| 2x6n |
Human foamy virus integrase - catalytic core. Manganese-bound structure. |
3 |
3 |
X-RAY DIFFRACTION |
| 2x6o |
Tet Repressor class D in complex with 7-chlor-2-cyano-iso- tetracycline |
1 |
1 |
X-RAY DIFFRACTION |
| 2x6p |
Crystal Structure of Coil Ser L19C |
1 |
1 |
X-RAY DIFFRACTION |
| 2x6q |
Crystal structure of trehalose synthase TreT from P.horikoshi |
2 |
2 |
X-RAY DIFFRACTION |
| 2x6r |
Crystal structure of trehalose synthase TreT from P.horikoshi produced by soaking in trehalose |
2 |
2 |
X-RAY DIFFRACTION |
| 2x6s |
Human foamy virus integrase - catalytic core. Magnesium-bound structure. |
3 |
3 |
X-RAY DIFFRACTION |
| 2x6t |
AGME bound to ADP-B-mannose |
10 |
10 |
X-RAY DIFFRACTION |
| 2x6u |
Crystal structure of human TBX5 in the DNA-free form |
1 |
1 |
X-RAY DIFFRACTION |
| 2x6v |
Crystal structure of human TBX5 in the DNA-bound and DNA-free form |
1 |
1 |
X-RAY DIFFRACTION |
| 2x6w |
Tailspike protein mutant E372Q of E.coli bacteriophage HK620 in complex with hexasaccharide |
1 |
1 |
X-RAY DIFFRACTION |
| 2x6x |
Tailspike protein mutant D339N of E.coli bacteriophage HK620 in complex with hexasaccharide |
1 |
1 |
X-RAY DIFFRACTION |
| 2x6y |
Tailspike protein mutant D339A of E.coli bacteriophage HK620 in complex with hexasaccharide |
1 |
1 |
X-RAY DIFFRACTION |
| 2x70 |
Crystal structure of MHC CLass I HLA-A2.1 bound to a photocleavable peptide |
2 |
2 |
X-RAY DIFFRACTION |
| 2x71 |
Structural basis for the interaction of lactivicins with serine beta- lactamases |
2 |
2 |
X-RAY DIFFRACTION |
| 2x72 |
CRYSTAL STRUCTURE OF THE CONSTITUTIVELY ACTIVE E113Q,D2C,D282C RHODOPSIN MUTANT WITH BOUND GALPHACT PEPTIDE. |
1 |
1 |
X-RAY DIFFRACTION |
| 2x74 |
Human foamy virus integrase - catalytic core. |
3 |
3 |
X-RAY DIFFRACTION |
| 2x75 |
Staphylococcus aureus adenylosuccinate lyase |
1 |
1 |
X-RAY DIFFRACTION |
| 2x76 |
The crystal structure of PhaZ7 at atomic (1.2 Angstrom) resolution reveals details of the active site and suggests a substrate binding mode |
1 |
1 |
X-RAY DIFFRACTION |
| 2x77 |
Crystal Structure of Leishmania major ADP ribosylation factor-like 1. |
1 |
1 |
X-RAY DIFFRACTION |
| 2x78 |
Human foamy virus integrase - catalytic core. |
2 |
2 |
X-RAY DIFFRACTION |
| 2x79 |
Inward facing conformation of Mhp1 |
1 |
1 |
X-RAY DIFFRACTION |
| 2x7a |
Structural basis of HIV-1 tethering to membranes by the Bst2-tetherin ectodomain |
6 |
6 |
X-RAY DIFFRACTION |
| 2x7b |
Crystal structure of the N-terminal acetylase Ard1 from Sulfolobus solfataricus P2 |
1 |
1 |
X-RAY DIFFRACTION |
| 2x7c |
Crystal structure of human kinesin Eg5 in complex with (S)-enastron |
2 |
2 |
X-RAY DIFFRACTION |
| 2x7d |
Crystal structure of human kinesin Eg5 in complex with (S)-dimethylenastron |
2 |
2 |
X-RAY DIFFRACTION |
| 2x7e |
Crystal structure of human kinesin Eg5 in complex with (R)-fluorastrol |
2 |
2 |
X-RAY DIFFRACTION |
| 2x7f |
Crystal structure of the kinase domain of human Traf2- and Nck- interacting Kinase with Wee1Chk1 inhibitor |
5 |
5 |
X-RAY DIFFRACTION |
| 2x7g |
Structure of human serine-arginine-rich protein-specific kinase 2 (SRPK2) bound to purvalanol B |
1 |
1 |
X-RAY DIFFRACTION |
| 2x7h |
Crystal structure of the human MGC45594 gene product in complex with fenoprofen |
2 |
2 |
X-RAY DIFFRACTION |
| 2x7i |
Crystal structure of mevalonate kinase from methicillin-resistant Staphylococcus aureus MRSA252 |
1 |
1 |
X-RAY DIFFRACTION |
| 2x7j |
Structure of the menaquinone biosynthesis protein MenD from Bacillus subtilis |
1 |
1 |
X-RAY DIFFRACTION |
| 2x7k |
The crystal structure of PPIL1 in complex with cyclosporine A suggests a binding mode for SKIP |
1 |
1 |
X-RAY DIFFRACTION |
| 2x7l |
Implications of the HIV-1 Rev dimer structure at 3.2A resolution for multimeric binding to the Rev response element |
6 |
6 |
X-RAY DIFFRACTION |
| 2x7m |
Crystal structure of Archaemetzincin (amzA) from Methanopyrus kandleri at 1.5 A resolution |
1 |
1 |
X-RAY DIFFRACTION |
| 2x7n |
Mechanism of eIF6s anti-association activity |
1 |
1 |
ELECTRON MICROSCOPY |
| 2x7o |
Crystal structure of TGFbRI complexed with an indolinone inhibitor |
5 |
5 |
X-RAY DIFFRACTION |
| 2x7p |
The Conserved Candida albicans CA3427 Gene Product Defines a New Family of Proteins Exhibiting the Generic Periplasmic Binding Protein Structural Fold |
1 |
1 |
X-RAY DIFFRACTION |
| 2x7q |
The conserved Candida albicans CA3427 gene product defines a new family of proteins exhibiting the generic periplasmic binding protein structural fold |
1 |
1 |
X-RAY DIFFRACTION |
| 2x7r |
Crystal structure of a late fusion intermediate of HIV-1 gp41 |
3 |
3 |
X-RAY DIFFRACTION |
| 2x7s |
Structures of human carbonic anhydrase II inhibitor complexes reveal a second binding site for steroidal and non-steroidal inhibitors. |
1 |
1 |
X-RAY DIFFRACTION |
| 2x7t |
Structures of human carbonic anhydrase II inhibitor complexes reveal a second binding site for steroidal and non-steroidal inhibitors. |
1 |
1 |
X-RAY DIFFRACTION |
| 2x7u |
Structures of human carbonic anhydrase II inhibitor complexes reveal a second binding site for steroidal and non-steroidal inhibitors. |
1 |
1 |
X-RAY DIFFRACTION |
| 2x7v |
Crystal structure of Thermotoga maritima endonuclease IV in the presence of zinc |
1 |
1 |
X-RAY DIFFRACTION |
| 2x7w |
Crystal structure of Thermotoga maritima endonuclease IV in the presence of cadmium and zinc |
1 |
1 |
X-RAY DIFFRACTION |
| 2x7x |
Fructose binding periplasmic domain of hybrid two component system BT1754 |
1 |
1 |
X-RAY DIFFRACTION |
| 2x7y |
P450 BM3 F87A in complex with DMSO |
2 |
2 |
X-RAY DIFFRACTION |
| 2x7z |
Crystal Structure of the SAP97 PDZ2 I342W C378A mutant protein domain |
1 |
1 |
X-RAY DIFFRACTION |
| 2x80 |
P450 BM3 F87A in complex with DMSO |
2 |
2 |
X-RAY DIFFRACTION |
| 2x81 |
STRUCTURE OF AURORA A IN COMPLEX WITH MLN8054 |
1 |
1 |
X-RAY DIFFRACTION |
| 2x82 |
Evolutionary basis of HIV restriction by the antiretroviral TRIMCyp |
2 |
2 |
X-RAY DIFFRACTION |