1fnk

CRYSTAL STRUCTURE ANALYSIS OF CHORISMATE MUTASE MUTANT C88K/R90S

Method: X-RAY DIFFRACTION Dmax: 51.3 Å Quality: REASONABLE

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

PROTEIN (CHORISMATE MUTASE)

Bacillus subtilis

UniProt P19080

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 1–127 Mutation:YES Non-standard monomer:Yes (specific site not provided by mmCIF) No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7;295 K;Protein solution: 10 mM Tris-HCl, 2mM DTT, 0.125 mM EDTA, Reservoir solution: 30% PEG 400, 50 mM Tris-HCl, 50 mM magnesium chloride, pH 7.0, VAPOR DIFFUSION, HANGING DROP, temperature 295K Resolution 2.00 Å R-free 0.251

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 22 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CHMU_BACSU
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–127; UniProt 1–127

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 1fnk

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id1fnk
Deposition date deposition_date2000-08-22
Structure title titleCRYSTAL STRUCTURE ANALYSIS OF CHORISMATE MUTASE MUTANT C88K/R90S
Keywords keywordsCHORISMATE MUTASE, PROTEIN, MUTANT, PSEUDO-ALPHA BETA-BARREL, TRIMER, ISOMERASE; ISOMERASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier15.58
Radius of gyration Rg (electron density) rg_electron14.17
Forward intensity I(0) i03477840.00
Molecular weight molecular_weight13145.0 kDa
Excluded volume excluded_volume16544 ų
Envelope volume envelope_volume19401 ų
Hydration-shell volume shell_volume11815 ų
Envelope diameter envelope_diameter51.3
Shell Rg shell_rg19.79
Envelope Rg envelope_rg14.56
Shape Rg shape_rg14.16
Total Rg total_rg15.43
Total atoms total_atoms917
Residues n_residues115
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 dmax51.3
Rg (real space) rg_real15.52
Rg uncertainty (real space) rg_real_error0.35
I(0) (real space) i0_real3.4780e+06
I(0) uncertainty (real space) i0_real_error4.3210e+04
Rg (reciprocal space) rg_reciprocal15.52
I(0) (reciprocal space) i0_reciprocal3478000.0000
Solution quality estimate total_estimate0.6347
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary18.2
Skewness Skewness skewness0.242
Kurtosis Kurtosis kurtosis-0.348
Angular range angular_range— – 0.5000 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha1174000.0000
Real-space data points n_real_points80
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.827; Stabil: 1.000; Sysdev: 0.256; Positv: 1.000; Valcen: 0.998; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1fnka_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.79 — Bacillus chorismate mutase-like
Superfamily Superfamily superfamilyd.79.1 — YjgF-like
Family Family familyd.79.1.2 — Chorismate mutase

CATH v4.4 (1 domains)

Domain ID domain_id1fnkA00
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology1330 — 60s Ribosomal Protein L30; Chain: A;
Homologous superfamily homologous superfamily40 — RutC-like

8. Citations (3)

9. Files and Curves (10)