8SR0: Therapeutic antibody
CryoEM structure of a therapeutic antibody (favezelimab) bound to human LAG3 local refined. Determined by electron microscopy at 3.53 Å resolution. Released 6 Sept 2023.
- Method
- Electron microscopy
- Resolution
- 3.53 Å
- Organisms
- Homo sapiens, Mus musculus
- Chains
- 6
- Atoms
- 5,988
- Mol. weight
- 221.78 kDa
- Ligands
- NAG
- Released
- 6 Sept 2023
Explore 8SR0 in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
8SR0 contains 10 α-helices and 84 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.
Chain D: 3 helices, 14 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 30 | 1 | |
| β-strand | 31 | 1 | 18 |
| β-strand | 40-42 | 3 | 19 |
| β-strand | 63-66 | 4 | 18 |
| β-strand | 100 | 1 | 18 |
| β-strand | 134-136 | 3 | 19 |
| α-helix | 141-143 | 3 | |
| β-strand | 146-149 | 4 | 18 |
| β-strand | 162-163 | 2 | 18 |
| β-strand | 171-173 | 3 | 20 |
| β-strand | 185-189 | 5 | 20 |
| α-helix | 196-197 | 2 | |
| β-strand | 199-202 | 4 | 21 |
| β-strand | 220-221 | 2 | 20 |
| β-strand | 226-228 | 3 | 20 |
| β-strand | 238-244 | 7 | 21 |
| β-strand | 251-256 | 6 | 21 |
Chain H: 0 helices, 10 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3-5 | 3 | 22 |
| β-strand | 20-25 | 6 | 22 |
| β-strand | 33-39 | 7 | 23 |
| β-strand | 45-51 | 7 | 23 |
| β-strand | 58-60 | 3 | 23 |
| β-strand | 70-73 | 4 | 22 |
| β-strand | 78-81 | 4 | 22 |
| β-strand | 93-100 | 8 | 23 |
| β-strand | 105-109 | 5 | 23 |
| β-strand | 114 | 1 | 23 |
Chain L: 2 helices, 12 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 5-7 | 3 | 24 |
| β-strand | 10-11 | 2 | 25 |
| β-strand | 19-20 | 2 | 26 |
| β-strand | 22-24 | 3 | 24 |
| β-strand | 37-42 | 6 | 25 |
| β-strand | 49-53 | 5 | 25 |
| β-strand | 57-58 | 2 | 25 |
| α-helix | 59 | 1 | |
| α-helix | 64-66 | 3 | |
| β-strand | 74 | 1 | 24 |
| β-strand | 78-79 | 2 | 26 |
| β-strand | 89-94 | 6 | 25 |
| β-strand | 101 | 1 | 25 |
| β-strand | 106-108 | 3 | 25 |
Chain X: 2 helices, 18 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 34-35 | 2 | 1 |
| β-strand | 40-43 | 4 | 2 |
| β-strand | 62-65 | 4 | 3 |
| β-strand | 99-102 | 4 | 3 |
| β-strand | 133-136 | 4 | 2 |
| β-strand | 147-150 | 4 | 3 |
| β-strand | 166-167 | 2 | 1 |
| β-strand | 171 | 1 | 4 |
| β-strand | 185-186 | 2 | 5 |
| β-strand | 189 | 1 | 4 |
| α-helix | 196-197 | 2 | |
| β-strand | 199-203 | 5 | 6 |
| β-strand | 212 | 1 | 6 |
| β-strand | 220-221 | 2 | 5 |
| β-strand | 226-228 | 3 | 5 |
| α-helix | 233-235 | 3 | |
| β-strand | 238 | 1 | 7 |
| β-strand | 240-244 | 5 | 6 |
| β-strand | 250-253 | 4 | 6 |
| β-strand | 256 | 1 | 7 |
Chain Y: 1 helix, 14 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3-4 | 2 | 8 |
| α-helix | 7-9 | 3 | |
| β-strand | 12 | 1 | 9 |
| β-strand | 18-21 | 4 | 10 |
| β-strand | 24-25 | 2 | 8 |
| β-strand | 34-39 | 6 | 11 |
| β-strand | 46-51 | 6 | 11 |
| β-strand | 58 | 1 | 11 |
| β-strand | 68-73 | 6 | 10 |
| β-strand | 78-83 | 6 | 10 |
| β-strand | 92-98 | 7 | 11 |
| β-strand | 108 | 1 | 11 |
| β-strand | 110 | 1 | 8 |
| β-strand | 113-115 | 3 | 11 |
| β-strand | 117 | 1 | 9 |
Chain Z: 2 helices, 16 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 5-7 | 3 | 12 |
| β-strand | 10-11 | 2 | 13 |
| β-strand | 19-20 | 2 | 14 |
| β-strand | 22-24 | 3 | 12 |
| β-strand | 38-42 | 5 | 15 |
| α-helix | 47-48 | 2 | |
| β-strand | 49-50 | 2 | 15 |
| β-strand | 52-53 | 2 | 16 |
| β-strand | 57-58 | 2 | 16 |
| α-helix | 59 | 1 | |
| β-strand | 67 | 1 | 14 |
| β-strand | 71 | 1 | 12 |
| β-strand | 74 | 1 | 12 |
| β-strand | 78-79 | 2 | 14 |
| β-strand | 89-93 | 5 | 15 |
| β-strand | 94 | 1 | 17 |
| β-strand | 101 | 1 | 17 |
| β-strand | 107-108 | 2 | 13 |
Molecules and chains
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|
| Lymphocyte activation gene 3 protein | D, X | protein | 525 | Homo sapiens | P18627 (AlphaFold model) |
| favezelimab Fab heavy chain | H, Y | protein | 252 | Mus musculus | |
| favezelimab Fab light chain | L, Z | protein | 238 | Mus musculus | |
Sequence of entity 1 (D, X), FASTA
>8SR0_1 Lymphocyte activation gene 3 protein (chains D, X)
MWEAQFLGLLFLQPLWVAPVKPLQPGAEVPVVWAQEGAPAQLPCSPTIPLQDLSLLRRAG
VTWQHQPDSGPPAAAPGHPLAPGPHPAAPSSWGPRPRRYTVLSVGPGGLRSGRLPLQPRV
QLDERGRQRGDFSLWLRPARRADAGEYRAAVHLRDRALSCRLRLRLGQASMTASPPGSLR
ASDWVILNCSFSRPDRPASVHWFRNRGQGRVPVRESPHHHLAESFLFLPQVSPMDSGPWG
CILTYRDGFNVSIMYNLTVLGLEPPTPLTVYAGAGSRVGLPCRLPAGVGTRSFLTAKWTP
PGGGPDLLVTGDNGDFTLRLEDVSQAQAGTYTCHIHLQEQQLNATVTLAIITVTPKSFGS
PGSLGKLLCEVTPVSGQERFVWSSLDTPSQRSFSGPWLEAQEAQLLSQPWQCQLYQGERL
LGAAVYFTELSSPGAQRSGRAPGALPAGHLLLFLILGVLSLLLLVTGAFGFHLWRRQWRP
RRFSALEQGIHPPQAQSKIEELEQEPEPEPEPEPEPEPEPEPEQL
Sequence of entity 2 (H, Y), FASTA
>8SR0_2 favezelimab Fab heavy chain (chains H, Y)
MGWTWIFLFFLSGTAGVLSEVLLLQSGPELVKPGTSVKIPCKASGYTFTDYNVDWVKQRH
GKGLEWIGDINPNNGGTIYSQKFKGKATLTVDKSSSTAFMELRSLTSEDTAVYFCARNYR
WFGAMDHWGQGTSVTVSSTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSG
ALTSGVHTFPAVLQSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKRVEPKSCD
KTAGWSHPQFEK
Sequence of entity 3 (L, Z), FASTA
>8SR0_3 favezelimab Fab light chain (chains L, Z)
METDTILLWVLLLWVPGSTGDIVLTQSPASLAVSPGQRATISCKASQSLDYEGDSDMNWY
QQKPGQPPRLLISGASNLESGIPARFSGSGSGTDFTVNIHPVEEEDAATYYCQQSTEDPR
TFGGGTKLEIKRTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPREAKYQWKVDNALQS
GNSQESVTEQDSKDSTYSLSSTLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC
Ligands and cofactors
| ID | Name | Formula | Copies |
|---|
| NAG | 2-acetamido-2-deoxy-beta-D-glucopyranose | C8 H15 N O6 | 2 |
Primary citation
CryoEM structure of a therapeutic antibody (favezelimab) bound to human LAG3 determined using a bivalent Fab as fiducial marker. Mishra, A.K., Shahid, S., Karade, S.S. et al. Structure (2023) 31:1149. DOI 10.1016/j.str.2023.07.013 · PubMed
Other PDB entries of the same protein (UniProt P18627 (AlphaFold model), which also has an AlphaFold model), best resolution first:
- 7UM3 2.4 Å, Crystal structure of a Fab in complex with a peptide derived from the LAG-3 D1 domain…
- 7TZH 2.43 Å, Structure of human LAG3 domains 3-4 in complex with antibody single chain-variable…
- 9BF9 3.4 Å, Human LAG-3-HLA-DR1 complex
- 8SO3 3.61 Å, CryoEM structure of a therapeutic antibody (favezelimab) bound to human LAG3
- 7TZG 3.71 Å, Structure of human LAG3 in complex with antibody single-chain variable fragment
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