| 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 |