3fp2

Crystal structure of Tom71 complexed with Hsp82 C-terminal fragment

Method: X-RAY DIFFRACTION Dmax: 114.2 Å Quality: GOOD

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

TPR repeat-containing protein YHR117W

Saccharomyces cerevisiae

UniProt P38825

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 107–639 Fragment:UNP residues 107-639 ATP-dependent molecular chaperone HSP82 × 1 (P02829) CL CHLORIDE ION × 1 MG MAGNESIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;PEG6K, Ethylene Glyco 5%, NaCl 0.15M, Tris 10mM, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K Resolution 1.98 Å R-free 0.236

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.

3 other PDB entries and 3 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name YHR7_YEAST
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 5–537; UniProt 107–639

ATP-dependent molecular chaperone HSP82

OrganismNot specified

UniProt P02829

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 Q; UniProt 698–709 Not recorded TPR repeat-containing protein YHR117W × 1 (P38825) CL CHLORIDE ION × 1 MG MAGNESIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 8;298 K;PEG6K, Ethylene Glyco 5%, NaCl 0.15M, Tris 10mM, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 298K Resolution 1.98 Å R-free 0.236

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.

47 other PDB entries and 61 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name HSP82_YEAST
Isoform
PDB entities 2
Chains and sequence ranges Author chain Q; PDBConstruct 1–12; UniProt 698–709

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 3fp2

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 3fp2
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2. Structure Basics 2. Structure Basics

Entry ID entry_id3fp2
Deposition date deposition_date2009-01-03
Structure title titleCrystal structure of Tom71 complexed with Hsp82 C-terminal fragment
Keywords keywords;Tom71, mitochondria translocation, chaperone, allosteric regulation, Phosphoprotein, TPR repeat, ATP-binding, Nucleotide-binding, Stress response, TRANSPORT PROTEIN ;; TRANSPORT PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier32.49
Radius of gyration Rg (electron density) rg_electron32.69
Forward intensity I(0) i047692600.00
Molecular weight molecular_weight55316.0 kDa
Excluded volume excluded_volume69716 ų
Envelope volume envelope_volume90587 ų
Hydration-shell volume shell_volume26198 ų
Envelope diameter envelope_diameter116.2
Shell Rg shell_rg34.81
Envelope Rg envelope_rg32.38
Shape Rg shape_rg32.71
Total Rg total_rg32.81
Total atoms total_atoms3901
Residues n_residues488
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 dmax114.2
Rg (real space) rg_real33.01
Rg uncertainty (real space) rg_real_error1.38
I(0) (real space) i0_real4.7690e+07
I(0) uncertainty (real space) i0_real_error8.5310e+05
Rg (reciprocal space) rg_reciprocal32.79
I(0) (reciprocal space) i0_reciprocal47680000.0000
Solution quality estimate total_estimate0.7966
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary30.3
Skewness Skewness skewness0.580
Kurtosis Kurtosis kurtosis-0.375
Angular range angular_range— – 0.2450 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha3350000.0000
Real-space data points n_real_points50
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.663; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 0.563; Smooth: 0.801

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

8. Citations (1)

9. Files and Curves (10)