2cit

Structure of the covalent intermediate of a family 26 lichenase

Method: X-RAY DIFFRACTION Dmax: 60.2 Å Quality: GOOD

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

ENDOGLUCANASE H

CLOSTRIDIUM THERMOCELLUM

UniProt P16218

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 26–304 Fragment:RESIDUES 26-304 Mutation:YES beta-D-glucopyranose-(1-4)-beta-D-glucopyranose-(1-3)-2-deoxy-2-fluoro-alpha-D-glucopyranose × 1 X-RAY DIFFRACTION X-ray crystallization conditions:pH 6.5;0.15 M AMMONIUM SULPHATE, 30 % PEG 5K MME BUFFERED TO PH 6.5 WITH 0.1 M MES Resolution 1.40 Å R-free 0.179

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.

19 other PDB entries and 26 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name GUNH_CLOTM
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 4–282; UniProt 26–304

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 2cit

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 2cit
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2. Structure Basics 2. Structure Basics

Entry ID entry_id2cit
Deposition date deposition_date2006-03-24
Structure title titleStructure of the covalent intermediate of a family 26 lichenase
Keywords keywords;LICHENASE, HYDROLASE, GLYCOSIDASE, POLYSACCHARIDE DEGRADATION, CELLULOSE DEGRADATION, CARBOHYDRATE METABOLISM, MICHAELIS COMPLEX, GLYCOSIDE HYDROLASE ;; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier19.11
Radius of gyration Rg (electron density) rg_electron17.76
Forward intensity I(0) i017261500.00
Molecular weight molecular_weight31677.0 kDa
Excluded volume excluded_volume39512 ų
Envelope volume envelope_volume42198 ų
Hydration-shell volume shell_volume19461 ų
Envelope diameter envelope_diameter58.8
Shell Rg shell_rg24.41
Envelope Rg envelope_rg18.00
Shape Rg shape_rg17.72
Total Rg total_rg18.75
Total atoms total_atoms2248
Residues n_residues274
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 dmax60.2
Rg (real space) rg_real18.97
Rg uncertainty (real space) rg_real_error0.34
I(0) (real space) i0_real1.7260e+07
I(0) uncertainty (real space) i0_real_error2.1000e+05
Rg (reciprocal space) rg_reciprocal19.00
I(0) (reciprocal space) i0_reciprocal17260000.0000
Solution quality estimate total_estimate0.8975
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary23.4
Skewness Skewness skewness0.117
Kurtosis Kurtosis kurtosis-0.510
Angular range angular_range— – 0.4150 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha3555000.0000
Real-space data points n_real_points73
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.891; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.992; Smooth: 0.997

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd2cita1
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.1 — TIM beta/alpha-barrel
Superfamily Superfamily superfamilyc.1.8 — (Trans)glycosidases
Family Family familyc.1.8.3 — beta-glycanases

CATH v4.4 (1 domains)

Domain ID domain_id2citA00
Class class3 — Alpha Beta
Architecture architecture20 — Alpha-Beta Barrel
Topology topology20 — TIM Barrel
Homologous superfamily homologous superfamily80 — Glycosidases

8. Citations (1)

9. Files and Curves (10)