Aminopeptidase O
Also known as: AOPEP, C9orf3, ONPEP
Function
Aminopeptidase which catalyzes the hydrolysis of amino acid residues from the N-terminus of peptide or protein substrates.
Classification
- Family (Pfam)
- PF09127 Leuk-A4-hydro_C, PF01433 Peptidase_M1
- InterPro
- Aminopeptidase_N-like_N_sf, AOPep, ARM-type_fold, M1_LTA-4_hydro/amino_C_sf, Peptidase_M1_C, Peptidase_M1_dom, Peptidase_M4/M1_CTD_sf
- Functional cluster
- Zinc-Finger & Chromatin Regulatory Proteins
Gene Ontology · 5
Disease associations
- dystonia 31 MONDO:0030455
Drugs targeting this protein · 1
- TOSEDOSTAT inhibitor
Related proteins · sequence + function similarity
- Aminopeptidase O 0.97
- Aminopeptidase O 0.96
- Transcription initiation factor TFIID subunit 2 0.59
- Aminopeptidase RNPEPL1 0.58
- Aminopeptidase RNPEPL1 0.57
- Aminopeptidase B 0.57
- Aminopeptidase B 0.56
- Prolyl endopeptidase-like 0.56
- Aminopeptidase B 0.55
- PHD finger protein 24 0.54
- Prolyl endopeptidase-like 0.54
- PHD finger protein 24 0.53
Co-cited proteins · studied together in the literature
- Aminopeptidase O 2 shared papers
Literature · 6 cited papers
- Biallelic AOPEP loss-of-function variants cause progressive dystonia with prominent limb involvement. Mov. Disord. · 2022
- PMID 30808004 J. Biol. Chem. · 2019
- Identification of human aminopeptidase O, a novel metalloprotease with structural similarity to aminopeptidase B and leukotriene A4 hydrolase. J. Biol. Chem. · 2005
- The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). Genome Res. · 2004
- DNA sequence and analysis of human chromosome 9. Nature · 2004
- Complete sequencing and characterization of 21,243 full-length human cDNAs. Nat. Genet. · 2004
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