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Leopard syndrome-associated SHP2/Q506P mutant

Analyse Leopard syndrome-associated SHP2/Q506P mutant in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4OHH
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
5 · best druggability 0.60

Structure

x-ray diffraction · 1 distinct chain · 29% helix, 26% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATyrosine-protein phosphatase non-receptor type 11 (EC 3.1.3.48)protein49429% helix, 26% strandQ06124

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13810.600.7739empty
2580.400.8120empty
31310.390.7428empty
4690.380.7919empty
5590.310.7618empty

Compared structures

  • 4OHH · LEOPARD Syndrome-Associated SHP2/Q506P mutant · the same entry in another collection · chain A against A, TM-score 1.00

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