8f8e

Crystal structure of the WDR domain of human DCAF1 in complex with OICR-8268 compound

Method: X-RAY DIFFRACTION Dmax: 86.7 Å Quality: EXCELLENT

1. Protein Identity and Related Structures Protein Identity & Related Structures

DDB1- and CUL4-associated factor 1

Homo sapiens

UniProt Q9Y4B6

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 1077–1390 Mutation:F1077A, R1079A XJI (3P)-N-[(1S)-3-amino-1-(3-chloro-4-fluorophenyl)-3-oxopropyl]-3-(4-chloro-2-fluorophenyl)-1H-pyrazole-4-carboxamide × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293 K;20% PEG3350, 0.2M di-Ammonium Citrate Resolution 1.55 Å R-free 0.209
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 1077–1390 Mutation:F1077A, R1079A XJI (3P)-N-[(1S)-3-amino-1-(3-chloro-4-fluorophenyl)-3-oxopropyl]-3-(4-chloro-2-fluorophenyl)-1H-pyrazole-4-carboxamide × 1 CIT CITRIC ACID × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;293 K;20% PEG3350, 0.2M di-Ammonium Citrate Resolution 1.55 Å R-free 0.209

Other States of the Same Protein in the Database

Each row is a biological assembly of the same UniProt protein in another PDB entry. The “Difference from current entry” column identifies evidence-level differences; no tag means the currently parsed fields agree.

46 other PDB entries and 59 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name DCAF1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–315; UniProt 1077–1390 Author chain B; PDBConstruct 2–315; UniProt 1077–1390

The page prioritizes protein identity, the current assembly, associated components, oligomeric state and cross-PDB links. Chain mapping and sequence ranges are retained as data evidence. Internal IDs, import timestamps and assembly operation expressions are maintenance fields and are not shown here.

SAXS scattering curve SAXS Profile

SAXS profile for 8f8e

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 8f8e
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2. Structure Basics 2. Structure Basics

Entry ID entry_id8f8e
Deposition date deposition_date2022-11-21
Structure title titleCrystal structure of the WDR domain of human DCAF1 in complex with OICR-8268 compound
Keywords keywordsWD-repeat, WDR, DCAF1, SGC, TRANSFERASE, Structural Genomics, Structural Genomics Consortium, TRANSFERASE-INHIBITOR complex; TRANSFERASE/INHIBITOR
Experimental Method methodX-RAY DIFFRACTION

3. SAXS Parameters (CRYSOL theoretical calculation) 3. SAXS Parameters (CRYSOL)

Radius of gyration Rg (Guinier) rg_guinier27.41
Radius of gyration Rg (electron density) rg_electron26.49
Forward intensity I(0) i074840400.00
Molecular weight molecular_weight66697.0 kDa
Excluded volume excluded_volume82801 ų
Envelope volume envelope_volume99590 ų
Hydration-shell volume shell_volume31458 ų
Envelope diameter envelope_diameter91.9
Shell Rg shell_rg33.69
Envelope Rg envelope_rg26.31
Shape Rg shape_rg26.47
Total Rg total_rg27.27
Total atoms total_atoms4691
Residues n_residues593
Spherical-harmonic order n_harmonics20
q range q_range— – 0.5000 −1
Data points n_points101
Shell type shell_typedirectional
Solvent electron density solvent_density0.3340 e/ų
Shell contrast contrast_shell0.0300 e/ų
CRYSOL version crysol_version4.1.3

4. P(r) Distance Distribution (GNOM inversion) 4. P(r) Analysis (GNOM)

Maximum dimension Dmax dmax86.7
Rg (real space) rg_real27.40
Rg uncertainty (real space) rg_real_error0.59
I(0) (real space) i0_real7.4840e+07
I(0) uncertainty (real space) i0_real_error1.1180e+06
Rg (reciprocal space) rg_reciprocal27.41
I(0) (reciprocal space) i0_reciprocal74840000.0000
Solution quality estimate total_estimate0.9000
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary29.9
Skewness Skewness skewness0.299
Kurtosis Kurtosis kurtosis-0.545
Angular range angular_range— – 0.2900 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha18450000.0000
Real-space data points n_real_points59
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.930; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.995; Smooth: 0.910

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 2 domains

CATH v4.4 (2 domains)

Domain ID domain_id8f8eA01
Class class2 — Mainly Beta
Architecture architecture130 — 7 Propeller
Topology topology10 — Methylamine Dehydrogenase; Chain H
Homologous superfamily homologous superfamily10 — YVTN repeat-like/Quinoprotein amine dehydrogenase
Domain ID domain_id8f8eB01
Class class2 — Mainly Beta
Architecture architecture130 — 7 Propeller
Topology topology10 — Methylamine Dehydrogenase; Chain H
Homologous superfamily homologous superfamily10 — YVTN repeat-like/Quinoprotein amine dehydrogenase

8. Citations (1)

9. Files and Curves (10)