Current Protein Identity:P04386 New Search
Main Difference Dimensions in This Set
Different construct Different mutation/modification Different assembly state Different ligand/ion Different experimental method Different experimental conditions Different structure-quality metrics

Difference tags compare only the current result set; every original PDB and assembly record remains separate.

Related-Structure Differences

Each row represents one biological assembly in one PDB entry; multiple monomers of the same protein are listed separately.

PDB Entry Assembly / Oligomeric State Construct Mutations and Modifications Ligands, Ions and Non-polymers Experimental Method Experimental Conditions Structure Quality
1AW6 GAL4 (CD), NMR, 24 STRUCTURES Deposited 1997-10-10 Assembly 1 Protein monomer Monomer;Protein × 1 PDB declaration: monomeric(1) Consistent with protein count
Chain A 1–43(43 aa) Fragment:DNA-BINDING DOMAIN
Not recorded CD CADMIUM ION × 2 SOLUTION NMR
NMR measurement conditions pH 7.2;298 K
Resolution not provided
1D66 DNA RECOGNITION BY GAL4: STRUCTURE OF A PROTEIN/DNA COMPLEX Deposited 1992-03-06 Assembly 1 Protein–DNA Homooligomer;Protein × 2 PDB declaration: tetrameric(4) Consistent with all polymers
Chain A 1–65(65 aa)
Chain B 1–65(65 aa)
Not recorded CD CADMIUM ION × 4 X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP;pH 6.8;pH 6.80, VAPOR DIFFUSION, HANGING DROP
Resolution 2.70 Å
1HBW Solution nmr structure of the dimerization domain of the yeast transcriptional activator Gal4 (residues 50-106) Deposited 2001-04-20 Assembly 1 Protein homooligomer Homooligomer;Protein × 2 PDB declaration: dimeric(2) Consistent with protein count
Chain A 50–106(57 aa) Fragment:DIMERIZATION DOMAIN RESIDUES 50-106
Chain B 50–106(57 aa) Fragment:DIMERIZATION DOMAIN RESIDUES 50-106
Mutation:YES Mutation:YES No recorded non-water small molecule SOLUTION NMR
NMR measurement conditions pH 7.4;308 K;Ionic strength (raw mmCIF value) 50 MM SODIUM PHOSPHATE
Resolution not provided
3BTS Crystal structure of a ternary complex of the transcriptional repressor Gal80p (Gal80S0 [G301R]) and the acidic activation domain of Gal4p (aa 854-874) from Saccharomyces cerevisiae with NAD Deposited 2007-12-30 Assembly 1 Protein heterocomplex Heteromer;Protein × 4 PDB declaration: tetrameric(4) Consistent with protein count
Chain E 854–874(21 aa) Fragment:S. cerevisiae Gal4p peptide; UNP residues 854-874
Chain F 854–874(21 aa) Fragment:S. cerevisiae Gal4p peptide; UNP residues 854-874
Not recorded NAD NICOTINAMIDE-ADENINE-DINUCLEOTIDE × 2 X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION, HANGING DROP;pH 8;290 K;20% PEG 3350, 0.15M Sodium fluoride, followed by soaking in NAD to a final concentration of 5mM, pH 8.0, VAPOR DIFFUSION, HANGING DROP, temperature 290K
Resolution 2.70 Å R-free 0.232
3COQ Structural Basis for Dimerization in DNA Recognition by Gal4 Deposited 2008-03-29 Assembly 1 Protein–DNA Homooligomer;Protein × 2 PDB declaration: tetrameric(4) Consistent with all polymers
Chain A 8–96(89 aa) Fragment:DNA binding domain with complete dimerization domain
Chain B 8–96(89 aa) Fragment:DNA binding domain with complete dimerization domain
Not recorded MPD (4S)-2-METHYL-2,4-PENTANEDIOL × 1 ZN ZINC ION × 4 X-RAY DIFFRACTION
X-ray crystallization conditions VAPOR DIFFUSION;pH 5.5;298 K;40mM Mg(OAc)2, 25mM sodium phosphate, 5% PEG400, 5% MPD, pH 5.5, VAPOR DIFFUSION, temperature 298K
Resolution 2.40 Å R-free 0.269
7UIK Mediator-PIC Early (Tail A + Upstream DNA & Activator) Deposited 2022-03-29 Assembly 1 Protein–DNA Heteromer;Protein × 8 PDB declaration: decameric(10) Consistent with all polymers
Chain T 1–147(147 aa)
Chain U 1–147(147 aa)
Not recorded ZN ZINC ION × 4 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.6
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 7.70 Å
7UIO Mediator-PIC Early (Composite Model) Deposited 2022-03-29 Assembly 1 Protein–DNA Heteromer;Protein × 78 PDB declaration: 80-meric(80) Consistent with all polymers
Chain GA 1–147(147 aa)
Chain GB 1–147(147 aa)
Not recorded ZN ZINC ION × 4 THR THREONINE × 1 ALA ALANINE × 1 ASP ASPARTIC ACID × 1 ELECTRON MICROSCOPY
cryo-EM buffer pH 7.6
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.30 Å