Datasets from the Institute of Biotechnology of the Czech Academy of Sciences




X-Ray Diffraction data from HIV-1 protease in complex with an ethyleneamine inhibitor ("WT-OE"), source of 1M0B structure

X-Ray Diffraction data from HIV-1 protease in complex with an ethyleneamine inhibitor ("WT-OE"), source of 1M0B structure


X-Ray Diffraction data from HIV-1 protease with a hydroxyethylamine peptidomimetic inhibitor ("WT-RE") , source of 1ZSF structure

X-Ray Diffraction data from HIV-1 protease with a hydroxyethylamine peptidomimetic inhibitor ("WT-RE") , source of 1ZSF structure


X-Ray Diffraction data from HIV-1 protease with a hydroxyethylamine peptidomimetic inhibitor ("WT-SQ"), source of 1IIQ structure

X-Ray Diffraction data from HIV-1 protease with a hydroxyethylamine peptidomimetic inhibitor ("WT-SQ"), source of 1IIQ structure


X-Ray Diffraction data from HIV-1 protease with a peptidomimetic inhibitor ("WT-SE"), source of 1FQX structure

X-Ray Diffraction data from HIV-1 protease with a peptidomimetic inhibitor ("WT-SE") , source of 1FQX structure


X-Ray Diffraction data from Monomeric form of human LLT1, a ligand for NKR-P1, source of 4QKG structure

X-Ray Diffraction data from monomeric form of human LLT1, a ligand for NKR-P1, source of 4QKG structure


X-Ray Diffraction data from mutant HIV-1 protease (A71V, V82T, I84V) with a hydroxyethylamine peptidomimetic inhibitor ("I8-SE"), source of 1ZJ7 structure

X-Ray Diffraction data from Mutant HIV-1 protease (A71V, V82T, I84V) with a hydroxyethylamine peptidomimetic inhibitor ("I8-SE"), source of 1ZJ7 structure


X-Ray Diffraction data from Glycosylated form of human LLT1, a ligand for NKR-P1, in this structure forming hexamers, source of 4QKJ structure

X-Ray Diffraction data from glycosylated form of human LLT1, a ligand for NKR-P1, in this structure forming hexamers, source of 4QKJ structure


X-Ray Diffraction data from Dimeric form of human LLT1, a ligand for NKR-P1, source of 4QKI structure

X-Ray Diffraction data from dimeric form of human LLT1, a ligand for NKR-P1, source of 4QKI structure


X-Ray Diffraction data from Dimeric form of human LLT1, a ligand for NKR-P1, source of 4QKH structure

X-Ray Diffraction data from dimeric form of human LLT1, a ligand for NKR-P1, source of 4QKH structure


X-Ray Diffraction data from Mutant HIV-1 protease (A71V, V82T, I84V) with a hydroxyethylamine peptidomimetic inhibitor ("I8-SQ"), source of 1ZLF structure

X-Ray Diffraction data from mutant HIV-1 protease (A71V, V82T, I84V) with a hydroxyethylamine peptidomimetic inhibitor ("I8-SQ"), source of 1ZLF structure


X-Ray Diffraction data from HIV-1 protease (A71V, V82T, I84V) with an inhibitor BOC-PHE-PSI[CH2CH2NH]-PHE-GLU-PHE-NH2 ("I8-OE"), source of 1LZQ structure

X-ray data of mutant HIV-1 protease (A71V, V82T, I84V) with an ethylenamine peptidomimetic inhibitor BOC-PHE-PSI[CH2CH2NH]-PHE-GLU-PHE-NH2 ("I8-OE"), source of 1LZQ structure


X-Ray Diffraction data from Laccase from Streptomyces coelicolor, source of 3CG8 structure

X-Ray Diffraction data of laccase from Streptomyces coelicolor, source of 3CG8 structure


X-Ray Diffraction data from Two-domain laccase from Streptomyces coelicolor at 2.3 A resolution, source of 3KW8 structure

X-Ray Diffraction data from Two-domain laccase from Streptomyces coelicolor at 2.3 A resolution, source of 3KW8 structure


X-Ray Diffraction data from Mouse Clr-g, a ligand for NK Cell activation receptor NKR-P1F, source of 3RS1 structure

X-ray data of mouse Clr-g, source of 3RS1 structure