2bmi

METALLO-BETA-LACTAMASE

Method: X-RAY DIFFRACTION Dmax: 82.0 Å Quality: GOOD

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

PROTEIN (CLASS B BETA-LACTAMASE)

Bacteroides fragilis

UniProt P25910

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 18–249 Chain B; UniProt 18–249 Not recorded ZN ZINC ION × 4 NA SODIUM ION × 2 X-RAY DIFFRACTION X-ray crystallization conditions:pH 9;FORM II CRYSTAL IN ACTA CRYST(1997) D53 485-487, pH 9.0 Resolution 2.00 Å R-free 0.262

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.

8 other PDB entries and 15 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BLAB_BACFR
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–232; UniProt 18–249 Author chain B; PDBConstruct 1–232; UniProt 18–249

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 2bmi

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id2bmi
Deposition date deposition_date1998-09-17
Structure title titleMETALLO-BETA-LACTAMASE
Keywords keywordsBETA-LACTAMASE, METALLO BETA-LACTAMASE, ZINC, HYDROLASE; HYDROLASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier25.05
Radius of gyration Rg (electron density) rg_electron24.05
Forward intensity I(0) i042506000.00
Molecular weight molecular_weight50185.0 kDa
Excluded volume excluded_volume62603 ų
Envelope volume envelope_volume73284 ų
Hydration-shell volume shell_volume25609 ų
Envelope diameter envelope_diameter87.3
Shell Rg shell_rg30.89
Envelope Rg envelope_rg24.50
Shape Rg shape_rg24.06
Total Rg total_rg24.81
Total atoms total_atoms3516
Residues n_residues458
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 dmax82.0
Rg (real space) rg_real25.08
Rg uncertainty (real space) rg_real_error0.53
I(0) (real space) i0_real4.2510e+07
I(0) uncertainty (real space) i0_real_error6.4760e+05
Rg (reciprocal space) rg_reciprocal25.07
I(0) (reciprocal space) i0_reciprocal42510000.0000
Solution quality estimate total_estimate0.8874
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary26.0
Skewness Skewness skewness0.371
Kurtosis Kurtosis kurtosis-0.440
Angular range angular_range— – 0.3150 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha13470000.0000
Real-space data points n_real_points64
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.865; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.948; Smooth: 0.991

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_idd2bmia_
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_idd2bmib_
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_id2bmiA00
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_id2bmiB00
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 (2)

9. Files and Curves (10)