XMAn_Disease_fasta.fasta (5.63 MB)
XMAn-A Homo sapiens Mutated Disease Peptides Database
Version 5 2016-08-16, 19:56
Version 4 2016-08-14, 02:53
Version 3 2016-08-14, 02:53
Version 2 2016-08-14, 02:51
Version 1 2016-08-13, 20:16
dataset
posted on 2016-08-16, 19:56 authored by Iulia M. LazarIulia M. LazarTo enable the identification of mutated peptide sequences in complex
biological samples, in this work, a disease protein database with
mutation information collected from several
public resources such as OMIM and UniProtKB, was
developed. In-house
developed Perl-scripts were used to search and process the data, and to
translate each gene-level mutation into a mutated peptide sequence. The disease mutation database comprises a total of 27,148 peptide entries
from 2913 protein IDs. A description
line for each entry provides the parent protein ID and name, the cDNA-
and
protein-level mutation site and type, the originating database, and the tissue type and corresponding hits. The database is FASTA
formatted to enable data retrieval by commonly used tandem MS search
engines.