5QGF: Tyrosine-protein phosphatase non-receptor type 1

PanDDA analysis group deposition -- Crystal structure of PTP1B in complex with compound_FMOOA000539a. Determined by X-ray diffraction at 1.51 Å resolution. Released 10 Oct 2018.

Method
X-ray diffraction
Resolution
1.51 Å
Organism
Homo sapiens
Chains
1
Atoms
8,968
Mol. weight
38 kDa
Ligands
F8D
Released
10 Oct 2018

Explore 5QGF in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

5QGF contains 14 α-helices and 13 β-strands across 1 chain. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 14 helices, 13 β-strands

ElementResiduesLengthSheet
α-helix3-1311
α-helix16-2611
α-helix38-436
α-helix53-553
β-strand56-5831
α-helix591
β-strand66-7491
β-strand79-8461
α-helix85-873
α-helix92-10110
β-strand10412
β-strand106-10941
β-strand114-11523
β-strand118-11923
β-strand133-13531
α-helix136-1383
β-strand140-149101
β-strand153-162101
β-strand168-17691
α-helix189-20012
β-strand20912
α-helix2101
β-strand211-21441
α-helix221-23717
α-helix241-2433
α-helix246-2538
α-helix264-28118

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Tyrosine-protein phosphatase non-receptor type 1Aprotein321Homo sapiensP18031 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>5QGF_1 Tyrosine-protein phosphatase non-receptor type 1 (chains A)
MEMEKEFEQIDKSGSWAAIYQDIRHEASDFPSRVAKLPKNKNRNRYRDVSPFDHSRIKLH
QEDNDYINASLIKMEEAQRSYILTQGPLPNTVGHFWEMVWEQKSRGVVMLNRVMEKGSLK
CAQYWPQKEEKEMIFEDTNLKLTLISEDIKSYYTVRQLELENLTTQETREILHFHYTTWP
DFGVPESPASFLNFLFKVRESGSLSPEHGPVVVHCSAGIGRSGTFCLADTCLLLMDKRKD
PSSVDIKKVLLEMRKFRMGLIQTADQLRFSYLAVIEGAKFIMGDSSVQDQWKELSHEDLE
PPPEHIPPPPRPPKRILEPHN

Ligands and cofactors

IDNameFormulaCopies
F8D1-[(3S,3aS,8bS)-7-chloro-3-(hydroxymethyl)-2,3,3a,8b-tetrahydro-1H-[1]benzofuro…C13 H14 Cl N O32

Water and common crystallization additives (TRS) are not listed.

Primary citation

An expanded allosteric network in PTP1B by multitemperature crystallography, fragment screening, and covalent tethering. Keedy, D.A., Hill, Z.B., Biel, J.T. et al. Elife (2018) 7. DOI 10.7554/eLife.36307 · PubMed

Other PDB entries of the same protein (UniProt P18031 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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