| 2wgx |
HUMAN P53 CORE DOMAIN MUTANT M133L-V203A-Y236F-N239Y-T253I-N268D |
2 |
2 |
X-RAY DIFFRACTION |
| 2wgy |
Crystal structure of the G243A mutant of CYP130 from M. tuberculosis |
1 |
1 |
X-RAY DIFFRACTION |
| 2wgz |
Crystal structure of alpha-1,3 galactosyltransferase (alpha3GT) in a complex with p-nitrophenyl-beta-galactoside (pNP-beta-Gal) |
1 |
1 |
X-RAY DIFFRACTION |
| 2wh0 |
Recognition of an intrachain tandem 14-3-3 binding site within protein kinase C epsilon |
2 |
2 |
X-RAY DIFFRACTION |
| 2wh5 |
Crystal structure of human acyl-CoA binding domain 4 complexed with stearoyl-CoA |
6 |
6 |
X-RAY DIFFRACTION |
| 2wh6 |
Crystal structure of anti-apoptotic BHRF1 in complex with the Bim BH3 domain |
1 |
1 |
X-RAY DIFFRACTION |
| 2wh7 |
The partial structure of a group A streptpcoccal phage-encoded tail fibre hyaluronate lyase Hylp2 |
1 |
1 |
X-RAY DIFFRACTION |
| 2wh8 |
Interaction of Mycobacterium tuberculosis CYP130 with heterocyclic arylamines |
4 |
4 |
X-RAY DIFFRACTION |
| 2wh9 |
Solution structure of GxTX-1E |
20 |
20 |
SOLUTION NMR |
| 2whb |
Truncation and Optimisation of Peptide Inhibitors of CDK2, Cyclin A Through Structure Guided Design |
2 |
2 |
X-RAY DIFFRACTION |
| 2whd |
Barley NADPH-dependent thioredoxin reductase 2 |
1 |
1 |
X-RAY DIFFRACTION |
| 2whe |
Structure of native Beta-Phosphoglucomutase in an open conformation without bound ligands. |
1 |
1 |
X-RAY DIFFRACTION |
| 2whf |
Interaction of Mycobacterium tuberculosis CYP130 with heterocyclic arylamines |
1 |
1 |
X-RAY DIFFRACTION |
| 2whg |
Crystal Structure of the Di-Zinc Metallo-beta-lactamase VIM-4 from Pseudomonas aeruginosa |
2 |
2 |
X-RAY DIFFRACTION |
| 2whh |
HIV-1 protease tethered dimer Q-product complex along with nucleophilic water molecule |
1 |
1 |
X-RAY DIFFRACTION |
| 2whi |
Crystal structure of Mycobacterium Tuberculosis Glutamine Synthetase in complex with a purine analogue inhibitor and L-methionine-S- sulfoximine phosphate. |
2 |
2 |
X-RAY DIFFRACTION |
| 2whj |
Understanding how diverse mannanases recognise heterogeneous substrates |
1 |
1 |
X-RAY DIFFRACTION |
| 2whk |
Structure of Bacillus subtilis mannanase man26 |
1 |
1 |
X-RAY DIFFRACTION |
| 2whl |
Understanding how diverse mannanases recognise heterogeneous substrates |
1 |
1 |
X-RAY DIFFRACTION |
| 2whm |
Cellvibrio japonicus Man26A E121A and E320G double mutant in complex with mannobiose |
1 |
1 |
X-RAY DIFFRACTION |
| 2whn |
N-terminal domain from the PilC type IV pilus biogenesis protein |
2 |
2 |
X-RAY DIFFRACTION |
| 2who |
CRYSTAL STRUCTURE OF HEPATITIS C VIRUS NS5B POLYMERASE FROM 1B GENOTYPE IN COMPLEX WITH A NON-NUCLEOSIDE INHIBITOR |
2 |
2 |
X-RAY DIFFRACTION |
| 2whp |
Crystal structure of acetylcholinesterase, phosphonylated by sarin and in complex with HI-6 |
2 |
2 |
X-RAY DIFFRACTION |
| 2whq |
Crystal structure of acetylcholinesterase, phosphonylated by sarin (aged) in complex with HI-6 |
1 |
1 |
X-RAY DIFFRACTION |
| 2whr |
Crystal structure of acetylcholinesterase in complex with K027 |
1 |
1 |
X-RAY DIFFRACTION |
| 2whs |
Fluorescent Protein mKeima at pH 3.8 |
4 |
4 |
X-RAY DIFFRACTION |
| 2wht |
Fluorescent Protein mKeima at pH 5.6 |
4 |
4 |
X-RAY DIFFRACTION |
| 2whu |
Fluorescent Protein mKeima at pH 8.0 |
4 |
4 |
X-RAY DIFFRACTION |
| 2whv |
CRYSTAL STRUCTURE OF MOUSE CADHERIN-23 EC1-2 (ALL CATION BINDING SITES OCCUPIED BY CALCIUM) |
1 |
1 |
X-RAY DIFFRACTION |
| 2whw |
Selective oxidation of carbolide C-H bonds by engineered macrolide P450 monooxygenase |
2 |
2 |
X-RAY DIFFRACTION |
| 2whx |
A second conformation of the NS3 protease-helicase from dengue virus |
1 |
1 |
X-RAY DIFFRACTION |
| 2why |
Crystal structure of the triscatecholate siderophore binding protein FeuA from Bacillus subtilis complexed with Ferri-Bacillibactin |
3 |
3 |
X-RAY DIFFRACTION |
| 2whz |
Dipeptide Inhibitors of Thermolysin |
1 |
1 |
X-RAY DIFFRACTION |
| 2wi0 |
Dipeptide Inhibitors of Thermolysin |
1 |
1 |
X-RAY DIFFRACTION |
| 2wi1 |
Orally Active 2-Amino Thienopyrimidine Inhibitors of the Hsp90 Chaperone |
1 |
1 |
X-RAY DIFFRACTION |
| 2wi2 |
Orally Active 2-Amino Thienopyrimidine Inhibitors of the Hsp90 Chaperone |
2 |
2 |
X-RAY DIFFRACTION |
| 2wi3 |
Orally Active 2-Amino Thienopyrimidine Inhibitors of the Hsp90 Chaperone |
1 |
1 |
X-RAY DIFFRACTION |
| 2wi4 |
Orally Active 2-Amino Thienopyrimidine Inhibitors of the Hsp90 Chaperone |
1 |
1 |
X-RAY DIFFRACTION |
| 2wi5 |
Orally Active 2-Amino Thienopyrimidine Inhibitors of the Hsp90 Chaperone |
1 |
1 |
X-RAY DIFFRACTION |
| 2wi6 |
Orally Active 2-Amino Thienopyrimidine Inhibitors of the Hsp90 Chaperone |
1 |
1 |
X-RAY DIFFRACTION |
| 2wi7 |
Orally Active 2-Amino Thienopyrimidine Inhibitors of the Hsp90 Chaperone |
1 |
1 |
X-RAY DIFFRACTION |
| 2wi8 |
Crystal structure of the triscatecholate siderophore binding protein FeuA from Bacillus subtilis |
1 |
1 |
X-RAY DIFFRACTION |
| 2wi9 |
Selective oxidation of carbolide C-H bonds by engineered macrolide P450 monooxygenase |
2 |
2 |
X-RAY DIFFRACTION |
| 2wia |
Crystal Structures of the N-terminal Intracellular Domain of FeoB from Klebsiella Pneumoniae in Apo Form |
4 |
4 |
X-RAY DIFFRACTION |
| 2wib |
Crystal Structures of the N-terminal Intracellular Domain of FeoB from Klebsiella Pneumoniae in GDP binding state |
2 |
2 |
X-RAY DIFFRACTION |
| 2wic |
Crystal Structures of the N-terminal Intracellular Domain of FeoB from Klebsiella Pneumoniae in GMPPNP binding state |
2 |
2 |
X-RAY DIFFRACTION |
| 2wid |
NONAGED FORM OF HUMAN BUTYRYLCHOLINESTERASE INHIBITED BY TABUN ANALOGUE TA1 |
1 |
1 |
X-RAY DIFFRACTION |
| 2wie |
High-resolution structure of the rotor ring from a proton dependent ATP synthase |
1 |
1 |
X-RAY DIFFRACTION |
| 2wif |
AGED FORM OF HUMAN BUTYRYLCHOLINESTERASE INHIBITED BY TABUN ANALOGUE TA1 |
1 |
1 |
X-RAY DIFFRACTION |
| 2wig |
NONAGED FORM OF HUMAN BUTYRYLCHOLINESTERASE INHIBITED BY TABUN ANALOGUE TA4 |
1 |
1 |
X-RAY DIFFRACTION |