9fbp

Deletion mutant MmChi60

Method: X-RAY DIFFRACTION Dmax: 125.4 Å Quality: GOOD

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

Chitinase 60

Moritella marina

UniProt B1VBB0

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 23–347 Chain A; UniProt 505–550 Not recorded NA SODIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;293 K;1.1 M sodium malonate, 0.5% Jeffamine ED-2001 and 0.1 M HEPES at pH 7.0 Resolution 1.84 Å R-free 0.219
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 23–347 Chain B; UniProt 505–550 Not recorded NA SODIUM ION × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7;293 K;1.1 M sodium malonate, 0.5% Jeffamine ED-2001 and 0.1 M HEPES at pH 7.0 Resolution 1.84 Å R-free 0.219

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.

11 other PDB entries and 12 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name B1VBB0_MORMI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–325; UniProt 23–347 Author chain A; PDBConstruct 326–371; UniProt 505–550 Author chain B; PDBConstruct 1–325; UniProt 23–347 Author chain B; PDBConstruct 326–371; UniProt 505–550

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 9fbp

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 9fbp
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2. Structure Basics 2. Structure Basics

Entry ID entry_id9fbp
Deposition date deposition_date2024-05-14
Structure title titleDeletion mutant MmChi60
Keywords keywordsChitinase, Deletion mutant, Psychrophilic protein, Protein engineering, HYDROLASE; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier34.37
Radius of gyration Rg (electron density) rg_electron34.39
Forward intensity I(0) i0109110000.00
Molecular weight molecular_weight83116.0 kDa
Excluded volume excluded_volume103540 ų
Envelope volume envelope_volume131800 ų
Hydration-shell volume shell_volume34206 ų
Envelope diameter envelope_diameter133.6
Shell Rg shell_rg37.68
Envelope Rg envelope_rg35.11
Shape Rg shape_rg34.39
Total Rg total_rg34.62
Total atoms total_atoms5884
Residues n_residues742
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 dmax125.4
Rg (real space) rg_real34.75
Rg uncertainty (real space) rg_real_error1.60
I(0) (real space) i0_real1.0910e+08
I(0) uncertainty (real space) i0_real_error2.2260e+06
Rg (reciprocal space) rg_reciprocal34.51
I(0) (reciprocal space) i0_reciprocal109100000.0000
Solution quality estimate total_estimate0.7999
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary30.0
Skewness Skewness skewness0.648
Kurtosis Kurtosis kurtosis-0.032
Angular range angular_range— – 0.2300 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha19930000.0000
Real-space data points n_real_points47
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.593; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.707; Smooth: 0.910

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

8. Citations (1)

9. Files and Curves (10)