Diversity structural

Box (1981) classified all of the different plant species into 16 different structural types (trees, small trees, etc.) and in turn into a total of 77 plant forms (e.g., evergreen tropical rainforest trees, mediterranean dwarf shrubs, etc.). This latter classification combines form, geographical distribution, and to a certain extent function (evergreen, deciduous, ephemeral). So fundamentally there are not too many different structural types of plants, as Theophrastus noted several millennia ago. These basic forms, when coalesced into communities, certainly have an influence on land surface/atmospheric models through turbulent transfer and boundary-layer effects that are often incorporated into atmospheric exchange models. 

The primary cell walls of most higher plant species contain XGs of the XXXG type, which bear trisaccharide side chains (8) on the backbone [247]. The seeds of many plants contain XXXG-type XGs, in which about 30% of the xylose units possess a /3-D-Galp residue attached to position 2. Several plant species produce XGs that lack fucose and galactose, and have a-L-Ara/ attached to 0-2 of some of the Xylp side-chains, such as XG isolated from olive fruit [262] and soybean (Glycine maxima) meal [263]. However, a-L-Ara/ residues occur also 2-linked directly to some of the Glcp residues of the backbone [154]. 

The cell walls of the Solanaceae plant species contain the XXGG type of XGs [247,275]. Suspension-cultured tobacco cells secrete a XG, bearing disaccharide side chains (11) [276], as similarly reported for XGs of other solana-ceous plants. The XG from suspension-cultured tomato cells is more complex, as it also contains the unusual / -L-Ara/-(1 3)-o -L-Ara/-(1 2)-a-D-Xylp trisaccharide side-chain (12) in addition to the prevaiUng dimeric moiety (13) [277]. 

Many XGs are acetylated [248,278,279]. XG isolated from the spent media of suspension-cultured sycamore cells Glcp contains acetyl groups at positions 3, 4, or 6 [2]. 

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Fig. 7. Structural diversity of marine sterols where R — a variety of unique side chains, including (a) cyclopropa(e)ne, (b) acetylene, (c) polyalhylated, and (d)...

VI Gillet, P Willett, I Bradshaw. The effectiveness of reactant pools for generating structurally-diverse combinatorial libraries. I Chem Inf Comput Sci 37 731-740, 1997. 

Although experimental studies of DNA and RNA structure have revealed the significant structural diversity of oligonucleotides, there are limitations to these approaches. X-ray crystallographic structures are limited to relatively small DNA duplexes, and the crystal lattice can impact the three-dimensional conformation [4]. NMR-based structural studies allow for the determination of structures in solution however, the limited amount of nuclear overhauser effect (NOE) data between nonadjacent stacked basepairs makes the determination of the overall structure of DNA difficult [5]. In addition, nanotechnology-based experiments, such as the use of optical tweezers and atomic force microscopy [6], have revealed that the forces required to distort DNA are relatively small, consistent with the structural heterogeneity observed in both DNA and RNA. 

The genes for MHC molecules, unlike immunoglobulin genes, do not undergo rearrangements to create structural diversity. The Pzm light chain is invariant, but the class I MHC heavy chain is the most genetically polymorphic... 

Similar structural diversity has been established for the heavier alkali metals also but it is unnecessary to deal with this in detail. The sUTictural chemistry of the organometallic compounds in particular, and of related complexes, has been well reviewed. 

Chain metasilicates Si03 formed by comersharing of Si04 tetrahedra arc particularly prevalent in nature and many important minerals have this basic structural unit (cf, polyphosphates, p, 528), Despite the apparent simplieily of their structure motif and stoichiometry considerable structural diversity is encountered because of the differing conformations that can be adopted by the linked tetrahedra. As a result, the repeat distance along the c -axis can be (1). 

Similar structural diversity characterizes the heavier halide complexes of the group. The... 

With such structural diversity it is perhaps not surprising that no certain method has been devised for theoretically predicting the mode of bonding to be expected in specific cases, although... 

The Jacobsen-Katsuki epoxidation reaction has been widely used for the preparation of a variety of structurally diverse complex molecules by both academia and the pharmaceutical industry. Summarized below are a few examples. 

Select a set of compounds resolved on a given CSP, calculate the similarity indices between all possible molecule pairs, and then use these indices to build a similarity matrix containing relevant information about the structural diversity within the set of samples separated on this CSP. 

Natural monomers and polymers present a scenario where they have a structural diversity and complexity that, with appropriate chemical modifications, and taking information from modern techniques of molecular and process designs could be utilized for transforming them into high-value polymers. This was exemplified by showing the example of a natural monomer, cardanol. 

Ionophores constitute a large collection of structurally diverse substances that share the ability to complex cations and to assist in the translocation of cations through a lipophilic interface.1 Using numerous Lewis-basic heteroatoms, an ionophore organizes itself around a cationic species such as an inorganic metal ion. This arrangement maximizes favorable ion-dipole interactions, while simultaneously exposing a relatively hydrophobic (lipophilic) exterior. 

Cytochrome P450 enzymes have been the subject of a number of recent reviews in which their mechanism and scope of action are covered in much detail [1, 6, 10, 11]. The reader is referred to these articles for a more thorough account of the mechanism and reactivity of cytochrome P450 enzymes, while we present a few representative examples of cytochrome P450-catalyzed epoxidation below. The enzymes we chose are all involved in the biosynthesis of polyketide natural products. Polyketides are a large, structurally diverse family of compounds and have provided a wealth of therapeutically useful drugs and drug leads. 

Blanco G et al (1998) Isozymes of the Na+-K+-ATPase heterogeneity in structure, diversity in function. Am J Physiol 275(5 Part 2) F633-F650... 

MAPK cascades are composed of three cytoplasmic kinases, the MAPKKK, MAPKK, and MAPK, that are regulated by phosphorylation (Fig. 1) [1, 2]. The MAPKKK, also called MEKK for MEK kinase, is a serine/threonine kinase. Selective activation of MAPKKKs by upstream cellular stimuli results in the phosphorylation of MAPKK, also called MEK for MAP/ERK kinase by the MAPKKK. MAPKKK members are structurally diverse and are differentially regulated by specific upstream stimuli. The MAPKK is phosphorylated by the MAPKKK on two specific serine/ threonine residues in its activation loop. The MAPKK family members are dual specificity kinases capable of phosphorylating critical threonine and tyrosine residues in the activation loop of the MAPKs. MAPKKs have the fewest members in the MAPK signaling module. MAPKs are a family of serine/threonine kinases that upon activation by their respective MAPKKs, are capable of phosphorylating cytoplasmic substrates as well as... 

The allyl sulphenate-allyl sulphoxide rearrangement is a general reaction and is applicable to structurally diverse allyl alcohols204,205 (Table 13). Mechanistically, it represents a typical example of a [2,3]-sigmatropic rearrangement as shown by the detailed investigations of Mislow and Braverman and their coworkers. 

Davis and coworkers40 have developed use of diastereomerically pure 2-sulfonyl and 2-sulfamyloxaziridines for asymmetric oxidation of sulfides into sulfoxides (equation 7). The best results (using the sulfamyloxaziridines) range from 38 to 68% enantiomeric purity of the resultant sulfoxides. The structural diversity of such substituted oxaziridines, their... 

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