|
News: 8th March 2012:Some modification have been added to xComb. (i) A reader for any FASTA file to accomodate any user format. (ii) Thermolysin and CNBr enzyme specificty 4th Jan 2011:A fix has been applied to xComb regarding issues with new lines with different OS formatted FASTA files. In case of strange caracters appearing (like ^M), please make sure to have your fasta file formatted in Linux (LF only for new line instead of CR LF for Dos or CR only for Mac) |
|
| Type of protein sequence format: DAT format considers UniProt protein annotations (e.g. removal of methionine or signal peptide) UniProt DAT (Flat file) UniProt FASTA Any FASTA Enzyme specificity: Number of missed cleavage (max = 3): This factor drastically affects the number of sequence permutations (recommended is 2) Input: Upload your file with .dat or .fasta extension, only letters, numbers, "-", "." and "_" symbol are allowed in file name (e.g. my_file_name.dat, my_file_name.fasta) | |
| Step 2: Define parameters for cross-linking database generation: | |
|---|---|
Type of database to be generated: Type of crosslinker used: Homo- or Heterobifunctional crosslinkers described by target1/target2 Specify whether amine cross-linking needs 1 trypsin missed cleavage at least: To be used with amine crosslinkers and trypsin (only peptides with at least one Lysine missed cleavage are consisered; e.g. xxxKxxxxK or xxxKxxxxR) Specify minimum peptide length for each peptide of the pair: Phenyx FASTA formatted output: Adds \AC= \ID= and \DE= Phenyx tags in FASTA header Test mode which adds "|" in between peptides: For database evaluation/checking/testing purposes only (e.g. MRALPICLLALMLGGCSMLSR|QAVCIGSALNISAK) | |
| Step 3: Download your database: | |