Hsp90b N-terminal domain in complex with 42C. Determined by X-ray diffraction at 1.82 Å resolution. Released 12 Apr 2023.
Explore 7ULJ in 3D Show helices and sheets RCSB PDB PDBe
7ULJ contains 40 α-helices and 32 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 | 12-16 | 5 | 1 |
| α-helix | 17-18 | 2 | |
| α-helix | 19-30 | 12 | |
| α-helix | 38-58 | 21 | |
| α-helix | 62-65 | 4 | |
| β-strand | 73-78 | 6 | 1 |
| β-strand | 83-88 | 6 | 1 |
| α-helix | 95-103 | 9 | |
| α-helix | 107-118 | 12 | |
| α-helix | 123-129 | 7 | |
| α-helix | 132-138 | 7 | |
| β-strand | 140-148 | 9 | 1 |
| β-strand | 155-159 | 5 | 1 |
| β-strand | 164-169 | 6 | 1 |
| β-strand | 178-185 | 8 | 1 |
| α-helix | 187-193 | 7 | |
| α-helix | 195-205 | 11 | |
| β-strand | 213-215 | 3 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 12-16 | 5 | 2 |
| α-helix | 17-18 | 2 | |
| α-helix | 19-30 | 12 | |
| α-helix | 38-60 | 23 | |
| α-helix | 62-65 | 4 | |
| β-strand | 73-78 | 6 | 2 |
| β-strand | 83-88 | 6 | 2 |
| α-helix | 95-103 | 9 | |
| α-helix | 106-118 | 13 | |
| α-helix | 123-129 | 7 | |
| α-helix | 132-138 | 7 | |
| β-strand | 140-148 | 9 | 2 |
| β-strand | 155-159 | 5 | 2 |
| β-strand | 164-169 | 6 | 2 |
| β-strand | 178-185 | 8 | 2 |
| α-helix | 187-193 | 7 | |
| α-helix | 195-205 | 11 | |
| β-strand | 213-215 | 3 | 2 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 12-16 | 5 | 3 |
| α-helix | 17-18 | 2 | |
| α-helix | 19-30 | 12 | |
| α-helix | 38-57 | 20 | |
| α-helix | 62-65 | 4 | |
| β-strand | 73-78 | 6 | 3 |
| β-strand | 83-88 | 6 | 3 |
| α-helix | 95-103 | 9 | |
| α-helix | 107-118 | 12 | |
| α-helix | 123-129 | 7 | |
| α-helix | 132-138 | 7 | |
| β-strand | 140-148 | 9 | 3 |
| β-strand | 155-159 | 5 | 3 |
| β-strand | 164-169 | 6 | 3 |
| β-strand | 178-185 | 8 | 3 |
| α-helix | 187-193 | 7 | |
| α-helix | 195-205 | 11 | |
| β-strand | 213-215 | 3 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 12-16 | 5 | 4 |
| α-helix | 17-18 | 2 | |
| α-helix | 19-30 | 12 | |
| α-helix | 38-60 | 23 | |
| α-helix | 62-65 | 4 | |
| β-strand | 73-78 | 6 | 4 |
| β-strand | 83-88 | 6 | 4 |
| α-helix | 95-103 | 9 | |
| α-helix | 107-118 | 12 | |
| α-helix | 123-129 | 7 | |
| α-helix | 132-138 | 7 | |
| β-strand | 140-148 | 9 | 4 |
| β-strand | 155-159 | 5 | 4 |
| β-strand | 164-169 | 6 | 4 |
| β-strand | 178-185 | 8 | 4 |
| α-helix | 187-193 | 7 | |
| α-helix | 195-205 | 11 | |
| β-strand | 213-215 | 3 | 4 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Heat shock protein HSP 90-beta | A, B, C, D | protein | 221 | Homo sapiens | P08238 (AlphaFold model) |
>7ULJ_1 Heat shock protein HSP 90-beta (chains A, B, C, D) GSHMPEEVHHGEEEVETFAFQAEIAQLMSLIINTFYSNKEIFLRELISNASDALDKIRYE SLTDPSKLDSGKELKIDIIPNPQERTLTLVDTGIGMTKADLINNLGTIAKSGTKAFMEAL QAGADISMIGQFGVGFYSAYLVAEKVVVITKHNDDEQYAWESSAGGSFTVRADHGEPIGR GTKVILHLKEDQTEYLEERRVKEVVKKHSQFIGYPITLYLE
| ID | Name | Formula | Copies |
|---|---|---|---|
| 42C | N,N-dimethyl-7H-purin-6-amine | C7 H9 N5 | 4 |
Water and common crystallization additives (GOL, MPD) are not listed.
Pan-HSP90 ligand binding reveals isoform-specific differences in plasticity and water networks. Stachowski, T.R., Nithianantham, S., Vanarotti, M. et al. Protein Sci (2023) 32:e4629-e4629. DOI 10.1002/pro.4629 · PubMed
Other PDB entries of the same protein (UniProt P08238 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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