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The structure of the SER128ALA point-mutant variant of cysg, the multifunctional METHYLTRANSFERASE/DEHYDROGENASE/FERROCHELATASE for siroheme synthesis

Analyse The structure of the SER128ALA point-mutant variant of cysg, the… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1PJT
Type
protein
Length
903 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Siroheme synthase
EC
2.1.1.107, 1.-.-.-, 4.99.1.-
UniProt
P25924
Ligands
SAH, PO4
Pockets
12 · best druggability 0.72

Structure

x-ray diffraction · 2 distinct chains · 38% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ASiroheme synthase (EC 2.1.1.107, 1.-.-.-, 4.99.1.-)protein44838% helix, 21% strandP25924
BSiroheme synthase (EC 2.1.1.107, 1.-.-.-, 4.99.1.-)protein45538% helix, 21% strandP25924

Ligands and binding sites

  • SAH · S-adenosyl-L-homocysteine · ligand · 2 copies · chains A, B
  • PO4 · Phosphate ion · ion · chains A, B

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

Pockets

12 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15800.720.8043PO4
22800.720.8532empty
35540.690.7951SAH
44940.680.7956SAH
53480.660.8158empty

Interfaces

1 interface between chains.

  • A–B · 6329 Ų buried · 96 hydrogen bonds · protein-protein

Compared structures

  • 1PJT · The structure of the Ser128Ala point-mutant variant of CysG, the multifunctional… · the same entry in another collection · chain A against A, TM-score 1.00
  • P25924 · AlphaFold monomer V2.0 prediction for siroheme synthase (P25924) · a predicted model of the same protein · chain B against A, TM-score 0.99

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