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1E67
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BU of 1e67 by Molmil
Zn-Azurin from Pseudomonas aeruginosa
Descriptor: AZURIN, NITRATE ION, ZINC ION
Authors:Nar, H, Messerschmidt, A.
Deposit date:2000-08-09
Release date:2000-08-16
Last modified:2017-07-12
Method:X-RAY DIFFRACTION (2.14 Å)
Cite:Characterization and Crystal Structure of Zinc Azurin, a by-Product of Heterologous Expression in Escherichia Coli of Pseudomonas Aeruginosa Copper Azurin
Eur.J.Biochem., 205, 1992
1E65
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Azurin from Pseudomonas aeruginosa, apo form
Descriptor: AZURIN
Authors:Nar, H, Messerschmidt, A.
Deposit date:2000-08-08
Release date:2000-08-16
Last modified:2017-07-12
Method:X-RAY DIFFRACTION (1.85 Å)
Cite:Crystal Structure of Pseudomonas Aeruginosa Apo-Azurin at 1.85 A Resolution.
FEBS Lett., 306, 1992
1E5Z
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BU of 1e5z by Molmil
Azurin from Pseudomonas aeruginosa, reduced form, pH 9.0
Descriptor: AZURIN, COPPER (II) ION, NITRATE ION
Authors:Nar, H, Messerschmidt, A.
Deposit date:2000-08-04
Release date:2000-08-19
Last modified:2017-07-05
Method:X-RAY DIFFRACTION (2 Å)
Cite:Rontgenkristallographische Strukturaufklarung Von Azurin Aus Pseudomonas Aeruginosa
Ph.D. Thesis, 1992
1E5Y
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BU of 1e5y by Molmil
Azurin from Pseudomonas aeruginosa, reduced form, pH 5.5
Descriptor: AZURIN, COPPER (II) ION, NITRATE ION
Authors:Nar, H, Messerschmidt, A.
Deposit date:2000-08-04
Release date:2000-08-19
Last modified:2017-07-12
Method:X-RAY DIFFRACTION (2 Å)
Cite:Rontgenkristallographische Strukturaufklarung Von Azurin Aus Pseudomonas Aeruginosa
Ph.D. Thesis, 1992
1JIZ
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BU of 1jiz by Molmil
Crystal Structure Analysis of human Macrophage Elastase MMP-12
Descriptor: CALCIUM ION, N-HYDROXY-2(R)-[[(4-METHOXYPHENYL)SULFONYL](3-PICOLYL)AMINO]-3-METHYLBUTANAMIDE HYDROCHLORIDE, ZINC ION, ...
Authors:Nar, H, Werle, K, Bauer, M.M.T, Dollinger, H, Jung, B.
Deposit date:2001-07-03
Release date:2002-07-03
Last modified:2024-02-07
Method:X-RAY DIFFRACTION (2.6 Å)
Cite:Crystal structure of human macrophage elastase (MMP-12) in complex with a hydroxamic acid inhibitor.
J.Mol.Biol., 312, 2001
1DB2
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BU of 1db2 by Molmil
CRYSTAL STRUCTURE OF NATIVE PLASMINOGEN ACTIVATOR INHIBITOR-1
Descriptor: PLASMINOGEN ACTIVATOR INHIBITOR-1
Authors:Nar, H, Bauer, M, Stassen, J.M, Lang, D, Gils, A, Declerck, P.
Deposit date:1999-11-02
Release date:1999-11-10
Last modified:2024-02-07
Method:X-RAY DIFFRACTION (2.7 Å)
Cite:Plasminogen activator inhibitor 1. Structure of the native serpin, comparison to its other conformers and implications for serpin inactivation.
J.Mol.Biol., 297, 2000
6Y0F
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BU of 6y0f by Molmil
Structure of human FAPalpha in complex with linagliptin
Descriptor: 2-acetamido-2-deoxy-beta-D-glucopyranose, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 8-[(3R)-3-Aminopiperidin-1-yl]-7-but-2-yn-1-yl-3-methyl-1-[(4-methylquinazolin-2-yl)methyl]-3,7-dihydro-1H-purine-2,6-d ione, ...
Authors:Nar, H, Schnapp, G, Schreiner, P.
Deposit date:2020-02-07
Release date:2021-02-17
Last modified:2024-01-24
Method:X-RAY DIFFRACTION (2.924 Å)
Cite:Structure of human FAPalpha in complex with linagliptin
To Be Published
1G36
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BU of 1g36 by Molmil
TRYPSIN INHIBITOR COMPLEX
Descriptor: 4-{[1-METHYL-5-(2-METHYL-BENZOIMIDAZOL-1-YLMETHYL)-1H-BENZOIMIDAZOL-2-YLMETHYL]-AMINO}-BENZAMIDINE, CALCIUM ION, SULFATE ION, ...
Authors:Nar, H.
Deposit date:2000-10-23
Release date:2001-10-23
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (1.9 Å)
Cite:Structural basis for inhibition promiscuity of dual specific thrombin and factor Xa blood coagulation inhibitors.
Structure, 9, 2001
1G2M
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FACTOR XA INHIBITOR COMPLEX
Descriptor: 4-{[1-METHYL-5-(2-METHYL-BENZOIMIDAZOL-1-YLMETHYL)-1H-BENZOIMIDAZOL-2-YLMETHYL]-AMINO}-BENZAMIDINE, CALCIUM ION, COAGULATION FACTOR X
Authors:Nar, H.
Deposit date:2000-10-20
Release date:2001-10-20
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (3.02 Å)
Cite:Structural basis for inhibition promiscuity of dual specific thrombin and factor Xa blood coagulation inhibitors.
Structure, 9, 2001
1G32
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THROMBIN INHIBITOR COMPLEX
Descriptor: 4-{[1-METHYL-5-(2-METHYL-BENZOIMIDAZOL-1-YLMETHYL)-1H-BENZOIMIDAZOL-2-YLMETHYL]-AMINO}-BENZAMIDINE, HIRUDIN IIB, PROTHROMBIN
Authors:Nar, H.
Deposit date:2000-10-23
Release date:2001-10-23
Last modified:2013-03-13
Method:X-RAY DIFFRACTION (1.9 Å)
Cite:Structural basis for inhibition promiscuity of dual specific thrombin and factor Xa blood coagulation inhibitors.
Structure, 9, 2001
1G2L
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FACTOR XA INHIBITOR COMPLEX
Descriptor: CALCIUM ION, COAGULATION FACTOR X, [(1-{2[(4-CARBAMIMIDOYL-PHENYLAMINO)-METHYL]-1-METHYL-1H-BENZOIMIDAZOL-5-YL}-CYCLOPROPYL)-PYRIDIN-2-YL-METHYLENEAMINOOXY]-ACETIC ACID ETHYL ESTER
Authors:Nar, H.
Deposit date:2000-10-20
Release date:2001-10-20
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (1.9 Å)
Cite:Structural basis for inhibition promiscuity of dual specific thrombin and factor Xa blood coagulation inhibitors.
Structure, 9, 2001
1G30
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THROMBIN INHIBITOR COMPLEX
Descriptor: HIRUDIN IIB, PROTHROMBIN, [(1-{2[(4-CARBAMIMIDOYL-PHENYLAMINO)-METHYL]-1-METHYL-1H-BENZOIMIDAZOL-5-YL}-CYCLOPROPYL)-PYRIDIN-2-YL-METHYLENEAMINOOXY]-ACETIC ACID ETHYL ESTER
Authors:Nar, H.
Deposit date:2000-10-23
Release date:2001-10-23
Last modified:2018-10-03
Method:X-RAY DIFFRACTION (2 Å)
Cite:Structural basis for inhibition promiscuity of dual specific thrombin and factor Xa blood coagulation inhibitors.
Structure, 9, 2001
6TL9
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CRYSTAL STRUCTURE OF LECTIN-LIKE OX-LDL RECEPTOR 1 IN COMPLEX WITH BI-0115
Descriptor: 9-chloranyl-5-propyl-11~{H}-pyrido[2,3-b][1,4]benzodiazepin-6-one, GLYCEROL, Oxidized low-density lipoprotein receptor 1
Authors:Nar, H, Fiegen, D, Schnapp, G.
Deposit date:2019-12-02
Release date:2020-07-22
Last modified:2024-01-24
Method:X-RAY DIFFRACTION (2.734 Å)
Cite:A small-molecule inhibitor of lectin-like oxidized LDL receptor-1 acts by stabilizing an inactive receptor tetramer state
Commun Chem, 2020
6TLA
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BU of 6tla by Molmil
CRYSTAL STRUCTURE OF LECTIN-LIKE OX-LDL RECEPTOR 1 (C 1 2 1)
Descriptor: 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, Oxidized low-density lipoprotein receptor 1
Authors:Nar, H, Fiegen, D, Schnapp, G.
Deposit date:2019-12-02
Release date:2020-07-22
Last modified:2024-01-24
Method:X-RAY DIFFRACTION (2.16 Å)
Cite:A small-molecule inhibitor of lectin-like oxidized LDL receptor-1 acts by stabilizing an inactive receptor tetramer state
Commun Chem, 2020
4AZU
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BU of 4azu by Molmil
CRYSTAL STRUCTURE ANALYSIS OF OXIDIZED PSEUDOMONAS AERUGINOSA AZURIN AT PH 5.5 AND PH 9.0. A PH-INDUCED CONFORMATIONAL TRANSITION INVOLVES A PEPTIDE BOND FLIP
Descriptor: AZURIN, COPPER (II) ION, NITRATE ION
Authors:Nar, H, Messerschmidt, A, Huber, R.
Deposit date:1993-06-23
Release date:1994-01-31
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (1.9 Å)
Cite:Crystal structure analysis of oxidized Pseudomonas aeruginosa azurin at pH 5.5 and pH 9.0. A pH-induced conformational transition involves a peptide bond flip.
J.Mol.Biol., 221, 1991
6TL7
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BU of 6tl7 by Molmil
CRYSTAL STRUCTURE OF LECTIN-LIKE OX-LDL RECEPTOR 1 (P212121)
Descriptor: NICKEL (II) ION, Oxidized low-density lipoprotein receptor 1
Authors:Nar, H, Fiegen, D, Schnapp, G.
Deposit date:2019-12-02
Release date:2020-07-22
Last modified:2024-01-24
Method:X-RAY DIFFRACTION (1.11 Å)
Cite:A small-molecule inhibitor of lectin-like oxidized LDL receptor-1 acts by stabilizing an inactive receptor tetramer state
Commun Chem, 2020
1OYQ
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BU of 1oyq by Molmil
TRYPSIN INHIBITOR COMPLEX
Descriptor: CALCIUM ION, SULFATE ION, Trypsin, ...
Authors:Nar, H.
Deposit date:2003-04-07
Release date:2003-04-29
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (1.9 Å)
Cite:Structural Basis for Inhibition Promiscuity of Dual Specific Thrombin and Factor Xa Blood Coagulation Inhibitors
Structure, 9, 2001
1GTP
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BU of 1gtp by Molmil
GTP CYCLOHYDROLASE I
Descriptor: GTP CYCLOHYDROLASE I, SULFATE ION
Authors:Nar, H, Huber, R, Meining, W, Bacher, A.
Deposit date:1995-09-16
Release date:1996-11-08
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (3 Å)
Cite:Atomic structure of GTP cyclohydrolase I.
Structure, 3, 1995
1GTQ
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BU of 1gtq by Molmil
6-PYRUVOYL TETRAHYDROPTERIN SYNTHASE
Descriptor: 6-PYRUVOYL TETRAHYDROPTERIN SYNTHASE, ZINC ION
Authors:Nar, H, Huber, R, Heizmann, C.W, Thoeny, B, Buergisser, D.
Deposit date:1995-09-16
Release date:1996-04-03
Last modified:2024-02-07
Method:X-RAY DIFFRACTION (2.3 Å)
Cite:Three-dimensional structure of 6-pyruvoyl tetrahydropterin synthase, an enzyme involved in tetrahydrobiopterin biosynthesis.
EMBO J., 13, 1994
5AZU
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BU of 5azu by Molmil
CRYSTAL STRUCTURE ANALYSIS OF OXIDIZED PSEUDOMONAS AERUGINOSA AZURIN AT PH 5.5 AND PH 9.0. A PH-INDUCED CONFORMATIONAL TRANSITION INVOLVES A PEPTIDE BOND FLIP
Descriptor: AZURIN, COPPER (II) ION, NITRATE ION
Authors:Nar, H, Messerschmidt, A, Huber, R.
Deposit date:1993-06-23
Release date:1994-01-31
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (1.9 Å)
Cite:Crystal structure analysis of oxidized Pseudomonas aeruginosa azurin at pH 5.5 and pH 9.0. A pH-induced conformational transition involves a peptide bond flip.
J.Mol.Biol., 221, 1991
2AZU
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BU of 2azu by Molmil
X-RAY CRYSTAL STRUCTURE OF THE TWO SITE-SPECIFIC MUTANTS HIS35*GLN AND HIS35*LEU OF AZURIN FROM PSEUDOMONAS AERUGINOSA
Descriptor: AZURIN, COPPER (II) ION, NITRATE ION
Authors:Nar, H, Messerschmidt, A, Huber, R.
Deposit date:1991-01-11
Release date:1993-07-15
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (1.9 Å)
Cite:X-ray crystal structure of the two site-specific mutants His35Gln and His35Leu of azurin from Pseudomonas aeruginosa.
J.Mol.Biol., 218, 1991
3NJW
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BU of 3njw by Molmil
First High Resolution Crystal Structure of a Lasso Peptide
Descriptor: Bicyclic peptide BI-32169
Authors:Nar, H, Schmid, A, Puder, C, Potterat, O.
Deposit date:2010-06-18
Release date:2010-09-01
Last modified:2011-08-10
Method:X-RAY DIFFRACTION (0.86 Å)
Cite:High-resolution crystal structure of a lasso Peptide.
Chemmedchem, 5, 2010
8P01
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Crystal structure of human STING ectodomain in complex with BI 7446, a potent cyclic dinucleotide STING agonist with broad-spectrum variant activity for the treatment of cancer
Descriptor: 3-[(1~{R},3~{R},6~{R},8~{R},9~{R},10~{R},12~{R},15~{R},17~{R},18~{R})-8-(6-aminopurin-9-yl)-9-fluoranyl-18-oxidanyl-3,12-bis(oxidanylidene)-3,12-bis(sulfanyl)-2,4,7,11,13,16-hexaoxa-3$l^{5},12$l^{5}-diphosphatricyclo[13.2.1.0^{6,10}]octadecan-17-yl]-6~{H}-imidazo[4,5-d]pyridazin-7-one, Stimulator of interferon genes protein
Authors:Nar, H.
Deposit date:2023-05-09
Release date:2023-07-26
Last modified:2023-08-09
Method:X-RAY DIFFRACTION (2.094 Å)
Cite:Discovery of BI 7446: A Potent Cyclic Dinucleotide STING Agonist with Broad-Spectrum Variant Activity for the Treatment of Cancer.
J.Med.Chem., 66, 2023
1KTS
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BU of 1kts by Molmil
Thrombin Inhibitor Complex
Descriptor: 3-({2-[(4-CARBAMIMIDOYL-PHENYLAMINO)-METHYL]-3-METHYL-3H-BENZOIMIDAZOLE-5-CARBONYL}-PYRIDIN-2-YL-AMINO)-PROPIONIC ACID ETHYL ESTER, hirudin IIB, thrombin
Authors:Nar, H.
Deposit date:2002-01-17
Release date:2002-02-06
Last modified:2013-03-13
Method:X-RAY DIFFRACTION (2.4 Å)
Cite:Structure-based design of novel potent nonpeptide thrombin inhibitors.
J.Med.Chem., 45, 2002
1KTT
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Thrombin inhibitor complex
Descriptor: 4-(5-BENZENESULFONYLAMINO-1-METHYL-1H-BENZOIMIDAZOL-2-YLMETHYL)-BENZAMIDINE, hirudin IIB, thrombin
Authors:Nar, H.
Deposit date:2002-01-17
Release date:2002-02-06
Last modified:2013-03-13
Method:X-RAY DIFFRACTION (2.1 Å)
Cite:Structure-based design of novel potent nonpeptide thrombin inhibitors.
J.Med.Chem., 45, 2002

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