CATH Classification
Level | CATH Code | Description |
---|---|---|
3 | Alpha Beta | |
3.30 | 2-Layer Sandwich | |
3.30.70 | Alpha-Beta Plaits | |
3.30.70.1470 | Caspase-like |
Domain Context
CATH Clusters
Superfamily | Caspase-like |
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 | 1F9E |
External Links | |
Method | X-RAY DIFFRACTION |
Organism | Escherichia |
Primary Citation |
Caspase-8 specificity probed at subsite S(4): crystal structure of the caspase-8-Z-DEVD-cho complex.
J.Mol.Biol.
|