BAFF in complex with belimumab. Determined by X-ray diffraction at 2.05 Å resolution. Released 21 Feb 2018.
Explore 5Y9J in 3D Show helices and sheets RCSB PDB PDBe
5Y9J contains 17 α-helices and 58 β-strands across 3 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 | 146-151 | 6 | 12 |
| β-strand | 158-160 | 3 | 13 |
| β-strand | 163-165 | 3 | 13 |
| β-strand | 168-174 | 7 | 12 |
| β-strand | 178-181 | 4 | 14 |
| β-strand | 184-187 | 4 | 14 |
| β-strand | 191-201 | 11 | 12 |
| β-strand | 207-215 | 9 | 14 |
| β-strand | 226-235 | 10 | 14 |
| β-strand | 243-253 | 11 | 12 |
| β-strand | 258-262 | 5 | 14 |
| β-strand | 263 | 1 | 13 |
| β-strand | 270 | 1 | 12 |
| β-strand | 278-283 | 6 | 12 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 4-6 | 3 | 7 |
| α-helix | 7-9 | 3 | |
| β-strand | 10-12 | 3 | 8 |
| β-strand | 18-24 | 7 | 7 |
| β-strand | 33-39 | 7 | 8 |
| β-strand | 45-51 | 7 | 8 |
| β-strand | 59-60 | 2 | 8 |
| β-strand | 68-73 | 6 | 7 |
| α-helix | 74-76 | 3 | |
| β-strand | 78-83 | 6 | 7 |
| α-helix | 88-90 | 3 | |
| β-strand | 92-99 | 8 | 8 |
| β-strand | 113 | 1 | 8 |
| β-strand | 117-121 | 5 | 8 |
| α-helix | 125-126 | 2 | |
| β-strand | 127 | 1 | 9 |
| α-helix | 128-129 | 2 | |
| β-strand | 130-134 | 5 | 10 |
| β-strand | 145-155 | 11 | 10 |
| β-strand | 156 | 1 | 9 |
| β-strand | 161-164 | 4 | 11 |
| α-helix | 165-167 | 3 | |
| β-strand | 173-175 | 3 | 10 |
| α-helix | 176-178 | 3 | |
| β-strand | 179-180 | 2 | 10 |
| β-strand | 186-195 | 10 | 10 |
| α-helix | 196-198 | 3 | |
| β-strand | 205-210 | 6 | 11 |
| α-helix | 211-213 | 3 | |
| β-strand | 215-220 | 6 | 11 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 5-6 | 2 | 1 |
| β-strand | 9-13 | 5 | 2 |
| β-strand | 18-23 | 6 | 1 |
| α-helix | 25-28 | 4 | |
| β-strand | 33-37 | 5 | 2 |
| β-strand | 44-47 | 4 | 2 |
| β-strand | 48 | 1 | 3 |
| β-strand | 52 | 1 | 3 |
| β-strand | 61-66 | 6 | 1 |
| β-strand | 69-74 | 6 | 1 |
| α-helix | 79-81 | 3 | |
| β-strand | 83-89 | 7 | 2 |
| β-strand | 98-99 | 2 | 2 |
| β-strand | 103-108 | 6 | 2 |
| α-helix | 110-112 | 3 | |
| β-strand | 113 | 1 | 4 |
| α-helix | 114-115 | 2 | |
| β-strand | 116-120 | 5 | 5 |
| α-helix | 121-123 | 3 | |
| α-helix | 124-128 | 5 | |
| β-strand | 132-141 | 10 | 5 |
| β-strand | 142 | 1 | 4 |
| β-strand | 147-152 | 6 | 6 |
| β-strand | 155-157 | 3 | 6 |
| β-strand | 161-163 | 3 | 5 |
| α-helix | 164-166 | 3 | |
| β-strand | 167-168 | 2 | 5 |
| β-strand | 174-182 | 9 | 5 |
| α-helix | 184-189 | 6 | |
| β-strand | 193-199 | 7 | 6 |
| β-strand | 202-208 | 7 | 6 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| belibumab light chain | L | protein | 214 | Homo sapiens | |
| belimumab heavy chain | H | protein | 235 | Homo sapiens | |
| Tumor necrosis factor ligand superfamily member 13B | A | protein | 152 | Homo sapiens | Q9Y275 (AlphaFold model) |
>5Y9J_1 belibumab light chain (chains L) SSELTQDPAVSVALGQTVRVTCQGDSLRSYYASWYQQKPGQAPVLVIYGKNNRPSGIPDR FSGSSSGNTASLTITGAQAEDEADYYCSSRDSSGNHWVFGGGTELTVLGQPKAAPSVTLF PPSSEELQANKATLVCLISDFYPGAVTVAWKADSSPVKAGVETTTPSKQSNNKYAASSYL SLTPEQWKSHRSYSCQVTHEGSTVEKTVAPTECS
>5Y9J_2 belimumab heavy chain (chains H) QVQLQQSGAEVKKPGSSVRVSCKASGGTFNNNAINWVRQAPGQGLEWMGGIIPMFGTAKY SQNFQGRVAITADESTGTASMELSSLRSEDTAVYYCARSRDLLLFPHHALSPWGRGTMVT VSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVL QSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTHHHHHH
>5Y9J_3 Tumor necrosis factor ligand superfamily member 13B (chains A) AVQGPEETVTQDCLQLIADSETPTIQKGSYTFVPWLLSFKRGSALEEKENKILVKETGYF FIYGQVLYTDKTYAMGHLIQRKKVHVFGDELSLVTLFRCIQNMPETLPNNSCYSAGIAKL EEGDELQLAIPRENAQISLDGDVTFFGALKLL
BAFF-neutralizing interaction of belimumab related to its therapeutic efficacy for treating systemic lupus erythematosus. Shin, W., Lee, H.T., Lim, H. et al. Nat Commun (2018) 9:1200-1200. DOI 10.1038/s41467-018-03620-2 · PubMed
Other PDB entries of the same protein (UniProt Q9Y275 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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