1g5j

COMPLEX OF BCL-XL WITH PEPTIDE FROM BAD

Method: SOLUTION NMR Dmax: 55.5 Å Quality: GOOD

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

APOPTOSIS REGULATOR BCL-X

Homo sapiens

UniProt Q07817

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 1–44 Chain A; UniProt 85–209 Fragment:RESIDUES 1-209 BAD PROTEIN × 1 (Q92934) SOLUTION NMR NMR measurement conditions:pH 7;303 K;Ionic strength (raw mmCIF value) 40 mM sodium phosphate;Pressure ambient NMR sample composition:15N-Bcl-xL/unlabeled Bad peptide; 15N,13C-Bcl-xL/unlabelled Bad peptide | H2O; 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.

123 other PDB entries and 195 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BCLX_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 5–48; UniProt 1–44 Author chain A; PDBConstruct 49–173; UniProt 85–209

BAD PROTEIN

OrganismNot specified

UniProt Q92934

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 B; UniProt 140–164 Fragment:RESIDUES 140-164 Mutation:E320K, G321D, G325K APOPTOSIS REGULATOR BCL-X × 1 (Q07817) SOLUTION NMR NMR measurement conditions:pH 7;303 K;Ionic strength (raw mmCIF value) 40 mM sodium phosphate;Pressure ambient NMR sample composition:15N-Bcl-xL/unlabeled Bad peptide; 15N,13C-Bcl-xL/unlabelled Bad peptide | H2O; 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.

2 other PDB entries and 2 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BAD_HUMAN
Isoform
PDB entities 2
Chains and sequence ranges Author chain B; PDBConstruct 1–25; UniProt 140–164

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 1g5j

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1g5j
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1g5j
Deposition date deposition_date2000-11-01
Structure title titleCOMPLEX OF BCL-XL WITH PEPTIDE FROM BAD
Keywords keywordscomplex, APOPTOSIS; APOPTOSIS
Experimental Method methodSOLUTION NMR

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

Radius of gyration Rg (Guinier) rg_guinier18.17
Radius of gyration Rg (electron density) rg_electron16.53
Forward intensity I(0) i010570600.00
Molecular weight molecular_weight23052.0 kDa
Excluded volume excluded_volume28441 ų
Envelope volume envelope_volume34357 ų
Hydration-shell volume shell_volume17065 ų
Envelope diameter envelope_diameter56.1
Shell Rg shell_rg22.95
Envelope Rg envelope_rg17.06
Shape Rg shape_rg16.48
Total Rg total_rg17.76
Total atoms total_atoms3164
Residues n_residues200
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 dmax55.5
Rg (real space) rg_real18.04
Rg uncertainty (real space) rg_real_error0.29
I(0) (real space) i0_real1.0570e+07
I(0) uncertainty (real space) i0_real_error1.1910e+05
Rg (reciprocal space) rg_reciprocal18.06
I(0) (reciprocal space) i0_reciprocal10570000.0000
Solution quality estimate total_estimate0.8215
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary24.0
Skewness Skewness skewness0.095
Kurtosis Kurtosis kurtosis-0.452
Angular range angular_range— – 0.4400 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha3154000.0000
Real-space data points n_real_points75
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.903; Stabil: 0.996; Sysdev: 1.000; Positv: 1.000; Valcen: 0.977; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (3 domains)

Domain ID domain_idd1g5ja1
Class classf — Membrane and cell surface proteins and peptides
Fold Fold foldf.1 — Toxins' membrane translocation domains
Superfamily Superfamily superfamilyf.1.4 — Bcl-2 inhibitors of programmed cell death
Family Family familyf.1.4.1 — Bcl-2 inhibitors of programmed cell death
Domain ID domain_idd1g5ja2
Class classl — Artifacts
Fold Fold foldl.1 — Tags
Superfamily Superfamily superfamilyl.1.1 — Tags
Family Family familyl.1.1.1 — Tags
Domain ID domain_idd1g5ja3
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_id1g5jA00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology437 — Apoptosis Regulator Bcl-x
Homologous superfamily homologous superfamily10 — Blc2-like

8. Citations (1)

9. Files and Curves (10)