6SC8: DAb3/HOIP-RBR-Ligand4

dAb3/HOIP-RBR-Ligand4. Determined by X-ray diffraction at 2.11 Å resolution. Released 27 Nov 2019.

Method
X-ray diffraction
Resolution
2.11 Å
Organisms
Homo sapiens, synthetic construct
Chains
3
Atoms
4,848
Mol. weight
70.62 kDa
Ligands
ZN, L6E
Released
27 Nov 2019

Explore 6SC8 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

6SC8 contains 24 α-helices and 40 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.

Chain A: 17 helices, 16 β-strands

ElementResiduesLengthSheet
α-helix708-7103
β-strand712-71321
β-strand720-72121
α-helix723-73614
α-helix739-7413
α-helix758-77215
α-helix775-78511
α-helix786-7905
β-strand796-79832
β-strand805-80732
β-strand814-81633
β-strand823-82533
β-strand83113
α-helix8321
α-helix834-8363
α-helix841-85111
α-helix853-8575
α-helix860-8667
β-strand87014
β-strand87714
β-strand887-88935
β-strand896-89835
β-strand90415
β-strand905-90626
β-strand923-92426
α-helix931-9344
α-helix939-9479
β-strand972-97657
β-strand981-98557
α-helix999-101214
α-helix1017-10204
α-helix1023-103412
α-helix1046-106015
Chain B: 3 helices, 13 β-strands
ElementResiduesLengthSheet
β-strand3-758
β-strand11-1229
β-strand17-2598
α-helix29-313
β-strand34-39610
α-helix44-452
β-strand46-51610
β-strand58-60310
β-strand6518
β-strand68-7368
β-strand78-8478
α-helix88-903
β-strand92-99810
β-strand107-110410
β-strand114-116310
β-strand117-11829
Chain C: 4 helices, 11 β-strands
ElementResiduesLengthSheet
β-strand3-7511
β-strand10-12310
β-strand18-25811
α-helix29-313
β-strand34-39610
β-strand45-51710
β-strand58-60310
α-helix62-643
β-strand68-73611
α-helix74-763
β-strand78-83611
α-helix88-903
β-strand92-99810
β-strand107-110410
β-strand114-118510

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
E3 ubiquitin-protein ligase RNF31Aprotein376Homo sapiensQ96EP0 (AlphaFold model)
Single domain antibodyB, Cprotein120synthetic construct
Sequence of entity 1 (A), FASTA
>6SC8_1 E3 ubiquitin-protein ligase RNF31 (chains A)
QECAVCGWALPHNRMQALTSCECTICPDCFRQHFTIALKEKHITDMVCPACGRPDLTDDT
QLLSYFSTLDIQLRESLEPDAYALFHKKLTEGVLMRDPKFLWCAQCSFGFIYEREQLEAT
CPQCHQTFCVRCKRQWEEQHRGRSCEDFQNWKRMNDPEYQAQGLAMYLQENGIDCPKCKF
SYALARGGCMHFHCTQCRHQFCSGCYNAFYAKNKCPEPNCRVKKSLHGHHPRDCLFYLRD
WTALRLQKLLQDNNVMFNTEPPAGARAVPGGGCRVIEQKEVPNGLRDEACGKETPAGYAG
LCQAHYKEYLVSLINAHSLDPATLYEVEELETATERYLHVRPQPLAGEDPPAYQARLLQK
LTEEVPLGQSIPRRRK
Sequence of entity 2 (B, C), FASTA
>6SC8_2 Single domain antibody (chains B, C)
EVQLLESGGGLVQPGGSLRLSCAASGFTFRGYSMAWVRQAPGKGLEWVSTISPIGTYTYY
ADSVKGRFTISRDNSKNTLYLQMNSLRAEDTAVYYCAKGSYSRGTPFDYWGQGTLVTVSS

Ligands and cofactors

IDNameFormulaCopies
ZNZinc ionZn8
L6E[2-(methylamino)-2-oxidanylidene-ethyl] (~{E})-4-[(2-oxidanylidene-5,6,7,8-tetr…C17 H21 N3 O51

Water and common crystallization additives (CL, SO4) are not listed.

Primary citation

Single-Domain Antibodies as Crystallization Chaperones to Enable Structure-Based Inhibitor Development for RBR E3 Ubiquitin Ligases. Tsai, Y.I., Johansson, H., Dixon, D. et al. Cell Chem Biol (2020) 27:83. DOI 10.1016/j.chembiol.2019.11.007 · PubMed

Other PDB entries of the same protein (UniProt Q96EP0 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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