Identification of 2-(4-pyridyl)thienopyridinones as GSK-3beta inhibitors. Determined by X-ray diffraction at 2.48 Å resolution. Released 29 Jun 2011.
Explore 3ZRL in 3D Show helices and sheets RCSB PDB PDBe
3ZRL contains 49 α-helices and 24 β-strands across 4 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 |
|---|---|---|---|
| β-strand | 38-44 | 7 | 1 |
| β-strand | 52-65 | 14 | 1 |
| β-strand | 68-75 | 8 | 1 |
| β-strand | 81-89 | 9 | 1 |
| α-helix | 96-103 | 8 | |
| β-strand | 109 | 1 | 2 |
| β-strand | 112-118 | 7 | 1 |
| β-strand | 126-133 | 8 | 1 |
| β-strand | 137-138 | 2 | 2 |
| α-helix | 139-148 | 10 | |
| α-helix | 152-154 | 3 | |
| α-helix | 155-173 | 19 | |
| β-strand | 177-178 | 2 | 3 |
| α-helix | 184-186 | 3 | |
| β-strand | 187-189 | 3 | 2 |
| β-strand | 196-198 | 3 | 2 |
| β-strand | 205-206 | 2 | 3 |
| α-helix | 220-222 | 3 | |
| α-helix | 225-228 | 4 | |
| α-helix | 237-252 | 16 | |
| α-helix | 262-273 | 12 | |
| α-helix | 275-277 | 3 | |
| α-helix | 278-284 | 7 | |
| α-helix | 297-300 | 4 | |
| α-helix | 301-304 | 4 | |
| α-helix | 311-318 | 8 | |
| α-helix | 325-327 | 3 | |
| α-helix | 329-330 | 2 | |
| α-helix | 331-335 | 5 | |
| α-helix | 338-344 | 7 | |
| α-helix | 354-356 | 3 | |
| α-helix | 364-367 | 4 | |
| α-helix | 371-373 | 3 | |
| α-helix | 374-377 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 38-44 | 7 | 4 |
| β-strand | 52-65 | 14 | 4 |
| β-strand | 68-75 | 8 | 4 |
| β-strand | 81-88 | 8 | 4 |
| α-helix | 96-101 | 6 | |
| β-strand | 109 | 1 | 5 |
| β-strand | 112-119 | 8 | 4 |
| β-strand | 126-133 | 8 | 4 |
| β-strand | 137-138 | 2 | 5 |
| α-helix | 139-148 | 10 | |
| α-helix | 152-154 | 3 | |
| α-helix | 155-173 | 19 | |
| β-strand | 177-178 | 2 | 6 |
| α-helix | 184-186 | 3 | |
| β-strand | 187-189 | 3 | 5 |
| β-strand | 196-198 | 3 | 5 |
| β-strand | 205-206 | 2 | 6 |
| α-helix | 220-222 | 3 | |
| α-helix | 225-228 | 4 | |
| α-helix | 237-252 | 16 | |
| α-helix | 262-273 | 12 | |
| α-helix | 276-277 | 2 | |
| α-helix | 278-284 | 7 | |
| α-helix | 297-300 | 4 | |
| α-helix | 301-304 | 4 | |
| α-helix | 311-320 | 10 | |
| α-helix | 325-327 | 3 | |
| α-helix | 329-330 | 2 | |
| α-helix | 331-335 | 5 | |
| α-helix | 338-340 | 3 | |
| α-helix | 341-344 | 4 | |
| α-helix | 354-356 | 3 | |
| α-helix | 371-373 | 3 | |
| α-helix | 374-377 | 4 | |
| α-helix | 380-382 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 201-209 | 9 | |
| α-helix | 212-220 | 9 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 202-209 | 8 | |
| α-helix | 212-220 | 9 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Glycogen synthase kinase-3 beta | A, B | protein | 371 | HOMO SAPIENS | P49841 (AlphaFold model) |
| Proto-oncogene FRAT1 | X, Y | protein | 32 | HOMO SAPIENS | Q92837 (AlphaFold model) |
>3ZRL_1 GLYCOGEN SYNTHASE KINASE-3 BETA (chains A, B) FGSMKVSRDKDGSKVTTVVATPGQGPDRPQEVSYTDTKVIGNGSFGVVYQAKLCDSGELV AIKKVLQDKRFKNRELQIMRKLDHCNIVRLRYFFYSSGEKKDEVYLNLVLDYVPETVYRV ARHYSRAKQTLPVIYVKLYMYQLFRSLAYIHSFGICHRDIKPQNLLLDPDTAVLKLCDFG SAKQLVRGEPNVSYICSRYYRAPELIFGATDYTSSIDVWSAGCVLAELLLGQPIFPGDSG VDQLVEIIKVLGTPTREQIREMNPNYTEFKFPQIKAHPWTKVFRPRTPPEAIALCSRLLE YTPTARLTPLEACAHSFFDELRDPNVKLPNGRDTPALFNFTTQELSSNPPLATILIPPHA RIQAAASTPTN
>3ZRL_2 PROTO-ONCOGENE FRAT1 (chains X, Y) MADDPHRLLQQLVLSGNLIKEAVRRLHSRRLQ
| ID | Name | Formula | Copies |
|---|---|---|---|
| ZRL | 7-bromo-2-pyridin-4-yl-5H-THIENO[3,2-c]pyridin-4-one | C12 H7 Br N2 O S | 2 |
Water and common crystallization additives (GOL, SO4) are not listed.
Identification of 2-(4-Pyridyl)Thienopyridinones as Gsk-3Beta Inhibitors. Gentile, G., Bernasconi, G., Pozzan, A. et al. Bioorg Med Chem Lett (2011) 21:4823. DOI 10.1016/J.BMCL.2011.06.050 · PubMed
Other PDB entries of the same protein (UniProt P49841 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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