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Crystal structure of the tyrosine phosphatase shp-2 with N308D mutation

Analyse Crystal structure of the tyrosine phosphatase shp-2 with N308D mutation in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4NWF
Type
protein
Length
985 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Tyrosine-protein phosphatase non-receptor type 11
EC
3.1.3.48
UniProt
Q06124
Pockets
11 · best druggability 0.74

Structure

x-ray diffraction · 2 distinct chains · 31% helix, 25% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATyrosine-protein phosphatase non-receptor type 11 (EC 3.1.3.48)protein48931% helix, 25% strandQ06124
BTyrosine-protein phosphatase non-receptor type 11 (EC 3.1.3.48)protein49631% helix, 25% strandQ06124

Ligands and binding sites

  • EDO · 1,2-ethanediol · additive · 7 copies · chains A, B
  • GOL · Glycerol · additive · chains A

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

Pockets

11 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111010.740.7786empty
23890.630.7833EDO
33380.620.7928empty
41840.440.7428empty
5990.420.7823empty

Interfaces

1 interface between chains.

  • A–B · 754 Ų buried · 10 hydrogen bonds · protein-protein

Compared structures

  • 4NWF · Crystal structure of the tyrosine phosphatase SHP-2 with N308D mutation · the same entry in another collection · chain A against A, TM-score 1.00

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