2ijj

Crystal structure analysis of ColE1 ROM mutant F14Y

Method: X-RAY DIFFRACTION Dmax: 63.0 Å Quality: GOOD

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

Regulatory protein rop

Escherichia coli

UniProt P03051

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 1–63 Chain B; UniProt 1–63 Mutation:M1G, F14Y No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 5.5;273 K;Well solution: 22% MPD, 0.1 M sodium acetate pH 5.5, 0.1 M sodium chloride. Protein solution: protein 2.5 mg/ml, 0.01 M Tris pH 6.5, 0.05 M sodium chloride. Drops: equal volumes of well and protein solutions., VAPOR DIFFUSION, HANGING DROP, temperature 273K Resolution 1.90 Å R-free 0.263
2 Protein homooligomer Homooligomer Protein × 2 PDB declaration: dimeric(2) Consistent with protein copy count Chain C; UniProt 1–63 Mutation:M1G, F14Y No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 5.5;273 K;Well solution: 22% MPD, 0.1 M sodium acetate pH 5.5, 0.1 M sodium chloride. Protein solution: protein 2.5 mg/ml, 0.01 M Tris pH 6.5, 0.05 M sodium chloride. Drops: equal volumes of well and protein solutions., VAPOR DIFFUSION, HANGING DROP, temperature 273K Resolution 1.90 Å R-free 0.263

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.

18 other PDB entries and 25 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name ROP_ECOLI
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 1–63; UniProt 1–63 Author chain B; PDBConstruct 1–63; UniProt 1–63 Author chain C; PDBConstruct 1–63; UniProt 1–63

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 2ijj

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id2ijj
Deposition date deposition_date2006-09-29
Structure title titleCrystal structure analysis of ColE1 ROM mutant F14Y
Keywords keywordsrop, rom, colE1, RNA-recognition, TRANSCRIPTION REGULATOR; TRANSCRIPTION REGULATOR
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier17.92
Radius of gyration Rg (electron density) rg_electron17.15
Forward intensity I(0) i07836780.00
Molecular weight molecular_weight19195.0 kDa
Excluded volume excluded_volume23517 ų
Envelope volume envelope_volume28083 ų
Hydration-shell volume shell_volume14392 ų
Envelope diameter envelope_diameter63.1
Shell Rg shell_rg22.53
Envelope Rg envelope_rg17.57
Shape Rg shape_rg17.13
Total Rg total_rg18.11
Total atoms total_atoms1343
Residues n_residues171
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 dmax63.0
Rg (real space) rg_real17.89
Rg uncertainty (real space) rg_real_error0.53
I(0) (real space) i0_real7.8370e+06
I(0) uncertainty (real space) i0_real_error9.7270e+04
Rg (reciprocal space) rg_reciprocal17.89
I(0) (reciprocal space) i0_reciprocal7837000.0000
Solution quality estimate total_estimate0.7833
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary23.0
Skewness Skewness skewness0.306
Kurtosis Kurtosis kurtosis-0.280
Angular range angular_range— – 0.4450 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha2276000.0000
Real-space data points n_real_points75
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.740; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.958; Smooth: 0.000

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 6 domains

SCOP 2.08 (3 domains)

Domain ID domain_idd2ijja_
Class classa — All alpha proteins
Fold Fold folda.30 — ROP-like
Superfamily Superfamily superfamilya.30.1 — ROP protein
Family Family familya.30.1.1 — ROP protein
Domain ID domain_idd2ijjb_
Class classa — All alpha proteins
Fold Fold folda.30 — ROP-like
Superfamily Superfamily superfamilya.30.1 — ROP protein
Family Family familya.30.1.1 — ROP protein
Domain ID domain_idd2ijjc_
Class classa — All alpha proteins
Fold Fold folda.30 — ROP-like
Superfamily Superfamily superfamilya.30.1 — ROP protein
Family Family familya.30.1.1 — ROP protein

CATH v4.4 (3 domains)

Domain ID domain_id2ijjA00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology287 — Helix Hairpins
Homologous superfamily homologous superfamily230
Domain ID domain_id2ijjB00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology287 — Helix Hairpins
Homologous superfamily homologous superfamily230
Domain ID domain_id2ijjC00
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology287 — Helix Hairpins
Homologous superfamily homologous superfamily230

8. Citations (1)

9. Files and Curves (10)