PDB: 10 resultsInfo pagesStatus searchChemie searchBIRD

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2PSG	REFINED STRUCTURE OF PORCINE PEPSINOGEN AT 1.8 ANGSTROMS RESOLUTION Descriptor: PEPSINOGEN Authors: James, M.N.G, Sielecki, A.R. Deposit date: 1991-01-23 Release date: 1992-10-15 Last modified: 2011-07-13 Method: X-RAY DIFFRACTION (1.8 Å) Cite: Refined structure of porcine pepsinogen at 1.8 A resolution. J.Mol.Biol., 219, 1991
3PSG	THE HIGH RESOLUTION CRYSTAL STRUCTURE OF PORCINE PEPSINOGEN Descriptor: PEPSINOGEN Authors: Hartsuck, J.A, Koelsch, G, Remington, S.J. Deposit date: 1991-09-03 Release date: 1993-01-15 Last modified: 2011-07-13 Method: X-RAY DIFFRACTION (1.65 Å) Cite: The high-resolution crystal structure of porcine pepsinogen. Proteins, 13, 1992
1HTR	CRYSTAL AND MOLECULAR STRUCTURES OF HUMAN PROGASTRICSIN AT 1.62 ANGSTROMS RESOLUTION Descriptor: GASTRICSIN, PROGASTRICSIN (PRO SEGMENT) Authors: Moore, S.A, Sielecki, A.R, James, M.N.G. Deposit date: 1994-10-21 Release date: 1995-01-26 Last modified: 2011-07-13 Method: X-RAY DIFFRACTION (1.62 Å) Cite: Crystal and molecular structures of human progastricsin at 1.62 A resolution. J.Mol.Biol., 247, 1995
1AVF	ACTIVATION INTERMEDIATE 2 OF HUMAN GASTRICSIN FROM HUMAN STOMACH Descriptor: GASTRICSIN, SODIUM ION Authors: Khan, A.R, Cherney, M.M, Tarasova, N.I, James, M.N.G. Deposit date: 1997-09-16 Release date: 1998-02-25 Last modified: 2023-08-02 Method: X-RAY DIFFRACTION (2.36 Å) Cite: Structural characterization of activation 'intermediate 2' on the pathway to human gastricsin. Nat.Struct.Biol., 4, 1997
1TZS	Crystal Structure of an activation intermediate of Cathepsin E Descriptor: 23-mer peptide from PelB-IgG kappa light chain fusion protein, Cathepsin E, activation peptide from Cathepsin E Authors: Ostermann, N, Gerhartz, B, Worpenberg, S, Trappe, J, Eder, J. Deposit date: 2004-07-12 Release date: 2005-07-12 Last modified: 2023-10-25 Method: X-RAY DIFFRACTION (2.35 Å) Cite: Crystal structure of an activation intermediate of cathepsin e J.Mol.Biol., 342, 2004
2X0B	Crystal structure of human angiotensinogen complexed with renin Descriptor: ANGIOTENSINOGEN, RENIN Authors: Zhou, A, Wei, Z, Yan, Y, Carrell, R.W, Read, R.J. Deposit date: 2009-12-08 Release date: 2010-10-20 Last modified: 2023-12-20 Method: X-RAY DIFFRACTION (4.33 Å) Cite: A Redox Switch in Angiotensinogen Modulates Angiotensin Release. Nature, 468, 2010
3VCM	Crystal structure of human prorenin Descriptor: 2-acetamido-2-deoxy-beta-D-glucopyranose, prorenin Authors: Morales, R, Watier, Y, Bocskei, Z. Deposit date: 2012-01-04 Release date: 2012-05-23 Last modified: 2024-03-06 Method: X-RAY DIFFRACTION (2.93 Å) Cite: Human Prorenin Structure Sheds Light on a Novel Mechanism of Its Autoinhibition and on Its Non-Proteolytic Activation by the (Pro)renin Receptor. J.Mol.Biol., 421, 2012
4AMT	Crystal structure at 2.6A of human prorenin Descriptor: RENIN, SULFATE ION, beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-[alpha-L-fucopyranose-(1-6)]2-acetamido-2-deoxy-beta-D-glucopyranose Authors: Zhou, A. Deposit date: 2012-03-13 Release date: 2013-03-20 Last modified: 2023-12-20 Method: X-RAY DIFFRACTION (2.6 Å) Cite: The Crystal Structure of Prorenin To be Published
5MKT	Crystal structure of mouse prorenin Descriptor: 2-acetamido-2-deoxy-beta-D-glucopyranose, Renin-1 Authors: Yan, Y, Read, R. Deposit date: 2016-12-05 Release date: 2017-12-20 Last modified: 2024-01-17 Method: X-RAY DIFFRACTION (3.2 Å) Cite: Crystal structure of mouse prorenin To Be Published
5UX4	Crystal Structure of Rat Cathepsin D with (5S)-3-(5,6-dihydro-2H-pyran-3-yl)-1-fluoro- 7-(2-fluoropyridin-3-yl)spiro[chromeno[2,3- c]pyridine-5,4'-[1,3]oxazol]-2'-amine Descriptor: (5S)-3-(5,6-dihydro-2H-pyran-3-yl)-1-fluoro-7-(2-fluoropyridin-3-yl)spiro[chromeno[2,3-c]pyridine-5,4'-[1,3]oxazol]-2'-amine, 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... Authors: Sickmier, A. Deposit date: 2017-02-22 Release date: 2018-06-13 Last modified: 2023-10-04 Method: X-RAY DIFFRACTION (2.805 Å) Cite: Development of 2-aminooxazoline 3-azaxanthene beta-amyloid cleaving enzyme (BACE) inhibitors with improved selectivity against Cathepsin D. Medchemcomm, 8, 2017