9ym3

Backbone Modification in the Villin Headpiece Miniprotein: HP35 with ACPC at Position 30

Method: SOLUTION NMR Dmax: 30.6 Å Quality: GOOD

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

Villin-1

OrganismNot specified

UniProt P02640

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 792–826 Non-standard monomer:Yes (specific site not provided by mmCIF) No other associated polymer SOLUTION NMR NMR measurement conditions:pH 5;288 K;Ionic strength (raw mmCIF value) 10;Pressure 1 NMR sample composition:1.0 mM Villin-1 headpiece: Met12Nle, Lys30ACPC, 0.2 mM DSS, 90% H2O/10% D2O | 90% H2O/10% 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.

45 other PDB entries and 51 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name VILI_CHICK
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–35; UniProt 792–826

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 9ym3

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9ym3
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9ym3
Deposition date deposition_date2025-10-09
Structure title titleBackbone Modification in the Villin Headpiece Miniprotein: HP35 with ACPC at Position 30
Keywords keywordsminiprotein, heterogeneous backbone, proteomimetic, STRUCTURAL PROTEIN; STRUCTURAL PROTEIN
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier9.40
Radius of gyration Rg (electron density) rg_electron9.14
Forward intensity I(0) i020045500.00
Molecular weight molecular_weight40257.0 kDa
Excluded volume excluded_volume51780 ų
Envelope volume envelope_volume7201 ų
Hydration-shell volume shell_volume6605 ų
Envelope diameter envelope_diameter31.8
Shell Rg shell_rg14.82
Envelope Rg envelope_rg10.09
Shape Rg shape_rg9.13
Total Rg total_rg9.55
Total atoms total_atoms5780
Residues n_residues330
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 dmax30.6
Rg (real space) rg_real9.35
Rg uncertainty (real space) rg_real_error0.33
I(0) (real space) i0_real2.0050e+07
I(0) uncertainty (real space) i0_real_error2.0230e+05
Rg (reciprocal space) rg_reciprocal9.35
I(0) (reciprocal space) i0_reciprocal20050000.0000
Solution quality estimate total_estimate0.8052
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary14.7
Skewness Skewness skewness-0.118
Kurtosis Kurtosis kurtosis-0.651
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha5261.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.523; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.949; Smooth: 0.945

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (1)

8. Citations (1)

9. Files and Curves (10)