1bc2

ZN-DEPENDENT METALLO-BETA-LACTAMASE FROM BACILLUS CEREUS

Method: X-RAY DIFFRACTION Dmax: 85.8 Å Quality: REASONABLE

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

METALLO-BETA-LACTAMASE II

OrganismNot specified

UniProt P04190

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 homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain A; UniProt 31–257 Chain B; UniProt 31–257 Not recorded ZN ZINC ION × 4 SO4 SULFATE ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 4.5;HANGING DROP METHOD. PROTEIN WAS DISSOLVED IN 10MM TRIS PH7, 1MM ZINC SULPHATE. WELL SOLUTION CONTAINED 100MM TRIS-HCL PH4.5, 75% AMMONIUM SULPHATE. 6UL DROPS WERE MADE WITH 3UL PROTEIN SOLUTION 50% DILUTED (WATER) WELL SOLUTION., vapor diffusion - hanging drop Resolution 1.90 Å R-free 0.279

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.

43 other PDB entries and 62 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BLA2_BACCE
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–227; UniProt 31–257 Author chain B; PDBConstruct 1–227; UniProt 31–257

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 1bc2

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1bc2
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1bc2
Deposition date deposition_date1997-04-11
Structure title titleZN-DEPENDENT METALLO-BETA-LACTAMASE FROM BACILLUS CEREUS
Keywords keywordsHYDROLASE, METALLO BETA-LACTAMASE, PENICILLINASE, ANTIBIOTIC RESISTANCE; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier25.97
Radius of gyration Rg (electron density) rg_electron25.65
Forward intensity I(0) i037475900.00
Molecular weight molecular_weight47908.0 kDa
Excluded volume excluded_volume60248 ų
Envelope volume envelope_volume72161 ų
Hydration-shell volume shell_volume24038 ų
Envelope diameter envelope_diameter88.3
Shell Rg shell_rg32.16
Envelope Rg envelope_rg25.53
Shape Rg shape_rg25.65
Total Rg total_rg26.39
Total atoms total_atoms3358
Residues n_residues432
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 dmax85.8
Rg (real space) rg_real26.09
Rg uncertainty (real space) rg_real_error0.70
I(0) (real space) i0_real3.7480e+07
I(0) uncertainty (real space) i0_real_error5.5900e+05
Rg (reciprocal space) rg_reciprocal26.06
I(0) (reciprocal space) i0_reciprocal37480000.0000
Solution quality estimate total_estimate0.6790
Solution quality rating solution_quality REASONABLE a REASONABLE solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary23.9
Skewness Skewness skewness0.415
Kurtosis Kurtosis kurtosis-0.562
Angular range angular_range— – 0.3050 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha17760000.0000
Real-space data points n_real_points62
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.778; Stabil: 1.000; Sysdev: 0.221; Positv: 1.000; Valcen: 0.869; Smooth: 0.957

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 4 domains

SCOP 2.08 (2 domains)

Domain ID domain_idd1bc2a_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.157 — Metallo-hydrolase/oxidoreductase
Superfamily Superfamily superfamilyd.157.1 — Metallo-hydrolase/oxidoreductase
Family Family familyd.157.1.1 — Zn metallo-beta-lactamase
Domain ID domain_idd1bc2b_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.157 — Metallo-hydrolase/oxidoreductase
Superfamily Superfamily superfamilyd.157.1 — Metallo-hydrolase/oxidoreductase
Family Family familyd.157.1.1 — Zn metallo-beta-lactamase

CATH v4.4 (2 domains)

Domain ID domain_id1bc2A00
Class class3 — Alpha Beta
Architecture architecture60 — 4-Layer Sandwich
Topology topology15 — Metallo-beta-lactamase; Chain A
Homologous superfamily homologous superfamily10 — Ribonuclease Z/Hydroxyacylglutathione hydrolase-like
Domain ID domain_id1bc2B00
Class class3 — Alpha Beta
Architecture architecture60 — 4-Layer Sandwich
Topology topology15 — Metallo-beta-lactamase; Chain A
Homologous superfamily homologous superfamily10 — Ribonuclease Z/Hydroxyacylglutathione hydrolase-like

8. Citations (1)

9. Files and Curves (10)