To specify which columns to display for peptide results, click the Pick Peptide Columns button in the View section of the MS2 Runs page (see Viewing an MS2 Run). On the Pick Columns page, you can see all available columns and select which to display in the current view. You can also set which columns are displayed by default.

The currently displayed columns appear in the Current field. You can edit the columns that appear in this list manually for finely tuned control over which columns are displayed in what order.

  • To display the most common columns in the current view, click the Pick button next to the Common list. To display the default column set in the current view, click the Pick button next to the Default list. Either of these options will replace the currently selected columns in the Current field.
  • To add a set of columns to the currently displayed set, click the Add button next to the list.
  • To apply the current column set only to the current run, click Pick Columns. To save the selected columns as the default set, click Save As Default.

Available Peptide Columns

The following table describes the available peptide columns which are applicable to all search engines.

Peptide Column Column Abbrev Description

Scan

 

The number of the machine scan from the run.

RetentionTime

RetTime The peptide's elution time.
Run   A unique integer identifying the run.
RunDescription   A description of the run, including the pep.xml file name and the search protocol name

Fraction

 

The id for a particular fraction, as assigned by the MS2 Viewer. Note that a single run can be comprised of multiple fractions (e.g., if a sample was fractionated to reduce its complexity, and the fractions were interrogated separately on the MS machine, a technician can combine the results for those fractions in a single run file for analysis and upload to the MS2 Viewer).

FractionName   The name specified for a given fraction.

Charge

Z

The assumed charge state of the peptide featured in the scan.

IonPercent

Ion%

The number of theoretical fragment ions that matched fragments in the experimental spectrum divided by the total number of theoretical fragment ions, multiplied by 100; higher value indicates a better match.

Mass

CalcMH+

The singly protonated mass of the peptide sequence in the database that was the best match.

DeltaMass

dMass

The difference between the MH+ observed mass and the MH+ theoretical mass of this peptide; a lower number indicates a better match.

DeltaMassPPM

dMassPPM

The difference between the theoretical m/z and the observed m/z , scaled by theoretical m/z and expressed in parts per million; this value gives a measure of the mass accuracy of the MS machine.

FractionalDeltaMass fdMass The LTQ-FT mass spectrometer may register the C13 peak in error in place of the monoisotopic peak. The FractionalDeltaMass indicates the absolute distance to nearest integer of the DeltaMass, thereby correcting for these errors.
FractionalDeltaMassPPM fdMassPPM The FractionalDeltaMass expressed in parts per million.

PrecursorMass

ObsMH+

The observed mass of the precursor ion, expressed as singly protonated (MH+).

MZ

ObsMZ

The mass-to-charge ratio of the peptide.

PeptideProphet PepProphet The score assigned by PeptideProphet. This score represents the probability that the peptide identification is correct. A higher score indicates a better match.

Peptide

 

The sequence of the peptide match.  The previous and next amino acids in the database sequence are printed before/after the identified peptide, separated by periods.

StrippedPeptide

 

The peptide sequence (including the previous amino acid and next amino acid, if applicable) filtered of all extra characters (no dot at the beginning or end, and no variable modification characters).

PrevAA

 

The amino acid immediately preceding the peptide in the protein sequence; peptides at the beginning of the protein sequence will have a dash (-) as this value.

TrimmedPeptide

 

The peptide sequence without the previous and next amino acids.

NextAA

 

The amino acid immediately following the peptide in the protein sequence; peptides at the end of the protein sequence will have a dash (-) as this value.

ProteinHits

SeqHits

The number of protein sequences in the protein database that contain the matched peptide sequence.

SequencePosition

SeqPos

The position in the protein sequence where the peptide begins.

H

 

Theoretical hydrophobicity of the peptide calculated using Krokhin’s algorithm (Anal. Chem. 2006, 78, 6265).

DeltaScan

dScan

The difference between actual and expected scan number, in standard deviations, based on theoretical hydrophobicity calculation.

Protein

 

A short name for the protein sequence identified by the search engine as a possible source for the identified peptide.

Description

 

A short phrase describing the protein sequence identified by the search engine. This name is derived from the UniProt XML or FASTA file from which the sequence was taken).

GeneName

 

The name of the gene that encodes for this protein sequence.

SeqId   A unique integer identifying the protein sequence.

Peptide Columns Populated by ProteinProphet

The following table describes the peptide columns that are populated by ProteinProphet.

Peptide Column Column Abbrev Description
NSPAdjustedProbability NSPAdjProb PeptideProphet probability adjusted for number of sibling peptides.
Weight   Share of peptide contributing to the protein identification.
NonDegenerateEvidence NonDegenEvid True/false value indicating whether peptide is unique to protein (true) or shared (false).
EnzymaticTermini   Number of expected cleavage termini (valid 0, 1 or 2) consistent with digestion enzyme.
SiblingPeptides SiblingPeps A calculation, based on peptide probabilities, to quantify sibling peptides (other peptides identified for this protein).
SiblingPeptidesBin SiblingPepsBin A bin or histogram value used by ProteinProphet.
Instances   Number of instances the peptide was identified.
ContributingEvidence ContribEvid True/false value indicating whether the peptide is contributing evidence to the protein identification.
CalcNeutralPepMass   Calculated neutral mass of peptide.

Peptide Columns Populated by Quantitation Analysis

The following table describes the peptide columns that are populated during the quantitation analysis.

Peptide Column Description
LightFirstScan Scan number of the start of the elution peak for the light-labeled precursor ion.
LightLastScan Scan number of the end of the elution peak for the light-labeled precursor ion
LightMass Precursor ion m/z of the isotopically light-labeled peptide.
HeavyFirstScan Scan number of the start of the elution peak for the heavy-labeled precursor ion.
HeavyLastScan Scan number of the end of the elution peak for the heavy-labeled precursor ion.
HeavyMass Precursor ion m/z of the isotopically heavy-labeled peptide.
Ratio Light-to-heavy ratio, based on elution peak areas.
Heavy2LightRatio Heavy-to-light ratio, based on elution peak areas.
LightArea Light elution peak area.
HeavyArea Heavy elution peak area.
DecimalRatio Light-to-heavy ratio expressed as a decimal value.

Peptide Columns Specific to X! Tandem

The following table describes the peptide columns that are specific to results generated by the X! Tandem search engine.

Peptide Column Description
Hyper Tandem’s hypergeometric score representing the quality of the match of the identified peptide; a higher score indicates a better match.
B Tandem’s b-ion score.
Next The hyperscore of the 2nd best scoring peptide.
Y Tandem’s y-ion score.
Expect Expectation value of the peptide hit.  This number represents how many identifications are expected by chance to have this hyperscore. The lower the value, the more likely it is that the match is not random.

Peptide Columns Specific to Mascot

The following table shows the scoring columns that are specific to Mascot:

Peptide Column Description

Ion

Mascot ions score representing the quality of the match of the identified peptide; a higher score indicates a better match.

Identity

Idenity threshold. An absolute threshold determines from the distribution of random scores to highlight the presence of non-random match. When ions score exceeds identity threshold, there is a 5% chance that the match is not exact.

Homology

Homology threshold. A lower, relative threshold determines from the distribution of random scores to highlight the presence of non-random outliners. When ions score exceeds homology threshold, the match is not random, spectrum may not fully define sequence and the sequence may be close but not exact.

Expect

Expectation value of the peptide hit. This number represents how many identifications are expected by chance to have this ion score or higher. The lower the value, the more likely it is that the match is significant.

Peptide Columns Specific to COMET

The following table shows the scoring columns that are specific to COMET:

Peptide Column Description

RawScore

Number between 0 and 1000 representing the quality of the match of the peptide feature in the scan to the top COMET database search result; higher score indicates a better match

ZScore

The number of standard deviations between the best peptide match's score and the mean of the top 100 peptide scores, calculated using the raw dot-product scores; higher score indicates a better match

DiffScore

The difference between the normalized (normalized from 0.0 to 1.0) RawScore values of the best peptide match and the second best peptide match; greater DiffScore tends to indicate a better match


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