| 1l0i |
Crystal structure of butyryl-ACP I62M mutant |
13.4 |
40.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l0j |
METHIONINE CORE MUTANT OF T4 LYSOZYME |
17.4 |
60.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1l0k |
METHIONINE CORE MUTANT OF T4 LYSOZYME |
17.4 |
58.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1l0l |
structure of bovine mitochondrial cytochrome bc1 complex with a bound fungicide famoxadone |
49.9 |
169.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l0m |
Solution structure of Bacteriorhodopsin |
18.2 |
59.8 |
SOLUTION NMR |
REASONABLE
|
| 1l0n |
native structure of bovine mitochondrial cytochrome bc1 complex |
49.5 |
165.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1l0o |
Crystal Structure of the Bacillus stearothermophilus Anti-Sigma Factor SpoIIAB with the Sporulation Sigma Factor SigmaF |
21.8 |
70.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1l0p |
CRYSTAL STRUCTURE ANALYSIS OF THE COMPLEX BETWEEN PSYCHROPHILIC ALPHA AMYLASE FROM PSEUDOALTEROMONAS HALOPLANCTIS AND NITRATE |
23.6 |
84.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1l0q |
Tandem YVTN beta-propeller and PKD domains from an archaeal surface layer protein |
46.3 |
176.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1l0r |
NMR Solution Structure of Nogalamycin Intercalation Between Co-Axially Stacked Hairpins |
10.8 |
30.6 |
SOLUTION NMR |
REASONABLE
|
| 1l0s |
Choristoneura fumiferana (spruce budworm) antifreeze protein isoform 337 |
24.1 |
82.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1l0v |
Quinol-Fumarate Reductase with Menaquinol Molecules |
45.4 |
144.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1l0w |
Aspartyl-tRNA synthetase-1 from space-grown crystals |
36.0 |
129.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l0x |
TCR beta chain complexed with streptococcal superantigen SpeA |
35.8 |
123.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1l0y |
T cell receptor beta chain complexed with superantigen SpeA soaked with zinc |
35.9 |
122.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l0z |
THE STRUCTURE OF PORCINE PANCREATIC ELASTASE COMPLEXED WITH XENON AND BROMIDE, CRYOPROTECTED WITH DRY PARAFFIN OIL |
18.2 |
54.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l10 |
;STRUCTURAL STUDIES OF MUTANTS OF THE LYSOZYME OF BACTERIOPHAGE T4. THE TEMPERATURE-SENSITIVE MUTANT PROTEIN THR157 (RIGHT ARROW) ILE
; |
17.5 |
58.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1l11 |
CONTRIBUTIONS OF HYDROGEN BONDS OF THR 157 TO THE THERMODYNAMIC STABILITY OF PHAGE T4 LYSOZYME |
17.5 |
58.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l12 |
CONTRIBUTIONS OF HYDROGEN BONDS OF THR 157 TO THE THERMODYNAMIC STABILITY OF PHAGE T4 LYSOZYME |
17.6 |
58.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l13 |
CONTRIBUTIONS OF HYDROGEN BONDS OF THR 157 TO THE THERMODYNAMIC STABILITY OF PHAGE T4 LYSOZYME |
17.6 |
60.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1l14 |
CONTRIBUTIONS OF HYDROGEN BONDS OF THR 157 TO THE THERMODYNAMIC STABILITY OF PHAGE T4 LYSOZYME |
17.5 |
58.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1l15 |
CONTRIBUTIONS OF HYDROGEN BONDS OF THR 157 TO THE THERMODYNAMIC STABILITY OF PHAGE T4 LYSOZYME |
17.5 |
58.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1l16 |
STRUCTURAL ANALYSIS OF THE TEMPERATURE-SENSITIVE MUTANT OF BACTERIOPHAGE T4 LYSOZYME, GLYCINE 156 (RIGHT ARROW) ASPARTIC ACID |
17.5 |
58.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1l17 |
HYDROPHOBIC STABILIZATION IN T4 LYSOZYME DETERMINED DIRECTLY BY MULTIPLE SUBSTITUTIONS OF ILE 3 |
17.5 |
57.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1l18 |
HYDROPHOBIC STABILIZATION IN T4 LYSOZYME DETERMINED DIRECTLY BY MULTIPLE SUBSTITUTIONS OF ILE 3 |
17.5 |
57.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1l19 |
ENHANCED PROTEIN THERMOSTABILITY FROM DESIGNED MUTATIONS THAT INTERACT WITH ALPHA-HELIX DIPOLES |
17.6 |
58.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1l1c |
Structure of the LicT Bacterial Antiterminator Protein in Complex with its RNA Target |
18.1 |
61.6 |
SOLUTION NMR |
GOOD
|
| 1l1d |
Crystal structure of the C-terminal methionine sulfoxide reductase domain (MsrB) of N. gonorrhoeae pilB |
23.2 |
85.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1l1e |
Crystal Structure of Mycolic Acid Cyclopropane Synthase PcaA Complexed with S-adenosyl-L-homocysteine |
25.9 |
89.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1l1f |
Structure of human glutamate dehydrogenase-apo form |
43.8 |
137.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l1g |
The Structure of Porcine Pancreatic Elastase Complexed with Xenon and Bromide, Cryoprotected with Glycerol |
17.7 |
54.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1l1h |
Crystal Structure of the Quadruplex DNA-Drug Complex |
11.4 |
36.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l1i |
Solution Structure of the Tenebrio molitor Antifreeze Protein |
12.2 |
49.9 |
SOLUTION NMR |
REASONABLE
|
| 1l1j |
Crystal structure of the protease domain of an ATP-independent heat shock protease HtrA |
29.7 |
95.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1l1k |
NMR Identification and Characterization of the Flexible Regions in the 160 KD Molten Globule-like Aggregate of Barstar at Low pH |
20.1 |
68.1 |
SOLUTION NMR |
REASONABLE
|
| 1l1l |
CRYSTAL STRUCTURE OF B-12 DEPENDENT (CLASS II) RIBONUCLEOTIDE REDUCTASE |
54.4 |
180.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1l1m |
SOLUTION STRUCTURE OF A DIMER OF LAC REPRESSOR DNA-BINDING DOMAIN COMPLEXED TO ITS NATURAL OPERATOR O1 |
21.4 |
72.6 |
SOLUTION NMR |
GOOD
|
| 1l1n |
POLIOVIRUS 3C PROTEINASE |
23.4 |
79.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1l1o |
Structure of the human Replication Protein A (RPA) trimerization core |
34.8 |
115.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1l1p |
Solution Structure of the PPIase Domain from E. coli Trigger Factor |
14.7 |
49.0 |
SOLUTION NMR |
GOOD
|
| 1l1q |
Crystal Structure of APRTase from Giardia lamblia Complexed with 9-deazaadenine |
16.9 |
54.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1l1r |
Crystal Structure of APRTase from Giardia lamblia Complexed with 9-deazaadenine, Mg2+ and PRPP |
16.8 |
54.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1l1s |
Structure of Protein of Unknown Function MTH1491 from Methanobacterium thermoautotrophicum |
14.8 |
53.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1l1t |
MutM (Fpg) Bound to Abasic-Site Containing DNA |
21.2 |
66.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l1v |
UNUSUAL ACTD/DNA_TA COMPLEX STRUCTURE |
8.5 |
33.1 |
SOLUTION NMR |
GOOD
|
| 1l1w |
NMR structure of a SRP19 binding domain in human SRP RNA |
14.8 |
39.3 |
SOLUTION NMR |
REASONABLE
|
| 1l1y |
;The Crystal Structure and Catalytic Mechanism of Cellobiohydrolase CelS, the Major Enzymatic Component of the Clostridium thermocellum cellulosome
; |
49.4 |
156.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l1z |
MutM (Fpg) Covalent-DNA Intermediate |
21.2 |
67.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l20 |
ENHANCED PROTEIN THERMOSTABILITY FROM DESIGNED MUTATIONS THAT INTERACT WITH ALPHA-HELIX DIPOLES |
17.5 |
58.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l21 |
CONTRIBUTIONS OF LEFT-HANDED HELICAL RESIDUES TO THE STRUCTURE AND STABILITY OF BACTERIOPHAGE T4 LYSOZYME |
17.5 |
57.0 |
X-RAY DIFFRACTION |
GOOD
|