1otm

Calcium-binding mutant of the internalin B LRR domain

Method: X-RAY DIFFRACTION Dmax: 69.6 Å Quality: GOOD

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

internalin B

Listeria monocytogenes

UniProt P25147

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 36–248 Fragment:LRR domain Mutation:D51A, D59A No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6.5;298 K;Peg 8000, Mes, Calcium acetate, DTT, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 298K Resolution 1.93 Å R-free 0.240

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.

16 other PDB entries and 34 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name INLB_LISMO
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 24–236; UniProt 36–248

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 1otm

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id1otm
Deposition date deposition_date2003-03-21
Structure title titleCalcium-binding mutant of the internalin B LRR domain
Keywords keywordsinternalin, InlB, calcium-binding, invasion, Listeria, CELL ADHESION; CELL ADHESION
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier19.75
Radius of gyration Rg (electron density) rg_electron18.90
Forward intensity I(0) i08725830.00
Molecular weight molecular_weight22944.0 kDa
Excluded volume excluded_volume29272 ų
Envelope volume envelope_volume33374 ų
Hydration-shell volume shell_volume15777 ų
Envelope diameter envelope_diameter70.8
Shell Rg shell_rg24.00
Envelope Rg envelope_rg19.24
Shape Rg shape_rg18.87
Total Rg total_rg19.83
Total atoms total_atoms1616
Residues n_residues207
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 dmax69.6
Rg (real space) rg_real19.87
Rg uncertainty (real space) rg_real_error0.45
I(0) (real space) i0_real8.7260e+06
I(0) uncertainty (real space) i0_real_error1.1020e+05
Rg (reciprocal space) rg_reciprocal19.85
I(0) (reciprocal space) i0_reciprocal8726000.0000
Solution quality estimate total_estimate0.8281
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary20.6
Skewness Skewness skewness0.515
Kurtosis Kurtosis kurtosis-0.105
Angular range angular_range— – 0.4050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha1371000.0000
Real-space data points n_real_points72
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.638; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.871; Smooth: 0.975

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_idd1otma_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.10 — Leucine-rich repeat, LRR (right-handed beta-alpha superhelix)
Superfamily Superfamily superfamilyc.10.2 — L domain-like
Family Family familyc.10.2.1 — Internalin LRR domain

CATH v4.4 (1 domains)

Domain ID domain_id1otmA00
Class class3 — Alpha Beta
Architecture architecture80 — Alpha-Beta Horseshoe
Topology topology10 — Leucine-rich repeat, LRR (right-handed beta-alpha superhelix)
Homologous superfamily homologous superfamily10 — Ribonuclease Inhibitor

8. Citations (1)

9. Files and Curves (10)