Wildtype PTP1b in complex with DES5743. Determined by X-ray diffraction at 1.53 Å resolution. Released 26 Apr 2023.
Explore 8G69 in 3D Show helices and sheets RCSB PDB PDBe
8G69 contains 25 α-helices and 26 β-strands across 2 chains. 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.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 3-13 | 11 | |
| α-helix | 16-26 | 11 | |
| α-helix | 38-43 | 6 | |
| β-strand | 56-58 | 3 | 1 |
| α-helix | 59 | 1 | |
| β-strand | 66-74 | 9 | 1 |
| β-strand | 79-84 | 6 | 1 |
| α-helix | 85-88 | 4 | |
| α-helix | 92-102 | 11 | |
| β-strand | 104 | 1 | 2 |
| β-strand | 106-109 | 4 | 1 |
| β-strand | 114-115 | 2 | 3 |
| β-strand | 118-119 | 2 | 3 |
| β-strand | 133-135 | 3 | 1 |
| β-strand | 140-149 | 10 | 1 |
| β-strand | 153-162 | 10 | 1 |
| β-strand | 168-176 | 9 | 1 |
| α-helix | 189-200 | 12 | |
| β-strand | 209 | 1 | 2 |
| α-helix | 210 | 1 | |
| β-strand | 211-214 | 4 | 1 |
| α-helix | 221-237 | 17 | |
| α-helix | 241-243 | 3 | |
| α-helix | 246-254 | 9 | |
| α-helix | 264-281 | 18 | |
| α-helix | 285-288 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 2-13 | 12 | |
| α-helix | 16-26 | 11 | |
| α-helix | 38-43 | 6 | |
| β-strand | 56-58 | 3 | 4 |
| α-helix | 59 | 1 | |
| β-strand | 66-74 | 9 | 4 |
| β-strand | 79-84 | 6 | 4 |
| α-helix | 85-88 | 4 | |
| α-helix | 92-102 | 11 | |
| β-strand | 104 | 1 | 5 |
| β-strand | 106-109 | 4 | 4 |
| β-strand | 114-115 | 2 | 6 |
| β-strand | 118-119 | 2 | 6 |
| β-strand | 133-135 | 3 | 4 |
| β-strand | 140-149 | 10 | 4 |
| β-strand | 153-162 | 10 | 4 |
| β-strand | 168-176 | 9 | 4 |
| α-helix | 189-200 | 12 | |
| β-strand | 209 | 1 | 5 |
| α-helix | 210 | 1 | |
| β-strand | 211-214 | 4 | 4 |
| α-helix | 221-237 | 17 | |
| α-helix | 241-243 | 3 | |
| α-helix | 246-253 | 8 | |
| α-helix | 264-281 | 18 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Tyrosine-protein phosphatase non-receptor type 1 | A, B | protein | 298 | Homo sapiens | P18031 (AlphaFold model) |
>8G69_1 Tyrosine-protein phosphatase non-receptor type 1 (chains A, B) MEMEKEFEQIDKSGSWAAIYQDIRHEASDFPCRVAKLPKNKNRNRYRDVSPFDHSRIKLH QEDNDYINASLIKMEEAQRSYILTQGPLPNTCGHFWEMVWEQKSRGVVMLNRVMEKGSLK CAQYWPQKEEKEMIFEDTNLKLTLISEDIKSYYTVRQLELENLTTQETREILHFHYTTWP DFGVPESPASFLNFLFKVRESGSLSPEHGPVVVHCSAGIGRSGTFCLADTCLLLMDKRKD PSSVDIKKVLLEMRKFRMGLIQTADQLRFSYLAVIEGAKFIMGDSSVQDQWKELSHED
Water and common crystallization additives (MPD) are not listed.
Discovery and Validation of the Binding Poses of Allosteric Fragment Hits to Protein Tyrosine Phosphatase 1b: From Molecular Dynamics Simulations to X-ray Crystallography. Greisman, J.B., Willmore, L., Yeh, C.Y. et al. J Chem Inf Model (2023) 63:2644-2650. DOI 10.1021/acs.jcim.3c00236 · PubMed
Other PDB entries of the same protein (UniProt P18031 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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