MARCKS
Myristoylated alanine-rich C-kinase substrate
Also known as: 80K-L, MACS, MARCS_HUMAN, PKCSL
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P29966
- Gene
- MARCKS
- Ensembl
- ENSG00000277443
- Chromosome
- 6
- Canonical length
- 332 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Endoplasmic reticulum,Plasma membrane,Cell Junctions,Primary cilium,Cytosol
OverviewNCBI Gene
The protein encoded by this gene is a substrate for protein kinase C. It is localized to the plasma membrane and is an actin filament crosslinking protein. Phosphorylation by protein kinase C or binding to calcium-calmodulin inhibits its association with actin and with the plasma membrane, leading to its presence in the cytoplasm. The protein is thought to be involved in cell motility, phagocytosis, membrane trafficking and mitogenesis. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
332 residues, UniProt reviewed canonical sequence.
>P29966|MARCKS
1 MGAQFSKTAA KGEAAAERPG EAAVASSPSK ANGQENGHVK VNGDASPAAA ESGAKEELQA
61 NGSAPAADKE EPAAAGSGAA SPSAAEKGEP AAAAAPEAGA SPVEKEAPAE GEAAEPGSPT
121 AAEGEAASAA SSTSSPKAED GATPSPSNET PKKKKKRFSF KKSFKLSGFS FKKNKKEAGE
181 GGEAEAPAAE GGKDEAAGGA AAAAAEAGAA SGEQAAAPGE EAAAGEEGAA GGDPQEAKPQ
241 EAAVAPEKPP ASDETKAAEE PSKVEEKKAE EAGASAAACE APSAAGPGAP PEQEAAPAEE
301 PAAAAASSAC AAPSQEAQPE CSPEAPPAEA AELocalizationUniProt · AlphaFold · HPA
Whether an antibody against MARCKS 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
- 0
- Mean surface accessibility (rSASA)
- 0.74
- Highest tissue expression
- 119 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 119 nTPM
- bone marrow: 99 nTPM
- urinary bladder: 81 nTPM
- cerebellum: 74 nTPM
- colon: 71 nTPM
- amygdala: 67 nTPM
Single-cell type
- neutrophils: 1,059 nCPM
- urothelial cells: 965 nCPM
- esophageal apical cells: 932 nCPM
- pancreatic acinar cells: 578 nCPM
- colonocytes: 514 nCPM
- suprabasal keratinocytes: 469 nCPM
Immune cell
- neutrophil: 19 nTPM
- intermediate monocyte: 13 nTPM
- non-classical monocyte: 7.5 nTPM
- memory B-cell: 4.6 nTPM
- classical monocyte: 3.9 nTPM
- naive B-cell: 1.9 nTPM
Brain region
- spinal cord: 225 nTPM
- white matter: 217 nTPM
- hypothalamus: 186 nTPM
- midbrain: 186 nTPM
- medulla oblongata: 170 nTPM
- thalamus: 153 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)
- 1.1
- gnomAD pLI
- 0.33
- gnomAD missense Z
- 0.29
- DepMap mean gene effect
- -0.1
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- actin crosslink formation
- actin filament bundle assembly
- actin filament organization
- apoptotic process
- central nervous system development
- mitochondrion organization
- neural tube development
- neurogenesis
- response to endoplasmic reticulum stress
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of MARCKS 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 MARCKS as an antibody target. Whether an autoantibody or antibody against MARCKS could matter depends on whether native MARCKS is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
MARCKS is annotated at the cell surface, where native MARCKS 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 MARCKS as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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