| 1r27 |
Crystal Structure of NarGH complex |
53.6 |
188.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1r28 |
Crystal Structure of the B-Cell Lymphoma 6 (BCL6) BTB domain to 2.2 Angstrom |
20.4 |
68.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1r29 |
Crystal Structure of the B-Cell Lymphoma 6 (BCL6) BTB Domain to 1.3 Angstrom |
16.8 |
58.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1r2a |
THE MOLECULAR BASIS FOR PROTEIN KINASE A ANCHORING REVEALED BY SOLUTION NMR |
16.3 |
66.8 |
SOLUTION NMR |
REASONABLE
|
| 1r2b |
Crystal structure of the BCL6 BTB domain complexed with a SMRT co-repressor peptide |
20.8 |
69.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1r2c |
PHOTOSYNTHETIC REACTION CENTER BLASTOCHLORIS VIRIDIS (ATCC) |
36.6 |
126.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1r2d |
Structure of Human Bcl-XL at 1.95 Angstroms |
15.7 |
48.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1r2e |
Human Bcl-XL containing a Glu to Leu mutation at position 92 |
15.8 |
48.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1r2f |
RIBONUCLEOTIDE REDUCTASE R2F PROTEIN FROM SALMONELLA TYPHIMURIUM |
26.4 |
85.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1r2g |
Human Bcl-XL containing a Phe to Trp mutation at position 97 |
15.7 |
48.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1r2h |
Human Bcl-XL containing an Ala to Leu mutation at position 142 |
15.8 |
48.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1r2i |
Human Bcl-XL containing a Phe to Leu mutation at position 146 |
15.8 |
48.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1r2j |
FkbI for Biosynthesis of Methoxymalonyl Extender Unit of Fk520 Polyketide Immunosuppresant |
21.5 |
80.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1r2k |
Crystal structure of MoaB from Escherichia coli |
23.9 |
63.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1r2l |
A parallel stranded DNA duplex with an A-G mismatch base-pair |
14.0 |
48.7 |
SOLUTION NMR |
GOOD
|
| 1r2m |
Atomic resolution structure of the HFBII hydrophobin: a self-assembling amphiphile |
17.8 |
60.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1r2n |
NMR structure of the all-trans retinal in dark-adapted Bacteriorhodopsin |
18.3 |
60.0 |
SOLUTION NMR |
GOOD
|
| 1r2o |
d(GCATGCT) + Ni2+ |
10.0 |
35.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1r2p |
Solution structure of domain 5 from the ai5(gamma) group II intron |
19.2 |
70.9 |
SOLUTION NMR |
REASONABLE
|
| 1r2q |
Crystal Structure of Human Rab5a GTPase Domain at 1.05 A resolution |
16.7 |
53.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1r2r |
CRYSTAL STRUCTURE OF RABBIT MUSCLE TRIOSEPHOSPHATE ISOMERASE |
33.3 |
111.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1r2s |
CRYSTAL STRUCTURE OF RABBIT MUSCLE TRIOSEPHOSPHATE ISOMERASE |
33.8 |
113.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1r2t |
CRYSTAL STRUCTURE OF RABBIT MUSCLE TRIOSEPHOSPHATE ISOMERASE |
25.2 |
80.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1r2u |
NMR structure of the N domain of trout cardiac troponin C at 30 C |
13.4 |
45.1 |
SOLUTION NMR |
GOOD
|
| 1r2w |
Coordinates of L11 with 58nts of 23S rRNA fitted into the cryo-EM map of the 70S ribosome |
19.5 |
59.5 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 1r2x |
Coordinates of L11 with 58nts of 23S rRNA fitted into the cryo-EM map of EF-Tu ternary complex (GDP.Kirromycin) bound 70S ribosome |
20.8 |
61.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 1r2y |
MutM (Fpg) bound to 8-oxoguanine (oxoG) containing DNA |
20.7 |
65.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1r2z |
MutM (Fpg) bound to 5,6-dihydrouracil (DHU) containing DNA |
20.8 |
66.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1r30 |
The Crystal Structure of Biotin Synthase, an S-Adenosylmethionine-Dependent Radical Enzyme |
29.4 |
102.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1r31 |
HMG-CoA reductase from Pseudomonas mevalonii complexed with HMG-CoA |
27.0 |
79.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1r33 |
Golgi alpha-mannosidase II complex with 5-thio-D-mannopyranosylamine |
30.5 |
101.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1r34 |
Golgi alpha-mannosidase II complex with 5-thio-D-mannopyranosylamidinium salt |
30.5 |
101.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1r35 |
MURINE INDUCIBLE NITRIC OXIDE SYNTHASE OXYGENASE DIMER, TETRAHYDROBIOPTERIN AND 4R-FLUORO-N6-ETHANIMIDOYL-L-LYSINE |
36.3 |
117.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1r36 |
NMR-based structure of autoinhibited murine Ets-1 deltaN301 |
14.5 |
42.8 |
SOLUTION NMR |
EXCELLENT
|
| 1r37 |
Alcohol dehydrogenase from sulfolobus solfataricus complexed with NAD(H) and 2-ethoxyethanol |
28.6 |
93.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1r38 |
Crystal structure of H114A mutant of Candida tenuis xylose reductase |
51.6 |
187.9 |
X-RAY DIFFRACTION |
SUSPICIOUS
|
| 1r39 |
THE STRUCTURE OF P38ALPHA |
22.9 |
75.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1r3b |
Solution structure of xenopus laevis Mob1 |
23.2 |
62.2 |
SOLUTION NMR |
REASONABLE
|
| 1r3c |
THE STRUCTURE OF P38ALPHA C162S MUTANT |
22.7 |
72.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1r3d |
Crystal structure of protein VC1974 from Vibrio cholerae, Pfam abhydrolase |
18.8 |
59.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1r3e |
;Crystal Structure of tRNA Pseudouridine Synthase TruB and Its RNA Complex: RNA-protein Recognition Through a Combination of Rigid Docking and Induced Fit
; |
26.6 |
97.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1r3f |
;Crystal Structure of tRNA Pseudouridine Synthase TruB and Its RNA Complex: RNA-protein Recognition Through a Combination of Rigid Docking and Induced Fit
; |
23.3 |
75.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1r3g |
;1.16A X-ray structure of the synthetic DNA fragment with the incorporated 2'-O-[(2-Guanidinium)ethyl]-5-methyluridine residues
; |
11.9 |
42.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1r3h |
Crystal Structure of T10 |
58.8 |
167.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1r3i |
potassium channel KcsA-Fab complex in Rb+ |
30.2 |
81.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1r3j |
potassium channel KcsA-Fab complex in high concentration of Tl+ |
31.1 |
127.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1r3k |
potassium channel KcsA-Fab complex in low concentration of Tl+ |
30.8 |
83.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1r3l |
potassium channel KcsA-Fab complex in Cs+ |
30.3 |
81.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1r3m |
Crystal structure of the dimeric unswapped form of bovine seminal ribonuclease |
21.2 |
74.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1r3n |
Crystal structure of beta-alanine synthase from Saccharomyces kluyveri |
61.2 |
203.4 |
X-RAY DIFFRACTION |
GOOD
|