| 1o7n |
NAPHTHALENE 1,2-DIOXYGENASE, TERNARY COMPLEX WITH DIOXYGEN AND INDOLE |
27.2 |
84.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1o7o |
Roles of Individual Residues of Alpha-1,3 Galactosyltransferases in Substrate Binding and Catalysis |
28.6 |
93.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1o7p |
NAPHTHALENE 1,2-DIOXYGENASE, PRODUCT COMPLEX |
27.2 |
84.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1o7q |
Roles of Individual Residues of Alpha-1,3 Galactosyltransferases in Substrate Binding and Catalysis |
29.0 |
95.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1o7s |
High resolution structure of Siglec-7 |
15.1 |
56.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1o7t |
Metal nanoclusters bound to the Ferric Binding Protein from Neisseria gonorrhoeae. |
58.8 |
185.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1o7u |
Radiation induced tryparedoxin-I |
15.7 |
47.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1o7v |
High resolution structure of Siglec-7 |
16.4 |
54.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1o7w |
NAPHTHALENE 1,2-DIOXYGENASE, FULLY REDUCED FORM |
27.2 |
83.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1o7x |
Citrate synthase from Sulfolobus solfataricus |
47.9 |
143.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1o7y |
Crystal structure of IP-10 M-form |
19.6 |
59.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1o7z |
Crystal structure of IP-10 T-form |
15.7 |
47.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1o80 |
Crystal structure of IP-10 H-Form |
16.4 |
50.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1o81 |
Tryparedoxin II from C.fasciculata solved by sulphur phasing |
21.4 |
69.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1o82 |
X-RAY STRUCTURE OF BACTERIOCIN AS-48 AT PH 4.5. SULPHATE BOUND FORM |
24.7 |
88.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1o83 |
Crystal Structure of Bacteriocin AS-48 at pH 7.5, phosphate bound. Crystal form I |
24.4 |
85.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1o84 |
Crystal Structure of Bacteriocin AS-48. N-decyl-beta-D-maltoside Bound. |
16.3 |
53.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1o85 |
Radiation-reduced Tryparedoxin-I |
15.8 |
48.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1o86 |
Crystal Structure of Human Angiotensin Converting Enzyme in complex with lisinopril. |
24.7 |
79.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1o87 |
A new MgGDP complex of the Ffh NG domain |
30.5 |
106.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1o88 |
Pectate Lyase C From Erwinia Chrysanthemi at pH 11.2 with 30mM Ca2+ |
20.4 |
70.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1o89 |
Crystal structure of E. COLI K-12 yhdH |
21.3 |
67.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1o8a |
Crystal Structure of Human Angiotensin Converting Enzyme (Native). |
24.9 |
78.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1o8b |
Structure of Escherichia coli ribose-5-phosphate isomerase, RpiA, complexed with arabinose-5-phosphate. |
22.8 |
83.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1o8c |
CRYSTAL STRUCTURE OF E. COLI K-12 YHDH WITH BOUND NADPH |
45.7 |
140.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1o8d |
Pectate Lyase C from Erwinia Chrysanthemi at pH 11.2 with 5mM CA2+ |
20.4 |
70.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1o8e |
Pectate Lyase C from Erwinia Chrysanthemi at pH 11.2 with 1mM Ca2+ |
20.3 |
70.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1o8f |
Pectate Lyase C from Erwinia Chrysanthemi at pH 9.5 with 30mM Ca2+ |
20.4 |
75.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1o8g |
Pectate Lyase C from Erwinia Chrysanthemi at pH 9.5 with 5mM Ca2+ |
20.4 |
69.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1o8h |
Pectate Lyase C from Erwinia Chrysanthemi at pH 9.5 with 0.3mM Ca2+ Added |
20.3 |
69.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1o8i |
Pectate Lyase C from Erwinia Chrysanthemi at pH 9.5 with no Ca2+ Added |
20.5 |
70.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1o8j |
Pectate Lyase C from Erwinia Chrysanthemi at pH 4.5 with 30mM CA2+ |
20.4 |
82.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1o8k |
Pectate Lyase C from Erwinia Chrysanthemi at pH 4.5 with 20mM CA2+ |
20.4 |
70.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1o8l |
Pectate Lyase C from Erwinia Chrysanthemi at pH 4.5 with 5mM CA2+ |
20.5 |
70.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1o8m |
Pectate Lyase C from Erwinia Chrysanthemi at pH 4.5 with no Ca2+ Added |
20.4 |
71.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1o8n |
The active site of the molybdenum cofactor biosynthetic protein domain Cnx1G |
23.9 |
74.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1o8o |
The active site of the molybdenum cofactor biosynthetic protein domain Cnx1G |
23.8 |
75.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1o8p |
Unbound structure of CsCBM6-3 from Clostridium stercorarium |
14.9 |
48.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1o8q |
The active site of the molybdenum cofactor biosenthetic protein domain Cnx1G |
37.9 |
120.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1o8r |
Solution structure of human proguanylin |
12.8 |
39.2 |
SOLUTION NMR |
GOOD
|
| 1o8s |
Structure of CsCBM6-3 from Clostridium stercorarium in complex with cellobiose |
15.1 |
48.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1o8t |
;Global Structure and Dynamics of Human Apolipoprotein CII in Complex with Micelles: Evidence for increased mobility of the helix involved in the activation of lipoprotein lipase
; |
20.5 |
70.7 |
SOLUTION NMR |
REASONABLE
|
| 1o8u |
The 2 Angstrom Structure of 6-Oxo Camphor Hydrolase: New Structural Diversity in the Crotonase Superfamily |
31.9 |
91.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1o8v |
The crystal structure of Echinococcus granulosus fatty-acid-binding protein 1 |
15.4 |
48.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1o8w |
Radiation-reduced Tryparedoxin-I |
15.8 |
48.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1o8x |
Mutant tryparedoxin-I Cys43Ala |
15.8 |
48.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1o8y |
Solution structure of SFTI-1(6,5), an acyclic permutant of the proteinase inhibitor SFTI-1, trans-trans-trans conformer (tt-A) |
7.0 |
29.8 |
SOLUTION NMR |
REASONABLE
|
| 1o8z |
Solution structure of SFTI-1(6,5), an acyclic permutant of the proteinase inhibitor SFTI-1, cis-trans-trans conformer (ct-A) |
6.2 |
17.5 |
SOLUTION NMR |
REASONABLE
|
| 1o90 |
Methionine Adenosyltransferase complexed with a L-methionine analogue |
25.8 |
78.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1o91 |
Crystal Structure of a Collagen VIII NC1 Domain Trimer |
20.2 |
59.2 |
X-RAY DIFFRACTION |
EXCELLENT
|