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Human tyrosine phosphatase 1B complexed with an inhibitor

Analyse Human tyrosine phosphatase 1B complexed with an inhibitor in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1KAK
Type
protein
Length
297 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Protein-tyrosine phosphatase, non-receptor type 1
EC
3.1.3.48
UniProt
P18031
Ligands
FNP

Structure

x-ray diffraction · 1 distinct chain · 37% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProtein-tyrosine phosphatase, non-receptor type 1 (EC 3.1.3.48)protein29737% helix, 21% strandP18031

Ligands and binding sites

  • FNP · {[7-(difluoro-phosphono-methyl)-naphthalen-2-yl]-difluoro-methyl}-phosphonic acid · ligand · chains A

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

Compared structures

  • 1KAK · Human Tyrosine Phosphatase 1B Complexed with an Inhibitor · the same entry in another collection · chain A against A, TM-score 1.00

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