ライフサイエンスコーパス: sn-1 position

1 % of dihydrosterculate was esterified to the sn-1 position.

2 lation of glycerol 3-phosphate (GPAT) at the sn-1 position.

3 n intermediate involved in remodeling at the sn-1 position.

4 and 1-20% of the total acyl groups from the sn-1 position.

5 rs, with the fatty acid predominately at the sn-1 position.

6 aining heterocyclic ring substituents at the sn-1 position.

7 y acyl chains esterified at the noncanonical sn-1 position.

8 3-phosphate substrates harboring 20:5 at the sn-1 position.

9 f saturated fatty acids is controlled at the sn-1 position.

10 ion of a second arachidonate moiety into the sn-1 position.

11 o discriminate the fatty acid linkage at the SN(1) position.

12 The ester moiety at the sn-1 position, a common feature in this template, is rel

13 euterated, saturated acyl chain (n:0) at the sn-1 position, adjacent to docosahexaenoic acid (DHA, 22

14 lcholine had about 21% less palmitate in the sn-1 position and 36 and 40%, respectively, more arachid

15 ly labile (Z)-vinyl ether substituent at the sn-1 position and a base-labile sn-2 acyl substituent th

16 log with a BODIPY-labeled alkyl ether at the sn-1 position and a N-(DNP)-8-amino-octanoyl group at th

17 tidylcholines containing stearic acid in the sn-1 position and an unsaturated fatty acid (either olei

18 plasmanylcholine containing palmitate at the sn-1 position and arachidonate at the sn-2 position were

19 have either 18:0 or 18:1 fatty acids in the sn-1 position and either 22:6 or 20:2 fatty acids in the

20 perdeuterated stearic acid, 18:0d35, in the sn-1 position and the fatty acid 18:0, 18:1 omega 9, 18:

21 ntained saturated stearic acid (18:0) in the sn-1 position and the monounsaturated oleic acid (18:1)

22 ated stearic acid (SA), respectively, at the sn-1 position and were synthesized with perdeuterated SA

23 cond myristate is then incorporated into the sn-1 position, but the mechanism has been unclear due to

24 osphate and dihydroxyacetonephosphate at the sn-1 position by glycerol-3-phosphate and dihydroxyaceto

25 The initial hydrolysis of DAG at the sn-1 position (by DAG lipase) will generate 2-arachidony

26 ro-3-phospho-(1'-myo-inositol), in which the sn-1 position contains an ether-linked C16:0 chain; they

27 acyl chains at the stereospecific numbering (sn)-1 position from PC and likely a channeling of lysoph

28 e highly purified fraction hydrolyzed at the sn-1 position, implying that this PLA2 also has some int

29 PagP transfers a palmitate residue from the sn-1 position of a phospholipid to the N-linked hydroxym

30 orated into the sn-2 position of PC, but the sn-1 position of de novo DAG and indicated similar rates

31 transfers a stearoyl or oleoyl chain to the sn-1 position of G3P and an oleyl chain to sn-2-LPA.

32 a classical one wherein the acylation of the sn-1 position of glycerol-3-phosphate (G3P) precedes tha

33 ing VLC-PUFAs, specifically contained in the sn-1 position of glycerophosphatidylcholine, implicating

34 yzing the transfer of an acyl group from the sn-1 position of lecithin to vitamin A to generate all-t

35 lyzes the transfer of an acyl group from the sn-1 position of lecithin to vitamin A to generate retin

36 yzes the transfer of an acyl moiety from the sn-1 position of lecithin to vitamin A, generating all-t

37 ed saturated acyl-CoAs specifically into the sn-1 position of lysophosphatidylethanolamine (LPE) rath

38 ether-linked aliphatic groups present in the sn-1 position of neutrophil plasmalogens.

39 double bond of oleic acid esterified to the sn-1 position of PC.

40 in planta, E. coli CPS acts primarily on the sn-1 position of PC; coexpression of SfLPAT results in t

41 ynthesized from oleic acid esterified at the sn-1 position of phosphatidylcholine (PC).

42 lyzes the transfer of an acyl group from the sn-1 position of phosphatidylcholine to all-trans-retino

43 lyzes the transfer of an acyl group from the sn-1 position of phosphatidylcholine to retinol.

44 acts by transferring an acyl group from the sn-1 position of phosphatidylcholine to retinol.

45 positioning of saturated fatty acids at the sn-1 position of phospholipids, and nutritional, hormona

46 onversely, PPL preferred hydrolysis from the sn-1 position of prochiral sn-1,3-DG regioisomer, wherea

47 Desaturation of oleate at the sn-1 position of PtdCho was also demonstrated after the

48 th the higher number of DBs are preferred in sn-1 position of TG enantiomers in hazelnut oil unlike t

49 erence of the fatty acyl hydrolysis from the sn-1 position of TG more pronounced for the substrates w

50 g OxPCs with palmitic acid esterified to the sn-1 position of the glycerol backbone yielded a NL of 2

51 phospholipids with a vinyl ether bond at the sn-1 position of the glycerol backbone.

52 by GC gave the composition of the FAs in the sn-1 position of the PC.

53 racterized by a fatty alcohol residue at the sn-1 position of their glycerol backbone.

54 s modified at the sn-2 position of PC to the sn-1 position of this molecule in plant cells).

55 Circulating [3H]PAM is incorporated into sn-1 positions of brain phospholipids, mainly phosphatid

56 mpanying 1,2-acyl migration from the sn-2 to sn-1 positions of glycerol.

57 ally hydrolyzes fatty acid from the sn-2 and sn-1 positions of phosphatidylcholine.

58 er linkage to the pro-S hydroxymethyl group (sn-1 position) of a glycerol backbone.

59 ert-butylamine, while the ester group at the sn-1-position remains unaffected.

60 hospholipids containing palmitic acid at the sn-1 position that could be exploited for the design of

61 tic G3P acyltransferases (GPATs) acylate the sn-1 position to produce lysophosphatidic acid (1-acyl-L

62 The selectivity of ATGL broadens to the sn-1 position upon stimulation of the enzyme by its co-a

63 gnificant percentage of acyl groups from the sn-1 position, when sn-2 is occupied by 18:0, 20:4, or 2

64 nt CPS prefers the stereospecific numbering (sn)-1 position whereas E. coli CPS acts on sn-2 of phosp