| 1hum |
SOLUTION STRUCTURE OF THE CHEMOKINE HMIP-1BETA(SLASH)ACT-2 BY MULTI-DIMENSIONAL NMR: A NOVEL CHEMOKINE DIMER |
19.2 |
65.4 |
SOLUTION NMR |
GOOD
|
| 1hun |
SOLUTION STRUCTURE OF THE CHEMOKINE HMIP-1BETA(SLASH)ACT-2 BY MULTI-DIMENSIONAL NMR: A NOVEL CHEMOKINE DIMER |
18.4 |
55.1 |
SOLUTION NMR |
GOOD
|
| 1huo |
CRYSTAL STRUCTURE OF DNA POLYMERASE BETA COMPLEXED WITH DNA AND CR-TMPPCP |
43.2 |
128.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1hup |
HUMAN MANNOSE BINDING PROTEIN CARBOHYDRATE RECOGNITION DOMAIN TRIMERIZES THROUGH A TRIPLE ALPHA-HELICAL COILED-COIL |
17.9 |
71.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1huq |
1.8A CRYSTAL STRUCTURE OF THE MONOMERIC GTPASE RAB5C (MOUSE) |
16.2 |
49.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1hur |
HUMAN ADP-RIBOSYLATION FACTOR 1 COMPLEXED WITH GDP, FULL LENGTH NON-MYRISTOYLATED |
23.4 |
75.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1hus |
RIBOSOMAL PROTEIN S7 |
17.1 |
60.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1hut |
THE STRUCTURE OF ALPHA-THROMBIN INHIBITED BY A 15-MER SINGLE-STRANDED DNA APTAMER |
20.8 |
69.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1huu |
DNA-BINDING PROTEIN HU FROM BACILLUS STEAROTHERMOPHILUS |
26.9 |
93.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1huv |
;CRYSTAL STRUCTURE OF A SOLUBLE MUTANT OF THE MEMBRANE-ASSOCIATED (S)-MANDELATE DEHYDROGENASE FROM PSEUDOMONAS PUTIDA AT 2.15A RESOLUTION
; |
21.1 |
79.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1huw |
THE CRYSTAL STRUCTURE OF AFFINITY-MATURED HUMAN GROWTH HORMONE AT 2 ANGSTROMS RESOLUTION |
17.7 |
64.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1hux |
CRYSTAL STRUCTURE OF THE ACIDAMINOCOCCUS FERMENTANS (R)-2-HYDROXYGLUTARYL-COA DEHYDRATASE COMPONENT A |
27.7 |
97.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1huy |
CRYSTAL STRUCTURE OF CITRINE, AN IMPROVED YELLOW VARIANT OF GREEN FLUORESCENT PROTEIN |
18.6 |
58.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1huz |
CRYSTAL STRUCTURE OF DNA POLYMERASE COMPLEXED WITH DNA AND CR-PCP |
42.9 |
126.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1hv0 |
DISSECTING ELECTROSTATIC INTERACTIONS AND THE PH-DEPENDENT ACTIVITY OF A FAMILY 11 GLYCOSIDASE |
16.3 |
47.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1hv1 |
DISSECTING ELECTROSTATIC INTERACTIONS AND THE PH-DEPENDENT ACTIVITY OF A FAMILY 11 GLYCOSIDASE |
16.3 |
48.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1hv2 |
SOLUTION STRUCTURE OF YEAST ELONGIN C IN COMPLEX WITH A VON HIPPEL-LINDAU PEPTIDE |
15.3 |
52.7 |
SOLUTION NMR |
GOOD
|
| 1hv4 |
CRYSTAL STRUCTURE ANALYSIS OF BAR-HEAD GOOSE HEMOGLOBIN (DEOXY FORM) |
39.4 |
132.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1hv5 |
CRYSTAL STRUCTURE OF THE STROMELYSIN-3 (MMP-11) CATALYTIC DOMAIN COMPLEXED WITH A PHOSPHINIC INHIBITOR |
56.7 |
161.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1hv6 |
CRYSTAL STRUCTURE OF ALGINATE LYASE A1-III COMPLEXED WITH TRISACCHARIDE PRODUCT. |
20.7 |
64.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1hv7 |
PORCINE PANCREATIC ELASTASE COMPLEXED WITH GW311616A |
17.8 |
55.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1hv8 |
CRYSTAL STRUCTURE OF A DEAD BOX PROTEIN FROM THE HYPERTHERMOPHILE METHANOCOCCUS JANNASCHII |
32.3 |
112.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1hv9 |
STRUCTURE OF E. COLI GLMU: ANALYSIS OF PYROPHOSPHORYLASE AND ACETYLTRANSFERASE ACTIVE SITES |
60.4 |
188.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1hva |
ENGINEERING THE ZINC BINDING SITE OF HUMAN CARBONIC ANHYDRASE II: STRUCTURE OF THE HIS-94-> CYS APOENZYME IN A NEW CRYSTALLINE FORM |
18.6 |
58.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1hvb |
CRYSTAL STRUCTURE OF STREPTOMYCES R61 DD-PEPTIDASE COMPLEXED WITH A NOVEL CEPHALOSPORIN ANALOG OF CELL WALL PEPTIDOGLYCAN |
19.9 |
59.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1hvc |
CRYSTAL STRUCTURE OF A TETHERED DIMER OF HIV-1 PROTEASE COMPLEXED WITH AN INHIBITOR |
18.3 |
60.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1hvd |
;STRUCTURAL AND ELECTROPHYSIOLOGICAL ANALYSIS OF ANNEXIN V MUTANTS. MUTAGENESIS OF HUMAN ANNEXIN V, AN IN VITRO VOLTAGE-GATED CALCIUM CHANNEL, PROVIDES INFORMATION ABOUT THE STRUCTURAL FEATURES OF THE ION PATHWAY, THE VOLTAGE SENSOR AND THE ION SELECTIVITY FILTER
; |
22.4 |
76.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1hve |
;STRUCTURAL AND ELECTROPHYSIOLOGICAL ANALYSIS OF ANNEXIN V MUTANTS. MUTAGENESIS OF HUMAN ANNEXIN V, AN IN VITRO VOLTAGE-GATED CALCIUM CHANNEL, PROVIDES INFORMATION ABOUT THE STRUCTURAL FEATURES OF THE ION PATHWAY, THE VOLTAGE SENSOR AND THE ION SELECTIVITY FILTER
; |
22.5 |
76.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1hvf |
;STRUCTURAL AND ELECTROPHYSIOLOGICAL ANALYSIS OF ANNEXIN V MUTANTS. MUTAGENESIS OF HUMAN ANNEXIN V, AN IN VITRO VOLTAGE-GATED CALCIUM CHANNEL, PROVIDES INFORMATION ABOUT THE STRUCTURAL FEATURES OF THE ION PATHWAY, THE VOLTAGE SENSOR AND THE ION SELECTIVITY FILTER
; |
22.5 |
76.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1hvg |
;STRUCTURAL AND ELECTROPHYSIOLOGICAL ANALYSIS OF ANNEXIN V MUTANTS. MUTAGENESIS OF HUMAN ANNEXIN V, AN IN VITRO VOLTAGE-GATED CALCIUM CHANNEL, PROVIDES INFORMATION ABOUT THE STRUCTURAL FEATURES OF THE ION PATHWAY, THE VOLTAGE SENSOR AND THE ION SELECTIVITY FILTER
; |
22.6 |
76.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1hvh |
NONPEPTIDE CYCLIC CYANOGUANIDINES AS HIV PROTEASE INHIBITORS |
18.2 |
59.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1hvi |
INFLUENCE OF STEREOCHEMISTRY ON ACTIVITY AND BINDING MODES FOR C2 SYMMETRY-BASED DIOL INHIBITORS OF HIV-1 PROTEASE |
18.2 |
61.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1hvj |
INFLUENCE OF STEREOCHEMISTRY ON ACTIVITY AND BINDING MODES FOR C2 SYMMETRY-BASED DIOL INHIBITORS OF HIV-1 PROTEASE |
18.3 |
65.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1hvk |
INFLUENCE OF STEREOCHEMISTRY ON ACTIVITY AND BINDING MODES FOR C2 SYMMETRY-BASED DIOL INHIBITORS OF HIV-1 PROTEASE |
18.2 |
70.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1hvl |
INFLUENCE OF STEREOCHEMISTRY ON ACTIVITY AND BINDING MODES FOR C2 SYMMETRY-BASED DIOL INHIBITORS OF HIV-1 PROTEASE |
18.2 |
61.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1hvn |
;ZINC-AND SEQUENCE-DEPENDENT BINDING TO NUCLEIC ACIDS BY THE N-TERMINAL ZINC FINGER DOMAIN OF THE HIV-1 NUCLEOCAPSID PROTEIN: NMR STRUCTURE OF THE COMPLEX WITH THE PSI-SITE ANALOG, D/ACGCC
; |
8.1 |
27.6 |
SOLUTION NMR |
GOOD
|
| 1hvo |
;ZINC-AND SEQUENCE-DEPENDENT BINDING TO NUCLEIC ACIDS BY THE N-TERMINAL ZINC FINGER DOMAIN OF THE HIV-1 NUCLEOCAPSID PROTEIN: NMR STRUCTURE OF THE COMPLEX WITH THE PSI-SITE ANALOG, D/ACGCC
; |
8.2 |
28.6 |
SOLUTION NMR |
GOOD
|
| 1hvq |
CRYSTAL STRUCTURES OF HEVAMINE, A PLANT DEFENCE PROTEIN WITH CHITINASE AND LYSOZYME ACTIVITY, AND ITS COMPLEX WITH AN INHIBITOR |
18.9 |
59.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1hvr |
RATIONAL DESIGN OF POTENT, BIOAVAILABLE, NONPEPTIDE CYCLIC UREAS AS HIV PROTEASE INHIBITORS |
18.3 |
61.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1hvs |
STRUCTURAL BASIS OF DRUG RESISTANCE FOR THE V82A MUTANT OF HIV-1 PROTEASE: BACKBONE FLEXIBILITY AND SUBSITE REPACKING |
18.2 |
61.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1hvu |
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 REVERSE TRANSCRIPTASE COMPLEXED WITH A 33-BASE NUCLEOTIDE RNA PSEUDOKNOT |
72.3 |
258.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1hvv |
SELF-ASSOCIATION OF THE H3 REGION OF SYNTAXIN 1A: IMPLICATIONS FOR SNARE COMPLEX ASSEMBLY |
27.6 |
103.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1hvw |
HAIRPINLESS MUTANT OF OMEGA-ATRACOTOXIN-HV1A |
6.7 |
23.4 |
SOLUTION NMR |
GOOD
|
| 1hvx |
BACILLUS STEAROTHERMOPHILUS ALPHA-AMYLASE |
25.3 |
85.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1hvy |
Human thymidylate synthase complexed with dUMP and Raltitrexed, an antifolate drug, is in the closed conformation |
41.9 |
135.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1hvz |
RTD-1, A CYCLIC ANTIMICROBIAL DEFENSIN FROM RHESUS MACAQUE LEUKOCYTES |
8.6 |
23.4 |
SOLUTION NMR |
REASONABLE
|
| 1hw1 |
THE FADR-DNA COMPLEX: TRANSCRIPTIONAL CONTROL OF FATTY ACID METABOLISM IN ESCHERICHIA COLI |
24.2 |
72.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1hw2 |
FADR-DNA COMPLEX: TRANSCRIPTIONAL CONTROL OF FATTY ACID METABOLISM IN ECHERICHIA COLI |
27.3 |
86.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1hw3 |
STRUCTURE OF HUMAN THYMIDYLATE SYNTHASE SUGGESTS ADVANTAGES OF CHEMOTHERAPY WITH NONCOMPETITIVE INHIBITORS |
19.9 |
60.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1hw4 |
STRUCTURE OF THYMIDYLATE SYNTHASE SUGGESTS ADVANTAGES OF CHEMOTHERAPY WITH NONCOMPETITIVE INHIBITORS |
19.9 |
59.7 |
X-RAY DIFFRACTION |
REASONABLE
|