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

PanDDA analysis group deposition -- Crystal structure of PTP1B in complex with compound_FMOPL000069a. Determined by X-ray diffraction at 1.55 Å resolution. Released 10 Oct 2018.

Method
X-ray diffraction
Resolution
1.55 Å
Organism
Homo sapiens
Chains
1
Atoms
7,703
Mol. weight
37.69 kDa
Ligands
JFS
Released
10 Oct 2018

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

Secondary structure: helices and β-sheets

5QDK contains 13 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: 13 helices, 13 β-strands

ElementResiduesLengthSheet
α-helix3-1311
α-helix16-2611
α-helix33-364
α-helix38-436
β-strand5611
α-helix57-593
β-strand69-7461
β-strand79-8461
α-helix85-884
α-helix92-10110
β-strand10412
β-strand106-10941
β-strand114-11523
β-strand118-11923
β-strand133-13531
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-helix264-28017

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Tyrosine-protein phosphatase non-receptor type 1Aprotein321Homo sapiensP18031 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>5QDK_1 Tyrosine-protein phosphatase non-receptor type 1 (chains A)
MEMEKEFEQIDKSGSWAAIYQDIRHEASDFPSRVAKLPKNKNRNRYRDVSPFDHSRIKLH
QEDNDYINASLIKMEEAQRSYILTQGPLPNTVGHFWEMVWEQKSRGVVMLNRVMEKGSLK
CAQYWPQKEEKEMIFEDTNLKLTLISEDIKSYYTVRQLELENLTTQETREILHFHYTTWP
DFGVPESPASFLNFLFKVRESGSLSPEHGPVVVHCSAGIGRSGTFCLADTCLLLMDKRKD
PSSVDIKKVLLEMRKFRMGLIQTADQLRFSYLAVIEGAKFIMGDSSVQDQWKELSHEDLE
PPPEHIPPPPRPPKRILEPHN

Ligands and cofactors

IDNameFormulaCopies
JFS[4-(1H-benzimidazol-1-yl)phenyl]methanolC14 H12 N2 O1

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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