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Leopard syndrome-associated SHP2/A461T mutant

Analyse Leopard syndrome-associated SHP2/A461T mutant in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4OHD
Type
protein
Length
494 residues
Chains
1
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
6 · best druggability 0.65

Structure

x-ray diffraction · 1 distinct chain · 29% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATyrosine-protein phosphatase non-receptor type 11 (EC 3.1.3.48)protein49429% helix, 28% strandQ06124

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13940.650.7940empty
22570.570.7843empty
32570.530.7634empty
4900.500.8323empty
5610.370.7912empty

Compared structures

  • 4OHD · LEOPARD Syndrome-Associated SHP2/A461T mutant · the same entry in another collection · chain A against A, TM-score 1.00

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