pVHL:EloB:EloC in complex with (4-(1H-pyrrol-1-yl)phenyl)methanol. Determined by X-ray diffraction at 1.75 Å resolution. Released 8 Aug 2018.
Explore 6GMR in 3D Show helices and sheets RCSB PDB PDBe
6GMR contains 20 α-helices and 31 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 | 2-9 | 8 | 1 |
| β-strand | 10 | 1 | 2 |
| β-strand | 12-19 | 8 | 1 |
| β-strand | 23 | 1 | 3 |
| α-helix | 24-35 | 12 | |
| α-helix | 39-41 | 3 | |
| β-strand | 42-46 | 5 | 1 |
| β-strand | 49-50 | 2 | 1 |
| α-helix | 51-52 | 2 | |
| β-strand | 56 | 1 | 3 |
| α-helix | 58-60 | 3 | |
| β-strand | 68 | 1 | 4 |
| β-strand | 71 | 1 | 4 |
| α-helix | 72 | 1 | |
| β-strand | 73-79 | 7 | 1 |
| β-strand | 80-81 | 2 | 5 |
| β-strand | 84-85 | 2 | 5 |
| α-helix | 86-88 | 3 | |
| β-strand | 90 | 1 | 2 |
| α-helix | 94-96 | 3 | |
| α-helix | 98-100 | 3 | |
| α-helix | 101-103 | 3 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 18-22 | 5 | 1 |
| β-strand | 28-32 | 5 | 1 |
| α-helix | 33-36 | 4 | |
| α-helix | 40-45 | 6 | |
| β-strand | 59-61 | 3 | 1 |
| α-helix | 67-83 | 17 | |
| α-helix | 89-92 | 4 | |
| α-helix | 97-110 | 14 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 565 | 1 | 6 |
| β-strand | 572-573 | 2 | 6 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 71-78 | 8 | 6 |
| α-helix | 83 | 1 | |
| β-strand | 84-89 | 6 | 7 |
| β-strand | 95-97 | 3 | 7 |
| β-strand | 101 | 1 | 7 |
| β-strand | 105-112 | 8 | 6 |
| β-strand | 116-121 | 6 | 7 |
| β-strand | 127 | 1 | 7 |
| β-strand | 129-130 | 2 | 6 |
| β-strand | 133 | 1 | 6 |
| β-strand | 136 | 1 | 7 |
| β-strand | 142 | 1 | 8 |
| β-strand | 145 | 1 | 8 |
| α-helix | 146 | 1 | |
| β-strand | 147-152 | 6 | 6 |
| α-helix | 158-169 | 12 | |
| α-helix | 172-177 | 6 | |
| α-helix | 183-189 | 7 | |
| α-helix | 194-207 | 14 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Elongin-B | B | protein | 118 | Homo sapiens | Q15370 (AlphaFold model) |
| Elongin-C | C | protein | 97 | Homo sapiens | Q15369 (AlphaFold model) |
| Hypoxia inducible factor 1alpha, residues 559-577 | H | protein | 19 | Homo sapiens | Q16665 (AlphaFold model) |
| von Hippel-Lindau disease tumor suppressor | V | protein | 163 | Homo sapiens | P40337 (AlphaFold model) |
>6GMR_1 Elongin-B (chains B) MDVFLMIRRHKTTIFTDAKESSTVFELKRIVEGILKRPPDEQRLYKDDQLLDDGKTLGEC GFTSQTARPQAPATVGLAFRADDTFEALCIEPFSSPPELPDVMKPQDSGSSANEQAVQ
>6GMR_2 Elongin-C (chains C) MMYVKLISSDGHEFIVKREHALTSGTIKAMLSGPGQFAENETNEVNFREIPSHVLSKVCM YFTYKVRYTNSSTEIPEFPIAPEIALELLMAANFLDC
>6GMR_3 Hypoxia inducible factor 1alpha, residues 559-577 (chains H) DEALAPYIPMDDDFQLRSF
>6GMR_4 von Hippel-Lindau disease tumor suppressor (chains V) GSHMEAGRPRPVLRSVNSREPSQVIFCNRSPRVVLPVWLNFDGEPQPYPTLPPGTGRRIH SYRGHLWLFRDAGTHDGLLVNQTELFVPSLNVDGQPIFANITLPVYTLKERCLQVVRSLV KPENYRRLDIVRSLYEDLEDHPNVQKDLERLTQERIAHQRMGD
| ID | Name | Formula | Copies |
|---|---|---|---|
| F4K | (4-pyrrol-1-ylphenyl)methanol | C11 H11 N O | 1 |
Water and common crystallization additives (SO4, GOL) are not listed.
Surface Probing by Fragment-Based Screening and Computational Methods Identifies Ligandable Pockets on the von Hippel-Lindau (VHL) E3 Ubiquitin Ligase. Lucas, X., Van Molle, I., Ciulli, A. J Med Chem (2018) 61:7387-7393. DOI 10.1021/acs.jmedchem.8b00842 · PubMed
Other PDB entries of the same protein (UniProt Q15370 (AlphaFold model), which also has an AlphaFold model), best resolution first:
MolViewer shows 6GMR directly in your browser with nothing to install. Switch between cartoon, ball-and-stick, spacefill and surface views, color by chain, secondary structure or B-factor, measure distances, angles and dihedrals, and share or embed the view.