| 2lhb |
REFINEMENT OF A MOLECULAR MODEL FOR LAMPREY HEMOGLOBIN FROM PETROMYZON MARINUS |
16.2 |
49.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2lhc |
Ga98 solution structure |
12.5 |
34.3 |
SOLUTION NMR |
REASONABLE
|
| 2lhd |
GB98 solution structure |
11.0 |
37.2 |
SOLUTION NMR |
GOOD
|
| 2lhe |
Gb98-T25I,L20A |
10.8 |
32.5 |
SOLUTION NMR |
GOOD
|
| 2lhf |
Solution structure of outer membrane protein H (OprH) from P. aeruginosa in DHPC micelles |
20.0 |
71.3 |
SOLUTION NMR |
GOOD
|
| 2lhg |
GB98-T25I solution structure |
10.9 |
41.7 |
SOLUTION NMR |
REASONABLE
|
| 2lhh |
Solution structure of Ca2+-bound yCaM |
15.2 |
56.6 |
SOLUTION NMR |
REASONABLE
|
| 2lhi |
Solution structure of Ca2+/CNA1 peptide-bound yCaM |
16.3 |
48.5 |
SOLUTION NMR |
EXCELLENT
|
| 2lhj |
NMR structure of the high mobility group protein-like protein NHP1 from Babesia bovis T2Bo (BaboA.00841.a) |
16.8 |
62.6 |
SOLUTION NMR |
GOOD
|
| 2lhk |
Structural analysis of a chaperone in type III secretion system |
29.6 |
107.7 |
SOLUTION NMR |
REASONABLE
|
| 2lhl |
Chemical Shift Assignments and solution structure of human apo-S100A1 E32Q mutant |
17.7 |
56.5 |
SOLUTION NMR |
GOOD
|
| 2lhm |
CRYSTAL STRUCTURES OF THE APO-AND HOLOMUTANT HUMAN LYSOZYMES WITH AN INTRODUCED CA2+ BINDING SITE |
15.4 |
50.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2lhn |
RNA-binding zinc finger protein |
12.8 |
49.6 |
SOLUTION NMR |
REASONABLE
|
| 2lho |
Solution Structure of a DNA duplex Containing an Unnatural, Hydrophobic Base Pair |
14.0 |
41.9 |
SOLUTION NMR |
GOOD
|
| 2lhp |
High resolution NMR solution structure of helix H1 of the chimpanzee HAR1 RNA |
18.8 |
66.1 |
SOLUTION NMR |
GOOD
|
| 2lhr |
Solution structure of Staphylococcus aureus IsdH linker domain |
18.4 |
49.7 |
SOLUTION NMR |
REASONABLE
|
| 2lhs |
Structure of the chitin binding protein 21 (CBP21) |
15.0 |
40.6 |
SOLUTION NMR |
GOOD
|
| 2lht |
Solution structure of Venturia inaequalis cellophane-induced 1 protein (ViCin1) domains 1 and 2 |
19.2 |
51.9 |
SOLUTION NMR |
REASONABLE
|
| 2lhu |
Structural Insight into the Unique Cardiac Myosin Binding Protein-C Motif: A Partially Folded Domain |
9.3 |
31.1 |
SOLUTION NMR |
GOOD
|
| 2lhv |
Mucin sequence based on MUC2 Mucin glycoprotein tandem repeat |
5.0 |
30.1 |
SOLUTION NMR |
REASONABLE
|
| 2lhw |
Tri-O-GalNAc glycosylated Mucin sequence based on MUC2 Mucin glycoprotein tandem repeat |
6.0 |
22.8 |
SOLUTION NMR |
REASONABLE
|
| 2lhx |
Di-O-GalNAc glycosylated Mucin sequence based on MUC2 Mucin glycoprotein tandem repeat |
5.5 |
19.0 |
SOLUTION NMR |
REASONABLE
|
| 2lhy |
Di-O-GalNAc glycosylated Mucin sequence based on MUC2 Mucin glycoprotein tandem repeat |
5.9 |
16.9 |
SOLUTION NMR |
REASONABLE
|
| 2lhz |
Di-O-GalNAc glycosylated Mucin sequence based on MUC2 Mucin glycoprotein tandem repeat |
5.6 |
15.4 |
SOLUTION NMR |
REASONABLE
|
| 2li0 |
Mono-O-GalNAc glycosylated Mucin sequence based on MUC2 Mucin glycoprotein tandem repeat |
5.1 |
14.6 |
SOLUTION NMR |
REASONABLE
|
| 2li1 |
Mono-O-GalNAc glycosylated Mucin sequence based on MUC2 Mucin glycoprotein tandem repeat |
5.6 |
31.4 |
SOLUTION NMR |
REASONABLE
|
| 2li2 |
Mono-O-GalNAc glycosylated Mucin sequence based on MUC2 Mucin glycoprotein tandem repeat |
5.5 |
26.8 |
SOLUTION NMR |
REASONABLE
|
| 2li3 |
;Structural and functional analysis of a novel potassium toxin argentinean scorpion Tityus trivittatus reveals a new kappa sub-family
; |
7.9 |
30.4 |
SOLUTION NMR |
GOOD
|
| 2li4 |
Solution structure of a shortened antiterminator hairpin from a Mg2+ riboswitch |
19.3 |
69.3 |
SOLUTION NMR |
REASONABLE
|
| 2li5 |
NMR structure of Atg8-Atg7C30 complex |
15.9 |
40.3 |
SOLUTION NMR |
REASONABLE
|
| 2li6 |
1H, 13C, and 15N Chemical Shift Assignments for yeast protein |
15.1 |
51.8 |
SOLUTION NMR |
GOOD
|
| 2li7 |
Solution Structure of CssII |
11.3 |
39.8 |
SOLUTION NMR |
GOOD
|
| 2li8 |
The solution structure of the Lin28-ZnF domains bound to AGGAGAU of pre-let-7 miRNA |
12.7 |
46.3 |
SOLUTION NMR |
GOOD
|
| 2li9 |
Metal binding domain of rat beta-amyloid |
8.5 |
31.7 |
SOLUTION NMR |
GOOD
|
| 2lia |
;Solution NMR structure of a DNA dodecamer containing the 7-aminomethyl-7-deaza-2'-deoxyguanosine adduct
; |
13.7 |
46.5 |
SOLUTION NMR |
GOOD
|
| 2lib |
DNA sequence context conceals alpha anomeric lesion |
12.5 |
40.5 |
SOLUTION NMR |
REASONABLE
|
| 2lic |
NMR Structure of the Polyserine Tract of Apis mellifera Vitellogenin, residues 358-392 |
17.0 |
45.8 |
SOLUTION NMR |
REASONABLE
|
| 2lid |
The polyserine tract of Nasonia vitripennis Vg residues 351-385 |
12.8 |
55.5 |
SOLUTION NMR |
REASONABLE
|
| 2lie |
NMR structure of the lectin CCL2 |
17.4 |
48.1 |
SOLUTION NMR |
REASONABLE
|
| 2lif |
Solution Structure of KKGF |
12.7 |
53.7 |
SOLUTION NMR |
REASONABLE
|
| 2lig |
THREE-DIMENSIONAL STRUCTURES OF THE LIGAND-BINDING DOMAIN OF THE BACTERIAL ASPARTATE RECEPTOR WITH AND WITHOUT A LIGAND |
22.5 |
84.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2lio |
Solution NMR Structure of BfR322 from Bacteroides fragilis, Northeast Structural Genomics Consortium Target BfR322 |
17.0 |
54.0 |
SOLUTION NMR |
GOOD
|
| 2lip |
PSEUDOMONAS LIPASE OPEN CONFORMATION |
19.6 |
64.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2liq |
Solution structure of CCL2 in complex with glycan |
17.4 |
49.0 |
SOLUTION NMR |
REASONABLE
|
| 2lir |
NMR Solution Structure of Yeast Iso-1-cytochrome c Mutant P71H in oxidized states |
13.0 |
40.4 |
SOLUTION NMR |
GOOD
|
| 2lis |
HIGH RESOLUTION STRUCTURE OF THE RED ABALONE LYSIN MONOMER |
17.5 |
68.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2lit |
NMR Solution Structure of Yeast Iso-1-cytochrome c Mutant P71H in reduced states |
13.3 |
41.5 |
SOLUTION NMR |
GOOD
|
| 2liu |
NMR structure of holo-ACPI domain from CurA module from Lyngbya majuscula |
13.7 |
43.1 |
SOLUTION NMR |
GOOD
|
| 2liv |
;PERIPLASMIC BINDING PROTEIN STRUCTURE AND FUNCTION. REFINED X-RAY STRUCTURES OF THE LEUCINE/ISOLEUCINE/VALINE-BINDING PROTEIN AND ITS COMPLEX WITH LEUCINE
; |
22.8 |
74.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2liw |
NMR structure of HMG-ACPI domain from CurA module from Lyngbya majuscula |
14.2 |
47.6 |
SOLUTION NMR |
GOOD
|