6VKD: Inhibitor JNJ-36689282

Crystal Structure of Inhibitor JNJ-36689282 in Complex with Prefusion RSV F Glycoprotein. Determined by X-ray diffraction at 2.5 Å resolution. Released 27 May 2020.

Method
X-ray diffraction
Resolution
2.5 Å
Organisms
Human respiratory syncytial virus, Human immunodeficiency virus 1
Chains
1
Atoms
3,558
Mol. weight
64.26 kDa
Ligands
R0P
Released
27 May 2020

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

Secondary structure: helices and β-sheets

6VKD contains 19 α-helices and 24 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 F: 19 helices, 24 β-strands

ElementResiduesLengthSheet
β-strand29-3351
β-strand38-60231
α-helix74-9623
α-helix139-1413
α-helix149-15810
α-helix163-1708
β-strand176-18051
β-strand186-19491
α-helix195-1984
α-helix199-2035
α-helix204-2085
α-helix217-23923
β-strand243-24421
α-helix254-26310
α-helix268-2758
α-helix278-2836
β-strand286-29381
β-strand296-318231
β-strand321-32222
β-strand333-33642
β-strand340-34561
β-strand348-35251
α-helix355-3573
β-strand359-36131
β-strand364-36851
α-helix369-3713
β-strand373-37531
α-helix377-3804
α-helix381-3844
β-strand394-39852
β-strand404-40743
β-strand411-41663
β-strand422-42654
β-strand430-43454
α-helix435-4362
β-strand438-44363
β-strand449-45244
β-strand455-45844
α-helix459-4602
β-strand465-46951
α-helix474-4774
β-strand487-49152
α-helix492-50413

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Prefusion RSV F (DS-Cav1)Fprotein568Human respiratory syncytial virus, Human immunodeficiency virus 1M1E1E4 (AlphaFold model), P03420
Sequence of entity 1 (F), FASTA
>6VKD_1 Prefusion RSV F (DS-Cav1) (chains F)
MELLILKANAITTILTAVTFCFASGQNITEEFYQSTCSAVSKGYLSALRTGWYTSVITIE
LSNIKENKCNGTDAKVKLIKQELDKYKNAVTELQLLMQSTPATNNRARRELPRFMNYTLN
NAKKTNVTLSKKRKRRFLGFLLGVGSAIASGVAVCKVLHLEGEVNKIKSALLSTNKAVVS
LSNGVSVLTFKVLDLKNYIDKQLLPILNKQSCSISNIETVIEFQQKNNRLLEITREFSVN
AGVTTPVSTYMLTNSELLSLINDMPITNDQKKLMSNNVQIVRQQSYSIMCIIKEEVLAYV
VQLPLYGVIDTPCWKLHTSPLCTTNTKEGSNICLTRTDRGWYCDNAGSVSFFPQAETCKV
QSNRVFCDTMNSLTLPSEVNLCNVDIFNPKYDCKIMTSKTDVSSSVITSLGAIVSCYGKT
KCTASNKNRGIIKTFSNGCDYVSNKGVDTVSVGNTLYYVNKQEGKSLYVKGEPIINFYDP
LVFPSDEFDASISQVNEKINQSLAFIRKSDELLSAIGGYIPEAPRDGQAYVRKDGEWVLL
STFLGGLVPRGSHHHHHHSAWSHPQFEK

Ligands and cofactors

IDNameFormulaCopies
R0P1-cyclopropyl-3-({1-[3-(methylsulfonyl)propyl]-1H-pyrrolo[3,2-c]pyridin-2-yl}me…C21 H23 N5 O3 S1

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

Primary citation

Discovery of 3-({5-Chloro-1-[3-(methylsulfonyl)propyl]-1H-indol-2-yl}methyl)-1-(2,2,2-trifluoroethyl)-1,3-dihydro-2H-imidazo[4,5-c]pyridin-2-one (JNJ-53718678), a Potent and Orally Bioavailable Fusion Inhibitor of Respiratory Syncytial Virus. Vendeville, S., Tahri, A., Hu, L. et al. J Med Chem (2020) 63:8046-8058. DOI 10.1021/acs.jmedchem.0c00226 · PubMed

Other PDB entries of the same protein (UniProt M1E1E4 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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