- An Oxygen-Sensing Diguanylate Cyclase and Phosphodiesterase Couple for c-di-GMP Control
[作者:Tuckerman, JR; Gonzalez, G; Sousa, EHS; Wan, XH; Saito, JA; Alam, M; Gilles-Gonzalez, MA,期刊:Biochemistry, 页码:9764-9774 , 文章类型: Article,,卷期:2009年48-41]
- A commonly observed coupling of sensory domains to GGDEF-class diguanylate cyclases and EAL-class phosphodiesterases has long suggested that c-di-GMP synthesizing and degrading enzyme sense environmental signals. Neverth...
- Novel Binding Motif of ACTH Analogues at the Melanocortin Receptors
[作者:Yang, YK; Hruby, VJ; Chen, M; Crasto, C; Cai, MY; Harmon, CM,期刊:Biochemistry, 页码:9775-9784 , 文章类型: Article,,卷期:2009年48-41]
- The melanocortin receptor (MCR) subtype family is a member of the GPCR superfamily, and each of them has a different pharmacological profile with regard to the relative potency of the endoganous and synthetic melanocorti...
- Anopheles gambiae Alkaline Phosphatase Is a Functional Receptor of Bacillus thuringiensis jegathesan Cry11Ba Toxin
[作者:Hua, G; Zhang, R; Bayyareddy, K; Adang, MJ,期刊:Biochemistry, 页码:9785-9793 , 文章类型: Article,,卷期:2009年48-41]
- Alkaline phosphatases (ALPs, EC 3131) isolated from lepidopteran and dipteran species are identified as receptors for Cry1Ac an Cry11Aa toxins, respectively [Jurat-Fuentes, J. L., and Adang, M.J. (2004) Eur. J. Biochem. ...
- Biochemical Characterization of the Multidrug Regulator QacR Distinguishes Residues That Are Crucial to Multidrug Binding and Induction of qacA Transcription
[作者:Peters, KM; Sharbeen, G; Theis, T; Skurray, RA; Brown, MH,期刊:Biochemistry, 页码:9794-9800 , 文章类型: Article,,卷期:2009年48-41]
- Slaphylococcus aureus transcription factor QacR regulates expression of the qacA multidrug efflux determinant. In response to binding cationic lipophilic compounds, including ethidium and rhodamine 60, QacR dissociates f...
- Disruption of the Proton Relay Network in the Class 2 Dihydroorotate Dehydrogenase from Escherichia coli
[作者:Kow, RL; Whicher, JR; McDonald, CA; Palfey, BA; Fagan, RL,期刊:Biochemistry, 页码:9801-9809 , 文章类型: Article,,卷期:2009年48-41]
- Dihydroorotate dehydrogenases (DHODs) are FMN-containing enzymes that catalyze the conversion of dihydroorotate (DHO) to orotate in the de novo synthesis of pyrimidines. During the reaction, a proton is transferred from ...
- Structure and Inhibition of Human Diamine Oxidase
[作者:McGrath, AP; Hilmer, KM; Collyer, CA; Shepard, EM; Elmore, BO; Brown, DE; Dooley, DM; Guss, JM,期刊:Biochemistry, 页码:9810-9822 , 文章类型: Article,,卷期:2009年48-41]
- Humans have three functioning genes that encode copper-containing amine oxidases. The product of the AOC1 gene is a so-called diamine oxidase (hDAO), named for its substrate preference for diamines, particularly histamin...
- Characterization of the CHK1 Allosteric Inhibitor Binding Site
[作者:Vanderpool, D; Johnson, TO; Ping, C; Bergqvist, S; Alton, G; Phonephaly, S; Rui, E; Luo, C; Deng, YL; Grant, S; Quenzer, T; Margosiak, S; Register, J; Brown, E; Ermolieff, J,期刊:Biochemistry, 页码:9823-9830 , 文章类型: Article,,卷期:2009年48-41]
- Checkpoint kinase 1 (CHK1) is a key element in the DNA damage response pathway and plays a crucial role in the S-G(2)-phase checkpoint, Inhibiting CHK1 is a therapeutic strategy involving abrogation of the G2/M mitotic c...
- Lipidic Sponge Phase Crystal Structure of a Photosynthetic Reaction Center Reveals Lipids on the Protein Surface
[作者:Wohri, AB; Wahlgren, WY; Malmerberg, E; Johansson, LC; Neutze, R; Katona, G,期刊:Biochemistry, 页码:9831-9838 , 文章类型: Article,,卷期:2009年48-41]
- Membrane proteins are embedded in a lipid bilayer and maintain strong interactions with lipid molecules, Tightly bound lipids are responsible for vertical positioning and integration of proteins in the membrane and for a...
- Matrix Metalloproteinase 2 Inhibition: Combined Quantum Mechanics and Molecular Mechanics Studies of the Inhibition Mechanism of (4-Phenoxyphenylsulfonyl)methylthiirane and Its Oxirane Analogue
[作者:Tao, P; Fisher, JF; Shi, QC; Vreven, T; Mobashery, S; Schlegel, HB,期刊:Biochemistry, 页码:9839-9847 , 文章类型: Article,,卷期:2009年48-41]
- The inhibition mechanism of matrix metalloproteinase 2 (MMP2) by the selective inhibitor (4-phenoxyphenylsulfonyl)methylthiirane (SB-3CT) and its oxirane analogue is investigated computationally. The inhibition mechanism...
- Effects of pH on the Rieske Protein from Thermus thermophilus: A Spectroscopic and Structural Analysis
[作者:Konkle, ME; Muellner, SK; Schwander, AL; Dious, MM; Pokhrel, R; Britt, RD; Taylor, AB; Hunsicker-Wang, LM,期刊:Biochemistry, 页码:9848-9857 , 文章类型: Article,,卷期:2009年48-41]
- The Rieske protein from Thermus, thermophilus (TtRp) and a truncated version OF the protein (truncTtRp), produced to achieve a low-pH crystallization condition, have been characterized using UV-visible and circular dichr...
- A New Class of Isothiocyanate-Based Irreversible Inhibitors of Macrophage Migration Inhibitory Factor
[作者:Ouertatani-Sakouhi, H; El-Turk, F; Fauvet, B; Roger, T; Le Roy, D; Karpinar, DP; Leng, L; Bucala, R; Zweckstetter, M; Calandra, T; Lashuel, HA,期刊:Biochemistry, 页码:9858-9870 , 文章类型: Article,,卷期:2009年48-41]
- Macrophage migration inhibitory factor (MIF) is a homotrimerte multifunctional proinflammatrory cytokine that has been implicated in the pathogenesis of several inflammatory and autoimmune diseases. Current therapeutic s...
- Structural Insights into Glucan Phosphatase Dynamics Using Amide Hydrogen-Deuterium Exchange Mass Spectrometry
[作者:Hsu, S; Kim, Y; Li, S; Durrant, ES; Pace, RM; Woods, VL; Gentry, MS,期刊:Biochemistry, 页码:9891-9902 , 文章类型: Article,,卷期:2009年48-41]
- Laforin an(l starch excess 4 (SEX4) are founding members of it class of phosphatases that dephosphorylate phosphoglucans. Each protein contains a carbohydrate binding module (CBM) and a dual specificity phosphatase (DSP)...
- Why the Extended-Spectrum beta-Lactamases SHV-2 and SHV-5 Are "Hypersusceptible" to Mechanism-Based Inhibitors
[作者:Kalp, M; Bethel, CR; Bonomo, RA; Carey, PR,期刊:Biochemistry, 页码:9912-9920 , 文章类型: Article,,卷期:2009年48-41]
- Extended-spectrum beta-lactamases (ESBLs) are derivatives of enzymes such as SHV-1 and TEM-1 that have undergone site-specific mutations that enable them to hydrolyze, and thus inactivate, oxyimino-cephalosporins, such a...
|