| 1dvc |
SOLUTION NMR STRUCTURE OF HUMAN STEFIN A AT PH 5.5 AND 308K, NMR, MINIMIZED AVERAGE STRUCTURE |
14.4 |
47.5 |
SOLUTION NMR |
GOOD
|
| 1dvd |
SOLUTION NMR STRUCTURE OF HUMAN STEFIN A AT PH 5.5 AND 308K, NMR, 17 STRUCTURES |
13.2 |
46.6 |
SOLUTION NMR |
GOOD
|
| 1dve |
CRYSTAL STRUCTURE OF RAT HEME OXYGENASE-1 IN COMPLEX WITH HEME |
18.0 |
57.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1dvf |
IDIOTOPIC ANTIBODY D1.3 FV FRAGMENT-ANTIIDIOTOPIC ANTIBODY E5.2 FV FRAGMENT COMPLEX |
24.6 |
84.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1dvg |
CRYSTAL STRUCTURE OF RAT HEME OXYGENASE-1 IN COMPLEX WITH HEME; SELELENO-METHIONINE DERIVATIVE, MUTATED AT M51T,M93L,M155L,M191L. |
26.3 |
84.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1dvh |
;STRUCTURE AND DYNAMICS OF FERROCYTOCHROME C553 FROM DESULFOVIBRIO VULGARIS STUDIED BY NMR SPECTROSCOPY AND RESTRAINED MOLECULAR DYNAMICS
; |
10.9 |
33.5 |
SOLUTION NMR |
GOOD
|
| 1dvi |
CALPAIN DOMAIN VI WITH CALCIUM BOUND |
21.8 |
76.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1dvj |
CRYSTAL STRUCTURE OF OROTIDINE MONOPHOSPHATE DECARBOXYLASE COMPLEXED WITH 6-AZAUMP |
43.7 |
142.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1dvk |
CRYSTAL STRUCTURE OF THE FUNCTIONAL DOMAIN OF THE SPLICING FACTOR PRP18 |
26.8 |
84.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1dvl |
CRYSTAL STRUCTURE OF THE 1:1 NETROPSIN-DECAMER D(CCIICICCII)2 COMPLEX WITH ONLY ONE DRUG BOUND AT ONE END |
12.1 |
39.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1dvm |
ACTIVE FORM OF HUMAN PAI-1 |
44.1 |
147.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1dvn |
LATENT FORM OF PLASMINOGEN ACTIVATOR INHIBITOR-1 (PAI-1) |
22.1 |
70.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1dvo |
THE X-RAY CRYSTAL STRUCTURE OF FINO, A REPRESSOR OF BACTERIAL CONJUGATION |
22.4 |
62.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1dvp |
CRYSTAL STRUCTURE OF THE VHS AND FYVE TANDEM DOMAINS OF HRS, A PROTEIN INVOLVED IN MEMBRANE TRAFFICKING AND SIGNAL TRANSDUCTION |
20.9 |
67.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1dvq |
CRYSTAL STRUCTURE OF HUMAN TRANSTHYRETIN |
18.8 |
61.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1dvr |
STRUCTURE OF A MUTANT ADENYLATE KINASE LIGATED WITH AN ATP-ANALOGUE SHOWING DOMAIN CLOSURE OVER ATP |
24.9 |
82.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1dvs |
CRYSTAL STRUCTURE OF HUMAN TRANSTHYRETIN IN COMPLEX WITH RESVERATROL |
18.8 |
61.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1dvt |
CRYSTAL STRUCTURE OF HUMAN TRANSTHYRETIN IN COMPLEX WITH FLURBIPROFEN |
18.8 |
60.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1dvu |
CRYSTAL STRUCTURE OF HUMAN TRANSTHYRETIN IN COMPLEX WITH DIBENZOFURAN-4,6-DICARBOXYLIC ACID |
18.9 |
60.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1dvv |
SOLUTION STRUCTURE OF THE QUINTUPLE MUTANT OF CYTOCHROME C-551 FROM PSEUDOMONAS AERUGINOSA |
11.4 |
31.7 |
SOLUTION NMR |
GOOD
|
| 1dvw |
NMR structure of 18 residue peptide from merp protein |
6.2 |
16.4 |
SOLUTION NMR |
REASONABLE
|
| 1dvx |
CRYSTAL STRUCTURE OF HUMAN TRANSTHYRETIN IN COMPLEX WITH DICLOFENAC |
18.7 |
60.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1dvy |
CRYSTAL STRUCTURE OF TRANSTHYRETIN IN COMPLEX WITH N-(M-TRIFLUOROMETHYLPHENYL) PHENOXAZINE-4,6-DICARBOXYLIC ACID |
18.9 |
61.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1dvz |
CRYSTAL STRUCTURE OF HUMAN TRANSTHYRETIN IN COMPLEX WITH O-TRIFLUOROMETHYLPHENYL ANTHRANILIC ACID |
18.8 |
60.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1dw0 |
STRUCTURE OF OXIDIZED SHP, AN OXYGEN BINDING CYTOCHROME C |
36.8 |
115.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1dw1 |
STRUCTURE OF THE CYANIDE COMPLEX OF SHP, AN OXYGEN BINDING CYTOCHROME C |
36.7 |
121.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1dw2 |
STRUCTURE OF THE NITRIC OXIDE COMPLEX OF REDUCED SHP, AN OXYGEN BINDING CYTOCHROME C |
36.6 |
121.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1dw3 |
STRUCTURE OF A REDUCED OXYGEN BINDING CYTOCHROME C |
36.7 |
121.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1dw4 |
NMR STRUCTURE OF OMEGA-CONOTOXIN MVIIA: CONSTRAINTS ON DISULPHIDE BRIDGES |
7.0 |
23.6 |
SOLUTION NMR |
GOOD
|
| 1dw5 |
NMR STRUCTURE OF OMEGA-CONOTOXIN MVIIA: NO CONSTRAINTS ON DISULPHIDE BRIDGES |
7.0 |
24.3 |
SOLUTION NMR |
GOOD
|
| 1dw6 |
Structural and kinetic analysis of drug resistant mutants of HIV-1 protease |
18.0 |
62.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1dw9 |
;Structure of cyanase reveals that a novel dimeric and decameric arrangement of subunits is required for formation of the enzyme active site
; |
33.2 |
97.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1dwa |
STUDY ON RADIATION DAMAGE ON A CRYOCOOLED CRYSTAL. PART 1: STRUCTURE PRIOR TO IRRADIATION |
23.8 |
78.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1dwb |
CRYSTALLOGRAPHIC ANALYSIS AT 3.0-ANGSTROMS RESOLUTION OF THE BINDING TO HUMAN THROMBIN OF FOUR ACTIVE SITE-DIRECTED INHIBITORS |
19.3 |
59.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1dwc |
CRYSTALLOGRAPHIC ANALYSIS AT 3.0-ANGSTROMS RESOLUTION OF THE BINDING TO HUMAN THROMBIN OF FOUR ACTIVE SITE-DIRECTED INHIBITORS |
19.3 |
59.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1dwd |
CRYSTALLOGRAPHIC ANALYSIS AT 3.0-ANGSTROMS RESOLUTION OF THE BINDING TO HUMAN THROMBIN OF FOUR ACTIVE SITE-DIRECTED INHIBITORS |
19.3 |
59.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1dwe |
Crystallographic analysis at 3.0-Angstroms resolution of the binding to human thrombin of four active site-directed inhibitors |
19.1 |
58.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1dwf |
Study on radiation damage on a cryocooled crystal. Part 2: Structure after irradiation with 9.1*10e15 photons/mm2 |
23.8 |
78.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1dwg |
STUDY ON RADIATION DAMAGE ON A CRYOCOOLED CRYSTAL: PART 3 STRUCTURE AFTER IRRADIATION WITH 18.2*10E15 PHOTONS/MM2. |
23.8 |
78.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1dwh |
Study on radiation damage on a cryocooled crystal. Part 4: Structure after irradiation with 27.2*10e15 photons/mm2 |
23.8 |
78.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1dwi |
Study on radiation damage on a cryocooled crystal. Part 5: Structure after irradiation with 54.0*10e15 photons/mm2 |
23.8 |
78.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1dwj |
study on radiation damage on a cryocooled crystal. Refined part 6: structure after a radiation dose of 54*10e15 photons/mm2 |
23.9 |
77.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1dwk |
STRUCTURE OF CYANASE WITH THE DI-ANION OXALATE BOUND AT THE ENZYME ACTIVE SITE |
33.2 |
97.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1dwl |
The Ferredoxin-Cytochrome complex using heteronuclear NMR and docking simulation |
14.7 |
50.5 |
— |
GOOD
|
| 1dwm |
Solution structure of Linum usitatissinum trypsin inhibitor (LUTI) |
11.7 |
42.1 |
SOLUTION NMR |
GOOD
|
| 1dwn |
Structure of bacteriophage PP7 from Pseudomonas aeruginosa at 3.7 A resolution |
28.6 |
92.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1dwo |
;Crystal Structure of Hydroxynitrile Lyase from Manihot esculenta in Complex with Substrates Acetone and Chloroacetone:Implications for the Mechanism of Cyanogenesis
; |
25.4 |
81.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1dwp |
Crystal Structure of Hydroxynitrile Lyase from Manihot esculenta at 2.2 Angstrom Resolution |
25.4 |
80.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1dwq |
;Crystal Structure of Hydroxynitrile Lyase from Manihot esculenta in Complex with Substrates Acetone and Chloroacetone:Implications for the Mechanism of Cyanogenesis
; |
25.4 |
80.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1dwr |
MYOGLOBIN (HORSE HEART) WILD-TYPE COMPLEXED WITH CO |
16.7 |
52.2 |
X-RAY DIFFRACTION |
GOOD
|