Gene/Proteome Database (LMPD)

LMPD ID
LMP012642
Gene ID
Species
Rattus norvegicus (Rat)
Gene Name
fatty acid synthase
Gene Symbol
Alternate Names
fatty acid synthase;
Chromosome
10
Map Location
chromosome:10
EC Number
2.3.1.85
Summary
plays a role in lipid biosynthesis [RGD, Feb 2006]
Orthologs

Proteins

fatty acid synthase
Refseq ID NP_059028
Protein GI 8394158
UniProt ID P12785
mRNA ID NM_017332
Length 2505
MEEVVIAGMSGKLPESENLQEFWANLIGGVDMVTDDDRRWKAGLYGLPKRSGKLKDLSKFDASFFGVHPKQAHTMDPQLRLLLEVSYEAIVDGGINPASLRGTNTGVWVGVSGSEASEALSRDPETLLGYSMVGCQRAMMANRLSFFFDFKGPSIALDTACSSSLLALQNAYQAIRSGECPAAIVGGINLLLKPNTSVQFMKLGMLSPDGTCRSFDDSGNGYCRAEAVVAVLLTKKSLARRVYATILNAGTNTDGCKEQGVTFPSGEAQEQLIRSLYQPGGVAPESLEYIEAHGTGTKVGDPQELNGITRSLCAFRQSPLLIGSTKSNMGHPEPASGLAALTKVLLSLENGVWAPNLHFHNPNPEIPALLDGRLQVVDRPLPVRGGIVGINSFGFGGANVHVILQPNTQQAPAPAPHAALPHLLHASGRTMEAVQGLLEQGRQHSQDLAFVSMLNDIAATPTAAMPFRGYTVLGVEGHVQEVQQVPASQRPLWFICSGMGTQWRGMGLSLMRLDSFRESILRSDEALKPLGVKVSDLLLSTDEHTFDDIVHSFVSLTAIQIALIDLLTSMGLKPDGIIGHSLGEVACGYADGCLSQREAVLAAYWRGQCIKDANLPAGSMAAVGLSWEECKQRCPPGVVPACHNSEDTVTISGPQAAVNEFVEQLKQEGVFAKEVRTGGLAFHSYFMEGIAPTLLQALKKVIREPRPRSARWLSTSIPEAQWQSSLARTSSAEYNVNNLVSPVLFQEALWHVPEHAVVLEIAPHALLQAVLKRGVKPSCTIIPLMKRDHKDNLEFFLTNLGKVHLTGIDINPNALFPPVEFPVPRGTPLISPHIKWDHSQTWDIPVAEDFPNGSSSSSATVYNIDASSESSDHYLVDHCIDGRVLFPGTGYLYLVWKTLARSLSLSLEETPVVFENVTFHQATILPRTGTVPLEVRLLEASHAFEVSDSGNLIVSGKVYQWEDPDSKLFDHPEVPIPAESESVSRLTQGEVYKELRLRGYDYGPHFQGVYEATLEGEQGKLLWKDNWVTFMDTMLQISILGFSKQSLQLPTRVTAIYIDPATHLQKVYMLEGDTQVADVTTSRCLGVTVSGGVYISRLQTTATSRRQQEQLVPTLEKFVFTPHVEPECLSESAILQKELQLCKGLAKALQTKATQQGLKMTVPGLEDLPQHGLPRLLAAACQLQLNGNLQLELGEVLARERLLLPEDPLISGLLNSQALKACIDTALENLSTLKMKVVEVLAGEGHLYSHISALLNTQPMLQLEYTATDRHPQALKDVQTKLQQHDVAQGQWDPSGPAPTNLGALDLVVCNCALATLGDPALALDNMVAALKDGGFLLMHTVLKGHALGETLACLPSEVQPGPSFLSQEEWESLFSRKALHLVGLKKSFYGTALFLCRRLSPQDKPIFLPVEDTSFQWVDSLKSILATSSSQPVWLTAMNCPTSGVVGLVNCLRKEPGGHRIRCILLSNLSSTSHVPKLDPGSSELQKVLESDLVMNVYRDGAWGAFRHFQLEQDKPEEQTAHAFVNVLTRGDLASIRWVSSPLKHMQPPSSSGAQLCTVYYASLNFRDIMLATGKLSPDAIPGKWASRDCMLGMEFSGRDKCGRRVMGLVPAEGLATSVLLSPDFLWDVPSSWTLEEAASVPVVYTTAYYSLVVRGRIQHGETVLIHSGSGGVGQAAISIALSLGCRVFTTVGSAEKRAYLQARFPQLDDTSFANSRDTSFEQHVLLHTGGKGVDLVLNSLAEEKLQASVRCLAQHGRFLEIGKFDLSNNHPLGMAIFLKNVTFHGILLDALFEGANDSWREVAELLKAGIRDGVVKPLKCTVFPKAQVEDAFRYMAQGKHIGKVLVQVREEEPEAMLPGAQPTLISAISKTFCPEHKSYIITGGLGGFGLELARWLVLRGAQRLVLTSRSGIRTGYQAKHVREWRRQGIHVLVSTSNVSSLEGARALIAEATKLGPVGGVFNLAMVLRDAMLENQTPELFQDVNKPKYNGTLNLDRATREACPELDYFVAFSSVSCGRGNAGQSNYGFANSTMERICEQRRHDGLPGLAVQWGAIGDVGIILEAMGTNDTVVGGTLPQRISSCMEVLDLFLNQPHAVLSSFVLVEKKAVAHGDGEAQRDLVKAVAHILGIRDLAGINLDSSLADLGLDSLMGVEVRQILEREHDLVLPIREVRQLTLRKLQEMSSKAGSDTELAAPKSKNDTSLKQAQLNLSILLVNPEGPTLTRLNSVQSSERPLFLVHPIEGSITVFHSLAAKLSVPTYGLQCTQAAPLDSIPNLAAYYIDCIKQVQPEGPHRVAGYSFGACVAFEMCSQLQAQQGPAPAHNNLFLFDGSHTYVLAYTQSYRAKLTPGCEAEAEAEAICFFIKQFVDAEHSKVLEALLPLKSLEDRVAAAVDLITRSHQSLDRRDLSFAAVSFYYKLRAADQYKPKAKYHGNVILLRAKTGGTYGEDLGADYNLSQVCDGKVSVHIIEGDHRTLLEGRGLESIINIIHSSLAEPRVSVREG

Gene Information

Entrez Gene ID
Gene Name
fatty acid synthase
Gene Symbol
Species
Rattus norvegicus

Gene Ontology (GO Annotations)

GO ID Source Type Description
GO:0005794 IEA:Ensembl C Golgi apparatus
GO:0070062 IEA:Ensembl C extracellular vesicular exosome
GO:0042587 IEA:Ensembl C glycogen granule
GO:0005739 IEA:Ensembl C mitochondrion
GO:0005886 IEA:Ensembl C plasma membrane
GO:0047451 IEA:UniProtKB-EC F 3-hydroxyoctanoyl-[acyl-carrier-protein] dehydratase activity
GO:0004317 IEA:InterPro F 3-hydroxypalmitoyl-[acyl-carrier-protein] dehydratase activity
GO:0004316 IEA:UniProtKB-EC F 3-oxoacyl-[acyl-carrier-protein] reductase (NADPH) activity
GO:0004315 IEA:UniProtKB-EC F 3-oxoacyl-[acyl-carrier-protein] synthase activity
GO:0070402 IDA:RGD F NADPH binding
GO:0004313 IEA:UniProtKB-EC F [acyl-carrier-protein] S-acetyltransferase activity
GO:0004314 IEA:UniProtKB-EC F [acyl-carrier-protein] S-malonyltransferase activity
GO:0008144 IDA:RGD F drug binding
GO:0047117 IEA:UniProtKB-EC F enoyl-[acyl-carrier-protein] reductase (NADPH, A-specific) activity
GO:0004319 IEA:InterPro F enoyl-[acyl-carrier-protein] reductase (NADPH, B-specific) activity
GO:0004312 IDA:RGD F fatty acid synthase activity
GO:0042802 IPI:IntAct F identical protein binding
GO:0016295 IEA:UniProtKB-EC F myristoyl-[acyl-carrier-protein] hydrolase activity
GO:0004320 IEA:UniProtKB-EC F oleoyl-[acyl-carrier-protein] hydrolase activity
GO:0016296 IEA:UniProtKB-EC F palmitoyl-[acyl-carrier-protein] hydrolase activity
GO:0044822 IEA:Ensembl F poly(A) RNA binding
GO:0042803 IDA:RGD F protein homodimerization activity
GO:0008270 IEA:InterPro F zinc ion binding
GO:0006084 IDA:RGD P acetyl-CoA metabolic process
GO:0071353 IEA:Ensembl P cellular response to interleukin-4
GO:0006633 IMP:RGD P fatty acid biosynthetic process
GO:0008610 TAS:RGD P lipid biosynthetic process
GO:0001649 IEA:Ensembl P osteoblast differentiation

KEGG Pathway Links

KEGG Pathway ID Description
ko04152 AMPK signaling pathway
rno04152 AMPK signaling pathway
ko00061 Fatty acid biosynthesis
rno00061 Fatty acid biosynthesis
M00083 Fatty acid biosynthesis, elongation
M00082 Fatty acid biosynthesis, initiation
ko01212 Fatty acid metabolism
rno01212 Fatty acid metabolism
ko04910 Insulin signaling pathway
rno04910 Insulin signaling pathway
rno01100 Metabolic pathways

REACTOME Pathway Links

REACTOME Pathway ID Description
5954496 Activation of gene expression by SREBF (SREBP)
5953760 ChREBP activates metabolic gene expression
5953298 Defective AMN causes hereditary megaloblastic anemia 1
5953308 Defective BTD causes biotidinase deficiency
5953307 Defective CD320 causes methylmalonic aciduria
5953299 Defective CUBN causes hereditary megaloblastic anemia 1
5953296 Defective GIF causes intrinsic factor deficiency
5953310 Defective HLCS causes multiple carboxylase deficiency
5953297 Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF
5953305 Defective MMAA causes methylmalonic aciduria type cblA
5953302 Defective MMAB causes methylmalonic aciduria type cblB
5953304 Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC
5953303 Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD
5953301 Defective MTR causes methylmalonic aciduria and homocystinuria type cblG
5953300 Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE
5953306 Defective MUT causes methylmalonic aciduria mut type
5953293 Defective TCN2 causes hereditary megaloblastic anemia
5953309 Defects in biotin (Btn) metabolism
5953294 Defects in cobalamin (B12) metabolism
5953295 Defects in vitamin and cofactor metabolism
5953253 Disease
5953463 Fatty Acyl-CoA Biosynthesis
5953288 Fatty acid, triacylglycerol, and ketone body metabolism
5953611 Integration of energy metabolism
5953250 Metabolism
5953289 Metabolism of lipids and lipoproteins
5953292 Metabolism of vitamins and cofactors
5953291 Metabolism of water-soluble vitamins and cofactors
5954497 Regulation of cholesterol biosynthesis by SREBP (SREBF)
5953464 Triglyceride Biosynthesis
5953985 Vitamin B5 (pantothenate) metabolism

Domain Information

InterPro Annotations

Accession Description
IPR009081 Acyl carrier protein-like
IPR014043 Acyl transferase
IPR001227 Acyl transferase domain
IPR016035 Acyl transferase/acyl hydrolase/lysophospholipase
IPR013149 Alcohol dehydrogenase, C-terminal
IPR029058 Alpha/Beta hydrolase fold
IPR014031 Beta-ketoacyl synthase, C-terminal
IPR014030 Beta-ketoacyl synthase, N-terminal
IPR018201 Beta-ketoacyl synthase, active site
IPR023102 Fatty acid synthase, domain 2
IPR011032 GroES (chaperonin 10)-like
IPR016036 Malonyl-CoA ACP transacylase, ACP-binding
IPR013217 Methyltransferase type 12
IPR016040 NAD(P)-binding domain
IPR006162 Phosphopantetheine attachment site
IPR020843 Polyketide synthase, enoylreductase domain
IPR013968 Polyketide synthase, ketoreductase domain
IPR029063 S-adenosyl-L-methionine-dependent methyltransferase
IPR001031 Thioesterase
IPR016039 Thiolase-like
IPR016038 Thiolase-like, subgroup

UniProt Annotations

Entry Information

Gene Name
fatty acid synthase
Protein Entry
FAS_RAT
UniProt ID
Species
Rat

Comments

Comment Type Description
Catalytic Activity (3R)-3-hydroxyacyl-[acyl-carrier-protein] + NADP(+) = 3-oxoacyl-[acyl-carrier-protein] + NADPH.
Catalytic Activity A (3R)-3-hydroxyacyl-[acyl-carrier protein] = a trans-2-enoyl-[acyl-carrier protein] + H(2)O.
Catalytic Activity Acetyl-CoA + [acyl-carrier-protein] = CoA + acetyl-[acyl-carrier-protein].
Catalytic Activity Acetyl-CoA + n malonyl-CoA + 2n NADPH = a long-chain fatty acid + (n+1) CoA + n CO(2) + 2n NADP(+).
Catalytic Activity Acyl-[acyl-carrier-protein] + malonyl-[acyl- carrier-protein] = 3-oxoacyl-[acyl-carrier-protein] + CO(2) + [acyl-carrier-protein].
Catalytic Activity An acyl-[acyl-carrier protein] + NADP(+) = a trans-2,3-dehydroacyl-[acyl-carrier protein] + NADPH.
Catalytic Activity Malonyl-CoA + an [acyl-carrier-protein] = CoA + a malonyl-[acyl-carrier-protein].
Catalytic Activity Oleoyl-[acyl-carrier-protein] + H(2)O = [acyl- carrier-protein] + oleate.
Function Fatty acid synthetase catalyzes the formation of long- chain fatty acids from acetyl-CoA, malonyl-CoA and NADPH. This multifunctional protein has 7 catalytic activities and an acyl carrier protein.
Induction Up-regulated in livers of rats fed on a high carbohydrate diet
Interaction Self; NbExp=8; IntAct=EBI-493558, EBI-493558;
Similarity Contains 1 acyl carrier domain. {ECO:0000255|PROSITE- ProRule:PRU00258}.
Subcellular Location Cytoplasm . Melanosome .
Subunit Homodimer which is arranged in a head to tail fashion.

Identical and Related Proteins

Unique RefSeq proteins for LMP012642 (as displayed in Record Overview)

Protein GI Database Accession Length Protein Name
8394158 RefSeq NP_059028 2505 fatty acid synthase

Identical Sequences to LMP012642 proteins

Reference Database Accession Length Protein Name
GI:8394158 GenBank AAA57219.1 2505 fatty acid synthase [Rattus norvegicus]
GI:8394158 GenBank AEK13591.1 2505 Sequence 3 from patent US 7972785

Related Sequences to LMP012642 proteins

Reference Database Accession Length Protein Name
GI:8394158 EMBL CAA44680.1 2505 fatty acid synthase [Rattus norvegicus]
GI:8394158 GenBank AAA57219.1 2505 fatty acid synthase [Rattus norvegicus]
GI:8394158 GenBank AEK13591.1 2505 Sequence 3 from patent US 7972785