Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
51
pubmed:dateCreated
2002-12-16
pubmed:databankReference
pubmed:abstractText
Metallocarboxypeptidase D (CPD), is a 180-kDa protein that contains three carboxypeptidase-like domains, a transmembrane domain, and a cytosolic tail and which functions in the processing of proteins that transit the secretory pathway. An initial report on the Drosophila melanogaster silver gene indicated a CPD-like protein with only two and a half carboxypeptidase-like domains with no transmembrane region (Settle, S. H., Jr., Green, M. M., and Burtis, K. C. (1995) Proc. Natl. Acad. Sci. U. S. A. 92, 9470-9474). A variety of bioinformatics and experimental approaches were used to determine that the Drosophila silver gene corresponds to a CPD-like protein with three carboxypeptidase-like domains, a transmembrane domain, and a cytosolic tail. In addition, two alternative exons were found, which result in proteins with different carboxypeptidase-like domains, termed domains 1A and 1B. Northern blot, reverse transcriptase PCR, and sequence analysis were used to confirm the presence of the various mRNA forms. Individual domains of Drosophila CPD were expressed in insect Sf9 cells using the baculovirus expression system. Media from domain 1B- and domain 2-expressing cells showed substantial enzymatic activity, whereas medium from domain 1A-expressing cells was no different from cells infected with wild-type virus. Domains 1B and 2 were purified, and the enzymatic properties were examined. Both enzymes cleaved substrates with C-terminal Arg or Lys, but not Leu, and were inhibited by conventional metallopeptidase inhibitors and some divalent cations. Drosophila domain 1B is more active at neutral pH and greatly prefers C-terminal Arg over Lys, whereas domain 2 is more active at pH 5-6 and slightly prefers C-terminal Lys over Arg. The differences in pH optima and substrate specificity between Drosophila domains 1B and 2 are similar to the differences between duck CPD domains 1 and 2, suggesting that these properties are essential to CPD function.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
20
pubmed:volume
277
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
49613-20
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:12393882-3' Untranslated Regions, pubmed-meshheading:12393882-Amino Acid Sequence, pubmed-meshheading:12393882-Animals, pubmed-meshheading:12393882-Arginine, pubmed-meshheading:12393882-Baculoviridae, pubmed-meshheading:12393882-Binding Sites, pubmed-meshheading:12393882-Blotting, Northern, pubmed-meshheading:12393882-Blotting, Western, pubmed-meshheading:12393882-Carboxypeptidases, pubmed-meshheading:12393882-Cations, pubmed-meshheading:12393882-Cell Line, pubmed-meshheading:12393882-Databases as Topic, pubmed-meshheading:12393882-Dose-Response Relationship, Drug, pubmed-meshheading:12393882-Drosophila melanogaster, pubmed-meshheading:12393882-Exons, pubmed-meshheading:12393882-Expressed Sequence Tags, pubmed-meshheading:12393882-Hydrogen-Ion Concentration, pubmed-meshheading:12393882-Insects, pubmed-meshheading:12393882-Introns, pubmed-meshheading:12393882-Kinetics, pubmed-meshheading:12393882-Lysine, pubmed-meshheading:12393882-Models, Genetic, pubmed-meshheading:12393882-Molecular Sequence Data, pubmed-meshheading:12393882-Phenotype, pubmed-meshheading:12393882-Protein Binding, pubmed-meshheading:12393882-Protein Structure, Tertiary, pubmed-meshheading:12393882-RNA, Messenger, pubmed-meshheading:12393882-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:12393882-Substrate Specificity, pubmed-meshheading:12393882-Time Factors
pubmed:year
2002
pubmed:articleTitle
Characterization of Drosophila carboxypeptidase D.
pubmed:affiliation
Department of Molecular Pharmacology, Albert Einstein College of Medicine, 1300 Morris Park Avenue, Bronx, NY 10461, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.