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FFUJ_02053 | Acetyl-coenzyme A synthetase. (663 aa) | ||||
FFUJ_02022 | Non-ribosomal peptide synthetase. (2560 aa) | ||||
FFUJ_00833 | Acetyl-coenzyme A synthetase. (719 aa) | ||||
FFUJ_01626 | Related to long-chain-fatty-acid CoA ligase FAA2. (708 aa) | ||||
FFUJ_00392 | Related to malonyl CoA synthetase. (596 aa) | ||||
apf1 | Apicidin F synthase; Non-ribosomal peptide synthetase; part of the gene cluster that mediates the biosynthesis of the cyclic tetrapeptide apicidin F (APF). The non-ribosomal peptide synthetase apf1 incorporates four different amino acids to produce apicidin F: L- phenylalanine, D-pipecolic acid (D-pip), N-methoxy-L-tryptophan and L- 2-aminooctanedioic acid. L-Phenylalanine is the only proteinogenic amino acid directly used by apf1. The 3 other apf1 substrates are non-proteinogenic and have to be modified by other enzymes of the cluster. Lysine is converted to delta-1-pyrroline-5-carbox [...] (5084 aa) | ||||
FFUJ_05273 | Probable phenylacetyl-CoA ligase. (579 aa) | ||||
FFUJ_04614 | Non-ribosomal peptide synthetase. (4834 aa) | ||||
FFUJ_00282 | Related to nonribosomal peptide synthetase. (1075 aa) | ||||
FFUJ_05240 | Probable phenylacetyl-CoA ligase. (578 aa) | ||||
FFUJ_00126 | Related to nonribosomal peptide synthetase. (1057 aa) | ||||
PKS-NRPS1 | Trichosetin synthetase PKS-NRPS1; Hybrid PKS-NRPS synthetase; part of the gene cluster that mediates the biosynthesis of trichosetin, a trans-fused decalin- containing tetramic acid with antimicrobial activity. The PKS module of PKS-NRPS1 together with the enoylreductase (ER) catalyze the formation of the polyketide unit which is then conjugated to L-serine by the condensation domain of the PKS-NRPS1 NRPS module (By similarity). Activity of the Dieckmann cyclase domain (RED) results in release of the intermediate N-desmethylequisetin also called trichosetin (By similarity). Diels-Alder [...] (3914 aa) | ||||
FFUJ_02440 | Related to non-ribosomal peptide synthetase. (986 aa) | ||||
FFUJ_03065 | Uncharacterized protein. (561 aa) | ||||
FFUJ_03184 | Related to AMP-binding protein. (588 aa) | ||||
FFUJ_02166 | Related to 4-coumarate-CoA ligase. (544 aa) | ||||
FFUJ_04275 | Related to long-chain fatty-acid-CoA ligase. (640 aa) | ||||
FFUJ_03602 | Related to coenzyme a synthetase. (1638 aa) | ||||
FFUJ_03641 | AM-toxin synthetase (AMT). (1226 aa) | ||||
FFUJ_02375 | Related to FAT1-very long-chain fatty acyl-CoA synthetase. (631 aa) | ||||
FFUJ_02913 | Probable alpha-aminoadipate reductase large subunit. (1167 aa) | ||||
FFUJ_13285 | Related to acetoacetyl-CoA synthetase. (697 aa) | ||||
FUB8 | Non-canonical non-ribosomal peptide synthetase FUB8; Non-canonical non-ribosomal peptide synthetase; part of the gene cluster that mediates the biosynthesis of fusaric acid, a mycotoxin with low to moderate toxicity to animals and humans, but with high phytotoxic properties. L-aspartate is suggested as fusaric acid amino acid precursor that is activated and further processed to O-acetyl-L-homoserine by cluster enzymes aspartate kinase FUB3 and homoserine O-acetyltransferase FUB5, as well as enzymes of the primary metabolism. The polyketide synthase (PKS) FUB1 generates the triketide tr [...] (1036 aa) | ||||
FFUJ_02242 | Related to malonyl CoA synthetase. (600 aa) | ||||
FFUJ_03358 | Acyl CoA ligase-like protein. (1841 aa) | ||||
FFUJ_03506 | Related to alpha-aminoadipate reductase large subunit. (1284 aa) | ||||
FFUJ_14790 | Non-ribosomal peptide synthetase. (1028 aa) | ||||
FFUJ_06720 | Related to AM-toxin synthetase (AMT). (994 aa) | ||||
FFUJ_05347 | Related to non-ribosomal peptide synthetase. (1549 aa) | ||||
FFUJ_07325 | Related to acetyl coenzyme A synthetase. (700 aa) | ||||
FFUJ_14588 | Related to nonribosomal peptide synthetase MxcG. (1061 aa) | ||||
FFUJ_14695 | Related to polyketide synthase. (4090 aa) | ||||
FFUJ_06929 | Non-ribosomal peptide synthetase. (2473 aa) | ||||
FFUJ_05339 | Related to AMP-dependent synthetase and ligase. (556 aa) | ||||
FFUJ_07083 | Probable fatty acid transporter FAT2. (515 aa) | ||||
FFUJ_05512 | Probable phenylacetyl-CoA ligase. (574 aa) | ||||
FFUJ_07188 | Related to 4-coumarate--CoA ligase. (568 aa) | ||||
FFUJ_06356 | Probable phenylacetyl-CoA ligase. (575 aa) | ||||
FFUJ_05443 | Related to phenylacetyl-CoA ligase. (556 aa) | ||||
FFUJ_05747 | Probable phenylacetyl-CoA ligase. (576 aa) | ||||
FFUJ_05804 | Related to long-chain-fatty-acid-CoA ligase. (1195 aa) | ||||
FFUJ_05957 | Related to long-chain-fatty-acid--CoA ligase. (697 aa) | ||||
FFUJ_12412 | Related to 4-coumarate--CoA ligase. (630 aa) | ||||
FFUJ_12741 | Related to 4-coumarate--CoA ligase. (571 aa) | ||||
FFUJ_12746 | Related to 4-coumarate--CoA ligase. (543 aa) | ||||
FFUJ_12756 | Probable phenylacetyl-CoA ligase. (487 aa) | ||||
FFUJ_12707 | Probable polyketide synthase. (3935 aa) | ||||
FFUJ_08113 | Related to non-ribosomal peptide synthetase. (7581 aa) | ||||
FFUJ_12813 | Related to acetoacetyl-CoA synthetase. (667 aa) | ||||
FFUJ_10155 | Related to long-chain-fatty-acid-CoA ligase. (605 aa) | ||||
FUS1 | Fusarin C synthetase; Fusarin C synthetase; part of the gene cluster that mediates the biosynthesis of the mycotoxin fusarin C. Within the cluster, FUS1, FUS2, FUS8 and FUS9 are sufficient for fusarin production. The roles of the other FUS members are yet undetermined. The fusarin C synthetase FUS1 is responsible for the condensation of one acetyl-coenzyme A (CoA) unit with six malonyl-CoA units and the amide linkage of the arising heptaketide and homoserine, subsequently releasing the first intermediate, prefusarin, as an alcohol with an open ring structure. The cytochrome P450 monoox [...] (3916 aa) | ||||
FFUJ_09796 | Related to long-chain-fatty-acid-CoA ligase. (575 aa) | ||||
FFUJ_09545 | Related to acetoacetyl-CoA synthetase. (676 aa) | ||||
FFUJ_09246 | Fumonisin cluster-fatty acyl-CoA Synthase. (499 aa) | ||||
FFUJ_12915 | Related to nonribosomal peptide synthetase MxcG. (557 aa) | ||||
FFUJ_10322 | AMP-binding domain-containing protein. (531 aa) | ||||
FFUJ_10392 | Probable phenylacetyl-CoA ligase. (568 aa) | ||||
FFUJ_10736 | Related to AM-toxin synthetase (AMT). (2067 aa) | ||||
FFUJ_10721 | Related to nonribosomal peptide synthetase MxcG. (1206 aa) | ||||
FFUJ_10900 | Related to nonribosomal peptide synthetase MxcG. (1085 aa) | ||||
FFUJ_12676 | Related to phenylacetyl-CoA ligase. (558 aa) | ||||
FFUJ_11296 | Related to 4-coumarate--CoA ligase. (534 aa) | ||||
FFUJ_10522 | Related to 4-coumarate--CoA ligase. (575 aa) | ||||
FFUJ_11603 | AMP-binding domain-containing protein. (537 aa) | ||||
FFUJ_11521 | Related to long-chain-fatty-acid--CoA ligase. (690 aa) | ||||
FFUJ_12005 | Probable phenylacetyl-CoA ligase. (649 aa) | ||||
FFUJ_11569 | Related to 4-coumarate--CoA ligase. (564 aa) | ||||
FFUJ_10934 | Non-ribosomal peptide synthetase. (992 aa) | ||||
FFUJ_12079 | Related to 4-coumarate-CoA ligase. (566 aa) | ||||
FFUJ_12038 | Related to long-chain-fatty-acid-CoA ligase. (1142 aa) | ||||
FFUJ_11742 | annotation not available (1222 aa) | ||||
FFUJ_12008 | Related to non-ribosomal peptide synthetase. (5756 aa) | ||||
BEA1 | Beauvericin nonribosomal cyclodepsipeptide synthetase BEA1; Beauvericin nonribosomal cyclodepsipeptide synthetase; part of the gene cluster that mediates the biosynthesis of beauvericin (BEA), a non-ribosomal cyclic hexadepsipeptide that shows antibiotic, antifungal, insecticidal, and cancer cell antiproliferative and antihaptotactic activity. Ketoisovalerate reductase BEA2 catalyzes the NADPH- specific reduction of ketoisovaleric acid to hydroxyisovalerate, a precursor for beauvericin biosynthesis (By similarity). The nonribosomal cyclodepsipeptide synthetase BEA1 then catalyzes the f [...] (3135 aa) | ||||
FFUJ_09252 | Fumonisin cluster-fatty acyl-CoA Synthase. (676 aa) |