2.A.50 The Glycerol Uptake (GUP) or Membrane-bound Acyl Transferase (MBOAT) Family

Yeast can use glycerol both as a carbon source and as an osmolyte. In Saccharomyces cerevisiae, glycerol has been reported to be actively taken up via two electrogenic H+ symporters, GUP1 (YGL084c) and GUP2 (YPL189w). These proteins were the first characterized members in a family of polytopic integral membrane proteins from fungi, animals and bacteria. Several of the bacterial proteins have been implicated in extracellular polysaccharide modification. One such protein, DltB (TC# 2.A.50.2.1; P39580) has been implicated in the transport of activated D-alanine across the bacterial cytoplasmic membrane for biosynthesis of D-alanine lipoteichoic acid. It is possible that proteins implicated in polysaccharide modification serve a similar role. Most of these proteins are of between 450 and 610 aas in length and exhibit 8-10 putative TMSs. One protein (spO09758) from Schizosaccharomyces pombe is half sized, having only 231aas with 4-5 putative TMSs. These proteins are members of the membrane-bound O acyl transferase (MBOAT) family. 

The Bacillus subtilis dlt operon (D-alanyl-lipoteichoic acid) is responsible for D-alanine esterification of both lipoteichoic acid (LTA) and wall teichoic acid (WTA). The dlt operon contains five genes, dltA-dltE. Insertional inactivation of dltA-dltD results in complete absence of D-alanine in both LTA and WTA. Based on protein sequence similarity with the Lactobacillus casei dlt gene products (Heaton and Neuhaus, 1992), dltA may encode the D-alanine-D-alanyl carrier protein ligase (Dcl) and dltC the D-alanyl carrier protein (Dcp). The products of dltB and dltD are concerned with the transport of activated D-alanine through the membrane and the final incorporation of D-alanine into LTA. The hydropathy profiles of the DltB and DltD suggest a transmembrane location for the former and an amino-terminal signal peptide for the latter (Perego et al., 1995).

Gup1 homologues of S. cerevisiae and Trypanosoma brucei are glycosyl phosphatidylinositol (GPI) remodelases (Jaquenoud et al., 2008; Ghugtyal et al., 2007). Lipids of Trypanosoma brucei undergo lipid remodelling, whereby longer fatty acids on the glycerol are replaced by myristate (C14:0). A similar process occurs on GPI proteins of Saccharomyces cerevisiae where Per1p first deacylates and Gup1p subsequently reacylates the anchor lipid, thus replacing a shorter fatty acid by C26:0 (Ghugtyal et al., 2007). Heterologous expression of the GUP1 homologue of T. brucei in Δgup1 yeast cells partially normalizes the Δgup1 phenotype and restores the transfer of labelled fatty acids from Coenzyme A to lyso-GPI proteins. Gup1p from T. brucei (tbGup1p) strongly prefers C14:0 and C12:0 over C16:0 and C18:0, whereas yeast Gup1p strongly prefers C16:0 and C18:0. This acyl specificity of tbGup1p closely matches the reported specificity of the reacylation of free lyso-GPI lipids in microsomes of T. brucei. Depletion of tbGup1p in trypanosomes by RNAi drastically reduces the rate of myristate incorporation into the sn-2 position of lyso-GPI lipids. Thus, tbGup1p is involved in the addition of myristate to sn-2 during GPI remodelling in T. brucei and can account for the fatty acid specificity of this process. tbGup1p can act on GPI proteins as well as on GPI lipids. These results and others put into doubt the original claim that GUP1 and GUP2 are glycerol transporters (Bleve et al., 2005; Bosson et al., 2006; Ferreira et al., 2006).

Mammalian glycerol uptake/transporter 1 (Gup1), a homolog of Saccharomyces cerevisiae Gup1, is predicted to be a member of the membrane-bound O-acyltransferase family and is highly homologous to mammalian hedgehog acyltransferase, known as Skn, the homolog of the Drosophila skinny hedgehog gene product. Although mammalian Gup1 has a sequence conserved among the membrane-bound O-acyltransferase family, the histidine residue in the motif that is indispensable to the acyltransferase activity of the family has been replaced with leucine. Abe et al. (2007) cloned Gup1 cDNA from adult mouse lung and examined whether it is involved in the regulation of N-terminal palmitoylation of Sonic hedgehog (Shh). Subcellular localization of mouse Gup1 was indistinguishable from that of mouse Skn. Gup1 and Skn co-localized with endoplasmic reticulum markers, suggesting that these two molecules interact with overlapped targets. Ectopic expression of Gup1 with full-length Shh in cells lacking endogenous Skn showed no hedgehog acyltransferase activity. On the other hand, Gup1 interfered with the palmitoylation of Shh catalyzed by endogenous Skn in COS7 and NSC34. Gup1 may thus be a negative regulator of N-terminal palmitoylation of Shh and may contribute to the variety of biological actions of Shh (Abe et al., 2007). MBOAT7 is anchared to endomembranes by a 6 TMS domain, and it functions in remodeling the acyl chain compositions of endomembranes (Caddeo et al. 2019).

Membrane-bound O-acyltransferases (MBOATs) are a superfamily of integral transmembrane enzymes that are found in all kingdoms of life. In bacteria, MBOATs modify protective cell-surface polymers while in vertebrates, some MBOAT enzymes - such as acyl-coenzyme A:cholesterol acyltransferase and diacylglycerol acyltransferase 1 - are responsible for lipid biosynthesis or phospholipid remodelling. Other MBOATs, including porcupine, hedgehog acyltransferase and ghrelin acyltransferase, catalyse essential lipid modifications of secreted proteins such as Wnt, hedgehog and ghrelin, respectively. Many MBOAT proteins are important drug targets. Ma et al. 2018 presented crystal structures of DltB, an MBOAT responsible for the D-alanylation of cell-wall teichoic acid, both alone and in complex with the D-alanyl donor protein DltC. DltB contains a ring of 11 peripheral transmembrane helices, which shield a highly conserved extracellular structural funnel extending into the middle of the lipid bilayer. The conserved catalytic histidine residue is located at the bottom of this funnel and is connected to the intracellular DltC through a narrow tunnel. Mutation of either the catalytic histidine or the DltC-binding site of DltB abolishes the D-alanylation of lipoteichoic acid and sensitizes B. subtilis to cell-wall stress, which suggests cross-membrane catalysis involving the tunnel. Structure-guided sequence comparisons among DltB and vertebrate MBOATs reveal a conserved structural core and suggests that MBOATs from different organisms have similar catalytic mechanisms. 

The protein, porcupine (2.A.50.3.1 and 2), is a  palmiteoyl transferase, known to acylate regulatory proteins such as Wnt.  It also regulates certain channel proteins.  For example it regulates the AMPA/TARP complex in a TARP-dependent manner (Kato and Witkin 2018).

Diacylglycerol O-acyltransferase 1, DGAT1 or AGRP1, of 488 aas and 9 TMSs, has been structurally solved by cryoEM (Wang et al. 2020). It synthesizes triacylglycerides and is required for dietary fat absorption and fat storage in humans. DGAT1 belongs to the membrane-bound O-acyltransferase (MBOAT) superfamily, members of which are found in all kingdoms of life and are involved in the acylation of lipids and proteins. Wang et al. 2020 addressed how human DGAT1 and other mammalian members of the MBOAT family recognize their substrates and catalyse their reactions. They revealed the structure of human DGAT1 in complex with oleoyl-CoA. Each DGAT1 protomer has nine TMSs, eight of which form a conserved structural fold, the MBOAT fold. It forms a hollow chamber in the membrane that encloses highly conserved catalytic residues. The chamber has separate entrances for each of the two substrates, fatty acyl-CoA and diacylglycerol. DGAT1 exists as either a homodimer or a homotetramer, and the two forms have similar enzymatic activities. The N terminus of DGAT1 interacts with the neighbouring protomer, and these interactions are required for enzymatic activity (Wang et al. 2020).

 

The transport reaction proposed to be catalyzed by GUP1 is:

Glycerol (out) + H+ (out) → glycerol (in) + H+ (in)


The transport reaction proposed to be catalyzed by DltB is:

DctC-alanine (in) + Teichoic acid (out) → Alanyl-teichoic acid (out) + DctC (in)


 

References:

Abe, Y., Y. Kita, and T. Niikura. (2008). Mammalian Gup1, a homolog of Saccharomyces cerevisiae glycerol uptake/transporter 1, acts as a negative regulator for N-terminal palmitoylation of Sonic hedgehog. F.E.B.S.J. 275: 318-331.

Bleve, G., G. Zacheo, M.S. Cappello, F. Dellaglio, and F. Grieco. (2005). Subcellular localization and functional expression of the glycerol uptake protein 1 (GUP1) of Saccharomyces cerevisiae tagged with green fluorescent protein. Biochem. J. 390: 145-155.

Bosson, R., M. Jaquenoud, and A. Conzelmann. (2006). GUP1 of Saccharomyces cerevisiae encodes an O-acyltransferase involved in remodeling of the GPI anchor. Mol. Biol. Cell 17: 2636-2645.

Caddeo, A., O. Jamialahmadi, G. Solinas, A. Pujia, R.M. Mancina, P. Pingitore, and S. Romeo. (2019). MBOAT7 is anchored to endomembranes by six transmembrane domains. J Struct Biol. [Epub: Ahead of Print]

Campaña, M.B., F.J. Irudayanathan, T.R. Davis, K.R. McGovern-Gooch, R. Loftus, M. Ashkar, N. Escoffery, M. Navarro, M.A. Sieburg, S. Nangia, and J.L. Hougland. (2019). The ghrelin -acyltransferase structure reveals a catalytic channel for transmembrane hormone acylation. J. Biol. Chem. [Epub: Ahead of Print]

Chamoun, Z., R.K. Mann, D. Nellen, D.P. von Kessler, M. Bellotto, P.A. Beachy, and K. Basler. (2001). Skinny hedgehog, an acyltransferase required for palmitoylation and activity of the hedgehog signal. Science 293: 2080-2084.

Coupland, C.E., S.A. Andrei, T.B. Ansell, L. Carrique, P. Kumar, L. Sefer, R.A. Schwab, E.F.X. Byrne, E. Pardon, J. Steyaert, A.I. Magee, T. Lanyon-Hogg, M.S.P. Sansom, E.W. Tate, and C. Siebold. (2021). Structure, mechanism, and inhibition of Hedgehog acyltransferase. Mol. Cell 81: 5025-5038.e10.

Di Sessa, A., S. Guarino, A.P. Passaro, L. Liguori, G.R. Umano, G. Cirillo, E. Miraglia Del Giudice, and P. Marzuillo. (2021). NAFLD and renal function in children: is there a genetic link? Expert Rev Gastroenterol Hepatol 1-10. [Epub: Ahead of Print]

Ferreira, C., S. Silva, F. van Voorst, C. Aguiar, M.C. Kielland-Brandt, A. Brandt, and C. Lucas. (2006). Absence of Gup1p in Saccharomyces cerevisiae results in defective cell wall composition, assembly, stability and morphology. FEMS Yeast Res. 6: 1027-1038.

Ghugtyal, V., C. Vionnet, C. Roubaty, and A. Conzelmann. (2007). CWH43 is required for the introduction of ceramides into GPI anchors in Saccharomyces cerevisiae. Mol. Microbiol. 65: 1493-1502.

Gutierrez, J.A., P.J. Solenberg, D.R. Perkins, J.A. Willency, M.D. Knierman, Z. Jin, D.R. Witcher, S. Luo, J.E. Onyia, and J.E. Hale. (2008). Ghrelin octanoylation mediated by an orphan lipid transferase. Proc. Natl. Acad. Sci. USA 105: 6320-6325.

Heaton, M.P. and F.C. Neuhaus. (1992). Biosynthesis of D-alanyl-lipoteichoic acid: cloning, nucleotide sequence, and expression of the Lactobacillus casei gene for the D-alanine-activating enzyme. J. Bacteriol. 174: 4707-4717.

Helsley, R.N., V. Venkateshwari, A.L. Brown, A.D. Gromovsky, R.C. Schugar, I. Ramachandiran, K. Fung, M.N. Kabbany, R. Banerjee, C.K. Neumann, C. Finney, P. Pathak, O. Danny, L.J. Osborn, W. Massey, R. Zhang, A. Kadam, B.E. Sansbury, C. Pan, J. Sacks, R.G. Lee, R.M. Crooke, M.J. Graham, M.E. Lemieux, V. Gogonea, J.P. Kirwan, D.S. Allende, M. Civelek, P.L. Fox, L.L. Rudel, A.J. Lusis, M. Spite, and J.M. Brown. (2019). Obesity-linked suppression of membrane-bound -Acyltransferase 7 (MBOAT7) drives non-alcoholic fatty liver disease. Elife 8:. [Epub: Ahead of Print]

Holst, B., C. Lunde, F. Lages, R. Oliveira, C. Lucas and M.C. Kielland-Brandt (2000). GUP1 and its close homologue GUP2, encoding multimembrane-spaning proteins involved in active glycerol uptake in Saccharomyces cerevisiae. Mol. Microbiol. 37: 108-124.

Jaquenoud, M., M. Pagac, A. Signorell, M. Benghezal, J. Jelk, P. Bütikofer, and A. Conzelmann. (2008). The Gup1 homologue of Trypanosoma brucei is a GPI glycosylphosphatidylinositol remodelase. Mol. Microbiol. 67: 202-212.

Jeppson, S., H. Mattisson, K. Demski, and I. Lager. (2020). A predicted transmembrane region in plant diacylglycerol acyltransferase 2 regulates specificity towards very long chain acyl-CoAs. J. Biol. Chem. [Epub: Ahead of Print]

Jiang, Y., T.L. Benz, and S.B. Long. (2021). Substrate and product complexes reveal mechanisms of Hedgehog acylation by HHAT. Science 372: 1215-1219.

Lee, H.C., T. Inoue, R. Imae, N. Kono, S. Shirae, S. Matsuda, K. Gengyo-Ando, S. Mitani, and H. Arai. (2008). Caenorhabditis elegans mboa-7, a member of the MBOAT family, is required for selective incorporation of polyunsaturated fatty acids into phosphatidylinositol. Mol. Biol. Cell 19: 1174-1184.

Lee, J.D. and J.E. Treisman. (2001). Sightless has homology to transmembrane acyltransferases and is required to generate active Hedgehog protein. Curr. Biol. 11: 1147-1152.

Longo, M., M. Meroni, E. Paolini, V. Erconi, F. Carli, F. Fortunato, D. Ronchi, R. Piciotti, S. Sabatini, C. Macchi, A. Alisi, L. Miele, G. Soardo, G.P. Comi, L. Valenti, M. Ruscica, A.L. Fracanzani, A. Gastaldelli, and P. Dongiovanni. (2021). TM6SF2/PNPLA3/MBOAT7 Loss-of-Function Genetic Variants Impact on NAFLD Development and Progression Both in Patients and in In Vitro Models. Cell Mol Gastroenterol Hepatol 13: 759-788. [Epub: Ahead of Print]

Lucas, C., C. Ferreira, G. Cazzanelli, R. Franco-Duarte, and J. Tulha. (2016). Yeast Gup1(2) Proteins Are Homologues of the Hedgehog Morphogens Acyltransferases HHAT(L): Facts and Implications. J Dev Biol 4:.

Ma, D., Z. Wang, C.N. Merrikh, K.S. Lang, P. Lu, X. Li, H. Merrikh, Z. Rao, and W. Xu. (2018). Crystal structure of a membrane-bound O-acyltransferase. Nature 562: 286-290.

Ma, Z., J.M. Onorato, L. Chen, D.W. Nelson, C.E. Yen, and D. Cheng. (2017). Synthesis of neutral ether lipid monoalkyl-diacylglycerol by lipid acyltransferases. J Lipid Res 58: 1091-1099.

Matsuda, S., T. Inoue, H.C. Lee, N. Kono, F. Tanaka, K. Gengyo-Ando, S. Mitani, and H. Arai. (2008). Member of the membrane-bound O-acyltransferase (MBOAT) family encodes a lysophospholipid acyltransferase with broad substrate specificity. Genes Cells 13: 879-888.

Perego, M., P. Glaser, A. Minutello, M.A. Strauch, K. Leopold, and W. Fischer W. (1995). Incorporation of D-alanine into lipoteichoic acid and wall teichoic acid in Bacillus subtilis. Identification of genes and regulation. J. Biol. Chem. 270: 15598-15606.

Wang, L., H. Qian, Y. Nian, Y. Han, Z. Ren, H. Zhang, L. Hu, B.V.V. Prasad, A. Laganowsky, N. Yan, and M. Zhou. (2020). Structure and mechanism of human diacylglycerol O-acyltransferase 1. Nature 581: 329-332.

Examples:

TC#NameOrganismal TypeExample
2.A.50.1.1

Putative glycerol:H+ symporter of 546 aas and 12 TMSs, GUP1.  In yeast, Gup1 is associated with a high number and diversity of biological functions, namely polarity establishment, secretory/endocytic pathway functionality, vacuole morphology, wall and membrane composition, structure and maintenance, cell death, morphogenesis and differentiation (Lucas et al. 2016). The protein HHAT (Hedgehog O-acyltransferase) modifies Hh morphogens prior to their secretion, while HHATL (Hh O-acyltransferase-like) negatively regulates the pathway. HHAT and HHATL are homologous to Saccharomyces cerevisiae Gup2 and Gup1, respectively (Lucas et al. 2016).

Yeast, fungi, animals, bacteria

GUP1 of Saccharomyces cerevisiae

 
2.A.50.1.2

Protein-cysteine N-palmitoyltransferase HHAT-like protein (Glycerol uptake/transporter homologue) (Hedgehog acyltransferase-like protein)

Animals

HHATL protein of Mus musculus

 
2.A.50.1.3Protein-cysteine N-palmitoyltransferase HHAT (EC 2.3.1.-) (Hedgehog acyltransferase) (Skinny hedgehog protein)AnimalsHhat of Mus musculus
 
2.A.50.1.4

SKI1, HHAT or MART2 (The Sonic Hedgehog) of 493 aas and 11 - 13 TMSs. Before they can function as signaling molecules, Hedgehog precursor proteins must undergo amino-terminal palmitoylation by Hedgehog acyltransferase (HHAT). Jiang et al. 2021 presented cryo-EM structures of human HHAT in complex with its palmitoyl-coenzyme A substrate and of a product complex with a palmitoylated Hedgehog peptide at resolutions of 2.7 and 3.2 angstroms, respectively. The structures revealed how HHAT overcomes the challenges of bringing together substrates that have different physiochemical properties from opposite sides of the endoplasmic reticulum membrane within a membrane-embedded active site for catalysis (Jiang et al. 2021). The Sonic Hedgehog (SHH) morphogen pathway is fundamental for embryonic development and stem cell maintenance and is implicated in various cancers. A key step in signaling is transfer of a palmitate group to the SHH N terminus, catalyzed by HHAT. Coupland et al. 2021 presented a high-resolution cryo-EM structure of HHAT bound to substrate analog palmityl-coenzyme A and a SHH-mimetic megabody, revealing a heme group bound to HHAT that is essential for HHAT function. A structure of HHAT bound to potent small-molecule inhibitor IMP-1575 revealed conformational changes in the active site that occlude substrate binding. The analysis provided a detailed view of the mechanism by which HHAT adapts the membrane environment to transfer an acyl chain across the endoplasmic reticulum membrane. This structure of a membrane-bound O-acyltransferase (MBOAT) superfamily member provides a blueprint for other protein-substrate MBOATs and a template for future drug discovery (Coupland et al. 2021).

SKI1 of Homo sapiens

 
2.A.50.1.5

Skinny or Sightless (Rasp, Cmn, Sit, Ski) of 500 aas and 12 TMSs.  It is required in hedgehog (hh) expressing cells for production of appropriate signaling activity in embryos and in the imaginal precursors of adult tissues. It acts within the secretory pathway to catalyze N-terminal palmitoylation of Hh; this lipid modification is required for the embryonic and larval patterning activities of the Hh signal, but is not required for Wg signaling (Chamoun et al. 2001; Lee and Treisman 2001).

Skinny of Drosophila melanogaster

 
Examples:

TC#NameOrganismal TypeExample
2.A.50.2.1

The alanyl teichoic acid synthesis protein, DltB of 395 aas and 12 TMSs. It may transport activated alanine across the membrane (Perego et al., 1995).  Crystal structures of DltB, a membrane-bound O-acyl transferase, MBOAT, responsible for the D-alanylation of cell-wall teichoic acid in Gram-positive bacteri, both alone and in complex with the D-alanyl donor protein DltC (an acyl carrier protein) have been solved (Ma et al. 2018). DltB contains a ring of 11 peripheral transmembrane helices, which shield a highly conserved extracellular structural funnel extending into the middle of the lipid bilayer. The conserved catalytic histidine residue is located at the bottom of this funnel and is connected to the intracellular DltC (acyl carrier protein) through a narrow tunnel. Mutation of either the catalytic histidine or the DltC-binding site of DltB abolishes D-alanylation of lipoteichoic acid and sensitizes Bacillus subtilis to cell-wall stress, which suggests cross-membrane catalysis involving the tunnel. Structure-guided sequence comparisons among DltB and vertebrate MBOATs reveals a conserved structural core and suggests that MBOATs from different organisms have similar catalytic mechanisms (Ma et al. 2018).

Bacteria

DltB of Bacillus subtilis (P39580)

DltC of Bacillus subtiois (P39579)

 
2.A.50.2.10

Lysophospholipid acyltransferase 1-like protein of 459 aas and ~ 10 TMSs.

AT of Solanum pennellii

 
2.A.50.2.2

MBOAT family protein of 494 aas and 10 - 12 TMSs.

MBOAT family protein of Leptospira santarosai

 
2.A.50.2.3

Uncharacterized MBOAT family protein of 461 aas and 12 TMSs, AlgI, possibly a poly(beta-D-mannuronate) O-acetylase.

UP of Lunatimonas lonarensis

 
2.A.50.2.4

Uncharacterized MBOAT family protein of 483 aas and 11 TMSs.

UP of Entamoeba histolytica

 
2.A.50.2.5

MBOAT7, also called BB1, LENG4, OCT7, of 472 aas and possibly 12 TMSs as 3 sets of 4 putative TMSs, where in each set, the last two TMSs are closs together.  Caddeo et al. 2019 reported that the protein is anchored to the endo membrane via a 6 TMS domain. The predicted catalytic dyad of the protein, composed of the conserved asparagine in position 321 (Asn-321) and the preserved histidine in position 356 (His-356), has a lumenal localization. This is compatible with the role of MBOAT7 in remodeling the acyl chain composition of endomembranes. Obesity-linked suppression of MBOAT7 drives non-alcoholic fatty liver disease (Helsley et al. 2019). It may be involved in nonalcoholic fatty liver disease (NAFLD) and chronic kidney disease (CKD) (Di Sessa et al. 2021; Longo et al. 2021).

MBOAT7 of Homo sapiens

 
2.A.50.2.6

MBOAT4, GOAT, or OACT4 of 435 aas and 7 - 9 TMSs in a 4 - 6 + 3 TMS arrangement.  It mediates the octanoylation of ghrelin at 'Ser-3',but can use a variety of fatty acids as substrates including octanoic acid, decanoic acid and tetradecanoic acid (Gutierrez et al. 2008). Campaña et al. 2019 reported a structural model of a eukaryotic membrane-bound O-acyltransferase (MBOAT), ghrelin O-acyltransferase (GOAT), which modifies the metabolism-regulating hormone, ghrelin. The proposed structure revealed a strategy for transmembrane protein acylation with catalysis occurring in an internal channel connecting the endoplasmic reticulum (ER) lumen and the cytoplasm (Campaña et al. 2019).

 

MBOAT4 of Homo sapiens

 
2.A.50.2.7

Uncharacterized membrane-bound O-acyltransferase domain-containing 2-like protein of 452 aas and 10 TMSs in a 7 + 3 TMS arrangement.

UAT of Amphimedon queenslandica

 
2.A.50.2.8

Uncharacterized membrane-bound O-acyl transferase, MBOAT of 511 aas and ~11 TMSs in a 7 - 9 + 3 - 4 TMS arrangement. MBOAT exhibits broad substrate specificity (Matsuda et al. 2008). It is required for incorporation of unsaturated fatty acids into phosphatidylinositol (Lee et al. 2008).

MBOAT of Caenorhabditis elegans

 
2.A.50.2.9

Uncharacterized acyltransferase of 461 aas and probably 10 TMSs in an 8 + 3 or 4 TMS arrangement.

U-AT of Paramecium tetraurelia

 
Examples:

TC#NameOrganismal TypeExample
2.A.50.3.1

Porcupine, a protein-serine O-palmitoleoyltransferase that acts as a key regulator of the Wnt signaling pathway by mediating the attachment of palmitoleate, a 16-carbon mono-unsaturated fatty acid (C16:1), to Wnt proteins. Serine palmitoleylation of WNT proteins is required for efficient binding to frizzled receptors (Caricasole et al. 2002Coombs et al. 2010; Gao and Hannoush 2014). It also regulates the AMPA/TARP complex in a TARP-dependent manner (Kato and Witkin 2018).

Porcupine of Homo sapiens

 
2.A.50.3.2

Porcupine (Por) of 525 aas and 9 - 11 TMSs. Por is a protein-serine O-palmitoleoyltransferase that acts as a key regulator of the Wnt signaling pathway by mediating the attachment of palmitoleate, a 16-carbon monounsaturated fatty acid (C16:1), to Wnt proteins. Serine palmitoleylation of Wnt proteins is required for efficient binding to frizzled receptors (Herr and Basler 2012)

Por of Drosophila melanogaster

 
2.A.50.3.3

Uncharacterized protein of 408 aas and 11 probable TMSs.

UP of Haemonchus placei

 
Examples:

TC#NameOrganismal TypeExample
2.A.50.4.1

Diacylglycerol O-acyltransferase 1, DGAT1 or AGRP1, of 488 aas and 9 TMSs. The cryoEM structure has been determined (Wang et al. 2020). It synthesizes triacylglycerides and is required for dietary fat absorption and fat storage in humans. DGAT1 belongs to the membrane-bound O-acyltransferase (MBOAT) superfamily, members of which are found in all kingdoms of life and are involved in the acylation of lipids and proteins. Wang et al. 2020 addressed how human DGAT1 and other mammalian members of the MBOAT family recognize their substrates and catalyse their reactions. They revealed the structure of human DGAT1 in complex with an oleoyl-CoA substrate. Each DGAT1 protomer has nine transmembrane helices, eight of which form a conserved structural fold, the MBOAT fold. It forms a hollow chamber in the membrane that encloses highly conserved catalytic residues. The chamber has separate entrances for each of the two substrates, fatty acyl-CoA and diacylglycerol. DGAT1 exists as either a homodimer or a homotetramer, and the two forms have similar enzymatic activities. The N terminus of DGAT1 interacts with the neighbouring protomer, and these interactions are required for enzymatic activity (Wang et al. 2020). In liver it plays a role in esterifying exogenous fatty acids to glycerol and is the major acyl-CoA retinol acyltransferase  in the skin, where it acts to maintain retinoid homeostasis and prevent retinoid toxicity, leading to skin and hair disorders. It exhibits additional acyltransferase activities, including acyl CoA:monoacylglycerol acyltransferase (MGAT), wax monoester and wax diester synthesis (Ma et al. 2017).

DGAT1 of Homo sapiens

 
2.A.50.4.10

Diacylglycerol O-acyltransferase 2, DGAT2, of 341 aas and 8 or 9 TMSs. It is involved in the pathway for triacylglycerol biosynthesis, which is important for providing triglycerides in seeds. A predicted transmembrane region in plant diacylglycerol acyltransferase 2 regulates specificity towards very long chain acyl-CoAs (Jeppson et al. 2020).

 

DGAT2 of Brassica napus

 
2.A.50.4.11

Sterol O-acyltransferase 2, SOAT2, ACAT2 or ACACT2, of 522 aas and 7 - 10 TMSs.  See also TC# 9.B.418.1.2.

SOAT2 of Homo sapiens

 
2.A.50.4.2

Diacylglycerol O-acyltransferase 1 of 742 aas and 4 or 5 TMSs. A predicted transmembrane region in plant diacylglycerol acyltransferase 2 regulates specificity towards very long chain acyl-CoAs (Jeppson et al. 2020).

Acyltransferase of Salvia splendens

 
2.A.50.4.3

Uncharacterized protein of 349 aas and 6 - 8 TMSs

UP of Ooceraea biroi (clonal raider ant)

 
2.A.50.4.4

Uncharacterized protein of 228 aas and 5 or 6 TMSs in a 2 or 3 + 3 TMS arrangement.

UP of Paramecium tetraurelia

 
2.A.50.4.5

Uncharacterized protein of 7 - 9 TMSs

UP of Coleophoma cylindrospora

 
2.A.50.4.6

Uncharacterized protein of 322 aas and 9 TMSs.

UP of Planctomycetes bacterium

 
2.A.50.4.7

Sterol or diacylglycerol O-acyltransferase of 785 aas and 10 or 11 TM

Acyltransferase of Ectocarpus siliculosus

 
2.A.50.4.8

Uncharacterized protein of 466 aas and 4 C-terminal TMSs

UP of Thalassiosira oceanica

 
2.A.50.4.9

Uncharacterized protein of 494 aas and 8 or 9 TMSs

UP of Fragilariopsis cylindrus