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MolNFT v1 · #104619 · protein

Crystal structure of phosphoglucomutase from leishmania major at 3.5 ångström resolution

4QG5 · Putative phosphoglucomutase: “Crystal structure of phosphoglucomutase from leishmania major at 3.5 ångström resolution”. X-ray diffraction, 1 ligand (MG), 20 pockets (best druggability 0.80). MolNFT v1 #104619 on GenesisL1: 3D…

PDB
4QG5
Type
protein
Length
2,244 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Putative phosphoglucomutase
EC
5.4.2.2
UniProt
Q4QCF1
Ligands
MG
Pockets
20 · best druggability 0.80

Structure

x-ray diffraction · 3 distinct chains · 28% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APutative phosphoglucomutase (EC 5.4.2.2)protein56530% helix, 19% strandQ4QCF1
B, DPutative phosphoglucomutase (EC 5.4.2.2)protein55927% helix, 21% strandQ4QCF1
CPutative phosphoglucomutase (EC 5.4.2.2)protein56128% helix, 21% strandQ4QCF1

Ligands and binding sites

  • 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

20 pockets found on a 1 Å grid, 15 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15050.800.8763empty
28600.760.7973empty
39470.750.7889empty
46490.750.8183empty
59410.750.7882empty

Interfaces

5 interfaces between chains.

  • A–D · 1044 Ų buried · 8 hydrogen bonds · protein-protein
  • B–C · 990 Ų buried · 9 hydrogen bonds · protein-protein
  • B–D · 778 Ų buried · 10 hydrogen bonds · protein-protein
  • A–B · 268 Ų buried · 0 hydrogen bonds · protein-protein
  • C–D · 220 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 4QG5 · Crystal structure of phosphoglucomutase from Leishmania major at 3.5 angstrom resolution · the same entry in another collection · chain A against A, TM-score 1.00

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