Detail Information for IndEnz0010000665
IED ID IndEnz0010000665
Enzyme Type ID esterase000665
Protein Name Compactin diketide synthase mlcB
EC 2.3.1.244
Compactin biosynthesis protein B
Gene Name mlcB
Organism Penicillium citrinum
Taxonomic Lineage cellular organisms Eukaryota Opisthokonta Fungi Dikarya Ascomycota saccharomyceta Pezizomycotina leotiomyceta Eurotiomycetes Eurotiomycetidae Eurotiales (green and blue molds) Aspergillaceae Penicillium Penicillium citrinum
Enzyme Sequence MNNTPAVTATATATATATAMAGSACSNTSTPIAIVGMGCRFAGDATSPQKLWEMVERGGSAWSKVPSSRFNVRGVYHPNGERVGSTHVKGGHFIDEDPALFDAAFFNMTTEVASCMDPQYRLMLEVVYESLESAGITIDGMAGSNTSVFGGVMYHDYQDSLNRDPETVPRYFITGNSGTMLSNRISHFYDLRGPSVTVDTACSTTLTALHLACQSLRTGESDTAIVIGANLLLNPDVFVTMSNLGFLSPDGISYSFDPRANGYGRGEGIAALVIKALPNALRDQDPIRAVIRETALNQDGKTPAITAPSDVAQKSLIQECYDKAGLDMSLTSYVEAHGTGTPTGDPLEISAISAAFKGHPLHLGSVKANIGHTEAASGLASIIKVALALEKGLIPPNARFLQKNSKLMLDQKNIKIPMSAQDWPVKDGTRRASVNNFGFGGSNAHVILESYDRASLALPEDQVHVNGNSEHGRVEDGSKQSRIYVVRAKDEQACRRTIASLRDYIKSVADIDGEPFLASLAYTLGSRRSILPWTSVYVADSLGGLVSALSDESNQPKRANEKVRLGFVFTGQGAQWHAMGRELVNTFPVFKQAILECDGYIKQLGASWNFMEELHRDELTTRVNDAEYSLPLSTAIQIALVRLLWSWGIRPTGITSHSSGEAAAAYAAGALSARSAIGITYIRGVLTTKPKPALAAKGGMMAVGLGRSETNVYISRLNQEDGCVVVGCINSQCSVTVSGDLGAIEKLEKLLHADGIFTRKLKVTEAFHSSHMRPMADAFGASLRDLFNSDNNNDNPNADTSKGVLYSSPKTGSRMTDLKLLLDPTHWMDSMLQPVEFESSLREMCFDPNTKEKAVDVIIEIGPHGALGGPINQVMQDLGLKGTDINYLSCLSRGRSSLETMYRAATELISKGYGLKMDAINFPHGRKEPRVKVLSDLPAYPWNHQTRYWREPRGSRESKQRTHPPHTLIGSRESLSPQFAPKWKHVLRLSDIPWIRDHVVGSSIIFPGAGFISMAIEGFSQVCPPVAGASINYNLRDVELAQALIIPADAEAEVDLRLTIRSCEERSLGTKNWHQFSVHSISGENNTWTEHCTGLIRSESERSHLDCSTVEASRRLNLGSDNRSIDPNDLWESLHANGICHGPIFQNIQRIQNNGQGSFCRFSIADTASAMPHSYENRHIVHPTTLDSVIQAAYTVLPYAGTRMKTAMVPRRLRNVKISSSLADLEAGDALDAQASIKDRNSQSFSTDLAVFDDYDSGSSPSDGIPVIEIEGLVFQSVGSSFSDQKSDSNDTENACSSWVWAPDISLGDSTWLKEKLSTEAETKETELMMDLRRCTINFIQEAVTDLTNSDIQHLDGHLQKYFDWMNVQLDLARQNKLSPASCDWLSDDAEQKKCLQARVAGESVNGEMISRLGPQLIAMLRRETEPLELMMQDQLLSRYYVNAIKWSRSNAQASELIRLCAHKNPRSRILEIGGGTGGCTKLIVNALGNTKPIDRYDFTDVSAGFFESAREQFADWQDVMTFKKLDIESDPEQQGFECATYDVVVACQVLHATRCMKRTLSNVRKLLKPGGNLILVETTRDQLDLFFTFGLLPGWWLSEEPERKSTPSLTTDLWNTMLDTSGFNGVELEVRDCEDDEFYMISTMLSTARKENTTPDTVAESEVLLLHGALRPPSSWLESLQAAICEKTSSSPSINALGEVDTTGRTCIFLGEMESSLLGEVGSETFKSITAMLNNCNALLWVSRGAAMSSEDPWKALHIGLLRTIRNENNGKEYVSLDLDPSRNAYTHESLYAICNIFNGRLGDLSEDKEFEFAERNGVIHVPRLFNDPHWKDQEAVEVTLQPFEQPGRRLRMEVETPGLLDSLQFRDDEGREGKDLPDDWVEIEPKAFGLNFRDVMVAMGQLEANRVMGFECAGVITKLGGAAAASQGLRLGDRVCALLKGHWATRTQTPYTNVVRIPDEMGFPEAASVPLAFTTAYIALYTTAKLRRGERVLIHSGAGGVGQAAIILSQLAGAEVFVTAGTQAKRDFVGDKFGINPDHIFSSRNDLFVDGIKAYTGGLGVHVVLNSLAGQLLQASFDCMAEFGRFVEIGKKDLEQNSRLDMLPFTRDVSFTSIDLLSWQRAKSEEVSEALNHVTKLLETKAIGLIGPIQQHSLSNIEKAFRTMQSGQHVGKVVVNVSGDELVPVGDGGFSLKLKPDSSYLVAGGLGGIGKQICQWLVDHGAKHLIILSRSAKASPFITSLQNQQCAVYLHACDISDQDQVTKVLRLCEEAHAPPIRGIIQGAMVLKDALLSRMTLDEFNAATRPKVQGSWYLHKIAQDVDFFVMLSSLVGVMGGAGQANYAAAGAFQDALAHHRRAHGMPAVTIDLGMVKSVGYVAETGRGVADRLARIGYKPMHEKDVMDVLEKAILCSSPQFPSPPAAVVTGINTSPGAHWTEANWIQEQRFVGLKYRQVLHADQSFVSSHKKGPDGVRAQLSRVTSHDEAISIVLKAMTEKLMRMFGLAEDDMSSSKNLAGVGVDSLVAIELRNWITSEIHVDVSIFELMNGNTIAGLVELVVAKCS
Enzyme Length 2563
Uniprot Accession Number Q8J0F5
Absorption
Active Site ACT_SITE 202; /note=For beta-ketoacyl synthase activity; /evidence=ECO:0000255|PROSITE-ProRule:PRU10022; ACT_SITE 658; /note=For malonyltransferase activity; /evidence=ECO:0000255|PROSITE-ProRule:PRU10022; ACT_SITE 998; /note=For beta-hydroxyacyl dehydratase activity; /evidence=ECO:0000255|PROSITE-ProRule:PRU10022
Activity Regulation
Binding Site
Calcium Binding
catalytic Activity CATALYTIC ACTIVITY: Reaction=3 H(+) + holo-[2-methylbutanoate polyketide synthase] + 2 malonyl-CoA + 2 NADPH + S-adenosyl-L-methionine = (S)-2-methylbutanoyl-[2-methylbutanoate polyketide synthase] + 2 CO2 + 2 CoA + H2O + 2 NADP(+) + S-adenosyl-L-homocysteine; Xref=Rhea:RHEA:42852, Rhea:RHEA-COMP:10260, Rhea:RHEA-COMP:10261, ChEBI:CHEBI:15377, ChEBI:CHEBI:15378, ChEBI:CHEBI:16526, ChEBI:CHEBI:57287, ChEBI:CHEBI:57384, ChEBI:CHEBI:57783, ChEBI:CHEBI:57856, ChEBI:CHEBI:58349, ChEBI:CHEBI:59789, ChEBI:CHEBI:64479, ChEBI:CHEBI:82764; EC=2.3.1.244; Evidence={ECO:0000269|PubMed:12172803};
DNA Binding
EC Number 2.3.1.244
Enzyme Function FUNCTION: Diketide synthase; part of the gene cluster that mediates the biosynthesis of compactin, also known as mevastatin or ML-236B, and which acts as a potent competitive inhibitor of HMG-CoA reductase (PubMed:12172803, PubMed:12242508). Compactin biosynthesis is performed in two stages (PubMed:12172803). The first stage is catalyzed by the nonaketide synthase mlcA, which belongs to type I polyketide synthases and catalyzes the iterative nine-step formation of the polyketide (PubMed:12172803). This PKS stage is completed by the action of dehydrogenase mlcG, which catalyzes the NADPH-dependent reduction of the unsaturated tetra-, penta- and heptaketide intermediates that arise during the mlcA-mediated biosynthesis of the nonaketide chain and leads to dihydro-ML-236C carboxylate (PubMed:12172803). Covalently bound dihydro-ML-236C carboxylate is released from mlcA by the mlcF esterase (PubMed:12172803). Conversion of dihydro-ML-236C carboxylate into ML-236A carboxylate is subsequently performed with the participation of molecular oxygen and P450 monoogygenase mlcC (PubMed:12172803). Finally, mlcH performs the conversion of ML-236A carboxylate to ML-236B/compactin carboxylate through the addition of the side-chain diketide moiety produced by the diketide synthase mlcB (PubMed:12172803). {ECO:0000269|PubMed:12172803, ECO:0000269|PubMed:12242508}.
Temperature Dependency
PH Dependency
Pathway PATHWAY: Polyketide biosynthesis. {ECO:0000305}.
nucleotide Binding
Features Active site (3); Chain (1); Domain (1); Modified residue (1); Region (5)
Keywords Acyltransferase;Methyltransferase;Multifunctional enzyme;NADP;Oxidoreductase;Phosphopantetheine;Phosphoprotein;S-adenosyl-L-methionine;Transferase
Interact With
Induction INDUCTION: Expression is induced at the beginning of the stationary phase, which is consistent with the timing of compactin production (PubMed:12172803). Expression is controlled by the ML-236B/compactin cluster transcription regulator mlcR (PubMed:12436257). {ECO:0000269|PubMed:12172803, ECO:0000269|PubMed:12436257}.
Subcellular Location
Modified Residue MOD_RES 2522; /note=O-(pantetheine 4'-phosphoryl)serine; /evidence=ECO:0000255|PROSITE-ProRule:PRU00258
Post Translational Modification
Signal Peptide
Structure 3D
Cross Reference PDB -
Mapped Pubmed ID -
Motif
Gene Encoded By
Mass 280,159
Kinetics
Metal Binding
Rhea ID RHEA:42852
Cross Reference Brenda