1zzf

The DNA-bound solution structure of HPV-16 E2 DNA-binding domain

Method: SOLUTION NMR Dmax: 54.8 Å Quality: GOOD

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

Regulatory protein E2

Human papillomavirus type 16

UniProt P03120

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 homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 286–365 Chain B; UniProt 286–365 Fragment:DNA-binding domain No other associated polymer SOLUTION NMR NMR measurement conditions:pH 5.6;318 K;Ionic strength (raw mmCIF value) 250 mM NaCl;Pressure ambient NMR sample composition:DNA-E2C complex (15N) 0.6mM, 25mM Acetate+ 10mM Phosphate, pH 5.6, NaCl 250mM, DTT 5mM | 95% H20, 5% D2O NMR sample composition:DNA-E2C complex (15N, 13C) 0.6mM, 25mM Acetate+ 10mM Phosphate, pH 5.6, NaCl 250mM, DTT 5mM | 95% H20, 5% D2O NMR sample composition:DNA-E2C complex (15N) 0.2mM, 25mM Acetate+ 10mM Phosphate, pH 5.6, NaCl 250mM, DTT 5mM, Philamentosus phage 17mg/ml | 95% H20, 5% D2O Resolution not provided

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.

6 other PDB entries and 7 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name VE2_HPV16
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–81; UniProt 286–365 Author chain B; PDBConstruct 2–81; UniProt 286–365

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 1zzf

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1zzf
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1zzf
Deposition date deposition_date2005-06-14
Structure title titleThe DNA-bound solution structure of HPV-16 E2 DNA-binding domain
Keywords keywordsdna-protein complex, papillomavirus transcription factor, dimeric beta-barrel, TRANSCRIPTION; TRANSCRIPTION
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier17.54
Radius of gyration Rg (electron density) rg_electron16.44
Forward intensity I(0) i06398410.00
Molecular weight molecular_weight18780.0 kDa
Excluded volume excluded_volume23758 ų
Envelope volume envelope_volume28689 ų
Hydration-shell volume shell_volume14866 ų
Envelope diameter envelope_diameter53.8
Shell Rg shell_rg22.05
Envelope Rg envelope_rg16.61
Shape Rg shape_rg16.40
Total Rg total_rg17.59
Total atoms total_atoms2664
Residues n_residues162
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 dmax54.8
Rg (real space) rg_real17.44
Rg uncertainty (real space) rg_real_error0.35
I(0) (real space) i0_real6.3980e+06
I(0) uncertainty (real space) i0_real_error7.9420e+04
Rg (reciprocal space) rg_reciprocal17.45
I(0) (reciprocal space) i0_reciprocal6398000.0000
Solution quality estimate total_estimate0.8927
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary21.9
Skewness Skewness skewness0.149
Kurtosis Kurtosis kurtosis-0.417
Angular range angular_range— – 0.4550 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha1003000.0000
Real-space data points n_real_points76
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.885; Stabil: 0.998; Sysdev: 1.000; Positv: 1.000; Valcen: 0.994; Smooth: 0.958

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (1)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd1zzfa_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.58 — Ferredoxin-like
Superfamily Superfamily superfamilyd.58.8 — Viral DNA-binding domain
Family Family familyd.58.8.1 — Viral DNA-binding domain
Domain ID domain_idd1zzfb_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.58 — Ferredoxin-like
Superfamily Superfamily superfamilyd.58.8 — Viral DNA-binding domain
Family Family familyd.58.8.1 — Viral DNA-binding domain

CATH v4.4 (2 domains)

Domain ID domain_id1zzfA00
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology70 — Alpha-Beta Plaits
Homologous superfamily homologous superfamily330 — RRM (RNA recognition motif) domain
Domain ID domain_id1zzfB00
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology70 — Alpha-Beta Plaits
Homologous superfamily homologous superfamily330 — RRM (RNA recognition motif) domain

8. Citations (1)

9. Files and Curves (10)