Source:HTTP://PATHWAYCOMMONS.ORG/PSI2BP#_8531834291321479954
Predicate | Object |
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rdf:type | |
biopax3:comment |
2010 publication year MI:0886,
Apoptosis - Interactions involving proteins with a function related to apoptosis dataset MI:0875,
Brieger A., Adryan B., Wolpert F., Passmann S., Zeuzem S., Trojan J. author-list MI:0636,
Cancer - Interactions investigated in the context of cancer dataset MI:0875,
Cytoskeletal scaffolding proteins interact with Lynch-Syndrome associated mismatch repair protein MLH1.,
Human colon plasmid cDNA library (obtained from normal colon tissue of a 59-year-old female). library-used MI:0672,
Only protein-protein interactions full coverage MI:0957,
Proteomics (1615-9853) journal MI:0885,
Several proteins identified by multiple transcripts. The entry for "protein":- FTHP1, (GenBank J04755), is stated to be a processed pseudogene, and no protein entry is available. According to the NCBI "Entry NM_001040070.1 was permanently suppressed because it is now thought that this gene is a pseudogene". Entry Z85636, does not contain a CDS. Entry AF471510 maps to Q0ZCG6 with only 82% identity, and has not been entered. Entry DQ840953, has only 92% identity with UniProt Q6PIK1 (amino acids 20-129) so has not been entered, Entry XM_001133484 has been removed from the NCBI website, but has 93% identity with P62249. Entry NC_001807.4 is obsolete and refers to a complete genome -i.e. several proteins. Entry DQ523681.1 also refers to a complete genome, so cannot be entered, similarly for entries DQ40444(4)7, DQ372886. Entry NM_001099081.1 refers to a Bovine protein, so has not been entered. Entry XM_001131713.1 has been removed from the NCBI site and cannot be uniquely identified on attempted remapping. data-processing MI:0633,
The column entitled "Protein length aa" most likely refers to the CDS (nucleotide) length, rather than the number of amino acids. caution MI:0618,
a.brieger@em.uni-frankfurt.de contact-email MI:0634,
imex curation MI:0959,
imex curation curation depth MI:0955
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biopax3:experimentalForm |