2wer

Yeast Hsp90 N-terminal domain LI-IV mutant with Radicicol

Method: X-RAY DIFFRACTION Dmax: 79.2 Å Quality: EXCELLENT

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

ATP-DEPENDENT MOLECULAR CHAPERONE HSP82

SACCHAROMYCES CEREVISIAE

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 homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 1–220 Fragment:N-TERMINAL DOMAIN, RESIDUES 1-220 Mutation:YES RDC RADICICOL × 2 X-RAY DIFFRACTION X-ray crystallization conditions:pH 7;pH 7 Resolution 1.60 Å R-free 0.273
2 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain B; UniProt 1–220 Fragment:N-TERMINAL DOMAIN, RESIDUES 1-220 Mutation:YES RDC RADICICOL × 2 X-RAY DIFFRACTION X-ray crystallization conditions:pH 7;pH 7 Resolution 1.60 Å R-free 0.273

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 60 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name HSP82_YEAST
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–220; UniProt 1–220 Author chain B; PDBConstruct 1–220; UniProt 1–220

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 2wer

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2wer
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2wer
Deposition date deposition_date2009-04-01
Structure title titleYeast Hsp90 N-terminal domain LI-IV mutant with Radicicol
Keywords keywordsATPASE, CHAPERONE, ATP-BINDING, PHOSPHOPROTEIN, STRESS RESPONSE, NUCLEOTIDE-BINDING; CHAPERONE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier25.38
Radius of gyration Rg (electron density) rg_electron24.47
Forward intensity I(0) i037371700.00
Molecular weight molecular_weight48308.0 kDa
Excluded volume excluded_volume60929 ų
Envelope volume envelope_volume74632 ų
Hydration-shell volume shell_volume25478 ų
Envelope diameter envelope_diameter80.7
Shell Rg shell_rg31.54
Envelope Rg envelope_rg24.49
Shape Rg shape_rg24.45
Total Rg total_rg25.37
Total atoms total_atoms3402
Residues n_residues428
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 dmax79.2
Rg (real space) rg_real25.36
Rg uncertainty (real space) rg_real_error0.49
I(0) (real space) i0_real3.7370e+07
I(0) uncertainty (real space) i0_real_error5.6180e+05
Rg (reciprocal space) rg_reciprocal25.37
I(0) (reciprocal space) i0_reciprocal37370000.0000
Solution quality estimate total_estimate0.9097
Solution quality rating solution_quality EXCELLENT a EXCELLENT solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary28.9
Skewness Skewness skewness0.273
Kurtosis Kurtosis kurtosis-0.560
Angular range angular_range— – 0.3150 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha6820000.0000
Real-space data points n_real_points64
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.951; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.986; Smooth: 0.982

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd2wera_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.122 — ATPase domain of HSP90 chaperone/DNA topoisomerase II/histidine kinase
Superfamily Superfamily superfamilyd.122.1 — ATPase domain of HSP90 chaperone/DNA topoisomerase II/histidine kinase
Family Family familyd.122.1.1 — Heat shock protein 90, HSP90, N-terminal domain
Domain ID domain_idd2werb_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.122 — ATPase domain of HSP90 chaperone/DNA topoisomerase II/histidine kinase
Superfamily Superfamily superfamilyd.122.1 — ATPase domain of HSP90 chaperone/DNA topoisomerase II/histidine kinase
Family Family familyd.122.1.1 — Heat shock protein 90, HSP90, N-terminal domain

CATH v4.4 (2 domains)

Domain ID domain_id2werA00
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology565 — Heat Shock Protein 90
Homologous superfamily homologous superfamily10 — Histidine kinase-like ATPase, C-terminal domain
Domain ID domain_id2werB00
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology565 — Heat Shock Protein 90
Homologous superfamily homologous superfamily10 — Histidine kinase-like ATPase, C-terminal domain

8. Citations (1)

9. Files and Curves (10)