4zam

Crystal structure of SHV-1 beta-lactamase bound to avibactam

Method: X-RAY DIFFRACTION Dmax: 62.0 Å Quality: GOOD

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

Beta-lactamase SHV-1

Klebsiella pneumoniae

UniProt P0AD64

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 22–286 Fragment:UNP residues 22-286 MA4 CYCLOHEXYL-HEXYL-BETA-D-MALTOSIDE × 2 NXL (2S,5R)-1-formyl-5-[(sulfooxy)amino]piperidine-2-carboxamide × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, SITTING DROP;pH 7.5;293 K;25% PEG6000, 100 mM Tris, pH 7.5, 0.56 mM Cymal-6 Resolution 1.42 Å R-free 0.193

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.

30 other PDB entries and 30 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BLA1_KLEPN
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–265; UniProt 22–286

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 4zam

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 4zam
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2. Structure Basics 2. Structure Basics

Entry ID entry_id4zam
Deposition date deposition_date2015-04-13
Structure title titleCrystal structure of SHV-1 beta-lactamase bound to avibactam
Keywords keywordsHYDROLASE-HYDROLASE INHIBITOR complex; HYDROLASE/HYDROLASE INHIBITOR
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier19.03
Radius of gyration Rg (electron density) rg_electron17.77
Forward intensity I(0) i016113700.00
Molecular weight molecular_weight29746.0 kDa
Excluded volume excluded_volume37052 ų
Envelope volume envelope_volume40879 ų
Hydration-shell volume shell_volume19009 ų
Envelope diameter envelope_diameter61.5
Shell Rg shell_rg24.36
Envelope Rg envelope_rg18.08
Shape Rg shape_rg17.80
Total Rg total_rg18.58
Total atoms total_atoms2083
Residues n_residues265
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 dmax62.0
Rg (real space) rg_real18.92
Rg uncertainty (real space) rg_real_error0.34
I(0) (real space) i0_real1.6110e+07
I(0) uncertainty (real space) i0_real_error1.9410e+05
Rg (reciprocal space) rg_reciprocal18.94
I(0) (reciprocal space) i0_reciprocal16110000.0000
Solution quality estimate total_estimate0.8810
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary24.1
Skewness Skewness skewness0.192
Kurtosis Kurtosis kurtosis-0.338
Angular range angular_range— – 0.4200 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha2945000.0000
Real-space data points n_real_points73
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.833; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.998; Smooth: 0.953

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (4)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd4zama_
Class classe — Multi-domain proteins (alpha and beta)
Fold Fold folde.3 — beta-lactamase/transpeptidase-like
Superfamily Superfamily superfamilye.3.1 — beta-lactamase/transpeptidase-like
Family Family familye.3.1.1 — beta-Lactamase/D-ala carboxypeptidase

CATH v4.4 (1 domains)

Domain ID domain_id4zamA00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology710 — Beta-lactamase
Homologous superfamily homologous superfamily10 — DD-peptidase/beta-lactamase superfamily

8. Citations (1)

9. Files and Curves (10)