Crystal structure of 10E8v4 Fab in complex with an HIV-1 gp41 peptide. Determined by X-ray diffraction at 2.4 Å resolution. Released 20 Apr 2016.
Explore 5IQ9 in 3D Show helices and sheets RCSB PDB PDBe
5IQ9 contains 31 α-helices and 89 β-strands across 6 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 | 3-7 | 5 | 1 |
| β-strand | 10-12 | 3 | 2 |
| β-strand | 18-25 | 8 | 1 |
| β-strand | 33-39 | 7 | 2 |
| β-strand | 46-51 | 6 | 2 |
| α-helix | 52B-53 | 3 | |
| β-strand | 57-59 | 3 | 2 |
| β-strand | 67-72 | 6 | 1 |
| β-strand | 77-82 | 6 | 1 |
| α-helix | 84-86 | 3 | |
| β-strand | 88-98 | 11 | 2 |
| β-strand | 100I-103 | 7 | 2 |
| β-strand | 107-111 | 5 | 2 |
| β-strand | 117 | 1 | 3 |
| α-helix | 118-119 | 2 | |
| β-strand | 120-128 | 9 | 4 |
| β-strand | 136-145 | 10 | 4 |
| β-strand | 146 | 1 | 3 |
| β-strand | 151-154 | 4 | 5 |
| α-helix | 155-157 | 3 | |
| β-strand | 163-165 | 3 | 4 |
| α-helix | 166-168 | 3 | |
| β-strand | 169-170 | 2 | 4 |
| α-helix | 171 | 1 | |
| β-strand | 176-184 | 9 | 4 |
| α-helix | 186-188 | 3 | |
| β-strand | 194-200 | 7 | 5 |
| α-helix | 201-203 | 3 | |
| β-strand | 205-211 | 7 | 5 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 5-6 | 2 | 6 |
| β-strand | 9-14 | 5 | 7 |
| β-strand | 19-24 | 6 | 6 |
| α-helix | 26-29 | 4 | |
| β-strand | 34-38 | 5 | 7 |
| β-strand | 45-48 | 4 | 7 |
| β-strand | 49 | 1 | 8 |
| β-strand | 53 | 1 | 8 |
| β-strand | 62-67 | 6 | 6 |
| β-strand | 70-75 | 6 | 6 |
| α-helix | 80-82 | 3 | |
| β-strand | 84-91 | 8 | 7 |
| β-strand | 96-98 | 3 | 7 |
| β-strand | 102-107 | 6 | 7 |
| β-strand | 112 | 1 | 9 |
| α-helix | 113-114 | 2 | |
| β-strand | 115-119 | 5 | 10 |
| α-helix | 120-122 | 3 | |
| α-helix | 123-127 | 5 | |
| β-strand | 131-140 | 10 | 10 |
| β-strand | 141 | 1 | 9 |
| β-strand | 146-151 | 6 | 11 |
| β-strand | 154-155 | 2 | 11 |
| α-helix | 156 | 1 | |
| β-strand | 160-162 | 3 | 10 |
| α-helix | 163-165 | 3 | |
| β-strand | 166-167 | 2 | 10 |
| β-strand | 173-181 | 9 | 10 |
| α-helix | 183-188 | 6 | |
| β-strand | 192-198 | 7 | 11 |
| β-strand | 201-207 | 7 | 11 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 672-683 | 12 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 3-7 | 5 | 12 |
| β-strand | 10-12 | 3 | 13 |
| β-strand | 18-25 | 8 | 12 |
| β-strand | 33-39 | 7 | 13 |
| β-strand | 46-51 | 6 | 13 |
| α-helix | 52B-53 | 3 | |
| β-strand | 57-59 | 3 | 13 |
| β-strand | 67-72 | 6 | 12 |
| β-strand | 77-82 | 6 | 12 |
| α-helix | 84-86 | 3 | |
| β-strand | 88-98 | 11 | 13 |
| β-strand | 100I-103 | 7 | 13 |
| β-strand | 107-111 | 5 | 13 |
| β-strand | 117 | 1 | 14 |
| α-helix | 118-119 | 2 | |
| β-strand | 120-128 | 9 | 15 |
| β-strand | 136-145 | 10 | 15 |
| β-strand | 146 | 1 | 14 |
| β-strand | 151-154 | 4 | 16 |
| α-helix | 155-157 | 3 | |
| β-strand | 159 | 1 | 16 |
| β-strand | 163-165 | 3 | 15 |
| α-helix | 166-168 | 3 | |
| β-strand | 169-170 | 2 | 15 |
| β-strand | 176-184 | 9 | 15 |
| α-helix | 186-188 | 3 | |
| β-strand | 194-200 | 7 | 16 |
| β-strand | 205-211 | 7 | 16 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 5-6 | 2 | 17 |
| β-strand | 9-13 | 4 | 18 |
| β-strand | 19-24 | 6 | 17 |
| α-helix | 26-29 | 4 | |
| β-strand | 34-38 | 5 | 18 |
| β-strand | 45-48 | 4 | 18 |
| β-strand | 49 | 1 | 19 |
| β-strand | 53 | 1 | 19 |
| β-strand | 62-67 | 6 | 17 |
| β-strand | 70-75 | 6 | 17 |
| α-helix | 80-82 | 3 | |
| β-strand | 84-91 | 8 | 18 |
| β-strand | 96-98 | 3 | 18 |
| β-strand | 102-106 | 5 | 18 |
| β-strand | 112 | 1 | 20 |
| α-helix | 113-114 | 2 | |
| β-strand | 115-119 | 5 | 21 |
| α-helix | 120-122 | 3 | |
| α-helix | 123-127 | 5 | |
| β-strand | 131-140 | 10 | 21 |
| β-strand | 141 | 1 | 20 |
| β-strand | 146-151 | 6 | 22 |
| β-strand | 154-155 | 2 | 22 |
| α-helix | 156 | 1 | |
| β-strand | 160-162 | 3 | 21 |
| β-strand | 166-167 | 2 | 21 |
| β-strand | 173-181 | 9 | 21 |
| α-helix | 183-186 | 4 | |
| β-strand | 192-198 | 7 | 22 |
| β-strand | 201-207 | 7 | 22 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| 10E8v4 Heavy Chain | A, H | protein | 232 | Homo sapiens | P01857 (AlphaFold model) |
| 10E8v4 Light Chain | B, L | protein | 210 | Homo sapiens | P0DOY2 (AlphaFold model) |
| gp41 MPER peptide | C, P | protein | 33 | Human immunodeficiency virus 1 | Q1HSF8 |
>5IQ9_1 10E8v4 Heavy Chain (chains A, H) EVRLVESGGGLVKPGGSLRLSCSASGFDFDNAWMTWVRQPPGKGLEWVGRITGPGEGWSV DYAESVKGRFTISRDNTKNTLYLEMNNVRTEDTGYYFCARTGKYYDFWSGYPPGEEYFQD WGQGTLVIVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSG VHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPK
>5IQ9_2 10E8v4 Light Chain (chains B, L) SELTQDPAVSVALKQTVTITCRGDSLRSHYASWYQKKPGQAPVLLFYGKNNRPSGIPDRF SGSASGNRASLTITGAQAEDEADYYCSSRDKSGSRLSVFGGGTKLTVLSQPKAAPSVTLF PPSSEELQANKATLVCLISDFYPGAVTVAWKADSSPVKAGVETTTPSKQSNNKYAASSYL SLTPEQWKSHRSYSCQVTHEGSTVEKTVAP
>5IQ9_3 gp41 MPER peptide (chains C, P) RRRNEQELLELDKWASLWNWFDITNWLWYIRRR
Optimization of the Solubility of HIV-1-Neutralizing Antibody 10E8 through Somatic Variation and Structure-Based Design. Kwon, Y.D., Georgiev, I.S., Ofek, G. et al. J Virol (2016) 90:5899-5914. DOI 10.1128/JVI.03246-15 · PubMed
Other PDB entries of the same protein (UniProt P01857 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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