CLZ1_COCLU
ID CLZ1_COCLU Reviewed; 277 AA.
AC A0A345BJN9;
DT 02-JUN-2021, integrated into UniProtKB/Swiss-Prot.
DT 07-NOV-2018, sequence version 1.
DT 25-MAY-2022, entry version 5.
DE RecName: Full=Zaragozic acid A biosynthesis cluster protein 1 {ECO:0000303|PubMed:28605916};
DE AltName: Full=Squalestatin S1 biosynthesis cluster protein clz1 {ECO:0000303|PubMed:28605916};
GN Name=clz1 {ECO:0000303|PubMed:28605916};
OS Cochliobolus lunatus (Filamentous fungus) (Curvularia lunata).
OC Eukaryota; Fungi; Dikarya; Ascomycota; Pezizomycotina; Dothideomycetes;
OC Pleosporomycetidae; Pleosporales; Pleosporineae; Pleosporaceae; Curvularia.
OX NCBI_TaxID=5503;
RN [1]
RP NUCLEOTIDE SEQUENCE [GENOMIC DNA], FUNCTION, AND PATHWAY.
RC STRAIN=ATCC 74067;
RX PubMed=28605916; DOI=10.1021/acs.orglett.7b01534;
RA Liu N., Hung Y.S., Gao S.S., Hang L., Zou Y., Chooi Y.H., Tang Y.;
RT "Identification and heterologous production of a benzoyl-primed
RT tricarboxylic acid polyketide intermediate from the zaragozic acid A
RT biosynthetic pathway.";
RL Org. Lett. 19:3560-3563(2017).
CC -!- FUNCTION: Part of the gene cluster that mediates the biosynthesis of
CC squalestatin S1 (SQS1, also known as zaragozic acid A), a heavily
CC oxidized fungal polyketide that offers potent cholesterol lowering
CC activity by targeting squalene synthase (SS) (PubMed:28605916). SQS1 is
CC composed of a 2,8-dioxobicyclic[3.2.1]octane-3,4,5-tricarboxyclic acid
CC core that is connected to two lipophilic polyketide arms
CC (PubMed:28605916). These initial steps feature the priming of an
CC unusual benzoic acid starter unit onto the highly reducing polyketide
CC synthase clz14, followed by oxaloacetate extension and product release
CC to generate a tricarboxylic acid containing product (PubMed:28605916).
CC The phenylalanine ammonia lyase (PAL) clz10 and the acyl-CoA ligase
CC clz12 are involved in transforming phenylalanine into benzoyl-CoA
CC (PubMed:28605916). The citrate synthase-like protein clz17 is involved
CC in connecting the C-alpha-carbons of the hexaketide chain and
CC oxaloacetate to afford the tricarboxylic acid unit (PubMed:28605916).
CC The potential hydrolytic enzymes, clz11 and clz13, are in close
CC proximity to pks2 and may participate in product release
CC (PubMed:28605916). On the other side, the tetraketide arm is
CC synthesized by a the squalestatin tetraketide synthase clz2 and
CC enzymatically esterified to the core in the last biosynthetic step, by
CC the acetyltransferase clz6 (By similarity). The biosynthesis of the
CC tetraketide must involve 3 rounds of chain extension (By similarity).
CC After the first and second rounds methyl-transfer occurs, and in all
CC rounds of extension the ketoreductase and dehydratase are active (By
CC similarity). The enoyl reductase and C-MeT of clz2 are not active in
CC the final round of extension (By similarity). The acetyltransferase
CC clz6 appears to have a broad substrate selectivity for its acyl CoA
CC substrate, allowing the in vitro synthesis of novel squalestatins (By
CC similarity). The biosynthesis of SQS1 requires several oxidative steps
CC likely performed by oxidoreductases clz3, clz15 and clz16 (Probable).
CC Finally, in support of the identification of the cluster as being
CC responsible for SQS1 production, the cluster contains a gene encoding a
CC putative squalene synthase (SS) clz20, suggesting a likely mechanism
CC for self-resistance (Probable). {ECO:0000250|UniProtKB:A0A3G1DJH7,
CC ECO:0000269|PubMed:28605916, ECO:0000305|PubMed:28605916}.
CC -!- PATHWAY: Secondary metabolite biosynthesis.
CC {ECO:0000305|PubMed:28605916}.
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DR EMBL; MF806533; AXF50652.1; -; Genomic_DNA.
DR AlphaFoldDB; A0A345BJN9; -.
PE 3: Inferred from homology;
FT CHAIN 1..277
FT /note="Zaragozic acid A biosynthesis cluster protein 1"
FT /id="PRO_0000452623"
SQ SEQUENCE 277 AA; 31370 MW; 9EE02410533CCB07 CRC64;
MRSPWADDVE YQKDPLFLNY EKRIWDNSTN QTTFSWHKDT REIASSSILA LALVHDVWGP
VIAACSIDAR WAASDIYVIP TNSTVVFSNT TDSLMESLRH SNQGNREANI AKYGLSRNPI
DIQLEWAEKL NRKYIFDLSV KPSQRMKAAP NEEINAIETF LMDIIPSMRV DPSVSTLLGL
IVSDSISRTI NTTRAPWGMV EEVDSNGSWN YSEVVRNSGN ENRPNPDDDN GYVMRVIADR
YGYGFALRVR FGVLYLESLP NGLVPIGDIF VLVWDLN