PDB_ID	PUBMED_CID	STRUCTURE TITLE	DEPOSITION DATE	RELEASE DATE	AUTHORS	CITATION TITLE	JOURNAL	YEAR	VOLUME	FIRST PAGE	LAST PAGE
1XKQ		Crystal Structure of Short-Chain Dehydrogenase/Reductase of unknown Function from Caenorhabditis Elegans with Cofactor	2004-09-29	2004-10-12	Schormann, N.,Zhou, J.,Karpova, E.,Zhang, Y.,Symersky, J.,Bunzel, B.,Huang, W.-Y.,Arabshahi, A.,Qiu, S.,Luan, C.-H.,Gray, R.,Carson, M.,Tsao, J.,Luo, M.,Johnson, D.,Lu, S.,Lin, G.,Luo, D.,Cao, Z.,Li, S.,McKinstry, A.,Shang, Q.,Chen, Y.-J.,Bray, T.,Nagy, L.,DeLucas, L.	Crystal Structure of Short-Chain Dehydrogenase/Reductase of unknown Function from Caenorhabditis Elegans with Cofactor	To be Published	0	0	0	0	
1Y1X		Structural analysis of a homolog of programmed cell death 6 protein from Leishmania major Friedlin	2004-11-19	2004-12-07	Robien, M.A.,Hol, W.G.J.,Structural Genomics of Pathogenic Protozoa Consortium (SGPP)	Structural analysis of a homolog of programmed cell death 6 protein from Leishmania major Friedlin	To be Published	0	0	0	0	
1YJ8		Initial structural analysis of Plasmodium falciparum Glycerol-3-phosphate dehydrogenase	2005-01-13	2005-02-01	Robien, M.A.,Hol, W.G.J.,Medical Structural Genomics of Pathogenic Protozoa	Initial structural analysis of Plasmodium falciparum Glycerol-3-phosphate dehydrogenase	To be Published	0	0	0	0	
1ZMS	16009714	LMP1 Protein binds to TRAF3 as a structural CD40	2005-05-10	2005-07-19	Wu, S.D.,Xie, P.,Welsh, K.,Li, C.,Ni, C.-Z.,Zhu, X.,Reed, J.C.,Satterthwait, A.C.,Bishop, G.A.,Ely, K.R.	LMP1 protein from the Epstein Barr virus is a structural CD40 decoy in B lymphocytes fro binding to TRAF3	J.Biol.Chem.	2005	39	33620	33626	
2AR1	16511295	Structure of Hypothetical protein from Leishmania major	2005-08-18	2005-08-30	Arakaki, T.,Le Trong, I.,Phizicky, E.,Quartley, E.,DeTitta, G.,Luft, J.,Lauricella, A.,Anderson, L.,Kalyuzhniy, O.,Worthey, E.,Myler, P.J.,Kim, D.,Baker, D.,Hol, W.G.,Merritt, E.A.	Structure of Lmaj006129AAA, a hypothetical protein from Leishmania major.	Acta Crystallogr.,Sect.F	2006	62	175	179	
2GQQ	17223133	Crystal Structure of E. coli Leucine-responsive regulatory protein (Lrp)	2006-04-21	2007-03-06	de Los Rios, S.,Perona, J.J.	Structure of the Escherichia coli Leucine-responsive Regulatory Protein Lrp Reveals a Novel Octameric Assembly.	J.Mol.Biol.	2007	366	1589	1602	
2PPA	18358002	Anaerobically manipulated wild type oxidized AfNiR bound to nitrous oxide	2007-04-28	2008-04-01	Tocheva, E.I.,Eltis, L.D.,Murphy, M.E.	Conserved active site residues limit inhibition of a copper-containing nitrite reductase by small molecules.	Biochemistry	2008	47	4452	4460	
2REZ	18388203	Tetracenomycin ARO/CYC NaI Structure	2007-09-27	2008-04-22	Ames, B.D.,Korman, T.P.,Zhang, W.,Smith, P.,Vu, T.,Tang, Y.,Tsai, S.C.	Crystal structure and functional analysis of tetracenomycin ARO/CYC: implications for cyclization specificity of aromatic polyketides.	Proc.Natl.Acad.Sci.Usa	2008	105	5349	5354	
3EZW	17441732	Crystal Structure of a Hyperactive Escherichia coli Glycerol Kinase Mutant Gly230 --> Asp Obtained Using Microfluidic Crystallization Devices	2008-10-23	2008-11-04	Anderson, M.J.,DeLabarre, B.,Raghunathan, A.,Palsson, B.O.,Brunger, A.T.,Quake, S.R.	Crystal structure of a hyperactive Escherichia coli glycerol kinase mutant Gly230 --> Asp obtained using microfluidic crystallization devices.	Biochemistry	2007	46	5722	5731	
3E13		Iron reconstituted ferric binding protein from Campylobacter jejuni	2008-08-01	2009-08-11	Tom-Yew, S.A.L.,Shilton, B.H.,Bekker, E.G.,Gaynor, E.C.,Murphy, M.E.P.	Small hinge motion by the anion-independent ferric binding protein from Campylobacter jejuni	To be Published	0	0	0	0	
2X05	19795054	Inhibition of the exo-beta-D-glucosaminidase CsxA by a glucosamine- configured castanospermine and an amino-australine analogue	2009-12-05	2009-12-15	Pluvinage, B.,Ghinet, M.G.,Brzezinski, R.,Boraston, A.B.,Stubbs, K.A.	Inhibition of the Exo-Beta-D-Glucosaminidase Csxa by a Glucosamine-Configured Castanospermine and an Amino-Australine Analogue.	Org.Biomol.Chem.	2009	7	4169	0	
4BBE	23127890	Aminoalkylpyrimidine Inhibitor Complexes with JAK2	2012-09-21	2012-11-21	Forsyth, T.,Kearney, P.C.,Kim, B.G.,Johnson, H.W.B.,Aay, N.,Arcalas, A.,Brown, D.S.,Chan, V.,Chen, J.,Du, H.,Epshteyn, S.,Galan, A.A.,Huynh, T.P.,Ibrahim, M.A.,Kane, B.,Koltun, E.,Mann, G.,Meyr, L.E.,Lee, M.S.,Lewis, G.L.,Noguchi, R.T.,Pack, M.,Ridgway, B.H.,Shi, X.,Takeuchi, C.S.,Zu, P.,Leahy, J.W.,Nuss, J.M.,Aoyama, R.,Engst, S.,Gendreau, S.B.,Kassees, R.,Li, J.,Lin, S.-H.,Martini, J.-F.,Stout, T.,Tong, P.,Woolfrey, J.,Zhang, W.,Yu, P.	Sar and in Vivo Evaluation of 4-Aryl-2-Aminoalkylpyrimidines as Potent and Selective Janus Kinase 2 (Jak2) Inhibitors	Bioorg.Med.Chem.Lett.	2012	22	7653	0