1wxv

Solution structure of the ubiquitin domain of BCL-2 binding athanogene-1

Method: SOLUTION NMR Dmax: 52.3 Å Quality: REASONABLE

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

BAG-family molecular chaperone regulator-1

Homo sapiens

UniProt Q99933

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 73–151 Fragment:ubiquitin-like domain No other associated polymer SOLUTION NMR NMR measurement conditions:pH 7;298 K;Ionic strength (raw mmCIF value) 100mM;Pressure ambient NMR sample composition:1.04mM ubiquitin domain U-13C, 15N; 20mM d-Tris-HCl; 100mM NaCl; 1mM d-DTT; 0.02 % NaN3 | 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.

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

View Construct and Data Evidence
UniProt name BAG1_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 8–86; UniProt 73–151

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 1wxv

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1wxv
Download Download

2. Structure Basics 2. Structure Basics

Entry ID entry_id1wxv
Deposition date deposition_date2005-02-02
Structure title titleSolution structure of the ubiquitin domain of BCL-2 binding athanogene-1
Keywords keywords;structural genomics, apoptosis, RIKEN Structural Genomics/Proteomics Initiative, RSGI, NPPSFA, National Project on Protein Structural and Functional Analyses ;; APOPTOSIS
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier13.63
Radius of gyration Rg (electron density) rg_electron13.02
Forward intensity I(0) i0548599000.00
Molecular weight molecular_weight192040.0 kDa
Excluded volume excluded_volume238560 ų
Envelope volume envelope_volume28349 ų
Hydration-shell volume shell_volume14420 ų
Envelope diameter envelope_diameter62.5
Shell Rg shell_rg22.69
Envelope Rg envelope_rg17.99
Shape Rg shape_rg13.01
Total Rg total_rg13.27
Total atoms total_atoms27100
Residues n_residues1840
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 dmax52.3
Rg (real space) rg_real13.64
Rg uncertainty (real space) rg_real_error0.58
I(0) (real space) i0_real5.4860e+08
I(0) uncertainty (real space) i0_real_error7.6770e+06
Rg (reciprocal space) rg_reciprocal13.64
I(0) (reciprocal space) i0_reciprocal548600000.0000
Solution quality estimate total_estimate0.6904
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary15.9
Skewness Skewness skewness0.400
Kurtosis Kurtosis kurtosis0.089
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha316400.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.370; Stabil: 0.998; Sysdev: 1.000; Positv: 1.000; Valcen: 0.867; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (1)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (3 domains)

Domain ID domain_idd1wxva1
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.15 — beta-Grasp (ubiquitin-like)
Superfamily Superfamily superfamilyd.15.1 — Ubiquitin-like
Family Family familyd.15.1.1 — Ubiquitin-related
Domain ID domain_idd1wxva2
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags
Domain ID domain_idd1wxva3
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags

CATH v4.4 (1 domains)

Domain ID domain_id1wxvA01
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology20 — Ubiquitin-like (UB roll)
Homologous superfamily homologous superfamily90 — Phosphatidylinositol 3-kinase Catalytic Subunit; Chain A, domain 1

8. Citations (1)

9. Files and Curves (10)