| 2bqb |
CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME |
15.5 |
50.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2bqc |
CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME |
15.4 |
51.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2bqd |
CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME |
15.5 |
57.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2bqe |
CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME |
15.5 |
50.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2bqf |
CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME |
15.5 |
50.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2bqg |
CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME |
15.5 |
50.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2bqh |
CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME |
15.5 |
50.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2bqi |
CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME |
15.5 |
50.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2bqj |
CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME |
15.5 |
50.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2bqk |
CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME |
15.5 |
51.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2bql |
CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME |
15.5 |
50.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2bqm |
CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME |
15.5 |
51.3 |
X-RAY DIFFRACTION |
GOOD
|
| 2bqn |
CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME |
15.4 |
50.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2bqo |
CONTRIBUTION OF HYDROPHOBIC EFFECT TO THE CONFORMATIONAL STABILITY OF HUMAN LYSOZYME |
15.4 |
51.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2bqp |
THE STRUCTURE OF THE PEA LECTIN-D-GLUCOPYRANOSE COMPLEX |
25.9 |
88.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2bqq |
X-ray Structure of the N-terminal Domain of Human Doublecortin |
14.7 |
47.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2bqr |
;DNA Adduct Bypass Polymerization by Sulfolobus solfataricus Dpo4. Analysis and Crystal Structures of Multiple Base-Pair Substitution and Frameshift Products with the Adduct 1,N2-Ethenoguanine
; |
23.7 |
74.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2bqu |
;DNA Adduct Bypass Polymerization by Sulfolobus solfataricus Dpo4. Analysis and Crystal Structures of Multiple Base-Pair Substitution and Frameshift Products with the Adduct 1,N2-Ethenoguanine
; |
23.7 |
73.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2bqv |
HIV-1 protease in complex with inhibitor AHA455 |
18.4 |
61.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2bqw |
CRYSTAL STRUCTURE OF FACTOR XA IN COMPLEX WITH COMPOUND 45 |
19.7 |
69.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2bqx |
Inorganic Pyrophosphatase from the Pathogenic Bacterium Helicobacter pylori-Kinetic and Structural Properties |
16.4 |
50.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2bqy |
Inorganic Pyrophosphatase from the Pathogenic Bacterium Helicobacter pylori-Kinetic and Structural Properties |
16.4 |
50.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2bqz |
Crystal structure of a ternary complex of the human histone methyltransferase Pr-SET7 (also known as SET8) |
24.9 |
85.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2br0 |
;DNA Adduct Bypass Polymerization by Sulfolobus solfataricus Dpo4. Analysis and Crystal Structures of Multiple Base-Pair Substitution and Frameshift Products with the Adduct 1,N2-Ethenoguanine
; |
23.5 |
73.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2br1 |
Structure-based Design of Novel Chk1 Inhibitors: Insights into Hydrogen Bonding and Protein-Ligand Affinity |
20.8 |
71.3 |
X-RAY DIFFRACTION |
GOOD
|
| 2br2 |
RNase PH core of the archaeal exosome |
57.3 |
175.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2br3 |
cmcI-D160 Mg |
36.9 |
109.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2br4 |
cmcI-D160 Mg-SAM |
36.7 |
109.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2br5 |
cmcI-N160 SAH |
36.6 |
106.3 |
X-RAY DIFFRACTION |
GOOD
|
| 2br6 |
Crystal Structure of Quorum-Quenching N-Acyl Homoserine Lactone Lactonase |
18.0 |
58.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2br7 |
Crystal Structure of Acetylcholine-binding Protein (AChBP) from Aplysia californica in complex with HEPES |
31.5 |
89.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2br8 |
Crystal Structure of Acetylcholine-binding Protein (AChBP) from Aplysia californica in complex with an alpha-conotoxin PnIA variant |
32.4 |
89.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2br9 |
14-3-3 Protein Epsilon (Human) Complexed to Peptide |
19.8 |
65.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2bra |
Structure of N-Terminal FAD Binding motif of mouse MICAL |
32.4 |
115.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2brb |
Structure-based Design of Novel Chk1 Inhibitors: Insights into Hydrogen Bonding and Protein-Ligand Affinity |
20.8 |
71.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2brc |
Structure of a Hsp90 Inhibitor bound to the N-terminus of Yeast Hsp90. |
18.1 |
62.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2brd |
CRYSTAL STRUCTURE OF BACTERIORHODOPSIN IN PURPLE MEMBRANE |
22.2 |
71.8 |
ELECTRON CRYSTALLOGRAPHY |
GOOD
|
| 2bre |
STRUCTURE OF A HSP90 INHIBITOR BOUND TO THE N-TERMINUS OF YEAST HSP90. |
26.0 |
89.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2brf |
;Crystal Structure of the FHA Domain of Human Polynucleotide Kinase 3' Phosphatase
; |
14.3 |
48.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2brg |
Structure-based Design of Novel Chk1 Inhibitors: Insights into Hydrogen Bonding and Protein-Ligand Affinity |
20.4 |
68.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2brh |
Structure-based Design of Novel Chk1 Inhibitors: Insights into Hydrogen Bonding and Protein-Ligand Affinity |
20.5 |
67.3 |
X-RAY DIFFRACTION |
GOOD
|
| 2bri |
UMP KINASE FROM PYROCOCCUS FURIOSUS COMPLEXED WITH ITS SUBSTRATE ANALOG AMPPNP |
25.3 |
81.3 |
X-RAY DIFFRACTION |
GOOD
|
| 2brj |
X-ray structure of the Allene Oxide Cyclase from Arabidopsis thaliana |
23.4 |
72.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2brk |
Crystal structure of Hepatitis C virus polymerase in complex with an allosteric inhibitor (compound 1) |
25.1 |
75.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2brl |
Crystal structure of Hepatitis C virus polymerase in complex with an allosteric inhibitor (compound 2) |
25.2 |
74.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2brm |
Structure-based Design of Novel Chk1 Inhibitors: Insights into Hydrogen Bonding and Protein-Ligand Affinity |
20.5 |
66.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2brn |
Structure-based Design of Novel Chk1 Inhibitors: Insights into Hydrogen Bonding and Protein-Ligand Affinity |
20.5 |
69.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2bro |
Structure-based Design of Novel Chk1 Inhibitors: Insights into Hydrogen Bonding and Protein-Ligand Affinity |
20.8 |
69.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2brp |
Crystal structure of S. pneumoniae hyaluronate lyase in complex with W249b |
28.4 |
91.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2brq |
Crystal structure of the filamin A repeat 21 complexed with the integrin beta7 cytoplasmic tail peptide |
19.7 |
63.9 |
X-RAY DIFFRACTION |
GOOD
|