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Cryo-EM structure of PCV2 replicase bound to ssdna

Analyse Cryo-EM structure of PCV2 replicase bound to ssdna in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7LAR
Type
protein + DNA
Length
1,104 residues
Chains
7
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
ATP-dependent helicase rep; DNA (5'-D(P*TP*TP*TP*TP*TP*T)-3')
EC
3.6.4.-
UniProt
Q6TC59
Ligands
ADP, MG
Pockets
20 · best druggability 0.88

Structure

electron microscopy · 2 distinct chains · 30% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, FATP-dependent helicase rep (EC 3.6.4.-)protein18330% helix, 21% strandQ6TC59
GDNA (5'-D(P*TP*TP*TP*TP*TP*T)-3')dna6——

Ligands and binding sites

  • ADP · Adenosine-5'-diphosphate · ligand · 4 copies · chains A, B, C, D, E
  • MG · Magnesium ion · metal · 4 copies · chains A, B, C, D, E

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

Pockets

20 pockets found on a 1 Å grid, 12 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110500.880.89127empty
25440.760.8358empty
31870.680.8728empty
41790.680.8729empty
57610.670.7559empty

Interfaces

12 interfaces between chains.

  • D–E · 1424 Ų buried · 6 hydrogen bonds · protein-protein
  • B–C · 1406 Ų buried · 2 hydrogen bonds · protein-protein
  • E–F · 1406 Ų buried · 6 hydrogen bonds · protein-protein
  • A–B · 1397 Ų buried · 5 hydrogen bonds · protein-protein
  • C–D · 1383 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 covalent (covalent ligand).

Compared structures

  • 7LAR · Cryo-EM structure of PCV2 Replicase bound to ssDNA · the same entry in another collection · chain A against A, TM-score 1.00

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