| 8q1d |
D10N variant of beta-phosphoglucomutase from Lactococcus lactis in complex with fructose 1,6-bisphosphate |
18.8 |
64.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8q1e |
D10N,P146A variant of beta-phosphoglucomutase from Lactococcus lactis in complex with fructose 1,6-bisphosphate |
18.7 |
62.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8q1f |
;D10N,P146A variant of beta-phosphoglucomutase from Lactococcus lactis in complex with native beta-glucose 1,6-bisphosphate intermediate
; |
26.6 |
91.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8q1g |
LSD1-CoREST bound to Acetylated K14 of Histone H3 |
42.7 |
155.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8q1h |
LSD1 Y391K-CoREST bound to Histone H3 N-terminal tail |
42.8 |
144.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8q1i |
Neck-tail junction of phage 812 after tail contraction (C6) |
51.4 |
185.0 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8q1j |
LSD1 Y391K-CoREST bound to Acetylated K14 of Histone H3 |
42.8 |
142.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8q1k |
;Structural analysis of PLD3 reveals insights into the mechanism of lysosomal 5' exonuclease-mediated nucleic acid degradation
; |
33.6 |
110.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8q1l |
NMR structure of arthrofactin A in micellar DPC solution |
4.2 |
20.9 |
SOLUTION NMR |
REASONABLE
|
| 8q1m |
Aplysia californica acetylcholine-binding protein in complex with Spiroimine (+)-4 R |
32.2 |
96.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8q1n |
Cyclic peptide binder of the WBM-site of WDR5 |
28.7 |
95.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8q1o |
S-layer protein SlpA from Lactobacillus amylovorus, domain I (aa 32-209), important for Self-assembly |
27.0 |
93.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8q1p |
Inward-facing, open2 proteoliposome complex I at 2.9 A, after deactivation treatment. Initially purified in LMNG. |
81.4 |
223.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q1q |
mouse Keap1 in complex with stapled peptide |
19.1 |
56.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8q1r |
mouse Keap1 in complex with stapled peptide |
18.9 |
56.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8q1s |
Pathogenic mutations of human phosphorylation sites affect protein-protein interactions |
27.5 |
83.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8q1u |
Inward-facing, open1 proteoliposome complex I at 3.3 A, after deactivation treatment. Initially purified in LMNG. |
80.9 |
218.2 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8q1v |
TtX183A - A c-type cytochrome domain from the Teredinibacter turnerae protein TERTU_2913 |
12.4 |
39.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8q1w |
TtX183B - A c-type cytochrome domain from the Teredinibacter turnerae protein TERTU_2913 |
20.2 |
62.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8q1x |
;Structural analysis of PLD3 reveals insights into the mechanism of lysosomal 5' exonuclease-mediated nucleic acid degradation
; |
33.6 |
109.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8q1y |
Outward-facing, open2 proteoliposome complex I at 2.6 A, after deactivation treatment. Initially purified in LMNG. |
81.6 |
218.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q1z |
Crystal Structure of Human Vaccinia-related kinase 2 (VRK-2) bound to JA-296 |
20.9 |
64.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8q20 |
Crystal structure of Vanadium-dependent haloperoxidase R425D mutant (A. marina) |
26.3 |
87.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8q21 |
Crystal structure of Vanadium-dependent haloperoxidase R425S mutant (A. marina) |
26.4 |
87.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8q22 |
Crystal structure of Vanadium-dependent haloperoxidase R425S mutant in complex with 1,3,5-trimethoxybenzene (A. marina) |
26.4 |
86.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8q23 |
HsNMT1 in complex with both MyrCoA and Ac-D-ORN-SFSKPR inhibitor peptide |
31.1 |
113.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8q24 |
HsNMT1 in complex with both MyrCoA and (DAB)SFSKPR inhibitor peptide |
31.0 |
112.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8q25 |
Outward-facing, open1 proteoliposome complex I at 2.8 A, after deactivation treatment. Initially purified in LMNG. |
81.2 |
219.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q26 |
HsNMT1 in complex with both MyrCoA and GNCFSKPR inhibitor peptide |
30.8 |
108.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8q27 |
Tau: AD-MIA1 |
41.8 |
130.4 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8q28 |
Se-Met labelled TtX122A - A domain of unknown function from the Teredinibacter turnerae protein TERTU_3803 |
24.5 |
79.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8q29 |
TtX122A - A domain of unknown function from the Teredinibacter turnerae protein TERTU_3803 |
24.5 |
80.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8q2a |
TtX122B - A domain of unknown function from the Teredinibacter turnerae protein TERTU_2913 |
28.9 |
86.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8q2b |
E. coli Adenylate Kinase variant D158A (AK D158A) showing significant changes to the stacking of catalytic arginine side chains |
26.5 |
92.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8q2c |
Crystal structure of the E. coli PqiC Lipoprotein |
22.2 |
74.6 |
X-RAY DIFFRACTION |
GOOD
|
| 8q2d |
Crystal structure of the E. coli PqiC Lipoprotein residues 17-187 |
29.4 |
91.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8q2e |
The 1.68-A X-ray crystal structure of Sporosarcina pasteurii urease inhibited by thiram and bound to dimethylditiocarbamate |
30.7 |
103.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8q2f |
Cytochrome P450 BM3 aMOx-A heme domain |
64.7 |
240.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8q2g |
X-ray structure of LysECD7 endolysin against Gram-negative bacteria |
15.5 |
50.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8q2h |
beta-galactosidase from Bacillus circulans |
35.9 |
115.9 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8q2i |
Crystal structure of Ser33 in complex 2HG (2-hydroxyglutarate) and Serine |
51.5 |
164.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8q2j |
Tau - AD-MIA2 |
34.2 |
115.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q2k |
Tau - AD-MIA3 |
34.4 |
122.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q2l |
Tau - AD-MIA4 |
32.4 |
113.7 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8q2m |
18mer DNA mimic Foldamer with an Aliphatic linker in complex with Sac7d V26A/M29A protein |
15.4 |
49.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8q2n |
Cas1-Cas2 CRISPR integrase bound to prespacer and target DNA, Streptococcus thermophilus DGCC 7710 CRISPR3 system |
46.0 |
153.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q2o |
Structure of alginate transporter AlgE from P. aeruginosa PAO1 by using Se-MAG for the the lipid cubic phase crystallization |
22.9 |
75.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8q2p |
;Structure of the membrane integral lipoprotein N-acyltransferase Lnt from E. coli by using Se-MAG for the the lipid cubic phase crystallization
; |
25.2 |
83.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8q2q |
Crystal structure of YTHDC1 in complex with Compound 2b (YL_32) |
23.8 |
78.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8q2r |
Crystal structure of YTHDC1 in complex with Compound 3 (ZA_431) |
23.9 |
77.0 |
X-RAY DIFFRACTION |
GOOD
|