1kaf

DNA Binding Domain Of The Phage T4 Transcription Factor MotA (AA105-211)

Method: X-RAY DIFFRACTION Dmax: 107.8 Å Quality: GOOD

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

Transcription regulatory protein MOTA

Enterobacteria phage T4

UniProt P22915

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 105–211 Fragment:DNA binding domain residues 105-211 No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6.5;298 K;from 19% PEG 8000, 35 mM potassium phosphate pH 5.0, 3% glycerol, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 298K Resolution 1.60 Å R-free 0.258
2 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain B; UniProt 105–211 Fragment:DNA binding domain residues 105-211 No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6.5;298 K;from 19% PEG 8000, 35 mM potassium phosphate pH 5.0, 3% glycerol, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 298K Resolution 1.60 Å R-free 0.258
3 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain C; UniProt 105–211 Fragment:DNA binding domain residues 105-211 No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6.5;298 K;from 19% PEG 8000, 35 mM potassium phosphate pH 5.0, 3% glycerol, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 298K Resolution 1.60 Å R-free 0.258
4 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain D; UniProt 105–211 Fragment:DNA binding domain residues 105-211 No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6.5;298 K;from 19% PEG 8000, 35 mM potassium phosphate pH 5.0, 3% glycerol, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 298K Resolution 1.60 Å R-free 0.258
5 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain E; UniProt 105–211 Fragment:DNA binding domain residues 105-211 No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6.5;298 K;from 19% PEG 8000, 35 mM potassium phosphate pH 5.0, 3% glycerol, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 298K Resolution 1.60 Å R-free 0.258
6 Protein monomer Monomer Protein × 1 PDB declaration: monomeric(1) Consistent with protein copy count Chain F; UniProt 105–211 Fragment:DNA binding domain residues 105-211 No other associated polymer X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 6.5;298 K;from 19% PEG 8000, 35 mM potassium phosphate pH 5.0, 3% glycerol, pH 6.5, VAPOR DIFFUSION, HANGING DROP, temperature 298K Resolution 1.60 Å R-free 0.258

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.

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

View Construct and Data Evidence
UniProt name MOTA_BPT4
Isoform
PDB entities 1
Chains and sequence ranges Author chain A; PDBConstruct 2–108; UniProt 105–211 Author chain B; PDBConstruct 2–108; UniProt 105–211 Author chain C; PDBConstruct 2–108; UniProt 105–211 Author chain D; PDBConstruct 2–108; UniProt 105–211 Author chain E; PDBConstruct 2–108; UniProt 105–211 Author chain F; PDBConstruct 2–108; UniProt 105–211

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 1kaf

P(r) Distance Distribution P(r) Distribution

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

Entry ID entry_id1kaf
Deposition date deposition_date2001-11-01
Structure title titleDNA Binding Domain Of The Phage T4 Transcription Factor MotA (AA105-211)
Keywords keywordsEscherichia coli; X-ray crystallography; protein-DNA interactions; structural genomics; eubacterial promoters., TRANSCRIPTION; TRANSCRIPTION
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier32.58
Radius of gyration Rg (electron density) rg_electron32.52
Forward intensity I(0) i086449500.00
Molecular weight molecular_weight73616.0 kDa
Excluded volume excluded_volume92338 ų
Envelope volume envelope_volume124830 ų
Hydration-shell volume shell_volume33841 ų
Envelope diameter envelope_diameter110.7
Shell Rg shell_rg37.45
Envelope Rg envelope_rg31.94
Shape Rg shape_rg32.52
Total Rg total_rg32.96
Total atoms total_atoms5142
Residues n_residues635
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 dmax107.8
Rg (real space) rg_real32.76
Rg uncertainty (real space) rg_real_error0.74
I(0) (real space) i0_real8.6450e+07
I(0) uncertainty (real space) i0_real_error1.3010e+06
Rg (reciprocal space) rg_reciprocal32.69
I(0) (reciprocal space) i0_reciprocal86440000.0000
Solution quality estimate total_estimate0.8740
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks1
Primary peak position r_peak_primary37.4
Skewness Skewness skewness0.430
Kurtosis Kurtosis kurtosis-0.438
Angular range angular_range— – 0.2450 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha12010000.0000
Real-space data points n_real_points50
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.856; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.930; Smooth: 0.859

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (2)

7. Fold Classification (SCOP + CATH) 12 domains

SCOP 2.08 (6 domains)

Domain ID domain_idd1kafa_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.199 — MotA C-terminal domain-like
Superfamily Superfamily superfamilyd.199.1 — DNA-binding C-terminal domain of the transcription factor MotA
Family Family familyd.199.1.1 — DNA-binding C-terminal domain of the transcription factor MotA
Domain ID domain_idd1kafb_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.199 — MotA C-terminal domain-like
Superfamily Superfamily superfamilyd.199.1 — DNA-binding C-terminal domain of the transcription factor MotA
Family Family familyd.199.1.1 — DNA-binding C-terminal domain of the transcription factor MotA
Domain ID domain_idd1kafc_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.199 — MotA C-terminal domain-like
Superfamily Superfamily superfamilyd.199.1 — DNA-binding C-terminal domain of the transcription factor MotA
Family Family familyd.199.1.1 — DNA-binding C-terminal domain of the transcription factor MotA
Domain ID domain_idd1kafd_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.199 — MotA C-terminal domain-like
Superfamily Superfamily superfamilyd.199.1 — DNA-binding C-terminal domain of the transcription factor MotA
Family Family familyd.199.1.1 — DNA-binding C-terminal domain of the transcription factor MotA
Domain ID domain_idd1kafe_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.199 — MotA C-terminal domain-like
Superfamily Superfamily superfamilyd.199.1 — DNA-binding C-terminal domain of the transcription factor MotA
Family Family familyd.199.1.1 — DNA-binding C-terminal domain of the transcription factor MotA
Domain ID domain_idd1kaff_
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.199 — MotA C-terminal domain-like
Superfamily Superfamily superfamilyd.199.1 — DNA-binding C-terminal domain of the transcription factor MotA
Family Family familyd.199.1.1 — DNA-binding C-terminal domain of the transcription factor MotA

CATH v4.4 (6 domains)

Domain ID domain_id1kafA00
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology1150 — Aspartate Aminotransferase, domain 1
Homologous superfamily homologous superfamily20 — Transcription regulator MotA, C-terminal domain
Domain ID domain_id1kafB00
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology1150 — Aspartate Aminotransferase, domain 1
Homologous superfamily homologous superfamily20 — Transcription regulator MotA, C-terminal domain
Domain ID domain_id1kafC00
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology1150 — Aspartate Aminotransferase, domain 1
Homologous superfamily homologous superfamily20 — Transcription regulator MotA, C-terminal domain
Domain ID domain_id1kafD00
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology1150 — Aspartate Aminotransferase, domain 1
Homologous superfamily homologous superfamily20 — Transcription regulator MotA, C-terminal domain
Domain ID domain_id1kafE00
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology1150 — Aspartate Aminotransferase, domain 1
Homologous superfamily homologous superfamily20 — Transcription regulator MotA, C-terminal domain
Domain ID domain_id1kafF00
Class class3 — Alpha Beta
Architecture architecture90 — Alpha-Beta Complex
Topology topology1150 — Aspartate Aminotransferase, domain 1
Homologous superfamily homologous superfamily20 — Transcription regulator MotA, C-terminal domain

8. Citations (1)

9. Files and Curves (10)