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1ONU
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NMDA RECEPTOR ANTAGONIST, CONANTOKIN-G, NMR, 17 STRUCTURES
Descriptor: CONANTOKIN-G
Authors:Skjaerbaek, N, Nielsen, K.J, Lewis, R.J, Alewood, P.F, Craik, D.J.
Deposit date:1996-08-27
Release date:1997-09-04
Last modified:2022-02-23
Method:SOLUTION NMR
Cite:Determination of the solution structures of conantokin-G and conantokin-T by CD and NMR spectroscopy.
J.Biol.Chem., 272, 1997
1ONV
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NMR Structure of a Complex Containing the TFIIF Subunit RAP74 and the RNAP II CTD Phosphatase FCP1
Descriptor: Transcription initiation factor IIF, alpha subunit, serine phosphatase FCP1a
Authors:Nguyen, B.D, Abbott, K.L, Potempa, K, Kobor, M.S, Archambault, J, Greenblatt, J, Legault, P, Omichinski, J.G.
Deposit date:2003-03-02
Release date:2003-05-20
Last modified:2024-05-22
Method:SOLUTION NMR
Cite:NMR Structure of a Complex Containing the TFIIF Subunit RAP74 and the RNA polymerase II carboxyl-terminal domain phosphatase FCP1
Proc.Natl.Acad.Sci.USA, 100, 2003
1ONW
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Crystal structure of Isoaspartyl Dipeptidase from E. coli
Descriptor: 1,2-ETHANEDIOL, CHLORIDE ION, Isoaspartyl dipeptidase, ...
Authors:Thoden, J.B, Marti-Arbona, R, Raushel, F.M, Holden, H.M.
Deposit date:2003-03-02
Release date:2003-05-06
Last modified:2017-10-11
Method:X-RAY DIFFRACTION (1.65 Å)
Cite:High Resolution X-ray Structure of Isoaspartyl Dipeptidase from Escherichia coli
Biochemistry, 42, 2003
1ONX
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Crystal structure of isoaspartyl dipeptidase from escherichia coli complexed with aspartate
Descriptor: ASPARTIC ACID, Isoaspartyl dipeptidase, ZINC ION
Authors:Thoden, J.B, Marti-Arbona, R, Raushel, F.M, Holden, H.M.
Deposit date:2003-03-02
Release date:2003-05-06
Last modified:2023-11-15
Method:X-RAY DIFFRACTION (2.1 Å)
Cite:High Resolution X-ray Structure of Isoaspartyl Dipeptidase from Escherichia coli
Biochemistry, 42, 2003
1ONY
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Oxalyl-Aryl-Amino Benzoic Acid inhibitors of PTP1B, compound 17
Descriptor: 2-{[2-(2-CARBAMOYL-VINYL)-4-(2-METHANESULFONYLAMINO-2-PENTYLCARBAMOYL-ETHYL)-PHENYL]-OXALYL-AMINO}-BENZOIC ACID, Protein-tyrosine phosphatase, non-receptor type 1
Authors:Liu, G, Szczepankiewicz, B.G, Pei, Z, Janowich, D.A, Xin, Z, Hadjuk, P.J, Abad-Zapatero, C, Liang, H, Hutchins, C.W, Fesik, S.W, Ballaron, S.J, Stashko, M.A, Lubben, T, Mika, A.K, Zinker, B.A, Trevillyan, J.M, Jirousek, M.R.
Deposit date:2003-03-02
Release date:2003-05-20
Last modified:2023-08-16
Method:X-RAY DIFFRACTION (2.15 Å)
Cite:Discovery and Structure-Activity Relationship of Oxalylarylaminobenzoic Acids as Inhibitors of Protein Tyrosine Phosphatase 1B
J.Med.Chem., 46, 2003
1ONZ
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Oxalyl-aryl-Amino Benzoic acid Inhibitors of PTP1B, compound 8b
Descriptor: 2-[(7-HYDROXY-NAPHTHALEN-1-YL)-OXALYL-AMINO]-BENZOIC ACID, Protein-tyrosine phosphatase, non-receptor type 1
Authors:Liu, G, Szczepankiewicz, B.G, Pei, Z, Janowich, D.A, Xin, Z, Hadjuk, P.J, Abad-Zapatero, C, Liang, H, Hutchins, C.W, Fesik, S.W, Ballaron, S.J, Stashko, M.A, Lubben, T, Mika, A.K, Zinker, B.A, Trevillyan, J.M, Jirousek, M.R.
Deposit date:2003-03-02
Release date:2003-05-20
Last modified:2023-08-16
Method:X-RAY DIFFRACTION (2.4 Å)
Cite:Discovery and Structure-Activity Relationship of Oxalylarylaminobenzoic Acids as Inhibitors of Protein Tyrosine Phosphatase 1B
J.Med.Chem., 46, 2003
1OO0
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Crystal structure of the Drosophila Mago nashi-Y14 complex
Descriptor: (4S)-2-METHYL-2,4-PENTANEDIOL, BETA-MERCAPTOETHANOL, CG8781-PA, ...
Authors:Shi, H, Xu, R.M.
Deposit date:2003-03-02
Release date:2003-05-27
Last modified:2024-02-14
Method:X-RAY DIFFRACTION (1.85 Å)
Cite:Crystal structure of the Drosophila Mago nashi-Y14 complex
Genes Dev., 17, 2003
1OO2
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Crystal structure of transthyretin from Sparus aurata
Descriptor: CADMIUM ION, transthyretin
Authors:Pasquato, N, Ramazzina, I, Folli, C, Battistutta, R, Berni, R, Zanotti, G.
Deposit date:2003-03-03
Release date:2004-01-20
Last modified:2023-08-16
Method:X-RAY DIFFRACTION (1.56 Å)
Cite:Distinctive binding and structural properties of piscine transthyretin.
Febs Lett., 555, 2003
1OO3
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P395S mutant of the p85 regulatory subunit of the N-terminal src homology 2 domain of PI3-Kinase
Descriptor: Phosphatidylinositol 3-kinase regulatory alpha subunit
Authors:Guenther, U.L, Weyrauch, B, Schaffhausen, B.
Deposit date:2003-03-03
Release date:2003-03-25
Last modified:2024-05-29
Method:SOLUTION NMR
Cite:Nuclear magnetic resonance structure of the P395S mutant of the N-SH2 domain of the p85 subunit of PI3 kinase: an SH2 domain with altered specificity
Biochemistry, 42, 2003
1OO4
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P395S mutant of the p85 regulatory subunit of the N-terminal src homology 2 domain of PI3-Kinase complexed to a peptide derived from PDGFr
Descriptor: 8-mer peptide from PDGFr, Phosphatidylinositol 3-kinase regulatory alpha subunit
Authors:Guenther, U.L, Weyrauch, B, Schaffhausen, B.
Deposit date:2003-03-03
Release date:2003-03-25
Last modified:2024-10-23
Method:SOLUTION NMR
Cite:Nuclear magnetic resonance structure of the P395S mutant of the N-SH2 domain of the p85 subunit of PI3 kinase: an SH2 domain with altered specificity
Biochemistry, 42, 2003
1OO5
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Studies on the Nitroreductase Prodrug-Activating System. Crystal Structures of the Enzyme Active Form and Complexes with the Inhibitor Dicoumarol and Dinitrobenzamide Prodrugs
Descriptor: FLAVIN MONONUCLEOTIDE, Oxygen-insensitive NAD(P)H nitroreductase
Authors:Johansson, E, Parkinson, G.N, Denny, W.A, Neidle, S.
Deposit date:2003-03-03
Release date:2003-04-08
Last modified:2023-08-16
Method:X-RAY DIFFRACTION (2.5 Å)
Cite:Studies on the Nitroreductase Prodrug-Activating System. Crystal Structures of Complexes with the Inhibitor Dicoumarol and Dinitrobenzamide Prodrugs and of the Enzyme Active Form
J.Med.Chem., 46, 2003
1OO6
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Nitroreductase from e-coli in complex with the dinitrobenzamide prodrug SN23862
Descriptor: 5-[BIS-2(CHLORO-ETHYL)-AMINO]-2,4-DINTRO-BENZAMIDE, FLAVIN MONONUCLEOTIDE, Oxygen-insensitive NAD(P)H nitroreductase
Authors:Johansson, E, Parkinson, G.N, Denny, W.A, Neidle, S.
Deposit date:2003-03-03
Release date:2003-04-08
Last modified:2023-08-16
Method:X-RAY DIFFRACTION (2 Å)
Cite:Studies on the Nitroreductase Prodrug-Activating System. Crystal Structures of Complexes with the Inhibitor Dicoumarol and Dinitrobenzamide Prodrugs and of the Enzyme Active Form
J.Med.Chem., 46, 2003
1OO7
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DNA.RNA HYBRID DUPLEX CONTAINING A 5-PROPYNE DNA STRAND AND PURINE-RICH RNA STRAND, NMR, 4 STRUCTURES
Descriptor: 5'-D(*GP*(5PC)P*(PDU)P*(PDU)P*(5PC)P*(PDU)P*(5PC)P*(PDU)P*(PDU)P*C)-3', 5'-R(*GP*AP*AP*GP*AP*GP*AP*AP*GP*C)-3'
Authors:Gyi, J.I, Gao, D, Conn, G.L, Trent, J.O, Brown, T, Lane, A.N.
Deposit date:2003-03-03
Release date:2003-11-11
Last modified:2024-05-01
Method:SOLUTION NMR
Cite:The solution structure of a DNA*RNA duplex containing 5-propynyl U and C; comparison with 5-Me modifications
Nucleic Acids Res., 31, 2003
1OO8
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CRYSTAL STRUCTURE OF A1PI-PITTSBURGH IN THE NATIVE CONFORMATION
Descriptor: Alpha-1-antitrypsin precursor
Authors:Dementiev, A, Simonovic, M, Volz, K, Gettins, P.G.
Deposit date:2003-03-03
Release date:2003-08-05
Last modified:2023-08-16
Method:X-RAY DIFFRACTION (2.65 Å)
Cite:Canonical inhibitor-like interactions explain reactivity of alpha1-proteinase inhibitor Pittsburgh and antithrombin with proteinases
J.Biol.Chem., 278, 2003
1OO9
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Orientation in Solution of MMP-3 Catalytic Domain and N-TIMP-1 from Residual Dipolar Couplings
Descriptor: Metalloproteinase inhibitor 1, Stromelysin-1
Authors:Arumugam, S, Van Doren, S.R.
Deposit date:2003-03-03
Release date:2003-07-29
Last modified:2022-02-23
Method:SOLUTION NMR
Cite:Global Orientation of Bound MMP-3 and N-TIMP-1 in Solution via Residual Dipolar Couplings
Biochemistry, 42, 2003
1OOA
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CRYSTAL STRUCTURE OF NF-kB(p50)2 COMPLEXED TO A HIGH-AFFINITY RNA APTAMER
Descriptor: Nuclear factor NF-kappa-B p105 subunit, RNA aptamer
Authors:Huang, D.B, Vu, D, Cassiday, L.A, Zimmerman, J.M, Maher III, L.J, Ghosh, G.
Deposit date:2003-03-03
Release date:2003-07-22
Last modified:2023-08-16
Method:X-RAY DIFFRACTION (2.45 Å)
Cite:Crystal structure of NF-kappaB (p50)2 complexed to a high-affinity RNA aptamer.
Proc.Natl.Acad.Sci.USA, 100, 2003
1OOC
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Mutations in the T1.5 loop of pectate lyase A
Descriptor: Pectate lyase A
Authors:Dehdashti, S.J, Doan, C.N, Chao, K, Vordtriede, P.B, Yoder, M.D.
Deposit date:2003-03-03
Release date:2004-03-16
Last modified:2024-10-16
Method:X-RAY DIFFRACTION (2.94 Å)
Cite:Effect of mutations in the T1.5 loop of pectate lyase A from Erwinia chrysanthemi EC16.
Acta Crystallogr.,Sect.D, 59, 2003
1OOE
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Structural Genomics of Caenorhabditis elegans : Dihydropteridine reductase
Descriptor: 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, Dihydropteridine reductase
Authors:Symersky, J, Li, S, Nagy, L, Qiu, S, Lin, G, Tsao, J, Luo, D, Carson, M, DeLucas, L, Luo, M, Southeast Collaboratory for Structural Genomics (SECSG)
Deposit date:2003-03-03
Release date:2003-03-18
Last modified:2023-08-16
Method:X-RAY DIFFRACTION (1.65 Å)
Cite:Structural genomics of Caenorhabditis elegans: structure of dihydropteridine reductase.
Proteins, 53, 2003
1OOF
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Complex of Drosophila odorant binding protein LUSH with ethanol
Descriptor: ACETATE ION, ETHANOL, odorant binding protein LUSH
Authors:Kruse, S.W, Zhao, R, Smith, D.P, Jones, D.N.M.
Deposit date:2003-03-03
Release date:2003-09-02
Last modified:2011-07-13
Method:X-RAY DIFFRACTION (1.49 Å)
Cite:Structure of a specific alcohol-binding site defined by the odorant binding protein LUSH from Drosophila melanogaster
Nat.Struct.Biol., 10, 2003
1OOG
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Complex of Drosophila odorant binding protein LUSH with propanol
Descriptor: ACETATE ION, N-PROPANOL, odorant binding protein LUSH
Authors:Kruse, S.W, Zhao, R, Smith, D.P, Jones, D.N.M.
Deposit date:2003-03-03
Release date:2003-09-02
Last modified:2024-10-16
Method:X-RAY DIFFRACTION (1.45 Å)
Cite:Structure of a specific alcohol-binding site defined by the odorant binding protein LUSH from Drosophila melanogaster
Nat.Struct.Biol., 10, 2003
1OOH
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Complex of Drosophila odorant binding protein LUSH with butanol
Descriptor: 1-BUTANOL, ACETATE ION, odorant binding protein LUSH
Authors:Kruse, S.W, Zhao, R, Smith, D.P, Jones, D.N.M.
Deposit date:2003-03-03
Release date:2003-09-02
Last modified:2023-08-16
Method:X-RAY DIFFRACTION (1.25 Å)
Cite:Structure of a specific alcohol-binding site defined by the odorant binding protein LUSH from Drosophila melanogaster
Nat.Struct.Biol., 10, 2003
1OOI
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Crystal structure of LUSH from Drosophila melanogaster at pH 6.5
Descriptor: odorant binding protein LUSH
Authors:Kruse, S.W, Zhao, R, Smith, D.P, Jones, D.N.M.
Deposit date:2003-03-03
Release date:2003-09-02
Last modified:2024-10-09
Method:X-RAY DIFFRACTION (2.04 Å)
Cite:Structure of a specific alcohol-binding site defined by the odorant binding protein LUSH from Drosophila melanogaster
Nat.Struct.Biol., 10, 2003
1OOJ
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Structural genomics of Caenorhabditis elegans : Calmodulin
Descriptor: CALCIUM ION, Calmodulin CMD-1
Authors:Symersky, J, Lin, G, Li, S, Qiu, S, Luan, C.-H, Luo, D, Tsao, J, Carson, M, DeLucas, L, Luo, M, Southeast Collaboratory for Structural Genomics (SECSG)
Deposit date:2003-03-03
Release date:2003-03-25
Last modified:2023-08-16
Method:X-RAY DIFFRACTION (2.11 Å)
Cite:Structural genomics of caenorhabditis elegans: crystal structure of calmodulin.
Proteins, 53, 2003
1OOK
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Crystal Structure of the Complex of Platelet Receptor GPIb-alpha and Human alpha-Thrombin
Descriptor: 2-acetamido-2-deoxy-beta-D-glucopyranose, CHLORIDE ION, Human Alpha Thrombin, ...
Authors:Varughese, K.I, Celikel, R, Ruggeri, Z.M.
Deposit date:2003-03-03
Release date:2003-07-22
Last modified:2024-10-30
Method:X-RAY DIFFRACTION (2.3 Å)
Cite:Modulation of alpha-thrombin function by distinct interactions with platelet glycoprotein Ibalpha
Science, 301, 2003
1OON
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Nitroreductase from e-coli in complex with the dinitrobenzamide prodrug SN27217
Descriptor: 2,4-DINITRO,5-[BIS(2-BROMOETHYL)AMINO]-N-(2',3'-DIOXOPROPYL)BENZAMIDE, FLAVIN MONONUCLEOTIDE, Oxygen-insensitive NAD(P)H nitroreductase
Authors:Johansson, E, Parkinson, G.N, Denny, W.A, Neidle, S.
Deposit date:2003-03-04
Release date:2003-04-08
Last modified:2023-08-16
Method:X-RAY DIFFRACTION (2.49 Å)
Cite:Studies on the Nitroreductase Prodrug-Activating System. Crystal Structures of Complexes with the Inhibitor Dicoumarol and Dinitrobenzamide Prodrugs and of the Enzyme Active Form
J.Med.Chem., 46, 2003

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