| 2f6w |
Protein tyrosine phosphatase 1B with sulfamic acid inhibitors |
1 |
1 |
X-RAY DIFFRACTION |
| 2f6x |
Crystal Structure of (S)-3-O-Geranylgeranylglyceryl Phosphate Synthase complexed with sn-G1P and MPD |
1 |
1 |
X-RAY DIFFRACTION |
| 2f6y |
Protein tyrosine phosphatase 1B with sulfamic acid inhibitors |
1 |
1 |
X-RAY DIFFRACTION |
| 2f6z |
Protein tyrosine phosphatase 1B with sulfamic acid inhibitors |
1 |
1 |
X-RAY DIFFRACTION |
| 2f70 |
Protein tyrosine phosphatase 1B with sulfamic acid inhibitors |
1 |
1 |
X-RAY DIFFRACTION |
| 2f71 |
Protein tyrosine phosphatase 1B with sulfamic acid inhibitors |
1 |
1 |
X-RAY DIFFRACTION |
| 2f73 |
Crystal structure of human fatty acid binding protein 1 (FABP1) |
8 |
8 |
X-RAY DIFFRACTION |
| 2f74 |
Murine MHC class I H-2Db in complex with human b2-microglobulin and LCMV-derived immunodminant peptide gp33 |
2 |
2 |
X-RAY DIFFRACTION |
| 2f76 |
Solution structure of the M-PMV wild type matrix protein (p10) |
20 |
20 |
SOLUTION NMR |
| 2f77 |
Solution structure of the R55F mutant of M-PMV matrix protein (p10) |
18 |
18 |
SOLUTION NMR |
| 2f78 |
BenM effector binding domain with its effector benzoate |
1 |
1 |
X-RAY DIFFRACTION |
| 2f7a |
BenM effector binding domain with its effector, cis,cis-muconate |
1 |
1 |
X-RAY DIFFRACTION |
| 2f7b |
CatM effector binding domain |
2 |
2 |
X-RAY DIFFRACTION |
| 2f7c |
CatM effector binding domain with its effector cis,cis-muconate |
1 |
1 |
X-RAY DIFFRACTION |
| 2f7d |
A mutant rabbit cathepsin K with a nitrile inhibitor |
1 |
1 |
X-RAY DIFFRACTION |
| 2f7e |
PKA complexed with (S)-2-(1H-Indol-3-yl)-1-(5-isoquinolin-6-yl-pyridin-3-yloxymethyl-etylamine |
1 |
1 |
X-RAY DIFFRACTION |
| 2f7f |
Crystal structure of Enterococcus faecalis putative nicotinate phosphoribosyltransferase, NEW YORK STRUCTURAL GENOMICS CONSORTIUM |
1 |
1 |
X-RAY DIFFRACTION |
| 2f7i |
Human transthyretin (TTR) complexed with diflunisal analogues- TTR. 2',6'-Difluorobiphenyl-4-carboxylic Acid |
1 |
1 |
X-RAY DIFFRACTION |
| 2f7k |
Crystal Structure of Human Pyridoxal Kinase |
1 |
1 |
X-RAY DIFFRACTION |
| 2f7l |
Crystal structure of Sulfolobus tokodaii phosphomannomutase/phosphoglucomutase |
3 |
3 |
X-RAY DIFFRACTION |
| 2f7m |
Crystal Structure of Unliganded Human FPPS |
1 |
1 |
X-RAY DIFFRACTION |
| 2f7n |
Structure of D. radiodurans Dps-1 |
2 |
2 |
X-RAY DIFFRACTION |
| 2f7o |
Golgi alpha-mannosidase II complex with mannostatin A |
1 |
1 |
X-RAY DIFFRACTION |
| 2f7p |
Golgi alpha-mannosidase II complex with benzyl-mannostatin A |
1 |
1 |
X-RAY DIFFRACTION |
| 2f7q |
Golgi alpha-mannosidase II complex with aminocyclopentitetrol |
1 |
1 |
X-RAY DIFFRACTION |
| 2f7r |
Golgi alpha-mannosidase II complex with benzyl-aminocyclopentitetrol |
1 |
1 |
X-RAY DIFFRACTION |
| 2f7s |
The crystal structure of human Rab27b bound to GDP |
1 |
1 |
X-RAY DIFFRACTION |
| 2f7t |
Crystal structure of the catalytic domain of Mos1 mariner transposase |
1 |
1 |
X-RAY DIFFRACTION |
| 2f7v |
Structure of acetylcitrulline deacetylase complexed with one Co |
1 |
1 |
X-RAY DIFFRACTION |
| 2f7w |
Crystal structure of Molybdenum cofactor biosynthesis protein Mog from Shewanella oneidensis |
1 |
1 |
X-RAY DIFFRACTION |
| 2f7x |
Protein Kinase A bound to (S)-2-(1H-Indol-3-yl)-1-[5-((E)-2-pyridin-4-yl-vinyl)-pyridin-3-yloxymethyl]-ethylamine |
1 |
1 |
X-RAY DIFFRACTION |
| 2f7y |
Crystal structure of Molybdenum cofactor biosynthesis protein Mog from Shewanella oneidensis |
1 |
1 |
X-RAY DIFFRACTION |
| 2f7z |
Protein Kinase A bound to (R)-1-(1H-Indol-3-ylmethyl)-2-(2-pyridin-4-yl-[1,7]naphtyridin-5-yloxy)-ehylamine |
1 |
1 |
X-RAY DIFFRACTION |
| 2f80 |
HIV-1 Protease mutant D30N complexed with inhibitor TMC114 |
2 |
2 |
X-RAY DIFFRACTION |
| 2f81 |
HIV-1 Protease mutant L90M complexed with inhibitor TMC114 |
1 |
1 |
X-RAY DIFFRACTION |
| 2f82 |
HMG-CoA synthase from Brassica juncea in the apo-form |
2 |
2 |
X-RAY DIFFRACTION |
| 2f84 |
Crystal Structure of an orotidine-5'-monophosphate decarboxylase homolog from P.falciparum |
1 |
1 |
X-RAY DIFFRACTION |
| 2f86 |
The Association Domain of C. elegans CaMKII |
1 |
1 |
X-RAY DIFFRACTION |
| 2f87 |
Solution structure of a GAAG tetraloop in SRP RNA from Pyrococcus furiosus |
13 |
13 |
SOLUTION NMR |
| 2f88 |
Solution NMR structure of domain 5 from the Pyaiella littoralis (PL) group II intron |
10 |
10 |
SOLUTION NMR |
| 2f89 |
Crystal structure of human FPPS in complex with pamidronate |
1 |
1 |
X-RAY DIFFRACTION |
| 2f8a |
Crystal structure of the selenocysteine to glycine mutant of human glutathione peroxidase 1 |
1 |
1 |
X-RAY DIFFRACTION |
| 2f8b |
NMR structure of the C-terminal domain (dimer) of HPV45 oncoprotein E7 |
15 |
15 |
SOLUTION NMR |
| 2f8c |
Crystal structure of FPPS in complex with Zoledronate |
1 |
1 |
X-RAY DIFFRACTION |
| 2f8d |
BenM effector-Binding domain crystallized from high pH conditions |
1 |
1 |
X-RAY DIFFRACTION |
| 2f8e |
Foot and Mouth Disease Virus RNA-dependent RNA polymerase in complex with uridylylated VPg protein |
1 |
1 |
X-RAY DIFFRACTION |
| 2f8f |
Crystal structure of the Y10F mutant of the gluathione s-transferase from schistosoma haematobium |
2 |
2 |
X-RAY DIFFRACTION |
| 2f8g |
HIV-1 protease mutant I50V complexed with inhibitor TMC114 |
1 |
1 |
X-RAY DIFFRACTION |
| 2f8h |
Structure of acetylcitrulline deacetylase from Xanthomonas campestris in metal-free form |
1 |
1 |
X-RAY DIFFRACTION |
| 2f8i |
Human transthyretin (TTR) complexed with Benzoxazole |
2 |
2 |
X-RAY DIFFRACTION |