Isoprenoids in three-dimensional space: the stereochemistry of terpene biosynthesis.
about
Hedycaryol synthase in complex with nerolidol reveals terpene cyclase mechanismInduced-fit mechanism in class I terpene cyclasesExperimental and Theoretical Studies on Corvol Ether Biosynthesis.Traversing the fungal terpenome.Volatile terpenes from actinomycetes: a biosynthetic study correlating chemical analyses to genome data.Purification and biochemical characterization of recombinant Persicaria minor β-sesquiphellandrene synthase.Diterpenoids of terrestrial origin.Sesquiterpenyl indoles.Bacterial terpene cyclases.Divergent Total Synthesis of Atisane-Type Diterpenoids.Propolis Diterpenes as a Remarkable Bio-Source for Drug Discovery Development: A Review.Structural Revision and Elucidation of the Biosynthesis of Hypodoratoxide by (13) C,(13) C COSY NMR Spectroscopy.A detailed view on 1,8-cineol biosynthesis by Streptomyces clavuligerus.The stereochemical course of tricho-acorenol biosynthesis.Rapid chemical characterization of bacterial terpene synthases.Improved selectivity of an engineered multi-product terpene synthase.Terpene Cyclases from Social Amoebae.Stereochemical assignment of fusiccocadiene from NMR shielding constants and vibrational circular dichroism spectroscopy.Substrate geometry controls the cyclization cascade in multiproduct terpene synthases from Zea mays.An improved technique for the rapid chemical characterisation of bacterial terpene cyclases.The stereochemical course and mechanism of the IspH reaction.
P2860
Q27688099-083AD8EC-D65C-4BF4-B7D1-36D1FE336ED7Q27690639-BE7912CB-E5B5-4902-BD9E-366FDBF18952Q31030129-5A81DDC0-27B5-4EF5-9EFD-B6ACFA1C3B11Q34204246-F7CCEF6F-F036-496D-8CFE-172B348DD62EQ35045304-C97BA02E-FE19-4048-8996-F43A37B7E03DQ37676965-E5109F59-12B3-462A-A684-D0A8D762D42AQ38018545-657A5720-6AEE-4E38-94FC-3E920028EF65Q38156579-2155BD5E-7E1D-47DD-8701-1BC48BB4D5D6Q38632052-FDD9F672-606C-4CB7-A69B-C5E60356D609Q39019501-3D86474B-833F-4EA5-BE89-91A6C6A143B3Q39383429-3720079D-76A9-4464-9F21-2F5F5A7E8A53Q41069472-11874FC5-D527-42C0-922C-BF330ACC8924Q41915006-8C6F77FB-5AFA-43C9-9806-808F51C34EE8Q44145049-E89040F5-B893-4296-BD8F-E18B6A286917Q44813455-6186BDA4-054F-438B-8FD9-DDA665F336CDQ46888620-9B594AA3-609B-4679-B4CB-4414779511D3Q48215049-C8C49D8E-3A64-4EEC-9DF5-9B54D6052970Q48352917-00C6982A-B30D-47BF-9958-3F2AF0039443Q51357791-EF03EC1C-A42E-449D-876C-B2D809C91E7EQ54294297-69C9DC3E-CF7E-48FA-8678-92D68028DEA0Q54340597-55BED298-4112-47B0-A565-873CB5C2FC82
P2860
Isoprenoids in three-dimensional space: the stereochemistry of terpene biosynthesis.
description
article científic
@ca
article scientifique
@fr
articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
@sq
artículo científico
@es
name
Isoprenoids in three-dimensional space: the stereochemistry of terpene biosynthesis.
@en
Isoprenoids in three-dimensional space: the stereochemistry of terpene biosynthesis.
@nl
type
label
Isoprenoids in three-dimensional space: the stereochemistry of terpene biosynthesis.
@en
Isoprenoids in three-dimensional space: the stereochemistry of terpene biosynthesis.
@nl
prefLabel
Isoprenoids in three-dimensional space: the stereochemistry of terpene biosynthesis.
@en
Isoprenoids in three-dimensional space: the stereochemistry of terpene biosynthesis.
@nl
P2860
P356
P1476
Isoprenoids in three-dimensional space: the stereochemistry of terpene biosynthesis.
@en
P2860
P304
P356
10.1039/C1NP00063B
P577
2011-10-07T00:00:00Z