| 2k2z |
Solution structure of the folded domain of intermediate IIIb of Tick Carboxypeptidase Inhibitor |
9.1 |
36.7 |
SOLUTION NMR |
GOOD
|
| 2k31 |
Solution Structure of cGMP-binding GAF domain of Phosphodiesterase 5 |
15.4 |
49.4 |
SOLUTION NMR |
REASONABLE
|
| 2k32 |
Truncated AcrA from Campylobacter jejuni for glycosylation studies |
20.0 |
53.5 |
SOLUTION NMR |
REASONABLE
|
| 2k33 |
Solution structure of an N-glycosylated protein using in vitro glycosylation |
19.8 |
81.2 |
SOLUTION NMR |
REASONABLE
|
| 2k35 |
Hydramacin-1: Structure and antibacterial activity of a peptide from the basal metazoan Hydra |
10.0 |
34.3 |
SOLUTION NMR |
REASONABLE
|
| 2k36 |
;Structure ensemble Backbone and side-chain 1H, 13C, and 15N Chemical Shift Assignments, 1H-15N RDCs and 1H-1H nOe restraints for protein K7 from the Vaccinia virus
; |
15.9 |
57.8 |
SOLUTION NMR |
GOOD
|
| 2k37 |
CsmA |
19.6 |
71.3 |
SOLUTION NMR |
GOOD
|
| 2k38 |
Cupiennin 1A, NMR, minimized average structure |
16.5 |
58.0 |
SOLUTION NMR |
REASONABLE
|
| 2k39 |
Recognition dynamics up to microseconds revealed from RDC derived ubiquitin ensemble in solution |
12.3 |
42.3 |
SOLUTION NMR |
GOOD
|
| 2k3a |
;NMR solution structure of Staphylococcus saprophyticus CHAP (cysteine, histidine-dependent amidohydrolases/peptidases) domain protein. Northeast Structural Genomics Consortium target SyR11
; |
25.8 |
51.6 |
SOLUTION NMR |
REASONABLE
|
| 2k3b |
Seeing the Invisible: Structures of Excited Protein States by Relaxation Dispersion NMR |
10.6 |
32.6 |
SOLUTION NMR |
GOOD
|
| 2k3c |
Structural and Functional Characterization of TM IX of the NHE1 Isoform of the Na+/H+ Exchanger |
14.9 |
36.4 |
SOLUTION NMR |
REASONABLE
|
| 2k3d |
;Solution NMR structure of the folded 79 residue fragment of Lin0334 from Listeria innocua. Northeast Structural Genomics Consortium target LkR15
; |
13.9 |
53.5 |
SOLUTION NMR |
GOOD
|
| 2k3f |
Ribosomal protein L11 from Thermotoga maritima |
18.0 |
62.7 |
SOLUTION NMR |
REASONABLE
|
| 2k3g |
NMR structure analysis of a BMP receptor |
17.0 |
45.8 |
SOLUTION NMR |
REASONABLE
|
| 2k3h |
Structural determinants for Ca2+ and PIP2 binding by the C2A domain of rabphilin-3A |
15.8 |
50.3 |
SOLUTION NMR |
GOOD
|
| 2k3i |
Solution NMR structure of protein yiiS from Shigella flexneri. Northeast Structural Genomics Consortium target SfR90 |
19.5 |
54.0 |
SOLUTION NMR |
REASONABLE
|
| 2k3j |
The solution structure of human Mia40 |
12.3 |
37.2 |
SOLUTION NMR |
EXCELLENT
|
| 2k3k |
Solution structure of Drosophila melanogaster SNF RBD1 |
14.4 |
54.5 |
SOLUTION NMR |
GOOD
|
| 2k3m |
Rv1761c |
16.6 |
50.4 |
SOLUTION NMR |
GOOD
|
| 2k3n |
Solution structure of the type 1 repetitive domain (TUSP1-RP1) of the egg case silk from Nephila Antipodiana |
19.7 |
54.6 |
SOLUTION NMR |
REASONABLE
|
| 2k3o |
Solution structure of the type 2 repetitive domain (TUSP1-RP2) of the egg case silk from Nephila Antipodiana |
14.4 |
53.4 |
SOLUTION NMR |
REASONABLE
|
| 2k3p |
Solution structure of the C-terminal domain (TUSP1-C) of the egg case silk from Nephila antipodiana |
21.7 |
60.9 |
SOLUTION NMR |
REASONABLE
|
| 2k3q |
Solution structure of the n-terminal domain (TUSP1-N) of the egg case silk from Nephila antipodiana |
15.9 |
63.4 |
SOLUTION NMR |
REASONABLE
|
| 2k3r |
Pfu Rpp21 structure and assignments |
14.7 |
54.3 |
SOLUTION NMR |
REASONABLE
|
| 2k3s |
HADDOCK-derived structure of the CH-domain of the smoothelin-like 1 complexed with the C-domain of apocalmodulin |
19.0 |
61.5 |
SOLUTION NMR |
GOOD
|
| 2k3t |
Solution Structure of IG-Like Domain 23 from Human Filamin A |
13.6 |
51.5 |
SOLUTION NMR |
GOOD
|
| 2k3u |
Structure of the tyrosine-sulfated C5a receptor N-terminus in complex with the immune evasion protein CHIPS. |
14.7 |
36.6 |
SOLUTION NMR |
REASONABLE
|
| 2k3v |
Solution Structure of a Tetrahaem Cytochrome from Shewanella Frigidimarina |
13.6 |
44.6 |
SOLUTION NMR |
GOOD
|
| 2k3w |
NMR structure of VPS4A-MIT-CHMP6 |
13.1 |
43.5 |
SOLUTION NMR |
GOOD
|
| 2k3x |
Solution structure of EAF3 chromo barrel domain |
14.4 |
48.4 |
SOLUTION NMR |
REASONABLE
|
| 2k3y |
Solution structure of EAF3 chromo barrel domain bound to histone h3 with a dimethyllysine analog H3K36ME2 |
16.2 |
56.9 |
SOLUTION NMR |
GOOD
|
| 2k3z |
NMR structure of adenosine bulged RNA duplex with C:G-A triple |
10.2 |
33.6 |
SOLUTION NMR |
GOOD
|
| 2k40 |
NMR structure of HESX-1 homeodomain double mutant R31L/E42L |
14.2 |
38.1 |
SOLUTION NMR |
REASONABLE
|
| 2k41 |
NMR structure of uridine bulged RNA duplex |
10.2 |
33.4 |
SOLUTION NMR |
GOOD
|
| 2k42 |
Solution Structure of the GTPase Binding Domain of WASP in Complex with EspFU, an EHEC Effector |
14.9 |
39.5 |
SOLUTION NMR |
REASONABLE
|
| 2k43 |
;Acidic fibroblast growth factor solution structure in the FGF-1-C2A binary complex: key component in the fibroblast growthfactor non-classical pathway
; |
14.2 |
46.6 |
SOLUTION NMR |
GOOD
|
| 2k44 |
Solution structure of a K+-channel voltage-sensor paddle domain |
8.8 |
30.9 |
SOLUTION NMR |
REASONABLE
|
| 2k45 |
;C2A domain of synaptototagmin I solution structure in the FGF-1-C2A binary complex: key component in the fibroblast growthfactor non-classical pathway
; |
14.8 |
46.2 |
SOLUTION NMR |
GOOD
|
| 2k46 |
Xenopus laevis malectin complexed with nigerose (Glcalpha1-3Glc) |
17.1 |
60.5 |
SOLUTION NMR |
GOOD
|
| 2k47 |
Solution structure of the C-terminal N-RNA binding domain of the Vesicular Stomatitis Virus Phosphoprotein |
12.4 |
39.4 |
SOLUTION NMR |
GOOD
|
| 2k48 |
NMR Structure of the N-terminal Coiled Coil Domain of the Andes Hantavirus Nucleocapsid Protein |
31.9 |
132.8 |
SOLUTION NMR |
REASONABLE
|
| 2k49 |
Solution NMR structure of UPF0339 protein SO3888 from Shewanella oneidensis. Northeast Structural Genomics Consortium target SoR190 |
14.8 |
47.4 |
SOLUTION NMR |
GOOD
|
| 2k4a |
FGF-1-C2A binary complex structure: a key component in the fibroblast growthfactor non-classical pathway |
19.8 |
65.3 |
SOLUTION NMR |
GOOD
|
| 2k4b |
CopR Repressor Structure |
13.3 |
52.2 |
SOLUTION NMR |
GOOD
|
| 2k4c |
tRNAPhe-based homology model for tRNAVal refined against base N-H RDCs in two media and SAXS data |
24.2 |
89.5 |
— |
GOOD
|
| 2k4d |
E2-c-Cbl recognition is necessary but not sufficient for ubiquitination activity |
18.4 |
72.8 |
SOLUTION NMR |
REASONABLE
|
| 2k4e |
Solution structure of the HIV-2 UNMYRISTOYLATED MATRIX PROTEIN |
19.9 |
55.2 |
SOLUTION NMR |
REASONABLE
|
| 2k4f |
Mouse CD3epsilon Cytoplasmic Tail |
16.7 |
68.6 |
SOLUTION NMR |
REASONABLE
|
| 2k4g |
Solution Structure of a Peptide Nucleic Acid Duplex, 10 structures |
11.9 |
50.7 |
SOLUTION NMR |
REASONABLE
|