CATH Classification

Domain Context

CATH Clusters

Superfamily 3.40.50.1460
Functional Family

Enzyme Information

3.4.22.61
Caspase-8.
based on mapping to UniProt Q14790
Strict requirement for Asp at position P1 and has a preferred cleavage sequence of (Leu/Asp/Val)-Glu-Thr-Asp-|-(Gly/Ser/Ala).
-!- Caspase-8 is an initiator caspase, as are caspase-2 (EC 3.4.22.55), caspase-9 (EC 3.4.22.62) and caspase-10 (EC 3.4.22.63). -!- Apical activator of the extrinsic (death receptor) apoptosis pathway, triggered by death receptor ligation. -!- Contains two tandem death effector domains (DEDs) in its N-terminal prodomain, which play a role in procaspase activation. -!- Linked to cell surface death receptors such as Fas. -!- When Fas is aggregated by the Fas ligand, procaspase-8 is recruited to the death receptor where it is activated. -!- Has a preference for Glu at P3 and prefers small residues, such as Gly, Ser and Ala at the P1' position. -!- Has very broad P4 specificity, tolerating substrates with Asp, Val or Leu in this position. -!- Endogenous substrates for caspase-8 include procaspase-3, the pro- apoptotic Bcl-2 family member Bid, RIP, PAK2 and the caspase-8 activity modulator FLIP(L). -!- Belongs to peptidase family C14.

UniProtKB Entries (1)

Q14790
CASP8_HUMAN
Homo sapiens
Caspase-8

PDB Structure

PDB 3KJN
External Links
Method X-RAY DIFFRACTION
Organism
Primary Citation
Kinetic and structural characterization of caspase-3 and caspase-8 inhibition by a novel class of irreversible inhibitors.
Wang, Z., Watt, W., Brooks, N.A., Harris, M.S., Urban, J., Boatman, D., McMillan, M., Kahn, M., Heinrikson, R.L., Finzel, B.C., Wittwer, A.J., Blinn, J., Kamtekar, S., Tomasselli, A.G.
Biochim.Biophys.Acta