Structure for peptidase C14.009: caspase-8
 
PDB | Organism | Resolution | Comment |
---|---|---|---|
1QDU | Homo sapiens | 2.80 Å | complex with tripeptide ketone inhibitor Z-Glu-Val-Asp-dichloromethylketone |
One heterodimer is shown. Catalytic residues are shown in ball-and-stick representation: His317 in purple and Cys360 in yellow. The inhibitor Glu-Val-dehydroxymethylaspartic acid is shown in ball-and-stick representation in grey. | |||
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TERTIARY STRUCTURE DATA | ||||||||
---|---|---|---|---|---|---|---|---|
Comment | Resolution | PDB | PDBe | SCOP | CATH | PDBSum | Proteopedia | Reference |
Homo sapiens | ||||||||
complex with Z-Asp-Glu-Val-Asp-CHO inhibitor | 2.90 Å | 1F9E | 1F9E | 1F9E | 1F9E | 1F9E | 1F9E | Blanchard et al., 2000 |
complex with baculovirus P35 inhibitor | 3.00 Å | 1I4E | 1I4E | 1I4E | 1I4E | 1I4E | 1I4E | Xu et al., 2001 |
complex with tripeptide ketone inhibitor Z-Glu-Val-Asp-dichloromethylketone | 2.80 Å | 1QDU | 1QDU | 1QDU | 1QDU | 1QDU | 1QDU | Blanchard et al., 1999 |
complex with acetyl-Ile-Glu-Thr-aspartic aldehyde | 1.20 Å | 1QTN | 1QTN | 1QTN | 1QTN | 1QTN | 1QTN | Watt et al., 1999 |
complex with | 1.95 Å | 2C2Z | 2C2Z | 2C2Z | 2C2Z | 2C2Z | 2C2Z | |
alternative p35-caspase-8 complex | 3.00 Å | 2FUN | 2FUN | 2FUN | 2FUN | 2FUN | 2FUN | Lu et al., 2006 |
complex with darpin-8.4 | 1.80 Å | 2Y1L | 2Y1L | 2Y1L | 2Y1L | 2Y1L | 2Y1L | |
zymogen; complex with c-flipl | 1.90 Å | 3H11 | 3H11 | 3H11 | 3H11 | 3H11 | 3H11 | Yu et al., 2009 |
complex with a covalent inhibitor | 1.80 Å | 3KJN | 3KJN | 3KJN | 3KJN | 3KJN | 3KJN | |
complex with a covalent inhibitor | 1.80 Å | 3KJQ | 3KJQ | 3KJQ | 3KJQ | 3KJQ | 3KJQ | |
caspase-3 specific unnatural amino acid-based peptides | 1.18 Å | 4JJ7 | 4JJ7 | 4JJ7 | 4JJ7 | 4JJ7 | 4JJ7 | |
caspase-8 specific unnatural amino acid peptides | 2.12 Å | 4PRZ | 4PRZ | 4PRZ | 4PRZ | 4PRZ | 4PRZ | |
caspase-8 specific unnatural amino acid peptides | 1.73 Å | 4PS1 | 4PS1 | 4PS1 | 4PS1 | 4PS1 | 4PS1 |