1.2 nTPM
Brain region
- medulla oblongata: 54 nTPM
- spinal cord: 51 nTPM
- midbrain: 46 nTPM
- hypothalamus: 46 nTPM
- cerebellum: 43 nTPM
- basal ganglia: 42 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)
- 0.49
- gnomAD pLI
- 0.59
- gnomAD missense Z
- 2.34
- DepMap mean gene effect
- -0.07
- DepMap dependency class
- selective
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
Biological processes
Molecular functions
- ATP binding
- metal ion binding
- N-acetyl-L-aspartate-L-glutamate ligase activity
- citrate-L-glutamate ligase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads RIMKLB as an antibody target. Whether an autoantibody or antibody against RIMKLB could matter depends on whether native RIMKLB is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RIMKLB 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 RIMKLB as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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