ESD
S-formylglutathione hydrolase
Also known as: ESTD_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P10768
- Gene
- ESD
- Ensembl
- ENSG00000139684
- Chromosome
- 13
- Canonical length
- 282 aa
- Protein class
- Enzymes, Metabolic proteins, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Golgi apparatus,Cytosol
- Quaternary structure
- Homodimer
OverviewNCBI Gene
This gene encodes a serine hydrolase that belongs to the esterase D family. The encoded enzyme is active toward numerous substrates including O-acetylated sialic acids, and it may be involved in the recycling of sialic acids. This gene is used as a genetic marker for retinoblastoma and Wilson's disease. [provided by RefSeq, Feb 2009]
Canonical amino-acid sequenceUniProt
282 residues, UniProt reviewed canonical sequence.
>P10768|ESD
1 MALKQISSNK CFGGLQKVFE HDSVELNCKM KFAVYLPPKA ETGKCPALYW LSGLTCTEQN
61 FISKSGYHQS ASEHGLVVIA PDTSPRGCNI KGEDESWDFG TGAGFYVDAT EDPWKTNYRM
121 YSYVTEELPQ LINANFPVDP QRMSIFGHSM GGHGALICAL KNPGKYKSVS AFAPICNPVL
181 CPWGKKAFSG YLGTDQSKWK AYDATHLVKS YPGSQLDILI DQGKDDQFLL DGQLLPDNFI
241 AACTEKKIPV VFRLQEGYDH SYYFIATFIT DHIRHHAKYL NALocalizationUniProt · AlphaFold · HPA
Whether an antibody against ESD 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)
- 0.2
- Highest tissue expression
- 259 nTPM
Expression across tissuesHPA
Tissue
- liver: 259 nTPM
- blood vessel: 248 nTPM
- kidney: 181 nTPM
- ovary: 178 nTPM
- tongue: 167 nTPM
- smooth muscle: 155 nTPM
Single-cell type
- decidual stromal cells: 428 nCPM
- hofbauer cells: 305 nCPM
- ovarian stromal cells: 303 nCPM
- esophageal basal cells: 297 nCPM
- late primary spermatocytes: 272 nCPM
- epididymal efferent duct absorptive cells: 263 nCPM
Immune cell
- plasmacytoid DC: 171 nTPM
- myeloid DC: 143 nTPM
- classical monocyte: 130 nTPM
- naive CD4 T-cell: 114 nTPM
- intermediate monocyte: 114 nTPM
- NK-cell: 110 nTPM
Brain region
- white matter: 85 nTPM
- hypothalamus: 85 nTPM
- spinal cord: 74 nTPM
- medulla oblongata: 66 nTPM
- choroid plexus: 60 nTPM
- cerebellum: 57 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)
- 1.15
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.4
- DepMap mean gene effect
- -0.02
- 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
- carboxylic ester hydrolase activity
- hydrolase activity, acting on ester bonds
- identical protein binding
- methylumbelliferyl-acetate deacetylase activity
- S-formylglutathione hydrolase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Alpha/Beta hydrolase fold
- Esterase-like
- S-formylglutathione hydrolase
- Putative esterase
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ESD 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 ESD as an antibody target. Whether an autoantibody or antibody against ESD could matter depends on whether native ESD is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ESD 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 ESD as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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