Springer Handbook of Enzymes Supplement Volume S1 Dietmar Schomburg and Ida Schomburg (Eds.) Springer Handbook of Enzymes Supplement Volume S1 Class 1 Oxidoreductases (cid:2) EC 1 coedited by Antje Chang Second Edition 1 3 Professor Dietmar Schomburg TechnicalUniversityBraunschweig e-mail: [email protected] Bioinformatics & Systems Biology Langer Kamp 19b Dr. Ida Schomburg 38106 Braunschweig e-mail: [email protected] Germany Dr. Antje Chang e-mail: [email protected] Library of Congress Control Number: 2008942397 ISBN 978-3-540-85187-5 2nd Edition Springer Berlin Heidelberg New York The first edition was published as the “Enzyme Handbook, edited by D. and I.Schomburg”. Thisworkissubjecttocopyright.Allrightsarereserved,whetherthewholeorpartofthematerialis concerned, specifically the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting,reproductiononmicrofilmorinanyotherway,andstorageindatabanks.Duplication ofthispublicationorpartsthereofispermittedonlyundertheprovisionsoftheGermanCopyright LawofSeptember9,1965,initscurrentversion,andpermissionforusemustalwaysbeobtained fromSpringer.ViolationsareliabletoprosecutionundertheGermanCopyrightLaw. SpringerisapartofSpringerScience+BusinessMedia springer.com #Springer-VerlagBerlinHeidelberg2009 PrintedinGermany Theuseofgeneraldescriptivenames,registerednames,etc.inthispublicationdoesnotimply,even intheabsenceofaspecificstatement,thatsuchnamesareexemptfromtherelevantprotectivelaws andregulationsandfreeforgeneraluse. Thepublishercannotassumeanylegalresponsibilityforgivendata,especiallyasfarasdirectionsfor theuseandthehandlingofchemicalsandbiologicalmaterialareconcerned.Thisinformationcanbe obtainedfromtheinstructionsonsafelaboratorypracticeandfromthemanufacturersofchemicals andlaboratoryequipment. Coverdesign:ErichKirchner,Heidelberg Typesetting:medionetPublishingServicesLtd.,Berlin Printedonacid-freepaper 2/3141m-543210 Preface Today, as the full information about the genome is becoming available for a rapidly increasing number of organisms and transcriptome and proteome analysesarebeginningtoprovideuswithamuchwiderimageofproteinregu- lationandfunction,itisobviousthattherearelimitationstoourabilitytoaccess functionaldata for the geneproducts –theproteinsand,inparticular,foren- zymes. Those data are inherently very difficult to collect, interpret and stan- dardizeastheyarewidelydistributedamongjournalsfromdifferentfieldsand areoftensubjectto experimentalconditions.Nevertheless asystematiccollec- tionisessentialforourinterpretationofgenomeinformationandmoresofor applicationsofthisknowledgeinthefieldsofmedicine,agriculture,etc.Progress onenzymeimmobilisation,enzymeproduction,enzymeinhibition,coenzyme regenerationandenzymeengineeringhasopenedupfascinatingnewfieldsfor thepotentialapplicationofenzymesinawiderangeofdifferentareas. ThedevelopmentoftheenzymedatainformationsystemBRENDAwasstartedin 1987 at the German National Research Centre for Biotechnology in Braun- schweig(GBF),continuedattheUniversityofColognefrom1996to2007,and then returned to Braunschweig, to the Technical University, Institute of Bio- informatics & Systems Biology. The present book “Springer Handbookof En- zymes”representstheprintedversionofthisdatabank.Theinformationsystem hasbeendevelopedintoafullmetabolicdatabase. The enzymes in this Handbook are arranged according to the Enzyme Com- mission list of enzymes. Some 4,000 “different” enzymes are covered. Fre- quently enzymes with very different properties are included under the same EC-number.Althoughweintendtogivearepresentativeoverviewonthechar- acteristicsandvariabilityofeachenzyme,theHandbookisnotacompendium. Thereaderwillhavetogototheprimaryliteratureformoredetailedinforma- tion.Naturallyit isnotpossibletocoverallthenumerousliteraturereferences foreachenzyme(forsomeenzymesupto40,000)ifthedatarepresentationisto beconciseasisintended. Itshouldbementionedherethatthedatahavebeenextractedfromtheliterature andcriticallyevaluatedbyqualified scientists.Ontheotherhand,theoriginal authors’ nomenclatureforenzyme formsand subunits is retained. Inorder to keepthetablesconcise,redundantinformationisavoidedasfaraspossible(e.g. if K values are measured inthe presence of an obvious cosubstrate, only the m nameofthecosubstrateisgiveninparenthesesasacommentarywithoutrefer- encetoitsspecificrole). Theauthorsaregratefultothefollowingbiologistsandchemistsforinvaluable helpinthecompilationofdata:CorneliaMunarettoandDr.AntjeChang. Braunschweig Autumn2008 DietmarSchomburg,IdaSchomburg VII List of Abbreviations A adenine Ac acetyl ADP adenosine5’-diphosphate Ala alanine All allose Alt altrose AMP adenosine5’-monophosphate Ara arabinose Arg arginine Asn asparagine Asp asparticacid ATP adenosine5’-triphosphate Bicine N,N’-bis(2-hydroxyethyl)glycine C cytosine cal calorie CDP cytidine5’-diphosphate CDTA trans-1,2-diaminocyclohexane-N,N,N,N-tetraaceticacid CMP cytidine5’-monophosphate CoA coenzymeA CTP cytidine5’-triphosphate Cys cysteine d deoxy- d- (andl-)prefixesindicatingconfiguration DFP diisopropylfluorophosphate DNA deoxyribonucleicacid DPN diphosphopyridiniumnucleotide(nowNAD+) DTNB 5,5’-dithiobis(2-nitrobenzoate) DTT dithiothreitol(i.e.Cleland’sreagent) EC numberofenzymeinEnzymeCommission’ssystem E.coli Escherichiacoli EDTA ethylenediaminetetraacetate EGTA ethyleneglycolbis(-aminoethylether)tetraacetate ER endoplasmicreticulum Et ethyl EXAFS extendedX-rayabsorptionfinestructure FAD flavin-adeninedinucleotide FMN flavinmononucleotide(riboflavin5’-monophosphate) Fru fructose Fuc fucose G guanine Gal galactose IX ListofAbbreviations GDP guanosine5’-diphosphate Glc glucose GlcN glucosamine GlcNAc N-acetylglucosamine Gln glutamine Glu glutamicacid Gly glycine GMP guanosine5’-monophosphate GSH glutathione GSSG oxidizedglutathione GTP guanosine5’-triphosphate Gul gulose h hour H4 tetrahydro HEPES 4-(2-hydroxyethyl)-1-piperazineethanesulfonicacid His histidine HPLC highperformanceliquidchromatography Hyl hydroxylysine Hyp hydroxyproline IAA iodoacetamide IC50 50%inhibitoryconcentration Ig immunoglobulin Ile isoleucine Ido idose IDP inosine5’-diphosphate IMP inosine5’-monophosphate ITP inosine5’-triphosphate K Michaelisconstant m l- (andd-)prefixesindicatingconfiguration Leu leucine Lys lysine Lyx lyxose M mol/l mM millimol/l m- meta- Man mannose MES 2-(N-morpholino)ethanesulfonate Met methionine min minute MOPS 3-(N-morpholino)propanesulfonate Mur muramicacid MW molecularweight NAD+ nicotinamide-adeninedinucleotide NADH reducedNAD NADP+ NADphosphate NADPH reducedNADP NAD(P)H indicateseitherNADHorNADPH X ListofAbbreviations NBS N-bromosuccinimide NDP nucleoside5’-diphosphate NEM N-ethylmaleimide Neu neuraminicacid NMN nicotinamidemononucleotide NMP nucleoside5’-monophosphate NTP nucleoside5’-triphosphate o- ortho- Orn ornithine p- para- PBS phosphate-bufferedsaline PCMB p-chloromercuribenzoate PEP phosphoenolpyruvate pH -log10[H+] Ph phenyl Phe phenylalanine PHMB p-hydroxymercuribenzoate PIXE proton-inducedX-rayemission PMSF phenylmethane-sulfonylfluoride p-NPP p-nitrophenylphosphate Pro proline (cid:3) Q factorforthechangeinreactionratefora10 Ctemperatureincrease 10 Rha rhamnose Rib ribose RNA ribonucleicacid mRNA messengerRNA rRNA ribosomalRNA tRNA transferRNA Sar N-methylglycine(sarcosine) SDS-PAGE sodiumdodecylsulfatepolyacrylamidegelelectrophoresis Ser serine T thymine t timeforhalf-completionofreaction H Tal talose TDP thymidine5’-diphosphate TEA triethanolamine Thr threonine TLCK Na-p-tosyl-l-lysinechloromethylketone T meltingtemperature m TMP thymidine5’-monophosphate Tos- tosyl-(p-toluenesulfonyl-) TPN triphosphopyridiniumnucleotide(nowNADP+) Tris tris(hydroxymethyl)-aminomethane Trp tryptophan TTP thymidine5’-triphosphate Tyr tyrosine U uridine XI ListofAbbreviations U/mg mmol/(mg*min) UDP uridine5’-diphosphate UMP uridine5’-monophosphate UTP uridine5’-triphosphate Val valine Xaa symbolforanaminoacidofunknownconstitutioninpeptideformula XAS X-rayabsorptionspectroscopy Xyl xylose XII Index of Recommended Enzyme Names EC-No. RecommendedName Page 1.14.13.93 (+)-abscisicacid8’-hydroxylase . . . . . . . . . . . . . . . . . 602 1.2.3.14 abscisic-aldehydeoxidase . . . . . . . . . . . . . . . . . . . . 176 1.13.11.53 acireductonedioxygenase(Ni2+-requiring). . . . . . . . . . . . . 470 1.13.11.54 acireductonedioxygenase[iron(II)-requiring] . . . . . . . . . . . 476 1.2.99.7 aldehydedehydrogenase(FAD-independent). . . . . . . . . . . . 219 1.2.7.5 aldehydeferredoxinoxidoreductase. . . . . . . . . . . . . . . . 188 1.3.99.23 all-trans-retinol13,14-reductase . . . . . . . . . . . . . . . . . 268 1.1.1.292 1,5-anhydro-D-fructosereductase(1,5-anhydro-D-mannitol-forming) . 80 1.3.1.77 anthocyanidinreductase . . . . . . . . . . . . . . . . . . . . 231 1.1.1.287 D-arabinitoldehydrogenase(NADP+). . . . . . . . . . . . . . . 64 1.3.1.78 arogenatedehydrogenase(NADP+). . . . . . . . . . . . . . . . 236 1.3.1.79 arogenatedehydrogenase[NAD(P)+] . . . . . . . . . . . . . . . 244 1.4.1.21 aspartatedehydrogenase . . . . . . . . . . . . . . . . . . . . 270 1.21.3.6 aureusidinsynthase . . . . . . . . . . . . . . . . . . . . . . 777 1.17.99.5 bile-acid7a-dehydroxylase . . . . . . . . . . . . . . . . . . . 774 1.17.1.6 bile-acid7a-dehydroxylase(transferredtoEC1.17.99.5(2006)). . . . 728 1.2.7.4 carbon-monoxidedehydrogenase(ferredoxin) . . . . . . . . . . . 179 1.1.1.294 chlorophyll(ide)breductase. . . . . . . . . . . . . . . . . . . 85 1.13.12.14 chlorophyllide-aoxygenase . . . . . . . . . . . . . . . . . . . 490 1.14.13.96 5b-cholestane-3a,7a-diol12a-hydroxylase. . . . . . . . . . . . . 615 1.14.13.98 cholesterol24-hydroxylase. . . . . . . . . . . . . . . . . . . . 623 1.14.99.38 cholesterol25-hydroxylase. . . . . . . . . . . . . . . . . . . . 668 1.13.11.51 9-cis-epoxycarotenoiddioxygenase . . . . . . . . . . . . . . . . 436 1.14.18.2 CMP-N-acetylneuraminatemonooxygenase . . . . . . . . . . . . 651 1.16.8.1 cob(II)yrinicacida,c-diamidereductase . . . . . . . . . . . . . 672 1.8.98.1 CoB-CoMheterodisulfidereductase. . . . . . . . . . . . . . . . 367 1.3.99.22 coproporphyrinogendehydrogenase . . . . . . . . . . . . . . . 262 1.14.11.26 deacetoxycephalosporin-Chydroxylase . . . . . . . . . . . . . . 514 1.1.1.285 3(cid:2)-deamino-3(cid:2)-oxonicotianaminereductase . . . . . . . . . . . . 59 1.14.11.24 2’-deoxymugineic-acid2’-dioxygenase . . . . . . . . . . . . . . 510 1.14.13.91 deoxysarpaginehydroxylase. . . . . . . . . . . . . . . . . . . 593 1.14.13.103 8-dimethylallylnaringenin2’-hydroxylase . . . . . . . . . . . . . 648 1.2.1.72 erythrose-4-phosphatedehydrogenase . . . . . . . . . . . . . . 171 1.14.11.22 flavonesynthase . . . . . . . . . . . . . . . . . . . . . . . . 500 1.14.13.88 flavonoid3’,5’-hydroxylase . . . . . . . . . . . . . . . . . . . 571 1.14.11.23 flavonolsynthase. . . . . . . . . . . . . . . . . . . . . . . . 504 1.3.3.12 L-galactonolactoneoxidase . . . . . . . . . . . . . . . . . . . 258 1.1.1.281 GDP-4-dehydro-6-deoxy-D-mannosereductase. . . . . . . . . . . 19 1.2.1.70 glutamyl-tRNAreductase . . . . . . . . . . . . . . . . . . . . 160 1.14.13.85 glyceollinsynthase . . . . . . . . . . . . . . . . . . . . . . . 556 1.2.7.6 glyceraldehyde-3-phosphatedehydrogenase(ferredoxin). . . . . . . 203 1.14.11.27 [histone-H3]-lysine-36demethylase. . . . . . . . . . . . . . . . 522 1.1.1.278 3b-hydroxy-5a-steroiddehydrogenase . . . . . . . . . . . . . . 10 1.1.1.277 3b-hydroxy-5b-steroiddehydrogenase. . . . . . . . . . . . . . . 8 1.14.13.84 4-hydroxyacetophenonemonooxygenase . . . . . . . . . . . . . 545 XIII IndexofRecommendedEnzymeNames 1.1.1.279 (R)-3-hydroxyacid-esterdehydrogenase . . . . . . . . . . . . . 14 1.1.1.280 (S)-3-hydroxyacid-esterdehydrogenase . . . . . . . . . . . . . 16 1.14.13.95 7a-hydroxycholest-4-en-3-one12a-hydroxylase. . . . . . . . . . 611 1.14.13.100 25-hydroxycholesterol7a-hydroxylase. . . . . . . . . . . . . . 633 1.14.13.99 24-hydroxycholesterol7a-hydroxylase. . . . . . . . . . . . . . 631 1.14.13.86 2-hydroxyisoflavanonesynthase . . . . . . . . . . . . . . . . 559 1.7.99.8 hydroxylamineoxidoreductase . . . . . . . . . . . . . . . . . 285 1.1.1.284 S-(hydroxymethyl)glutathionedehydrogenase. . . . . . . . . . . 38 1.1.1.291 2-hydroxymethylglutaratedehydrogenase . . . . . . . . . . . . 78 1.17.3.3 6-hydroxynicotinatedehydrogenase . . . . . . . . . . . . . . . 757 1.13.11.52 indoleamine2,3-dioxygenase. . . . . . . . . . . . . . . . . . 445 1.2.7.8 indolepyruvateferredoxinoxidoreductase . . . . . . . . . . . . 213 1.1.1.286 isocitrate-homoisocitratedehydrogenase. . . . . . . . . . . . . 61 1.14.13.89 isoflavone2’-hydroxylase . . . . . . . . . . . . . . . . . . . 582 1.14.21.6 lathosteroloxidase . . . . . . . . . . . . . . . . . . . . . . 662 1.14.13.87 licodionesynthase . . . . . . . . . . . . . . . . . . . . . . 568 1.14.13.94 lithocholate6b-hydroxylase . . . . . . . . . . . . . . . . . . 608 1.4.3.20 L-lysine6-oxidase. . . . . . . . . . . . . . . . . . . . . . . 275 1.1.99.31 (S)-mandelatedehydrogenase. . . . . . . . . . . . . . . . . . 144 1.8.4.14 L-methionine(R)-S-oxidereductase. . . . . . . . . . . . . . . 361 1.8.4.13 L-methionine(S)-S-oxidereductase . . . . . . . . . . . . . . . 357 1.2.7.7 3-methyl-2-oxobutanoatedehydrogenase(ferredoxin) . . . . . . . 207 1.5.7.1 methylenetetrahydrofolatereductase(ferredoxin) . . . . . . . . . 279 1.1.1.283 methylglyoxalreductase(NADPH-dependent) . . . . . . . . . . 32 1.14.11.25 mugineic-acid3-dioxygenase. . . . . . . . . . . . . . . . . . 512 1.17.1.5 nicotinatedehydrogenase . . . . . . . . . . . . . . . . . . . 719 1.13.12.13 Oplophorus-luciferin2-monooxygenase . . . . . . . . . . . . . 488 1.1.99.30 2-oxo-acidreductase . . . . . . . . . . . . . . . . . . . . . 134 1.2.7.9 2-oxoglutarateferredoxinoxidoreductase(deleted2005) . . . . . . 217 1.8.4.12 peptide-methionine(R)-S-oxidereductase . . . . . . . . . . . . 328 1.8.4.11 peptide-methionine(S)-S-oxidereductase . . . . . . . . . . . . 291 1.11.1.15 peroxiredoxin . . . . . . . . . . . . . . . . . . . . . . . . 403 1.14.13.92 phenylacetonemonooxygenase . . . . . . . . . . . . . . . . . 595 1.17.5.1 phenylacetyl-CoAdehydrogenase . . . . . . . . . . . . . . . . 761 1.14.12.19 3-phenylpropanoatedioxygenase . . . . . . . . . . . . . . . . 529 1.14.12.20 pheophorbideaoxygenase. . . . . . . . . . . . . . . . . . . 532 1.1.1.290 4-phosphoerythronatedehydogenase . . . . . . . . . . . . . . 75 1.3.1.76 precorrin-2dehydrogenase. . . . . . . . . . . . . . . . . . . 226 1.14.13.83 precorrin-3Bsynthase. . . . . . . . . . . . . . . . . . . . . 541 1.7.1.13 preQ1synthase. . . . . . . . . . . . . . . . . . . . . . . . 282 1.14.11.28 proline3-hydroxylase . . . . . . . . . . . . . . . . . . . . . 524 1.14.13.102 psoralensynthase. . . . . . . . . . . . . . . . . . . . . . . 643 1.1.99.29 pyranosedehydrogenase(acceptor) . . . . . . . . . . . . . . . 124 1.5.1.35 1-pyrrolinedehydrogenase(deleted,identicalto1.2.1.19) . . . . . . 278 1.3.3.11 pyrroloquinoline-quinonesynthase . . . . . . . . . . . . . . . 255 1.1.1.282 quinate/shikimatedehydrogenase . . . . . . . . . . . . . . . . 22 1.1.5.2 quinoproteinglucosedehydrogenase . . . . . . . . . . . . . . 88 1.3.1.80 redchlorophyllcatabolitereductase. . . . . . . . . . . . . . . 246 1.10.99.2 ribosyldihydronicotinamidedehydrogenase(quinone). . . . . . . 383 1.97.1.9 selenatereductase. . . . . . . . . . . . . . . . . . . . . . . 782 1.14.13.101 senecionineN-oxygenase . . . . . . . . . . . . . . . . . . . 638 1.1.1.276 serine3-dehydrogenase . . . . . . . . . . . . . . . . . . . . 3 1.1.99.32 L-sorbose1-dehydrogenase. . . . . . . . . . . . . . . . . . . 159 XIV