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Structure of radical S-adenosylmethionine methyltransferase, tsrm, from kitasatospora setae with tryptophan substrate and SAM analog (aza-SAM) bound

Analyse Structure of radical S-adenosylmethionine methyltransferase, tsrm, from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6WTF
Type
protein
Length
1,081 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Tryptophan-C2-methyltransferase containing B12-binding domain
UniProt
E4N8S5
Ligands
SF4, B12, SA8, TRP
Pockets
9 · best druggability 0.88

Structure

x-ray diffraction · 2 distinct chains · 38% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATryptophan-C2-methyltransferase containing B12-binding domainprotein54238% helix, 16% strandE4N8S5
BTryptophan-C2-methyltransferase containing B12-binding domainprotein53938% helix, 17% strandE4N8S5

Ligands and binding sites

  • SF4 · Iron/sulfur cluster · ligand · 2 copies · chains A, B
  • B12 · Cobalamin · ligand · 2 copies · chains A, B
  • SA8 · S-5'-azamethionine-5'-deoxyadenosine · ligand · 2 copies · chains A, B
  • TRP · Tryptophan · ligand · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111110.880.9092SF4, B12, SA8, TRP
211630.880.8995SF4, B12, SA8, TRP
35920.750.8244empty
41470.380.7224empty
51000.380.7515empty

Interfaces

1 interface between chains.

  • A–B · 607 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 6WTF · Structure of radical S-adenosylmethionine methyltransferase, TsrM, from Kitasatospora… · the same entry in another collection · chain A against A, TM-score 1.00

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