| 1ag2 |
PRION PROTEIN DOMAIN PRP(121-231) FROM MOUSE, NMR, 2 MINIMIZED AVERAGE STRUCTURE |
15.0 |
47.9 |
SOLUTION NMR |
GOOD
|
| 1ag3 |
DUPLEX OLIGODEOXYNUCLEOTIDE CONTAINING PROPANODEOXYGUANOSINE OPPOSITE A TWO-BASE DELETION, NMR, MINIMIZED AVERAGE STRUCTURE |
13.9 |
48.5 |
SOLUTION NMR |
GOOD
|
| 1ag4 |
NMR STRUCTURE OF SPHERULIN 3A (S3A) FROM PHYSARUM POLYCEPHALUM, MINIMIZED AVERAGE STRUCTURE |
14.3 |
45.3 |
SOLUTION NMR |
GOOD
|
| 1ag5 |
THE SOLUTION STRUCTURE OF AN AFLATOXIN B1 EPOXIDE ADDUCT AT THE N7 POSITION OF GUANINE OPPOSITE AN ADENINE IN THE COMPLEMENTARY STRAND OF AN OLIGODEOXYNUCLEOTIDE DUPLEX, NMR, MINIMIZED AVERAGE STRUCTURE |
13.0 |
45.6 |
SOLUTION NMR |
GOOD
|
| 1ag6 |
PLASTOCYANIN FROM SPINACH |
13.9 |
43.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1ag7 |
CONOTOXIN GS, NMR, 20 STRUCTURES |
9.1 |
31.6 |
SOLUTION NMR |
GOOD
|
| 1ag8 |
ALDEHYDE DEHYDROGENASE FROM BOVINE MITOCHONDRIA |
36.5 |
110.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1ag9 |
FLAVODOXINS THAT ARE REQUIRED FOR ENZYME ACTIVATION: THE STRUCTURE OF OXIDIZED FLAVODOXIN FROM ESCHERICHIA COLI AT 1.8 ANGSTROMS RESOLUTION. |
23.9 |
88.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1aga |
THE AGAROSE DOUBLE HELIX AND ITS FUNCTION IN AGAROSE GEL STRUCTURE |
8.8 |
32.3 |
FIBER DIFFRACTION |
REASONABLE
|
| 1agb |
ANTAGONIST HIV-1 GAG PEPTIDES INDUCE STRUCTURAL CHANGES IN HLA B8-HIV-1 GAG PEPTIDE (GGRKKYKL-3R MUTATION) |
24.2 |
82.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1agc |
ANTAGONIST HIV-1 GAG PEPTIDES INDUCE STRUCTURAL CHANGES IN HLA B8-HIV-1 GAG PEPTIDE (GGKKKYQL-7Q MUTATION) |
23.9 |
74.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1agd |
ANTAGONIST HIV-1 GAG PEPTIDES INDUCE STRUCTURAL CHANGES IN HLA B8-HIV-1 GAG PEPTIDE (GGKKKYKL-INDEX PEPTIDE) |
24.1 |
75.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1age |
ANTAGONIST HIV-1 GAG PEPTIDES INDUCE STRUCTURAL CHANGES IN HLA B8-HIV-1 GAG PEPTIDE (GGKKKYRL-7R MUTATION) |
24.1 |
75.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1agf |
ANTAGONIST HIV-1 GAG PEPTIDES INDUCE STRUCTURAL CHANGES IN HLA B8-HIV-1 GAG PEPTIDE (GGKKRYKL-5R MUTATION) |
24.0 |
75.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1agg |
THE SOLUTION STRUCTURE OF OMEGA-AGA-IVB, A P-TYPE CALCIUM CHANNEL ANTAGONIST FROM THE VENOM OF AGELENOPSIS APERTA |
11.2 |
29.5 |
SOLUTION NMR |
REASONABLE
|
| 1agh |
THE SOLUTION STRUCTURE OF AN 11 BASE-PAIR OLIGONUCLEOTIDE DUPLEX CODING FOR AMINO ACIDS 60-62 OF THE PRODUCT OF THE N-RAS PROTOONCOGENE, NMR, MINIMIZED AVERAGE STRUCTURE |
12.8 |
44.0 |
SOLUTION NMR |
GOOD
|
| 1agi |
CRYSTAL STRUCTURE OF BOVINE ANGIOGENIN AT 1.5 ANGSTROMS RESOLUTION |
16.0 |
53.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1agj |
EPIDERMOLYTIC TOXIN A FROM STAPHYLOCOCCUS AUREUS |
29.1 |
90.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1agk |
THE SOLUTION NMR STRUCTURE OF AN (R)-A-(N6-ADENYL)-STYRENE OXIDE-RAS61 OLIGODEOXYNUCLEOTIDE MODIFIED AT THE SECOND POSITION OF THE CODON 61 REGION, MINIMIZED AVERAGE STRUCTURE |
12.8 |
43.6 |
SOLUTION NMR |
GOOD
|
| 1agl |
STRUCTURE OF A DNA-BISDAUNOMYCIN COMPLEX |
9.7 |
33.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1agm |
Refined structure for the complex of acarbose with glucoamylase from Aspergillus awamori var. x100 to 2.4 angstroms resolution |
22.5 |
68.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1agn |
X-RAY STRUCTURE OF HUMAN SIGMA ALCOHOL DEHYDROGENASE |
42.9 |
149.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1ago |
THE SOLUTION NMR STRUCTURE OF AN (S)-A-(N6-ADENYL)-STYRENE OXIDE-RAS61 OLIGODEOXYNUCLEOTIDE MODIFIED AT THE THIRD POSITION OF THE CODON 61 REGION, MINIMIZED AVERAGE STRUCTURE |
12.8 |
43.5 |
SOLUTION NMR |
GOOD
|
| 1agp |
THREE-DIMENSIONAL STRUCTURES AND PROPERTIES OF A TRANSFORMING AND A NONTRANSFORMING GLY-12 MUTANT OF P21-H-RAS |
16.3 |
48.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1agq |
GLIAL CELL-DERIVED NEUROTROPHIC FACTOR FROM RAT |
27.7 |
82.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1agr |
COMPLEX OF ALF4-ACTIVATED GI-ALPHA-1 WITH RGS4 |
34.9 |
122.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1ags |
A SURFACE MUTANT (G82R) OF A HUMAN ALPHA-GLUTATHIONE S-TRANSFERASE SHOWS DECREASED THERMAL STABILITY AND A NEW MODE OF MOLECULAR ASSOCIATION IN THE CRYSTAL |
22.4 |
75.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1agt |
SOLUTION STRUCTURE OF THE POTASSIUM CHANNEL INHIBITOR AGITOXIN 2: CALIPER FOR PROBING CHANNEL GEOMETRY |
8.7 |
35.1 |
SOLUTION NMR |
GOOD
|
| 1agu |
THE SOLUTION NMR STRUCTURE OF THE C10R ADDUCT OF BENZO[A]PYRENE-DIOL-EPOXIDE AT THE N6 POSITION OF ADENINE OF AN 11 BASE-PAIR OLIGONUCLEOTIDE SEQUENCE CODING FOR AMINO ACIDS 60-62 OF THE PRODUCT OF THE N-RAS PROTOONCOGENE, MINIMIZED AVERAGE STRUCTURE |
13.6 |
46.9 |
SOLUTION NMR |
GOOD
|
| 1agw |
CRYSTAL STRUCTURE OF THE TYROSINE KINASE DOMAIN OF FIBROBLAST GROWTH FACTOR RECEPTOR 1 IN COMPLEX WITH SU4984 INHIBITOR |
30.5 |
107.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1agx |
REFINED CRYSTAL STRUCTURE OF ACINETOBACTER GLUTAMINASIFICANS GLUTAMINASE-ASPARAGINASE |
21.3 |
69.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1agy |
The 1.15 angstrom refined structure of fusarium solani pisi cutinase |
16.5 |
52.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1agz |
THE SOLUTION NMR STRUCTURE OF AN (R)-A-(N6-ADENYL)-STYRENE OXIDE-RAS61 OLIGODEOXYNUCLEOTIDE MODIFIED AT THE THIRD POSITION OF THE CODON 61 REGION, MINIMIZED AVERAGE STRUCTURE |
13.1 |
45.5 |
SOLUTION NMR |
GOOD
|
| 1ah0 |
PIG ALDOSE REDUCTASE COMPLEXED WITH SORBINIL |
19.8 |
60.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1ah1 |
CTLA-4, NMR, 20 STRUCTURES |
17.0 |
65.2 |
SOLUTION NMR |
GOOD
|
| 1ah2 |
SERINE PROTEASE PB92 FROM BACILLUS ALCALOPHILUS, NMR, 18 STRUCTURES |
17.3 |
49.2 |
SOLUTION NMR |
GOOD
|
| 1ah3 |
ALDOSE REDUCTASE COMPLEXED WITH TOLRESTAT INHIBITOR |
19.9 |
60.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1ah4 |
PIG ALDOSE REDUCTASE, HOLO FORM |
19.9 |
60.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1ah5 |
REDUCED FORM SELENOMETHIONINE-LABELLED HYDROXYMETHYLBILANE SYNTHASE DETERMINED BY MAD |
20.4 |
64.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1ah6 |
STRUCTURE OF THE TETRAGONAL FORM OF THE N-TERMINAL DOMAIN OF THE YEAST HSP90 CHAPERONE |
17.8 |
59.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1ah7 |
PHOSPHOLIPASE C FROM BACILLUS CEREUS |
18.5 |
66.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1ah8 |
STRUCTURE OF THE ORTHORHOMBIC FORM OF THE N-TERMINAL DOMAIN OF THE YEAST HSP90 CHAPERONE |
26.1 |
89.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1ah9 |
THE STRUCTURE OF THE TRANSLATIONAL INITIATION FACTOR IF1 FROM ESCHERICHIA COLI, NMR, 19 STRUCTURES |
12.0 |
42.2 |
SOLUTION NMR |
GOOD
|
| 1aha |
THE N-GLYCOSIDASE MECHANISM OF RIBOSOME-INACTIVATING PROTEINS IMPLIED BY CRYSTAL STRUCTURES OF ALPHA-MOMORCHARIN |
19.0 |
61.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1ahb |
THE N-GLYCOSIDASE MECHANISM OF RIBOSOME-INACTIVATING PROTEINS IMPLIED BY CRYSTAL STRUCTURES OF ALPHA-MOMORCHARIN |
18.9 |
61.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1ahc |
THE N-GLYCOSIDASE MECHANISM OF RIBOSOME-INACTIVATING PROTEINS IMPLIED BY CRYSTAL STRUCTURES OF ALPHA-MOMORCHARIN |
19.1 |
61.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1ahd |
DETERMINATION OF THE NMR SOLUTION STRUCTURE OF AN ANTENNAPEDIA HOMEODOMAIN-DNA COMPLEX |
15.7 |
54.2 |
SOLUTION NMR |
GOOD
|
| 1ahe |
ASPARTATE AMINOTRANSFERASE HEXAMUTANT |
28.4 |
100.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1ahf |
ASPARTATE AMINOTRANSFERASE HEXAMUTANT |
28.5 |
95.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1ahg |
ASPARTATE AMINOTRANSFERASE HEXAMUTANT |
28.6 |
95.7 |
X-RAY DIFFRACTION |
GOOD
|