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Crystal structure of schistosoma mansoni arginase in complex with L- lysine

Analyse Crystal structure of schistosoma mansoni arginase in complex with L- lysine in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4Q41
Type
protein
Length
1,331 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Arginase
EC
3.5.3.1
UniProt
Q6WVP6
Ligands
LYS, MN
Pockets
8 · best druggability 0.71

Structure

x-ray diffraction · 4 distinct chains · 41% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AArginase (EC 3.5.3.1)protein33342% helix, 16% strandQ6WVP6
BArginase (EC 3.5.3.1)protein33642% helix, 16% strandQ6WVP6
CArginase (EC 3.5.3.1)protein33342% helix, 16% strandQ6WVP6
DArginase (EC 3.5.3.1)protein32939% helix, 17% strandQ6WVP6

Ligands and binding sites

  • LYS · Lysine · ligand · 2 copies · chains A, B
  • MN · Manganese (II) ion · metal · 8 copies · chains A, B, C, D
  • GOL · Glycerol · additive · 6 copies · chains A, B, C

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
15440.710.8048empty
2940.440.8023LYS
31670.430.7425empty
4880.420.7922empty
5980.420.7919LYS

Interfaces

3 interfaces between chains.

  • B–C · 284 Ų buried · 7 hydrogen bonds · protein-protein
  • A–B · 244 Ų buried · 0 hydrogen bonds · protein-protein
  • A–D · 67 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 4Q41 · Crystal structure of Schistosoma mansoni arginase in complex with L-lysine · the same entry in another collection · chain B against B, TM-score 1.00

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