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Crystal structure of C-terminal domain of precorrin-6Y C5,15- methyltransferase from rhodobacter capsulatus

Analyse Crystal structure of C-terminal domain of precorrin-6Y C5,15- methyltransferase… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3NJR
Type
protein
Length
368 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Precorrin-6Y methylase
EC
2.1.1.132
UniProt
O68099
Ligands
SAH
Pockets
3 · best druggability 0.65

Structure

x-ray diffraction · 1 distinct chain · 34% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BPrecorrin-6Y methylase (EC 2.1.1.132)protein18434% helix, 27% strandO68099

Ligands and binding sites

  • SAH · S-adenosyl-L-homocysteine · ligand · 2 copies · chains A, B
  • GOL · Glycerol · additive · 2 copies · chains A, B
  • PG4 · Tetraethylene glycol · additive · chains B

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

Pockets

3 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14520.650.7876SAH
24890.650.7773SAH, GOL
3530.320.7821empty

Interfaces

1 interface between chains.

  • A–B · 1515 Ų buried · 19 hydrogen bonds · protein-protein

Compared structures

  • 3NJR · Crystal structure of C-terminal domain of precorrin-6Y C5,15-methyltransferase from… · the same entry in another collection · chain B against B, TM-score 1.00

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