9cbe

Structure of a type III antifreeze protein isoform HPLC12 re-refined using standard protocols

Method: X-RAY DIFFRACTION Dmax: 41.6 Å Quality: GOOD

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

Type-3 ice-structuring protein HPLC 12

Zoarces americanus

UniProt P19614

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 1–63 Not recorded No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:PROTEIN WAS CRYSTALLIZED IN 50-55% AMMONIUM SULFATE, 0.1 M SODIUM ACETATE PH 4-4.5 Resolution 1.90 Å R-free 0.189

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.

34 other PDB entries and 38 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name ANP12_ZOAAM
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–64; UniProt 1–63

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 9cbe

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id9cbe
Deposition date deposition_date2024-06-19
最后修订 last_revision2024-07-17
Structure title titleStructure of a type III antifreeze protein isoform HPLC12 re-refined using standard protocols
Keywords keywordsRe-refinement, ANTIFREEZE PROTEIN; ANTIFREEZE PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier12.13
Radius of gyration Rg (electron density) rg_electron10.79
Forward intensity I(0) i01097790.00
Molecular weight molecular_weight7096.0 kDa
Excluded volume excluded_volume8985 ų
Envelope volume envelope_volume9532 ų
Hydration-shell volume shell_volume7858 ų
Envelope diameter envelope_diameter39.1
Shell Rg shell_rg16.08
Envelope Rg envelope_rg11.11
Shape Rg shape_rg10.76
Total Rg total_rg12.30
Total atoms total_atoms491
Residues n_residues66
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 dmax41.6
Rg (real space) rg_real12.07
Rg uncertainty (real space) rg_real_error0.27
I(0) (real space) i0_real1.0980e+06
I(0) uncertainty (real space) i0_real_error1.1410e+04
Rg (reciprocal space) rg_reciprocal12.07
I(0) (reciprocal space) i0_reciprocal1098000.0000
Solution quality estimate total_estimate0.8508
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary15.3
Skewness Skewness skewness0.224
Kurtosis Kurtosis kurtosis-0.087
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha239400.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.698; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.999; Smooth: 0.962

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

8. Citations (2)

9. Files and Curves (10)