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Page 1099 of 5099 · 254917 entries
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| PDB ID | Title | official curves | Structure unit | Experimental Method |
|---|---|---|---|---|
| 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 |