2znd

Crystal structure of Ca2+-free form of des3-20ALG-2

Method: X-RAY DIFFRACTION Dmax: 61.7 Å Quality: GOOD

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

Programmed cell death protein 6

Homo sapiens

UniProt O75340

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 20–191 Fragment:residues 20-191 MRD (4R)-2-METHYLPENTANE-2,4-DIOL × 10 PO4 PHOSPHATE ION × 4 NA SODIUM ION × 6 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6.5;277 K;40% 2-methyl-2,4-pentanediol, 0.1M Na2HPO4-KH2PO4, 2mM EDTA, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 277K Resolution 1.70 Å R-free 0.222

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.

9 other PDB entries and 19 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name PDCD6_HUMAN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–172; UniProt 20–191

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 2znd

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id2znd
Deposition date deposition_date2008-04-22
Structure title titleCrystal structure of Ca2+-free form of des3-20ALG-2
Keywords keywordsPENTA-EF-HAND PROTEIN, CALCIUM BINDING PROTEIN, Apoptosis, Calcium, Endoplasmic reticulum, Membrane, Nucleus, Polymorphism; APOPTOSIS
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier19.03
Radius of gyration Rg (electron density) rg_electron17.92
Forward intensity I(0) i07703720.00
Molecular weight molecular_weight20501.0 kDa
Excluded volume excluded_volume25668 ų
Envelope volume envelope_volume30781 ų
Hydration-shell volume shell_volume15040 ų
Envelope diameter envelope_diameter64.0
Shell Rg shell_rg23.15
Envelope Rg envelope_rg18.28
Shape Rg shape_rg17.94
Total Rg total_rg18.73
Total atoms total_atoms1444
Residues n_residues167
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 dmax61.7
Rg (real space) rg_real19.00
Rg uncertainty (real space) rg_real_error0.53
I(0) (real space) i0_real7.7040e+06
I(0) uncertainty (real space) i0_real_error9.7750e+04
Rg (reciprocal space) rg_reciprocal19.00
I(0) (reciprocal space) i0_reciprocal7704000.0000
Solution quality estimate total_estimate0.8186
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary21.4
Skewness Skewness skewness0.263
Kurtosis Kurtosis kurtosis-0.397
Angular range angular_range— – 0.4200 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha863400.0000
Real-space data points n_real_points73
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.883; Stabil: 0.999; Sysdev: 1.000; Positv: 1.000; Valcen: 0.991; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd2znda_
Class classa — All alpha proteins
Fold Fold folda.39 — EF Hand-like
Superfamily Superfamily superfamilya.39.1 — EF-hand
Family Family familya.39.1.0 — automated matches

CATH v4.4 (1 domains)

Domain ID domain_id2zndA00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology238 — Recoverin; domain 1
Homologous superfamily homologous superfamily10 — EF-hand

8. Citations (2)

9. Files and Curves (10)