6che

Selenomethionine mutant (A34Sem) of protein GB1 examined by X-ray diffraction

Method: X-RAY DIFFRACTION Dmax: 40.7 Å Quality: GOOD

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

Immunoglobulin G-binding protein G

Streptococcus sp. group G

UniProt P19909

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 304–357 Mutation:A34Sem Non-standard monomer:Yes (specific site not provided by mmCIF) MPD (4S)-2-METHYL-2,4-PENTANEDIOL × 2 IMD IMIDAZOLE × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 4.9;283.15 K;49% MPD 20% IPA 25 mM sodium acetate pH 4.9 20 mg/ml protein in 25 mM sodium acetate buffer pH 5.5 and 2 mM TCEP Resolution 1.10 Å R-free 0.147

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.

76 other PDB entries and 116 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name SPG2_STRSG
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 3–56; UniProt 304–357

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 6che

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 6che
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2. Structure Basics 2. Structure Basics

Entry ID entry_id6che
Deposition date deposition_date2018-02-22
Structure title titleSelenomethionine mutant (A34Sem) of protein GB1 examined by X-ray diffraction
Keywords keywordsImmunoglobulin G-binding protein domain B1, IMMUNE SYSTEM; IMMUNE SYSTEM
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier11.88
Radius of gyration Rg (electron density) rg_electron10.62
Forward intensity I(0) i01001330.00
Molecular weight molecular_weight6558.0 kDa
Excluded volume excluded_volume8178 ų
Envelope volume envelope_volume8927 ų
Hydration-shell volume shell_volume7495 ų
Envelope diameter envelope_diameter37.9
Shell Rg shell_rg15.75
Envelope Rg envelope_rg11.00
Shape Rg shape_rg10.59
Total Rg total_rg12.10
Total atoms total_atoms909
Residues n_residues55
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 dmax40.7
Rg (real space) rg_real11.83
Rg uncertainty (real space) rg_real_error0.26
I(0) (real space) i0_real1.0010e+06
I(0) uncertainty (real space) i0_real_error1.1500e+04
Rg (reciprocal space) rg_reciprocal11.84
I(0) (reciprocal space) i0_reciprocal1001000.0000
Solution quality estimate total_estimate0.8647
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary14.4
Skewness Skewness skewness0.226
Kurtosis Kurtosis kurtosis-0.241
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha231500.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.748; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.995; Smooth: 0.997

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 3 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd6chea1
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.15 — beta-Grasp (ubiquitin-like)
Superfamily Superfamily superfamilyd.15.7 — Immunoglobulin-binding domains
Family Family familyd.15.7.1 — Immunoglobulin-binding domains
Domain ID domain_idd6chea2
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_id6cheA00
Class class3 — Alpha Beta
Architecture architecture10 — Roll
Topology topology20 — Ubiquitin-like (UB roll)
Homologous superfamily homologous superfamily10

8. Citations (1)

9. Files and Curves (10)