AMY2A
Pancreatic alpha-amylase
Also known as: AMY2, AMYP_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P04746
- Gene
- AMY2A
- Ensembl
- ENSG00000243480
- Chromosome
- 1
- Canonical length
- 511 aa
- Protein class
- Enzymes, FDA approved drug targets, Metabolic proteins, Predicted secreted proteins
- Subcellular location
- Golgi apparatus,Cytosol
- Secretome location
- Secreted to digestive system
OverviewNCBI Gene
This gene encodes a member of the alpha-amylase family of proteins. Amylases are secreted proteins that hydrolyze 1,4-alpha-glucoside bonds in oligosaccharides and polysaccharides, catalyzing the first step in digestion of dietary starch and glycogen. This gene and several family members are present in a gene cluster on chromosome 1. This gene encodes an amylase isoenzyme produced by the pancreas. [provided by RefSeq, Jan 2015]
Canonical amino-acid sequenceUniProt
511 residues, UniProt reviewed canonical sequence.
>P04746|AMY2A
1 MKFFLLLFTI GFCWAQYSPN TQQGRTSIVH LFEWRWVDIA LECERYLAPK GFGGVQVSPP
61 NENVAIYNPF RPWWERYQPV SYKLCTRSGN EDEFRNMVTR CNNVGVRIYV DAVINHMCGN
121 AVSAGTSSTC GSYFNPGSRD FPAVPYSGWD FNDGKCKTGS GDIENYNDAT QVRDCRLTGL
181 LDLALEKDYV RSKIAEYMNH LIDIGVAGFR LDASKHMWPG DIKAILDKLH NLNSNWFPAG
241 SKPFIYQEVI DLGGEPIKSS DYFGNGRVTE FKYGAKLGTV IRKWNGEKMS YLKNWGEGWG
301 FVPSDRALVF VDNHDNQRGH GAGGASILTF WDARLYKMAV GFMLAHPYGF TRVMSSYRWP
361 RQFQNGNDVN DWVGPPNNNG VIKEVTINPD TTCGNDWVCE HRWRQIRNMV IFRNVVDGQP
421 FTNWYDNGSN QVAFGRGNRG FIVFNNDDWS FSLTLQTGLP AGTYCDVISG DKINGNCTGI
481 KIYVSDDGKA HFSISNSAED PFIAIHAESK LLocalizationUniProt · AlphaFold · HPA
Whether an antibody against AMY2A 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
- 0
- Mean surface accessibility (rSASA)
- 0.21
- Highest tissue expression
- 145,041 nTPM
Expression across tissuesHPA
Tissue
- pancreas: 145,041 nTPM
- ovary: 31 nTPM
- salivary gland: 29 nTPM
- heart muscle: 26 nTPM
- duodenum: 22 nTPM
- small intestine: 10 nTPM
Single-cell type
- pancreatic acinar cells: 865 nCPM
- pancreatic duct cells: 4 nCPM
- salivary acinar cells: 1.2 nCPM
- early spermatids: 0.7 nCPM
- monocytes: 0.6 nCPM
- mast cells: 0.4 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- basal ganglia: 1.6 nTPM
- amygdala: 1.4 nTPM
- cerebral cortex: 1.3 nTPM
- hippocampal formation: 1.3 nTPM
- white matter: 1 nTPM
- hypothalamus: 0.8 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)
- 1.68
- gnomAD pLI
- 0
- gnomAD missense Z
- -1.02
- DepMap mean gene effect
- -0.36
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads AMY2A as an antibody target. Whether an autoantibody or antibody against AMY2A could matter depends on whether native AMY2A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
AMY2A is annotated as secreted, so native AMY2A 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 AMY2A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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