Structure of Unliganded Hsp90-Beta N-Terminal Domain. Determined by X-ray diffraction at 3.09 Å resolution. Released 3 Jul 2019.
Explore 6N8W in 3D Show helices and sheets RCSB PDB PDBe
6N8W contains 40 α-helices and 34 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 | 1-6 | 6 | 1 |
| β-strand | 13-16 | 4 | 2 |
| α-helix | 19-30 | 12 | |
| α-helix | 38-56 | 19 | |
| α-helix | 57-59 | 3 | |
| α-helix | 62-65 | 4 | |
| β-strand | 73-78 | 6 | 2 |
| β-strand | 83-88 | 6 | 2 |
| α-helix | 95-103 | 9 | |
| α-helix | 107-117 | 11 | |
| α-helix | 123-129 | 7 | |
| α-helix | 132-138 | 7 | |
| β-strand | 140-148 | 9 | 2 |
| β-strand | 154-159 | 6 | 2 |
| β-strand | 164-169 | 6 | 2 |
| β-strand | 178-185 | 8 | 2 |
| α-helix | 190-193 | 4 | |
| α-helix | 195-204 | 10 | |
| β-strand | 213-215 | 3 | 2 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 12-14 | 3 | 3 |
| α-helix | 19-28 | 10 | |
| α-helix | 38-56 | 19 | |
| α-helix | 62-65 | 4 | |
| β-strand | 73-78 | 6 | 3 |
| β-strand | 83-88 | 6 | 3 |
| α-helix | 95-103 | 9 | |
| α-helix | 107-117 | 11 | |
| α-helix | 123-129 | 7 | |
| α-helix | 134-138 | 5 | |
| β-strand | 140-148 | 9 | 3 |
| β-strand | 154-159 | 6 | 3 |
| β-strand | 166-169 | 4 | 3 |
| β-strand | 178-185 | 8 | 3 |
| α-helix | 191-193 | 3 | |
| α-helix | 195-204 | 10 | |
| β-strand | 213-217 | 5 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 12-16 | 5 | 1 |
| α-helix | 19-30 | 12 | |
| α-helix | 38-57 | 20 | |
| α-helix | 62-66 | 5 | |
| β-strand | 73-76 | 4 | 1 |
| β-strand | 85-88 | 4 | 1 |
| α-helix | 95-99 | 5 | |
| α-helix | 100-104 | 5 | |
| α-helix | 108-117 | 10 | |
| α-helix | 123-125 | 3 | |
| α-helix | 127-129 | 3 | |
| α-helix | 132-138 | 7 | |
| β-strand | 140-148 | 9 | 1 |
| β-strand | 154-159 | 6 | 1 |
| β-strand | 164-168 | 5 | 1 |
| β-strand | 178-185 | 8 | 1 |
| α-helix | 190-193 | 4 | |
| α-helix | 195-204 | 10 | |
| β-strand | 213-217 | 5 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 1-6 | 6 | 3 |
| β-strand | 13-16 | 4 | 4 |
| α-helix | 19-30 | 12 | |
| α-helix | 38-59 | 22 | |
| α-helix | 62-65 | 4 | |
| β-strand | 73-78 | 6 | 4 |
| β-strand | 83-88 | 6 | 4 |
| α-helix | 95-100 | 6 | |
| α-helix | 101-105 | 5 | |
| α-helix | 107-117 | 11 | |
| α-helix | 123-129 | 7 | |
| α-helix | 132-138 | 7 | |
| β-strand | 140-148 | 9 | 4 |
| β-strand | 154-159 | 6 | 4 |
| β-strand | 164-168 | 5 | 4 |
| β-strand | 178-185 | 8 | 4 |
| α-helix | 190-193 | 4 | |
| α-helix | 195-204 | 10 | |
| β-strand | 213-215 | 3 | 4 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Heat shock protein HSP 90-beta | A, B, C, D | protein | 251 | Homo sapiens | P08238 (AlphaFold model) |
>6N8W_1 Heat shock protein HSP 90-beta (chains A, B, C, D) MGSSHHHHHHSSGLVPRGSHMPEEVHHGEEEVETFAFQAEIAQLMSLIINTFYSNKEIFL RELISNASDALDKIRYESLTDPSKLDSGKELKIDIIPNPQERTLTLVDTGIGMTKADLIN NLGTIAKSGTKAFMEALQAGADISMIGQFGVGFYSAYLVAEKVVVITKHNDDEQYAWESS AGGSFTVRADHGEPIGRGTKVILHLKEDQTEYLEERRVKEVVKKHSQFIGYPITLYLEKE REKEISDDEAE
Structures of Hsp90 alpha and Hsp90 beta bound to a purine-scaffold inhibitor reveal an exploitable residue for drug selectivity. Huck, J.D., Que, N.L.S., Sharma, S. et al. Proteins (2019) 87:869-877. DOI 10.1002/prot.25750 · 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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