KEGG   ENZYME: 4.2.1.181
Entry
EC 4.2.1.181                Enzyme                                 
Name
3-carboxymethyl-3-hydroxy-acyl-[acp] dehydratase;
aprF (gene name);
corF (gene name);
curE (gene name);
pedL (gene name);
3-carboxymethyl-3-hydroxy-acyl-[acyl-carrier protein] dehydratase
Class
Lyases;
Carbon-oxygen lyases;
Hydro-lyases
Sysname
3-carboxymethyl-3-hydroxy-acyl-[acyl-carrier protein] hydro-lyase
Reaction(IUBMB)
a 3-carboxymethyl-3-hydroxy-acyl-[acyl-carrier protein] = a 4-carboxy-3-alkylbut-2-enoyl-[acyl-carrier protein] + H2O [RN:R13242]
Reaction(KEGG)
R13242
Substrate
3-carboxymethyl-3-hydroxy-acyl-[acyl-carrier protein] [CPD:C22847]
Product
4-carboxy-3-alkylbut-2-enoyl-[acyl-carrier protein] [CPD:C22835];
H2O [CPD:C00001]
Comment
This family of enzymes participates in a process that introduces a methyl branch into nascent polyketide products. The process begins with EC 4.1.1.124, malonyl-[acp] decarboxylase, which converts the common extender unit malonyl-[acp] to acetyl-[acp]. The enzyme is a mutated form of a ketosynthase enzyme, in which a Cys residue in the active site is modified to a Ser residue, leaving the decarboxylase function intact, but nulifying the ability of the enzyme to form a carbon-carbon bond. Next, EC 2.3.3.22, 3-carboxymethyl-3-hydroxy-acyl-[acp] synthase, utilizes the acetyl group to introduce the branch at the beta position of 3-oxoacyl intermediates attached to a polyketide synthase, forming a 3-hydroxy-3-carboxymethyl intermediate. This is followed by dehydration catalysed by EC 4.2.1.181, 3-carboxymethyl-3-hydroxy-acyl-[acp] dehydratase (often referred to as an ECH1 domain), leaving a 3-carboxymethyl group and forming a double bond between the alpha and beta carbons. The process concludes with decarboxylation catalysed by EC 4.1.1.125, 4-carboxy-3-alkylbut-2-enoyl-[acp] decarboxylase (often referred to as an ECH2 domain), leaving a methyl branch at the beta carbon. The enzymes are usually encoded by a cluster of genes referred to as an "HMGS cassette", based on the similarity of the key enzyme to EC 2.3.3.10, hydroxymethylglutaryl-CoA synthase. cf. EC 4.2.1.18, methylglutaconyl-CoA hydratase.
History
EC 4.2.1.181 created 2023
Orthology
K15312  3-carboxymethyl-3-hydroxy-acyl-[acp] dehydratase
Genes
SRLSOD_c22840(pksH)
DZCW909_17800
DSOA4U42_06465
DDQDDI_2628
DDADd703_1417
XNMXNC2_1717
LEMLEN_2590(pksH)
LFLIM816_06320
TAMNN4264_14655
PSEPC4K39_4883
PAEWKIH87_10490 KIH87_12130
MOZMoryE10_19250
TIGTHII_2220
GSNYC6258_03056
CVCBKX93_02970
CHROCXB49_16055
CHICN8I74_03990
BMABMAA1215
BMVBMASAVP1_0182
BMLBMA10229_0458
BMNBMA10247_A1117
BMALDM55_4298
BMAEDM78_3872
BMAQDM76_3250
BMAIDM57_10930
BMAFDM51_4878
BMAZBM44_4261
BMABBM45_3384
BPSBPSS1001
BPMBURPS1710b_A2612(pksH)
BPLBURPS1106A_A1383
BPDBURPS668_A1469
BPSEBDL_4295
BPSMBBQ_5133
BPSUBBN_4463
BPSDBBX_6136
BPZBP1026B_II1096
BPQBPC006_II1390
BPKBBK_6146
BPSHDR55_4332
BPSABBU_5028
BPSOX996_4240
BUTX994_6119
BTEBTH_II1669
BTQBTQ_4957
BTJBTJ_3582
BTZBTL_4430
BTDBTI_4277
BTVBTHA_5788
BTHEBTN_4081
BTHMBTRA_4012
BTHADR62_4116
BTHLBG87_4413
BHGI6G56_31645
BUDAQ610_21810
BGDbgla_1g21590 bgla_2g02230
BGOBM43_4521
BULBW21_3817
MNRACZ75_05395
MASSCR152_21530
MFLAGO485_00275
DZOSR858_09950
ETBN7L95_29195
SSDCSSDC_00715(dipC)
ECAAJ3R84_37520
LABPFJ695_03615
SIWGH266_20505
ABQABAZ39_27210
AARED3093_32525
MGYMGMSRv2__1639(pksH)
MGRYMSR1_15750(pksH)
THALA1OE_416
EFKP856_247
MXAMXAN_3940
SCLsce3180
SCUSCE1572_03950
PAUUE8A73_037860
BSUBSU17160(pksH)
BSRI33_1903
BSLA7A1_3370
BSHBSU6051_17160(pksH)
BSYI653_08805
BSUTBSUB_01847(pksH)
BSULBSUA_01847(pksH)
BSUSQ433_09760(baeH)
BSNBSn5_20700
BSQB657_17160(pksH)
BSXC663_1759(pksH)
BSPU712_08995
BSSBSUW23_08825(pksH)
BSTGYO_2071
BITBIS30_19445
BAYRBAM_016960
BAQBACAU_1668(baeH)
BYABANAU_1672(baeH)
BAMPB938_08795(baeH)
BQYMUS_1874(pksH)
BAMLBAM5036_1638(baeH)
BAMARBAU_1677(baeH)
BAMNBASU_1656(baeH)
BAMBBAPNAU_2051(baeH)
BAMTAJ82_09640
BAMYV529_06440(caiD) V529_16560(baeH)
BMPNG74_01763(pksH)
BAOBAMF_1784(baeH)
BAZBAMTA208_08575(baeH)
BQLLL3_01871(baeH)
BXHBAXH7_01748(baeH)
BAMIKSO_010865
BAMCU471_17380
BAMFU722_08990
BSIACWD84_12705
BAEBATR1942_06385
BVMB9C48_08665
BHTDIC78_00755
BIQAN935_11435
BSTRQI003_09265 QI003_12690
BCABEFK13_09420
BRYM0696_09260
BJSMY9_1866
BACPSB24_01205
BACBOY17_11585
BACYQF06_07625
BACLBS34A_18850(pksH)
BALMBsLM_1813
BACSAUL54_02025
BGIBGM20_02980
BRWGOP56_01500 GOP56_04020
PPYPPE_03014
PPMPPSC2_15890(pksH)
PPOPPM_3220(pksH)
PPOLX809_32360
PPQPPSQR21_031850
PPOYRE92_20825
PDUPDUR_14140
PBDPBOR_19395
PAENP40081_13250 P40081_19720
PAEQR50912_18030
PAEAR70723_17165
PPEOABE82_16380
PDHB9T62_00975
PLUTEI981_06660
STRGSRT_10950(corF)
RPAYP0092_11515
LACYA4V08_01180
ACELacsn021_15640(pksH)
VGUHYG85_05760
PFTJBW_04335
MANAMAMMFC1_03230(pksH_1) MAMMFC1_04168(pksH_2)
MSTOMSTO_24510
STREGZL_06866
STRMM444_04630
SPRISPRI_0245 SPRI_7108
SLEsle_09510(sle_09510)
SBYH7H31_30825
SFUGCNQ36_00280
SXNIAG42_36035 IAG42_36330 IAG42_36680
SRUGF0345_27485
SGKPET44_03200
SYUNMOV08_10115
SLAIP8A22_02220
STRZOYE22_30155
PPCHMPREF9154_1025
NAKEKGD83_16505
MHAIOHB01_35460
SENSACE_4571(echA7)
SESPBN6_46210
MAUMicau_3898
MILML5_4519
MTUACSH63_06135
AMSAMIS_50370
DVCDvina_37710
DMATDmats_32740
CAICaci_2596
ACTCCHIBA101_1317
CYNCyan7425_2883
MPROBJP34_29100
NPUNpun_F3166
CSGCylst_1893
CPICpin_5294
CHFKTO58_09940
FUALVD17_26900
KANIMCC3317_14470(pksH_1)
 » show all
Reference
1  [PMID:16834357]
  Authors
Gu L, Jia J, Liu H, Hakansson K, Gerwick WH, Sherman DH.
  Title
Metabolic coupling of dehydration and decarboxylation in the curacin A pathway: functional identification of a mechanistically diverse enzyme pair.
  Journal
J Am Chem Soc 128:9014-5 (2006)
DOI:10.1021/ja0626382
Reference
2  [PMID:19494914]
  Authors
Gu L, Wang B, Kulkarni A, Geders TW, Grindberg RV, Gerwick L, Hakansson K, Wipf P, Smith JL, Gerwick WH, Sherman DH.
  Title
Metamorphic enzyme assembly in polyketide diversification.
  Journal
Nature 459:731-5 (2009)
DOI:10.1038/nature07870
Reference
3  [PMID:20503218]
  Authors
Erol O, Schaberle TF, Schmitz A, Rachid S, Gurgui C, El Omari M, Lohr F, Kehraus S, Piel J, Muller R, Konig GM.
  Title
Biosynthesis of the myxobacterial antibiotic corallopyronin A.
  Journal
Chembiochem 11:1253-65 (2010)
DOI:10.1002/cbic.201000085
  Sequence
Reference
4  [PMID:21533272]
  Authors
Grindberg RV, Ishoey T, Brinza D, Esquenazi E, Coates RC, Liu WT, Gerwick L, Dorrestein PC, Pevzner P, Lasken R, Gerwick WH.
  Title
Single cell genome amplification accelerates identification of the apratoxin biosynthetic pathway from a complex microbial assemblage.
  Journal
PLoS One 6:e18565 (2011)
DOI:10.1371/journal.pone.0018565
  Sequence
Other DBs
ExplorEnz - The Enzyme Database: 4.2.1.181
IUBMB Enzyme Nomenclature: 4.2.1.181
ExPASy - ENZYME nomenclature database: 4.2.1.181
BRENDA, the Enzyme Database: 4.2.1.181

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