The number of protein and peptide structures included in Protein
Data Bank (PDB) and Gen Bank without functional annotation has increased.
Consequently, there is a high demand for theoretical models to predict
these functions. Here, we trained and validated, with an external
set, a Markov Chain Model (MCM) that classifies proteins by their
possible mechanism of action according to Enzyme Classification (EC)
number. The methodology proposed is essentially new, and enables prediction
of all EC classes with a single equation without the need for an equation
for each class or nonlinear models with multiple outputs. In addition,
the model may be used to predict whether one peptide presents a positive
or negative contribution of the activity of the same EC class. The
model predicts the first EC number for 106 out of 151 (70.2%) oxidoreductases,
178/178 (100%) transferases, 223/223 (100%) hydrolases, 64/85 (75.3%)
lyases, 74/74 (100%) isomerases, and 100/100 (100%) ligases, as well
as 745/811 (91.9%) nonenzymes. It is important to underline that this
method may help us predict new enzyme proteins or select peptide candidates
that improve enzyme activity, which may be of interest for the prediction
of new drugs or drug targets. To illustrate the model’s application,
we report the 2D-Electrophoresis (2DE) isolation from Leishmania
infantum as well as MADLI TOF Mass Spectra characterization
and theoretical study of the Peptide Mass Fingerprints (PMFs) of a
new protein sequence. The theoretical study focused on MASCOT, BLAST
alignment, and alignment-free QSAR prediction of the contribution
of 29 peptides found in the PMF of the new protein to specific enzyme
action. This combined strategy may be used to identify and predict
peptides of prokaryote and eukaryote parasites and their hosts as
well as other superior organisms, which may be of interest in drug
development or target identification.