Interpreting ConSurf Results

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This page discusses how to decide whether a ConSurf result is optimal for the questions you wish to ask about a protein. It assumes that you already have one or more completed ConSurf results. For background principles and instructions on how to get a ConSurf result, please see ConSurf/Index.

Breadth of the MSABreadth of the MSA

A ConSurf result depends crucially on the sequences included in the multiple sequence alignment (MSA). The optimal breadth of coverage of those sequences depends on your goal. The breadth of an MSA is represented in the #Average Pairwise Distance (APD).

For more about this, see What is the best way to collect homologous sequences in order to construct an MSA? at the ConSurf Server.

Average Pairwise DistanceAverage Pairwise Distance

The average pairwise distance (APD) in a multiple sequence alignment (MSA) is a measure of the evolutionary breadth of the range of sequences included. The APD is "The average number of replacements between any two sequences in the alignment; A distance of 0.01 means that on average, the expected replacement for every 100 positions is 1." (quoted from the ConSurf Server).

Generally, an APD of ≲1 is consistent with an MSA whose sequences are limited to proteins with one specific function. As the APD climbs above 1, it is more likely that proteins of multiple functions are included in the MSA.

ExampleExample

At the ConSurf Server, click on Gallery, then MHC Class I heavy chain (2VAA). In the finished results for chain A of 2VAA, under the subheading Sequence Data, click on Sequences Used.

The APD is 0.99. The MSA has 150 sequences, largely limited to sequences for major histocompatibility complex class I proteins. There is only one class II protein sequence. Three sequences are labeled "zinc-alpha-2-glycoprotein", clearly a different function. There are 22 sequences labeled "uncharacterized protein" which nevertheless have high similarity to the query. 19 sequences are labeled "UPI000... related cluster".

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Eric Martz