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Introduction to Enzyme and Coenzyme Chemistry - E-Library Home

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Index 291<br />

riboflavin 123, 129, 141<br />

ribonuclease A 104–7<br />

ribonucleic acid see RNA<br />

ribonucleotide reductase 244–5<br />

ribosomes 11, 258–9<br />

ribozymes 255–9<br />

ribulose biphosphate carboxylase/oxygenase<br />

(Rubisco) 171–3<br />

RNA<br />

catalytic 255–9<br />

cleavage 104–6<br />

types 11, 255<br />

Rubisco 171–3<br />

S-adenosyl homocysteine 113<br />

S-adenosyl homocysteine hydrolase 207<br />

S-adenosyl methionine (SAM) 112–13,<br />

246<br />

S-adenosyl methionine (SAM)-dependent radical<br />

reactions 246–9<br />

salutaridine sythase 185<br />

sarin 116<br />

scurvy 148<br />

secondary deuterium iso<strong>to</strong>pe effect 73–4<br />

secondary metabolites 156<br />

secondary structures, proteins 13–16<br />

selectivity<br />

defined 30<br />

enzyme-substrate interactions 19–22<br />

prochiral 62–7<br />

self-splicing reaction 255–7<br />

sequence alignment 12–13<br />

serine hydroxymethyltransferase 114–15, 215,<br />

220–21<br />

serine proteases 84–9<br />

evolution 90–91<br />

inhibition 86–7<br />

sero<strong>to</strong>nin 214–15<br />

shikimate pathway 193<br />

side chains 8–10<br />

nucleophilic catalysis 43<br />

sinapyl alcohol 186<br />

site-directed mutagenesis 2, 77<br />

specific activity 53<br />

specificity<br />

defined 30<br />

glycosidase enzymes 110<br />

phosphodiesterases 104–5<br />

steady state approximation 55<br />

stereochemical course of reactions 60–68<br />

at glycosyl centre 111–12<br />

chiral products 61–2<br />

of phosphate release 67<br />

prochiral selectivity 62–7<br />

pyruvate carboxylase reaction 172<br />

stereochemical nomenclature 272–3<br />

stereoselectivity<br />

defined 61<br />

hydrolysis 30<br />

stereospecificity, defined 51<br />

s<strong>to</strong>pped flow 59–60, 68<br />

strain energy <strong>and</strong> catalysis 45–6, 111<br />

structure <strong>and</strong> function of enzymes 19–26<br />

strychnine 222, 223, 224<br />

subtilisin 88<br />

sucrose phosphorylase 112<br />

sulochrin oxidase 185<br />

sulphur insertion reactions 249–50<br />

superoxide dismutase 19<br />

synthetic enzyme models 265–70<br />

tau<strong>to</strong>merases, ke<strong>to</strong>-enol 230–31<br />

taxol 5<br />

terpene cyclases 179–83<br />

terpenes 179–80<br />

tertiary structures, protein 16–19<br />

tetrahydrofolate 113–14, 220<br />

Tetrahymena thermophila ribozyme 255–7<br />

thalidomide 6<br />

thermodynamic model of catalysis 31<br />

thermolysin 42, 92, 93, 94<br />

thiamine 3, 250<br />

thiamine pyrophoshate (TPP) 176, 178, 179<br />

thiamine pyrophosphate-dependent<br />

enzymes 176–9<br />

thio-uridine 250<br />

threonine b-epimerase 224<br />

threonine dehydratase 218–19<br />

thymine hydroxylase 153<br />

TPQ 251<br />

trans-2-phenylcylcopropylamine 132<br />

transamination of amino acids 214, 215–18<br />

transcarboxylase 188<br />

transfer reactions<br />

acyl group 99–102<br />

glycosyl group 109<br />

methyl group 112–13<br />

methylene <strong>and</strong> methyne groups 113–15<br />

phosphoryl group 102–6<br />

transke<strong>to</strong>lase enzymes 179

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