| 2l3u |
;Solution Structure of Domain IV from the YbbR family protein of Desulfitobacterium hafniense: Northeast Structural Genomics Consortium target DhR29A
; |
19.0 |
71.7 |
SOLUTION NMR |
REASONABLE
|
| 2l3w |
;Solution NMR Structure of the PBS linker domain of phycobilisome rod linker polypeptide from Synechococcus elongatus, Northeast Structural Genomics Consortium Target SnR168A
; |
15.7 |
50.5 |
SOLUTION NMR |
GOOD
|
| 2l3x |
villin head piece domain of human ABLIM2 |
12.0 |
38.8 |
SOLUTION NMR |
GOOD
|
| 2l3y |
Solution structure of mouse IL-6 |
18.3 |
69.7 |
SOLUTION NMR |
REASONABLE
|
| 2l3z |
Proton-Detected 4D DREAM Solid-State NMR Structure of Ubiquitin |
12.8 |
45.8 |
SOLID-STATE NMR |
GOOD
|
| 2l40 |
Mouse prion protein (121-231) containing the substitution Y169A |
15.8 |
55.4 |
SOLUTION NMR |
GOOD
|
| 2l41 |
Nab3 RRM - UCUU complex |
13.2 |
49.0 |
SOLUTION NMR |
GOOD
|
| 2l42 |
The solution structure of Rap1 BRCT domain from Saccharomyces cerevisiae |
14.7 |
62.6 |
SOLUTION NMR |
REASONABLE
|
| 2l43 |
Structural basis for histone code recognition by BRPF2-PHD1 finger |
14.9 |
39.1 |
SOLUTION NMR |
REASONABLE
|
| 2l44 |
C-terminal zinc knuckle of the HIVNCp7 |
7.0 |
19.3 |
SOLUTION NMR |
REASONABLE
|
| 2l45 |
C-terminal zinc knuckle of the HIVNCp7 with DNA |
9.1 |
35.1 |
SOLUTION NMR |
GOOD
|
| 2l46 |
C-terminal zinc finger of the HIVNCp7 with platinated DNA |
8.8 |
33.6 |
SOLUTION NMR |
GOOD
|
| 2l47 |
Solution structure of the PlyG catalytic domain |
14.9 |
52.3 |
SOLUTION NMR |
GOOD
|
| 2l48 |
Solution structure of the PlyG cell wall binding domain |
20.1 |
52.9 |
SOLUTION NMR |
REASONABLE
|
| 2l49 |
The solution structure of the P2 C,the immunity repressor of the P2 bacteriophage |
18.4 |
47.2 |
SOLUTION NMR |
REASONABLE
|
| 2l4a |
NMR structure of the DNA-binding domain of E.coli Lrp |
11.1 |
38.0 |
SOLUTION NMR |
GOOD
|
| 2l4b |
;Solution structure of a putative acyl carrier protein from Anaplasma phagocytophilum. Seattle Structural Genomics Center for Infectious Disease target AnphA.01018.a
; |
13.2 |
41.5 |
SOLUTION NMR |
GOOD
|
| 2l4c |
Solution Structure of the b domain of Human ERp27 |
14.4 |
38.9 |
SOLUTION NMR |
REASONABLE
|
| 2l4d |
cytochrome c domain of pp3183 protein from Pseudomonas putida |
14.5 |
55.8 |
SOLUTION NMR |
REASONABLE
|
| 2l4e |
NMR structure of the UBA domain of S. cerevisiae Dcn1 |
12.7 |
33.7 |
SOLUTION NMR |
REASONABLE
|
| 2l4f |
NMR structure of the UBA domain of S. cerevisiae Dcn1 bound to ubiquitin |
12.4 |
32.5 |
SOLUTION NMR |
REASONABLE
|
| 2l4g |
Influenza Haemagglutinin fusion peptide mutant G13A |
8.0 |
32.3 |
SOLUTION NMR |
REASONABLE
|
| 2l4h |
The Solution Structure of Calcium Bound CIB1 |
19.1 |
64.4 |
SOLUTION NMR |
REASONABLE
|
| 2l4i |
The Solution Structure of Magnesium bound CIB1 |
17.9 |
60.8 |
SOLUTION NMR |
GOOD
|
| 2l4j |
Yap ww2 |
13.0 |
50.1 |
SOLUTION NMR |
REASONABLE
|
| 2l4k |
Water refined solution structure of the human Grb7-SH2 domain in complex with the 10 amino acid peptide pY1139 |
16.3 |
45.2 |
SOLUTION NMR |
REASONABLE
|
| 2l4l |
;Structural insights into the cTAR DNA recognition by the HIV-1 Nucleocapsid protein: role of sugar deoxyriboses in the binding polarity of NC
; |
11.2 |
46.1 |
SOLUTION NMR |
REASONABLE
|
| 2l4m |
Solution structure of the Zbeta domain of human DAI and its binding modes to B- and Z-DNA |
12.3 |
47.8 |
SOLUTION NMR |
REASONABLE
|
| 2l4n |
Solution Structure of the Chemokine CCL21 |
12.4 |
43.9 |
SOLUTION NMR |
REASONABLE
|
| 2l4o |
Solution structure of the Streptococcus pneumoniae RrgB pilus backbone D1 domain |
17.2 |
44.2 |
SOLUTION NMR |
REASONABLE
|
| 2l4q |
Solution Structures of Oxidized and Reduced Thioredoxin C from M. tb |
14.2 |
51.2 |
SOLUTION NMR |
GOOD
|
| 2l4r |
NMR solution structure of the N-terminal PAS domain of hERG |
17.9 |
46.9 |
SOLUTION NMR |
REASONABLE
|
| 2l4s |
Promiscuous Binding at the Crossroads of Numerous Cancer Pathways: Insight from the Binding of GIP with Glutaminase L |
15.7 |
63.2 |
SOLUTION NMR |
GOOD
|
| 2l4t |
GIP/Glutaminase L peptide complex |
16.1 |
42.5 |
SOLUTION NMR |
REASONABLE
|
| 2l4u |
Solution structure of Ste5PM24 in the presence of SDS micelle |
10.8 |
43.4 |
SOLUTION NMR |
REASONABLE
|
| 2l4v |
Three Dimensional Structure of Pineapple Cystatin |
14.6 |
47.4 |
SOLUTION NMR |
GOOD
|
| 2l4w |
NMR structure of the Xanthomonas VirB7 |
28.0 |
167.1 |
SOLUTION NMR |
REASONABLE
|
| 2l4x |
Solution Structure of apo-IscU(WT) |
17.4 |
46.2 |
SOLUTION NMR |
REASONABLE
|
| 2l4z |
NMR structure of fusion of CtIP (641-685) to LMO4-LIM1 (18-82) |
20.6 |
54.5 |
SOLUTION NMR |
REASONABLE
|
| 2l50 |
Solution structure of apo S100A16 |
18.1 |
56.2 |
SOLUTION NMR |
GOOD
|
| 2l51 |
Solution structure of calcium bound S100A16 |
17.7 |
51.8 |
SOLUTION NMR |
GOOD
|
| 2l52 |
Solution structure of the small archaeal modifier protein 1 (SAMP1) from Methanosarcina acetivorans |
13.6 |
46.0 |
SOLUTION NMR |
GOOD
|
| 2l53 |
Solution NMR Structure of apo-calmodulin in complex with the IQ motif of Human Cardiac Sodium Channel NaV1.5 |
22.7 |
74.2 |
SOLUTION NMR |
GOOD
|
| 2l54 |
Solution structure of the Zalpha domain mutant of ADAR1 (N43A,Y47A) |
11.9 |
39.7 |
SOLUTION NMR |
GOOD
|
| 2l55 |
Solution structure of the C-terminal domain of SilB from Cupriavidus metallidurans |
12.2 |
45.8 |
SOLUTION NMR |
REASONABLE
|
| 2l56 |
NMR structure of the GCN4 trigger peptide refined using biased molecular dynamics simulations |
8.0 |
32.7 |
SOLUTION NMR |
REASONABLE
|
| 2l57 |
Solution Structure of an Uncharacterized Thioredoin-like Protein from Clostridium perfringens |
15.1 |
60.2 |
SOLUTION NMR |
GOOD
|
| 2l58 |
Solution structure of the cytosolic fragment 22-53 of Bcl-2 member Harakiri |
14.9 |
59.1 |
SOLUTION NMR |
REASONABLE
|
| 2l59 |
Solution Structures of Oxidized and Reduced Thioredoxin C from M. tb |
14.2 |
51.7 |
SOLUTION NMR |
GOOD
|
| 2l5a |
Structural basis for recognition of centromere specific histone H3 variant by nonhistone Scm3 |
19.4 |
68.3 |
SOLUTION NMR |
GOOD
|