Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2006-2-14
pubmed:abstractText
The amino acid sequence of methylamine oxidase (MeAO) from the fungus Aspergillus niger was analyzed using mass spectrometry (MS). First, MeAO was characterized by an accurate molar mass of 72.4 kDa of the monomer measured using MALDI-TOF-MS and by a pI value of 5.8 determined by isoelectric focusing. MALDI-TOF-MS revealed a clear peptide mass fingerprint after tryptic digestion, which did not provide any relevant hit when searched against a nonredundant protein database and was different from that of A. niger amine oxidase AO-I. Tandem mass spectrometry with electrospray ionization coupled to liquid chromatography allowed unambiguous reading of six peptide sequences (11-19 amino acids) and seven sequence tags (4-15 amino acids), which were used for MS BLAST homology searching. MeAO was found to be largely homologous to a hypothetical protein AN7641.2 (EMBL/GenBank protein-accession code EAA61827) from Aspergillus nidulans FGSC A4 with a theoretical molar mass of 76.46 kDa and pI 6.14, which belongs to the superfamily of copper amine oxidases. The protein AN7641.2 is only little homologous to the amine oxidase AO-I (32% identity, 49 % similarity).
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0015-5632
pubmed:author
pubmed:issnType
Print
pubmed:volume
50
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
401-8
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:16475499-Amino Acid Sequence, pubmed-meshheading:16475499-Aspergillus niger, pubmed-meshheading:16475499-Chromatography, Liquid, pubmed-meshheading:16475499-Computational Biology, pubmed-meshheading:16475499-Copper, pubmed-meshheading:16475499-Dihydroxyphenylalanine, pubmed-meshheading:16475499-Isoelectric Focusing, pubmed-meshheading:16475499-Isoelectric Point, pubmed-meshheading:16475499-Molecular Sequence Data, pubmed-meshheading:16475499-Molecular Weight, pubmed-meshheading:16475499-Oxidoreductases Acting on CH-NH Group Donors, pubmed-meshheading:16475499-Peptide Mapping, pubmed-meshheading:16475499-Sequence Analysis, Protein, pubmed-meshheading:16475499-Sequence Homology, Amino Acid, pubmed-meshheading:16475499-Spectrometry, Mass, Electrospray Ionization, pubmed-meshheading:16475499-Spectrometry, Mass, Matrix-Assisted Laser..., pubmed-meshheading:16475499-Trypsin
pubmed:year
2005
pubmed:articleTitle
Mapping the primary structure of copper/topaquinone-containing methylamine oxidase from Aspergillus niger.
pubmed:affiliation
Laboratory of Growth Regulators, Faculty of Science, Palacký University, 783 71 Olomouc, Czechia.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't