These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 28251412)

  • 1. Insight into the orientational versatility of steroid substrates-a docking and molecular dynamics study of a steroid receptor and steroid monooxygenase.
    Panek A; Świzdor A; Milecka-Tronina N; Panek JJ
    J Mol Model; 2017 Mar; 23(3):96. PubMed ID: 28251412
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Exploring the structural basis of substrate preferences in Baeyer-Villiger monooxygenases: insight from steroid monooxygenase.
    Franceschini S; van Beek HL; Pennetta A; Martinoli C; Fraaije MW; Mattevi A
    J Biol Chem; 2012 Jun; 287(27):22626-34. PubMed ID: 22605340
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Baeyer-Villiger oxidation of progesterone by Aspergillus sojae PTCC 5196.
    Javid M; Nickavar B; Vahidi H; Faramarzi MA
    Steroids; 2018 Dec; 140():52-57. PubMed ID: 30055193
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel steroid hydroxylase from Nigrospora sphaerica with various hydroxylation capabilities to different steroid substrates.
    Li S; Chang Y; Liu Y; Tian W; Chang Z
    J Steroid Biochem Mol Biol; 2023 Mar; 227():106236. PubMed ID: 36563764
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The significance of the 20-carbonyl group of progesterone in steroid receptor binding: a molecular dynamics and structure-based ligand design study.
    Hillisch A; von Langen J; Menzenbach B; Droescher P; Kaufmann G; Schneider B; Elger W
    Steroids; 2003 Nov; 68(10-13):869-78. PubMed ID: 14667979
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Theoretical and experimental evaluation of a CYP106A2 low homology model and production of mutants with changed activity and selectivity of hydroxylation.
    Lisurek M; Simgen B; Antes I; Bernhardt R
    Chembiochem; 2008 Jun; 9(9):1439-49. PubMed ID: 18481342
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Multiple steroid-binding orientations: alteration of regiospecificity of dehydroepiandrosterone 2- and 7-hydroxylase activities of cytochrome P-450 2a-5 by mutation of residue 209.
    Iwasaki M; Davis DG; Darden TA; Pedersen LG; Negishi M
    Biochem J; 1995 Feb; 306 ( Pt 1)(Pt 1):29-33. PubMed ID: 7864823
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hydroxylation of steroids by Fusarium oxysporum, Exophiala jeanselmei and Ceratocystis paradoxa.
    Peart PC; McCook KP; Russell FA; Reynolds WF; Reese PB
    Steroids; 2011 Nov; 76(12):1317-30. PubMed ID: 21763336
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Inherent versatility of P-450 oxygenase. Conferring dehydroepiandrosterone hydroxylase activity to P-450 2a-4 by a single amino acid mutation at position 117.
    Iwasaki M; Darden TA; Parker CE; Tomer KB; Pedersen LG; Negishi M
    J Biol Chem; 1994 Mar; 269(12):9079-83. PubMed ID: 8132645
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Steroid conversion with CYP106A2 - production of pharmaceutically interesting DHEA metabolites.
    Schmitz D; Zapp J; Bernhardt R
    Microb Cell Fact; 2014 Jun; 13():81. PubMed ID: 24903845
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Structural and dynamic basis of human cytochrome P450 7B1: a survey of substrate selectivity and major active site access channels.
    Cui YL; Zhang JL; Zheng QC; Niu RJ; Xu Y; Zhang HX; Sun CC
    Chemistry; 2013 Jan; 19(2):549-57. PubMed ID: 23180418
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Transformation of some 3alpha-substituted steroids by Aspergillus tamarii KITA reveals stereochemical restriction of steroid binding orientation in the minor hydroxylation pathway.
    Christy Hunter A; Khuenl-Brady H; Barrett P; Dodd HT; Dedi C
    J Steroid Biochem Mol Biol; 2010 Feb; 118(3):171-6. PubMed ID: 20026270
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Biotransformation of dehydro-epi-androsterone by Aspergillus parasiticus: Metabolic evidences of BVMO activity.
    Mascotti ML; Palazzolo MA; Bisogno FR; Kurina-Sanz M
    Steroids; 2016 May; 109():44-9. PubMed ID: 27025973
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Structures of human steroidogenic cytochrome P450 17A1 with substrates.
    Petrunak EM; DeVore NM; Porubsky PR; Scott EE
    J Biol Chem; 2014 Nov; 289(47):32952-64. PubMed ID: 25301938
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Microbial Modifications of Androstane and Androstene Steroids by
    Panek A; Łyczko P; Świzdor A
    Molecules; 2020 Sep; 25(18):. PubMed ID: 32942593
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mammalian Cells Engineered To Produce New Steroids.
    Spady ES; Wyche TP; Rollins NJ; Clardy J; Way JC; Silver PA
    Chembiochem; 2018 Sep; 19(17):1827-1833. PubMed ID: 29931794
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A DFT-D investigation of the mechanisms for activation of the wild-type and S810L mutated mineralocorticoid receptor by steroid hormones.
    Riley KE; Hobza P
    J Phys Chem B; 2008 Mar; 112(10):3157-63. PubMed ID: 18284228
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular dynamics of substrate complexes with hamster cytochrome P450c17 (CYP17): mechanistic approach to understanding substrate binding and activities.
    Mathieu AP; LeHoux JG; Auchus RJ
    Biochim Biophys Acta; 2003 Feb; 1619(3):291-300. PubMed ID: 12573489
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A nucleotide-gated molecular pore selects sulfotransferase substrates.
    Cook I; Wang T; Falany CN; Leyh TS
    Biochemistry; 2012 Jul; 51(28):5674-83. PubMed ID: 22703301
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Synthesis, molecular docking, molecular dynamics and evaluation of Drug-Likeness properties of the fused
    Çapan İ; Shehu A; Sert Y; Çelik İ; Erol M; Koca İ; Servi S
    J Biomol Struct Dyn; 2023 Apr; 41(6):2492-2503. PubMed ID: 35132941
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.