1ojn

SPECIFICITY AND MECHANISM OF STREPTOCOCCUS PNEUMONIAE HYALURONATE LYASE: COMPLEX OF THE TYR408PHE MUTANT WITH 6-SULPHATED CHONDROITIN DISACCHARIDE

Method: X-RAY DIFFRACTION Dmax: 95.5 Å Quality: GOOD

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

HYALURONATE LYASE

STREPTOCOCCUS PNEUMONIAE

UniProt Q54873

State in the Current Structure

Assembly Oligomeric State Construct Mutations and Modifications Ligands, Ions and Associated Components Method and Experimental Conditions Structure Quality
1 Other combination Monomer Protein × 1 其他Polymer 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain A; UniProt 285–1009 Fragment:HYALURONATE LYASE, RESIDUES 285-1009 Mutation:YES 4-deoxy-alpha-L-threo-hex-4-enopyranuronic acid-(1-3)-2-acetamido-2-deoxy-6-O-sulfo-beta-D-galactopyranose × 1 SO4 SULFATE ION × 4 X-RAY DIFFRACTION X-ray crystallization conditions:pH 6;3.5M AMMONIUM SULFATE, 200MM SODIUM CACODYLATE, PH 6.0 Resolution 1.60 Å R-free 0.209

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.

14 other PDB entries and 15 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name HYSA_STRPN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–725; UniProt 285–1009

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 1ojn

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id1ojn
Deposition date deposition_date2003-07-11
Structure title titleSPECIFICITY AND MECHANISM OF STREPTOCOCCUS PNEUMONIAE HYALURONATE LYASE: COMPLEX OF THE TYR408PHE MUTANT WITH 6-SULPHATED CHONDROITIN DISACCHARIDE
Keywords keywordsLYASE, PROTEIN-CARBOHYDRATE COMPLEX; LYASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier28.38
Radius of gyration Rg (electron density) rg_electron27.57
Forward intensity I(0) i0116056000.00
Molecular weight molecular_weight83161.0 kDa
Excluded volume excluded_volume103130 ų
Envelope volume envelope_volume122260 ų
Hydration-shell volume shell_volume36538 ų
Envelope diameter envelope_diameter100.2
Shell Rg shell_rg35.48
Envelope Rg envelope_rg27.75
Shape Rg shape_rg27.55
Total Rg total_rg28.35
Total atoms total_atoms5849
Residues n_residues723
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 dmax95.5
Rg (real space) rg_real28.37
Rg uncertainty (real space) rg_real_error0.56
I(0) (real space) i0_real1.1610e+08
I(0) uncertainty (real space) i0_real_error1.4720e+06
Rg (reciprocal space) rg_reciprocal28.38
I(0) (reciprocal space) i0_reciprocal116100000.0000
Solution quality estimate total_estimate0.8764
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary32.4
Skewness Skewness skewness0.374
Kurtosis Kurtosis kurtosis-0.333
Angular range angular_range— – 0.2800 −1
Current regularization parameter α current_alpha0.0001
Highest regularization parameter α highest_alpha32370000.0000
Real-space data points n_real_points57
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.802; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.988; Smooth: 0.995

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 6 domains

SCOP 2.08 (3 domains)

Domain ID domain_idd1ojna1
Class classa — All alpha proteins
Fold Fold folda.102 — alpha/alpha toroid
Superfamily Superfamily superfamilya.102.3 — Chondroitin AC/alginate lyase
Family Family familya.102.3.2 — Hyaluronate lyase-like catalytic, N-terminal domain
Domain ID domain_idd1ojna2
Class classb — All beta proteins
Fold Fold foldb.24 — Hyaluronate lyase-like, C-terminal domain
Superfamily Superfamily superfamilyb.24.1 — Hyaluronate lyase-like, C-terminal domain
Family Family familyb.24.1.1 — Hyaluronate lyase-like, C-terminal domain
Domain ID domain_idd1ojna3
Class classb — All beta proteins
Fold Fold foldb.30 — Supersandwich
Superfamily Superfamily superfamilyb.30.5 — Galactose mutarotase-like
Family Family familyb.30.5.2 — Hyaluronate lyase-like, central domain

CATH v4.4 (3 domains)

Domain ID domain_id1ojnA01
Class class2 — Mainly Beta
Architecture architecture70 — Distorted Sandwich
Topology topology98 — Beta-galactosidase; Chain A, domain 5
Homologous superfamily homologous superfamily10
Domain ID domain_id1ojnA02
Class class1 — Mainly Alpha
Architecture architecture50 — Alpha/alpha barrel
Topology topology10 — Glycosyltransferase
Homologous superfamily homologous superfamily100 — Chondroitin AC/alginate lyase
Domain ID domain_id1ojnA03
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology220 — Chondroitinase Ac; Chain A, domain 3
Homologous superfamily homologous superfamily10 — Polysaccharide lyase family 8-like, C-terminal

8. Citations (2)

9. Files and Curves (10)