1cla

EVIDENCE FOR TRANSITION-STATE STABILIZATION BY SERINE-148 IN THE CATALYTIC MECHANISM OF CHLORAMPHENICOL ACETYLTRANSFERASE

Method: X-RAY DIFFRACTION Dmax: 63.1 Å Quality: GOOD

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

TYPE III CHLORAMPHENICOL ACETYLTRANSFERASE

Escherichia coli

UniProt P00484

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 × 3 PDB declaration: trimeric(3) Consistent with protein copy count Chain A; UniProt 1–213 Not recorded CO COBALT (II) ION × 6 CLM CHLORAMPHENICOL × 3 X-RAY DIFFRACTION mmCIF provides none of the parsed experimental conditions Resolution 2.34 Å
2 Protein homooligomer Homooligomer Protein × 6 PDB declaration: hexameric(6) Consistent with protein copy count Chain A; UniProt 1–213 Not recorded CO COBALT (II) ION × 12 CLM CHLORAMPHENICOL × 6 X-RAY DIFFRACTION mmCIF provides none of the parsed experimental conditions Resolution 2.34 Å

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.

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

View Construct and Data Evidence
UniProt name CAT3_ECOLI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–213; UniProt 1–213

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 1cla

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id1cla
Deposition date deposition_date1989-10-16
Structure title titleEVIDENCE FOR TRANSITION-STATE STABILIZATION BY SERINE-148 IN THE CATALYTIC MECHANISM OF CHLORAMPHENICOL ACETYLTRANSFERASE
Keywords keywordsTRANSFERASE (ACYLTRANSFERASE); TRANSFERASE (ACYLTRANSFERASE)
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier18.73
Radius of gyration Rg (electron density) rg_electron17.47
Forward intensity I(0) i010556700.00
Molecular weight molecular_weight24524.0 kDa
Excluded volume excluded_volume30803 ų
Envelope volume envelope_volume35581 ų
Hydration-shell volume shell_volume17199 ų
Envelope diameter envelope_diameter58.9
Shell Rg shell_rg23.57
Envelope Rg envelope_rg17.74
Shape Rg shape_rg17.48
Total Rg total_rg18.47
Total atoms total_atoms1726
Residues n_residues213
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 dmax63.1
Rg (real space) rg_real18.63
Rg uncertainty (real space) rg_real_error0.44
I(0) (real space) i0_real1.0560e+07
I(0) uncertainty (real space) i0_real_error1.3760e+05
Rg (reciprocal space) rg_reciprocal18.65
I(0) (reciprocal space) i0_reciprocal10560000.0000
Solution quality estimate total_estimate0.8013
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary62.2
Skewness Skewness skewness0.184
Kurtosis Kurtosis kurtosis-0.378
Angular range angular_range— – 0.4250 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha1854000.0000
Real-space data points n_real_points74
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.804; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 1.000; Smooth: 0.000

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_idd1claa_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.43 — CoA-dependent acyltransferases
Superfamily Superfamily superfamilyc.43.1 — CoA-dependent acyltransferases
Family Family familyc.43.1.1 — CAT-like

CATH v4.4 (1 domains)

Domain ID domain_id1claA00
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology559 — Chloramphenicol Acetyltransferase
Homologous superfamily homologous superfamily10 — Chloramphenicol acetyltransferase-like domain

8. Citations (6)

9. Files and Curves (10)