KEGG   ENZYME: 1.1.1.365
Entry
EC 1.1.1.365                Enzyme                                 
Name
D-galacturonate reductase;
GalUR;
gar1 (gene name)
Class
Oxidoreductases;
Acting on the CH-OH group of donors;
With NAD+ or NADP+ as acceptor
Sysname
L-galactonate:NADP+ oxidoreductase
Reaction(IUBMB)
L-galactonate + NADP+ = D-galacturonate + NADPH + H+ [RN:R07676]
Reaction(KEGG)
R07676
Substrate
L-galactonate [CPD:C15930];
NADP+ [CPD:C00006]
Product
D-galacturonate [CPD:C00333];
NADPH [CPD:C00005];
H+ [CPD:C00080]
Comment
The enzyme from plants is involved in ascorbic acid (vitamin C) biosynthesis [1,2]. The enzyme from the fungus Trichoderma reesei (Hypocrea jecorina) is involved in a eukaryotic degradation pathway of D-galacturonate. It is also active with D-glucuronate and glyceraldehyde [3]. Neither enzyme shows any activity with NADH.
History
EC 1.1.1.365 created 2013
Pathway
ec00040  Pentose and glucuronate interconversions
ec00053  Ascorbate and aldarate metabolism
ec01100  Metabolic pathways
Orthology
K19634  D-galacturonate reductase
K19642  D-galacturonate reductase
Genes
TCC18609968 18609969 18609970
GRA105794339
GHI107909951 107948305
GAB108488709
HSYR120124831
DZI111287841 111318131
EGR104432997
RARG115727805 115727814
QSAO6P43_026045
FVE101312822
AANS126791378
RCN112179335 112180478 112197683
PPER18792656
PMUM103320996 103320997
PAVI110762797 110762798
PDUL117615044
MDM103403467 103403490 114820654
MSYL126597321 126606293 126608385
PXB103943126 103943129
PCOX137731748 137731749 137736573
CSAV115723940
CSV101206206 101220899 105434417
CMO103485931 103504508 127151316
BHJ120079163 120082065
MCHA111023026
CMAX111487459
CMOS111447573
CPEP111776980
MEAN126680207
HBR110634149
MESC110604780 110605509
JRE108996990
CILL122309300
QSU112039299 136062987
QLO115979225 115982098
TWL120013951
VVI100233130 100254148
VRI117912187 117914996 117915195
SLY101256763
SPEN107016409
SOT102586306
SSTN125856242 125856604
SDUL129869902
LBB132614896
NTA107770207 107822373
NSY104245176
NAU109216145
INI109166850
ITR116003821
SIND105160165 105160170 105160182
OEU111399339
EGT105954242
SSPL121793704 121798253 121807646
SMIL130993240
SHIS125204589 125212614
APAN127244994
PEBU140809318 140841874
HAN110870024 110872872 110872873 110872885 110872886 110894612 110894613 110894616 110894617
ECAD122578637 122581227 122586087 122608799 122610221
LSV111905193 111918309 111918314
CSIN114311083
RVL131301271 131301441
AEW130756771 130766070 130781069 130781622 130795620
DLT127809200
MOF131153318
NNU104588465
MING122078230
PSOM113293294 113360647
NCRNCU01906
NTENEUTE1DRAFT126627(NEUTE1DRAFT_126627)
SMP10806512(SMAC4_06811)
PANPODANSg077
PBELQC761_121080(GAR1_1)
PPSDQC762_121080(GAR1_1)
PPSPQC763_121080(GAR1_1)
PPSAQC764_121080(GAR1_1)
TTTTHITE_2111398
MTMMYCTH_110022
CTHRCTHT_0011490
RTHE98122374(VTJ83DRAFT_1558)
MGRMGG_02921
PPEIPpBr36_09319
PGRIPgNI_10451
TMNUCRPA7_7443
SSCKSPSK_06425
FGRFGSG_08941
FPUFPSE_08888
FPOAFPOAC1_005103(GAR1)
FVNFVRRES_05631
FVRFVEG_02550
FOXFOXG_03675
NHENECHADRAFT_67734
FFCNCS54_00441100
FKRNCS57_00448000
FMUJ7337_008889(GAR1_2)
TRETRIREDRAFT_22004(gar1)
TRRM419DRAFT_140803
TATV25781814(TrAtP1_002151)
TASP36607497(GAR1_1)
MAW19252904(GAR1_6)
MAJMAA_08724
MBRN26243754(gar1_1)
PCHMVFPPC_06692
CMTCCM_06560
AMUSLMH87_001790
PLJ28892593(PLICBS_006383)
PTKZJDV02_008185(GAR1_2)
VALVDBG_01939
VDAVDAG_04951
CFJCFIO01_08025
CLUPCLUP02_14820
CHIGCH63R_10014
CDET87938679(CDEST_02176) 87951139(CDEST_14639)
SAPOSAPIO_CDS5111
ELAUCREL1_6384
PFYPFICI_07059
BFUBCIN_06g04660(Bcgar1)
MBEMBM_07852
PSCOLY89DRAFT_621151
GLZGLAREA_12027
ANIANIA_05986
AFMAFUA_2G10220
ACTACLA_069240
NFINFIA_085610
AORAO090011000614
ANGAn16g04770
AFVAFLA_008017
ALUCAKAW2_70408S(GAR1_2)
ACHEACHE_40996S(GAR1_2)
APUUAPUU_11031S(GAR1_1)
PCSN7525_004331
PDPPDIP_64420
POUPOX_f07916
TMFEYB26_003473
TRGTRUGW13939_01503 TRUGW13939_07843
CIMCIMG_04373
CPW9697318(GAR1_2)
UREUREG_01614
PNOSNOG_07475
PTEPTT_19219
PTRR6344358(PtrM4_101730)
BZECOCCADRAFT_2924
BSCCOCSADRAFT_32054
BORCOCMIDRAFT_879
AALTCC77DRAFT_451953
ADAC96089223(ACET3X_008901)
ARABEKO05_0006326
ZTRMYCGRDRAFT_98587
PFJMYCFIDRAFT_85826
FFUCLAFUR5_00543
CBETCB0940_01403
BCOMBAUCODRAFT_518265
NPAUCRNP2_8170
TMLGSTUM_00008536001
 » show all
Reference
1  [PMID:13363799]
  Authors
ISHERWOOD FA, MAPSON LW
  Title
Biological synthesis of ascorbic acid: the conversion of derivatives of D-galacturonic acid into L-ascorbic acid by plant extracts.
  Journal
Biochem J 64:13-22 (1956)
DOI:10.1042/bj0640013
Reference
2  [PMID:12524550]
  Authors
Agius F, Gonzalez-Lamothe R, Caballero JL, Munoz-Blanco J, Botella MA, Valpuesta V
  Title
Engineering increased vitamin C levels in plants by overexpression of a D-galacturonic acid reductase.
  Journal
Nat Biotechnol 21:177-81 (2003)
DOI:10.1038/nbt777
  Sequence
Reference
3  [PMID:16101307]
  Authors
Kuorelahti S, Kalkkinen N, Penttila M, Londesborough J, Richard P
  Title
Identification in the mold Hypocrea jecorina of the first fungal D-galacturonic acid reductase.
  Journal
Biochemistry 44:11234-40 (2005)
DOI:10.1021/bi050792f
  Sequence
Reference
4  [PMID:18768163]
  Authors
Martens-Uzunova ES, Schaap PJ
  Title
An evolutionary conserved d-galacturonic acid metabolic pathway operates across filamentous fungi capable of pectin degradation.
  Journal
Fungal Genet Biol 45:1449-57 (2008)
DOI:10.1016/j.fgb.2008.08.002
Other DBs
ExplorEnz - The Enzyme Database: 1.1.1.365
IUBMB Enzyme Nomenclature: 1.1.1.365
ExPASy - ENZYME nomenclature database: 1.1.1.365
BRENDA, the Enzyme Database: 1.1.1.365
LinkDB

DBGET integrated database retrieval system