Protein tyrosine binding (PTB) and 'post synaptic density disc-large t
o-1' (PDZ) domains bind to short peptidic ligands by augmentation of o
ne of the domain's beta sheets and other recognition mechanisms, The t
wo domain classes have a superficial resemblance to each other, even t
hough no sequential homology exists. The structural bases of the inter
actions are well understood for the few domains now experimentally det
ermined, and ligand-target pairs can probably be identified in favorab
le cases by analogy with the known domains. For both PTB and PDZ class
es, functional activities are still not fully defined: it is possible
that these domain classes, along with pleckstrin homology domains, hav
e multiple roles. (C) Current Biology Ltd ISSN 0959-440X.