| 2ami |
Solution Structure Of The Calcium-loaded N-Terminal Sensor Domain Of Centrin |
12.7 |
43.7 |
SOLUTION NMR |
GOOD
|
| 2amj |
Crystal Structure of Modulator of Drug Activity B from Escherichia coli O157:H7 |
32.0 |
110.3 |
X-RAY DIFFRACTION |
GOOD
|
| 2aml |
Crystal structure of Lmo0035 protein (46906266) from LISTERIA MONOCYTOGENES 4b F2365 at 1.50 A resolution |
26.0 |
79.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2amm |
Crystal structure of L122V/L132V mutant of nitrophorin 2 |
16.5 |
48.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2amn |
Solution structure of Fowlicidin-1, a novel Cathelicidin antimicrobial peptide from chicken |
11.6 |
30.2 |
SOLUTION NMR |
REASONABLE
|
| 2amo |
Loose Dimer of a Bacillus subtilis Nitric Oxide Synthase |
36.9 |
124.4 |
X-RAY DIFFRACTION |
GOOD
|
| 2amp |
Crystal Structure Of Porcine Transmissible Gastroenteritis Virus Mpro in Complex with an Inhibitor N1 |
26.4 |
82.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2amq |
Crystal Structure Of SARS_CoV Mpro in Complex with an Inhibitor N3 |
26.4 |
81.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2ams |
Structure of the oxidized Hipip from thermochromatium tepidum at 1.4 angstrom resolution |
12.5 |
40.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2amt |
Structure of 2C-Methyl-D-Erythritol 2,4-Clycodiphosphate Synthase complexed with a CDP derived fluorescent inhibitor |
30.1 |
94.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2amu |
CRYSTAL STRUCTURE OF A PUTATIVE SUPEROXIDE REDUCTASE (TM0658) FROM THERMOTOGA MARITIMA AT 2.00 A RESOLUTION |
17.4 |
61.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2amv |
THE STRUCTURE OF GLYCOGEN PHOSPHORYLASE B WITH AN ALKYL-DIHYDROPYRIDINE-DICARBOXYLIC ACID |
28.6 |
90.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2amx |
Crystal structure of Plasmodium Yoelii Adenosine deaminase (PY02076) |
— |
— |
X-RAY DIFFRACTION |
—
|
| 2amy |
X-Ray Structure of Human Phosphomannomutase 2 (PMM2) |
20.6 |
66.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2an0 |
Crystal Structure of the P332G mutant of the Bacillus subtilis NOS |
22.9 |
80.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2an1 |
Structural Genomics, The crystal structure of a putative kinase from Salmonella typhimurim LT2 |
33.8 |
104.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2an2 |
P332G, A333S Double mutant of the Bacillus subtilis Nitric Oxide Synthase |
22.7 |
79.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2an3 |
Structure of PNMT with S-adenosyl-L-homocysteine and the semi-rigid analogue acceptor substrate cis-(1R,2S)-2-amino-1-tetralol. |
28.3 |
96.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2an4 |
Structure of PNMT complexed with S-adenosyl-L-homocysteine and the acceptor substrate octopamine |
28.4 |
94.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2an5 |
Structure of human PNMT complexed with S-adenosyl-homocysteine and an inhibitor, trans-(1S,2S)-2-amino-1-tetralol |
28.3 |
100.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2an6 |
Protein-peptide complex |
31.9 |
108.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2an7 |
Solution structure of the bacterial antidote ParD |
22.5 |
78.1 |
SOLUTION NMR |
REASONABLE
|
| 2an9 |
Crystal Structure Of Oligomeric E.coli Guanylate Kinase In Complex With GDP |
26.7 |
88.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2ana |
THE CRYSTAL STRUCTURE OF D(G-G-G-G-C-C-C-C). A MODEL FOR POLY(DG).POLY(DC) |
11.1 |
36.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2anb |
Crystal Structure Of Oligomeric E.coli Guanylate Kinase In Complex With GMP |
18.9 |
76.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2anc |
Crystal Structure Of Unliganded Form Of Oligomeric E.coli Guanylate Kinase |
33.6 |
100.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2ane |
Crystal structure of N-terminal domain of E.Coli Lon Protease |
36.9 |
120.7 |
X-RAY DIFFRACTION |
GOOD
|
| 2ang |
CRYSTAL STRUCTURE OF HUMAN ANGIOGENIN OF THE MET(-1) FORM |
15.6 |
49.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2anh |
ALKALINE PHOSPHATASE (D153H) |
28.2 |
99.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2ani |
Crystal structure of the F127Y mutant of Ribonucleotide Reductase R2 from Chlamydia trachomatis |
22.0 |
82.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2anj |
;Crystal Structure of the Glur2 Ligand Binding Core (S1S2J-Y450W) Mutant in Complex With the Partial Agonist Kainic Acid at 2.1 A Resolution
; |
20.0 |
65.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2ank |
orally active thrombin inhibitors in complex with thrombin and an exosite decapeptide |
19.3 |
60.3 |
X-RAY DIFFRACTION |
GOOD
|
| 2anl |
;X-ray crystal structure of the aspartic protease plasmepsin 4 from the malarial parasite plasmodium malariae bound to an allophenylnorstatine based inhibitor
; |
31.8 |
104.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2anm |
Ternary complex of an orally active thrombin inhibitor with human thrombin and a c-terminal hirudin derived exo-sit inhibitor |
18.9 |
57.6 |
X-RAY DIFFRACTION |
GOOD
|
| 2ann |
Crystal structure (I) of Nova-1 KH1/KH2 domain tandem with 25 nt RNA hairpin |
20.7 |
70.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2ano |
Crystal structure of E.coli dihydrofolate reductase in complex with NADPH and the inhibitor MS-SH08-17 |
16.6 |
50.9 |
X-RAY DIFFRACTION |
GOOD
|
| 2anp |
Functional Glutamate 151 to Histidine mutant of the aminopeptidase from Aeromonas Proteolytica. |
18.4 |
57.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2anq |
Crystal Structure of E.coli DHFR in complex with NADPH and the inhibitor compound 10a. |
16.6 |
54.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2anr |
Crystal structure (II) of Nova-1 KH1/KH2 domain tandem with 25nt RNA hairpin |
21.3 |
72.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2ans |
ADIPOCYTE LIPID BINDING PROTEIN COMPLEXED WITH 1-ANILINO-8-NAPHTHALENE SULFONATE |
20.1 |
62.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2ant |
THE 2.6 A STRUCTURE OF ANTITHROMBIN INDICATES A CONFORMATIONAL CHANGE AT THE HEPARIN BINDING SITE |
32.7 |
107.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2anu |
Crystal structure of Predicted metal-dependent phosphoesterase (PHP family) (tm0559) from THERMOTOGA MARITIMA at 2.40 A resolution |
41.8 |
127.2 |
X-RAY DIFFRACTION |
GOOD
|
| 2anv |
crystal structure of P22 lysozyme mutant L86M |
21.7 |
69.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 2anw |
;Expression, crystallization and three-dimensional structure of the catalytic domain of human plasma kallikrein: Implications for structure-based design of protease inhibitors
; |
18.1 |
53.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 2anx |
crystal structure of bacteriophage P22 lysozyme mutant L87M |
21.7 |
72.0 |
X-RAY DIFFRACTION |
GOOD
|
| 2any |
;Expression, Crystallization and the Three-dimensional Structure of the Catalytic Domain of Human Plasma Kallikrein: Implications for Structure-Based Design of Protease Inhibitors
; |
18.3 |
57.8 |
X-RAY DIFFRACTION |
GOOD
|
| 2anz |
cytochrome c peroxidase in complex with 2,6-diaminopyridine |
19.4 |
61.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2ao2 |
;The 2.07 Angstrom crystal structure of Mycobacterium tuberculosis chorismate mutase reveals unexpected gene duplication and suggests a role in host-pathogen interactions
; |
32.1 |
111.5 |
X-RAY DIFFRACTION |
GOOD
|
| 2ao5 |
Crystal structure of an RNA duplex r(GGCGBrUGCGCU)2 with terminal and internal tandem G-U base pairs |
18.9 |
59.1 |
X-RAY DIFFRACTION |
GOOD
|
| 2ao6 |
Crystal structure of the human androgen receptor ligand binding domain bound with TIF2(iii) 740-753 peptide and R1881 |
19.1 |
59.6 |
X-RAY DIFFRACTION |
GOOD
|