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VCAM4I restriction endonuclease in complex with 5MC-modified dsdna

Analyse VCAM4I restriction endonuclease in complex with 5MC-modified dsdna in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6YMG
Type
protein + DNA
Length
662 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hnh endonuclease; DNA (5'-D(*CP*CP*AP*TP*GP*(5CM)P*GP*CP*TP*GP*A)-3'); DNA…
UniProt
A0A344KQF3
Ligands
SO4, CL
Pockets
9 · best druggability 0.80

Structure

x-ray diffraction · 3 distinct chains · 39% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BHnh endonucleaseprotein30939% helix, 18% strandA0A344KQF3
C, EDNA (5'-D(*CP*CP*AP*TP*GP*(5CM)P*GP*CP*TP*GP*A)-3')dna11——
D, FDNA (5'-D(P*CP*AP*GP*CP*GP*CP*AP*TP*GP*G)-3')dna11——

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 9 copies · chains A, B, D
  • CL · Chloride ion · ion · chains A

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

Pockets

9 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111300.800.8186SO4
2970.620.8919empty
31220.610.8721empty
42730.550.7723empty
51830.450.7523empty

Interfaces

7 interfaces between chains.

  • A–B · 2345 Ų buried · 31 hydrogen bonds · protein-protein
  • A–C · 797 Ų buried · 27 hydrogen bonds · protein-nucleic
  • B–E · 794 Ų buried · 26 hydrogen bonds · protein-nucleic
  • E–F · 524 Ų buried · 44 hydrogen bonds · nucleic-nucleic
  • C–D · 523 Ų buried · 44 hydrogen bonds · nucleic-nucleic

Modifications

Observed in the structure: 2 modified (nucleotide modification).

Compared structures

  • 6YMG · VcaM4I restriction endonuclease in complex with 5mC-modified dsDNA · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

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