1dah

DETHIOBIOTIN SYNTHETASE COMPLEXED WITH 7,8-DIAMINO-NONANOIC ACID, 5'-ADENOSYL-METHYLENE-TRIPHOSPHATE, AND MANGANESE

Method: X-RAY DIFFRACTION Dmax: 56.9 Å Quality: GOOD

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

DETHIOBIOTIN SYNTHETASE

Escherichia coli

UniProt P13000

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 1–224 Not recorded MN MANGANESE (II) ION × 2 DNN 7,8-DIAMINO-NONANOIC ACID × 2 ACP PHOSPHOMETHYLPHOSPHONIC ACID ADENYLATE ESTER × 2 X-RAY DIFFRACTION mmCIF provides none of the parsed experimental conditions Resolution 1.64 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.

12 other PDB entries and 13 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name BIOD_ECOLI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–224; UniProt 1–224

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 1dah

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id1dah
Deposition date deposition_date1995-05-08
Structure title titleDETHIOBIOTIN SYNTHETASE COMPLEXED WITH 7,8-DIAMINO-NONANOIC ACID, 5'-ADENOSYL-METHYLENE-TRIPHOSPHATE, AND MANGANESE
Keywords keywordsLIGASE, BIOTIN BIOSYNTHESIS, MAGNESIUM, ATP-BINDING; LIGASE
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier17.90
Radius of gyration Rg (electron density) rg_electron16.83
Forward intensity I(0) i011138600.00
Molecular weight molecular_weight24753.0 kDa
Excluded volume excluded_volume30941 ų
Envelope volume envelope_volume34967 ų
Hydration-shell volume shell_volume17244 ų
Envelope diameter envelope_diameter58.1
Shell Rg shell_rg23.28
Envelope Rg envelope_rg17.19
Shape Rg shape_rg16.84
Total Rg total_rg17.82
Total atoms total_atoms1737
Residues n_residues224
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 dmax56.9
Rg (real space) rg_real17.79
Rg uncertainty (real space) rg_real_error0.33
I(0) (real space) i0_real1.1140e+07
I(0) uncertainty (real space) i0_real_error1.4420e+05
Rg (reciprocal space) rg_reciprocal17.80
I(0) (reciprocal space) i0_reciprocal11140000.0000
Solution quality estimate total_estimate0.8071
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks3
Primary peak position r_peak_primary23.1
Skewness Skewness skewness0.179
Kurtosis Kurtosis kurtosis-0.313
Angular range angular_range— – 0.4450 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha2463000.0000
Real-space data points n_real_points75
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.835; Stabil: 0.997; Sysdev: 1.000; Positv: 1.000; Valcen: 0.990; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (5)

7. Fold Classification (SCOP + CATH) 2 domains

SCOP 2.08 (1 domains)

Domain ID domain_idd1daha_
Class classc — Alpha and beta proteins (a/b)
Fold Fold foldc.37 — P-loop containing nucleoside triphosphate hydrolases
Superfamily Superfamily superfamilyc.37.1 — P-loop containing nucleoside triphosphate hydrolases
Family Family familyc.37.1.10 — Nitrogenase iron protein-like

CATH v4.4 (1 domains)

Domain ID domain_id1dahA00
Class class3 — Alpha Beta
Architecture architecture40 — 3-Layer(aba) Sandwich
Topology topology50 — Rossmann fold
Homologous superfamily homologous superfamily300 — P-loop containing nucleotide triphosphate hydrolases

8. Citations (2)

9. Files and Curves (10)