7VAZ: Antibody 14A
Crystal structure of antibody 14A in complex with MUC1 glycopeptide(GlycoS). Determined by X-ray diffraction at 2.73 Å resolution. Released 31 Aug 2022.
- Method
- X-ray diffraction
- Resolution
- 2.73 Å
- Organisms
- Mus musculus, Homo sapiens
- Chains
- 9
- Atoms
- 9,884
- Mol. weight
- 148.12 kDa
- Ligands
- NGA
- Released
- 31 Aug 2022
Explore 7VAZ in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
7VAZ contains 55 α-helices and 135 β-strands across 9 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 A: 8 helices, 21 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 4-6 | 3 | 11 |
| β-strand | 9-12 | 4 | 12 |
| β-strand | 17-24 | 8 | 11 |
| α-helix | 31-33 | 3 | |
| β-strand | 36-41 | 6 | 12 |
| β-strand | 45-51 | 7 | 12 |
| β-strand | 55-56 | 2 | 12 |
| α-helix | 57 | 1 | |
| β-strand | 64-69 | 6 | 11 |
| β-strand | 72-78 | 7 | 11 |
| α-helix | 82-84 | 3 | |
| β-strand | 86-93 | 8 | 12 |
| β-strand | 98-100 | 3 | 12 |
| β-strand | 104-108 | 5 | 12 |
| β-strand | 114 | 1 | 13 |
| α-helix | 115-116 | 2 | |
| β-strand | 117-121 | 5 | 14 |
| α-helix | 122-124 | 3 | |
| α-helix | 125-129 | 5 | |
| β-strand | 132-142 | 11 | 14 |
| β-strand | 143 | 1 | 13 |
| β-strand | 148-153 | 6 | 15 |
| β-strand | 156-157 | 2 | 15 |
| β-strand | 162-166 | 5 | 14 |
| α-helix | 167-170 | 4 | |
| β-strand | 176-185 | 10 | 14 |
| α-helix | 186-191 | 6 | |
| β-strand | 194-200 | 7 | 15 |
| β-strand | 208-213 | 6 | 15 |
Chain B: 9 helices, 24 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 4-9 | 6 | 16 |
| β-strand | 12-13 | 2 | 17 |
| β-strand | 19-26 | 8 | 16 |
| α-helix | 30-32 | 3 | |
| β-strand | 34-40 | 7 | 18 |
| β-strand | 46-52 | 7 | 18 |
| β-strand | 59-61 | 3 | 18 |
| α-helix | 63-65 | 3 | |
| β-strand | 69-74 | 6 | 16 |
| β-strand | 79-84 | 6 | 16 |
| α-helix | 89-91 | 3 | |
| β-strand | 93-100 | 8 | 18 |
| β-strand | 104-107 | 4 | 18 |
| β-strand | 108 | 1 | 16 |
| β-strand | 111-113 | 3 | 18 |
| β-strand | 114-115 | 2 | 17 |
| α-helix | 118-120 | 3 | |
| β-strand | 121 | 1 | 19 |
| α-helix | 122-123 | 2 | |
| β-strand | 124-128 | 5 | 20 |
| β-strand | 135-136 | 2 | 20 |
| β-strand | 139-149 | 11 | 20 |
| β-strand | 150 | 1 | 19 |
| β-strand | 155-158 | 4 | 21 |
| α-helix | 159-161 | 3 | |
| β-strand | 167-169 | 3 | 20 |
| α-helix | 170-172 | 3 | |
| β-strand | 173-174 | 2 | 20 |
| β-strand | 180-189 | 10 | 20 |
| α-helix | 190-194 | 5 | |
| β-strand | 199-204 | 6 | 21 |
| α-helix | 205-207 | 3 | |
| β-strand | 209-214 | 6 | 21 |
Chain C: 8 helices, 21 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 4-6 | 3 | 1 |
| β-strand | 9-12 | 4 | 2 |
| β-strand | 18-24 | 7 | 1 |
| α-helix | 31-33 | 3 | |
| β-strand | 36-41 | 6 | 2 |
| β-strand | 45-51 | 7 | 2 |
| β-strand | 55-56 | 2 | 2 |
| α-helix | 57 | 1 | |
| β-strand | 64-69 | 6 | 1 |
| β-strand | 72-77 | 6 | 1 |
| α-helix | 82-84 | 3 | |
| β-strand | 86-93 | 8 | 2 |
| β-strand | 98-100 | 3 | 2 |
| β-strand | 104-108 | 5 | 2 |
| β-strand | 114 | 1 | 3 |
| α-helix | 115-116 | 2 | |
| β-strand | 117-121 | 5 | 4 |
| α-helix | 122-124 | 3 | |
| α-helix | 125-129 | 5 | |
| β-strand | 132-142 | 11 | 4 |
| β-strand | 143 | 1 | 3 |
| β-strand | 148-153 | 6 | 5 |
| β-strand | 156-157 | 2 | 5 |
| β-strand | 162-166 | 5 | 4 |
| α-helix | 167-170 | 4 | |
| β-strand | 176-185 | 10 | 4 |
| α-helix | 186-191 | 6 | |
| β-strand | 194-200 | 7 | 5 |
| β-strand | 208-213 | 6 | 5 |
Chain D: 10 helices, 23 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 4-8 | 5 | 6 |
| β-strand | 11-13 | 3 | 7 |
| β-strand | 19-26 | 8 | 6 |
| α-helix | 30-32 | 3 | |
| β-strand | 35-40 | 6 | 7 |
| β-strand | 46-52 | 7 | 7 |
| β-strand | 59-61 | 3 | 7 |
| α-helix | 63-65 | 3 | |
| β-strand | 69-74 | 6 | 6 |
| α-helix | 75-77 | 3 | |
| β-strand | 79-84 | 6 | 6 |
| α-helix | 89-91 | 3 | |
| β-strand | 93-100 | 8 | 7 |
| β-strand | 104-107 | 4 | 7 |
| β-strand | 111-115 | 5 | 7 |
| α-helix | 118-120 | 3 | |
| β-strand | 121 | 1 | 8 |
| α-helix | 122-123 | 2 | |
| β-strand | 124-128 | 5 | 9 |
| β-strand | 136 | 1 | 9 |
| β-strand | 139-149 | 11 | 9 |
| β-strand | 150 | 1 | 8 |
| β-strand | 155-158 | 4 | 10 |
| α-helix | 159-161 | 3 | |
| β-strand | 163 | 1 | 10 |
| β-strand | 167-169 | 3 | 9 |
| α-helix | 170-172 | 3 | |
| β-strand | 173-174 | 2 | 9 |
| β-strand | 180-189 | 10 | 9 |
| α-helix | 191-194 | 4 | |
| β-strand | 198-204 | 7 | 10 |
| α-helix | 205-207 | 3 | |
| β-strand | 209-215 | 7 | 10 |
Chain E: 1 helix, 0 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 7-10 | 4 | |
Chain F: 8 helices, 21 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 4-6 | 3 | 22 |
| β-strand | 9-12 | 4 | 23 |
| β-strand | 17-24 | 8 | 22 |
| α-helix | 31-33 | 3 | |
| β-strand | 36-41 | 6 | 23 |
| β-strand | 45-51 | 7 | 23 |
| β-strand | 55-56 | 2 | 23 |
| α-helix | 57 | 1 | |
| β-strand | 64-69 | 6 | 22 |
| β-strand | 72-78 | 7 | 22 |
| α-helix | 82-84 | 3 | |
| β-strand | 86-93 | 8 | 23 |
| β-strand | 98-100 | 3 | 23 |
| β-strand | 104-108 | 5 | 23 |
| β-strand | 114 | 1 | 24 |
| α-helix | 115-116 | 2 | |
| β-strand | 117-121 | 5 | 25 |
| α-helix | 122-124 | 3 | |
| α-helix | 127-129 | 3 | |
| β-strand | 132-142 | 11 | 25 |
| β-strand | 143 | 1 | 24 |
| β-strand | 147-153 | 7 | 26 |
| β-strand | 156-157 | 2 | 26 |
| β-strand | 162-166 | 5 | 25 |
| α-helix | 167-170 | 4 | |
| β-strand | 176-185 | 10 | 25 |
| α-helix | 186-191 | 6 | |
| β-strand | 195-201 | 7 | 26 |
| β-strand | 208-212 | 5 | 26 |
Chains G and I: 1 helix, 0 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 8-10 | 3 | |
Chain H: 9 helices, 25 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 4-8 | 5 | 27 |
| β-strand | 12-13 | 2 | 28 |
| β-strand | 18-26 | 9 | 27 |
| α-helix | 30-32 | 3 | |
| β-strand | 35-40 | 6 | 29 |
| β-strand | 46-52 | 7 | 29 |
| β-strand | 59-61 | 3 | 29 |
| α-helix | 63-65 | 3 | |
| β-strand | 69-74 | 6 | 27 |
| β-strand | 79-85 | 7 | 27 |
| α-helix | 89-91 | 3 | |
| β-strand | 93-100 | 8 | 29 |
| β-strand | 104-107 | 4 | 29 |
| β-strand | 111-113 | 3 | 29 |
| β-strand | 114-115 | 2 | 28 |
| α-helix | 118-120 | 3 | |
| β-strand | 121 | 1 | 30 |
| α-helix | 122-123 | 2 | |
| β-strand | 124-127 | 4 | 31 |
| α-helix | 136-138 | 3 | |
| β-strand | 139-149 | 11 | 31 |
| β-strand | 150 | 1 | 30 |
| β-strand | 155-158 | 4 | 32 |
| α-helix | 159-161 | 3 | |
| β-strand | 163 | 1 | 32 |
| β-strand | 167-169 | 3 | 31 |
| α-helix | 170-172 | 3 | |
| β-strand | 173-174 | 2 | 31 |
| β-strand | 180-189 | 10 | 31 |
| β-strand | 193 | 1 | 33 |
| β-strand | 196 | 1 | 33 |
| β-strand | 200-204 | 5 | 32 |
| α-helix | 205-207 | 3 | |
| β-strand | 209-213 | 5 | 32 |
Molecules and chains
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|
| 14A fab light chain | A, C, F | protein | 217 | Mus musculus | |
| 14A fab heavy chain | B, D, H | protein | 229 | Mus musculus | |
| Mucin-1 subunit alpha | E, G, I | protein | 13 | Homo sapiens | P15941 (AlphaFold model) |
Sequence of entity 1 (A, C, F), FASTA
>7VAZ_1 14A fab light chain (chains A, C, F)
QAVVTQESALTTSPGETVTLTCRSSTGAVTTSNYANWVQEKPDHLFTGLIGRTNNRVPGV
PARFSGSLIGDKAALTITGAQTEDEAIYFCALWYSNHFIFGSGTKVTVLKRTVAAPSVFI
FPPSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLSS
TLTLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC
Sequence of entity 2 (B, D, H), FASTA
>7VAZ_2 14A fab heavy chain (chains B, D, H)
MEVKLLQSGGGLVQPGGSLKLSCAASGIDFSGYWMSWVRRAPGKGLEWIGEITPDSSTIN
YAPSLKDEFIISRDNAKNTLYLQMTKVRSDDTALYYCVSYYEGFAYWGQGTLVTVSAAST
KGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGLY
SLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEPKSCDKTENLYFQ
Sequence of entity 3 (E, G, I), FASTA
>7VAZ_3 Mucin-1 subunit alpha (chains E, G, I)
RPAPGSTAPPAHG
Ligands and cofactors
| ID | Name | Formula | Copies |
|---|
| NGA | 2-acetamido-2-deoxy-beta-D-galactopyranose | C8 H15 N O6 | 1 |
Primary citation
Site-specific GalNAc modification on a MUC1 neoantigen epitope forms a basis for high-affinity antibody binding. Han, Y.B., Xu, L. To be published.
Other PDB entries of the same protein (UniProt P15941 (AlphaFold model), which also has an AlphaFold model), best resolution first:
- 6BSC 1.3 Å, Crystal structure of the Mucin-1 SEA domain
- 7V64 1.56 Å, Crystal structure of Antibody 16A in complex with MUC1 Glycopeptide(GlycoT)
- 6BSB 1.6 Å, Crystal structure of the Mucin-1 SEA domain, L1105M mutant, Selenium-derivative
- 6FZQ 1.7 Å, Crystal structure of scFv-SM3 in complex with compound 3
- 8S6K 1.75 Å, Crystal structure of ScFv-G2D11 complexed to a bis-Tn glycopeptide
- 6KX1 1.77 Å, Crystal structure of SN-101 mAb in complex with MUC1 glycopeptide
- 6FZR 1.8 Å, Crystal structure of scFv-SM3 in complex with compound 2
- 8AXH 1.85 Å, Crystal structure of a MUC1-like glycopeptide containing the unnatural…
- 8S6T 1.85 Å, Crystal structure of Fab-3F1 complexed to a bis-STn glycopeptide
- 1SM3 1.95 Å, Crystal structure of the tumor specific antibody SM3 complex with its peptide epitope
- 8S6V 1.95 Å, Crystal structure of Fab-2D9 chimera complexed to a bis-Tn glycopeptide
- 5T6P 1.97 Å, Crystal structure of therapeutic mAB AR20.5 in complex with MUC1 peptide
Browse structure collections
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