Copy of Data panel

In the data panel you will see several columns of data:

• Gene name (symbol)
• Gene ID (see details in Search)
• UniProt ID
• Organism
• Protein name
  (This information was extracted from the ProteinName field of the FASTA header in the UniProt protein FASTA file (https://www.uniprot.org/help/fasta-headers).
• Gene functional annotations (GO aspects Molecular Function (F) and Biological Process (P))
  This information was extracted from GOC (http://geneontology.org/). Annotation supported by Experimental Evidence (one of the evidence code listed below) is indicated by a yellow flask icon. Annotation propagated from ancestral genes (GO evidence code IBA) is indicated by a green tree glyph.
• Experimental Evidence includes:
  • IDA: direct assay
  • IMP: mutant phenotype
  • IGI: genetic interaction
  • IPI: physical interaction
  • IEP: expression pattern

  • EXP: experimental evidence

 

Each subheader under Known Function is a distinct known function reported for at least one member of the gene family. If a YELLOW colored circle appears in a gene row under a subheader that indicates presence of that particular known function for that gene. Clicking on a YELLOW circle will open a popup window where details about the function annotation can be found. The columns in the popup include:

• 
  
  • GO term: Shows the GO term name, which is hyperlinked to the term detail page in QuickGO.
  • Evidence description: Shows the experimental evidence that supports the annotation of the GO term to the gene/protein.
  • Reference: Shows the publication(s) containing the experimental evidence supporting the GO annotation.  We use digits (i.e., 1, 2, etc.) to indicate each distinct reference. Each number is a hyperlink to the PubMed record for the article.
  • With/From: Displays other gene(s) that support the annotation. You will usually find it for annotations that were supported by physical interaction or genetic interaction evidence.
    
  • Source: QuickGO. Clicking here takes you to the complete annotation record of the gene (UniProt protein) in QuickGO. Annotations displayed there are not limited to molecular functions that are supported by experimental evidence.You will likely find annotations to molecular functions with other types of evidence, and annotations to biological processes, or cellular components. 
    
• Subfamily name
  Subfamilies within each family are groups of genes that share a particularly high degree of similarity due to limited divergence from their common ancestor. Subfamilies are, in general, closely-related orthologs. More about subfamilies

Toggle to see the multiple sequence alignment (MSA) of a gene family

The MSA is built using the MAFFT software and represents an alignment across the entire length of all protein sequences in a PANTHER family (please see here for difference between a PANTHER family and a PhyloGenes family.) The sequence of an internal node is deduced from all of its child nodes, and is shown in the MSA when the child nodes are collapsed in the gene family tree.

• an uppercase letter: the residue is shared by at least 30% of sequences at the same position. It is considered more conserved (aka match state). Only match state residues are used in constructing PANTHER HMMs. When looking at the sequence of an internal node, the uppercase letter X indicates an undetermined ancestral residue.
• a lowercase letter: less conserved amino acid residue (aka non-match state). The lower case letter x represents an undetermined ancestral residue.
• a dash symbol (-): a gap in a match state site
• a dot symbol (.): a gap in a non-match state site

Higher sequence similarities shared among proteins in a PhyloGenes family are indicated with color shadings in MSA.

• a darker shading over an amino acid residue indicates that the residue is shared by 90% or more sequences at the same position.
• a lighter shading indicates a residue shared by more than 50% but less than 90% of sequences. 
• the identity is calculated by including all protein sequences in a PhyloGenes family.
• sequence similarity is recalculated when a user chooses to run ‘prune tree by organism’. The pruned protein sequences are excluded in recalculating sequence similarity.