7L9X: VPS4B

Structure of VPS4B in complex with an allele-specific covalent inhibitor. Determined by X-ray diffraction at 2.81 Å resolution. Released 14 Apr 2021.

Method
X-ray diffraction
Resolution
2.81 Å
Organism
Homo sapiens
Chains
1
Atoms
2,326
Mol. weight
50.04 kDa
Ligands
XQV
Released
14 Apr 2021

Explore 7L9X in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

7L9X contains 19 α-helices and 11 β-strands across 1 chain. 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 A: 19 helices, 11 β-strands

ElementResiduesLengthSheet
α-helix133-1353
α-helix140-1467
α-helix147-1515
α-helix152-1554
β-strand169-17351
α-helix180-19112
β-strand196-19941
α-helix214-22512
β-strand229-23351
α-helix236-2383
α-helix251-2544
α-helix257-2626
β-strand272-27871
α-helix286-2894
β-strand294-29741
α-helix299-3024
α-helix303-31210
β-strand31912
α-helix323-33210
α-helix338-35821
β-strand361-36883
β-strand376-38383
β-strand392-39323
α-helix396-3983
α-helix401-4033
β-strand40413
α-helix406-4083
β-strand40912
α-helix411-4188
α-helix427-43913

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Vacuolar protein sorting-associated protein 4BAprotein446Homo sapiensO75351 (AlphaFold model)
Sequence of entity 1 (A), FASTA
>7L9X_1 Vacuolar protein sorting-associated protein 4B (chains A)
SHMSSTSPNLQKAIDLASKAAQEDKAGNYEEALQLYQHAVQYFLHVVKYEAQGDKAKQSI
RAKCTEYLDRAEKLKEYLKNKEKKAQKPVKEGQPSPADEKGNDSDGEGESDDPEKKKLQN
QLQGAIVIERPNVKWSCVAGLEGAKEALKEAVILPIKFPHLFTGKRTPWRGILLFGPPGT
GKSYLAKAVATEANNSTFFSISSSDLVSKWLGESEKLVKNLFQLARENKPSIIFIDEIDS
LCGSRSENESEAARRIKTEFLVQMQGVGVDNDGILVLGATNIPWVLDSAIRRRFEKRIYI
PLPEPHARAAMFKLHLGTTQNSLTEADFRELGRKTDGYSGADISIIVRDALMQPVRKVQS
ATHFKKVRGPSRADPNHLVDDLLTPCSPGDPGAIEMTWMDVPGDKLLEPVVSMSDMLRSL
SNTKPTVNEHDLLKLKKFTEDFGQEG

Ligands and cofactors

IDNameFormulaCopies
XQVN-{3-[(8-phenyl[1,2,4]triazolo[1,5-a]pyridin-2-yl)amino]phenyl}propanamideC21 H19 N5 O1

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

Primary citation

A chemical genetics approach to examine the functions of AAA proteins. Cupido, T., Jones, N.H., Grasso, M.J. et al. Nat Struct Mol Biol (2021) 28:388-397. DOI 10.1038/s41594-021-00575-9 · PubMed

Other PDB entries of the same protein (UniProt O75351 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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