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5099
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Page 1111 of 5099 · 254917 entries
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| PDB ID | Title | official curves | Structure unit | Experimental Method |
|---|---|---|---|---|
| 2xof | Ribonucleotide reductase Y122NO2Y modified R2 subunit of E. coli | 1 | 1 | X-RAY DIFFRACTION |
| 2xog | Functional and Structural Analyses of N-Acylsulfonamide-Linked Dinucleoside Inhibitors of Ribonuclease A | 2 | 2 | X-RAY DIFFRACTION |
| 2xoi | Functional and Structural Analyses of N-Acylsulfonamide-Linked Dinucleoside Inhibitors of Ribonuclease A | 2 | 2 | X-RAY DIFFRACTION |
| 2xok | Refined structure of yeast F1c10 ATPase complex to 3 A resolution | 1 | 1 | X-RAY DIFFRACTION |
| 2xol | High resolution structure of TtrD from Archaeoglobus fulgidus | 1 | 1 | X-RAY DIFFRACTION |
| 2xom | Atomic resolution structure of TmCBM61 in complex with beta-1,4- galactotriose | 1 | 1 | X-RAY DIFFRACTION |
| 2xon | Structure of TmCBM61 in complex with beta-1,4-galactotriose at 1.4 A resolution | 2 | 2 | X-RAY DIFFRACTION |
| 2xot | Crystal structure of neuronal leucine rich repeat protein AMIGO-1 | 1 | 1 | X-RAY DIFFRACTION |
| 2xov | Crystal Structure of E.coli rhomboid protease GlpG, native enzyme | 1 | 1 | X-RAY DIFFRACTION |
| 2xow | Structure of GlpG in complex with a mechanism-based isocoumarin inhibitor | 1 | 1 | X-RAY DIFFRACTION |
| 2xox | Crystal structure of pteridine reductase (PTR1) from Leishmania donovani | 1 | 1 | X-RAY DIFFRACTION |
| 2xoy | C-terminal cysteine-rich domain of human CHFR bound to P(1),P(2)- Diadenosine-5'-pyrophosphate | 2 | 2 | X-RAY DIFFRACTION |
| 2xoz | C-terminal cysteine rich domain of human CHFR bound to AMP | 2 | 2 | X-RAY DIFFRACTION |
| 2xp0 | C-terminal cysteine-rich domain of human CHFR | 2 | 2 | X-RAY DIFFRACTION |
| 2xp1 | Structure of the tandem SH2 domains from Antonospora locustae transcription elongation factor Spt6 | 1 | 1 | X-RAY DIFFRACTION |
| 2xp2 | Structure of the Human Anaplastic Lymphoma Kinase in Complex with Crizotinib (PF-02341066) | 1 | 1 | X-RAY DIFFRACTION |
| 2xp3 | DISCOVERY OF CELL-ACTIVE PHENYL-IMIDAZOLE PIN1 INHIBITORS BY STRUCTURE-GUIDED FRAGMENT EVOLUTION | 1 | 1 | X-RAY DIFFRACTION |
| 2xp4 | DISCOVERY OF CELL-ACTIVE PHENYL-IMIDAZOLE PIN1 INHIBITORS BY STRUCTURE-GUIDED FRAGMENT EVOLUTION | 1 | 1 | X-RAY DIFFRACTION |
| 2xp5 | DISCOVERY OF CELL-ACTIVE PHENYL-IMIDAZOLE PIN1 INHIBITORS BY STRUCTURE-GUIDED FRAGMENT EVOLUTION | 1 | 1 | X-RAY DIFFRACTION |
| 2xp6 | DISCOVERY OF CELL-ACTIVE PHENYL-IMIDAZOLE PIN1 INHIBITORS BY STRUCTURE-GUIDED FRAGMENT EVOLUTION | 1 | 1 | X-RAY DIFFRACTION |
| 2xp7 | DISCOVERY OF CELL-ACTIVE PHENYL-IMIDAZOLE PIN1 INHIBITORS BY STRUCTURE-GUIDED FRAGMENT EVOLUTION | 1 | 1 | X-RAY DIFFRACTION |
| 2xp8 | DISCOVERY OF CELL-ACTIVE PHENYL-IMIDAZOLE PIN1 INHIBITORS BY STRUCTURE-GUIDED FRAGMENT EVOLUTION | 1 | 1 | X-RAY DIFFRACTION |
| 2xp9 | DISCOVERY OF CELL-ACTIVE PHENYL-IMIDAZOLE PIN1 INHIBITORS BY STRUCTURE-GUIDED FRAGMENT EVOLUTION | 1 | 1 | X-RAY DIFFRACTION |
| 2xpa | DISCOVERY OF CELL-ACTIVE PHENYL-IMIDAZOLE PIN1 INHIBITORS BY STRUCTURE-GUIDED FRAGMENT EVOLUTION | 1 | 1 | X-RAY DIFFRACTION |
| 2xpb | DISCOVERY OF CELL-ACTIVE PHENYL-IMIDAZOLE PIN1 INHIBITORS BY STRUCTURE-GUIDED FRAGMENT EVOLUTION | 1 | 1 | X-RAY DIFFRACTION |
| 2xpc | Second-generation sulfonamide inhibitors of MurD: Activity optimisation with conformationally rigid analogues of D-glutamic acid | 1 | 1 | X-RAY DIFFRACTION |
| 2xpd | Reduced Thiol peroxidase (Tpx) from yersinia Pseudotuberculosis | 3 | 3 | X-RAY DIFFRACTION |
| 2xpe | Oxidised Thiol peroxidase (Tpx) from Yersinia pseudotuberculosis | 1 | 1 | X-RAY DIFFRACTION |
| 2xpg | Crystal structure of a MHC class I-peptide complex | 1 | 1 | X-RAY DIFFRACTION |
| 2xph | Crystal structure of human SENP1 with the bound cobalt | 2 | 2 | X-RAY DIFFRACTION |
| 2xpi | Crystal structure of APC/C hetero-tetramer Cut9-Hcn1 | 1 | 1 | X-RAY DIFFRACTION |
| 2xpj | Crystal structure of Physalis Mottle Virus with intact ordered RNA | 1 | 5 | X-RAY DIFFRACTION |
| 2xpk | Cell-penetrant, nanomolar O-GlcNAcase inhibitors selective against lysosomal hexosaminidases | 1 | 1 | X-RAY DIFFRACTION |
| 2xpl | Crystal structure of Iws1(Spn1) conserved domain from Encephalitozoon cuniculi | 1 | 1 | X-RAY DIFFRACTION |
| 2xpn | Crystal structure of a Spt6-Iws1(Spn1) complex from Encephalitozoon cuniculi, Form I | 1 | 1 | X-RAY DIFFRACTION |
| 2xpo | Crystal structure of a Spt6-Iws1(Spn1) complex from Encephalitozoon cuniculi, Form II | 2 | 2 | X-RAY DIFFRACTION |
| 2xpp | Crystal structure of a Spt6-Iws1(Spn1) complex from Encephalitozoon cuniculi, Form III | 1 | 1 | X-RAY DIFFRACTION |
| 2xpu | TetR(D) in complex with anhydrotetracycline. | 2 | 2 | X-RAY DIFFRACTION |
| 2xpv | TetR(D) in complex with minocycline and magnesium. | 1 | 1 | X-RAY DIFFRACTION |
| 2xpw | TetR(D) in complex with oxytetracycline and magnesium. | 1 | 1 | X-RAY DIFFRACTION |
| 2xpx | Crystal structure of BHRF1:Bak BH3 complex | 1 | 1 | X-RAY DIFFRACTION |
| 2xpy | Structure of Native Leukotriene A4 Hydrolase from Saccharomyces cerevisiae | 1 | 1 | X-RAY DIFFRACTION |
| 2xpz | Structure of native yeast LTA4 hydrolase | 1 | 1 | X-RAY DIFFRACTION |
| 2xq0 | Structure of yeast LTA4 hydrolase in complex with Bestatin | 1 | 1 | X-RAY DIFFRACTION |
| 2xq1 | Crystal structure of peroxisomal catalase from the yeast Hansenula polymorpha | 4 | 4 | X-RAY DIFFRACTION |
| 2xq2 | Structure of the K294A mutant of vSGLT | 1 | 1 | X-RAY DIFFRACTION |
| 2xq3 | Pentameric ligand gated ion channel GLIC in complex with Br-lidocaine | 1 | 1 | X-RAY DIFFRACTION |
| 2xq4 | Pentameric ligand gated ion channel GLIC in complex with tetramethylarsonium (TMAs) | 1 | 1 | X-RAY DIFFRACTION |
| 2xq5 | Pentameric ligand gated ion channel GLIC in complex with tetraethylarsonium (TEAs) | 1 | 1 | X-RAY DIFFRACTION |
| 2xq6 | Pentameric ligand gated ion channel GLIC in complex with cesium ion (Cs+) | 1 | 1 | X-RAY DIFFRACTION |