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Crystal structure of the F316A mutant of goxa soaked with glycine

Analyse Crystal structure of the F316A mutant of goxa soaked with glycine in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6VMW
Type
protein
Length
3,076 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Glycine oxidase
UniProt
A0A161XU12
Ligands
MG, NA
Pockets
20 · best druggability 0.88

Structure

x-ray diffraction · 4 distinct chains · 32% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
BGlycine oxidaseprotein78432% helix, 20% strandA0A161XU12
AGlycine oxidaseprotein76431% helix, 21% strandA0A161XU12
CGlycine oxidaseprotein76932% helix, 21% strandA0A161XU12
DGlycine oxidaseprotein75932% helix, 21% strandA0A161XU12

Ligands and binding sites

  • MG · Magnesium ion · metal · 4 copies · chains B, A, C, D
  • NA · Sodium ion · metal · chains B

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

Pockets

20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16420.880.9277empty
24820.860.9355empty
39140.800.83101empty
45710.780.8580empty
51470.760.9423empty

Interfaces

6 interfaces between chains.

  • C–D · 3142 Ų buried · 63 hydrogen bonds · protein-protein
  • B–A · 3083 Ų buried · 65 hydrogen bonds · protein-protein
  • B–C · 2510 Ų buried · 40 hydrogen bonds · protein-protein
  • A–D · 2474 Ų buried · 41 hydrogen bonds · protein-protein
  • B–D · 236 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 modified (nonstandard).

Compared structures

  • 6VMW · Crystal structure of the F316A mutant of GoxA soaked with glycine · the same entry in another collection · chain B against B, TM-score 1.00

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