1d2p

CRYSTAL STRUCTURE OF TWO B REPEAT UNITS (B1B2) OF THE COLLAGEN BINDING PROTEIN (CNA) OF STAPHYLOCOCCUS AUREUS

Method: X-RAY DIFFRACTION Dmax: 102.1 Å Quality: GOOD

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

COLLAGEN ADHESIN

Staphylococcus aureus

UniProt Q53654

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 533–905 Fragment:B REPEAT REGIONS No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 7.5;298 K;PEG6000, Calcium chloride, sodium cacodylate , pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 298K Resolution 2.50 Å R-free 0.245

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.

4 other PDB entries and 6 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name CNA_STAAU
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–373; UniProt 533–905

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 1d2p

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1d2p
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1d2p
Deposition date deposition_date1999-09-25
Structure title titleCRYSTAL STRUCTURE OF TWO B REPEAT UNITS (B1B2) OF THE COLLAGEN BINDING PROTEIN (CNA) OF STAPHYLOCOCCUS AUREUS
Keywords keywordsCOLLAGEN, IGG, IGSF, MSCRAMM, CNA, STAPHYLOCOCCUS AUREUS, STRUCTURAL PROTEIN; STRUCTURAL PROTEIN
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier30.47
Radius of gyration Rg (electron density) rg_electron30.47
Forward intensity I(0) i031715600.00
Molecular weight molecular_weight42341.0 kDa
Excluded volume excluded_volume52298 ų
Envelope volume envelope_volume69723 ų
Hydration-shell volume shell_volume21022 ų
Envelope diameter envelope_diameter107.0
Shell Rg shell_rg34.08
Envelope Rg envelope_rg30.23
Shape Rg shape_rg30.45
Total Rg total_rg30.89
Total atoms total_atoms2986
Residues n_residues373
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 dmax102.1
Rg (real space) rg_real30.86
Rg uncertainty (real space) rg_real_error1.00
I(0) (real space) i0_real3.1720e+07
I(0) uncertainty (real space) i0_real_error5.3350e+05
Rg (reciprocal space) rg_reciprocal30.70
I(0) (reciprocal space) i0_reciprocal31710000.0000
Solution quality estimate total_estimate0.7721
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary23.6
Skewness Skewness skewness0.495
Kurtosis Kurtosis kurtosis-0.616
Angular range angular_range— – 0.2600 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha3874000.0000
Real-space data points n_real_points53
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.658; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.398; Smooth: 0.660

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 8 domains

SCOP 2.08 (4 domains)

Domain ID domain_idd1d2pa1
Class classb — All beta proteins
Fold Fold foldb.3 — Prealbumin-like
Superfamily Superfamily superfamilyb.3.5 — Cna protein B-type domain
Family Family familyb.3.5.1 — Cna protein B-type domain
Domain ID domain_idd1d2pa2
Class classb — All beta proteins
Fold Fold foldb.3 — Prealbumin-like
Superfamily Superfamily superfamilyb.3.5 — Cna protein B-type domain
Family Family familyb.3.5.1 — Cna protein B-type domain
Domain ID domain_idd1d2pa3
Class classb — All beta proteins
Fold Fold foldb.3 — Prealbumin-like
Superfamily Superfamily superfamilyb.3.5 — Cna protein B-type domain
Family Family familyb.3.5.1 — Cna protein B-type domain
Domain ID domain_idd1d2pa4
Class classb — All beta proteins
Fold Fold foldb.3 — Prealbumin-like
Superfamily Superfamily superfamilyb.3.5 — Cna protein B-type domain
Family Family familyb.3.5.1 — Cna protein B-type domain

CATH v4.4 (4 domains)

Domain ID domain_id1d2pA01
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily1140 — Collagen-binding surface protein Cna, B-type domain
Domain ID domain_id1d2pA02
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily1140 — Collagen-binding surface protein Cna, B-type domain
Domain ID domain_id1d2pA03
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily1140 — Collagen-binding surface protein Cna, B-type domain
Domain ID domain_id1d2pA04
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily1140 — Collagen-binding surface protein Cna, B-type domain

8. Citations (1)

9. Files and Curves (10)