calpain 1

Summary
Gene Symbol
  • CAPN1
Organism
Homo sapiens (human)
NCBI Gene
823
PubChem
823
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Acetylation
  • Autocatalytic cleavage
  • Calcium
  • Cell membrane
  • Cytoplasm
  • Disease variant
  • Hereditary spastic paraplegia
  • Metal-binding
  • Phosphoprotein
  • Reference proteome
  • Repeat
  • Thiol protease
Proteins
Displaying all 3 entries
UniProt Protein Name
B4DWH5
  • Calcium-activated neutral proteinase 1
  • Calpain mu-type
  • Calpain-1 large subunit
  • Micromolar-calpain
B2RDI5
  • Calcium-activated neutral proteinase 1
  • Calpain mu-type
  • Calpain-1 large subunit
  • Micromolar-calpain
P07384
  • Calcium-activated neutral proteinase 1
  • Calpain mu-type
  • Calpain-1 large subunit
  • Cell proliferation-inducing gene 30 protein
  • Micromolar-calpain
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
calpain
Functional Category
  • K: Transcription
  • O: Posttranslational modification, protein turnover, chaperones
  • Q: Secondary metabolites biosynthesis, transport and catabolism
Disease
Disease Ontology
Displaying all 9 entries
DO ID Disease Name Source
DOID:0081292 traumatic brain injury
DOID:0110821 hereditary spastic paraplegia 76
DOID:10230 aortic atherosclerosis
DOID:10652 Alzheimer's disease
DOID:11446 sciatic neuropathy
DOID:11723 Duchenne muscular dystrophy
DOID:1826 epilepsy
DOID:2476 hereditary spastic paraplegia
DOID:3021 acute kidney failure

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: February 17, 2025