×

Network disruptions

We have been experiencing disruptions on our local network which has affected the stability of these web pages. We have been working with IT support team to get this fixed as a matter of urgency and apologise for any inconvenience.

CATH Classification

Domain Context

CATH Clusters

Superfamily K Homology domain, type 1
Functional Family Fragile X mental retardation 1, isoform CRA_e

Enzyme Information

UniProtKB Entries (1)

Q06787
FMR1_HUMAN
Homo sapiens
Synaptic functional regulator FMR1

PDB Structure

PDB 2FMR
External Links
Method SOLUTION NMR
Organism Escherichia
Primary Citation
The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome.
Musco, G., Kharrat, A., Stier, G., Fraternali, F., Gibson, T.J., Nilges, M., Pastore, A.
Nat.Struct.Biol.
CATH-Gene3D is a Global Biodata Core Resource Learn more...