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Spua mutant - H221N with glu

Analyse Spua mutant - H221N with glu in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7D53
Type
protein
Length
992 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Probable glutamine amidotransferase
UniProt
Q9I6J4
Ligands
GLU, MG
Pockets
7 · best druggability 0.74

Structure

x-ray diffraction · 3 distinct chains · 34% helix, 24% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, DProbable glutamine amidotransferaseprotein24933% helix, 24% strandQ9I6J4
BProbable glutamine amidotransferaseprotein24635% helix, 24% strandQ9I6J4
CProbable glutamine amidotransferaseprotein24834% helix, 24% strandQ9I6J4

Ligands and binding sites

  • GLU · Glutamic acid · ligand · 4 copies · chains A, B, C, D
  • MG · Magnesium ion · metal · 4 copies · chains A, B, C, D

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

Pockets

7 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18160.740.7970empty
23920.660.7953empty
34020.630.7856GLU
42680.610.8038GLU
51880.490.7638GLU

Interfaces

5 interfaces between chains.

  • A–B · 1579 Ų buried · 13 hydrogen bonds · protein-protein
  • A–C · 317 Ų buried · 2 hydrogen bonds · protein-protein
  • B–D · 268 Ų buried · 3 hydrogen bonds · protein-protein
  • C–D · 153 Ų buried · 0 hydrogen bonds · protein-protein
  • A–D · 34 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 7D53 · SpuA mutant - H221N with Glu · the same entry in another collection · chain A against A, TM-score 1.00

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