CES2
Cocaine esterase
Also known as: CE-2, CES2A1, EST2_HUMAN, iCE
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O00748
- Gene
- CES2
- Ensembl
- ENSG00000172831
- Chromosome
- 16
- Canonical length
- 559 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Subcellular location
- Endoplasmic reticulum,Golgi apparatus,Cytosol
- Secretome location
- Intracellular and membrane
OverviewNCBI Gene
This gene encodes a member of the carboxylesterase large family. The family members are responsible for the hydrolysis or transesterification of various xenobiotics, such as cocaine and heroin, and endogenous substrates with ester, thioester, or amide bonds. They may participate in fatty acyl and cholesterol ester metabolism, and may play a role in the blood-brain barrier system. The protein encoded by this gene is the major intestinal enzyme and functions in intestine drug clearance. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Oct 2010]
Canonical amino-acid sequenceUniProt
559 residues, UniProt reviewed canonical sequence.
>O00748|CES2
1 MRLHRLRARL SAVACGLLLL LVRGQGQDSA SPIRTTHTGQ VLGSLVHVKG ANAGVQTFLG
61 IPFAKPPLGP LRFAPPEPPE SWSGVRDGTT HPAMCLQDLT AVESEFLSQF NMTFPSDSMS
121 EDCLYLSIYT PAHSHEGSNL PVMVWIHGGA LVFGMASLYD GSMLAALENV VVVIIQYRLG
181 VLGFFSTGDK HATGNWGYLD QVAALRWVQQ NIAHFGGNPD RVTIFGESAG GTSVSSLVVS
241 PISQGLFHGA IMESGVALLP GLIASSADVI STVVANLSAC DQVDSEALVG CLRGKSKEEI
301 LAINKPFKMI PGVVDGVFLP RHPQELLASA DFQPVPSIVG VNNNEFGWLI PKVMRIYDTQ
361 KEMDREASQA ALQKMLTLLM LPPTFGDLLR EEYIGDNGDP QTLQAQFQEM MADSMFVIPA
421 LQVAHFQCSR APVYFYEFQH QPSWLKNIRP PHMKADHGDE LPFVFRSFFG GNYIKFTEEE
481 EQLSRKMMKY WANFARNGNP NGEGLPHWPL FDQEEQYLQL NLQPAVGRAL KAHRLQFWKK
541 ALPQKIQELE EPEERHTELLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CES2 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)
- 0.23
- Highest tissue expression
- 662 nTPM
Expression across tissuesHPA
Tissue
- duodenum: 662 nTPM
- small intestine: 543 nTPM
- liver: 323 nTPM
- colon: 179 nTPM
- rectum: 168 nTPM
- esophagus: 162 nTPM
Single-cell type
- enterocytes: 571 nCPM
- colonocytes: 119 nCPM
- esophageal apical cells: 112 nCPM
- enteric transient amplifying cells: 86 nCPM
- hepatocytes: 79 nCPM
- esophageal suprabasal cells: 66 nCPM
Immune cell
- memory CD8 T-cell: 5.8 nTPM
- classical monocyte: 5.4 nTPM
- gdT-cell: 5.1 nTPM
- naive CD4 T-cell: 4.8 nTPM
- naive CD8 T-cell: 4.6 nTPM
- MAIT T-cell: 4.5 nTPM
Brain region
- choroid plexus: 36 nTPM
- cerebellum: 32 nTPM
- cerebral cortex: 30 nTPM
- hippocampal formation: 28 nTPM
- thalamus: 26 nTPM
- amygdala: 26 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)
- 1.29
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.37
- DepMap mean gene effect
- -0.07
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 8% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cocaine catabolic process
- prostaglandin metabolic process
- xenobiotic metabolic process
- detoxification
- morphine catabolic process
Molecular functions
- carboxylesterase activity
- carboxylic ester hydrolase activity
- methylumbelliferyl-acetate deacetylase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CES2 as an antibody target. Whether an autoantibody or antibody against CES2 could matter depends on whether native CES2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CES2 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 CES2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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