| 1pwm |
Crystal structure of human Aldose Reductase complexed with NADP and Fidarestat |
1 |
1 |
X-RAY DIFFRACTION |
| 1pwo |
Crystal Structure of Phospholipase A2 (MIPLA2) from Micropechis Ikaheka |
1 |
1 |
X-RAY DIFFRACTION |
| 1pwp |
Crystal Structure of the Anthrax Lethal Factor complexed with Small Molecule Inhibitor NSC 12155 |
2 |
2 |
X-RAY DIFFRACTION |
| 1pwq |
Crystal structure of Anthrax Lethal Factor complexed with Thioacetyl-Tyr-Pro-Met-Amide, a metal-chelating peptidyl small molecule inhibitor |
2 |
2 |
X-RAY DIFFRACTION |
| 1pwt |
THERMODYNAMIC ANALYSIS OF ALPHA-SPECTRIN SH3 AND TWO OF ITS CIRCULAR PERMUTANTS WITH DIFFERENT LOOP LENGTHS: DISCERNING THE REASONS FOR RAPID FOLDING IN PROTEINS |
1 |
1 |
X-RAY DIFFRACTION |
| 1pwu |
Crystal Structure of Anthrax Lethal Factor complexed with (3-(N-hydroxycarboxamido)-2-isobutylpropanoyl-Trp-methylamide), a known small molecule inhibitor of matrix metalloproteases. |
2 |
2 |
X-RAY DIFFRACTION |
| 1pwv |
Crystal structure of Anthrax Lethal Factor wild-type protein complexed with an optimised peptide substrate. |
3 |
3 |
X-RAY DIFFRACTION |
| 1pww |
Crystal structure of Anthrax Lethal Factor active site mutant protein complexed with an optimised peptide substrate in the presence of zinc. |
3 |
3 |
X-RAY DIFFRACTION |
| 1pwx |
Crystal structure of the haloalcohol dehalogenase HheC complexed with bromide |
1 |
1 |
X-RAY DIFFRACTION |
| 1pwy |
CRYSTAL STRUCTURE OF HUMAN PNP COMPLEXED WITH ACYCLOVIR |
1 |
1 |
X-RAY DIFFRACTION |
| 1pwz |
Crystal structure of the haloalcohol dehalogenase HheC complexed with (R)-styrene oxide and chloride |
1 |
1 |
X-RAY DIFFRACTION |
| 1px0 |
Crystal structure of the haloalcohol dehalogenase HheC complexed with the haloalcohol mimic (R)-1-para-nitro-phenyl-2-azido-ethanol |
1 |
1 |
X-RAY DIFFRACTION |
| 1px2 |
Crystal Structure of Rat Synapsin I C Domain Complexed to Ca.ATP (Form 1) |
1 |
1 |
X-RAY DIFFRACTION |
| 1px3 |
E. COLI (LACZ) BETA-GALACTOSIDASE (G794A) |
1 |
1 |
X-RAY DIFFRACTION |
| 1px4 |
E. COLI (LACZ) BETA-GALACTOSIDASE (G794A) WITH IPTG BOUND |
1 |
1 |
X-RAY DIFFRACTION |
| 1px5 |
Crystal structure of the 2'-specific and double-stranded RNA-activated interferon-induced antiviral protein 2'-5'-oligoadenylate synthetase |
2 |
2 |
X-RAY DIFFRACTION |
| 1px6 |
A folding mutant of human class pi glutathione transferase, created by mutating aspartate 153 of the wild-type protein to asparagine |
1 |
1 |
X-RAY DIFFRACTION |
| 1px7 |
A folding mutant of human class pi glutathione transferase, created by mutating aspartate 153 of the wild-type protein to glutamate |
1 |
1 |
X-RAY DIFFRACTION |
| 1px8 |
Crystal structure of beta-D-xylosidase from Thermoanaerobacterium saccharolyticum, a family 39 glycoside hydrolase |
1 |
1 |
X-RAY DIFFRACTION |
| 1px9 |
Solution structure of the native CnErg1 Ergtoxin, a highly specific inhibitor of HERG channel |
1 |
1 |
SOLUTION NMR |
| 1pxa |
CRYSTAL STRUCTURES OF MUTANT PSEUDOMONAS AERUGINOSA P-HYDROXYBENZOATE HYDROXYLASE: THE TYR201PHE, TYR385PHE, AND ASN300ASP VARIANTS |
1 |
1 |
X-RAY DIFFRACTION |
| 1pxb |
CRYSTAL STRUCTURES OF MUTANT PSEUDOMONAS AERUGINOSA P-HYDROXYBENZOATE HYDROXYLASE: THE TYR201PHE, TYR385PHE, AND ASN300ASP VARIANTS |
1 |
1 |
X-RAY DIFFRACTION |
| 1pxc |
CRYSTAL STRUCTURES OF MUTANT PSEUDOMONAS AERUGINOSA P-HYDROXYBENZOATE HYDROXYLASE: THE TYR201PHE, TYR385PHE, AND ASN300ASP VARIANTS |
1 |
1 |
X-RAY DIFFRACTION |
| 1pxd |
Crystal structure of the complex of jacalin with meso-tetrasulphonatophenylporphyrin. |
1 |
1 |
X-RAY DIFFRACTION |
| 1pxe |
Solution Structure of a CCHHC Domain of Neural Zinc Finger Factor-1 |
21 |
21 |
SOLUTION NMR |
| 1pxg |
Crystal structure of the mutated tRNA-guanine transglycosylase (TGT) D280E complexed with preQ1 |
1 |
1 |
X-RAY DIFFRACTION |
| 1pxh |
Crystal structure of protein tyrosine phosphatase 1B with potent and selective bidentate inhibitor compound 2 |
1 |
1 |
X-RAY DIFFRACTION |
| 1pxi |
HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR 4-(2,5-Dichloro-thiophen-3-yl)-pyrimidin-2-ylamine |
1 |
1 |
X-RAY DIFFRACTION |
| 1pxj |
HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR 4-(2,4-Dimethyl-thiazol-5-yl)-pyrimidin-2-ylamine |
1 |
1 |
X-RAY DIFFRACTION |
| 1pxk |
HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR N-[4-(2,4-Dimethyl-thiazol-5-yl)pyrimidin-2-yl]-N'-hydroxyiminoformamide |
1 |
1 |
X-RAY DIFFRACTION |
| 1pxl |
HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR [4-(2,4-Dimethyl-thiazol-5-yl)-pyrimidin-2-yl]-(4-trifluoromethyl-phenyl)-amine |
1 |
1 |
X-RAY DIFFRACTION |
| 1pxm |
HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR 3-[4-(2,4-Dimethyl-thiazol-5-yl)-pyrimidin-2-ylamino]-phenol |
1 |
1 |
X-RAY DIFFRACTION |
| 1pxn |
HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR 4-[4-(4-Methyl-2-methylamino-thiazol-5-yl)-pyrimidin-2-ylamino]-phenol |
1 |
1 |
X-RAY DIFFRACTION |
| 1pxo |
HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR [4-(2-Amino-4-methyl-thiazol-5-yl)-pyrimidin-2-yl]-(3-nitro-phenyl)-amine |
1 |
1 |
X-RAY DIFFRACTION |
| 1pxp |
HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR N-[4-(2,4-Dimethyl-thiazol-5-yl)-pyrimidin-2-yl]-N',N'-dimethyl-benzene-1,4-diamine |
1 |
1 |
X-RAY DIFFRACTION |
| 1pxq |
Structure of Subtilisin A |
8 |
8 |
SOLUTION NMR |
| 1pxr |
Structure of Pro50Ala mutant of Bacteriorhodopsin |
2 |
2 |
X-RAY DIFFRACTION |
| 1pxs |
Structure of Met56Ala mutant of Bacteriorhodopsin |
2 |
2 |
X-RAY DIFFRACTION |
| 1pxt |
THE 2.8 ANGSTROMS STRUCTURE OF PEROXISOMAL 3-KETOACYL-COA THIOLASE OF SACCHAROMYCES CEREVISIAE: A FIVE LAYERED A-B-A-B-A STRUCTURE, CONSTRUCTED FROM TWO CORE DOMAINS OF IDENTICAL TOPOLOGY |
1 |
1 |
X-RAY DIFFRACTION |
| 1pxu |
Crystal structure of chicken NtA from a eukaryotic source at 2.2A resolution |
1 |
1 |
X-RAY DIFFRACTION |
| 1pxv |
The staphostatin-staphopain complex: a forward binding inhibitor in complex with its target cysteine protease |
4 |
4 |
X-RAY DIFFRACTION |
| 1pxw |
Crystal structure of L7Ae sRNP core protein from Pyrococcus abyssii |
2 |
2 |
X-RAY DIFFRACTION |
| 1pxx |
CRYSTAL STRUCTURE OF DICLOFENAC BOUND TO THE CYCLOOXYGENASE ACTIVE SITE OF COX-2 |
2 |
2 |
X-RAY DIFFRACTION |
| 1pxy |
Crystal structure of the actin-crosslinking core of Arabidopsis fimbrin |
2 |
2 |
X-RAY DIFFRACTION |
| 1pxz |
1.7 Angstrom Crystal Structure of jun a 1, the major allergen from cedar pollen |
2 |
2 |
X-RAY DIFFRACTION |
| 1py0 |
Crystal structure of E51C/E54C Psaz from A.faecalis with CLaNP probe |
1 |
1 |
X-RAY DIFFRACTION |
| 1py1 |
Complex of GGA1-VHS domain and beta-secretase C-terminal phosphopeptide |
2 |
2 |
X-RAY DIFFRACTION |
| 1py2 |
Structure of a 60 nM Small Molecule Bound to a Hot Spot on IL-2 |
6 |
6 |
X-RAY DIFFRACTION |
| 1py3 |
Crystal structure of Ribonuclease Sa2 |
3 |
3 |
X-RAY DIFFRACTION |
| 1py4 |
Beta2 microglobulin mutant H31Y displays hints for amyloid formations |
4 |
4 |
X-RAY DIFFRACTION |