SLC16A3
Monocarboxylate transporter 4
Also known as: MCT3, MCT4, MOT4_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O15427
- Gene
- SLC16A3
- Ensembl
- ENSG00000141526
- Chromosome
- 17
- Canonical length
- 465 aa
- Protein class
- Metabolic proteins, Predicted membrane proteins, Transporters
- Subcellular location
- Nuclear membrane,Plasma membrane
OverviewNCBI Gene
Lactic acid and pyruvate transport across plasma membranes is catalyzed by members of the proton-linked monocarboxylate transporter (MCT) family, which has been designated solute carrier family-16. Each MCT appears to have slightly different substrate and inhibitor specificities and transport kinetics, which are related to the metabolic requirements of the tissues in which it is found. The MCTs, which include MCT1 (SLC16A1; MIM 600682) and MCT2 (SLC16A7; MIM 603654), are characterized by 12 predicted transmembrane domains (Price et al., 1998 [PubMed 9425115]).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
465 residues, UniProt reviewed canonical sequence.
>O15427|SLC16A3
1 MGGAVVDEGP TGVKAPDGGW GWAVLFGCFV ITGFSYAFPK AVSVFFKELI QEFGIGYSDT
61 AWISSILLAM LYGTGPLCSV CVNRFGCRPV MLVGGLFASL GMVAASFCRS IIQVYLTTGV
121 ITGLGLALNF QPSLIMLNRY FSKRRPMANG LAAAGSPVFL CALSPLGQLL QDRYGWRGGF
181 LILGGLLLNC CVCAALMRPL VVTAQPGSGP PRPSRRLLDL SVFRDRGFVL YAVAASVMVL
241 GLFVPPVFVV SYAKDLGVPD TKAAFLLTIL GFIDIFARPA AGFVAGLGKV RPYSVYLFSF
301 SMFFNGLADL AGSTAGDYGG LVVFCIFFGI SYGMVGALQF EVLMAIVGTH KFSSAIGLVL
361 LMEAVAVLVG PPSGGKLLDA THVYMYVFIL AGAEVLTSSL ILLLGNFFCI RKKPKEPQPE
421 VAAAEEEKLH KPPADSGVDL REVEHFLKAE PEKNGEVVHT PETSVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SLC16A3 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 12
- Mean surface accessibility (rSASA)
- 0.28
- Highest tissue expression
- 134 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 134 nTPM
- tongue: 68 nTPM
- spleen: 40 nTPM
- lung: 33 nTPM
- esophagus: 29 nTPM
- blood vessel: 29 nTPM
Single-cell type
- extravillous trophoblasts: 2,421 nCPM
- syncytiotrophoblasts: 885 nCPM
- neutrophils: 850 nCPM
- retinal pigment epithelial cells: 661 nCPM
- esophageal apical cells: 585 nCPM
- epicardial cells: 380 nCPM
Immune cell
- neutrophil: 110 nTPM
- eosinophil: 92 nTPM
- basophil: 57 nTPM
- classical monocyte: 33 nTPM
- non-classical monocyte: 32 nTPM
- intermediate monocyte: 31 nTPM
Brain region
- medulla oblongata: 43 nTPM
- white matter: 37 nTPM
- thalamus: 36 nTPM
- pons: 31 nTPM
- cerebral cortex: 27 nTPM
- spinal cord: 24 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)
- 1.17
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.05
- DepMap mean gene effect
- -0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- lactate transmembrane transport
- monocarboxylic acid transport
- plasma membrane lactate transport
- pyruvate catabolic process
- pyruvate transmembrane transport
Molecular functions
- lactate:proton symporter activity
- monocarboxylic acid transmembrane transporter activity
- pyruvate transmembrane transporter activity
- RNA binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SLC16A3 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 SLC16A3 as an antibody target. Whether an autoantibody or antibody against SLC16A3 could matter depends on whether native SLC16A3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SLC16A3 is annotated at the cell surface, where native SLC16A3 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label SLC16A3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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