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CD10 (neprilysin, neutral endopeptidase, enkephalinase, common acute lymphoblastic leukemia antigen, CALLA, atriopeptidase, MME, EPN)
Function:
- thermolysin-like specificity
- preferential cleavage of polypeptides between hydrophobic residues, particularly with Phe or Tyr at P1
- substrates are polypeptides < 5 kD
a) endorphins, enkephalins, cleavage of a Gly-Phe bond
b) substance P, kinins
c) somatostatin
d) atrial natriuretic factor (ANF)
e) amyloid A4 peptide
- degrades amyloid beta-peptide (A4 amyloid peptide) [7,8,9] of senile plaques in Alzheimer's disease; [5]
- it is thought that neprilysin & insulin-degrading enzyme may be major enzymes degrading the amyloid beta-peptide [6]
Cofactor: binds 1 Zn+2 per subunit
Structure: belongs to the peptidase M13 family
Compartment:
- plasma membrane
- internal membranes
- axonally transported; present in presynaptic membrane [7]
Expression:
- widely distributed
- follicular center cells, pre-B cells, granulocytes cortical thymocytes, lympho-hematopoietic precursors
- endometrial stroma, male GU epithelium, mesonephric remnants, liver, brush border in small bowel mucosa, placenta choroid plexus, brain, ovary, adrenal cortex
Pathology:
- expressed in many tumors including: follicular center cell lymphomas pre-B ALL ~75% CML in blast crisis ~90% hepatocellular carcinoma (canalicular pattern) ~68% sensitive, >95% specific with canalicular pattern mesonephric tumors renal cell carcinoma urothelial carcinoma prostate carcinoma pancreatic carcinoma uterine carcinoma endometrial stromal tumors smooth muscle tumors sarcomas melanomas microvillous inclusion disease
- myeloid & erythroid precursors & female genital tract tumors stain negatively with antibody
Interactions
molecular events
Related
CD10 (neprilysin) Ag in tissue
CD10 blasts in blood
CD10 blasts in bone marrow
CD10 cells in blood
General
cluster-of-differentiation antigen; cluster designation antigen; CD antigen
zinc metalloprotease
Properties
SIZE: entity length = 750 aa
MW = 86 kD
COMPARTMENT: plasma membrane
MOTIF: Stop-transfer sequence {16-23}
transmembrane domain {29-51}
cysteine residue {C57}
MODIFICATION: cysteine residue {C62}
cysteine residue {C62}
MODIFICATION: cysteine residue {C57}
cysteine residue {C80}
MODIFICATION: cysteine residue {C735}
cysteine residue {C88}
MODIFICATION: cysteine residue {C695}
binding site
SITE: 103-103
FOR-BINDING-OF: Substrate carboxyl
cysteine residue {C143}
MODIFICATION: cysteine residue {C411}
N-glycosylation site {N145}
cysteine residue {C234}
MODIFICATION: cysteine residue {C242}
cysteine residue {C242}
MODIFICATION: cysteine residue {C234}
N-glycosylation site {N285}
N-glycosylation site {N325}
cysteine residue {C411}
MODIFICATION: cysteine residue {C143}
Zn+2-binding site
SITE: 584-584
Zn+2-binding site
SITE: 588-588
aspartate residue {D591}
cysteine residue {C621}
MODIFICATION: cysteine residue {C747}
N-glycosylation site {N628}
Zn+2-binding site
SITE: 647-647
aspartate residue {D651}
cysteine residue {C695}
MODIFICATION: cysteine residue {C88}
cysteine residue {C735}
MODIFICATION: cysteine residue {C80}
cysteine residue {C747}
MODIFICATION: cysteine residue {C621}
Database Correlations
OMIM 120520
UniProt P08473
PFAM correlations
Entrez Gene 4311
Kegg hsa:4311
ENZYME 3.4.24.11
References
- Cotran et al Robbins Pathologic Basis of Disease,
W.B. Saunders Co, Philadelphia, PA 1989 pg 165
- UniProt :accession Q00973
- Journal Watch 20(5):38, 2000
Iwata N, Tsubuki S, Takaki Y, Watanabe K, Sekiguchi M,
Hosoki E, Kawashima-Morishima M, Lee HJ, Hama E,
Sekine-Aizawa Y, Saido TC.
Identification of the major Abeta1-42-degrading catabolic
pathway in brain parenchyma: suppression leads to
biochemical and pathological deposition.
Nat Med. 2000 Feb;6(2):143-50.
PMID: 10655101
- Selkoe DJ.
Clearing the brain's amyloid cobwebs.
Neuron. 2001 Oct 25;32(2):177-80. Review.
PMID: 11683988
- http://www.pathologyoutlines.com/cdmarkers.html
15 October 2002
- Greg Gole, UCLA Sepulveda VA, 02/12/2004, personal
communication
- Iwata N, Mizukami H, Shirotani K, Takaki Y, Muramatsu S,
Lu B, Gerard NP, Gerard C, Ozawa K, Saido TC.
Presynaptic localization of neprilysin contributes to
efficient clearance of amyloid-beta peptide in mouse brain.
J Neurosci. 2004 Jan 28;24(4):991-8.
PMID: 14749444
- Marr RA, Guan H, Rockenstein E, Kindy M, Gage FH, Verma I,
Masliah E, Hersh LB.
Neprilysin regulates amyloid Beta peptide levels.
J Mol Neurosci. 2004;22(1-2):5-11.
PMID: 14742905
- Atlas of genetics & cytogenetics in oncology & haematology
http://atlasgeneticsoncology.org/genes/MMEID41386ch3q25.html