Hello, I have a question about the semantics of different possible versions of proteins. In mice, a particular protein will have a given amino acid sequence, so when I talk about say Il-10 in C57/Bl6 mice it's referring to a specific primary structure.
My confusion is about the human correlate of this - different alleles of a gene can code for different versions of a protein with slightly different amino acid sequences. So when people refer to Il-10 (or another protein) in humans either on Wikipedia or clinical studies, what version of the protein are they talking about? Are they talking about the most common (wild-type) version of the protein or just all major polymorphisms assuming they don't differ much in function (as say APOE versions would)? You can look up a human protein on UniProt and it'll give you the amino acid length, where it's phosphorylated etc but is this for a particular version of the protein coded by a certain allele, or is this describing all variants of a given protein?
I guess more specifically, how can a study describe the structure of a given human protein (amino acid sequence, secondary structure etc.) if these proteins can exist as different versions through different alleles in a population?
I hope that makes sense - thanks in advance!
I've often encountered (and myself used) the term isoforms for proteins derived from different alleles or gene duplications. However, I'm told this is old school and Joe's definition seems the accepted one nowadays. Just beware when reading the old literature :)