Ms Macphisto: It was more like ‘made up without bothering to check’. I’m not surprised that Rel is a real gene, being a three-letter name. But “part of the NF-kB family” (how did you make a kappa?) illustrates my point. If I say that a molecule is an alkylpyridine or a benzylcyclohexyloxetane, someone who knows something about chemical nomenclature can understand those names without having heard of the particular family of molecules I’m discussing. You can’t know what NF-kB is without having heard of it in detail. Really, this is just a property of genes – genomics, like anatomy, deals with things that are difficult to name systematically. Chemistry deals with things that are inherently possible to break down into fragments and name.
mnemosyne: I’d be happy if nomenclature was the only outdated part of biochemistry. They also love to draw molecules with 90° bond angles and like to write carbons and hydrogens explicitly. To make it even worse, the system of drawing mechanisms is different in biochemistry than in organic chemistry – they like to draw arrows from atoms rather than bonds. Having to learn two ways of drawing arrows is very annoying. I lost large numbers of marks for drawing arrows in biochemical mechanisms as if they were organic reactions.
Trivial names (like CoA) are acceptable and often necessary for anything biological. I agree that the D,L system should no longer be used, but in a lot of cases it’s only practical to give a +,- designator for a large molecule. For some biomolecules, using R,S would mean having to assign 20 or 30 stereocenters. That might not even be of much use if the numbering of the molecule wasn’t clear. So it’s probably better to use a relative stereochemical label and remember the absolute stereochemistry of the stereocenter of interest separately.
Technically, those amino acid structures you saw did include stereochemical information. They’re Fischer projections of the D[sub]S[/sub],L[sub]S[/sub] type, showing the molecule’s stereochemistry relative to glycine. (Rather than glyceraldehyde, the usual basis for Fischer projections.) Now, as you probably know, Fischer projections are evil and confusing – two adjacent stereocenters which have the same orientation on paper in a Fischer projection actually have the opposite orientation in a molecule. (I believe that anyone who draws a Fischer projection in the twenty-first century should be stripped of their degrees.)
In some of my courses, amino acids were drawn in the biochemical manner, with 90° bond angles, explicit C and H – Fischer projections, basically. In others, they were drawn properly – zigzag structures with dashed and wedged bonds to indicated 3D orientation. The difference is one of biochemistry versus biological chemistry.
This reminds me of one time I was asked to give the IUPAC name for alanine. I know “(2S)-2-aminopropanoic acid” was the correct answer, and I gave it. But “(2S)-alanine” is also correct, because ‘alanine’ is a reserved name according to the IUPAC Blue Book (1993).