3jzq

Human MDMX liganded with a 12mer peptide inhibitor (pDIQ)

Method: X-RAY DIFFRACTION Dmax: 69.4 Å Quality: GOOD

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

Protein Mdm4

Homo sapiens

UniProt O15151

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 heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 23–111 Not recorded pDIQ peptide (12mer) × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.4;292 K;2.1 M ammonium sulfate, 10 mM Tris HCl, pH 7.4, VAPOR DIFFUSION, HANGING DROP, temperature 292K Resolution 1.80 Å R-free 0.224
2 Protein heterocomplex Heteromer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 23–111 Not recorded pDIQ peptide (12mer) × 1 SO4 SULFATE ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.4;292 K;2.1 M ammonium sulfate, 10 mM Tris HCl, pH 7.4, VAPOR DIFFUSION, HANGING DROP, temperature 292K Resolution 1.80 Å R-free 0.224

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.

36 other PDB entries and 65 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name MDM4_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–89; UniProt 23–111 Author chain B; PDBConstruct 1–89; UniProt 23–111

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 3jzq

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3jzq
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3jzq
Deposition date deposition_date2009-09-24
Structure title titleHuman MDMX liganded with a 12mer peptide inhibitor (pDIQ)
Keywords keywords;CELL CYCLE, P53-BINDING PROTEIN MDM4, DOUBLE MINUTE 4 PROTEIN, Alternative splicing, Metal-binding, Nucleus, Polymorphism, Zinc, Zinc-finger ;; CELL CYCLE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier20.23
Radius of gyration Rg (electron density) rg_electron19.24
Forward intensity I(0) i09011630.00
Molecular weight molecular_weight22732.0 kDa
Excluded volume excluded_volume28670 ų
Envelope volume envelope_volume34009 ų
Hydration-shell volume shell_volume15587 ų
Envelope diameter envelope_diameter69.2
Shell Rg shell_rg24.39
Envelope Rg envelope_rg19.52
Shape Rg shape_rg19.21
Total Rg total_rg20.15
Total atoms total_atoms1596
Residues n_residues195
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 dmax69.4
Rg (real space) rg_real20.27
Rg uncertainty (real space) rg_real_error0.56
I(0) (real space) i0_real9.0120e+06
I(0) uncertainty (real space) i0_real_error1.2950e+05
Rg (reciprocal space) rg_reciprocal20.27
I(0) (reciprocal space) i0_reciprocal9012000.0000
Solution quality estimate total_estimate0.8671
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary20.8
Skewness Skewness skewness0.385
Kurtosis Kurtosis kurtosis-0.388
Angular range angular_range— – 0.3950 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha1769000.0000
Real-space data points n_real_points71
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.787; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.944; Smooth: 0.964

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd3jzqa_
Class classa — All alpha proteins
Fold Fold folda.42 — SWIB/MDM2 domain
Superfamily Superfamily superfamilya.42.1 — SWIB/MDM2 domain
Family Family familya.42.1.0 — automated matches
Domain ID domain_idd3jzqb_
Class classa — All alpha proteins
Fold Fold folda.42 — SWIB/MDM2 domain
Superfamily Superfamily superfamilya.42.1 — SWIB/MDM2 domain
Family Family familya.42.1.0 — automated matches

CATH v4.4 (2 domains)

Domain ID domain_id3jzqA00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology245 — MDM2
Homologous superfamily homologous superfamily10 — SWIB/MDM2 domain
Domain ID domain_id3jzqB00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology245 — MDM2
Homologous superfamily homologous superfamily10 — SWIB/MDM2 domain

8. Citations (1)

9. Files and Curves (10)