| 1l6i |
;Crystal Structure of the Maltodextrin Phosphorylase complexed with the products of the enzymatic reaction between glucose-1-phosphate and maltopentaose
; |
39.0 |
130.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1l6j |
Crystal structure of human matrix metalloproteinase MMP9 (gelatinase B). |
24.6 |
78.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l6m |
;Neutrophil Gelatinase-associated Lipocalin is a Novel Bacteriostatic Agent that Interferes with Siderophore-mediated Iron Acquisition
; |
30.3 |
95.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1l6n |
STRUCTURE OF THE N-TERMINAL 283-RESIDUE FRAGMENT OF THE HIV-1 GAG POLYPROTEIN |
52.5 |
204.2 |
SOLUTION NMR |
REASONABLE
|
| 1l6o |
XENOPUS DISHEVELLED PDZ DOMAIN |
21.9 |
77.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l6p |
N-terminal of DsbD (residues 20-144) from E. coli. |
16.7 |
62.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1l6r |
Crystal Structure of Thermoplasma acidophilum 0175 (APC0014) |
23.6 |
71.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l6s |
Crystal Structure of Porphobilinogen Synthase Complexed with the Inhibitor 4,7-Dioxosebacic Acid |
27.2 |
84.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1l6t |
STRUCTURE OF ALA24/ASP61 TO ASP24/ASN61 SUBSTITUTED SUBUNIT C OF ESCHERICHIA COLI ATP SYNTHASE |
18.3 |
50.0 |
SOLUTION NMR |
REASONABLE
|
| 1l6u |
NMR STRUCTURE OF OXIDIZED ADRENODOXIN |
13.7 |
48.8 |
SOLUTION NMR |
REASONABLE
|
| 1l6v |
STRUCTURE OF REDUCED BOVINE ADRENODOXIN |
13.2 |
42.9 |
SOLUTION NMR |
GOOD
|
| 1l6w |
Fructose-6-phosphate aldolase |
39.9 |
116.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1l6x |
FC FRAGMENT OF RITUXIMAB BOUND TO A MINIMIZED VERSION OF THE B-DOMAIN FROM PROTEIN A CALLED Z34C |
22.6 |
72.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l6y |
Crystal Structure of Porphobilinogen Synthase Complexed with the Inhibitor 4-Oxosebacic Acid |
27.3 |
86.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l6z |
CRYSTAL STRUCTURE OF MURINE CEACAM1A[1,4]: A CORONAVIRUS RECEPTOR AND CELL ADHESION MOLECULE IN THE CEA FAMILY |
26.1 |
94.0 |
X-RAY DIFFRACTION |
SUSPICIOUS
|
| 1l70 |
;MULTIPLE STABILIZING ALANINE REPLACEMENTS WITHIN ALPHA-HELIX 126-134 OF T4 LYSOZYME HAVE INDEPENDENT, ADDITIVE EFFECTS ON BOTH STRUCTURE AND STABILITY
; |
17.4 |
59.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l71 |
;MULTIPLE STABILIZING ALANINE REPLACEMENTS WITHIN ALPHA-HELIX 126-134 OF T4 LYSOZYME HAVE INDEPENDENT, ADDITIVE EFFECTS ON BOTH STRUCTURE AND STABILITY
; |
17.4 |
60.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1l72 |
;MULTIPLE STABILIZING ALANINE REPLACEMENTS WITHIN ALPHA-HELIX 126-134 OF T4 LYSOZYME HAVE INDEPENDENT, ADDITIVE EFFECTS ON BOTH STRUCTURE AND STABILITY
; |
17.4 |
59.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1l73 |
;MULTIPLE STABILIZING ALANINE REPLACEMENTS WITHIN ALPHA-HELIX 126-134 OF T4 LYSOZYME HAVE INDEPENDENT, ADDITIVE EFFECTS ON BOTH STRUCTURE AND STABILITY
; |
17.4 |
58.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1l74 |
;MULTIPLE STABILIZING ALANINE REPLACEMENTS WITHIN ALPHA-HELIX 126-134 OF T4 LYSOZYME HAVE INDEPENDENT, ADDITIVE EFFECTS ON BOTH STRUCTURE AND STABILITY
; |
17.4 |
57.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1l75 |
;MULTIPLE STABILIZING ALANINE REPLACEMENTS WITHIN ALPHA-HELIX 126-134 OF T4 LYSOZYME HAVE INDEPENDENT, ADDITIVE EFFECTS ON BOTH STRUCTURE AND STABILITY
; |
17.3 |
58.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1l76 |
;TOLERANCE OF T4 LYSOZYME TO PROLINE SUBSTITUTIONS WITHIN THE LONG INTERDOMAIN ALPHA-HELIX ILLUSTRATES THE ADAPTABILITY OF PROTEINS TO POTENTIALLY DESTABILIZING LESIONS
; |
17.4 |
58.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1l77 |
DESIGN AND STRUCTURAL ANALYSIS OF ALTERNATIVE HYDROPHOBIC CORE PACKING ARRANGEMENTS IN BACTERIOPHAGE T4 LYSOZYME |
17.5 |
60.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1l79 |
DESIGN AND STRUCTURAL ANALYSIS OF ALTERNATIVE HYDROPHOBIC CORE PACKING ARRANGEMENTS IN BACTERIOPHAGE T4 LYSOZYME |
17.4 |
58.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1l7a |
structural Genomics, crystal structure of Cephalosporin C deacetylase |
27.8 |
88.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l7b |
Solution NMR Structure of BRCT Domain of T. Thermophilus: Northeast Structural Genomics Consortium Target WR64TT |
14.1 |
52.2 |
SOLUTION NMR |
GOOD
|
| 1l7c |
alpha-catenin fragment, residues 385-651 |
30.1 |
98.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1l7d |
Crystal Structure of R. rubrum Transhydrogenase Domain I without Bound NAD(H) |
41.6 |
134.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1l7e |
Crystal Structure of R. rubrum Transhydrogenase Domain I with Bound NADH |
41.6 |
128.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1l7f |
Crystal structure of influenza virus neuraminidase in complex with BCX-1812 |
21.3 |
77.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l7g |
Crystal structure of E119G mutant influenza virus neuraminidase in complex with BCX-1812 |
21.3 |
77.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1l7h |
Crystal structure of R292K mutant influenza virus neuraminidase in complex with BCX-1812 |
21.3 |
80.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l7i |
Crystal Structure of the anti-ErbB2 Fab2C4 |
25.1 |
77.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l7j |
X-ray structure of galactose mutarotase from Lactococcus lactis (apo) |
28.9 |
93.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l7k |
x-ray structure of galactose mutarotase from Lactococcus lactis complexed with galactose |
29.4 |
95.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1l7l |
Crystal structure of Pseudomonas aeruginosa lectin 1 determined by single wavelength anomalous scattering phasing method |
15.2 |
50.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l7m |
HIGH RESOLUTION LIGANDED STRUCTURE OF PHOSPHOSERINE PHOSPHATASE (PI COMPLEX) |
27.5 |
94.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l7n |
TRANSITION STATE ANALOGUE OF PHOSPHOSERINE PHOSPHATASE (ALUMINUM FLUORIDE COMPLEX) |
27.5 |
94.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1l7o |
CRYSTAL STRUCTURE OF PHOSPHOSERINE PHOSPHATASE IN APO FORM |
26.6 |
90.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l7p |
SUBSTRATE BOUND PHOSPHOSERINE PHOSPHATASE COMPLEX STRUCTURE |
27.5 |
92.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1l7q |
Ser117Ala Mutant of Bacterial Cocaine Esterase cocE |
25.1 |
80.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1l7r |
Tyr44Phe Mutant of Bacterial Cocaine Esterase cocE |
25.2 |
81.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l7t |
Crystal Structure Analysis of the anti-testosterone Fab fragment |
25.7 |
82.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l7v |
Bacterial ABC Transporter Involved in B12 Uptake |
33.2 |
105.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l7x |
Human liver glycogen phosphorylase b complexed with caffeine, N-acetyl-beta-D-glucopyranosylamine, and CP-403,700 |
38.2 |
126.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1l7y |
Solution NMR Structure of C. elegans Protein ZK652.3. NORTHEAST STRUCTURAL GENOMICS CONSORTIUM TARGET WR41. |
13.5 |
36.2 |
SOLUTION NMR |
REASONABLE
|
| 1l7z |
Crystal structure of Ca2+/Calmodulin complexed with myristoylated CAP-23/NAP-22 peptide |
16.8 |
51.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1l80 |
DESIGN AND STRUCTURAL ANALYSIS OF ALTERNATIVE HYDROPHOBIC CORE PACKING ARRANGEMENTS IN BACTERIOPHAGE T4 LYSOZYME |
17.5 |
58.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l81 |
DESIGN AND STRUCTURAL ANALYSIS OF ALTERNATIVE HYDROPHOBIC CORE PACKING ARRANGEMENTS IN BACTERIOPHAGE T4 LYSOZYME |
17.5 |
58.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1l82 |
DESIGN AND STRUCTURAL ANALYSIS OF ALTERNATIVE HYDROPHOBIC CORE PACKING ARRANGEMENTS IN BACTERIOPHAGE T4 LYSOZYME |
17.4 |
60.1 |
X-RAY DIFFRACTION |
REASONABLE
|