| 1tei |
STRUCTURE OF CONCANAVALIN A COMPLEXED TO BETA-D-GLCNAC (1,2)ALPHA-D-MAN-(1,6)[BETA-D-GLCNAC(1,2)ALPHA-D-MAN (1,6)]ALPHA-D-MAN |
45.1 |
147.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1tej |
Crystal structure of a disintegrin heterodimer at 1.9 A resolution. |
20.2 |
67.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1tel |
Crystal structure of a RubisCO-like protein from Chlorobium tepidum |
28.9 |
96.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1tem |
6 ALPHA HYDROXYMETHYL PENICILLOIC ACID ACYLATED ON THE TEM-1 BETA-LACTAMASE FROM ESCHERICHIA COLI |
18.9 |
61.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1ten |
STRUCTURE OF A FIBRONECTIN TYPE III DOMAIN FROM TENASCIN PHASED BY MAD ANALYSIS OF THE SELENOMETHIONYL PROTEIN |
14.4 |
47.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1teq |
Effect of Shuttle Location and pH Environment on H+ Transfer in Human Carbonic Anhydrase II |
18.8 |
58.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1ter |
SOLUTION STRUCTURE OF TERTIAPIN DETERMINED USING NUCLEAR MAGNETIC RESONANCE AND DISTANCE GEOMETRY |
6.5 |
23.4 |
SOLUTION NMR |
GOOD
|
| 1tes |
OXYGEN BINDING MUSCLE PROTEIN |
16.7 |
50.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1tet |
CRYSTAL STRUCTURE OF AN ANTICHOLERA TOXIN PEPTIDE COMPLEX AT 2.3 ANGSTROMS |
25.8 |
87.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1teu |
Effect of Shuttle Location and pH Environment on H+ Transfer in Human Carbonic Anhydrase II |
18.8 |
58.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1tev |
Crystal structure of the human UMP/CMP kinase in open conformation |
18.6 |
57.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1tew |
STRUCTURE OF HEXAGONAL TURKEY EGG WHITE LYSOZYME AT 1.65 ANGSTROMS RESOLUTION |
15.0 |
48.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1tex |
Mycobacterium smegmatis Stf0 Sulfotransferase with Trehalose |
37.3 |
126.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1tey |
NMR structure of human histone chaperone, ASF1A |
17.5 |
61.6 |
SOLUTION NMR |
GOOD
|
| 1tez |
COMPLEX BETWEEN DNA AND THE DNA PHOTOLYASE FROM ANACYSTIS NIDULANS |
53.5 |
191.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1tf0 |
Crystal structure of the GA module complexed with human serum albumin |
28.0 |
93.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1tf1 |
Crystal Structure of the E. coli Glyoxylate Regulatory Protein Ligand Binding Domain |
29.6 |
91.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1tf2 |
Crystal structure of SecA:ADP in an open conformation from Bacillus Subtilis |
33.0 |
108.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1tf3 |
TFIIIA FINGER 1-3 BOUND TO DNA, NMR, 22 STRUCTURES |
16.3 |
52.4 |
SOLUTION NMR |
REASONABLE
|
| 1tf4 |
ENDO/EXOCELLULASE FROM THERMOMONOSPORA |
42.7 |
138.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1tf5 |
Crystal structure of SecA in an open conformation from Bacillus Subtilis |
33.1 |
109.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1tf6 |
CO-CRYSTAL STRUCTURE OF XENOPUS TFIIIA ZINC FINGER DOMAIN BOUND TO THE 5S RIBOSOMAL RNA GENE INTERNAL CONTROL REGION |
35.0 |
111.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1tf7 |
Crystal Structure of Circadian Clock Protein KaiC |
42.1 |
120.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1tf8 |
Streptomyces griseus aminopeptidase complexed with L-tryptophan |
18.2 |
55.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1tf9 |
Streptomyces griseus aminopeptidase complexed with P-Iodo-L-Phenylalanine |
18.0 |
55.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1tfa |
OVOTRANSFERRIN, N-TERMINAL LOBE, APO FORM |
22.4 |
72.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1tfb |
NMR STUDIES OF HUMAN GENERAL TRANSCRIPTION FACTOR TFIIB: DYNAMICS AND INTERACTION WITH VP16 ACTIVATION DOMAIN, 20 STRUCTURES |
17.2 |
60.4 |
SOLUTION NMR |
GOOD
|
| 1tfc |
;CRYSTAL STRUCTURE OF THE LIGAND-BINDING DOMAIN OF THE ESTROGEN-RELATED RECEPTOR GAMMA IN COMPLEX WITH A STEROID RECEPTOR COACTIVATOR-1 PEPTIDE
; |
23.8 |
70.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1tfd |
;HIGH-RESOLUTION X-RAY STUDIES ON RABBIT SERUM TRANSFERRIN: PRELIMINARY STRUCTURE ANALYSIS OF THE N-TERMINAL HALF-MOLECULE AT 2.3 ANGSTROMS RESOLUTION
; |
20.4 |
70.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1tfe |
DIMERIZATION DOMAIN OF EF-TS FROM T. THERMOPHILUS |
18.9 |
67.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1tff |
Structure of Otubain-2 |
19.3 |
61.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1tfg |
AN UNUSUAL FEATURE REVEALED BY THE CRYSTAL STRUCTURE AT 2.2 ANGSTROMS RESOLUTION OF HUMAN TRANSFORMING GROWTH FACTOR-BETA2 |
17.9 |
66.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1tfh |
EXTRACELLULAR DOMAIN OF HUMAN TISSUE FACTOR |
41.3 |
118.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1tfi |
;A NOVEL ZN FINGER MOTIF IN THE BASAL TRANSCRIPTIONAL MACHINERY: THREE-DIMENSIONAL NMR STUDIES OF THE NUCLEIC-ACID BINDING DOMAIN OF TRANSCRIPTIONAL ELONGATION FACTOR TFIIS
; |
12.1 |
50.2 |
SOLUTION NMR |
REASONABLE
|
| 1tfj |
Crystal structure of Bovine Glycolipid transfer protein in complex with a fatty acid |
18.9 |
62.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1tfk |
Ribonuclease from Escherichia coli complexed with its inhibtor protein |
17.1 |
58.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1tfm |
CRYSTAL STRUCTURE OF A RIBOSOME INACTIVATING PROTEIN IN ITS NATURALLY INHIBITED FORM |
26.2 |
85.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1tfn |
STRUCTURE REFINEMENT FOR A 24-NUCLEOTIDE RNA HAIRPIN, NMR, MINIMIZED AVERAGE STRUCTURE |
13.6 |
46.6 |
SOLUTION NMR |
GOOD
|
| 1tfo |
Ribonuclease from Escherichia coli complexed with its inhibitor protein |
17.2 |
54.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1tfp |
TRANSTHYRETIN (FORMERLY KNOWN AS PREALBUMIN) |
18.8 |
58.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1tfq |
NMR Structure of an Antagonists of the XIAP-Caspase-9 Interaction Complexed to the BIR3 domain of XIAP |
18.4 |
70.1 |
SOLUTION NMR |
GOOD
|
| 1tfr |
RNASE H FROM BACTERIOPHAGE T4 |
21.3 |
70.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1tfs |
;NMR AND RESTRAINED MOLECULAR DYNAMICS STUDY OF THE THREE-DIMENSIONAL SOLUTION STRUCTURE OF TOXIN FS2, A SPECIFIC BLOCKER OF THE L-TYPE CALCIUM CHANNEL, ISOLATED FROM BLACK MAMBA VENOM
; |
10.7 |
33.7 |
SOLUTION NMR |
REASONABLE
|
| 1tft |
NMR Structure of an Antagonists of the XIAP-Caspase-9 Interaction Complexed to the BIR3 domain of XIAP |
18.2 |
67.3 |
SOLUTION NMR |
GOOD
|
| 1tfu |
phosphopantetheine adenylyltransferase from Mycobacterium tuberculosis |
16.7 |
54.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1tfv |
CRYSTAL STRUCTURE OF A BUFFALO SIGNALING GLYCOPROTEIN (SPB-40) SECRETED DURING INVOLUTION |
21.6 |
70.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1tfw |
;How CCA is added to the 3' end of immature tRNA without the use of an oligonucleotide template
; |
49.5 |
183.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1tfx |
COMPLEX OF THE SECOND KUNITZ DOMAIN OF TISSUE FACTOR PATHWAY INHIBITOR WITH PORCINE TRYPSIN |
32.4 |
109.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1tfy |
;How CCA is added to the 3' end of immature tRNA without the use of an oligonucleotide template
; |
48.8 |
180.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1tfz |
;Structural basis for herbicidal inhibitor selectivity revealed by comparison of crystal structures of plant and mammalian 4-hydroxyphenylpyruvate dioxygenases
; |
21.5 |
72.8 |
X-RAY DIFFRACTION |
GOOD
|