6XEA: PTP1B YopH WPD loop Chimera 3

Crystal Structure of the PTP1B YopH WPD loop Chimera 3 bound to vanadate. Determined by X-ray diffraction at 1.55 Å resolution. Released 15 Dec 2021.

Method
X-ray diffraction
Resolution
1.55 Å
Organism
Homo sapiens
Chains
1
Atoms
2,676
Mol. weight
37.71 kDa
Ligands
VO4, BEN, MG
Released
15 Dec 2021

Explore 6XEA in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

6XEA 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-helix2-1312
α-helix16-2611
α-helix38-436
α-helix53-553
β-strand56-5831
α-helix591
β-strand66-7491
β-strand79-8461
α-helix85-884
α-helix92-10211
β-strand10412
β-strand106-10941
β-strand114-11523
β-strand118-11923
β-strand133-13531
β-strand140-149101
β-strand153-162101
β-strand168-17691
α-helix188-20013
β-strand20912
α-helix2101
β-strand211-21441
α-helix221-23818
α-helix241-2433
α-helix246-2538
α-helix264-28118
α-helix287-2959

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Tyrosine-protein phosphatase non-receptor type 1Aprotein321Homo sapiensP18031 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>6XEA_1 Tyrosine-protein phosphatase non-receptor type 1 (chains A)
MEMEKEFEQIDKSGSWAAIYQDIRHEASDFPCRVAKLPKNKNRNRYRDVSPFDHSRIKLH
QEDNDYINASLIKMEEAQRSYILTQGPLPNTCGHFWEMVWEQKSRGVVMLNRVMEKGSLK
CAQYWPQKEEKEMIFEDTNLKLTLISEDIKSYYTVRQLELENLTTQETREILHFHYGNWP
DQTAPESPASFLNFLFKVRESGSLSPEHGPVVVHCSAGIGRSGTFCLADTCLLLMDKRKD
PSSVDIKKVLLEMRKFRMGLIQTADQLRFSYLAVIEGAKFIMGDSSVQDQWKELSHEDLE
PPPEHIPPPPRPPKRILEPHN

Ligands and cofactors

IDNameFormulaCopies
VO4Vanadate ionO4 V1
BENBenzamidineC7 H8 N21
MGMagnesium ionMg1

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

Primary citation

Insights into the importance of WPD-loop sequence for activity and structure in protein tyrosine phosphatases. Shen, R., Crean, R.M., Olsen, K.J. et al. Chem Sci (2022) 13:13524-13540. DOI 10.1039/d2sc04135a · 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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