Dear Modellers,
Our lab is studying the structure of the rod and cone photoreceptor
phosphodiesterase that is central to the visual signaling pathway. The
rod enzyme contains a regulatory tandem GAF domain (GAFa-GAFb) and a
catalytic domain, and exists as a heterodimer
(PDE6A and PDE6B).
There are currently no full length crystal structures for this
catalytic heterodimer, only a structure for the GAFa regulatory domain
of cone PDE6C, the GAF domain that binds cGMP noncatalytically.
The most homologous protein to PDE6 is the PDE that is abundant in
vascular smooth muscle and is the target for Viagra, PDE5 (a catalytic
homodimer). There is a dimeric structure for the PDE5 tandem GAF domains
(GAFa-GAFb) and for the isolated, monomeric
catalytic domain, but no full-length structures. cGMP binds to the GAFa
domain of PDE5, the same as PDE6.
A more distantly related PDE, PDE2, has a crystal structure of the
nearly full-length, dimeric protein, but unfortunately the GAF domains
of PDE2 occur in an opposite order compared to PDE5 and PDE6 (i.e., the
cGMP binding site is in GAFb).
See the attached diagram for a visual description of the domain organization of the three PDEs.
We are trying to build a homology model for PDE6 heterodimer. The
homology model when PDE6 is threaded onto the PDE2 structure is poor. In
contrast, structural homology modeling of PDE6 GAF and catalytic
domains using PDE5 as a template gives excellent
results. Unfortunately, it is only in the PDE2 structure that the
molecular architecture of the nearly full-length dimer has been
determined, namely the region between the GAF and catalytic domains and
the relationship of the two catalytic domains.
Is there some way to rearrange (cut-and-past) the individual
domains in the sequence alignment to allow PDE5 to serve for the
template for those domains that have been determined, while still using
the PDE2 template to thread the PDE6 linker region and
to define the relationship of the two catalytic domains with each other?
Could you kindly give us some advice on how to do the alignment and build the model? I would greatly appreciate your help.
Best,
Xiongzhuo Gao
Molecular, Cellular and Biomedical Sciences Department
University of New Hampshire
Durham, New Hampshire 03824
