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MolNFT v1 · #75483 · protein

Structural analysis of a viral otu domain protease from the crimean- congo hemorrhagic fever virus in complex with human ubiquitin

3PRM · L protein: “Structural analysis of a viral otu domain protease from the crimean- congo hemorrhagic fever virus in complex…”. X-ray diffraction, 1 ligand (3CN), 3 pockets (best druggability 0.63). MolNFT v1 #75483 on GenesisL1: 3D…

PDB
3PRM
Type
protein
Length
472 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
L protein; Ubiquitin
EC
3.4.19.12
UniProt
Q6TFZ7, P0CG48
Ligands
3CN
Pockets
3 · best druggability 0.63

Structure

x-ray diffraction · 2 distinct chains · 34% helix, 29% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CL proteinprotein16139% helix, 25% strandQ6TFZ7
B, DUbiquitin (EC 3.4.19.12)protein7524% helix, 36% strandP0CG48

Ligands and binding sites

  • 3CN · 3-aminopropane · ligand · 2 copies · chains A, B, C, D

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

3 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13850.630.7842empty
21580.490.7725empty
31360.430.7622empty

Interfaces

5 interfaces between chains.

  • A–B · 1073 Ų buried · 12 hydrogen bonds · protein-protein
  • C–D · 1033 Ų buried · 14 hydrogen bonds · protein-protein
  • B–C · 476 Ų buried · 11 hydrogen bonds · protein-protein
  • A–D · 458 Ų buried · 11 hydrogen bonds · protein-protein
  • A–C · 144 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 8 modified, 3 covalent (engineered, covalent ligand).

Compared structures

  • 3PRM · Structural analysis of a viral OTU domain protease from the Crimean-Congo Hemorrhagic… · the same entry in another collection · chain A against A, TM-score 1.00

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