| 1cjt |
;COMPLEX OF GS-ALPHA WITH THE CATALYTIC DOMAINS OF MAMMALIAN ADENYLYL CYCLASE: COMPLEX WITH BETA-L-2',3'-DIDEOXYATP, MN, AND MG
; |
32.0 |
102.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1cju |
;COMPLEX OF GS-ALPHA WITH THE CATALYTIC DOMAINS OF MAMMALIAN ADENYLYL CYCLASE: COMPLEX WITH BETA-L-2',3'-DIDEOXYATP AND MG
; |
32.1 |
100.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1cjv |
;COMPLEX OF GS-ALPHA WITH THE CATALYTIC DOMAINS OF MAMMALIAN ADENYLYL CYCLASE: COMPLEX WITH BETA-L-2',3'-DIDEOXYATP, MG, AND ZN
; |
32.0 |
102.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1cjw |
SEROTONIN N-ACETYLTRANSFERASE COMPLEXED WITH A BISUBSTRATE ANALOG |
16.5 |
55.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1cjx |
CRYSTAL STRUCTURE OF PSEUDOMONAS FLUORESCENS HPPD |
40.0 |
129.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1cjy |
HUMAN CYTOSOLIC PHOSPHOLIPASE A2 |
73.3 |
234.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1ck0 |
ANTI-ANTI-IDIOTYPIC ANTIBODY AGAINST HUMAN ANGIOTENSIN II, UNLIGANDED FORM |
25.3 |
80.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1ck1 |
STRUCTURE OF STAPHYLOCOCCAL ENTEROTOXIN C3 |
19.2 |
59.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1ck2 |
YEAST (SACCHAROMYCES CEREVISIAE) RIBOSOMAL PROTEIN L30 |
14.1 |
43.0 |
SOLUTION NMR |
GOOD
|
| 1ck3 |
N276D MUTANT OF ESCHERICHIA COLI TEM-1 BETA-LACTAMASE |
18.8 |
58.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1ck4 |
CRYSTAL STRUCTURE OF RAT A1B1 INTEGRIN I-DOMAIN. |
25.3 |
85.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1ck6 |
BINDING MODE OF SALICYLHYDROXAMIC ACID TO ARTHROMYCES RAMOSUS PEROXIDASE |
20.5 |
63.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1ck7 |
GELATINASE A (FULL-LENGTH) |
28.2 |
95.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1cka |
STRUCTURAL BASIS FOR THE SPECIFIC INTERACTION OF LYSINE-CONTAINING PROLINE-RICH PEPTIDES WITH THE N-TERMINAL SH3 DOMAIN OF C-CRK |
12.4 |
38.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1ckb |
STRUCTURAL BASIS FOR THE SPECIFIC INTERACTION OF LYSINE-CONTAINING PROLINE-RICH PEPTIDES WITH THE N-TERMINAL SH3 DOMAIN OF C-CRK |
12.2 |
36.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1ckc |
T43A MUTANT HUMAN LYSOZYME |
15.5 |
50.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1ckd |
T43V MUTANT HUMAN LYSOZYME |
15.5 |
51.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1cke |
CMP KINASE FROM ESCHERICHIA COLI FREE ENZYME STRUCTURE |
18.7 |
60.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1ckf |
T52A MUTANT HUMAN LYSOZYME |
15.5 |
50.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1ckg |
T52V MUTANT HUMAN LYSOZYME |
22.1 |
70.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1ckh |
T70V MUTANT HUMAN LYSOZYME |
15.5 |
53.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1cki |
RECOMBINANT CASEIN KINASE I DELTA TRUNCATION MUTANT CONTAINING RESIDUES 1-317 |
28.8 |
99.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1ckj |
CASEIN KINASE I DELTA TRUNCATION MUTANT CONTAINING RESIDUES 1-317 COMPLEX WITH BOUND TUNGSTATE |
28.9 |
101.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1ckk |
CALMODULIN/RAT CA2+/CALMODULIN DEPENDENT PROTEIN KINASE FRAGMENT |
16.7 |
52.1 |
SOLUTION NMR |
GOOD
|
| 1ckl |
N-TERMINAL TWO DOMAINS OF HUMAN CD46 (MEMBRANE COFACTOR PROTEIN, MCP) |
33.5 |
106.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1ckm |
STRUCTURE OF TWO DIFFERENT CONFORMATIONS OF MRNA CAPPING ENZYME IN COMPLEX WITH GTP |
27.6 |
86.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1ckn |
STRUCTURE OF GUANYLYLATED MRNA CAPPING ENZYME COMPLEXED WITH GTP |
27.4 |
86.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1cko |
STRUCTURE OF MRNA CAPPING ENZYME IN COMPLEX WITH THE CAP ANALOG GPPPG |
21.9 |
69.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1ckp |
HUMAN CYCLIN DEPENDENT KINASE 2 COMPLEXED WITH THE INHIBITOR PURVALANOL B |
20.6 |
65.8 |
X-RAY DIFFRACTION |
GOOD
|
| 1ckq |
PRE-TRANSITION STATE ECO RI ENDONUCLEASE/COGNATE DNA (TCGCGAATTCGCG) COMPLEX |
22.6 |
77.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1ckr |
;HIGH RESOLUTION SOLUTION STRUCTURE OF THE HEAT SHOCK COGNATE-70 KD SUBSTRATE BINDING DOMAIN OBTAINED BY MULTIDIMENSIONAL NMR TECHNIQUES
; |
17.0 |
72.9 |
SOLUTION NMR |
REASONABLE
|
| 1cks |
HUMAN CKSHS2 ATOMIC STRUCTURE: A ROLE FOR ITS HEXAMERIC ASSEMBLY IN CELL CYCLE CONTROL |
23.7 |
70.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1ckt |
CRYSTAL STRUCTURE OF HMG1 DOMAIN A BOUND TO A CISPLATIN-MODIFIED DNA DUPLEX |
17.4 |
56.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1cku |
AB INITIO SOLUTION AND REFINEMENT OF TWO HIGH POTENTIAL IRON PROTEIN STRUCTURES AT ATOMIC RESOLUTION |
16.5 |
55.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1ckv |
STRUCTURE OF THE SOLUBLE METHANE MONOOXYGENASE REGULATORY PROTEIN B |
21.8 |
58.8 |
SOLUTION NMR |
REASONABLE
|
| 1ckw |
;CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR: SOLUTION STRUCTURES OF PEPTIDES BASED ON THE PHE508 REGION, THE MOST COMMON SITE OF DISEASE-CAUSING DELTA-F508 MUTATION
; |
10.8 |
44.5 |
SOLUTION NMR |
REASONABLE
|
| 1ckx |
;Cystic fibrosis transmembrane conductance regulator: Solution structures of peptides based on the Phe508 region, the most common site of disease-causing Delta-F508 mutation
; |
10.8 |
44.4 |
SOLUTION NMR |
REASONABLE
|
| 1cky |
;CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR: SOLUTION STRUCTURES OF PEPTIDES BASED ON THE PHE508 REGION, THE MOST COMMON SITE OF DISEASE-CAUSING DELTA-F508 MUTATION
; |
11.4 |
30.8 |
SOLUTION NMR |
REASONABLE
|
| 1ckz |
;CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR: SOLUTION STRUCTURES OF PEPTIDES BASED ON THE PHE508 REGION, THE MOST COMMON SITE OF DISEASE-CAUSING DELTA-F508 MUTATION
; |
12.9 |
56.2 |
SOLUTION NMR |
REASONABLE
|
| 1cl0 |
CRYSTAL STRUCTURE OF REDUCED THIOREDOXIN REDUCTASE FROM ESCHERICHIA COLI. |
22.4 |
74.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1cl1 |
CYSTATHIONINE BETA-LYASE (CBL) FROM ESCHERICHIA COLI |
34.0 |
107.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1cl2 |
CYSTATHIONINE BETA-LYASE (CBL) FROM ESCHERICHIA COLI IN COMPLEX WITH AMINOETHOXYVINYLGLYCINE |
33.8 |
106.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1cl3 |
MOLECULAR INSIGHTS INTO PEBP2/CBF-SMMHC ASSOCIATED ACUTE LEUKEMIA REVEALED FROM THE THREE-DIMENSIONAL STRUCTURE OF PEBP2/CBF BETA |
17.7 |
52.6 |
SOLUTION NMR |
GOOD
|
| 1cl4 |
NUCLEOCAPSID PROTEIN FROM MASON-PFIZER MONKEY VIRUS (MPMV) |
9.0 |
31.6 |
SOLUTION NMR |
GOOD
|
| 1cl5 |
CRYSTAL STRUCTURE OF PHOSPHOLIPASE A2 FROM DABOIA RUSSELLI PULCHELLA |
19.0 |
59.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1cl6 |
CRYSTAL STRUCTURES OF FERRIC-NO COMPLEXES OF FUNGAL NITRIC OXIDE REDUCTASE AND ITS SER286 MUTANTS AT CRYOGENIC TEMPERATURE |
22.2 |
69.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1cl7 |
ANTI HIV1 PROTEASE FAB |
26.0 |
79.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1cl8 |
A PRE-TRANSITION STATE ECO RI ENDONUCLEASE/COGNATE DNA (TCGCGAPTTCGCG) COMPLEX WITH DNA BASE ANALOG PURINE (P) |
22.5 |
76.6 |
X-RAY DIFFRACTION |
GOOD
|
| 1cla |
EVIDENCE FOR TRANSITION-STATE STABILIZATION BY SERINE-148 IN THE CATALYTIC MECHANISM OF CHLORAMPHENICOL ACETYLTRANSFERASE |
18.7 |
63.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1clb |
Determination of the solution structure of apo calbindin D9K by nmr spectroscopy |
11.9 |
40.2 |
SOLUTION NMR |
GOOD
|