SPACA3
Sperm acrosome membrane-associated protein 3
Also known as: ALLP17, CT54, LYC3, LYZL3, SACA3_HUMAN, SLLP1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8IXA5
- Gene
- SPACA3
- Ensembl
- ENSG00000141316
- Chromosome
- 17
- Canonical length
- 215 aa
- Protein class
- Predicted intracellular proteins, Predicted membrane proteins, Predicted secreted proteins
- Subcellular location
- Acrosome
- Secretome location
- Secreted in male reproductive system
OverviewNCBI Gene
The protein encoded by this gene is a sperm surface protein that may be involved in adhesion to the egg prior to fertilization. While the encoded protein has significant similarity to lysozyme at the amino acid level, it has no detectable bacteriocidal activity. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]
Canonical amino-acid sequenceUniProt
215 residues, UniProt reviewed canonical sequence.
>Q8IXA5|SPACA3
1 MVSALRGAPL IRVHSSPVSS PSVSGPRRLV SCLSSQSSAL SQSGGGSTSA AGIEARSRAL
61 RRRWCPAGIM LLALVCLLSC LLPSSEAKLY GRCELARVLH DFGLDGYRGY SLADWVCLAY
121 FTSGFNAAAL DYEADGSTNN GIFQINSRRW CSNLTPNVPN VCRMYCSDLL NPNLKDTVIC
181 AMKITQEPQG LGYWEAWRHH CQGKDLTEWV DGCDFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SPACA3 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.44
- Highest tissue expression
- 118 nTPM
Expression across tissuesHPA
Tissue
- testis: 118 nTPM
- pancreas: 20 nTPM
- choroid plexus: 1.7 nTPM
- bone marrow: 0.3 nTPM
- small intestine: 0.3 nTPM
- epididymis: 0.2 nTPM
Single-cell type
- early spermatids: 1,521 nCPM
- late spermatids: 1,393 nCPM
- late primary spermatocytes: 614 nCPM
- pancreatic acinar cells: 21 nCPM
- sertoli cells: 8.6 nCPM
- leydig cells: 5.2 nCPM
Immune cell
- memory B-cell: 1.2 nTPM
- plasmacytoid DC: 0.2 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- cerebellum: 2.9 nTPM
- amygdala: 1.9 nTPM
- cerebral cortex: 1.9 nTPM
- hippocampal formation: 1.8 nTPM
- pons: 1.8 nTPM
- choroid plexus: 1.7 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)
- 1.39
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.38
- 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
- fusion of sperm to egg plasma membrane involved in single fertilization
- monocyte activation
- positive regulation of macrophage activation
- positive regulation of phagocytosis
- sperm-egg recognition
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SPACA3 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 SPACA3 as an antibody target. Whether an autoantibody or antibody against SPACA3 could matter depends on whether native SPACA3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SPACA3 is annotated as secreted, so native SPACA3 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label SPACA3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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