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1JUL
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BU of 1jul by Molmil
INDOLE-3-GLYCEROLPHOSPHATE SYNTHASE FROM SULFOLOBUS SOLFATARICUS IN A SECOND ORTHORHOMBIC CRYSTAL FORM
分子名称: 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, INDOLE-3-GLYCEROL PHOSPHATE SYNTHASE
著者Knoechel, T.R, Hennig, M, Merz, A, Darimont, B, Kirschner, K, Jansonius, J.N.
登録日1996-05-03
公開日1997-07-07
最終更新日2024-05-22
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献The crystal structure of indole-3-glycerol phosphate synthase from the hyperthermophilic archaeon Sulfolobus solfataricus in three different crystal forms: effects of ionic strength.
J.Mol.Biol., 262, 1996
1MEG
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BU of 1meg by Molmil
CRYSTAL STRUCTURE OF A CARICAIN D158E MUTANT IN COMPLEX WITH E-64
分子名称: CARICAIN, ETHANOL, N-[N-[1-HYDROXYCARBOXYETHYL-CARBONYL]LEUCYLAMINO-BUTYL]-GUANIDINE
著者Katerelos, N.A.
登録日1996-05-04
公開日1997-01-11
最終更新日2021-11-03
実験手法X-RAY DIFFRACTION (2 Å)
主引用文献Crystal structure of a caricain D158E mutant in complex with E-64.
FEBS Lett., 392, 1996
1GNO
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BU of 1gno by Molmil
HIV-1 PROTEASE (WILD TYPE) COMPLEXED WITH U89360E (INHIBITOR)
分子名称: HIV-1 PROTEASE, N-[[1-[N-ACETAMIDYL]-[1-CYCLOHEXYLMETHYL-2-HYDROXY-4-ISOPROPYL]-BUT-4-YL]-CARBONYL]-GLUTAMINYL-ARGINYL-AMIDE
著者Hong, L, Treharne, A, Hartsuck, J.A, Foundling, S, Tang, J.
登録日1996-05-04
公開日1996-11-08
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Crystal structures of complexes of a peptidic inhibitor with wild-type and two mutant HIV-1 proteases.
Biochemistry, 35, 1996
1GNN
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BU of 1gnn by Molmil
HIV-1 PROTEASE MUTANT WITH VAL 82 REPLACED BY ASN (V82N) COMPLEXED WITH U89360E (INHIBITOR)
分子名称: HIV-1 PROTEASE, N-[[1-[N-ACETAMIDYL]-[1-CYCLOHEXYLMETHYL-2-HYDROXY-4-ISOPROPYL]-BUT-4-YL]-CARBONYL]-GLUTAMINYL-ARGINYL-AMIDE
著者Hong, L, Treharne, A, Hartsuck, J.A, Foundling, S, Tang, J.
登録日1996-05-04
公開日1996-11-08
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Crystal structures of complexes of a peptidic inhibitor with wild-type and two mutant HIV-1 proteases.
Biochemistry, 35, 1996
1GNM
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BU of 1gnm by Molmil
HIV-1 PROTEASE MUTANT WITH VAL 82 REPLACED BY ASP (V82D) COMPLEXED WITH U89360E (INHIBITOR)
分子名称: HIV-1 PROTEASE, N-[[1-[N-ACETAMIDYL]-[1-CYCLOHEXYLMETHYL-2-HYDROXY-4-ISOPROPYL]-BUT-4-YL]-CARBONYL]-GLUTAMINYL-ARGINYL-AMIDE
著者Hong, L, Treharne, A, Hartsuck, J.A, Foundling, S, Tang, J.
登録日1996-05-04
公開日1996-11-08
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (2.3 Å)
主引用文献Crystal structures of complexes of a peptidic inhibitor with wild-type and two mutant HIV-1 proteases.
Biochemistry, 35, 1996
1KXA
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BU of 1kxa by Molmil
SINDBIS VIRUS CAPSID, (WILD-TYPE) RESIDUES 106-264, TETRAGONAL CRYSTAL FORM
分子名称: SINDBIS VIRUS CAPSID PROTEIN
著者Choi, H.-K, Rossmann, M.G.
登録日1996-05-05
公開日1996-11-08
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (3.1 Å)
主引用文献Structural analysis of Sindbis virus capsid mutants involving assembly and catalysis.
J.Mol.Biol., 262, 1996
1KXC
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BU of 1kxc by Molmil
SINDBIS VIRUS CAPSID (N190K MUTANT), TETRAGONAL CRYSTAL FORM
分子名称: SINDBIS VIRUS CAPSID PROTEIN
著者Choi, H.-K, Rossmann, M.G.
登録日1996-05-05
公開日1996-11-08
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (3.1 Å)
主引用文献Structural analysis of Sindbis virus capsid mutants involving assembly and catalysis.
J.Mol.Biol., 262, 1996
1KXD
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BU of 1kxd by Molmil
SINDBIS VIRUS CAPSID (N222L MUTANT), TETRAGONAL CRYSTAL FORM
分子名称: SINDBIS VIRUS CAPSID PROTEIN
著者Choi, H.-K, Rossmann, M.G.
登録日1996-05-05
公開日1996-11-08
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (3 Å)
主引用文献Structural analysis of Sindbis virus capsid mutants involving assembly and catalysis.
J.Mol.Biol., 262, 1996
1KXB
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BU of 1kxb by Molmil
SINDBIS VIRUS CAPSID (S215A MUTANT), TETRAGONAL CRYSTAL FORM
分子名称: SINDBIS VIRUS CAPSID PROTEIN
著者Choi, H.-K, Rossmann, M.G.
登録日1996-05-05
公開日1996-11-08
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (2.9 Å)
主引用文献Structural analysis of Sindbis virus capsid mutants involving assembly and catalysis.
J.Mol.Biol., 262, 1996
1KXE
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BU of 1kxe by Molmil
SINDBIS VIRUS CAPSID (Y180S, E183G DOUBLE MUTANT), TETRAGONAL CRYSTAL FORM
分子名称: SINDBIS VIRUS CAPSID PROTEIN
著者Choi, H.-K, Rossmann, M.G.
登録日1996-05-05
公開日1996-11-08
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (3.2 Å)
主引用文献Structural analysis of Sindbis virus capsid mutants involving assembly and catalysis.
J.Mol.Biol., 262, 1996
1KXF
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BU of 1kxf by Molmil
SINDBIS VIRUS CAPSID, (WILD-TYPE) RESIDUES 1-264, TETRAGONAL CRYSTAL FORM (FORM II)
分子名称: SINDBIS VIRUS CAPSID PROTEIN
著者Choi, H.-K, Rossmann, M.G.
登録日1996-05-05
公開日1996-12-07
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (2.38 Å)
主引用文献Structural analysis of Sindbis virus capsid mutants involving assembly and catalysis.
J.Mol.Biol., 262, 1996
1PAX
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BU of 1pax by Molmil
THE CATALYTIC FRAGMENT OF POLY(ADP-RIBOSE) POLYMERASE COMPLEXED WITH 3,4-DIHYDRO-5-METHYL-ISOQUINOLINONE
分子名称: 3,4-DIHYDRO-5-METHYL-ISOQUINOLINONE, POLY(ADP-RIBOSE) POLYMERASE
著者Ruf, A, Schulz, G.E.
登録日1996-05-06
公開日1997-05-15
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (2.4 Å)
主引用文献Structure of the catalytic fragment of poly(ADP-ribose) polymerase from chicken.
Proc.Natl.Acad.Sci.USA, 93, 1996
1ZFO
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BU of 1zfo by Molmil
AMINO-TERMINAL LIM-DOMAIN PEPTIDE OF LASP-1, NMR
分子名称: LASP-1, ZINC ION
著者Hammarstrom, A, Berndt, K.D, Sillard, R, Adermann, K, Otting, G.
登録日1996-05-06
公開日1996-11-08
最終更新日2022-03-02
実験手法SOLUTION NMR
主引用文献Solution structure of a naturally-occurring zinc-peptide complex demonstrates that the N-terminal zinc-binding module of the Lasp-1 LIM domain is an independent folding unit.
Biochemistry, 35, 1996
1TES
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BU of 1tes by Molmil
OXYGEN BINDING MUSCLE PROTEIN
分子名称: METHYLETHYLAMINE, MYOGLOBIN, PROTOPORPHYRIN IX CONTAINING FE, ...
著者Smith, R.D, Phillips Jr, G.N, Olson, J.S.
登録日1996-05-06
公開日1996-11-08
最終更新日2024-02-14
実験手法X-RAY DIFFRACTION (1.7 Å)
主引用文献Mechanism of NO-induced oxidation of myoglobin and hemoglobin.
Biochemistry, 35, 1996
1SON
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BU of 1son by Molmil
ADENYLOSUCCINATE SYNTHETASE IN COMPLEX WITH THE NATURAL FEEDBACK INHIBITOR AMP
分子名称: ADENOSINE MONOPHOSPHATE, ADENYLOSUCCINATE SYNTHETASE, BETA-MERCAPTOETHANOL
著者Cowan-Jacob, S.W.
登録日1996-05-07
公開日1997-09-04
最終更新日2023-08-09
実験手法X-RAY DIFFRACTION (2.55 Å)
主引用文献The mode of action and the structure of a herbicide in complex with its target: binding of activated hydantocidin to the feedback regulation site of adenylosuccinate synthetase.
Proc.Natl.Acad.Sci.USA, 93, 1996
1EBP
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BU of 1ebp by Molmil
COMPLEX BETWEEN THE EXTRACELLULAR DOMAIN OF ERYTHROPOIETIN (EPO) RECEPTOR [EBP] AND AN AGONIST PEPTIDE [EMP1]
分子名称: EPO MIMETICS PEPTIDE 1, EPO RECEPTOR
著者Livnah, O, Stura, E.A, Wilson, I.A.
登録日1996-05-07
公開日1997-07-29
最終更新日2024-06-05
実験手法X-RAY DIFFRACTION (2.8 Å)
主引用文献Functional mimicry of a protein hormone by a peptide agonist: the EPO receptor complex at 2.8 A.
Science, 273, 1996
1SOO
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BU of 1soo by Molmil
ADENYLOSUCCINATE SYNTHETASE INHIBITED BY HYDANTOCIDIN 5'-MONOPHOSPHATE
分子名称: ADENYLOSUCCINATE SYNTHETASE, BETA-MERCAPTOETHANOL, HYDANTOCIDIN-5'-PHOSPHATE, ...
著者Cowan-Jacob, S.W.
登録日1996-05-07
公開日1997-09-04
最終更新日2023-08-09
実験手法X-RAY DIFFRACTION (2.6 Å)
主引用文献The mode of action and the structure of a herbicide in complex with its target: binding of activated hydantocidin to the feedback regulation site of adenylosuccinate synthetase.
Proc.Natl.Acad.Sci.USA, 93, 1996
1BGK
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BU of 1bgk by Molmil
SEA ANEMONE TOXIN (BGK) WITH HIGH AFFINITY FOR VOLTAGE DEPENDENT POTASSIUM CHANNEL, NMR, 15 STRUCTURES
分子名称: BGK
著者Dauplais, M, Lecoq, A, Song, J, Cotton, J, Jamin, N, Gilquin, B, Roumestand, C, Vita, C, Harvey, A, Menez, A.
登録日1996-05-08
公開日1997-01-27
最終更新日2022-02-16
実験手法SOLUTION NMR
主引用文献On the convergent evolution of animal toxins. Conservation of a diad of functional residues in potassium channel-blocking toxins with unrelated structures.
J.Biol.Chem., 272, 1997
1WKT
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BU of 1wkt by Molmil
WILLIOPSIS MRAKII KILLER TOXIN, NMR SOLUTION STRUCTURE
分子名称: YEAST KILLER TOXIN
著者Antuch, W, Guntert, P, Wuthrich, K.
登録日1996-05-08
公開日1996-11-08
最終更新日2022-03-02
実験手法SOLUTION NMR
主引用文献Ancestral beta gamma-crystallin precursor structure in a yeast killer toxin.
Nat.Struct.Biol., 3, 1996
1GFQ
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BU of 1gfq by Molmil
OMPF PORIN (MUTANT R82C)
分子名称: (HYDROXYETHYLOXY)TRI(ETHYLOXY)OCTANE, MATRIX PORIN OUTER MEMBRANE PROTEIN F
著者Lou, K.-L, Schirmer, T.
登録日1996-05-08
公開日1996-12-07
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (2.8 Å)
主引用文献Structural and functional characterization of OmpF porin mutants selected for larger pore size. I. Crystallographic analysis.
J.Biol.Chem., 271, 1996
1GFM
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OMPF PORIN (MUTANT D113G)
分子名称: (HYDROXYETHYLOXY)TRI(ETHYLOXY)OCTANE, MATRIX PORIN OUTER MEMBRANE PROTEIN F
著者Lou, K.-L, Schirmer, T.
登録日1996-05-08
公開日1996-12-07
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (3.5 Å)
主引用文献Structural and functional characterization of OmpF porin mutants selected for larger pore size. I. Crystallographic analysis.
J.Biol.Chem., 271, 1996
1GFP
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BU of 1gfp by Molmil
OMPF PORIN (MUTANT R42C)
分子名称: (HYDROXYETHYLOXY)TRI(ETHYLOXY)OCTANE, MATRIX PORIN OUTER MEMBRANE PROTEIN F
著者Lou, K.-L, Schirmer, T.
登録日1996-05-08
公開日1996-12-07
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (2.7 Å)
主引用文献Structural and functional characterization of OmpF porin mutants selected for larger pore size. I. Crystallographic analysis.
J.Biol.Chem., 271, 1996
1GFN
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OMPF PORIN DELETION (MUTANT DELTA 109-114)
分子名称: (HYDROXYETHYLOXY)TRI(ETHYLOXY)OCTANE, MATRIX PORIN OUTER MEMBRANE PROTEIN F
著者Lou, K.-L, Schirmer, T.
登録日1996-05-08
公開日1996-12-07
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (3.1 Å)
主引用文献Structural and functional characterization of OmpF porin mutants selected for larger pore size. I. Crystallographic analysis.
J.Biol.Chem., 271, 1996
1COW
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BU of 1cow by Molmil
BOVINE MITOCHONDRIAL F1-ATPASE COMPLEXED WITH AUROVERTIN B
分子名称: ADENOSINE-5'-DIPHOSPHATE, AUROVERTIN B, BOVINE MITOCHONDRIAL F1-ATPASE, ...
著者van Raaij, M.J, Abrahams, J.P, Leslie, A.G.W, Walker, J.E.
登録日1996-05-08
公開日1996-08-17
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (3.1 Å)
主引用文献The structure of bovine F1-ATPase complexed with the antibiotic inhibitor aurovertin B.
Proc.Natl.Acad.Sci.USA, 93, 1996
1GFO
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BU of 1gfo by Molmil
OMPF PORIN (MUTANT R132P)
分子名称: (HYDROXYETHYLOXY)TRI(ETHYLOXY)OCTANE, MATRIX PORIN OUTER MEMBRANE PROTEIN F
著者Lou, K.-L, Schirmer, T.
登録日1996-05-08
公開日1996-12-07
最終更新日2024-02-07
実験手法X-RAY DIFFRACTION (3.3 Å)
主引用文献Structural and functional characterization of OmpF porin mutants selected for larger pore size. I. Crystallographic analysis.
J.Biol.Chem., 271, 1996

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