| 1hsz |
HUMAN BETA-1 ALCOHOL DEHYDROGENASE (ADH1B*1) |
29.7 |
103.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1ht0 |
HUMAN GAMMA-2 ALCOHOL DEHYDROGENSE |
29.6 |
107.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1ht1 |
Nucleotide-Dependent Conformational Changes in a Protease-Associated ATPase HslU |
78.5 |
237.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1ht2 |
Nucleotide-Dependent Conformational Changes in a Protease-Associated ATPase HslU |
— |
295.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1ht3 |
;MERCURY INDUCED MODIFICATIONS IN THE STEREOCHEMISTRY OF THE ACTIVE SITE THROUGH CYS-73 IN A SERINE PROTEASE: CRYSTAL STRUCTURE OF THE COMPLEX OF A PARTIALLY MODIFIED PROTEINASE K WITH MERCURY AT 1.8 A RESOLUTION
; |
17.7 |
56.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1ht4 |
;SOLUTION STRUCTURE OF A BISTRAND ABASIC SITE LESION STAGGERED IN A 3'-ORIENTATION.
; |
13.2 |
44.7 |
SOLUTION NMR |
GOOD
|
| 1ht5 |
THE 2.75 ANGSTROM RESOLUTION MODEL OF OVINE COX-1 COMPLEXED WITH METHYL ESTER FLURBIPROFEN |
32.2 |
100.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1ht6 |
CRYSTAL STRUCTURE AT 1.5A RESOLUTION OF THE BARLEY ALPHA-AMYLASE ISOZYME 1 |
22.8 |
78.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1ht7 |
;STRUCTURE OF A DNA DUPLEX CONTAINING A BISTRAND ABASIC SITE LESION STAGGERED IN A 5'-ORIENTATION.
; |
13.2 |
47.8 |
SOLUTION NMR |
GOOD
|
| 1ht8 |
THE 2.7 ANGSTROM RESOLUTION MODEL OF OVINE COX-1 COMPLEXED WITH ALCLOFENAC |
32.2 |
100.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1ht9 |
DOMAIN SWAPPING EF-HANDS |
18.2 |
57.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1hta |
CRYSTAL STRUCTURE OF THE HISTONE HMFA FROM METHANOTHERMUS FERVIDUS |
16.4 |
57.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1htb |
;CRYSTALLIZATION OF HUMAN BETA3 ALCOHOL DEHYDROGENASE (10 MG/ML) IN 100 MM SODIUM PHOSPHATE (PH 7.5), 7.5 MM NAD+ AND 1 MM 4-IODOPYRAZOLE AT 25 C
; |
29.6 |
102.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1htd |
STRUCTURAL INTERACTION OF NATURAL AND SYNTHETIC INHIBITORS WITH THE VENOM METALLOPROTEINASE, ATROLYSIN C (HT-D) |
25.5 |
82.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1hte |
X-RAY CRYSTALLOGRAPHIC STUDIES OF A SERIES OF PENICILLIN-DERIVED ASYMMETRIC INHIBITORS OF HIV-1 PROTEASE |
18.1 |
60.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1htf |
X-RAY CRYSTALLOGRAPHIC STUDIES OF A SERIES OF PENICILLIN-DERIVED ASYMMETRIC INHIBITORS OF HIV-1 PROTEASE |
18.3 |
60.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1htg |
X-RAY CRYSTALLOGRAPHIC STUDIES OF A SERIES OF PENICILLIN-DERIVED ASYMMETRIC INHIBITORS OF HIV-1 PROTEASE |
18.0 |
61.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1hth |
The solution structure of cyclic human parathyroid hormone fragment 1-34, NMR, 10 structures |
16.0 |
62.2 |
SOLUTION NMR |
REASONABLE
|
| 1hti |
;CRYSTAL STRUCTURE OF RECOMBINANT HUMAN TRIOSEPHOSPHATE ISOMERASE AT 2.8 ANGSTROMS RESOLUTION. TRIOSEPHOSPHATE ISOMERASE RELATED HUMAN GENETIC DISORDERS AND COMPARISON WITH THE TRYPANOSOMAL ENZYME
; |
25.2 |
80.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1htj |
STRUCTURE OF THE RGS-LIKE DOMAIN FROM PDZ-RHOGEF |
17.7 |
58.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1htl |
;MUTATION OF A BURIED RESIDUE CAUSES LACK OF ACTIVITY BUT NO CONFORMATIONAL CHANGE: CRYSTAL STRUCTURE OF E. COLI HEAT-LABILE ENTEROTOXIN MUTANT VAL 97--> LYS
; |
28.3 |
86.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1htm |
STRUCTURE OF INFLUENZA HAEMAGGLUTININ AT THE PH OF MEMBRANE FUSION |
28.2 |
101.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1htn |
HUMAN TETRANECTIN, A TRIMERIC PLASMINOGEN BINDING PROTEIN WITH AN ALPHA-HELICAL COILED COIL |
18.4 |
74.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1hto |
CRYSTALLOGRAPHIC STRUCTURE OF A RELAXED GLUTAMINE SYNTHETASE FROM MYCOBACTERIUM TUBERCULOSIS |
80.6 |
286.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1htp |
;REFINED STRUCTURES AT 2 ANGSTROMS AND 2.2 ANGSTROMS OF THE TWO FORMS OF THE H-PROTEIN, A LIPOAMIDE-CONTAINING PROTEIN OF THE GLYCINE DECARBOXYLASE COMPLEX
; |
15.0 |
48.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1htq |
Multicopy crystallographic structure of a relaxed glutamine synthetase from Mycobacterium tuberculosis |
80.6 |
286.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1htr |
CRYSTAL AND MOLECULAR STRUCTURES OF HUMAN PROGASTRICSIN AT 1.62 ANGSTROMS RESOLUTION |
21.4 |
67.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1htt |
HISTIDYL-TRNA SYNTHETASE |
41.8 |
142.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1htv |
CRYSTAL STRUCTURE OF DESTRIPEPTIDE (B28-B30) INSULIN |
20.0 |
57.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1htw |
COMPLEX OF HI0065 WITH ADP AND MAGNESIUM |
27.4 |
89.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1htx |
SOLUTION STRUCTURE OF THE MAIN ALPHA-AMYLASE INHIBITOR FROM AMARANTH SEEDS |
8.0 |
28.6 |
SOLUTION NMR |
GOOD
|
| 1hty |
GOLGI ALPHA-MANNOSIDASE II |
30.4 |
100.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1htz |
CRYSTAL STRUCTURE OF TEM52 BETA-LACTAMASE |
41.1 |
139.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1hu0 |
CRYSTAL STRUCTURE OF AN HOGG1-DNA BOROHYDRIDE TRAPPED INTERMEDIATE COMPLEX |
22.7 |
75.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1hu3 |
MIDDLE DOMAIN OF HUMAN EIF4GII |
20.0 |
72.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1hu5 |
SOLUTION STRUCTURE OF OVISPIRIN-1 |
14.5 |
52.9 |
SOLUTION NMR |
GOOD
|
| 1hu6 |
SOLUTION STRUCTURE OF G10 NOVISPIRIN |
16.2 |
59.6 |
SOLUTION NMR |
GOOD
|
| 1hu7 |
SOLUTION STRUCTURE OF T7 NOVISPIRIN |
15.6 |
52.3 |
SOLUTION NMR |
GOOD
|
| 1hu8 |
CRYSTAL STRUCTURE OF THE MOUSE P53 CORE DNA-BINDING DOMAIN AT 2.7A RESOLUTION |
28.2 |
84.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1hu9 |
LIPOXYGENASE-3 (SOYBEAN) COMPLEX WITH 4-HYDROPEROXY-2-METHOXY-PHENOL |
29.4 |
99.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1hua |
THE SOLUTION CONFORMATION OF HYALURONAN: A COMBINED NMR AND MOLECULAR DYNAMICS STUDY |
5.9 |
21.2 |
SOLUTION NMR |
GOOD
|
| 1huc |
THE REFINED 2.15 ANGSTROMS X-RAY CRYSTAL STRUCTURE OF HUMAN LIVER CATHEPSIN B: THE STRUCTURAL BASIS FOR ITS SPECIFICITY |
29.8 |
96.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1hue |
HISTONE-LIKE PROTEIN |
20.9 |
77.9 |
SOLUTION NMR |
GOOD
|
| 1huf |
CRYSTAL STRUCTURE OF THE N-TERMINAL DOMAIN OF THE TYROSINE PHOSPHATASE YOPH FROM YERSINIA PESTIS. |
14.9 |
48.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1hug |
;Differences in anionic inhibition of Human Carbonic Anhydrase I revealed from the structures of iodide and gold cyanide inhibitor complexes
; |
18.6 |
59.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1huh |
;DIFFERENCES IN ANIONIC INHIBITION OF HUMAN CARBONIC ANHYDRASE I REVEALED FROM THE STRUCTURES OF IODIDE AND GOLD CYANIDE INHIBITOR COMPLEXES
; |
18.5 |
58.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1hui |
INSULIN MUTANT (B1, B10, B16, B27)GLU, DES-B30, NMR, 25 STRUCTURES |
11.2 |
45.1 |
SOLUTION NMR |
GOOD
|
| 1huj |
REFINED STRUCTURE OF YEAST INORGANIC PYROPHOSPHATASE AND ITS K61R MUTANT |
27.5 |
92.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1huk |
REFINED STRUCTURE OF YEAST INORGANIC PYROPHOSPHATASE AND ITS K61R MUTANT |
27.5 |
89.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1hul |
A NOVEL DIMER CONFIGURATION REVEALED BY THE CRYSTAL STRUCTURE AT 2.4 ANGSTROMS RESOLUTION OF HUMAN INTERLEUKIN-5 |
20.7 |
68.6 |
X-RAY DIFFRACTION |
GOOD
|