PDB ID Title official curves Structure unit Experimental Method
2we1 EBV dUTPase mutant Asp131Asn with bound dUMP 1 1 X-RAY DIFFRACTION
2we2 EBV dUTPase double mutant Gly78Asp-Asp131Ser with dUMP 1 1 X-RAY DIFFRACTION
2we3 EBV dUTPase inactive mutant deleted of motif V 1 1 X-RAY DIFFRACTION
2we4 Carbamate kinase from Enterococcus faecalis bound to a sulfate ion and two water molecules, which mimic the substrate carbamyl phosphate 2 2 X-RAY DIFFRACTION
2we5 Carbamate kinase from Enterococcus faecalis bound to MgADP 2 2 X-RAY DIFFRACTION
2we6 Crystal Structure of Plasmodium falciparum Ubiquitin Carboxyl- terminal Hydrolase 3 (UCHL3) 2 2 X-RAY DIFFRACTION
2we7 Crystal structure of Mycobacterium tuberculosis Rv0376c homologue from Mycobacterium smegmatis 2 2 X-RAY DIFFRACTION
2we8 Crystal structure of Mycobacterium tuberculosis Rv0376c homologue from Mycobacterium smegmatis 2 2 X-RAY DIFFRACTION
2we9 Crystal structure of Rv0371c from Mycobacterium tuberculosis H37Rv 2 2 X-RAY DIFFRACTION
2wea ACID PROTEINASE (PENICILLOPEPSIN) (E.C.3.4.23.20) COMPLEX WITH PHOSPHONATE INHIBITOR: METHYL[CYCLO-7[(2R)-((N-VALYL) AMINO)-2-(HYDROXYL-(1S)-1-METHYOXYCARBONYL-2-PHENYLETHOXY) PHOSPHINYLOXY-ETHYL]-1-NAPHTHALENEACETAMIDE], SODIUM SALT 1 1 X-RAY DIFFRACTION
2web ACID PROTEINASE (PENICILLOPEPSIN) (E.C.3.4.23.20) COMPLEX WITH PHOSPHONATE INHIBITOR: METHYL(2S)-[1-(((N-FORMYL)-L-VALYL)AMINO-2-(2-NAPHTHYL)ETHYL)HYDROXYPHOSPHINYLOXY]-3-PHENYLPROPANOATE, SODIUM SALT 1 1 X-RAY DIFFRACTION
2wec ACID PROTEINASE (PENICILLOPEPSIN) (E.C.3.4.23.20) COMPLEX WITH PHOSPHONATE INHIBITOR: METHYL(2S)-[1-(((N-(1-NAPHTHALENEACETYL))-L-VALYL)AMINOMETHYL)HYDROXY PHOSPHINYLOXY]-3-PHENYLPROPANOATE, SODIUM SALT 1 1 X-RAY DIFFRACTION
2wed ACID PROTEINASE (PENICILLOPEPSIN) (E.C.3.4.23.20) COMPLEX WITH PHOSPHONATE MACROCYCLIC INHIBITOR:METHYL[CYCLO-7[(2R)-((N-VALYL)AMINO)-2-(HYDROXYL-(1S)-1-METHYOXYCARBONYL-2-PHENYLETHOXY)PHOSPHINYLOXY-ETHYL]-1-NAPHTHALENEACETAMIDE], SODIUM SALT 1 1 X-RAY DIFFRACTION
2wee Crystal structure of Rv0371c from Mycobacterium tuberculosis H37Rv 2 2 X-RAY DIFFRACTION
2wef Human 3'(2'), 5'-bisphosphate nucleotidase 1 (BPNT1) in complex with AMP, PO4 and Magnesium 1 1 X-RAY DIFFRACTION
2weg Thermodynamic Optimisation of Carbonic Anhydrase Fragment Inhibitors 1 1 X-RAY DIFFRACTION
2weh Thermodynamic Optimisation of Carbonic Anhydrase Fragment Inhibitors 1 1 X-RAY DIFFRACTION
2wei Crystal structure of the kinase domain of Cryptosporidium parvum calcium dependent protein kinase in complex with 3-MB-PP1 1 1 X-RAY DIFFRACTION
2wej Thermodynamic Optimisation of Carbonic Anhydrase Fragment Inhibitors 1 1 X-RAY DIFFRACTION
2wek Crystal structure of the human MGC45594 gene product in complex with diclofenac 2 2 X-RAY DIFFRACTION
2wel Crystal structure of SU6656-bound calcium/calmodulin-dependent protein kinase II delta in complex with calmodulin 1 1 X-RAY DIFFRACTION
2weo Thermodynamic Optimisation of Carbonic Anhydrase Fragment Inhibitors 1 1 X-RAY DIFFRACTION
2wep Yeast Hsp90 N-terminal domain LI-IV mutant with ADP 1 1 X-RAY DIFFRACTION
2weq Yeast Hsp90 N-terminal domain LI-IV mutant with Geldanamycin 1 1 X-RAY DIFFRACTION
2wer Yeast Hsp90 N-terminal domain LI-IV mutant with Radicicol 2 2 X-RAY DIFFRACTION
2wes Crystal structures of mutant E46Q of tryptophan 5-halogenase (PyrH) 2 2 X-RAY DIFFRACTION
2wet Crystal structure of tryptophan 5-halogenase (PyrH) complex with FAD (tryptophan) 2 2 X-RAY DIFFRACTION
2weu Crystal structure of tryptophan 5-halogenase (PyrH) complex with substrate tryptophan 2 2 X-RAY DIFFRACTION
2wev Truncation and Optimisation of Peptide Inhibitors of CDK2, Cyclin A Through Structure Guided Design 2 2 X-RAY DIFFRACTION
2wew Crystal structure of human apoM in complex with myristic acid 1 1 X-RAY DIFFRACTION
2wex Crystal structure of human apoM in complex with glycerol 1- myristic acid 1 1 X-RAY DIFFRACTION
2wey Human PDE-papaverine complex obtained by ligand soaking of cross- linked protein crystals 2 2 X-RAY DIFFRACTION
2wez Human BACE-1 in complex with 1-ethyl-N-((1S,2R)-2-hydroxy-3-(((3-(methyloxy)phenyl)methyl)amino)-1-(phenylmethyl)propyl)-4-(2-oxo-1- pyrrolidinyl)-1H-indole-6-carboxamide 1 1 X-RAY DIFFRACTION
2wf0 Human BACE-1 in complex with 4-ethyl-N-((1S,2R)-2-hydroxy-1-(phenylmethyl)-3-(((3-(trifluoromethyl)phenyl)methyl)amino)propyl)-8-(2-oxo-1-pyrrolidinyl)-6-quinolinecarboxamide 1 1 X-RAY DIFFRACTION
2wf1 Human BACE-1 in complex with 7-ethyl-N-((1S,2R)-2-hydroxy-3-(((3-(methyloxy)phenyl(methyl)amino)-1-(phenylmethyl)propyl)-1-methyl-3,4- dihydro-1H-(1,2,5)thiadiazepino(3,4,5-hi)indole-9-carboxamide 2,2- dioxide 1 1 X-RAY DIFFRACTION
2wf2 Human BACE-1 in complex with 8-ethyl-N-((1S,2R)-2-hydroxy-3-(((3-(methyloxy)phenyl)methyl)amino)-1-(phenylmethyl)propyl)-1-methyl-3,4,7, 8-tetrahydro-1H,6H-(1,2,5)thiadiazepino(5,4,3-de)quinoxaline-10- carboxamide 2,2-dioxide 1 1 X-RAY DIFFRACTION
2wf3 Human BACE-1 in complex with 6-(ethylamino)-N-((1S,2R)-2-hydroxy-3-(((3-(methyloxy)phenyl)methyl)amino)-1-(phenylmethyl)propyl)-1-methyl-1, 3,4,5-tetrahydro-2,1-benzothiazepine-8-carboxamide 2,2-dioxide 1 1 X-RAY DIFFRACTION
2wf4 Human BACE-1 in complex with 6-ethyl-1-methyl-N-((1S)-2-oxo-1-(phenylmethyl)-3-(tetrahydro-2H-pyran-4-ylamino)propyl)-1,3,4,6- tetrahydro(1,2)thiazepino(5,4,3-cd)indole-8-carboxamide 2,2-dioxide 1 1 X-RAY DIFFRACTION
2wf5 Structure of Beta-Phosphoglucomutase inhibited with Glucose-6-phosphate and trifluoromagnesate 1 1 X-RAY DIFFRACTION
2wf6 Structure of Beta-Phosphoglucomutase inhibited with Glucose-6-phosphate and Aluminium tetrafluoride 1 1 X-RAY DIFFRACTION
2wf7 Structure of Beta-Phosphoglucomutase inhibited with Glucose-6- phosphonate and Aluminium tetrafluoride 1 1 X-RAY DIFFRACTION
2wf8 Structure of Beta-Phosphoglucomutase inhibited with Glucose-6- phosphate, Glucose-1-phosphate and Beryllium trifluoride 1 1 X-RAY DIFFRACTION
2wf9 Structure of Beta-Phosphoglucomutase inhibited with Glucose-6- phosphate, and Beryllium trifluoride, crystal form 2 1 1 X-RAY DIFFRACTION
2wfa Structure of Beta-Phosphoglucomutase inhibited with Beryllium trifluoride, in an open conformation. 1 1 X-RAY DIFFRACTION
2wfb High resolution structure of the apo form of the orange protein (ORP) from Desulfovibrio gigas 1 1 X-RAY DIFFRACTION
2wfc Crystal structure of peroxiredoxin 5 from Arenicola Marina 2 2 X-RAY DIFFRACTION
2wfd Structure of the human cytosolic leucyl-tRNA synthetase editing domain 1 1 X-RAY DIFFRACTION
2wfe Structure of the Candida albicans cytosolic leucyl-tRNA synthetase editing domain 4 4 X-RAY DIFFRACTION
2wff Equine Rhinitis A Virus 1 5 X-RAY DIFFRACTION
2wfg Structure of the Candida albicans cytosolic leucyl-tRNA synthetase editing domain bound to a benzoxaborole-AMP adduct 1 1 X-RAY DIFFRACTION