6GMR: PVHL:EloB:EloC

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.

Method
X-ray diffraction
Resolution
1.75 Å
Organism
Homo sapiens
Chains
4
Atoms
3,249
Mol. weight
45.58 kDa
Ligands
F4K
Released
8 Aug 2018

Explore 6GMR in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

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.

Chain B: 9 helices, 13 β-strands

ElementResiduesLengthSheet
β-strand2-981
β-strand1012
β-strand12-1981
β-strand2313
α-helix24-3512
α-helix39-413
β-strand42-4651
β-strand49-5021
α-helix51-522
β-strand5613
α-helix58-603
β-strand6814
β-strand7114
α-helix721
β-strand73-7971
β-strand80-8125
β-strand84-8525
α-helix86-883
β-strand9012
α-helix94-963
α-helix98-1003
α-helix101-1033
Chain C: 5 helices, 3 β-strands
ElementResiduesLengthSheet
β-strand18-2251
β-strand28-3251
α-helix33-364
α-helix40-456
β-strand59-6131
α-helix67-8317
α-helix89-924
α-helix97-11014
Chain H: 0 helices, 2 β-strands
ElementResiduesLengthSheet
β-strand56516
β-strand572-57326
Chain V: 6 helices, 13 β-strands
ElementResiduesLengthSheet
β-strand71-7886
α-helix831
β-strand84-8967
β-strand95-9737
β-strand10117
β-strand105-11286
β-strand116-12167
β-strand12717
β-strand129-13026
β-strand13316
β-strand13617
β-strand14218
β-strand14518
α-helix1461
β-strand147-15266
α-helix158-16912
α-helix172-1776
α-helix183-1897
α-helix194-20714

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Elongin-BBprotein118Homo sapiensQ15370 (AlphaFold model)
Elongin-CCprotein97Homo sapiensQ15369 (AlphaFold model)
Hypoxia inducible factor 1alpha, residues 559-577Hprotein19Homo sapiensQ16665 (AlphaFold model)
von Hippel-Lindau disease tumor suppressorVprotein163Homo sapiensP40337 (AlphaFold model)
Sequence of entity 1 (B), FASTA
>6GMR_1 Elongin-B (chains B)
MDVFLMIRRHKTTIFTDAKESSTVFELKRIVEGILKRPPDEQRLYKDDQLLDDGKTLGEC
GFTSQTARPQAPATVGLAFRADDTFEALCIEPFSSPPELPDVMKPQDSGSSANEQAVQ
Sequence of entity 2 (C), FASTA
>6GMR_2 Elongin-C (chains C)
MMYVKLISSDGHEFIVKREHALTSGTIKAMLSGPGQFAENETNEVNFREIPSHVLSKVCM
YFTYKVRYTNSSTEIPEFPIAPEIALELLMAANFLDC
Sequence of entity 3 (H), FASTA
>6GMR_3 Hypoxia inducible factor 1alpha, residues 559-577 (chains H)
DEALAPYIPMDDDFQLRSF
Sequence of entity 4 (V), FASTA
>6GMR_4 von Hippel-Lindau disease tumor suppressor (chains V)
GSHMEAGRPRPVLRSVNSREPSQVIFCNRSPRVVLPVWLNFDGEPQPYPTLPPGTGRRIH
SYRGHLWLFRDAGTHDGLLVNQTELFVPSLNVDGQPIFANITLPVYTLKERCLQVVRSLV
KPENYRRLDIVRSLYEDLEDHPNVQKDLERLTQERIAHQRMGD

Ligands and cofactors

IDNameFormulaCopies
F4K(4-pyrrol-1-ylphenyl)methanolC11 H11 N O1

Water and common crystallization additives (SO4, GOL) are not listed.

Primary citation

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:

Browse structure collections

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