Crystal structure of 4E10 modified with pyrene acetamide. Determined by X-ray diffraction at 1.45 Å resolution. Released 11 Aug 2021.
Explore 7EKB in 3D Show helices and sheets RCSB PDB PDBe
7EKB contains 19 α-helices and 44 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 | 3-6 | 4 | 1 |
| α-helix | 7-9 | 3 | |
| β-strand | 10-12 | 3 | 2 |
| β-strand | 18-25 | 8 | 1 |
| β-strand | 34-39 | 6 | 2 |
| β-strand | 45-52 | 8 | 2 |
| β-strand | 56-59 | 4 | 2 |
| α-helix | 61-63 | 3 | |
| β-strand | 67-72 | 6 | 1 |
| β-strand | 77-82 | 6 | 1 |
| α-helix | 84-86 | 3 | |
| β-strand | 88-97 | 10 | 2 |
| β-strand | 100F-103 | 8 | 2 |
| β-strand | 107-111 | 5 | 2 |
| β-strand | 117 | 1 | 3 |
| α-helix | 118-119 | 2 | |
| β-strand | 120-124 | 5 | 4 |
| β-strand | 137-147 | 11 | 4 |
| β-strand | 148 | 1 | 3 |
| β-strand | 153-157 | 4 | 5 |
| α-helix | 162-164 | 3 | |
| β-strand | 166 | 1 | 5 |
| β-strand | 171-173 | 3 | 4 |
| α-helix | 174-176 | 3 | |
| β-strand | 177-178 | 2 | 4 |
| β-strand | 185-194 | 10 | 4 |
| α-helix | 195-197 | 3 | |
| β-strand | 207-212 | 6 | 5 |
| α-helix | 213-215 | 3 | |
| β-strand | 217-222 | 6 | 5 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 4-5 | 2 | 6 |
| β-strand | 10-13 | 4 | 7 |
| β-strand | 19-25 | 7 | 6 |
| α-helix | 27A-28 | 2 | |
| α-helix | 29-31 | 3 | |
| β-strand | 33-38 | 6 | 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 | 85-90 | 6 | 7 |
| β-strand | 97-98 | 2 | 7 |
| β-strand | 102-106 | 5 | 7 |
| β-strand | 111 | 1 | 9 |
| α-helix | 112-113 | 2 | |
| β-strand | 114-118 | 5 | 10 |
| α-helix | 119-121 | 3 | |
| α-helix | 122-125 | 4 | |
| β-strand | 129-139 | 11 | 10 |
| β-strand | 140 | 1 | 9 |
| β-strand | 145-150 | 6 | 11 |
| β-strand | 153-154 | 2 | 11 |
| α-helix | 155 | 1 | |
| β-strand | 159-163 | 5 | 10 |
| α-helix | 164-167 | 4 | |
| β-strand | 173-182 | 10 | 10 |
| α-helix | 183-186 | 4 | |
| β-strand | 191-197 | 7 | 11 |
| β-strand | 205-210 | 6 | 11 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| α-helix | 672-674 | 3 | |
| α-helix | 675-684 | 10 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Fab region of the heavy chain of broadly neutralizing antibody anti-HIV-1 4E10 | H | protein | 228 | Homo sapiens | |
| Fab region of the light chain of the broadly neutralizing anti-HIV-1 antibody 4E10 | L | protein | 214 | Homo sapiens | |
| MPER region of the HIV-1 envelope glycoprotein protein gp41 | P | protein | 16 | Human immunodeficiency virus 1 | P04578 (AlphaFold model) |
>7EKB_1 Fab region of the heavy chain of broadly neutralizing antibody anti-HIV-1 4E10 (chains H) QVQLVQSGAEVKRPGSSVTVSCKASGGSFSTYALSWVRQAPGRGLEWMGGVIPLLTITNY APRFQGRITITADRSTSTAYLELNSLRPEDTAVYYCAREGTTGWGCLGKPIGAFAHWGQG TLVTVSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTF PAVLQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPK
>7EKB_2 Fab region of the light chain of the broadly neutralizing anti-HIV-1 antibody 4E10 (chains L) EIVLTQSPGTQSLSPGERATLSCRASQSVGNNKLAWYQQRPGQAPRLLIYGASSRPSGVA DRFSGSGSGTDFTLTISRLEPEDFAVYYCQQYGQSLSTFGQGTKVEVKRTVAAPSVFIFP PSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLSSTL TLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGE
>7EKB_3 MPER region of the HIV-1 envelope glycoprotein protein gp41 (chains P) NWFDITNWLWYIKKKK
Focal accumulation of aromaticity at the CDRH3 loop mitigates 4E10 polyreactivity without altering its HIV neutralization profile. Rujas, E., Leaman, D.P., Insausti, S. et al. iScience (2021) 24:102987-102987. DOI 10.1016/j.isci.2021.102987 · PubMed
Other PDB entries of the same protein (UniProt P04578 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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