| 1xku |
Crystal structure of the dimeric protein core of decorin, the archetypal small leucine-rich repeat proteoglycan |
23.8 |
79.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1xkv |
Crystal Structure Of ATP-Dependent Phosphoenolpyruvate Carboxykinase From Thermus thermophilus HB8 |
32.8 |
103.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1xkw |
Pyochelin outer membrane receptor FptA from Pseudomonas aeruginosa |
26.2 |
85.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1xkx |
;Kinetic and crystallographic studies on 2-(beta-D-glucopyranosyl)-5-methyl-1,3,4-oxadiazole,-benzothiazole, and-benzimidazole, inhibitors of muscle glycogen phosphorylase b. Evidence for a new binding site.
; |
28.3 |
90.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1xky |
Crystal Structure of Dihydrodipicolinate Synthase DapA-2 (BA3935) from Bacillus Anthracis at 1.94A Resolution. |
32.4 |
93.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1xkz |
Crystal structure of the acylated beta-lactam sensor domain of Blar1 from S. aureus |
35.4 |
114.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1xl0 |
;Kinetic and crystallographic studies on 2-(beta-D-glucopyranosyl)-5-methyl-1,3,4-oxadiazole,-benzothiazole, and-benzimidazole, inhibitors of muscle glycogen phosphorylase b. Evidence for a new binding site.
; |
28.2 |
89.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1xl1 |
;Kinetic and crystallographic studies on 2-(beta-D-glucopyranosyl)-5-methyl-1,3,4-oxadiazole,-benzothiazole, and-benzimidazole, inhibitors of muscle glycogen phosphorylase b. Evidence for a new binding site.
; |
28.2 |
90.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1xl2 |
HIV-1 Protease in complex with pyrrolidinmethanamine |
18.2 |
61.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1xl3 |
Complex structure of Y.pestis virulence Factors YopN and TyeA |
32.9 |
123.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1xl4 |
Intermediate gating structure 1 of the inwardly rectifying K+ channel KirBac3.1 |
32.0 |
103.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1xl5 |
HIV-1 Protease in complex with amidhyroxysulfone |
18.2 |
65.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1xl6 |
Intermediate gating structure 2 of the inwardly rectifying K+ channel KirBac3.1 |
32.1 |
109.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1xl7 |
Crystal Structure of Mouse Carnitine Octanoyltransferase |
62.3 |
198.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1xl8 |
Crystal structure of mouse carnitine octanoyltransferase in complex with octanoylcarnitine |
62.7 |
199.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1xl9 |
Crystal Structure of Dihydrodipicolinate Synthase DapA-2 (BA3935) from Bacillus Anthracis. |
32.5 |
94.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1xla |
MECHANISM FOR ALDOSE-KETOSE INTERCONVERSION BY D-XYLOSE ISOMERASE INVOLVING RING OPENING FOLLOWED BY A 1,2-HYDRIDE SHIFT |
30.8 |
96.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1xlb |
MECHANISM FOR ALDOSE-KETOSE INTERCONVERSION BY D-XYLOSE ISOMERASE INVOLVING RING OPENING FOLLOWED BY A 1,2-HYDRIDE SHIFT |
30.7 |
96.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1xlc |
MECHANISM FOR ALDOSE-KETOSE INTERCONVERSION BY D-XYLOSE ISOMERASE INVOLVING RING OPENING FOLLOWED BY A 1,2-HYDRIDE SHIFT |
30.7 |
98.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1xld |
MECHANISM FOR ALDOSE-KETOSE INTERCONVERSION BY D-XYLOSE ISOMERASE INVOLVING RING OPENING FOLLOWED BY A 1,2-HYDRIDE SHIFT |
30.6 |
97.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1xle |
MECHANISM FOR ALDOSE-KETOSE INTERCONVERSION BY D-XYLOSE ISOMERASE INVOLVING RING OPENING FOLLOWED BY A 1,2-HYDRIDE SHIFT |
30.7 |
99.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1xlf |
MECHANISM FOR ALDOSE-KETOSE INTERCONVERSION BY D-XYLOSE ISOMERASE INVOLVING RING OPENING FOLLOWED BY A 1,2-HYDRIDE SHIFT |
30.8 |
99.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1xlg |
MECHANISM FOR ALDOSE-KETOSE INTERCONVERSION BY D-XYLOSE ISOMERASE INVOLVING RING OPENING FOLLOWED BY A 1,2-HYDRIDE SHIFT |
30.7 |
95.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1xlh |
MECHANISM FOR ALDOSE-KETOSE INTERCONVERSION BY D-XYLOSE ISOMERASE INVOLVING RING OPENING FOLLOWED BY A 1,2-HYDRIDE SHIFT |
30.8 |
98.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1xli |
MECHANISM FOR ALDOSE-KETOSE INTERCONVERSION BY D-XYLOSE ISOMERASE INVOLVING RING OPENING FOLLOWED BY A 1,2-HYDRIDE SHIFT |
30.6 |
98.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1xlj |
MECHANISM FOR ALDOSE-KETOSE INTERCONVERSION BY D-XYLOSE ISOMERASE INVOLVING RING OPENING FOLLOWED BY A 1,2-HYDRIDE SHIFT |
30.8 |
98.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1xlk |
MECHANISM FOR ALDOSE-KETOSE INTERCONVERSION BY D-XYLOSE ISOMERASE INVOLVING RING OPENING FOLLOWED BY A 1,2-HYDRIDE SHIFT |
30.7 |
95.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1xll |
MECHANISM FOR ALDOSE-KETOSE INTERCONVERSION BY D-XYLOSE ISOMERASE INVOLVING RING OPENING FOLLOWED BY A 1,2-HYDRIDE SHIFT |
30.7 |
97.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1xlm |
D254E, D256E MUTANT OF D-XYLOSE ISOMERASE COMPLEXED WITH AL3 AND XYLITOL |
30.8 |
96.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1xln |
Crystal structure of oxidized C73S/C85S putidaredoxin, a [2Fe-2S] ferredoxin from Pseudomonas putida |
19.8 |
66.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1xlo |
Structure of reduced C73S/C85S putidaredoxin, a [2Fe-2S] ferredoxin from Pseudomonas putida |
19.8 |
66.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1xlp |
Structure of oxidized C73S putidaredoxin from Pseudomonas putida |
23.8 |
76.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1xlq |
Crystal structure of reduced C73S putidaredoxin from Pseudomonas putida |
22.9 |
75.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1xlr |
CHORISMATE LYASE WITH INHIBITOR VANILLATE |
16.5 |
50.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1xls |
Crystal structure of the mouse CAR/RXR LBD heterodimer bound to TCPOBOP and 9cRA and a TIF2 peptide containg the third LXXLL motifs |
46.5 |
151.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1xlt |
Crystal structure of Transhydrogenase [(domain I)2:domain III] heterotrimer complex |
50.7 |
174.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1xlu |
X-Ray Structure Of Di-Isopropyl-Phosphoro-Fluoridate (Dfp) Inhibited Butyrylcholinesterase after Aging |
24.1 |
75.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1xlv |
Ethylphosphorylated Butyrylcholinesterase (Aged) Obtained By Reaction With Echothiophate |
24.2 |
76.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1xlw |
Diethylphosphorylated Butyrylcholinesterase (Nonaged) Obtained By Reaction With Echothiophate |
24.3 |
77.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1xlx |
Catalytic Domain Of Human Phosphodiesterase 4B In Complex With Cilomilast |
29.0 |
92.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1xly |
X-RAY STRUCTURE OF THE RNA-BINDING PROTEIN SHE2p |
23.5 |
80.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1xlz |
Catalytic Domain Of Human Phosphodiesterase 4B In Complex With Filaminast |
29.0 |
92.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1xm1 |
Nonbasic Thrombin Inhibitor Complex |
19.2 |
59.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1xm2 |
Crystal structure of Human PRL-1 |
35.6 |
120.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1xm3 |
Crystal structure of Northeast Structural Genomics Target SR156 |
30.8 |
94.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1xm4 |
Catalytic Domain Of Human Phosphodiesterase 4B In Complex With Piclamilast |
29.1 |
91.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1xm5 |
Crystal structure of metal-dependent hydrolase ybeY from E. coli, Pfam UPF0054 |
27.0 |
79.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1xm6 |
Catalytic Domain Of Human Phosphodiesterase 4B In Complex With (R)-Mesopram |
28.9 |
91.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1xm7 |
The Crystal Structure of the Protein of Unknown Function AQ665 from Aquifex aeolicus |
27.1 |
91.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1xm8 |
X-RAY STRUCTURE OF GLYOXALASE II FROM ARABIDOPSIS THALIANA GENE AT2G31350 |
24.4 |
77.8 |
X-RAY DIFFRACTION |
GOOD
|