| 2lix |
Solution structure Analysis of the ImKTx104 |
7.7 |
30.5 |
SOLUTION NMR |
REASONABLE
|
| 2liy |
Plant peptide hormone regulating stomatal density |
12.9 |
46.3 |
SOLUTION NMR |
GOOD
|
| 2liz |
NMR solution structure of C-terminal domain of SARS-CoV main protease in 2.5M urea |
15.5 |
58.7 |
SOLUTION NMR |
REASONABLE
|
| 2lj0 |
The third SH3 domain of R85FL |
11.3 |
39.0 |
SOLUTION NMR |
GOOD
|
| 2lj1 |
The third SH3 domain of R85FL with ataxin-7 PRR |
12.0 |
44.2 |
SOLUTION NMR |
REASONABLE
|
| 2lj2 |
Integral membrane core domain of the mercury transporter MerF in lipid bilayer membranes |
14.9 |
55.1 |
SOLID-STATE NMR |
REASONABLE
|
| 2lj3 |
PFBD: High-throughput Strategy of Backbone fold Determination for small well-folded proteins in less than a day |
12.0 |
42.2 |
SOLUTION NMR |
GOOD
|
| 2lj4 |
Solution structure of the TbPIN1 |
13.8 |
51.5 |
SOLUTION NMR |
GOOD
|
| 2lj5 |
Description of the Structural fluctuations of proteins from structure-based calculations of Residual dipolar couplings |
12.2 |
39.9 |
SOLUTION NMR |
GOOD
|
| 2lj6 |
Solution Structure and DNA-binding Properties of the Phosphoesterase Domain of DNA Ligase D |
14.8 |
54.0 |
SOLUTION NMR |
REASONABLE
|
| 2lj7 |
3D solution structure of plant defensin Lc-def |
9.7 |
34.1 |
SOLUTION NMR |
GOOD
|
| 2lj8 |
Solution structure of ADF/Cofilin from trypanosoma brucei |
15.5 |
52.1 |
SOLUTION NMR |
GOOD
|
| 2lj9 |
Partial 3d structure of the c-terminal part of the free arabidopsis thaliana cp12-2 in its oxidized form |
8.5 |
31.4 |
SOLUTION NMR |
GOOD
|
| 2lja |
Solution Structure of a putative thiol-disulfide oxidoreductase from Bacteroides vulgatus |
16.5 |
65.1 |
SOLUTION NMR |
REASONABLE
|
| 2ljb |
Structure of the influenza AM2-BM2 chimeric channel |
16.1 |
60.1 |
SOLUTION NMR |
REASONABLE
|
| 2ljc |
Structure of the influenza AM2-BM2 chimeric channel bound to rimantadine |
15.7 |
57.3 |
SOLUTION NMR |
REASONABLE
|
| 2ljd |
monophosphorylated (747pY) beta3 integrin cytoplasmic tail under membrane mimetic conditions |
10.5 |
34.8 |
SOLUTION NMR |
GOOD
|
| 2lje |
Biphosphorylated (747pY, 759pY) beta3 integrin cytoplasmic tail under membrane mimetic conditions |
11.5 |
42.3 |
SOLUTION NMR |
GOOD
|
| 2ljf |
Monophosphorylated (747pY) beta3 integrin cytoplasmic tail under aqueous conditions |
10.4 |
41.6 |
SOLUTION NMR |
GOOD
|
| 2ljh |
NMR structure of Double-stranded RNA-specific editase Adar |
15.0 |
37.9 |
SOLUTION NMR |
REASONABLE
|
| 2lji |
Structure of a protein from Haloferax volcanii |
12.5 |
36.6 |
SOLUTION NMR |
REASONABLE
|
| 2ljj |
The structure of subdomain IV-B from the CVB-3 IRES |
14.7 |
49.9 |
SOLUTION NMR |
GOOD
|
| 2ljk |
Solution structure of the oncogenic-potential MIEN1 protein |
17.1 |
44.0 |
SOLUTION NMR |
REASONABLE
|
| 2ljl |
NMR structure of Hsp12 in the presence of DPC |
54.4 |
265.1 |
SOLUTION NMR |
REASONABLE
|
| 2ljm |
Solution Structure of CssII |
16.4 |
45.2 |
SOLUTION NMR |
REASONABLE
|
| 2ljp |
Backbone 1H, 13C, and 15N Chemical Shift Assignments for E.coli Ribonuclease P protein |
16.1 |
59.4 |
SOLUTION NMR |
GOOD
|
| 2ljq |
(C9S, C14S)-leucocin A |
11.4 |
41.1 |
SOLUTION NMR |
GOOD
|
| 2ljr |
GLUTATHIONE TRANSFERASE APO-FORM FROM HUMAN |
23.0 |
74.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2ljs |
Solution structure of MCoTI-V |
7.8 |
30.2 |
SOLUTION NMR |
GOOD
|
| 2ljt |
C9L,C14L-LeuA |
13.5 |
54.1 |
SOLUTION NMR |
REASONABLE
|
| 2lju |
;Solution structure of putative oxidoreductase from Ehrlichia chaffeensis, Seattle Structural Genomics Center for Infectious Disease (SSGCID)
; |
23.0 |
63.8 |
SOLUTION NMR |
REASONABLE
|
| 2ljv |
Solution structure of Rhodostomin G50L mutant |
13.8 |
52.2 |
SOLUTION NMR |
GOOD
|
| 2ljw |
Solution NMR structure of Alr2454 protein from Nostoc sp. strain PCC 7120, Northeast Structural Genomics Consortium Target NsR264 |
14.6 |
56.3 |
SOLUTION NMR |
GOOD
|
| 2ljx |
Structure of the monomeric N-terminal domain of HPV16 E6 oncoprotein |
12.7 |
53.0 |
SOLUTION NMR |
REASONABLE
|
| 2ljy |
Haddock model structure of the N-terminal domain dimer of HPV16 E6 |
18.6 |
64.7 |
SOLUTION NMR |
GOOD
|
| 2ljz |
Structure of the C-terminal domain of HPV16 E6 oncoprotein |
11.8 |
40.1 |
SOLUTION NMR |
GOOD
|
| 2lk0 |
Solution structure and binding studies of the RanBP2-type zinc finger of RBM5 |
8.1 |
30.2 |
SOLUTION NMR |
GOOD
|
| 2lk1 |
Solution structure and binding studies of the RanBP2-type zinc finger of RBM5 |
8.3 |
29.5 |
SOLUTION NMR |
GOOD
|
| 2lk2 |
;Solution NMR structure of homeobox domain (171-248) of human homeobox protein TGIF1, Northeast Structural Genomics Consortium Target HR4411B
; |
15.6 |
42.1 |
SOLUTION NMR |
REASONABLE
|
| 2lk3 |
U2/U6 Helix I |
12.5 |
41.3 |
SOLUTION NMR |
GOOD
|
| 2lk4 |
Structural and mechanistic insights into the interaction between PAT Pyk2 and Paxillin LD motif |
17.7 |
66.5 |
SOLUTION NMR |
REASONABLE
|
| 2lk5 |
Solution structure of the Zn(II) form of Desulforedoxin |
10.6 |
30.1 |
SOLUTION NMR |
EXCELLENT
|
| 2lk6 |
NMR determination of the global structure of the Cd-113 derivative of desulforedoxin |
10.6 |
31.9 |
SOLUTION NMR |
GOOD
|
| 2lk7 |
;Monomer-dimer equilibrium for 5'-5' stacking of propeller-type parallel-stranded G-quadruplexes: NMR structural study
; |
10.6 |
41.1 |
SOLUTION NMR |
GOOD
|
| 2lk9 |
Structure of BST-2/Tetherin Transmembrane Domain |
11.7 |
45.8 |
SOLUTION NMR |
REASONABLE
|
| 2lkb |
Evolutionary diversification of Mesobuthus alpha-scorpion toxins affecting sodium channels |
11.0 |
37.5 |
SOLUTION NMR |
GOOD
|
| 2lkc |
Free B.st IF2-G2 |
16.4 |
54.3 |
SOLUTION NMR |
REASONABLE
|
| 2lkd |
IF2-G2 GDP complex |
16.4 |
54.6 |
SOLUTION NMR |
GOOD
|
| 2lke |
Structures and Interaction Analyses of the Integrin Alpha-M Beta-2 Cytoplasmic Tails |
8.0 |
30.5 |
SOLUTION NMR |
GOOD
|
| 2lkf |
LEUKOCIDIN F (HLGB) FROM STAPHYLOCOCCUS AUREUS |
23.0 |
82.8 |
X-RAY DIFFRACTION |
GOOD
|