GPM #:
Keyword:


# GPM # proteins Description
1. GPM10100155757
peptide
model
gel
aaa
go
mh 		1018
  1. BRENDA cell culture: none
  2. BRENDA tissue: none
  3. CELL cell type: CL:0000057 
  4. GO subcellular: GO:0005623 
  5. email:
  6. institution: Vanderbilt University
  7. name: W Luo et al.
  8. project: Global Impact of Oncogenic Src on a Phosphotyrosine Proteome
  9. project comment: Nontransformed Trypsin pY4G10 Tranche  These files are associated with the article Global Impact of Oncogenic Src on a Phosphotyrosine Proteome by W Luo et al, J. Proteome Res., 7(8), 3447-3460, 2008. This publication can be retrieved at the following URL: http://dx.doi.org/10.1021/pr800187n. Files are organized into the following directories, reflecting the experiment design: I. Nontransformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 II. Src-transformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 Nontransformed and Src-transformed are mouse fibroblast cell lines that differ by whether or not SRC-F529 transformation has taken place. Chymotrypsin and trypsin reflect the digestion enzymes used to cleave the proteins to peptides. The use of two different enzymes enabled some phosphorylations to be identified from overlapping peptides. pY4G10 and pY100 are two commercially available antibodies with affinity to phosphorylated tyrosines. Each directory contains either four or five Thermo RAW files, each representing an RPLC of the phos-Tyr peptides. Proteins were reduced with DTT and alkylated with iodoacetamide. These files were produced in one of two different Thermo LTQ instruments at the Vanderbilt Mass Spectrometry Research Center. Each RAW contains approximately 10,000 tandem mass spectra. Each MS was followed by five MS/MS scans, with the exception that an MS/MS/MS scan was captured when the presence of a -98 or -80 Da neutral loss was detected in a MS/MS scan.
2. GPM10100155758
peptide
model
gel
aaa
go
mh 		1121
  1. BRENDA cell culture: none
  2. BRENDA tissue: none
  3. CELL cell type: CL:0000057  fibroblast
  4. GO subcellular: GO:0005623  cell
  5. email:
  6. institution: Vanderbilt University
  7. name: W Luo et al.
  8. project: Global Impact of Oncogenic Src on a Phosphotyrosine Proteome
  9. project comment: Nontransformed Trypsin pY100 Tranche  These files are associated with the article Global Impact of Oncogenic Src on a Phosphotyrosine Proteome by W Luo et al, J. Proteome Res., 7(8), 3447-3460, 2008. This publication can be retrieved at the following URL: http://dx.doi.org/10.1021/pr800187n. Files are organized into the following directories, reflecting the experiment design: I. Nontransformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 II. Src-transformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 Nontransformed and Src-transformed are mouse fibroblast cell lines that differ by whether or not SRC-F529 transformation has taken place. Chymotrypsin and trypsin reflect the digestion enzymes used to cleave the proteins to peptides. The use of two different enzymes enabled some phosphorylations to be identified from overlapping peptides. pY4G10 and pY100 are two commercially available antibodies with affinity to phosphorylated tyrosines. Each directory contains either four or five Thermo RAW files, each representing an RPLC of the phos-Tyr peptides. Proteins were reduced with DTT and alkylated with iodoacetamide. These files were produced in one of two different Thermo LTQ instruments at the Vanderbilt Mass Spectrometry Research Center. Each RAW contains approximately 10,000 tandem mass spectra. Each MS was followed by five MS/MS scans, with the exception that an MS/MS/MS scan was captured when the presence of a -98 or -80 Da neutral loss was detected in a MS/MS scan.
3. GPM10100155759
peptide
model
gel
aaa
go
mh 		1075
  1. BRENDA cell culture: none
  2. BRENDA tissue: none
  3. CELL cell type: CL:0000057 
  4. GO subcellular: GO:0005623 
  5. email:
  6. institution: Vanderbilt University
  7. name: W Luo et al.
  8. project: Global Impact of Oncogenic Src on a Phosphotyrosine Proteome
  9. project comment: Nontransformed Trypsin pY4G10 Tranche  These files are associated with the article Global Impact of Oncogenic Src on a Phosphotyrosine Proteome by W Luo et al, J. Proteome Res., 7(8), 3447-3460, 2008. This publication can be retrieved at the following URL: http://dx.doi.org/10.1021/pr800187n. Files are organized into the following directories, reflecting the experiment design: I. Nontransformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 II. Src-transformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 Nontransformed and Src-transformed are mouse fibroblast cell lines that differ by whether or not SRC-F529 transformation has taken place. Chymotrypsin and trypsin reflect the digestion enzymes used to cleave the proteins to peptides. The use of two different enzymes enabled some phosphorylations to be identified from overlapping peptides. pY4G10 and pY100 are two commercially available antibodies with affinity to phosphorylated tyrosines. Each directory contains either four or five Thermo RAW files, each representing an RPLC of the phos-Tyr peptides. Proteins were reduced with DTT and alkylated with iodoacetamide. These files were produced in one of two different Thermo LTQ instruments at the Vanderbilt Mass Spectrometry Research Center. Each RAW contains approximately 10,000 tandem mass spectra. Each MS was followed by five MS/MS scans, with the exception that an MS/MS/MS scan was captured when the presence of a -98 or -80 Da neutral loss was detected in a MS/MS scan.
4. GPM10100155760
peptide
model
gel
aaa
go
mh 		978
  1. BRENDA cell culture: none
  2. BRENDA tissue: none
  3. CELL cell type: CL:0000057  fibroblast
  4. GO subcellular: GO:0005623  cell
  5. email:
  6. institution: Vanderbilt University
  7. name: W Luo et al.
  8. project: Global Impact of Oncogenic Src on a Phosphotyrosine Proteome
  9. project comment: Nontransformed Trypsin pY100 Tranche  These files are associated with the article Global Impact of Oncogenic Src on a Phosphotyrosine Proteome by W Luo et al, J. Proteome Res., 7(8), 3447-3460, 2008. This publication can be retrieved at the following URL: http://dx.doi.org/10.1021/pr800187n. Files are organized into the following directories, reflecting the experiment design: I. Nontransformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 II. Src-transformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 Nontransformed and Src-transformed are mouse fibroblast cell lines that differ by whether or not SRC-F529 transformation has taken place. Chymotrypsin and trypsin reflect the digestion enzymes used to cleave the proteins to peptides. The use of two different enzymes enabled some phosphorylations to be identified from overlapping peptides. pY4G10 and pY100 are two commercially available antibodies with affinity to phosphorylated tyrosines. Each directory contains either four or five Thermo RAW files, each representing an RPLC of the phos-Tyr peptides. Proteins were reduced with DTT and alkylated with iodoacetamide. These files were produced in one of two different Thermo LTQ instruments at the Vanderbilt Mass Spectrometry Research Center. Each RAW contains approximately 10,000 tandem mass spectra. Each MS was followed by five MS/MS scans, with the exception that an MS/MS/MS scan was captured when the presence of a -98 or -80 Da neutral loss was detected in a MS/MS scan.
5. GPM10100155761
peptide
model
gel
aaa
go
mh 		1248
  1. BRENDA cell culture: none
  2. BRENDA tissue: none
  3. CELL cell type: CL:0000057 
  4. GO subcellular: GO:0005623 
  5. email:
  6. institution: Vanderbilt University
  7. name: W Luo et al.
  8. project: Global Impact of Oncogenic Src on a Phosphotyrosine Proteome
  9. project comment: Nontransformed Trypsin pY4G10 Tranche  These files are associated with the article Global Impact of Oncogenic Src on a Phosphotyrosine Proteome by W Luo et al, J. Proteome Res., 7(8), 3447-3460, 2008. This publication can be retrieved at the following URL: http://dx.doi.org/10.1021/pr800187n. Files are organized into the following directories, reflecting the experiment design: I. Nontransformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 II. Src-transformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 Nontransformed and Src-transformed are mouse fibroblast cell lines that differ by whether or not SRC-F529 transformation has taken place. Chymotrypsin and trypsin reflect the digestion enzymes used to cleave the proteins to peptides. The use of two different enzymes enabled some phosphorylations to be identified from overlapping peptides. pY4G10 and pY100 are two commercially available antibodies with affinity to phosphorylated tyrosines. Each directory contains either four or five Thermo RAW files, each representing an RPLC of the phos-Tyr peptides. Proteins were reduced with DTT and alkylated with iodoacetamide. These files were produced in one of two different Thermo LTQ instruments at the Vanderbilt Mass Spectrometry Research Center. Each RAW contains approximately 10,000 tandem mass spectra. Each MS was followed by five MS/MS scans, with the exception that an MS/MS/MS scan was captured when the presence of a -98 or -80 Da neutral loss was detected in a MS/MS scan.
6. GPM10100155762
peptide
model
gel
aaa
go
mh 		932
  1. BRENDA cell culture: none
  2. BRENDA tissue: none
  3. CELL cell type: CL:0000057 
  4. GO subcellular: GO:0005623 
  5. email:
  6. institution: Vanderbilt University
  7. name: W Luo et al.
  8. project: Global Impact of Oncogenic Src on a Phosphotyrosine Proteome
  9. project comment: Nontransformed Trypsin pY4G10 Tranche  These files are associated with the article Global Impact of Oncogenic Src on a Phosphotyrosine Proteome by W Luo et al, J. Proteome Res., 7(8), 3447-3460, 2008. This publication can be retrieved at the following URL: http://dx.doi.org/10.1021/pr800187n. Files are organized into the following directories, reflecting the experiment design: I. Nontransformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 II. Src-transformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 Nontransformed and Src-transformed are mouse fibroblast cell lines that differ by whether or not SRC-F529 transformation has taken place. Chymotrypsin and trypsin reflect the digestion enzymes used to cleave the proteins to peptides. The use of two different enzymes enabled some phosphorylations to be identified from overlapping peptides. pY4G10 and pY100 are two commercially available antibodies with affinity to phosphorylated tyrosines. Each directory contains either four or five Thermo RAW files, each representing an RPLC of the phos-Tyr peptides. Proteins were reduced with DTT and alkylated with iodoacetamide. These files were produced in one of two different Thermo LTQ instruments at the Vanderbilt Mass Spectrometry Research Center. Each RAW contains approximately 10,000 tandem mass spectra. Each MS was followed by five MS/MS scans, with the exception that an MS/MS/MS scan was captured when the presence of a -98 or -80 Da neutral loss was detected in a MS/MS scan.
7. GPM10100155763
peptide
model
gel
aaa
go
mh 		872
  1. BRENDA cell culture: none
  2. BRENDA tissue: none
  3. CELL cell type: CL:0000057  fibroblast
  4. GO subcellular: GO:0005623  cell
  5. email:
  6. institution: Vanderbilt University
  7. name: W Luo et al.
  8. project: Global Impact of Oncogenic Src on a Phosphotyrosine Proteome
  9. project comment: Nontransformed Trypsin pY100 Tranche  These files are associated with the article Global Impact of Oncogenic Src on a Phosphotyrosine Proteome by W Luo et al, J. Proteome Res., 7(8), 3447-3460, 2008. This publication can be retrieved at the following URL: http://dx.doi.org/10.1021/pr800187n. Files are organized into the following directories, reflecting the experiment design: I. Nontransformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 II. Src-transformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 Nontransformed and Src-transformed are mouse fibroblast cell lines that differ by whether or not SRC-F529 transformation has taken place. Chymotrypsin and trypsin reflect the digestion enzymes used to cleave the proteins to peptides. The use of two different enzymes enabled some phosphorylations to be identified from overlapping peptides. pY4G10 and pY100 are two commercially available antibodies with affinity to phosphorylated tyrosines. Each directory contains either four or five Thermo RAW files, each representing an RPLC of the phos-Tyr peptides. Proteins were reduced with DTT and alkylated with iodoacetamide. These files were produced in one of two different Thermo LTQ instruments at the Vanderbilt Mass Spectrometry Research Center. Each RAW contains approximately 10,000 tandem mass spectra. Each MS was followed by five MS/MS scans, with the exception that an MS/MS/MS scan was captured when the presence of a -98 or -80 Da neutral loss was detected in a MS/MS scan.
8. GPM10100155764
peptide
model
gel
aaa
go
mh 		1016
  1. BRENDA cell culture: none
  2. BRENDA tissue: none
  3. CELL cell type: CL:0000057 
  4. GO subcellular: GO:0005623 
  5. email:
  6. institution: Vanderbilt University
  7. name: W Luo et al.
  8. project: Global Impact of Oncogenic Src on a Phosphotyrosine Proteome
  9. project comment: Nontransformed Trypsin pY4G10 Tranche  These files are associated with the article Global Impact of Oncogenic Src on a Phosphotyrosine Proteome by W Luo et al, J. Proteome Res., 7(8), 3447-3460, 2008. This publication can be retrieved at the following URL: http://dx.doi.org/10.1021/pr800187n. Files are organized into the following directories, reflecting the experiment design: I. Nontransformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 II. Src-transformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 Nontransformed and Src-transformed are mouse fibroblast cell lines that differ by whether or not SRC-F529 transformation has taken place. Chymotrypsin and trypsin reflect the digestion enzymes used to cleave the proteins to peptides. The use of two different enzymes enabled some phosphorylations to be identified from overlapping peptides. pY4G10 and pY100 are two commercially available antibodies with affinity to phosphorylated tyrosines. Each directory contains either four or five Thermo RAW files, each representing an RPLC of the phos-Tyr peptides. Proteins were reduced with DTT and alkylated with iodoacetamide. These files were produced in one of two different Thermo LTQ instruments at the Vanderbilt Mass Spectrometry Research Center. Each RAW contains approximately 10,000 tandem mass spectra. Each MS was followed by five MS/MS scans, with the exception that an MS/MS/MS scan was captured when the presence of a -98 or -80 Da neutral loss was detected in a MS/MS scan.
9. GPM10100155765
peptide
model
gel
aaa
go
mh 		934
  1. BRENDA cell culture: none
  2. BRENDA tissue: none
  3. CELL cell type: CL:0000057  fibroblast
  4. GO subcellular: GO:0005623  cell
  5. email:
  6. institution: Vanderbilt University
  7. name: W Luo et al.
  8. project: Global Impact of Oncogenic Src on a Phosphotyrosine Proteome
  9. project comment: Nontransformed Trypsin pY100 Tranche  These files are associated with the article Global Impact of Oncogenic Src on a Phosphotyrosine Proteome by W Luo et al, J. Proteome Res., 7(8), 3447-3460, 2008. This publication can be retrieved at the following URL: http://dx.doi.org/10.1021/pr800187n. Files are organized into the following directories, reflecting the experiment design: I. Nontransformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 II. Src-transformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 Nontransformed and Src-transformed are mouse fibroblast cell lines that differ by whether or not SRC-F529 transformation has taken place. Chymotrypsin and trypsin reflect the digestion enzymes used to cleave the proteins to peptides. The use of two different enzymes enabled some phosphorylations to be identified from overlapping peptides. pY4G10 and pY100 are two commercially available antibodies with affinity to phosphorylated tyrosines. Each directory contains either four or five Thermo RAW files, each representing an RPLC of the phos-Tyr peptides. Proteins were reduced with DTT and alkylated with iodoacetamide. These files were produced in one of two different Thermo LTQ instruments at the Vanderbilt Mass Spectrometry Research Center. Each RAW contains approximately 10,000 tandem mass spectra. Each MS was followed by five MS/MS scans, with the exception that an MS/MS/MS scan was captured when the presence of a -98 or -80 Da neutral loss was detected in a MS/MS scan.
10. GPM10100155766
peptide
model
gel
aaa
go
mh 		1222
  1. BRENDA cell culture: none
  2. BRENDA tissue: none
  3. CELL cell type: CL:0000057  fibroblast
  4. GO subcellular: GO:0005623  cell
  5. email:
  6. institution: Vanderbilt University
  7. name: W Luo et al.
  8. project: Global Impact of Oncogenic Src on a Phosphotyrosine Proteome
  9. project comment: Nontransformed Trypsin pY100 Tranche  These files are associated with the article Global Impact of Oncogenic Src on a Phosphotyrosine Proteome by W Luo et al, J. Proteome Res., 7(8), 3447-3460, 2008. This publication can be retrieved at the following URL: http://dx.doi.org/10.1021/pr800187n. Files are organized into the following directories, reflecting the experiment design: I. Nontransformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 II. Src-transformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 Nontransformed and Src-transformed are mouse fibroblast cell lines that differ by whether or not SRC-F529 transformation has taken place. Chymotrypsin and trypsin reflect the digestion enzymes used to cleave the proteins to peptides. The use of two different enzymes enabled some phosphorylations to be identified from overlapping peptides. pY4G10 and pY100 are two commercially available antibodies with affinity to phosphorylated tyrosines. Each directory contains either four or five Thermo RAW files, each representing an RPLC of the phos-Tyr peptides. Proteins were reduced with DTT and alkylated with iodoacetamide. These files were produced in one of two different Thermo LTQ instruments at the Vanderbilt Mass Spectrometry Research Center. Each RAW contains approximately 10,000 tandem mass spectra. Each MS was followed by five MS/MS scans, with the exception that an MS/MS/MS scan was captured when the presence of a -98 or -80 Da neutral loss was detected in a MS/MS scan.
11. GPM10100155767
peptide
model
gel
aaa
go
mh 		939
  1. BRENDA cell culture: none
  2. BRENDA tissue: none
  3. CELL cell type: CL:0000057 
  4. GO subcellular: GO:0005623 
  5. email:
  6. institution: Vanderbilt University
  7. name: W Luo et al.
  8. project: Global Impact of Oncogenic Src on a Phosphotyrosine Proteome
  9. project comment: Src-transformed Trypsin pY4G10 Tranche  These files are associated with the article Global Impact of Oncogenic Src on a Phosphotyrosine Proteome by W Luo et al, J. Proteome Res., 7(8), 3447-3460, 2008. This publication can be retrieved at the following URL: http://dx.doi.org/10.1021/pr800187n. Files are organized into the following directories, reflecting the experiment design: I. Nontransformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 II. Src-transformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 Nontransformed and Src-transformed are mouse fibroblast cell lines that differ by whether or not SRC-F529 transformation has taken place. Chymotrypsin and trypsin reflect the digestion enzymes used to cleave the proteins to peptides. The use of two different enzymes enabled some phosphorylations to be identified from overlapping peptides. pY4G10 and pY100 are two commercially available antibodies with affinity to phosphorylated tyrosines. Each directory contains either four or five Thermo RAW files, each representing an RPLC of the phos-Tyr peptides. Proteins were reduced with DTT and alkylated with iodoacetamide. These files were produced in one of two different Thermo LTQ instruments at the Vanderbilt Mass Spectrometry Research Center. Each RAW contains approximately 10,000 tandem mass spectra. Each MS was followed by five MS/MS scans, with the exception that an MS/MS/MS scan was captured when the presence of a -98 or -80 Da neutral loss was detected in a MS/MS scan.
12. GPM10100155768
peptide
model
gel
aaa
go
mh 		1004
  1. BRENDA cell culture: none
  2. BRENDA tissue: none
  3. CELL cell type: CL:0000057 
  4. GO subcellular: GO:0005623 
  5. email:
  6. institution: Vanderbilt University
  7. name: W Luo et al.
  8. project: Global Impact of Oncogenic Src on a Phosphotyrosine Proteome
  9. project comment: Src-transformed Trypsin pY4G10 Tranche  These files are associated with the article Global Impact of Oncogenic Src on a Phosphotyrosine Proteome by W Luo et al, J. Proteome Res., 7(8), 3447-3460, 2008. This publication can be retrieved at the following URL: http://dx.doi.org/10.1021/pr800187n. Files are organized into the following directories, reflecting the experiment design: I. Nontransformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 II. Src-transformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 Nontransformed and Src-transformed are mouse fibroblast cell lines that differ by whether or not SRC-F529 transformation has taken place. Chymotrypsin and trypsin reflect the digestion enzymes used to cleave the proteins to peptides. The use of two different enzymes enabled some phosphorylations to be identified from overlapping peptides. pY4G10 and pY100 are two commercially available antibodies with affinity to phosphorylated tyrosines. Each directory contains either four or five Thermo RAW files, each representing an RPLC of the phos-Tyr peptides. Proteins were reduced with DTT and alkylated with iodoacetamide. These files were produced in one of two different Thermo LTQ instruments at the Vanderbilt Mass Spectrometry Research Center. Each RAW contains approximately 10,000 tandem mass spectra. Each MS was followed by five MS/MS scans, with the exception that an MS/MS/MS scan was captured when the presence of a -98 or -80 Da neutral loss was detected in a MS/MS scan.
13. GPM10100155769
peptide
model
gel
aaa
go
mh 		974
  1. BRENDA cell culture: none
  2. BRENDA tissue: none
  3. CELL cell type: CL:0000057 
  4. GO subcellular: GO:0005623 
  5. email:
  6. institution: Vanderbilt University
  7. name: W Luo et al.
  8. project: Global Impact of Oncogenic Src on a Phosphotyrosine Proteome
  9. project comment: Src-transformed Trypsin pY4G10 Tranche  These files are associated with the article Global Impact of Oncogenic Src on a Phosphotyrosine Proteome by W Luo et al, J. Proteome Res., 7(8), 3447-3460, 2008. This publication can be retrieved at the following URL: http://dx.doi.org/10.1021/pr800187n. Files are organized into the following directories, reflecting the experiment design: I. Nontransformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 II. Src-transformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 Nontransformed and Src-transformed are mouse fibroblast cell lines that differ by whether or not SRC-F529 transformation has taken place. Chymotrypsin and trypsin reflect the digestion enzymes used to cleave the proteins to peptides. The use of two different enzymes enabled some phosphorylations to be identified from overlapping peptides. pY4G10 and pY100 are two commercially available antibodies with affinity to phosphorylated tyrosines. Each directory contains either four or five Thermo RAW files, each representing an RPLC of the phos-Tyr peptides. Proteins were reduced with DTT and alkylated with iodoacetamide. These files were produced in one of two different Thermo LTQ instruments at the Vanderbilt Mass Spectrometry Research Center. Each RAW contains approximately 10,000 tandem mass spectra. Each MS was followed by five MS/MS scans, with the exception that an MS/MS/MS scan was captured when the presence of a -98 or -80 Da neutral loss was detected in a MS/MS scan.
14. GPM10100155770
peptide
model
gel
aaa
go
mh 		928
  1. BRENDA cell culture: none
  2. BRENDA tissue: none
  3. CELL cell type: CL:0000057 
  4. GO subcellular: GO:0005623 
  5. email:
  6. institution: Vanderbilt University
  7. name: W Luo et al.
  8. project: Global Impact of Oncogenic Src on a Phosphotyrosine Proteome
  9. project comment: Src-transformed Trypsin pY4G10 Tranche  These files are associated with the article Global Impact of Oncogenic Src on a Phosphotyrosine Proteome by W Luo et al, J. Proteome Res., 7(8), 3447-3460, 2008. This publication can be retrieved at the following URL: http://dx.doi.org/10.1021/pr800187n. Files are organized into the following directories, reflecting the experiment design: I. Nontransformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 II. Src-transformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 Nontransformed and Src-transformed are mouse fibroblast cell lines that differ by whether or not SRC-F529 transformation has taken place. Chymotrypsin and trypsin reflect the digestion enzymes used to cleave the proteins to peptides. The use of two different enzymes enabled some phosphorylations to be identified from overlapping peptides. pY4G10 and pY100 are two commercially available antibodies with affinity to phosphorylated tyrosines. Each directory contains either four or five Thermo RAW files, each representing an RPLC of the phos-Tyr peptides. Proteins were reduced with DTT and alkylated with iodoacetamide. These files were produced in one of two different Thermo LTQ instruments at the Vanderbilt Mass Spectrometry Research Center. Each RAW contains approximately 10,000 tandem mass spectra. Each MS was followed by five MS/MS scans, with the exception that an MS/MS/MS scan was captured when the presence of a -98 or -80 Da neutral loss was detected in a MS/MS scan.
15. GPM10100155771
peptide
model
gel
aaa
go
mh 		890
  1. BRENDA cell culture: none
  2. BRENDA tissue: none
  3. CELL cell type: CL:0000057 
  4. GO subcellular: GO:0005623 
  5. email:
  6. institution: Vanderbilt University
  7. name: W Luo et al.
  8. project: Global Impact of Oncogenic Src on a Phosphotyrosine Proteome
  9. project comment: Src-transformed Trypsin pY4G10 Tranche  These files are associated with the article Global Impact of Oncogenic Src on a Phosphotyrosine Proteome by W Luo et al, J. Proteome Res., 7(8), 3447-3460, 2008. This publication can be retrieved at the following URL: http://dx.doi.org/10.1021/pr800187n. Files are organized into the following directories, reflecting the experiment design: I. Nontransformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 II. Src-transformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 Nontransformed and Src-transformed are mouse fibroblast cell lines that differ by whether or not SRC-F529 transformation has taken place. Chymotrypsin and trypsin reflect the digestion enzymes used to cleave the proteins to peptides. The use of two different enzymes enabled some phosphorylations to be identified from overlapping peptides. pY4G10 and pY100 are two commercially available antibodies with affinity to phosphorylated tyrosines. Each directory contains either four or five Thermo RAW files, each representing an RPLC of the phos-Tyr peptides. Proteins were reduced with DTT and alkylated with iodoacetamide. These files were produced in one of two different Thermo LTQ instruments at the Vanderbilt Mass Spectrometry Research Center. Each RAW contains approximately 10,000 tandem mass spectra. Each MS was followed by five MS/MS scans, with the exception that an MS/MS/MS scan was captured when the presence of a -98 or -80 Da neutral loss was detected in a MS/MS scan.
16. GPM10100155772
peptide
model
gel
aaa
go
mh 		732
  1. BRENDA cell culture: none
  2. BRENDA tissue: none
  3. CELL cell type: CL:0000057 
  4. GO subcellular: GO:0005623 
  5. email:
  6. institution: Vanderbilt University
  7. name: W Luo et al.
  8. project: Global Impact of Oncogenic Src on a Phosphotyrosine Proteome
  9. project comment: Src-transformed Trypsin pY100 Tranche  These files are associated with the article Global Impact of Oncogenic Src on a Phosphotyrosine Proteome by W Luo et al, J. Proteome Res., 7(8), 3447-3460, 2008. This publication can be retrieved at the following URL: http://dx.doi.org/10.1021/pr800187n. Files are organized into the following directories, reflecting the experiment design: I. Nontransformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 II. Src-transformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 Nontransformed and Src-transformed are mouse fibroblast cell lines that differ by whether or not SRC-F529 transformation has taken place. Chymotrypsin and trypsin reflect the digestion enzymes used to cleave the proteins to peptides. The use of two different enzymes enabled some phosphorylations to be identified from overlapping peptides. pY4G10 and pY100 are two commercially available antibodies with affinity to phosphorylated tyrosines. Each directory contains either four or five Thermo RAW files, each representing an RPLC of the phos-Tyr peptides. Proteins were reduced with DTT and alkylated with iodoacetamide. These files were produced in one of two different Thermo LTQ instruments at the Vanderbilt Mass Spectrometry Research Center. Each RAW contains approximately 10,000 tandem mass spectra. Each MS was followed by five MS/MS scans, with the exception that an MS/MS/MS scan was captured when the presence of a -98 or -80 Da neutral loss was detected in a MS/MS scan.
17. GPM10100155773
peptide
model
gel
aaa
go
mh 		727
  1. BRENDA cell culture: none
  2. BRENDA tissue: none
  3. CELL cell type: CL:0000057 
  4. GO subcellular: GO:0005623 
  5. email:
  6. institution: Vanderbilt University
  7. name: W Luo et al.
  8. project: Global Impact of Oncogenic Src on a Phosphotyrosine Proteome
  9. project comment: Src-transformed Trypsin pY100 Tranche  These files are associated with the article Global Impact of Oncogenic Src on a Phosphotyrosine Proteome by W Luo et al, J. Proteome Res., 7(8), 3447-3460, 2008. This publication can be retrieved at the following URL: http://dx.doi.org/10.1021/pr800187n. Files are organized into the following directories, reflecting the experiment design: I. Nontransformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 II. Src-transformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 Nontransformed and Src-transformed are mouse fibroblast cell lines that differ by whether or not SRC-F529 transformation has taken place. Chymotrypsin and trypsin reflect the digestion enzymes used to cleave the proteins to peptides. The use of two different enzymes enabled some phosphorylations to be identified from overlapping peptides. pY4G10 and pY100 are two commercially available antibodies with affinity to phosphorylated tyrosines. Each directory contains either four or five Thermo RAW files, each representing an RPLC of the phos-Tyr peptides. Proteins were reduced with DTT and alkylated with iodoacetamide. These files were produced in one of two different Thermo LTQ instruments at the Vanderbilt Mass Spectrometry Research Center. Each RAW contains approximately 10,000 tandem mass spectra. Each MS was followed by five MS/MS scans, with the exception that an MS/MS/MS scan was captured when the presence of a -98 or -80 Da neutral loss was detected in a MS/MS scan.
18. GPM10100155774
peptide
model
gel
aaa
go
mh 		892
  1. BRENDA cell culture: none
  2. BRENDA tissue: none
  3. CELL cell type: CL:0000057 
  4. GO subcellular: GO:0005623 
  5. email:
  6. institution: Vanderbilt University
  7. name: W Luo et al.
  8. project: Global Impact of Oncogenic Src on a Phosphotyrosine Proteome
  9. project comment: Src-transformed Trypsin pY100 Tranche  These files are associated with the article Global Impact of Oncogenic Src on a Phosphotyrosine Proteome by W Luo et al, J. Proteome Res., 7(8), 3447-3460, 2008. This publication can be retrieved at the following URL: http://dx.doi.org/10.1021/pr800187n. Files are organized into the following directories, reflecting the experiment design: I. Nontransformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 II. Src-transformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 Nontransformed and Src-transformed are mouse fibroblast cell lines that differ by whether or not SRC-F529 transformation has taken place. Chymotrypsin and trypsin reflect the digestion enzymes used to cleave the proteins to peptides. The use of two different enzymes enabled some phosphorylations to be identified from overlapping peptides. pY4G10 and pY100 are two commercially available antibodies with affinity to phosphorylated tyrosines. Each directory contains either four or five Thermo RAW files, each representing an RPLC of the phos-Tyr peptides. Proteins were reduced with DTT and alkylated with iodoacetamide. These files were produced in one of two different Thermo LTQ instruments at the Vanderbilt Mass Spectrometry Research Center. Each RAW contains approximately 10,000 tandem mass spectra. Each MS was followed by five MS/MS scans, with the exception that an MS/MS/MS scan was captured when the presence of a -98 or -80 Da neutral loss was detected in a MS/MS scan.
19. GPM10100155775
peptide
model
gel
aaa
go
mh 		707
  1. BRENDA cell culture: none
  2. BRENDA tissue: none
  3. CELL cell type: CL:0000057 
  4. GO subcellular: GO:0005623 
  5. email:
  6. institution: Vanderbilt University
  7. name: W Luo et al.
  8. project: Global Impact of Oncogenic Src on a Phosphotyrosine Proteome
  9. project comment: Src-transformed Trypsin pY100 Tranche  These files are associated with the article Global Impact of Oncogenic Src on a Phosphotyrosine Proteome by W Luo et al, J. Proteome Res., 7(8), 3447-3460, 2008. This publication can be retrieved at the following URL: http://dx.doi.org/10.1021/pr800187n. Files are organized into the following directories, reflecting the experiment design: I. Nontransformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 II. Src-transformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 Nontransformed and Src-transformed are mouse fibroblast cell lines that differ by whether or not SRC-F529 transformation has taken place. Chymotrypsin and trypsin reflect the digestion enzymes used to cleave the proteins to peptides. The use of two different enzymes enabled some phosphorylations to be identified from overlapping peptides. pY4G10 and pY100 are two commercially available antibodies with affinity to phosphorylated tyrosines. Each directory contains either four or five Thermo RAW files, each representing an RPLC of the phos-Tyr peptides. Proteins were reduced with DTT and alkylated with iodoacetamide. These files were produced in one of two different Thermo LTQ instruments at the Vanderbilt Mass Spectrometry Research Center. Each RAW contains approximately 10,000 tandem mass spectra. Each MS was followed by five MS/MS scans, with the exception that an MS/MS/MS scan was captured when the presence of a -98 or -80 Da neutral loss was detected in a MS/MS scan.
20. GPM10100155776
peptide
model
gel
aaa
go
mh 		919
  1. BRENDA cell culture: none
  2. BRENDA tissue: none
  3. CELL cell type: CL:0000057 
  4. GO subcellular: GO:0005623 
  5. email:
  6. institution: Vanderbilt University
  7. name: W Luo et al.
  8. project: Global Impact of Oncogenic Src on a Phosphotyrosine Proteome
  9. project comment: Src-transformed Trypsin pY100 Tranche  These files are associated with the article Global Impact of Oncogenic Src on a Phosphotyrosine Proteome by W Luo et al, J. Proteome Res., 7(8), 3447-3460, 2008. This publication can be retrieved at the following URL: http://dx.doi.org/10.1021/pr800187n. Files are organized into the following directories, reflecting the experiment design: I. Nontransformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 II. Src-transformed A. Chymotrypsin 1. pY4G10 2. pY100 B. Trypsin 1. pY4G10 2. pY100 Nontransformed and Src-transformed are mouse fibroblast cell lines that differ by whether or not SRC-F529 transformation has taken place. Chymotrypsin and trypsin reflect the digestion enzymes used to cleave the proteins to peptides. The use of two different enzymes enabled some phosphorylations to be identified from overlapping peptides. pY4G10 and pY100 are two commercially available antibodies with affinity to phosphorylated tyrosines. Each directory contains either four or five Thermo RAW files, each representing an RPLC of the phos-Tyr peptides. Proteins were reduced with DTT and alkylated with iodoacetamide. These files were produced in one of two different Thermo LTQ instruments at the Vanderbilt Mass Spectrometry Research Center. Each RAW contains approximately 10,000 tandem mass spectra. Each MS was followed by five MS/MS scans, with the exception that an MS/MS/MS scan was captured when the presence of a -98 or -80 Da neutral loss was detected in a MS/MS scan.

Page 1 of 2 | 1 | 2 |
Key word(s): YW6GL39ADLkNzvlfVwpMJ1JrgnASGdMAS0451JIhR8j12KojOulXI1ghbRY5WKpo6 ...
Total protein ids = 21417
If you do not see a red dot in the square brackets [], you will need Adobe's SVG plugin to view this site properly.













dblist_gpmnotes.pl, v. 2010.07.06