3rau

Crystal structure of the HD-PTP Bro1 domain

Method: X-RAY DIFFRACTION Dmax: 122.4 Å Quality: GOOD

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

Tyrosine-protein phosphatase non-receptor type 23

Homo sapiens

UniProt Q9H3S7

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 2–361 Chain B; UniProt 2–361 Fragment:UNP residues 2-361 ACT ACETATE ION × 8 EDO 1,2-ETHANEDIOL × 2 GOL GLYCEROL × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 5.5;291 K;0.1M MES pH5.5, 16% PEG3350, 0.3M Magnesium Acetate, VAPOR DIFFUSION, HANGING DROP, temperature 291K Resolution 1.95 Å R-free 0.215

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.

10 other PDB entries and 25 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PTN23_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 4–363; UniProt 2–361 Author chain B; PDBConstruct 4–363; UniProt 2–361

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 3rau

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id3rau
Deposition date deposition_date2011-03-28
Structure title titleCrystal structure of the HD-PTP Bro1 domain
Keywords keywordsBro1 domain, HYDROLASE; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier32.19
Radius of gyration Rg (electron density) rg_electron31.96
Forward intensity I(0) i0100893000.00
Molecular weight molecular_weight81231.0 kDa
Excluded volume excluded_volume102310 ų
Envelope volume envelope_volume127260 ų
Hydration-shell volume shell_volume34777 ų
Envelope diameter envelope_diameter129.8
Shell Rg shell_rg36.81
Envelope Rg envelope_rg31.91
Shape Rg shape_rg31.98
Total Rg total_rg32.29
Total atoms total_atoms5709
Residues n_residues715
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 dmax122.4
Rg (real space) rg_real32.47
Rg uncertainty (real space) rg_real_error1.41
I(0) (real space) i0_real1.0090e+08
I(0) uncertainty (real space) i0_real_error1.8090e+06
Rg (reciprocal space) rg_reciprocal32.35
I(0) (reciprocal space) i0_reciprocal100900000.0000
Solution quality estimate total_estimate0.8107
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary35.0
Skewness Skewness skewness0.579
Kurtosis Kurtosis kurtosis0.080
Angular range angular_range— – 0.2450 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha24580000.0000
Real-space data points n_real_points50
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.608; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.726; Smooth: 0.985

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd3raua_
Class classa — All alpha proteins
Fold Fold folda.118 — alpha-alpha superhelix
Superfamily Superfamily superfamilya.118.8 — TPR-like
Family Family familya.118.8.0 — automated matches
Domain ID domain_idd3raub_
Class classa — All alpha proteins
Fold Fold folda.118 — alpha-alpha superhelix
Superfamily Superfamily superfamilya.118.8 — TPR-like
Family Family familya.118.8.0 — automated matches

CATH v4.4 (2 domains)

Domain ID domain_id3rauA00
Class class1 — Mainly Alpha
Architecture architecture25 — Alpha Horseshoe
Topology topology40 — Serine Threonine Protein Phosphatase 5, Tetratricopeptide repeat
Homologous superfamily homologous superfamily280 — alix/aip1 like domains
Domain ID domain_id3rauB00
Class class1 — Mainly Alpha
Architecture architecture25 — Alpha Horseshoe
Topology topology40 — Serine Threonine Protein Phosphatase 5, Tetratricopeptide repeat
Homologous superfamily homologous superfamily280 — alix/aip1 like domains

8. Citations (1)

9. Files and Curves (10)