2HBZ: Human caspase-1

Crystal structure of human caspase-1 (Arg286->Ala, Glu390->Ala) in complex with 3-[2-(2-benzyloxycarbonylamino-3-methyl-butyrylamino)-propionylamino]-4-oxo-pentanoic acid (z-VAD-FMK). Determined by X-ray diffraction at 1.9 Å resolution. Released 27 Jun 2006.

Method
X-ray diffraction
Resolution
1.9 Å
Organism
Homo sapiens
Chains
3
Atoms
2,210
Mol. weight
30.46 kDa
Released
27 Jun 2006

Explore 2HBZ in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

2HBZ contains 11 α-helices and 17 β-strands across 3 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 9 helices, 9 β-strands

ElementResiduesLengthSheet
α-helix133-1353
α-helix138-1447
β-strand15211
α-helix153-1575
β-strand164-16962
α-helix182-19514
β-strand199-20462
α-helix208-21912
α-helix222-2265
β-strand230-23562
β-strand238-23923
β-strand242-24433
α-helix2451
β-strand255-25623
α-helix258-2647
α-helix271-2733
β-strand278-28362
β-strand28914
Chain B: 2 helices, 7 β-strands
ElementResiduesLengthSheet
β-strand327-33152
β-strand33714
β-strand34015
β-strand341-34226
β-strand346-34726
α-helix348-36013
α-helix366-37611
β-strand388-39032
β-strand39711
Chain C: 0 helices, 1 β-strand
ElementResiduesLengthSheet
β-strand315

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Caspase-1Aprotein178Homo sapiensP29466 (AlphaFold model)
Caspase-1Bprotein88Homo sapiensP29466 (AlphaFold model)
PHQ-VAD-fluoromethylketone inhibitorCprotein5
Sequence of entity 1 (A), FASTA
>2HBZ_1 Caspase-1 (chains A)
NPAMPTSSGSEGNVKLCSLEEAQRIWKQKSAEIYPIMDKSSRTRLALIICNEEFDSIPRR
TGAEVDITGMTMLLQNLGYSVDVKKNLTASDMTTELEAFAHRPEHKTSDSTFLVFMSHGI
REGICGKKHSEQVPDILQLNAIFNMLNTKNCPSLKDKPKVIIIQACAGDSPGVVWFKD
Sequence of entity 2 (B), FASTA
>2HBZ_2 Caspase-1 (chains B)
AIKKAHIEKDFIAFCSSTPDNVSWRHPTMGSVFIGRLIEHMQEYACSCDVEEIFRKVRFS
FEQPDGRAQMPTTARVTLTRCFYLFPGH
Sequence of entity 3 (C), FASTA
>2HBZ_3 PHQ-VAD-fluoromethylketone inhibitor (chains C)
XVADX

Primary citation

A Common Allosteric Site and Mechanism in Caspases. Scheer, J.M., Romanowski, M.J., Wells, J.A. Proc Natl Acad Sci U S A (2006) 103:7595-7600. DOI 10.1073/pnas.0602571103 · PubMed

Other PDB entries of the same protein (UniProt P29466 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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