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Sequences defined

ChemSketch has some special-purpose building functions. The peptide builder creates a line structure from the protein sequence defined with the typical three-letter abbreviations. The carbohydrate builder creates a structure from a text string description of the molecule. The nucleic acid builder creates a structure from the typical one-letter abbreviations. There is a function to clean up the shape of the structure (i.e., make bond lengths equivalent). There is also a three-dimensional optimization routine, which uses a proprietary modification of the CHARMM force field. It is possible to set the molecule line drawing mode to obey the conventions of several different publishers. [Pg.326]

Suppose we define as pjj the probability that a unit of type i is followed in the polymer by a unit of type j, where both i and j can be either 1 or 2. Since an i unit must be followed by either an i or a j, the fraction of ij sequences out of all possible sequences defines p ... [Pg.448]

The discretized symbol-sequence defined in equation 8.39 suggests that we might use two other familiar measures of complexity to characterize the various dynamical regimes of behavior namely, the pattern entropy and dynamical entropy. [Pg.395]

Fig. 7 Sequence alignment of GPR motifs. Consensus amino acids are red chemically similar amino acids are blue. Consensus I refers to the conserved sequence defined with die family of AGS3-related proteins. Consensus II refers to the conserved sequence defined widi all known GPR proteins. Consensus II amino acid groupings are. =any, +=positive (HKR), —negative (DE), h=hydrophobic (ACFILMVWY), u=tiny (AGS), p=polar (CDEHKNQRST), and l=aliphatic (ILV). (C.e. C. elegans, D.m. D. melanogaster, A.t.. A. thaliand) The core GPR motif is as defined in Peterson et al. 2002. This figure is ad ted from die thesis of Dr. Yuri Peterson. Fig. 7 Sequence alignment of GPR motifs. Consensus amino acids are red chemically similar amino acids are blue. Consensus I refers to the conserved sequence defined with die family of AGS3-related proteins. Consensus II refers to the conserved sequence defined widi all known GPR proteins. Consensus II amino acid groupings are. =any, +=positive (HKR), —negative (DE), h=hydrophobic (ACFILMVWY), u=tiny (AGS), p=polar (CDEHKNQRST), and l=aliphatic (ILV). (C.e. C. elegans, D.m. D. melanogaster, A.t.. A. thaliand) The core GPR motif is as defined in Peterson et al. 2002. This figure is ad ted from die thesis of Dr. Yuri Peterson.
Most methods are mainly suited to either assembled (A) or sequential (S) epitopes Some methods are applicable only to Ags expressed from cloned cDNA (R, recombinant), whereas others need purified protein (P) Resolution of mapping may be low (L, sequences not defined), medium (M, sequence defined to within 10-100 ammo acids), or high (H, individual amino acids defined) Some methods are particularly expensive (E) or cheap (C) in terms of the equipment and/or skilled labor required Finally (not shown in the table), some methods may not be usefiil for your particular Ab-Ag combination... [Pg.163]

Mammalian MT synthesis is regulated at the transcriptional level. A series of ds-acting control sequences has been identified and can be attributed to the range of effectors described above (see Hamer, 1986). Among these are sequences defined as metal-responsive elements (MREs). In the mouse MTI gene is a pair of MREs which are imperfectly duplicated 12 bp sequences, at -46 (relative to the start of transcription) and -114 further partial repeats are centred at positions -160, -134 and -62. The requirement for such sequences in metal regulation is proven for the mouse MTI promoter, Zn and Cd induction requires two or more MREs (Searle et al., 1985). [Pg.12]

Sequence-Defined Polymers Allow Synthetically Controlled Functionality. 239... [Pg.228]

One step further, namely to monomeric sequence-defined polymeric vehicles, leads to the synthetic strategy based on standard peptide solid phase chemistry. [Pg.239]

Hartmann L, Krause E, Antonietti M et al (2006) Solid-phase supported polymer synthesis of sequence-defined, multifunctional poly(amidoamines). Biomacromolecules 7 1239-1244... [Pg.248]

The response of the plant host to rhizobial LPS is an area that requires more investigation. The availability of numerous rhizobial symbiont genome sequences, defined LPS mutants and isolated structures from these mutants, as well as a number of legume host sequences (i.e. M. truncatula, Glcyine max, and Lotus japonicus) offer the tools required to define the structure-function aspects that rhizobial LPS play during symbiosis. [Pg.377]

Fig. 4.14. Diagram showing origin of sequences from cloned Alul fragment (cf. Plate I). The dashed underlined sequence is seen to correspond to the underlined bands in Plate I and represents the sequence around the EcofU site in the vector. The third C of the sequence -CCC- defines the start of the cloned Alul fragment and the first G of the -GGG- sequence defines its end. Fig. 4.14. Diagram showing origin of sequences from cloned Alul fragment (cf. Plate I). The dashed underlined sequence is seen to correspond to the underlined bands in Plate I and represents the sequence around the EcofU site in the vector. The third C of the sequence -CCC- defines the start of the cloned Alul fragment and the first G of the -GGG- sequence defines its end.
The sequence of nucleotides in mRNA is converted through the translation machinery into a sequence of amino acids that constitutes a polypeptide. This machinery includes tRNA and ribosomes (which contain rRNA and a collection of unique proteins). The function of tRNA is to act as an adapter between the nucleotide sequence (defining the order of codons) and the amino acid sequence to be assembled into a polypeptide. [Pg.500]

Accordingly, protocols for activating monoesters such as adenosine-5 -phosphate would soon be developed and these breakthroughs would eventually pave the way for H. Khorana and his colleagues pioneering work on phosphodiester chemistry and sequence-defined synthetic oligonucleotides at the University of Wisconsin, Madison. [Pg.105]

The reagents should be added to a new plastic tube, in the sequence defined in Fig. 4.2 and the procedure, as depicted, followed precisely. [Pg.113]

Hays FA, Teegarden AT, Jones ZJR, Harms M, Raup D, Watson J, Cavaliere E, Ho PS. How does sequence define structure A crystallographic map of DNA structure and conformation. Proc. Natl. Acad. Sci. U.S.A. 2005 102 7157-7162. [Pg.1511]

PROOF The Hom-Ext exact sequence defined ty the last row of the diagram splices ... [Pg.60]


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See also in sourсe #XX -- [ Pg.40 ]




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Sequence group, defined

Sequence-defined oligonucleotides

Sequence-defined structures

Tandem sequences defined

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