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Crystal structure of complex of SAM and BVU_3255, a methyltransferase from bacteroides vulgatus atcc 8482

Analyse Crystal structure of complex of SAM and BVU_3255, a methyltransferase from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3T7S
Type
protein
Length
965 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Putative methyltransferase
UniProt
A6L5C0
Ligands
SAM
Pockets
11 · best druggability 0.72

Structure

x-ray diffraction · 4 distinct chains · 42% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APutative methyltransferaseprotein24644% helix, 23% strandA6L5C0
BPutative methyltransferaseprotein23941% helix, 24% strandA6L5C0
CPutative methyltransferaseprotein24543% helix, 24% strandA6L5C0
DPutative methyltransferaseprotein23540% helix, 25% strandA6L5C0

Ligands and binding sites

  • SAM · S-adenosylmethionine · ligand · 4 copies · chains A, B, C, D

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

Pockets

11 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17150.720.7882empty
28700.710.7758empty
34080.670.7944SAM
43660.660.8044SAM
53070.640.8045SAM

Interfaces

5 interfaces between chains.

  • C–D · 973 Ų buried · 8 hydrogen bonds · protein-protein
  • A–B · 841 Ų buried · 11 hydrogen bonds · protein-protein
  • B–C · 228 Ų buried · 3 hydrogen bonds · protein-protein
  • A–D · 201 Ų buried · 0 hydrogen bonds · protein-protein
  • A–C · 119 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 3T7S · Crystal structure of complex of SAM and BVU_3255, a methyltransferase from Bacteroides… · the same entry in another collection · chain A against A, TM-score 1.00

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