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1-72 of about 72 matches for site:www.ncbi.nlm.nih.gov side-chain
https://www.ncbi.nlm.nih.gov/books/NBK453048/
Figure 3.1 . An N-glycan makes a glycosidic bond with the side-chain nitrogen of
https://www.ncbi.nlm.nih.gov/books/NBK20734/
the species. Modifications of the C9 hydroxyl group on the side chain of sialic
https://www.ncbi.nlm.nih.gov/books/NBK20724/
the fact that the O-acetyl esters can migrate along the side chain (from the
https://www.ncbi.nlm.nih.gov/books/NBK215044/
may be classified into two groups based on molecular weight. Accordingly, low-molecular-weight phthalates (ester side-chain lengths, one to
https://www.ncbi.nlm.nih.gov/books/NBK92775/
urine, suggesting that [6]-gingerol undergoes conjugation and oxidation of its phenolic side chain ( Nakazawa and
https://www.ncbi.nlm.nih.gov/gtr/conditions/C0085859/
Abnormality of the immune system See: Feature record | Search on this feature Anti-side-chain cleavage enzyme antibody
https://www.ncbi.nlm.nih.gov/books/NBK453082/
carried on one monosaccharide, including a carboxylic acid, a 3-carbon exocyclic side chain, and often
https://www.ncbi.nlm.nih.gov/books/NBK453092/
3 , bottom). Loop A contains an invariant aspartate, which forms hydrogen bonds between its side chain and the
https://www.ncbi.nlm.nih.gov/books/NBK453021/
and glycolipids involves glycosyltransferases that attach sugars to either a polypeptide side chain or a
https://www.ncbi.nlm.nih.gov/books/NBK20722/
Figure 39.1 . The most commonly used protocol involves amino acids that have their side-chain functional groups (amines
https://www.ncbi.nlm.nih.gov/books/NBK453049/
HG). The borate ester is formed between the apiosyl residue in side chain A of
https://www.ncbi.nlm.nih.gov/books/NBK548287/
1979, 2001, N). The synthetic quaternary ammonium derivatives have a bulky ammonium side chain that makes them
https://www.ncbi.nlm.nih.gov/gene/1591
the physiologically active form of vitamin D3, by hydroxylation of the side chain. In regulating
https://www.ncbi.nlm.nih.gov/gene/1591
the physiologically active form of vitamin D3, by hydroxylation of the side chain. In regulating
https://www.ncbi.nlm.nih.gov/books/NBK453073/
G β-strands that interact with the N-acetyl group and glycerol side chain of Sia
https://www.ncbi.nlm.nih.gov/books/NBK453068/
example, in Leishmania majo r, the PG repeats bear β1-3-galactosyl side-chain modifications, which provide
https://www.ncbi.nlm.nih.gov/books/NBK453072/
terminal GPI-addition signal peptide, and (3) lipid remodeling and/or carbohydrate side-chain modifications in
https://www.ncbi.nlm.nih.gov/books/NBK279150/
forms of vitamin D, although the differences in the side chain (double bond at
https://www.ncbi.nlm.nih.gov/books/NBK92775/
urine, suggesting that [6]-gingerol undergoes conjugation and oxidation of its phenolic side chain ( Nakazawa and
https://www.ncbi.nlm.nih.gov/books/NBK26928/
them in the process. Both the backbone and the side-chain sugars vary according
https://www.ncbi.nlm.nih.gov/books/NBK572151/
the amino acid sequence of mammalian GLP-1. A free fatty acid side chain is attached to
https://www.ncbi.nlm.nih.gov/books/NBK278951/
factor I; PTX, pentraxin; TNFAIP6, tumor necrosis factor-induced protein 6; LH, luteinizing hormone; P450SCC, P450 side chain cleavage; P450AROM, P450
https://www.ncbi.nlm.nih.gov/books/NBK453041/
the transfer of the glycan to proteins. Defects in side-chain modifications ( PIGN and
https://www.ncbi.nlm.nih.gov/books/NBK279000/
contributes ( 8 ). Testosterone biosynthesis involves two multifunctional cytochrome P-450 complexes involving hydroxylations and side-chain scissions (cholesterol side
https://www.ncbi.nlm.nih.gov/books/NBK279129/
step in biodegradation. After several further hydroxylations, cleavage of the secosteroid side chain occurs between carbons
https://www.ncbi.nlm.nih.gov/books/NBK453078/
ligand in the binding site, mitigating the problem of optimizing side chain conformations. For
https://www.ncbi.nlm.nih.gov/books/NBK548287/
1979, 2001, N). The synthetic quaternary ammonium derivatives have a bulky ammonium side chain that makes them
https://www.ncbi.nlm.nih.gov/books/NBK279000/
contributes ( 8 ). Testosterone biosynthesis involves two multifunctional cytochrome P-450 complexes involving hydroxylations and side-chain scissions (cholesterol side
https://www.ncbi.nlm.nih.gov/books/NBK26911/
elastase, and other serine proteases (see Figure 3-14). The aspartic acid side chain (Asp 102) induces
https://www.ncbi.nlm.nih.gov/medgen/83341
C0342474 • Disease or Syndrome Synonyms: ADRENAL HYPERPLASIA I; Cholesterol Desmolase-Deficient Congenital Adrenal Hyperplasia; Cholesterol monooxygenase (side-chain cleaving) deficiency; Congenital
https://www.ncbi.nlm.nih.gov/books/NBK557435/
of 17 alpha-hydroxylase, 3 beta-hydroxysteroid dehydrogenase, steroid acute regulatory protein, P450 oxidoreductase, P450 side-chain cleaving enzyme. Measurement
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r20
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r24
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r1
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r16
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r8
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r11
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r7
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r23
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r17
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#__NBK551616_dtls__
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r12
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r14
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r10
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r2
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r6
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r18
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r19
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r25
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r13
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r15
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r9
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r21
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#maincontent
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#__NBK551616_ai__
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r4
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r5
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r22
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK551616/#article-26396.r3
supplements, accumulating evidence favors the use of cholecalciferol over ergocalciferol because its side chain has a
https://www.ncbi.nlm.nih.gov/books/NBK92776/
et al. 1983 ; Figure 8.1a ). The chemical structure of the side chain at the
https://www.ncbi.nlm.nih.gov/medgen/18705
133-142. Epub 2023 Jan 20 doi: 10.1016/j.ygyno.2022.12.008. PMID: 36682091 Side-chain cleavage enzyme deficiency
https://www.ncbi.nlm.nih.gov/tools/msaviewer/embedding-api/
from blosum80.iij BLOSUM Clustered Scoring Matrix in 1/2 Bit Units hydropathy – Protein: Side chain hydropathy, corrected for
https://www.ncbi.nlm.nih.gov/Structure/structure_news.html
angstrom from the SNP, uses rotamer libraries to predict the side chain conformation, and
https://www.ncbi.nlm.nih.gov/books/NBK557435/
of 17 alpha-hydroxylase, 3 beta-hydroxysteroid dehydrogenase, steroid acute regulatory protein, P450 oxidoreductase, P450 side-chain cleaving enzyme. Measurement
https://www.ncbi.nlm.nih.gov/books/NBK26921/
immune response on its own, when it is coupled covalently to a lysine side chain on a
https://www.ncbi.nlm.nih.gov/tools/msaviewer/tutorial1/
rows in the alignment at that position. Hydropathy Scale This coloration method reflects side chain hydropathy, with very
https://www.ncbi.nlm.nih.gov/tools/sviewer/embedding-api/
the quality scoring is above (or below) a given threshold Hydropathy Scale Protein: Side chain hydropathy, corrected for
https://www.ncbi.nlm.nih.gov/Structure/VAST/vasthelp.html
fraction of residues with missing coordinates Low fraction of residues with incomplete side-chain coordinates High resolution
https://www.ncbi.nlm.nih.gov/books/NBK26829/
activation. The two-step process in which an amino acid (with its side chain denoted by R
https://www.ncbi.nlm.nih.gov/Structure/MMDB/docs/mmdb_news.html
angstrom from the SNP, uses rotamer libraries to predict the side chain conformation, and