Mass spectrometric analysis was conducted as previously described (Zhang et al., 2016).
Their structures were determined based on comprehensive spectroscopic and mass spectrometric analysis.
The mass spectrometric analysis of the purified β-xylosidase from Pseudozyma hubeiensis NCIM 3574.
Therefore mass spectrometric analysis for these proteases should be further elaborated to obtain their full sequences.
Mass spectrometric analysis suggested that Mis17 might contain phosphorylated sites.
Bioinformatics modeling investigations also supported the pattern of disulfide connectivity obtained by Mass spectrometric analysis.
Data obtained from mass spectrometric analysis was further confirmed by homology modeling.
Gel bands for mass spectrometric analysis were basically processed according to Shevchenko et al. [22].
Mass spectrometric analysis of the tryptic digests of a glycoprotein with multiple glycosylation sites is complicated.
Mass spectrometric analysis of these bands revealed their identity as Cul1, Cul2, Cul3, and Cul5.
HPLC and mass spectrometric analysis of bacterial products were performed as described elsewhere [44].
