8S6F: Protease 3C

A Structural Investigation of the Interaction between a GC-376-Based Peptidomimetic PROTAC and Its Precursor with the Viral Main Protease of Coxsackievirus B3. Determined by X-ray diffraction at 1.93 Å resolution. Released 4 Dec 2024.

Method
X-ray diffraction
Resolution
1.93 Å
Organism
Coxsackievirus B3
Chains
1
Atoms
1,496
Mol. weight
20.39 kDa
Ligands
VQR
Released
4 Dec 2024

Explore 8S6F in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

8S6F contains 7 α-helices and 17 β-strands across 1 chain. 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: 7 helices, 17 β-strands

ElementResiduesLengthSheet
α-helix2-1413
β-strand15-2061
β-strand23-3191
β-strand3212
β-strand34-3851
α-helix39-413
β-strand46-4941
β-strand52-63121
β-strand69-7791
α-helix821
β-strand8312
α-helix841
α-helix87-893
β-strand9011
β-strand9113
β-strand97-10481
β-strand112-127161
β-strand130-13891
α-helix1491
β-strand150-15341
β-strand156-16381
β-strand169-17351
β-strand17513
α-helix176-1794

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Protease 3CAprotein180Coxsackievirus B3P03313
Sequence of entity 1 (A), FASTA
>8S6F_1 Protease 3C (chains A)
GPAFEFAVAMMKRNSSTVKTEYGEFTMLGIYDRWAVLPRHAKPGPTILMNDQEVGVLDAK
ELVDKDGTNLELTLLKLNRNEKFRDIRGFLAKEEVEVNEAVLAINTSKFPNMYIPVGQVT
EYGFLNLGGTPTKRMLMYNFPTRAGQCGGVLMSTGKVLGIHVGGNGHQGFSAALLKHYFN

Ligands and cofactors

IDNameFormulaCopies
VQRmethyl (4~{S})-4-[[(2~{S})-4-methyl-2-(phenylmethoxycarbonylamino)pentanoyl]ami…C24 H35 N3 O61

Primary citation

A Structural Investigation of the Interaction between a GC-376-Based Peptidomimetic PROTAC and Its Precursor with the Viral Main Protease of Coxsackievirus B3. De Santis, A., Grifagni, D., Orsetti, A. et al. Biomolecules (2024) 14. DOI 10.3390/biom14101260 · PubMed

Other PDB entries of the same protein (UniProt P03313), best resolution first:

Browse structure collections

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