ACCS
1-aminocyclopropane-1-carboxylate synthase-like protein 1
Also known as: 1A1L1_HUMAN, ACS, PHACS
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96QU6
- Gene
- ACCS
- Ensembl
- ENSG00000110455
- Chromosome
- 11
- Canonical length
- 501 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Golgi apparatus
OverviewNCBI Gene
Enables identical protein binding activity. Predicted to be involved in amino acid metabolic process. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
501 residues, UniProt reviewed canonical sequence.
>Q96QU6|ACCS
1 MFTLPQKDFR APTTCLGPTC MQDLGSSHGE DLEGECSRKL DQKLPELRGV GDPAMISSDT
61 SYLSSRGRMI KWFWDSAEEG YRTYHMDEYD EDKNPSGIIN LGTSENKLCF DLLSWRLSQR
121 DMQRVEPSLL QYADWRGHLF LREEVAKFLS FYCKSPVPLR PENVVVLNGG ASLFSALATV
181 LCEAGEAFLI PTPYYGAITQ HVCLYGNIRL AYVYLDSEVT GLDTRPFQLT VEKLEMALRE
241 AHSEGVKVKG LILISPQNPL GDVYSPEELQ EYLVFAKRHR LHVIVDEVYM LSVFEKSVGY
301 RSVLSLERLP DPQRTHVMWA TSKDFGMSGL RFGTLYTENQ DVATAVASLC RYHGLSGLVQ
361 YQMAQLLRDR DWINQVYLPE NHARLKAAHT YVSEELRALG IPFLSRGAGF FIWVDLRKYL
421 PKGTFEEEML LWRRFLDNKV LLSFGKAFEC KEPGWFRFVF SDQVHRLCLG MQRVQQVLAG
481 KSQVAEDPRP SQSQEPSDQR RLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ACCS 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.29
- Highest tissue expression
- 18 nTPM
Expression across tissuesHPA
Tissue
- liver: 18 nTPM
- adrenal gland: 17 nTPM
- fallopian tube: 15 nTPM
- spleen: 13 nTPM
- endometrium: 13 nTPM
- thyroid gland: 12 nTPM
Single-cell type
- platelets: 47 nCPM
- choroid plexus epithelial cells: 31 nCPM
- sertoli cells: 30 nCPM
- fibro-adipogenic progenitors: 28 nCPM
- proximal tubule cells: 23 nCPM
- microglia: 23 nCPM
Immune cell
- eosinophil: 5.7 nTPM
- myeloid DC: 4.4 nTPM
- plasmacytoid DC: 3.3 nTPM
- classical monocyte: 3.1 nTPM
- intermediate monocyte: 3.1 nTPM
- non-classical monocyte: 2.5 nTPM
Brain region
- choroid plexus: 17 nTPM
- hypothalamus: 6.6 nTPM
- thalamus: 6.6 nTPM
- medulla oblongata: 6.2 nTPM
- cerebral cortex: 6 nTPM
- midbrain: 6 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)
- 0.84
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.23
- DepMap mean gene effect
- 0.03
- DepMap dependency class
- none
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
Molecular functions
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ACCS as an antibody target. Whether an autoantibody or antibody against ACCS could matter depends on whether native ACCS is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ACCS 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 ACCS as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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