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MolNFT v1 · #43564 · protein

Feedback inhibition of fully unadenylylated glutamine synthetase from salmonella typhimurium by glycine, alanine, and serine

2LGS: “Feedback inhibition of fully unadenylylated glutamine synthetase from salmonella typhimurium by glycine…”. X-ray diffraction, 2 ligands (GLU, MN), 20 pockets (best druggability 0.78). MolNFT v1 #43564 on GenesisL1: 3D structure…

PDB
2LGS
Type
protein
Length
5,340 residues
Chains
12
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Glutamine synthetase
EC
6.3.1.2
UniProt
P06201
Ligands
GLU, MN
Pockets
20 · best druggability 0.78

Structure

x-ray diffraction · 1 distinct chain · 37% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, F, G, H, I, J, K, LGlutamine synthetase (EC 6.3.1.2)protein44537% helix, 23% strandP06201

Ligands and binding sites

  • GLU · Glutamic acid · ligand · 12 copies · chains A, B, C, D, E, F, G, H, I, J, K, L
  • MN · Manganese (II) ion · metal · 24 copies · chains A, B, C, D, E, F, G, H, I, J, K, L

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
13340.780.8927empty
23750.780.8835empty
33350.780.8826empty
49930.780.8076MN, GLU
59730.770.8077MN, GLU

Interfaces

24 interfaces between chains.

  • A–G · 2829 Ų buried · 32 hydrogen bonds · protein-protein
  • E–I · 2828 Ų buried · 32 hydrogen bonds · protein-protein
  • B–L · 2828 Ų buried · 32 hydrogen bonds · protein-protein
  • F–H · 2822 Ų buried · 32 hydrogen bonds · protein-protein
  • C–K · 2815 Ų buried · 32 hydrogen bonds · protein-protein

Compared structures

  • 2LGS · Feedback inhibition of fully unadenylylated glutamine synthetase from salmonella… · the same entry in another collection · chain F against F, TM-score 1.00

Analyse

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