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AfCS Yeast 2-Hybrid: Interaction Data

Protein short name:
Protein name/synonyms:
Entrez Gene ID:
AfCS ID:
Intact protein length:

1 This column shows the bait name and the amino (N)- and carboxy (C)-terminal amino acid coordinates of the bait protein region used to isolate the interacting prey protein. Fragments of proteins representing folded domains are often more effective than the full-length protein in identifying physiologically relevant interactions in this assay. If the domain structure of a given bait protein was already established, specific baits were designed to represent one or more folded domains. In cases where domain structure was not available, a variety of secondary structure prediction algorithms were used to predict domains and thus direct bait design.

2Top AfCS BLAST hit obtained by comparing the bait sequence against the AfCS database, restricted to hits with at least 90% identity over 90% of the sequence.

3 This column shows the prey name and the amino (N)- and carboxy (C)-terminal amino acid coordinates of the prey protein region identified in the screen. In cases where the nucleotide sequence of the prey fragment began upstream of the initiation codon, the N-terminal coordinate is 1. Similarly, in cases where the nucleotide sequence of the prey fragment finishes downstream of the termination codon, the C-terminal coordinate corresponds to the last amino acid of the protein.

4Top AfCS BLAST hit obtained by comparing the prey sequence against the AfCS database, restricted to hits with at least 90% identity over 90% of the sequence.

5 This column denotes the activation domain library used for identifying the bait-prey interaction. Screening of an activation domain library derived from a specific cell type may permit the identification of protein interactions that are unique to that cell type. The AfCS has isolated mRNA from several sources, which Myriad has used to prepare the following specific activation domain libraries:

  • Macrophage (Resting RAW264.7 cells + RAW264.7 cells stimulated with a cocktail of lipopolysaccharide (5mg/ml) and interferon gamma (5nM) for 18 hours + Murine primary bone marrow-derived macrophages)
  • Embryo (derived from mRNA isolated from mouse embryos at multiple developmental stages)
  • B cell (Resting primary B cells + stimulated primary B cells (4 hour incubation with anti-IgM [0.06 microM], anti-CD40 [0.06 microM], and IL-4 [0.011 nM] + WEHI-231 B cell line)
  • Primary cardiac myocytes (Note that this library contains high levels of mitochondrial DNA and consequently gives fewer interactions)
  • Nk-TAg myocyte cell line

6 Date on which interaction was first identified

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