| 1l51 |
STRUCTURAL AND THERMODYNAMIC ANALYSIS OF THE PACKING OF TWO ALPHA-HELICES IN BACTERIOPHAGE T4 LYSOZYME |
17.5 |
57.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l52 |
STRUCTURAL AND THERMODYNAMIC ANALYSIS OF THE PACKING OF TWO ALPHA-HELICES IN BACTERIOPHAGE T4 LYSOZYME |
17.5 |
58.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1l53 |
STRUCTURAL AND THERMODYNAMIC ANALYSIS OF THE PACKING OF TWO ALPHA-HELICES IN BACTERIOPHAGE T4 LYSOZYME |
17.4 |
57.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l54 |
THE STRUCTURAL AND THERMODYNAMIC CONSEQUENCES OF BURYING A CHARGED RESIDUE WITHIN THE HYDROPHOBIC CORE OF T4 LYSOZYME |
17.5 |
60.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l55 |
;ANALYSIS OF THE INTERACTION BETWEEN CHARGED SIDE CHAINS AND THE ALPHA-HELIX DIPOLE USING DESIGNED THERMOSTABLE MUTANTS OF PHAGE T4 LYSOZYME
; |
17.4 |
58.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1l56 |
;ANALYSIS OF THE INTERACTION BETWEEN CHARGED SIDE CHAINS AND THE ALPHA-HELIX DIPOLE USING DESIGNED THERMOSTABLE MUTANTS OF PHAGE T4 LYSOZYME
; |
17.5 |
60.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l57 |
;ANALYSIS OF THE INTERACTION BETWEEN CHARGED SIDE CHAINS AND THE ALPHA-HELIX DIPOLE USING DESIGNED THERMOSTABLE MUTANTS OF PHAGE T4 LYSOZYME
; |
17.5 |
58.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1l58 |
;ANALYSIS OF THE INTERACTION BETWEEN CHARGED SIDE CHAINS AND THE ALPHA-HELIX DIPOLE USING DESIGNED THERMOSTABLE MUTANTS OF PHAGE T4 LYSOZYME
; |
17.5 |
57.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1l59 |
;ANALYSIS OF THE INTERACTION BETWEEN CHARGED SIDE CHAINS AND THE ALPHA-HELIX DIPOLE USING DESIGNED THERMOSTABLE MUTANTS OF PHAGE T4 LYSOZYME
; |
17.5 |
59.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1l5a |
Crystal Structure of VibH, an NRPS Condensation Enzyme |
37.5 |
113.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l5b |
DOMAIN-SWAPPED CYANOVIRIN-N DIMER |
19.0 |
56.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l5c |
Solution Structure of the Monomeric Form of a Mutant Unliganded Bovine Neurophysin, 20 Structures |
12.1 |
41.4 |
SOLUTION NMR |
GOOD
|
| 1l5d |
Solution Structure of the Monomeric Form of a Mutant Unliganded Bovine Neurophysin, Minimized Average Structure |
13.3 |
48.3 |
SOLUTION NMR |
GOOD
|
| 1l5e |
The domain-swapped dimer of CV-N in solution |
19.4 |
77.3 |
SOLUTION NMR |
REASONABLE
|
| 1l5f |
Crystal Structure of CobT complexed with benzimidazole |
20.9 |
75.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l5g |
CRYSTAL STRUCTURE OF THE EXTRACELLULAR SEGMENT OF INTEGRIN AVB3 IN COMPLEX WITH AN ARG-GLY-ASP LIGAND |
40.1 |
129.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1l5h |
FeMo-cofactor Deficient Nitrogenase MoFe Protein |
29.6 |
92.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l5i |
;30-CONFORMER NMR ENSEMBLE OF THE N-TERMINAL, DNA-BINDING DOMAIN OF THE REPLICATION INITIATION PROTEIN FROM A GEMINIVIRUS (TOMATO YELLOW LEAF CURL VIRUS-SARDINIA)
; |
14.9 |
53.5 |
SOLUTION NMR |
GOOD
|
| 1l5j |
CRYSTAL STRUCTURE OF E. COLI ACONITASE B. |
39.8 |
135.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l5k |
;Crystal Structure of CobT complexed with N1-(5'-phosphoribosyl)-benzimidazole and nicotinate
; |
20.8 |
73.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l5l |
;Crystal Structure of CobT complexed with N7-(5'-phosphoribosyl)purine and nicotinate
; |
20.9 |
76.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1l5m |
;Crystal Structure of CobT complexed with N7-(5'-phosphoribosyl)-2-aminopurine and nicotinate
; |
20.6 |
73.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1l5n |
Crystal Structure of CobT complexed with imidazole |
21.0 |
75.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1l5o |
Crystal Structure of CobT complexed with 3,4-dimethylphenol and nicotinate mononucleotide |
20.9 |
74.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l5p |
Crystal Structure of Trichomonas vaginalis Ferredoxin |
24.1 |
73.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l5q |
Human liver glycogen phosphorylase a complexed with caffeine, N-Acetyl-beta-D-glucopyranosylamine, and CP-403700 |
38.3 |
126.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1l5r |
Human liver glycogen phosphorylase a complexed with riboflavin, N-Acetyl-beta-D-Glucopyranosylamine and CP-403,700 |
38.3 |
126.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1l5s |
Human liver glycogen phosphorylase complexed with uric acid, N-Acetyl-beta-D-glucopyranosylamine, and CP-403,700 |
38.1 |
126.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1l5t |
;Crystal Structure of a Domain-Opened Mutant (R121D) of the Human Lactoferrin N-lobe Refined From a Merohedrally-Twinned Crystal Form.
; |
57.6 |
159.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l5u |
;Crystal Structure of Bacillus DNA Polymerase I Fragment product complex with 12 base pairs of duplex DNA following addition of a dTTP, a dATP, and a dCTP residue.
; |
27.3 |
85.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1l5v |
Crystal Structure of the Maltodextrin Phosphorylase complexed with Glucose-1-phosphate |
38.9 |
130.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1l5w |
;Crystal Structure of the Maltodextrin Phosphorylase Complexed with the Products of the Enzymatic Reaction between Glucose-1-phosphate and Maltotetraose
; |
38.7 |
129.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1l5x |
The 2.0-Angstrom resolution crystal structure of a survival protein E (SurE) homolog from Pyrobaculum aerophilum |
25.4 |
95.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1l5y |
CRYSTAL STRUCTURE OF MG2+ / BEF3-BOUND RECEIVER DOMAIN OF SINORHIZOBIUM MELILOTI DCTD |
24.9 |
82.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1l5z |
CRYSTAL STRUCTURE OF THE E121K SUBSTITUTION OF THE RECEIVER DOMAIN OF SINORHIZOBIUM MELILOTI DCTD |
17.6 |
68.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l60 |
;ANALYSIS OF THE INTERACTION BETWEEN CHARGED SIDE CHAINS AND THE ALPHA-HELIX DIPOLE USING DESIGNED THERMOSTABLE MUTANTS OF PHAGE T4 LYSOZYME
; |
17.5 |
58.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1l61 |
;ANALYSIS OF THE INTERACTION BETWEEN CHARGED SIDE CHAINS AND THE ALPHA-HELIX DIPOLE USING DESIGNED THERMOSTABLE MUTANTS OF PHAGE T4 LYSOZYME
; |
17.5 |
58.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1l62 |
;ANALYSIS OF THE INTERACTION BETWEEN CHARGED SIDE CHAINS AND THE ALPHA-HELIX DIPOLE USING DESIGNED THERMOSTABLE MUTANTS OF PHAGE T4 LYSOZYME
; |
17.5 |
57.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l63 |
;ANALYSIS OF THE INTERACTION BETWEEN CHARGED SIDE CHAINS AND THE ALPHA-HELIX DIPOLE USING DESIGNED THERMOSTABLE MUTANTS OF PHAGE T4 LYSOZYME
; |
17.4 |
58.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1l64 |
;TOLERANCE OF T4 LYSOZYME TO MULTIPLE XAA (RIGHT ARROW) ALA SUBSTITUTIONS: A POLYALANINE ALPHA-HELIX CONTAINING TEN CONSECUTIVE ALANINES
; |
17.2 |
60.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l65 |
;TOLERANCE OF T4 LYSOZYME TO MULTIPLE XAA (RIGHT ARROW) ALA SUBSTITUTIONS: A POLYALANINE ALPHA-HELIX CONTAINING TEN CONSECUTIVE ALANINES
; |
17.4 |
58.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1l66 |
;TOLERANCE OF T4 LYSOZYME TO MULTIPLE XAA (RIGHT ARROW) ALA SUBSTITUTIONS: A POLYALANINE ALPHA-HELIX CONTAINING TEN CONSECUTIVE ALANINES
; |
17.4 |
58.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l67 |
;TOLERANCE OF T4 LYSOZYME TO MULTIPLE XAA (RIGHT ARROW) ALA SUBSTITUTIONS: A POLYALANINE ALPHA-HELIX CONTAINING TEN CONSECUTIVE ALANINES
; |
17.4 |
58.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1l68 |
;TOLERANCE OF T4 LYSOZYME TO MULTIPLE XAA (RIGHT ARROW) ALA SUBSTITUTIONS: A POLYALANINE ALPHA-HELIX CONTAINING TEN CONSECUTIVE ALANINES
; |
17.4 |
61.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1l69 |
;MULTIPLE STABILIZING ALANINE REPLACEMENTS WITHIN ALPHA-HELIX 126-134 OF T4 LYSOZYME HAVE INDEPENDENT, ADDITIVE EFFECTS ON BOTH STRUCTURE AND STABILITY
; |
17.5 |
58.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1l6b |
CRYSTAL STRUCTURE ANALYSIS OF THE ALL DNA HOLLIDAY JUNCTION STRUCTURE OF CCGGTACM5CGG |
13.4 |
43.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l6e |
;Solution structure of the docking and dimerization domain of protein kinase A II-alpha (RIIalpha D/D). Alternatively called the N-terminal dimerization domain of the regulatory subunit of protein kinase A.
; |
15.3 |
61.2 |
SOLUTION NMR |
GOOD
|
| 1l6f |
;Alanine racemase bound with N-(5'-phosphopyridoxyl)-L-alanine
; |
28.4 |
92.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l6g |
;Alanine racemase bound with N-(5'-phosphopyridoxyl)-D-alanine
; |
28.3 |
89.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l6h |
Solution Structure of Plant nsLTP2 purified from Rice (oryza Sativa) |
11.9 |
37.5 |
SOLUTION NMR |
GOOD
|