CST Guide:
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Section III: Workflow Tools<br />
chapter 17: Exploration<br />
Protein Page<br />
Provides information about a protein and its PTMs.<br />
Modification Site Page<br />
Summarizes information on single site from all records.<br />
C. Overview:<br />
• Brief description of protein function<br />
• Protein type and cellular component<br />
• Chromosomal location of human<br />
ortholog<br />
• Molecular function and<br />
biological process<br />
• Accession IDs, synonyms,<br />
and gene symbols<br />
• Molecular weight, isoelectric<br />
point, and pI calculator<br />
• Associated molecular structures<br />
and viewer<br />
• <strong>CST</strong> pathways and antibodies<br />
• Structural viewer<br />
D. Linked Resources Include:<br />
• Pathways: STRING, Reactome,<br />
NetworKIN<br />
• Expression: Protein Atlas, BioGPS<br />
• Scansite: Predictor of Kinases and<br />
Interactors<br />
• KinBase: Kinase Database at The<br />
Salk Institute<br />
• Structures: RCSB PDB, Pfam<br />
• NextGen Protein Resource: neXtProt<br />
E. Sites Implicated In:<br />
• Biological and molecular regulation,<br />
with links to associated site pages<br />
F. Modification Sites<br />
and Domains:<br />
• Zoomable linear diagram<br />
with sequence<br />
• Domains and modification<br />
sites mapped<br />
• Domain names linked to Pfam<br />
C<br />
D<br />
E<br />
F<br />
H<br />
I<br />
J<br />
Curated Information Page<br />
Experimental details on all sites in a single record.<br />
H. Site Information:<br />
•For most sites identified at <strong>CST</strong>, links<br />
to MS/MS spectra are included<br />
• Scansite predictions provide potential<br />
kinases and binding partners<br />
• Blast links allow site comparison<br />
against NCBI, UniProt, or PDB<br />
I. Experimental Summary<br />
Sections:<br />
May include information about how<br />
the site was experimentally characterized;<br />
diseases, cell lines and tissues<br />
in which it was observed; upstream<br />
control by treatments, receptors and<br />
other cellular proteins, and enzymes<br />
that may directly modify the site<br />
(in vivo and in vitro)<br />
J. References:<br />
Information curated from the literature<br />
contains links to the PubMed entry.<br />
Information curated from MS/MS<br />
experiments at <strong>CST</strong> or other institutions<br />
indicates the biological sample studied<br />
and treatments. If performed at <strong>CST</strong><br />
with PTMScan ® Technology, the<br />
antibody used for peptide enrichment<br />
prior to MS/MS is indicated.<br />
Links to the Curated Information Page<br />
are provided for most modification sites.<br />
G. Table of Sites, Sequences,<br />
and References:<br />
• Modification sites and surrounding<br />
sequences (+/- 7 AA) from parent<br />
protein, orthologs, and isoforms<br />
• Red characters indicate modified<br />
sites with links to associated records<br />
• First column (SS): the number<br />
of records using site-specific,<br />
low-throughput techniques<br />
• Second column (MS): the number of<br />
records using mass spectrometrybased<br />
high-throughput techniques<br />
G<br />
Download PyMOL and/or Chimera script<br />
Highlight modified residues<br />
K<br />
L<br />
K. Record and Sites:<br />
Standard bibliographic information<br />
about the record links to its PubMed<br />
entry. A list of modification sites<br />
associated with this record links to<br />
the the details curated for each site.<br />
L. Details Curated for<br />
each Modification Site:<br />
• Methods used to characterize site<br />
• Upstream Regulation<br />
– Kinases, phosphatases, receptors<br />
and signaling intermediates<br />
that regulate modification<br />
– Treatments that regulate<br />
modification<br />
• Downstream Regulation<br />
– Effects on protein function and<br />
biological processes due to<br />
modification<br />
– Protein-protein interactions directly<br />
influenced by modification<br />
• Disease Relevance of Modification<br />
252 For Research Use Only. Not For Use in Diagnostic Procedures. See pages 302 & 303 for Pathway Diagrams, Application, and Reactivity keys.<br />
www.cellsignal.com/exploration<br />
253