5VEB: Anti-CDH6 Fab heavy chain
Crystal structure of a Fab binding to extracellular domain 5 of Cadherin-6. Determined by X-ray diffraction at 2.34 Å resolution. Released 7 Jun 2017.
- Method
- X-ray diffraction
- Resolution
- 2.34 Å
- Organism
- Homo sapiens
- Chains
- 6
- Atoms
- 8,497
- Mol. weight
- 123.01 kDa
- Ligands
- A2G
- Released
- 7 Jun 2017
Explore 5VEB in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
5VEB contains 31 α-helices and 104 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 A: 8 helices, 24 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3-7 | 5 | 1 |
| β-strand | 10-12 | 3 | 2 |
| β-strand | 18-25 | 8 | 1 |
| α-helix | 29-31 | 3 | |
| β-strand | 32 | 1 | 3 |
| β-strand | 34-39 | 6 | 2 |
| β-strand | 45-51 | 7 | 2 |
| β-strand | 58-60 | 3 | 2 |
| β-strand | 69-73 | 5 | 1 |
| β-strand | 78-83 | 6 | 1 |
| α-helix | 88-90 | 3 | |
| β-strand | 92-100 | 9 | 2 |
| β-strand | 104-108 | 5 | 2 |
| β-strand | 112-116 | 5 | 2 |
| α-helix | 120-121 | 2 | |
| β-strand | 122 | 1 | 4 |
| α-helix | 123-124 | 2 | |
| β-strand | 125-129 | 5 | 5 |
| β-strand | 137 | 1 | 5 |
| β-strand | 140-150 | 11 | 5 |
| β-strand | 151 | 1 | 4 |
| β-strand | 156-159 | 4 | 6 |
| α-helix | 160-162 | 3 | |
| β-strand | 164 | 1 | 6 |
| β-strand | 168-170 | 3 | 5 |
| α-helix | 171-173 | 3 | |
| β-strand | 174-175 | 2 | 5 |
| β-strand | 181-190 | 10 | 5 |
| α-helix | 191-193 | 3 | |
| β-strand | 200-205 | 6 | 6 |
| α-helix | 206-208 | 3 | |
| β-strand | 210-215 | 6 | 6 |
Chains B and L: 7 helices, 20 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 4-7 | 4 | 7 |
| β-strand | 10-13 | 4 | 2 |
| β-strand | 19-29 | 11 | 7 |
| β-strand | 33-38 | 6 | 2 |
| β-strand | 45-49 | 5 | 2 |
| β-strand | 53-55 | 3 | 2 |
| β-strand | 62-75 | 14 | 7 |
| α-helix | 80-82 | 3 | |
| β-strand | 84-90 | 7 | 2 |
| β-strand | 98-99 | 2 | 2 |
| β-strand | 103-107 | 5 | 2 |
| β-strand | 112 | 1 | 8 |
| α-helix | 113-114 | 2 | |
| β-strand | 115-119 | 5 | 9 |
| α-helix | 120-122 | 3 | |
| α-helix | 123-126 | 4 | |
| β-strand | 130-140 | 11 | 9 |
| β-strand | 141 | 1 | 8 |
| β-strand | 146-151 | 6 | 10 |
| β-strand | 154-155 | 2 | 10 |
| α-helix | 156 | 1 | |
| β-strand | 160-164 | 5 | 9 |
| α-helix | 165-168 | 4 | |
| β-strand | 174-183 | 10 | 9 |
| α-helix | 184-188 | 5 | |
| β-strand | 192-198 | 7 | 10 |
| β-strand | 206-211 | 6 | 10 |
Chain H: 7 helices, 23 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3-7 | 5 | 11 |
| β-strand | 10-12 | 3 | 12 |
| β-strand | 18-25 | 8 | 11 |
| α-helix | 29-31 | 3 | |
| β-strand | 34-39 | 6 | 12 |
| β-strand | 45-51 | 7 | 12 |
| β-strand | 58-60 | 3 | 12 |
| β-strand | 69-73 | 5 | 11 |
| β-strand | 78-83 | 6 | 11 |
| α-helix | 88-90 | 3 | |
| β-strand | 92-100 | 9 | 12 |
| β-strand | 104-108 | 5 | 12 |
| β-strand | 112-116 | 5 | 12 |
| β-strand | 122 | 1 | 13 |
| α-helix | 123-124 | 2 | |
| β-strand | 125-129 | 5 | 14 |
| β-strand | 137 | 1 | 14 |
| β-strand | 140-150 | 11 | 14 |
| β-strand | 151 | 1 | 13 |
| β-strand | 156-159 | 4 | 15 |
| α-helix | 160-162 | 3 | |
| β-strand | 164 | 1 | 15 |
| β-strand | 168-170 | 3 | 14 |
| α-helix | 171-173 | 3 | |
| β-strand | 174-175 | 2 | 14 |
| β-strand | 181-190 | 10 | 14 |
| α-helix | 191-193 | 3 | |
| β-strand | 199-205 | 7 | 15 |
| α-helix | 206-208 | 3 | |
| β-strand | 210-216 | 7 | 15 |
Chain X: 1 helix, 9 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 495-497 | 3 | 21 |
| α-helix | 500-501 | 2 | |
| β-strand | 505-512 | 8 | 2 |
| β-strand | 524-527 | 4 | 21 |
| β-strand | 537-541 | 5 | 2 |
| β-strand | 546-551 | 6 | 2 |
| β-strand | 563-571 | 9 | 21 |
| β-strand | 573 | 1 | 3 |
| β-strand | 579-589 | 11 | 21 |
| β-strand | 609-612 | 4 | 2 |
Chain Y: 1 helix, 8 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 493-497 | 5 | 22 |
| α-helix | 500-501 | 2 | |
| β-strand | 505-512 | 8 | 17 |
| β-strand | 524-527 | 4 | 22 |
| β-strand | 537-541 | 5 | 17 |
| β-strand | 546-551 | 6 | 17 |
| β-strand | 563-571 | 9 | 22 |
| β-strand | 579-589 | 11 | 22 |
| β-strand | 609-612 | 4 | 17 |
Molecules and chains
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|
| anti-CDH6 Fab heavy chain | A | protein | 225 | Homo sapiens | S6B291 (AlphaFold model) |
| anti-CDH6 Fab light chain | B, L | protein | 215 | Homo sapiens | P01834 (AlphaFold model) |
| anti-CDH6 Fab heavy chain | H | protein | 225 | Homo sapiens | S6B291 (AlphaFold model) |
| Cadherin-6 | X, Y | protein | 125 | Homo sapiens | P55285 (AlphaFold model) |
Sequence of entity 1 (A), FASTA
>5VEB_1 anti-CDH6 Fab heavy chain (chains A)
QVQLLESGGGLVQPGGSLRLSCAASGFTFSSHGMHWVRQAPGKGLEWVSVISGSGSNTGY
ADSVXGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARQWGSYAFDSWGQGTLVTVSSAS
TKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGL
YSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKRVEPKSCDKTH
Sequence of entity 2 (B, L), FASTA
>5VEB_2 anti-CDH6 Fab light chain (chains B, L)
DIQMTQSPSSLSASVGDRVTITCRASQSISSYLNWYQQKPGKAPKLLIYAVSTLQSGVPS
RFSGSGSGTDFTLTISSLQPEDFATYYCQQSGTFPPTTFGQGTKVEIKRTVAAPSVFIFP
PSDEQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLSSTL
TLSKADYEKHKVYACEVTHQGLSSPVTKSFNRGEC
Sequence of entity 3 (H), FASTA
>5VEB_3 anti-CDH6 Fab heavy chain (chains H)
QVQLLESGGGLVQPGGSLRLSCAASGFTFSSHGMHWVRQAPGKGLEWVSVISGSGSNTGY
ADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCARQWGSYAFDSWGQGTLVTVSSAS
TKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSSGL
YSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKRVEPKSCDKTH
Sequence of entity 4 (X, Y), FASTA
>5VEB_4 Cadherin-6 (chains X, Y)
EFYETFVCEKAKADQLIQTLHAVDKDDPYSGHQFSFSLAPEAASGSNFTIQDNKDNTAGI
LTRKNGYNRHEMSTYLLPVVISDNDYPVQSSTGTVTVRVCACDHHGNMQSCHAEALIHPL
EVLFQ
Ligands and cofactors
| ID | Name | Formula | Copies |
|---|
| A2G | 2-acetamido-2-deoxy-alpha-D-galactopyranose | C8 H15 N O6 | 4 |
Primary citation
Discovery and Optimization of HKT288, a Cadherin-6-Targeting ADC for the Treatment of Ovarian and Renal Cancers. Bialucha, C.U., Collins, S.D., Li, X. et al. Cancer Discov (2017) 7:1030-1045. DOI 10.1158/2159-8290.CD-16-1414 · PubMed
Other PDB entries of the same protein (UniProt S6B291 (AlphaFold model), which also has an AlphaFold model), best resolution first:
- 4LLY 1.6 Å, Crystal structure of Pertuzumab Clambda Fab with variable and constant domain redesigns…
- 3MNZ 1.8 Å, Crystal structure of the non-neutralizing HIV antibody 13H11 Fab fragment with a gp41…
- 6B9Z 1.82 Å, Trastuzumab Fab v3
- 4LLW 1.95 Å, Crystal structure of Pertuzumab Clambda Fab with variable domain redesign (VRD2) at 1.95A
- 6BAE 2.14 Å, Trastuzumab Fab v3 in complex with CQFDLSTRRLKC
- 3MNW 2.2 Å, Crystal structure of the non-neutralizing HIV antibody 13H11 Fab fragment with a gp41…
- 6AZK 2.48 Å, Structure of cetuximab with aminoheptanoic acid-linked N-(3-hydroxypropyl)-L-arginine…
- 6AYN 2.48 Å, Structure of cetuximab with aminoheptanoic acid-linked N-(3-aminopropyl)-L-arginine…
- 6AZL 2.48 Å, Structure of cetuximab with aminoheptanoic acid-linked N-carboxyethylarginine meditope…
- 6AU5 2.48 Å, Structure of cetuximab with aminoheptanoic acid-linked n-butylarginine meditope variant
- 6AXP 2.48 Å, Structure of cetuximab with aminoheptanoic acid-linked n-octylarginine meditope variant
- 6VTU 2.61 Å, DH717.1 Fab monomer in complex with man9 glycan
Browse structure collections
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