7GP2: Protease 3C

PanDDA analysis group deposition -- Crystal Structure of Enterovirus D68 3C Protease in complex with Z425757818. Determined by X-ray diffraction at 1.31 Å resolution. Released 29 Nov 2023.

Method
X-ray diffraction
Resolution
1.31 Å
Organism
Human Enterovirus D68
Chains
2
Atoms
3,242
Mol. weight
40.74 kDa
Ligands
LPU
Released
29 Nov 2023

Explore 7GP2 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

7GP2 contains 13 α-helices and 28 β-strands across 2 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: 7 helices, 14 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-strand97-10481
β-strand112-127161
β-strand130-13891
α-helix1491
β-strand150-15341
β-strand156-16491
β-strand169-17351
α-helix176-1794
Chain B: 6 helices, 14 β-strands
ElementResiduesLengthSheet
α-helix3-1412
β-strand15-2061
β-strand23-3191
β-strand3213
β-strand34-3851
α-helix39-413
β-strand46-4941
β-strand52-63121
β-strand69-78101
β-strand8313
α-helix84-852
α-helix87-893
β-strand97-10481
β-strand112-127161
β-strand130-139101
β-strand150-15341
β-strand156-16491
β-strand168-17361
α-helix1741
α-helix176-1783

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Protease 3CA, Bprotein182Human Enterovirus D68Q68T42 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>7GP2_1 Protease 3C (chains A, B)
MGPGFDFAQAIMKKNTVIARTEKGEFTMLGVYDRVAVIPTHASVGEIIYINDVETRVLDA
CALRDLTDTNLEITIVKLDRNQKFRDIRHFLPRCEDDYNDAVLSVHTSKFPNMYIPVGQV
TNYGFLNLGGTPTHRILMYNFPTRAGQCGGVVTTTGKVIGIHVGGNGAQGFAAMLLHSYF
TD

Ligands and cofactors

IDNameFormulaCopies
LPU1-(methanesulfonyl)piperidin-4-olC6 H13 N O3 S1

Water and common crystallization additives (DMS) are not listed.

Primary citation

Crystallographic Fragment Screen of Coxsackievirus A16 2A Protease identifies new opportunities for the development of broad-spectrum anti-enterovirals. Lithgo, R.M., Tomlinson, C.W.E., Fairhead, M. et al. bioRxiv (2024). DOI 10.1101/2024.04.29.591684 · PubMed

Other PDB entries of the same protein (UniProt Q68T42 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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