1bf5

TYROSINE PHOSPHORYLATED STAT-1/DNA COMPLEX

Method: X-RAY DIFFRACTION Dmax: 133.8 Å Quality: GOOD

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

SIGNAL TRANSDUCER AND ACTIVATOR OF TRANSCRIPTION 1-ALPHA/BETA

Homo sapiens

UniProt P42224

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–DNA Homooligomer Protein × 2 DNA 2 PDB declaration: tetrameric(4) Consistent with all polymer counts Chain A; UniProt 136–683 Fragment:RESIDUES 136-710 Mutation:PHOSPHORYLATED TYR 701 Non-standard monomer:Yes (specific site not provided by mmCIF) ;DNA (5'-D(*AP*CP*AP*GP*TP*TP*TP*CP*CP*CP*GP*TP*AP*AP*AP*TP*G P*C)-3') ; × 1 ;DNA (5'-D(*TP*GP*CP*AP*TP*TP*TP*AP*CP*GP*GP*GP*AP*AP*AP*CP*T P*G)-3') ; × 1 X-RAY DIFFRACTION X-ray crystallization conditions:VAPOR DIFFUSION, HANGING DROP;pH 5;277 K;pH 5.00, VAPOR DIFFUSION, HANGING DROP, temperature 277.00K Resolution 2.90 Å R-free 0.293

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.

9 other PDB entries and 16 assemblies. Open the comparison page and filter oligomeric states

View Construct and Data Evidence
UniProt name STAT1_HUMAN
Isoform
PDB entities 3
Chains and sequence ranges Author chain A; PDBConstruct 1–575; UniProt 136–683

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 1bf5

P(r) Distance Distribution P(r) Distribution

P(r) distribution for 1bf5
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2. Structure Basics 2. Structure Basics

Entry ID entry_id1bf5
Deposition date deposition_date1998-05-27
Structure title titleTYROSINE PHOSPHORYLATED STAT-1/DNA COMPLEX
Keywords keywordsCOMPLEX (SH2 DOMAIN-DNA), SH2 DOMAIN, TRANSCRIPTION FACTOR, GENE REGULATION-DNA COMPLEX; GENE REGULATION/DNA
Experimental Method methodX-RAY DIFFRACTION

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

Radius of gyration Rg (Guinier) rg_guinier33.74
Radius of gyration Rg (electron density) rg_electron33.89
Forward intensity I(0) i098380000.00
Molecular weight molecular_weight73239.0 kDa
Excluded volume excluded_volume89228 ų
Envelope volume envelope_volume119690 ų
Hydration-shell volume shell_volume32366 ų
Envelope diameter envelope_diameter141.7
Shell Rg shell_rg36.60
Envelope Rg envelope_rg34.55
Shape Rg shape_rg33.89
Total Rg total_rg34.09
Total atoms total_atoms5117
Residues n_residues580
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 dmax133.8
Rg (real space) rg_real34.12
Rg uncertainty (real space) rg_real_error1.75
I(0) (real space) i0_real9.8380e+07
I(0) uncertainty (real space) i0_real_error1.9180e+06
Rg (reciprocal space) rg_reciprocal33.88
I(0) (reciprocal space) i0_reciprocal98360000.0000
Solution quality estimate total_estimate0.7505
Solution quality rating solution_quality GOOD a GOOD solution
P(r) peaks n_peaks2
Primary peak position r_peak_primary34.2
Skewness Skewness skewness0.715
Kurtosis Kurtosis kurtosis0.294
Angular range angular_range— – 0.2350 −1
Current regularization parameter α current_alpha0.0000
Highest regularization parameter α highest_alpha9097000.0000
Real-space data points n_real_points48
GNOM version gnom_version4.1.3
Quality Criteria quality_criteria AN1: 0.000; Oscil: 0.471; Stabil: 1.000; Sysdev: 1.000; Positv: 1.000; Valcen: 0.388; Smooth: 0.952

5. Crystallography and Experiment 5. Crystallography & Experiment

6. Entities and Polymers Entities & Polymers (3)

7. Fold Classification (SCOP + CATH) 7 domains

SCOP 2.08 (3 domains)

Domain ID domain_idd1bf5a1
Class classa — All alpha proteins
Fold Fold folda.47 — STAT-like
Superfamily Superfamily superfamilya.47.1 — STAT
Family Family familya.47.1.1 — STAT
Domain ID domain_idd1bf5a2
Class classb — All beta proteins
Fold Fold foldb.2 — Common fold of diphtheria toxin/transcription factors/cytochrome f
Superfamily Superfamily superfamilyb.2.5 — p53-like transcription factors
Family Family familyb.2.5.5 — STAT DNA-binding domain
Domain ID domain_idd1bf5a3
Class classd — Alpha and beta proteins (a+b)
Fold Fold foldd.93 — SH2-like
Superfamily Superfamily superfamilyd.93.1 — SH2 domain
Family Family familyd.93.1.1 — SH2 domain

CATH v4.4 (4 domains)

Domain ID domain_id1bf5A01
Class class1 — Mainly Alpha
Architecture architecture20 — Up-down Bundle
Topology topology1050 — Glutathione S-transferase Yfyf (Class Pi); Chain A, domain 2
Homologous superfamily homologous superfamily20 — STAT transcription factor, all-alpha domain
Domain ID domain_id1bf5A02
Class class2 — Mainly Beta
Architecture architecture60 — Sandwich
Topology topology40 — Immunoglobulin-like
Homologous superfamily homologous superfamily630 — STAT transcription factor, DNA-binding domain
Domain ID domain_id1bf5A03
Class class1 — Mainly Alpha
Architecture architecture10 — Orthogonal Bundle
Topology topology238 — Recoverin; domain 1
Homologous superfamily homologous superfamily10 — EF-hand
Domain ID domain_id1bf5A04
Class class3 — Alpha Beta
Architecture architecture30 — 2-Layer Sandwich
Topology topology505 — SHC Adaptor Protein
Homologous superfamily homologous superfamily10 — SH2 domain

8. Citations (1)

9. Files and Curves (10)