KEGG   ENZYME: 4.1.2.10
Entry
EC 4.1.2.10                 Enzyme                                 
Name
(R)-mandelonitrile lyase;
(R)-oxynitrilase;
oxynitrilase;
D-oxynitrilase;
D-alpha-hydroxynitrile lyase;
mandelonitrile benzaldehyde-lyase;
PaHNL;
AtHNL;
PhaMDL;
(R)-HNL;
(R)-PeHNL;
(R)-hydroxynitrile lyase;
R-selective hydroxynitrile lyase;
R-selective HNL;
(R)-(+)-mandelonitrile lyase
Class
Lyases;
Carbon-carbon lyases;
Aldehyde-lyases
Sysname
(R)-mandelonitrile benzaldehyde-lyase (cyanide-forming)
Reaction(IUBMB)
(R)-mandelonitrile = cyanide + benzaldehyde [RN:R01767]
Reaction(KEGG)
R01767;
(other) R01409 R02811
Substrate
(R)-mandelonitrile [CPD:C00561]
Product
cyanide [CPD:C00177];
benzaldehyde [CPD:C00261]
Comment
A variety of enzymes from different sources and with different properties. Some are flavoproteins, others are not. Active towards a number of aromatic and aliphatic hydroxynitriles (cyanohydrins).
History
EC 4.1.2.10 created 1961, modified 1999, modified 2011
Pathway
ec00460  Cyanoamino acid metabolism
ec01100  Metabolic pathways
ec01110  Biosynthesis of secondary metabolites
Orthology
K08248  (R)-mandelonitrile lyase
K20802  (R)-mandelonitrile lyase
Genes
ATHAT1G73050 AT5G10300(MES5)
ALY9309518 9324968
CRB17882602 17894548
CSAT104701992 104708070 104712914 104735043 104751159 104769234
EUSEUTSA_v10014451mg EUTSA_v10018360mg
BRP103831793 103846819 103852822
BNA106354249 106372481 106381275 106402693 106404872
BOE106299217 106312968 106327722
RSZ108814498 108841961 108841964
THJ104798892 104812207
CPAP110824699 110824820
CIT102626291
CICCICLE_v10025302mg
PVY116104932
MINC123212454 123212483
TCC18595196
GRA105767552
GHI107906346 107958501
GAB108453003 108465479
HSYR120133426 120148998 120191477
DZI111280688
EGR104423258
GMX100820069
GSJ114419167
PVUPHAVU_010G162900g
VRA106773780
VAR108320669
VUN114165905
VUM124835873
CCAJ109808261
APRC113857241
MTR11434866
TPRA123923187
CAM101508164
PSAT127107124
VVO131606069
LJALj3g3v2040180.1(Lj3g3v2040180.1)
ADU107482361
AIP107635832
AHF112740806 112795530
LANG109356592
PCIN129287440 129291371 129295005
QSAO6P43_017898 O6P43_027981
FVE101298340 101314080
RCN112189159 112195896 112199010 112200405
PPER109946273 109946518 109946533 109946707 109946708 109946737 109948219 109948555 18788267 18788307 18789360 18790170 18790921 18792725 18792970
PMUM103323319 103323417 103323418 103323458 103323460 103323461 103323462 103323463 103323464 103323465 103323466 103328816 103344346 103344354
PAVI110748378 110749710 110752511 110752512 110752514 110752517 110752520 110752523 110752528 110752533 110752546 110767481 110772812 110774301
PDUL117614487 117614647 117614649 117615086 117615220 117615239 117615281 117615325 117615505 117617267 117623911 117635510
MDM103404510 103416927 103417232 103417299 103420796 103429895 103429959 103443315 103447443 103447445 103447446 114819207 114823910
MSYL126583382 126591179 126591180 126591181 126591182 126595139 126606559 126607412 126610129 126616874 126616875 126616876
PXB103926833 103926855 103931741 103944089 103944905 103944906 103944908 103954303 108867073
ZJU107405884 107405886 107405923 107405924 107405925 107405927 107407673 107410829 107410921 107411003 107414212 107414223 107414239 107414267 107414317 107414349 107414388 107415173 107428185 107432121 107432123 107432124 112493444 125418345 125423758 125424306 132799199 132800150 132800219 132800225 132800258 132800283 132800336 132800337 132800343 132800347 132800821 132803410 132805279 132805365 132805367 132805371
MNT21388472 21405661 21405817 21405818 21405819
CSAV115694894 115694898 115695176 115695919 115695926 115695941 115714652 115718612 115724435 115724498 115724686 115725080 115725081 115725720
CSV101211615 101212821 101213062 101213549 101213785 101214030 101214272 101214723 101218493 116401960 116401973 116401986
CMO103493044 103493053 103493064 103493073 103493083 103493093 103493130 103493164 103493179 103493189 103500635
BHJ120079226 120079227 120079228 120079550 120080282 120080549 120086734
MCHA111020834 111020835 111020836 111020841
CMAX111465496 111465498 111488606 111492330 111492348 111494473
CMOS111436113 111436125 111436223 111444087 111444097 111450816 111456379 111464460
CPEP111779136 111799103 111804863 111805062 111805571 111805875 111807599
RCU107260750
JCU105643749
HBR110655857
MESC110603558 110628615
POP7490862
PEU105131644 105141162
PALZ118045144 118059813
JRE108983056 109004998
CILL122300687 122300854
CAVE132187742
QSU112001779
QLO115989370
TWL120008047 120011473
VVI100254058
VRI117905746
SLY101250204
SPEN107014093
SOT102580581
SSTN125857664
SDUL129896937
CANN107865788
LBB132634393
NTA107771021 107780107
NSY104246964
NTO104107041
NAU109224695
INI109187446 109187563 109192240
ITR115996468 116011297
SIND105157899
OEU111401494
EGT105954354
SSPL121778127 121781122
SMIL131013069
APAN127241769
HAN110874223 110877473 110877524 110877525 110886397 110886885 110886886 110894152 110913082 110916839 110917615 110929299 110929300 110929307 110929308 110931731
ECAD122589929 122597922 122599479 122600961
LSV111879508 111909027 111910381 111915295
CCAV112504716 112509255 112517338
DCR108225454 108227163
CSIN114311932
RVL131335570
AEW130796241
BVG104901404
SOE110785208
CQI110706134 110713236
ATRI130824369
MOF131157848 131159594 131159597 131159600
NNU104599090
MING122073004
TSS122657587
PSOM113275657 113277545
OSA9266710
DOSAOs06t0656000-00(Os06g0656000)
OBR102719124
OGL127775358
BDI100822804
ATS109783110
TDC119333926 119339393
TAES123154811 123160447 123171371
TUA125525090
LPER127311746
LRD124684348 124684531
SBI8069366
ZMA100382914
SITA101763110
SVS117853312
PVIR120671531 120704924
PHAI112888364
PDA103715972
EGU105039402
MUS103977401
DCT110096808
AOF109842577 109842578 109842616
MSIN131256359 131256384
NCOL116250416
ATR18438828 18440898
 » show all
Reference
1  [PMID:18540101]
  Authors
Ueatrongchit T, Kayo A, Komeda H, Asano Y, H-Kittikun A
  Title
Purification and characterization of a novel (R)-hydroxynitrile lyase from Eriobotrya japonica (Loquat).
  Journal
Biosci Biotechnol Biochem 72:1513-22 (2008)
DOI:10.1271/bbb.80023
Reference
2
  Authors
Lin, G., Han, S. and Li, Z.
  Title
Enzymic synthesis of (R)-cyanohydrins by three (R)-oxynitrilase sources in micro-aqueous organic medium.
  Journal
Tetrahedron 55:3531-3540 (1999)
Reference
3
  Authors
de Gonzalo, G., Brieva, R. and Gotor, V.
  Title
(R)-Oxynitrilase-catalyzed transformation of omega-hydroxyalkanals.
  Journal
J Mol Catal B 19-20:223-230 (2002)
Reference
4  [PMID:25919621]
  Authors
Ueatrongchit T, Tamura K, Ohmiya T, H-Kittikun A, Asano Y
  Title
Hydroxynitrile lyase from Passiflora edulis: Purification, characteristics and application in asymmetric synthesis of (R)-mandelonitrile.
  Journal
Enzyme Microb Technol 46:456-65 (2010)
DOI:10.1016/j.enzmictec.2010.02.008
Reference
5  [PMID:17907254]
  Authors
Andexer J, von Langermann J, Mell A, Bocola M, Kragl U, Eggert T, Pohl M
  Title
An R-selective hydroxynitrile lyase from Arabidopsis thaliana with an alpha/beta-hydrolase fold.
  Journal
Angew Chem Int Ed Engl 46:8679-81 (2007)
DOI:10.1002/anie.200701455
  Sequence
[ath:AT5G10300]
Reference
6  [PMID:19433222]
  Authors
Guterl JK, Andexer JN, Sehl T, von Langermann J, Frindi-Wosch I, Rosenkranz T, Fitter J, Gruber K, Kragl U, Eggert T, Pohl M
  Title
Uneven twins: comparison of two enantiocomplementary hydroxynitrile lyases with alpha/beta-hydrolase fold.
  Journal
J Biotechnol 141:166-73 (2009)
DOI:10.1016/j.jbiotec.2009.03.010
  Sequence
[ath:AT5G10300]
Other DBs
ExplorEnz - The Enzyme Database: 4.1.2.10
IUBMB Enzyme Nomenclature: 4.1.2.10
ExPASy - ENZYME nomenclature database: 4.1.2.10
BRENDA, the Enzyme Database: 4.1.2.10
CAS: 9024-43-5
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