Ebola virus VP35 bound to small molecule. Determined by X-ray diffraction at 1.75 Å resolution. Released 26 Feb 2014.
Explore 4IBB in 3D Show helices and sheets RCSB PDB PDBe
4IBB contains 21 α-helices and 8 β-strands across 2 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 |
|---|---|---|---|
| α-helix | 221-229 | 9 | |
| α-helix | 238-252 | 15 | |
| α-helix | 256-268 | 13 | |
| α-helix | 273-283 | 11 | |
| α-helix | 285-287 | 3 | |
| α-helix | 290-293 | 4 | |
| β-strand | 294-297 | 4 | 1 |
| α-helix | 300-302 | 3 | |
| α-helix | 305-310 | 6 | |
| β-strand | 311-312 | 2 | 1 |
| α-helix | 313-315 | 3 | |
| α-helix | 320-322 | 3 | |
| β-strand | 324-330 | 7 | 1 |
| β-strand | 335-339 | 5 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 218-220 | 3 | |
| α-helix | 221-229 | 9 | |
| α-helix | 238-252 | 15 | |
| α-helix | 256-268 | 13 | |
| α-helix | 273-283 | 11 | |
| α-helix | 285-287 | 3 | |
| α-helix | 290-293 | 4 | |
| β-strand | 294-297 | 4 | 2 |
| α-helix | 300-302 | 3 | |
| α-helix | 305-310 | 6 | |
| β-strand | 311-312 | 2 | 2 |
| α-helix | 313-315 | 3 | |
| α-helix | 320-322 | 3 | |
| β-strand | 324-330 | 7 | 2 |
| β-strand | 335-339 | 5 | 2 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Polymerase cofactor VP35 | A, B | protein | 129 | Ebola virus | Q05127 (AlphaFold model) |
>4IBB_1 Polymerase cofactor VP35 (chains A, B) GHMGKPDISAKDLRNIMYDHLPGFGTAFHQLVQVICKLGKDSNSLDIIHAEFQASLAEGD SPQCALIQITKRVPIFQDAAPPVIHIRSRGDIPRACQKSLRPVPPSPKIDRGWVCVFQLQ DGKTLGLKI
| ID | Name | Formula | Copies |
|---|---|---|---|
| 1DK | {4-[(5R)-3-hydroxy-2-oxo-4-(thiophen-2-ylcarbonyl)-5-(2,4,5-trimethylphenyl)-2,… | C26 H23 N O5 S | 2 |
In Silico Derived Small Molecules Bind the Filovirus VP35 Protein and Inhibit Its Polymerase Cofactor Activity. Brown, C.S., Lee, M.S., Leung, D.W. et al. J Mol Biol (2014) 426:2045-2058. DOI 10.1016/j.jmb.2014.01.010 · PubMed
Other PDB entries of the same protein (UniProt Q05127 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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