MLST8
Target of rapamycin complex subunit LST8
Also known as: GbetaL, GBL, Lst8, LST8_HUMAN, Pop3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BVC4
- Gene
- MLST8
- Ensembl
- ENSG00000167965
- Chromosome
- 16
- Canonical length
- 326 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Golgi apparatus,Cell Junctions
OverviewNCBI Gene
Enables protein serine/threonine kinase activator activity and protein-macromolecule adaptor activity. Involved in TOR signaling; positive regulation of TOR signaling; and regulation of actin cytoskeleton organization. Part of TORC1 complex; TORC2 complex; and serine/threonine protein kinase complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
326 residues, UniProt reviewed canonical sequence.
>Q9BVC4|MLST8
1 MNTSPGTVGS DPVILATAGY DHTVRFWQAH SGICTRTVQH QDSQVNALEV TPDRSMIAAA
61 GYQHIRMYDL NSNNPNPIIS YDGVNKNIAS VGFHEDGRWM YTGGEDCTAR IWDLRSRNLQ
121 CQRIFQVNAP INCVCLHPNQ AELIVGDQSG AIHIWDLKTD HNEQLIPEPE VSITSAHIDP
181 DASYMAAVNS TGNCYVWNLT GGIGDEVTQL IPKTKIPAHT RYALQCRFSP DSTLLATCSA
241 DQTCKIWRTS NFSLMTELSI KSGNPGESSR GWMWGCAFSG DSQYIVTASS DNLARLWCVE
301 TGEIKREYGG HQKAVVCLAF NDSVLGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against MLST8 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.24
- Highest tissue expression
- 49 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 49 nTPM
- hippocampal formation: 42 nTPM
- amygdala: 42 nTPM
- cerebellum: 39 nTPM
- basal ganglia: 38 nTPM
- pancreas: 37 nTPM
Single-cell type
- late spermatids: 181 nCPM
- late primary spermatocytes: 79 nCPM
- esophageal basal cells: 76 nCPM
- migrating cytotrophoblasts: 76 nCPM
- cytotrophoblasts: 74 nCPM
- esophageal suprabasal cells: 62 nCPM
Immune cell
- non-classical monocyte: 30 nTPM
- intermediate monocyte: 30 nTPM
- classical monocyte: 25 nTPM
- myeloid DC: 25 nTPM
- total PBMC: 21 nTPM
- memory CD8 T-cell: 15 nTPM
Brain region
- cerebral cortex: 47 nTPM
- white matter: 38 nTPM
- thalamus: 37 nTPM
- pons: 35 nTPM
- hippocampal formation: 35 nTPM
- amygdala: 34 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)
- 0.67
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 1.38
- DepMap mean gene effect
- -0.47
- 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
- cellular response to hypoxia
- cellular response to nutrient levels
- cellular response to osmotic stress
- cytoskeleton organization
- DNA damage response
- negative regulation of apoptotic process
- negative regulation of autophagy
- positive regulation of actin filament polymerization
- positive regulation of cell growth
- positive regulation of glycolytic process
- positive regulation of lipid biosynthetic process
- positive regulation of pentose-phosphate shunt
- positive regulation of TOR signaling
- regulation of actin cytoskeleton organization
- TOR signaling
- TORC1 signaling
- TORC2 signaling
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MLST8 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 MLST8 as an antibody target. Whether an autoantibody or antibody against MLST8 could matter depends on whether native MLST8 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MLST8 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 MLST8 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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