Crystal structure of GSK-3/Axin complex bound to phosphorylated N-terminal auto-inhibitory pS9 peptide. Determined by X-ray diffraction at 2.1 Å resolution. Released 26 Mar 2014.
Explore 4NM3 in 3D Show helices and sheets RCSB PDB PDBe
4NM3 contains 22 α-helices and 13 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 |
|---|---|---|---|
| β-strand | 27-29 | 3 | 1 |
| β-strand | 37-44 | 8 | 1 |
| β-strand | 52-63 | 12 | 1 |
| β-strand | 69-75 | 7 | 1 |
| β-strand | 81-88 | 8 | 1 |
| α-helix | 97-101 | 5 | |
| β-strand | 109 | 1 | 2 |
| β-strand | 112-118 | 7 | 1 |
| β-strand | 127-133 | 7 | 1 |
| β-strand | 137-138 | 2 | 2 |
| α-helix | 139-148 | 10 | |
| α-helix | 155-173 | 19 | |
| β-strand | 177-178 | 2 | 3 |
| α-helix | 184-186 | 3 | |
| β-strand | 187-190 | 4 | 2 |
| β-strand | 195-198 | 4 | 2 |
| β-strand | 205-206 | 2 | 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 | 286-288 | 3 | |
| α-helix | 296-300 | 5 | |
| 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 | 338-344 | 7 | |
| α-helix | 354-356 | 3 | |
| α-helix | 371-373 | 3 | |
| α-helix | 374-377 | 4 | |
| α-helix | 380-383 | 4 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 385-400 | 16 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Glycogen synthase kinase-3 beta | A | protein | 389 | Homo sapiens | P49841 (AlphaFold model) |
| Axin-1 | B | protein | 24 | Homo sapiens | O15169 (AlphaFold model) |
>4NM3_1 Glycogen synthase kinase-3 beta (chains A) MSGRPRTTSFAESCKPVQQPSAFGSMKVSRDKDGSKVTTVVATPGQGPDRPQEVSYTDTK VIGNGSFGVVYQAKLCDSGELVAIKKVLQDKRFKNRELQIMRKLDHCNIVRLRYFFYSSG EKKDEVYLNLVLDYVPETVYRVARHYSRAKQTLPVIYVKLYMYQLFRSLAYIHSFGICHR DIKPQNLLLDPDTAVLKLCDFGSAKQLVRGEPNVSYICSRYYRAPELIFGATDYTSSIDV WSAGCVLAELLLGQPIFPGDSGVDQLVEIIKVLGTPTREQIREMNPNYTEFKFPQIKAHP WTKVFRPRTPPEAIALCSRLLEYTPTARLTPLEACAHSFFDELRDPNVKLPNGRDTPALF NFTTQELSSNPPLATILIPPHARHHHHHH
>4NM3_2 Axin-1 (chains B) GGILVEPQKFAEELIHRLEAVQRT
| ID | Name | Formula | Copies |
|---|---|---|---|
| MG | Magnesium ion | Mg | 2 |
| DTT | 2,3-dihydroxy-1,4-dithiobutane | C4 H10 O2 S2 | 1 |
| ADP | Adenosine-5'-diphosphate | C10 H15 N5 O10 P2 | 1 |
Water and common crystallization additives (GOL, CL) are not listed.
Structural basis of GSK-3 inhibition by N-terminal phosphorylation and by the Wnt receptor LRP6. Stamos, J.L., Chu, M.L., Enos, M.D. et al. Elife (2014) 3:e01998-e01998. 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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