8CAF: N8C_Fab3b
N8C_Fab3b in complex with NEDD8-CUL1(WHB). Determined by X-ray diffraction at 2.66 Å resolution. Released 13 Sept 2023.
- Method
- X-ray diffraction
- Resolution
- 2.66 Å
- Organism
- Homo sapiens
- Chains
- 8
- Atoms
- 8,808
- Mol. weight
- 128.53 kDa
- Released
- 13 Sept 2023
Explore 8CAF in 3D
Show helices and sheets
RCSB PDB
PDBe
Secondary structure: helices and β-sheets
8CAF contains 45 α-helices and 108 β-strands across 8 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: 9 helices, 21 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 4-7 | 4 | 1 |
| β-strand | 10-14 | 5 | 2 |
| β-strand | 19-25 | 7 | 1 |
| β-strand | 33-38 | 6 | 2 |
| α-helix | 43-44 | 2 | |
| β-strand | 45-49 | 5 | 2 |
| β-strand | 53-54 | 2 | 2 |
| α-helix | 55 | 1 | |
| β-strand | 62-67 | 6 | 1 |
| β-strand | 70-75 | 6 | 1 |
| α-helix | 80-82 | 3 | |
| β-strand | 84-91 | 8 | 2 |
| β-strand | 96-98 | 3 | 2 |
| β-strand | 102-107 | 6 | 2 |
| β-strand | 111 | 1 | 3 |
| α-helix | 112-113 | 2 | |
| β-strand | 114-118 | 5 | 4 |
| α-helix | 119-121 | 3 | |
| α-helix | 122-127 | 6 | |
| β-strand | 129-139 | 11 | 4 |
| β-strand | 140 | 1 | 3 |
| β-strand | 145-150 | 6 | 5 |
| β-strand | 153-154 | 2 | 5 |
| α-helix | 155 | 1 | |
| β-strand | 159-163 | 5 | 4 |
| α-helix | 164-167 | 4 | |
| β-strand | 173-182 | 10 | 4 |
| α-helix | 183-187 | 5 | |
| β-strand | 191-197 | 7 | 5 |
| β-strand | 205-210 | 6 | 5 |
Chain B: 6 helices, 22 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3-7 | 5 | 6 |
| β-strand | 10-12 | 3 | 7 |
| β-strand | 18-25 | 8 | 6 |
| α-helix | 29-31 | 3 | |
| β-strand | 33-39 | 7 | 7 |
| β-strand | 45-52 | 8 | 7 |
| β-strand | 58-60 | 3 | 7 |
| α-helix | 62-64 | 3 | |
| β-strand | 68-73 | 6 | 6 |
| β-strand | 78-83 | 6 | 6 |
| α-helix | 88-90 | 3 | |
| β-strand | 92-99 | 8 | 7 |
| β-strand | 112-113 | 2 | 7 |
| β-strand | 117-121 | 5 | 7 |
| α-helix | 125-126 | 2 | |
| β-strand | 127 | 1 | 8 |
| β-strand | 130-134 | 5 | 9 |
| β-strand | 146-155 | 10 | 9 |
| β-strand | 156 | 1 | 8 |
| β-strand | 161-164 | 4 | 10 |
| β-strand | 169 | 1 | 10 |
| β-strand | 173-175 | 3 | 9 |
| α-helix | 176-178 | 3 | |
| β-strand | 179-180 | 2 | 9 |
| β-strand | 186-194 | 9 | 9 |
| β-strand | 205-210 | 6 | 10 |
| α-helix | 211-213 | 3 | |
| β-strand | 215-220 | 6 | 10 |
Chain C: 7 helices, 21 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 4-7 | 4 | 11 |
| β-strand | 10-13 | 4 | 12 |
| β-strand | 19-25 | 7 | 11 |
| β-strand | 33-38 | 6 | 12 |
| β-strand | 45-49 | 5 | 12 |
| β-strand | 53-54 | 2 | 12 |
| α-helix | 55 | 1 | |
| β-strand | 62-67 | 6 | 11 |
| β-strand | 70-75 | 6 | 11 |
| α-helix | 80-82 | 3 | |
| β-strand | 85-91 | 7 | 12 |
| β-strand | 96-98 | 3 | 12 |
| β-strand | 102-106 | 5 | 12 |
| β-strand | 111 | 1 | 13 |
| α-helix | 112-113 | 2 | |
| β-strand | 114-118 | 5 | 14 |
| α-helix | 119-121 | 3 | |
| α-helix | 122-125 | 4 | |
| β-strand | 129-139 | 11 | 14 |
| β-strand | 140 | 1 | 13 |
| β-strand | 145-150 | 6 | 15 |
| β-strand | 153-154 | 2 | 15 |
| β-strand | 159-163 | 5 | 14 |
| α-helix | 164-167 | 4 | |
| β-strand | 173-182 | 10 | 14 |
| α-helix | 183-188 | 6 | |
| β-strand | 191-197 | 7 | 15 |
| β-strand | 205-210 | 6 | 15 |
Chain D: 8 helices, 24 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 3-7 | 5 | 16 |
| β-strand | 10-12 | 3 | 17 |
| β-strand | 18-25 | 8 | 16 |
| α-helix | 29-31 | 3 | |
| β-strand | 33-39 | 7 | 17 |
| β-strand | 46-52 | 7 | 17 |
| β-strand | 58-60 | 3 | 17 |
| α-helix | 62-64 | 3 | |
| β-strand | 68-73 | 6 | 16 |
| β-strand | 78-83 | 6 | 16 |
| α-helix | 88-90 | 3 | |
| β-strand | 92-99 | 8 | 17 |
| β-strand | 112-113 | 2 | 17 |
| β-strand | 117-121 | 5 | 17 |
| β-strand | 127 | 1 | 18 |
| α-helix | 128-129 | 2 | |
| β-strand | 130-134 | 5 | 19 |
| β-strand | 146-155 | 10 | 19 |
| β-strand | 156 | 1 | 18 |
| β-strand | 161-164 | 4 | 20 |
| α-helix | 165-167 | 3 | |
| β-strand | 169 | 1 | 20 |
| β-strand | 173-175 | 3 | 19 |
| α-helix | 176-178 | 3 | |
| β-strand | 179-180 | 2 | 19 |
| β-strand | 186-194 | 9 | 19 |
| α-helix | 196-198 | 3 | |
| β-strand | 199 | 1 | 21 |
| β-strand | 202 | 1 | 21 |
| β-strand | 205-210 | 6 | 20 |
| α-helix | 211-213 | 3 | |
| β-strand | 215-220 | 6 | 20 |
Chain E: 4 helices, 3 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 699-722 | 24 | |
| β-strand | 724-726 | 3 | 22 |
| α-helix | 727-738 | 12 | |
| α-helix | 746-758 | 13 | |
| β-strand | 762-764 | 3 | 22 |
| α-helix | 765 | 1 | |
| β-strand | 771-774 | 4 | 22 |
Chain F: 4 helices, 7 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 2-6 | 5 | 23 |
| β-strand | 12-16 | 5 | 23 |
| β-strand | 22 | 1 | 24 |
| α-helix | 23-34 | 12 | |
| α-helix | 38-40 | 3 | |
| β-strand | 41-45 | 5 | 23 |
| β-strand | 48-49 | 2 | 23 |
| α-helix | 50-51 | 2 | |
| β-strand | 55 | 1 | 24 |
| α-helix | 57-59 | 3 | |
| β-strand | 66-71 | 6 | 23 |
Chain G: 4 helices, 7 β-strands
| Element | Residues | Length | Sheet |
|---|
| β-strand | 2-7 | 6 | 25 |
| β-strand | 12-16 | 5 | 25 |
| β-strand | 22 | 1 | 26 |
| α-helix | 23-34 | 12 | |
| α-helix | 38-40 | 3 | |
| β-strand | 41-45 | 5 | 25 |
| β-strand | 48-49 | 2 | 25 |
| α-helix | 50-51 | 2 | |
| β-strand | 55 | 1 | 26 |
| α-helix | 57-59 | 3 | |
| β-strand | 66-71 | 6 | 25 |
Chain H: 3 helices, 3 β-strands
| Element | Residues | Length | Sheet |
|---|
| α-helix | 703-722 | 20 | |
| β-strand | 724-726 | 3 | 27 |
| α-helix | 727-738 | 12 | |
| α-helix | 746-758 | 13 | |
| β-strand | 762-764 | 3 | 27 |
| β-strand | 771-774 | 4 | 27 |
Molecules and chains
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|
| Fab Light Chain | A, C | protein | 211 | Homo sapiens | |
| Fab Heavy Chain | B, D | protein | 223 | Homo sapiens | |
| Cullin-1 | E, H | protein | 79 | Homo sapiens | Q13616 (AlphaFold model) |
| NEDD8 | F, G | protein | 76 | Homo sapiens | Q15843 (AlphaFold model) |
Sequence of entity 1 (A, C), FASTA
>8CAF_1 Fab Light Chain (chains A, C)
DIQMTQSPSSLSASVGDRVTITCRASQSVSSAVAWYQQKPGKAPKLLIYSASSLYSGVPS
RFSGSRSGTDFTLTISSLQPEDFATYYCQQSSYSLITFGQGTKVEIKRTVAAPSVFIFPP
SDSQLKSGTASVVCLLNNFYPREAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLSSTLT
LSKADYEKHKVYACEVTHQGLSSPVTKSFNR
Sequence of entity 2 (B, D), FASTA
>8CAF_2 Fab Heavy Chain (chains B, D)
EVQLVESGGGLVQPGGSLRLSCAASGFNFSSSSIHWVRQAPGKGLEWVASISSSYGYTYY
ADSVKGRFTISADTSKNTAYLQMNSLRAEDTAVYYCARDPFGWAAHGVGLDYWGQGTLVT
VSSASTKGPSVFPLAPSSKSTSGGTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVL
QSSGLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEP
Sequence of entity 3 (E, H), FASTA
>8CAF_3 Cullin-1 (chains E, H)
TTHKNIEEDRKLLIQAAIVRIMKMRKVLKHQQLLGEVLTQLSSRFKPRVPVIKKCIDILI
EKEYLERVDGEKDTYSYLA
Sequence of entity 4 (F, G), FASTA
>8CAF_4 NEDD8 (chains F, G)
MLIKVKTLTGKEIEIDIEPTDKVERIKERVEEKEGIPPQQQRLIYSGKQMNDEKTAADYK
ILGGSVLHLVLALRGG
Primary citation
Activity-based profiling of cullin-RING E3 networks by conformation-specific probes. Henneberg, L.T., Singh, J., Duda, D.M. et al. Nat Chem Biol (2023) 19:1513-1523. DOI 10.1038/s41589-023-01392-5 · PubMed
Other PDB entries of the same protein (UniProt Q13616 (AlphaFold model), which also has an AlphaFold model), best resolution first:
- 3TDU 1.5 Å, N-terminal acetylation acts as an avidity enhancer within an interconnected multiprotein…
- 5V89 1.55 Å, Structure of DCN4 PONY domain bound to CUL1 WHB
- 3TDZ 2.0 Å, N-terminal acetylation acts as an avidity enhancer within an interconnected multiprotein…
- 7Z8R 2.7 Å, CAND1-CUL1-RBX1
- 7Z8V 2.7 Å, CAND1-SCF-SKP2 (SKP1deldel) CAND1 engaged SCF rocked
- 8OR3 2.9 Å, CAND1-CUL1-RBX1-SKP1-SKP2-DCNL1
- 9QO4 2.95 Å, Dissociation-state-3 of 9-subunit CSN and SCF (SKP1-SKP2-CKS1) complex
- 1LDJ 3.0 Å, Structure of the Cul1-Rbx1-Skp1-F boxSkp2 SCF Ubiquitin Ligase Complex
- 4F52 3.0 Å, Structure of a Glomulin-RBX1-CUL1 complex
- 7Z8T 3.0 Å, CAND1-SCF-SKP2 CAND1 engaged SCF rocked
- 9XZL 3.0 Å, Cryo-EM structure of F-box helicase 1 (FBH1) bound to an SCF ubiquitin ligase complex…
- 9EFV 3.03 Å, Cryo-EM structure of CSN-N8CUL1 in complex with CSN5i-3
Browse structure collections
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