| 1l3i |
MT0146, THE PRECORRIN-6Y METHYLTRANSFERASE (CBIT) HOMOLOG FROM M. THERMOAUTOTROPHICUM, ADOHCY BINARY COMPLEX |
38.1 |
126.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1l3j |
Crystal Structure of Oxalate Decarboxylase Formate Complex |
24.4 |
89.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l3k |
UP1, THE TWO RNA-RECOGNITION MOTIF DOMAIN OF HNRNP A1 |
20.0 |
72.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1l3l |
Crystal structure of a bacterial quorum-sensing transcription factor complexed with pheromone and DNA |
44.1 |
155.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1l3m |
The Solution Structure of [d(CGC)r(amamam)d(TTTGCG)]2 |
13.8 |
44.6 |
SOLUTION NMR |
GOOD
|
| 1l3n |
The Solution Structure of Reduced Dimeric Copper Zinc SOD: the Structural Effects of Dimerization |
19.9 |
61.2 |
SOLUTION NMR |
EXCELLENT
|
| 1l3o |
;SOLUTION STRUCTURE DETERMINATION OF THE FULLY OXIDIZED DOUBLE MUTANT K9-10A CYTOCHROME C7 FROM DESULFUROMONAS ACETOXIDANS, ENSEMBLE OF 35 STRUCTURES
; |
11.7 |
36.4 |
SOLUTION NMR |
GOOD
|
| 1l3p |
CRYSTAL STRUCTURE OF THE FUNCTIONAL DOMAIN OF THE MAJOR GRASS POLLEN ALLERGEN Phl p 5b |
14.4 |
48.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l3q |
H. rufescens abalone shell Lustrin A consensus repeat, FPGKNVNCTSGE, pH 7.4, 1-H NMR structure |
8.1 |
26.7 |
SOLUTION NMR |
GOOD
|
| 1l3r |
Crystal Structure of a Transition State Mimic of the Catalytic Subunit of cAMP-dependent Protein Kinase |
21.0 |
66.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l3s |
Crystal Structure of Bacillus DNA Polymerase I Fragment complexed to 9 base pairs of duplex DNA. |
27.1 |
84.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1l3t |
;Crystal Structure of Bacillus DNA Polymerase I Fragment product complex with 10 base pairs of duplex DNA following addition of a single dTTP residue
; |
27.1 |
87.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l3u |
;Crystal Structure of Bacillus DNA Polymerase I Fragment product complex with 11 base pairs of duplex DNA following addition of a dTTP and a dATP residue.
; |
27.1 |
85.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l3v |
;Crystal Structure of Bacillus DNA Polymerase I Fragment product complex with 15 base pairs of duplex DNA following addition of dTTP, dATP, dCTP, and dGTP residues.
; |
27.8 |
84.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l3w |
C-cadherin Ectodomain |
62.6 |
200.1 |
X-RAY DIFFRACTION |
SUSPICIOUS
|
| 1l3x |
Solution Structure of Novel Disintegrin Salmosin |
11.3 |
39.0 |
SOLUTION NMR |
REASONABLE
|
| 1l3y |
INTEGRIN EGF-LIKE MODULE 3 FROM THE BETA-2 SUBUNIT |
9.7 |
35.1 |
SOLUTION NMR |
GOOD
|
| 1l3z |
Crystal Structure Analysis of an RNA Heptamer |
12.7 |
43.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1l40 |
CONTRIBUTIONS OF ENGINEERED SURFACE SALT BRIDGES TO THE STABILITY OF T4 LYSOZYME DETERMINED BY DIRECTED MUTAGENESIS |
17.6 |
58.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1l41 |
CONTRIBUTIONS OF ENGINEERED SURFACE SALT BRIDGES TO THE STABILITY OF T4 LYSOZYME DETERMINED BY DIRECTED MUTAGENESIS |
17.4 |
57.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1l42 |
;CUMULATIVE SITE-DIRECTED CHARGE-CHANGE REPLACEMENTS IN BACTERIOPHAGE T4 LYSOZYME SUGGEST THAT LONG-RANGE ELECTROSTATIC INTERACTIONS CONTRIBUTE LITTLE TO PROTEIN STABILITY
; |
17.6 |
58.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l43 |
;CUMULATIVE SITE-DIRECTED CHARGE-CHANGE REPLACEMENTS IN BACTERIOPHAGE T4 LYSOZYME SUGGEST THAT LONG-RANGE ELECTROSTATIC INTERACTIONS CONTRIBUTE LITTLE TO PROTEIN STABILITY
; |
17.5 |
57.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l44 |
;CUMULATIVE SITE-DIRECTED CHARGE-CHANGE REPLACEMENTS IN BACTERIOPHAGE T4 LYSOZYME SUGGEST THAT LONG-RANGE ELECTROSTATIC INTERACTIONS CONTRIBUTE LITTLE TO PROTEIN STABILITY
; |
17.4 |
57.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1l45 |
;CUMULATIVE SITE-DIRECTED CHARGE-CHANGE REPLACEMENTS IN BACTERIOPHAGE T4 LYSOZYME SUGGEST THAT LONG-RANGE ELECTROSTATIC INTERACTIONS CONTRIBUTE LITTLE TO PROTEIN STABILITY
; |
17.5 |
57.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l46 |
;CUMULATIVE SITE-DIRECTED CHARGE-CHANGE REPLACEMENTS IN BACTERIOPHAGE T4 LYSOZYME SUGGEST THAT LONG-RANGE ELECTROSTATIC INTERACTIONS CONTRIBUTE LITTLE TO PROTEIN STABILITY
; |
17.5 |
57.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1l47 |
;CUMULATIVE SITE-DIRECTED CHARGE-CHANGE REPLACEMENTS IN BACTERIOPHAGE T4 LYSOZYME SUGGEST THAT LONG-RANGE ELECTROSTATIC INTERACTIONS CONTRIBUTE LITTLE TO PROTEIN STABILITY
; |
17.5 |
57.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1l48 |
STRUCTURAL AND THERMODYNAMIC ANALYSIS OF THE PACKING OF TWO ALPHA-HELICES IN BACTERIOPHAGE T4 LYSOZYME |
17.5 |
58.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1l49 |
STRUCTURAL AND THERMODYNAMIC ANALYSIS OF THE PACKING OF TWO ALPHA-HELICES IN BACTERIOPHAGE T4 LYSOZYME |
17.5 |
58.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l4a |
X-RAY STRUCTURE OF THE NEURONAL COMPLEXIN/SNARE COMPLEX FROM THE SQUID LOLIGO PEALEI |
29.4 |
120.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l4b |
Crystal Structure of CobT in apo state |
20.5 |
70.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1l4d |
CRYSTAL STRUCTURE OF MICROPLASMINOGEN-STREPTOKINASE ALPHA DOMAIN COMPLEX |
23.3 |
75.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l4e |
;The crystal structure of CobT complexed with alpha-ribazole-5'-phosphate
; |
21.0 |
76.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l4f |
The crystal structure of CobT complexed with 4,5-dimethyl-1,2-phenylenediamine and nicotinate mononucleotide |
20.9 |
75.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l4g |
Crystal Structure of CobT complexed with 4-methylcatechol and nicotinate mononucleotide |
20.9 |
74.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l4h |
Crystal Structure of CobT complexed with indole and nicotinate mononucleotide |
20.9 |
75.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1l4i |
Crystal Structure of the Periplasmic Chaperone SfaE |
22.7 |
68.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1l4j |
Holliday Junction TCGGTACCGA with Na and Ca Binding Sites. |
15.4 |
52.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1l4k |
Crystal Structure of CobT complexed with 3,4-dimethylaniline and nicotinate mononucleotide |
20.9 |
75.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l4l |
Crystal Structure of CobT complexed with 2,5-dimethylaniline and nicotinate mononucleotide |
20.9 |
75.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l4m |
Crystal Structure of CobT complexed with 2-amino-p-cresol and nicotinate mononucleotide |
20.9 |
75.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1l4n |
Crystal Structure of CobT complexed with 2-aminophenol |
21.0 |
75.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1l4s |
Solution structure of ribosome associated factor Y |
19.8 |
53.5 |
SOLUTION NMR |
REASONABLE
|
| 1l4t |
SOLUTION NMR STRUCTURE OF THE CCK2E3 |
11.2 |
38.0 |
SOLUTION NMR |
GOOD
|
| 1l4u |
CRYSTAL STRUCTURE OF SHIKIMATE KINASE FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH MGADP AND PT(II) AT 1.8 ANGSTROM RESOLUTION |
16.5 |
49.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1l4v |
SOLUTION STRUCTURE OF SAPECIN |
9.4 |
36.3 |
SOLUTION NMR |
REASONABLE
|
| 1l4w |
NMR structure of an AChR-peptide (Torpedo Californica, alpha-subunit residues 182-202) in complex with alpha-Bungarotoxin |
15.1 |
53.3 |
SOLUTION NMR |
GOOD
|
| 1l4x |
Octameric de novo designed peptide |
15.8 |
48.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1l4y |
CRYSTAL STRUCTURE OF SHIKIMATE KINASE FROM MYCOBACTERIUM TUBERCULOSIS IN COMPLEX WITH MGADP AT 2.0 ANGSTROM RESOLUTION |
16.4 |
49.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1l4z |
X-RAY CRYSTAL STRUCTURE OF THE COMPLEX OF MICROPLASMINOGEN WITH ALPHA DOMAIN OF STREPTOKINASE IN THE PRESENCE CADMIUM IONS |
23.3 |
75.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1l50 |
STRUCTURAL AND THERMODYNAMIC ANALYSIS OF THE PACKING OF TWO ALPHA-HELICES IN BACTERIOPHAGE T4 LYSOZYME |
17.5 |
57.7 |
X-RAY DIFFRACTION |
GOOD
|