Current Protein Identity:P05386 New Search
Main Difference Dimensions in This Set
Different construct Different mutation/modification Different assembly state 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
2LBF Solution structure of the dimerization domain of human ribosomal protein P1/P2 heterodimer Deposited 2011-03-30 Assembly 1 Protein heterocomplex Heteromer;Protein × 2 PDB declaration: dimeric(2) Consistent with protein count
Chain A 1–69(69 aa) Fragment:UNP residues 1-69
Not recorded No recorded non-water small molecule SOLUTION NMR
NMR measurement conditions pH 6.5;298 K;Ionic strength (raw mmCIF value) 0.15;Pressure ambient
NMR sample composition 1 mM [U-100% 13C; U-100% 15N] protein_1-1, 1 mM [U-100% 13C; U-100% 15N] protein_2-2, 90% H2O/10% D2O | 90% H2O/10% D2O
Resolution not provided
4BEH Solution structure of human ribosomal protein P1.P2 heterodimer Deposited 2013-03-10 Assembly 1 Protein heterocomplex Heteromer;Protein × 2 PDB declaration: dimeric(2) Consistent with protein count
Chain A 1–114(114 aa)
Not recorded No recorded non-water small molecule SOLUTION NMR
NMR measurement conditions pH 6.5;298 K;Ionic strength (raw mmCIF value) 150;Pressure 1.0
NMR sample composition 10% WATER/90% D2O
Resolution not provided
4V6X Structure of the human 80S ribosome Deposited 2013-02-27 Assembly 1 Protein–RNA Heteromer;Protein × 84 PDB declaration: 89-meric(89) Consistent with all polymers
Chain Cs 1–114(114 aa)
Chain Ct 1–114(114 aa)
Not recorded No recorded non-water small molecule ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5
cryo-EM vitrification conditions Cryogen ETHANE;Blot for 3 seconds using two pieces of filter paper, then plunge into liquid ethane (FEI VITROBOT MARK IV).
Resolution 5.00 Å