LATS2
Serine/threonine-protein kinase LATS2
Also known as: LATS2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9NRM7
- Gene
- LATS2
- Ensembl
- ENSG00000150457
- Chromosome
- 13
- Canonical length
- 1088 aa
- Protein class
- Cancer-related genes, Enzymes, Predicted intracellular proteins
- Subcellular location
- Centriolar satellite,Cytosol
OverviewNCBI Gene
This gene encodes a serine/threonine protein kinase belonging to the LATS tumor suppressor family. The protein localizes to centrosomes during interphase, and early and late metaphase. It interacts with the centrosomal proteins aurora-A and ajuba and is required for accumulation of gamma-tubulin and spindle formation at the onset of mitosis. It also interacts with a negative regulator of p53 and may function in a positive feedback loop with p53 that responds to cytoskeleton damage. Additionally, it can function as a co-repressor of androgen-responsive gene expression. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
1088 residues, UniProt reviewed canonical sequence.
>Q9NRM7|LATS2
1 MRPKTFPATT YSGNSRQRLQ EIREGLKQPS KSSVQGLPAG PNSDTSLDAK VLGSKDATRQ
61 QQQMRATPKF GPYQKALREI RYSLLPFANE SGTSAAAEVN RQMLQELVNA GCDQEMAGRA
121 LKQTGSRSIE AALEYISKMG YLDPRNEQIV RVIKQTSPGK GLMPTPVTRR PSFEGTGDSF
181 ASYHQLSGTP YEGPSFGADG PTALEEMPRP YVDYLFPGVG PHGPGHQHQH PPKGYGASVE
241 AAGAHFPLQG AHYGRPHLLV PGEPLGYGVQ RSPSFQSKTP PETGGYASLP TKGQGGPPGA
301 GLAFPPPAAG LYVPHPHHKQ AGPAAHQLHV LGSRSQVFAS DSPPQSLLTP SRNSLNVDLY
361 ELGSTSVQQW PAATLARRDS LQKPGLEAPP RAHVAFRPDC PVPSRTNSFN SHQPRPGPPG
421 KAEPSLPAPN TVTAVTAAHI LHPVKSVRVL RPEPQTAVGP SHPAWVPAPA PAPAPAPAPA
481 AEGLDAKEEH ALALGGAGAF PLDVEYGGPD RRCPPPPYPK HLLLRSKSEQ YDLDSLCAGM
541 EQSLRAGPNE PEGGDKSRKS AKGDKGGKDK KQIQTSPVPV RKNSRDEEKR ESRIKSYSPY
601 AFKFFMEQHV ENVIKTYQQK VNRRLQLEQE MAKAGLCEAE QEQMRKILYQ KESNYNRLKR
661 AKMDKSMFVK IKTLGIGAFG EVCLACKVDT HALYAMKTLR KKDVLNRNQV AHVKAERDIL
721 AEADNEWVVK LYYSFQDKDS LYFVMDYIPG GDMMSLLIRM EVFPEHLARF YIAELTLAIE
781 SVHKMGFIHR DIKPDNILID LDGHIKLTDF GLCTGFRWTH NSKYYQKGSH VRQDSMEPSD
841 LWDDVSNCRC GDRLKTLEQR ARKQHQRCLA HSLVGTPNYI APEVLLRKGY TQLCDWWSVG
901 VILFEMLVGQ PPFLAPTPTE TQLKVINWEN TLHIPAQVKL SPEARDLITK LCCSADHRLG
961 RNGADDLKAH PFFSAIDFSS DIRKQPAPYV PTISHPMDTS NFDPVDEESP WNDASEGSTK
1021 AWDTLTSPNN KHPEHAFYEF TFRRFFDDNG YPFRCPKPSG AEASQAESSD LESSDLVDQT
1081 EGCQPVYVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LATS2 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)
- 0.52
- Highest tissue expression
- 24 nTPM
Expression across tissuesHPA
Tissue
- blood vessel: 24 nTPM
- adipose tissue: 19 nTPM
- skeletal muscle: 16 nTPM
- bone marrow: 14 nTPM
- gallbladder: 14 nTPM
- testis: 14 nTPM
Single-cell type
- neutrophils: 446 nCPM
- early spermatids: 250 nCPM
- endometrial luminal cells: 220 nCPM
- endometrial glandular cells: 211 nCPM
- syncytiotrophoblasts: 183 nCPM
- myonuclei: 178 nCPM
Immune cell
- MAIT T-cell: 0.9 nTPM
- neutrophil: 0.9 nTPM
- classical monocyte: 0.5 nTPM
- eosinophil: 0.5 nTPM
- gdT-cell: 0.4 nTPM
- intermediate monocyte: 0.4 nTPM
Brain region
- choroid plexus: 15 nTPM
- medulla oblongata: 10 nTPM
- thalamus: 10 nTPM
- hippocampal formation: 10 nTPM
- cerebellum: 8.8 nTPM
- midbrain: 8.6 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about LATS2.
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 166 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
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)
- 0.3
- gnomAD pLI
- 0.99
- gnomAD missense Z
- 2.21
- DepMap mean gene effect
- -0.01
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- canonical Wnt signaling pathway
- cell division
- G1/S transition of mitotic cell cycle
- hippo signaling
- hormone-mediated signaling pathway
- inner cell mass cell fate commitment
- inner cell mass cellular morphogenesis
- intracellular protein localization
- intracellular signal transduction
- keratinocyte differentiation
- negative regulation of canonical Wnt signaling pathway
- negative regulation of cell growth involved in contact inhibition
- negative regulation of cyclin-dependent protein serine/threonine kinase activity
- negative regulation of protein localization to nucleus
- positive regulation of apoptotic process
- positive regulation of NLRP3 inflammasome complex assembly
- protein phosphorylation
- regulation of organ growth
- regulation of transforming growth factor beta receptor signaling pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Protein kinase domain
- AGC-kinase, C-terminal
- Serine/threonine-protein kinase, active site
- UBA-like superfamily
- Protein kinase-like domain superfamily
- Ubiquitin-associated domain
- Protein kinase, ATP binding site
- Protein kinase, C-terminal
- Serine/threonine-protein kinases, AGC
- Protein kinase domain
- Protein kinase C terminal domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of LATS2 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 LATS2 as an antibody target. Whether an autoantibody or antibody against LATS2 could matter depends on whether native LATS2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LATS2 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 LATS2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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