| 1pwm |
Crystal structure of human Aldose Reductase complexed with NADP and Fidarestat |
19.9 |
62.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1pwo |
Crystal Structure of Phospholipase A2 (MIPLA2) from Micropechis Ikaheka |
26.0 |
86.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1pwp |
Crystal Structure of the Anthrax Lethal Factor complexed with Small Molecule Inhibitor NSC 12155 |
38.3 |
115.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1pwq |
;Crystal structure of Anthrax Lethal Factor complexed with Thioacetyl-Tyr-Pro-Met-Amide, a metal-chelating peptidyl small molecule inhibitor
; |
38.3 |
117.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 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
; |
12.5 |
40.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1pwu |
;Crystal Structure of Anthrax Lethal Factor complexed with (3-(N-hydroxycarboxamido)-2-isobutylpropanoyl-Trp-methylamide), a known small molecule inhibitor of matrix metalloproteases.
; |
38.4 |
118.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1pwv |
Crystal structure of Anthrax Lethal Factor wild-type protein complexed with an optimised peptide substrate. |
38.1 |
117.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1pww |
;Crystal structure of Anthrax Lethal Factor active site mutant protein complexed with an optimised peptide substrate in the presence of zinc.
; |
38.1 |
117.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1pwx |
Crystal structure of the haloalcohol dehalogenase HheC complexed with bromide |
28.9 |
91.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1pwy |
CRYSTAL STRUCTURE OF HUMAN PNP COMPLEXED WITH ACYCLOVIR |
19.2 |
62.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1pwz |
Crystal structure of the haloalcohol dehalogenase HheC complexed with (R)-styrene oxide and chloride |
25.2 |
77.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1px0 |
Crystal structure of the haloalcohol dehalogenase HheC complexed with the haloalcohol mimic (R)-1-para-nitro-phenyl-2-azido-ethanol |
29.0 |
91.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1px2 |
Crystal Structure of Rat Synapsin I C Domain Complexed to Ca.ATP (Form 1) |
26.5 |
81.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1px3 |
E. COLI (LACZ) BETA-GALACTOSIDASE (G794A) |
52.1 |
172.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1px4 |
E. COLI (LACZ) BETA-GALACTOSIDASE (G794A) WITH IPTG BOUND |
52.0 |
172.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1px5 |
;Crystal structure of the 2'-specific and double-stranded RNA-activated interferon-induced antiviral protein 2'-5'-oligoadenylate synthetase
; |
32.6 |
106.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1px6 |
;A folding mutant of human class pi glutathione transferase, created by mutating aspartate 153 of the wild-type protein to asparagine
; |
21.9 |
64.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1px7 |
A folding mutant of human class pi glutathione transferase, created by mutating aspartate 153 of the wild-type protein to glutamate |
22.0 |
64.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1px8 |
Crystal structure of beta-D-xylosidase from Thermoanaerobacterium saccharolyticum, a family 39 glycoside hydrolase |
34.2 |
109.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1px9 |
Solution structure of the native CnErg1 Ergtoxin, a highly specific inhibitor of HERG channel |
10.3 |
36.0 |
SOLUTION NMR |
GOOD
|
| 1pxa |
CRYSTAL STRUCTURES OF MUTANT PSEUDOMONAS AERUGINOSA P-HYDROXYBENZOATE HYDROXYLASE: THE TYR201PHE, TYR385PHE, AND ASN300ASP VARIANTS |
22.8 |
73.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1pxb |
CRYSTAL STRUCTURES OF MUTANT PSEUDOMONAS AERUGINOSA P-HYDROXYBENZOATE HYDROXYLASE: THE TYR201PHE, TYR385PHE, AND ASN300ASP VARIANTS |
22.7 |
73.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1pxc |
CRYSTAL STRUCTURES OF MUTANT PSEUDOMONAS AERUGINOSA P-HYDROXYBENZOATE HYDROXYLASE: THE TYR201PHE, TYR385PHE, AND ASN300ASP VARIANTS |
22.7 |
72.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1pxd |
Crystal structure of the complex of jacalin with meso-tetrasulphonatophenylporphyrin. |
17.1 |
54.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1pxe |
Solution Structure of a CCHHC Domain of Neural Zinc Finger Factor-1 |
9.4 |
37.4 |
SOLUTION NMR |
GOOD
|
| 1pxg |
Crystal structure of the mutated tRNA-guanine transglycosylase (TGT) D280E complexed with preQ1 |
21.7 |
67.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1pxh |
Crystal structure of protein tyrosine phosphatase 1B with potent and selective bidentate inhibitor compound 2 |
20.2 |
67.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1pxi |
HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR 4-(2,5-Dichloro-thiophen-3-yl)-pyrimidin-2-ylamine |
20.6 |
66.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1pxj |
HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR 4-(2,4-Dimethyl-thiazol-5-yl)-pyrimidin-2-ylamine |
20.7 |
65.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1pxk |
;HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR N-[4-(2,4-Dimethyl-thiazol-5-yl)pyrimidin-2-yl]-N'-hydroxyiminoformamide
; |
20.6 |
66.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1pxl |
;HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR [4-(2,4-Dimethyl-thiazol-5-yl)-pyrimidin-2-yl]-(4-trifluoromethyl-phenyl)-amine
; |
20.5 |
66.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1pxm |
HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR 3-[4-(2,4-Dimethyl-thiazol-5-yl)-pyrimidin-2-ylamino]-phenol |
20.5 |
65.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1pxn |
HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR 4-[4-(4-Methyl-2-methylamino-thiazol-5-yl)-pyrimidin-2-ylamino]-phenol |
20.6 |
65.5 |
X-RAY DIFFRACTION |
GOOD
|
| 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
; |
20.8 |
66.4 |
X-RAY DIFFRACTION |
GOOD
|
| 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
; |
20.7 |
65.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1pxq |
Structure of Subtilisin A |
10.6 |
39.8 |
SOLUTION NMR |
REASONABLE
|
| 1pxr |
Structure of Pro50Ala mutant of Bacteriorhodopsin |
25.0 |
80.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1pxs |
Structure of Met56Ala mutant of Bacteriorhodopsin |
25.1 |
79.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 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
; |
25.7 |
83.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1pxu |
Crystal structure of chicken NtA from a eukaryotic source at 2.2A resolution |
15.8 |
49.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1pxv |
The staphostatin-staphopain complex: a forward binding inhibitor in complex with its target cysteine protease |
28.9 |
99.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1pxw |
Crystal structure of L7Ae sRNP core protein from Pyrococcus abyssii |
30.4 |
93.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1pxx |
CRYSTAL STRUCTURE OF DICLOFENAC BOUND TO THE CYCLOOXYGENASE ACTIVE SITE OF COX-2 |
45.4 |
150.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1pxy |
Crystal structure of the actin-crosslinking core of Arabidopsis fimbrin |
33.5 |
108.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1pxz |
1.7 Angstrom Crystal Structure of jun a 1, the major allergen from cedar pollen |
28.7 |
87.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1py0 |
Crystal structure of E51C/E54C Psaz from A.faecalis with CLaNP probe |
15.2 |
51.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1py1 |
Complex of GGA1-VHS domain and beta-secretase C-terminal phosphopeptide |
37.8 |
117.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1py2 |
Structure of a 60 nM Small Molecule Bound to a Hot Spot on IL-2 |
39.9 |
117.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1py3 |
Crystal structure of Ribonuclease Sa2 |
23.6 |
82.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1py4 |
Beta2 microglobulin mutant H31Y displays hints for amyloid formations |
26.8 |
83.8 |
X-RAY DIFFRACTION |
EXCELLENT
|