Yes, it is in there.

David

On Mon, Oct 30, 2017 at 5:52 AM, Adam R <[email protected]> wrote:

> Hi David,
>
> Just wanted to ask if the release candidate version that you posted here
> in this post (https://groups.google.com/d/msg/spctools-discuss/5NwyzUw3mH
> A/ZP8AazR0AwAJ)
> contains an updated version of PeptideProphet with an extended mass model
> to handle MSFragger processed files? What settings do you recommend
> starting with when processing MSFragger output with PeptideProphet?
>
> Best,
>
> Adam
>
> On Tuesday, September 26, 2017 at 11:00:24 AM UTC-5, David Shteynberg
> wrote:
>>
>> Hi Adam,
>>
>> Yes there is a mode in PTMProphet you can enable called MASSDIFFMODE, it
>> will localize the mass difference like a PTM.  I have tried this using
>> MSFragger and tier-wise open mass searching using SpectraST.
>>
>> -David
>>
>> On Mon, Sep 25, 2017 at 11:09 AM, Adam R <[email protected]> wrote:
>>
>>> Hi David,
>>>
>>> Thank you for the prompt response! I will give it a try from the command
>>> line. I also have a follow-up question to ask to this as I have been
>>> wondering about other ways to tackle the data.
>>>
>>> Gygi's group published a paper in 2015 (http://www.nature.com/nbt/jou
>>> rnal/v33/n7/abs/nbt.3267.html) about using wide mass tolerance windows
>>> for searching spectra (+/- 500 Da windows) to identify modifications in
>>> unassigned spectra. They went on to use the Ascore algorithm to identify
>>> the sites of modifcation. I'm wondering whether this would be possible to
>>> perform with the current iteration of TPP? (i.e. wide mass tolerant search
>>> with comet followed by site analysis by PTM Prophet) PTM Prophet's input
>>> requires the amino acid and the mass shifts for PTMs but I'm wondering
>>> whether it could be utilized to identify "un-specified" mods on any amino
>>> acid.
>>>
>>> Best,
>>>
>>> Adam
>>>
>>> On Monday, September 25, 2017 at 11:47:39 AM UTC-5, David Shteynberg
>>> wrote:
>>>>
>>>> There are a couple things wrong here.  Primarily there is a bug in
>>>> current distributed version of PTMProphet that prevents it from being run
>>>> through the web-interface.  There is already a fix available, however, you
>>>> will probably want to run this from the command line because of reasons
>>>> that follow.  Your command needs some adjustment.  As is it will try to
>>>> localize a different "PTM" on the amino acids you have specified for each
>>>> set of amino acids, when what you want it to localize on any amino acid.
>>>> You can try the following in a command terminal
>>>>
>>>> cd c:\TPP\data\[YOUR_DATA_DIRECTORY]
>>>>
>>>> PTMProphetParser MZTOL=0.2 ABCDEFGHIJKLMNOPQRSTUVXWYZ:639.3169
>>>> [YOUR_INPUT_PEPXML] [YOUR_OUTPUT_PEPXML]
>>>>
>>>>
>>>> Thank you for reporting the issue.
>>>>
>>>> -David
>>>>
>>>>
>>>> On Sun, Sep 24, 2017 at 11:19 AM, wicher89 <[email protected]> wrote:
>>>>
>>>>> Hi Everyone,
>>>>>
>>>>> I am analyzing peptides from cells that have been treated with a UV
>>>>> crosslinker attached to a small molecule (ABPP method). This results in
>>>>> mono-linked peptides. Because the UV cross-linker is not residue specific,
>>>>> I am forced to search the data in comet with a modification of 639.3118 Da
>>>>> on any amino acid other than those with fixed modifications. I am able to
>>>>> process the output files until the iProphet step, but am running into
>>>>> command failure at PTM Prophet. Is there a maximum limit on the number of
>>>>> amino acids used at once in a single line entry for a modification? I have
>>>>> attached screenshots of the parameters used and the command failure 
>>>>> output.
>>>>>
>>>>> Thanks!
>>>>>
>>>>>
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>>>>>
>>>>
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>>
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