ライフサイエンスコーパス: Drosophila protein

1 , PITALRE, could be the human homolog of the Drosophila protein.

2 share 55-58% amino acid similarity with the Drosophila protein.

3 hedgehog, a homolog of hedgehog, a secreted Drosophila protein.

4 e highest degree of sequence homology to the Drosophila protein.

5 human HIWI protein was 52% homologous to the Drosophila protein.

6 to the N-terminal 406 amino acid residues in Drosophila protein.

7 rly 5,000 individual, FLAG-HA epitope-tagged Drosophila proteins.

8 s in the amino termini of both the human and Drosophila proteins.

9 alogous to interactions observed between the Drosophila proteins.

10 e we demonstrate that a second IL-1R-related Drosophila protein, 18-Wheeler (18W), is a critical comp

11 Coracle, a Drosophila protein 4.1 homologue, is required during emb

12 Studies of coracle, a Drosophila Protein 4.1 homologue, provide an opportunity

13 we show that, unlike other learning-related Drosophila proteins, AMN is not preferentially expressed

14 Similarity between the Drosophila protein and the topoisomerase IIIbetas is par

15 Using in vitro assays with purified Drosophila proteins and stabilized microtubules, we foun

16 OAP reveals functional analogies between the Drosophila proteins and subunits of the yeast and mammal

17 The product of the egl-46 gene, two Drosophila proteins, and two proteins in human and mice

18 age variants of lacZalpha and 74 challenging Drosophila protein antigens, which were then screened fo

19 The available fraction of Drosophila proteins appears to lack representatives of m

20 iguingly, a large majority of the identified Drosophila proteins are essential developmental proteins

21 eta-catenin (the vertebrate homologue of the Drosophila protein Armadillo), a critical effector of th

22 sphorylation site, which is conserved in the Drosophila protein armadillo.

23 simultaneously binds to two molecules of the Drosophila protein B52 and two copies of streptavidin, t

24 The LZIP-related Drosophila protein BBF-2/dCREB-A contains this HCF-bindi

25 is protein, Bicd2, is a human homolog of the Drosophila protein Bicaudal D, a coiled-coil protein.

26 LexA protein fused to the Drosophila protein bicoid (LexA-bicoid) failed to intera

27 Hairless (H), a novel Drosophila protein, binds to Su(H) and has been proposed

28 We show that a locust ortholog of the Drosophila protein Bruchpilot is localized to the presyn

29 d multiple long homopeptides in about 12% of Drosophila proteins but in only about 1.7% of human, mou

30 This protein is 57% homologous to a Drosophila protein called heix.

31 the physiological properties of three other Drosophila proteins (CG17137, CG17139, and CG17140) whos

32 The Drosophila protein Chip potentiates activation by severa

33 For example, the Drosophila proteins Clock (Clk) and Cycle (Cyc) activate

34 RNA-seq, we then identified >400 additional Drosophila protein-coding genes whose expression increas

35 on blocks Integrator function at a subset of Drosophila protein-coding genes, although having no effe

36 pansions were engineered into Dishevelled, a Drosophila protein containing a naturally occurring poly

37 In Drosophila, proteins containing leucine-rich repeats (LR

38 The Drosophila protein Cortex (Cort) is a female, meiosis-sp

39 sis of an overgrowth phenotype driven by the Drosophila protein Crumbs (Crb), which nucleates an apic

40 resence of 18 chitinase-like proteins in the Drosophila protein database.

41 concentration; a well-studied example is the Drosophila protein decapentaplegic (DPP) acting in the w

42 SATB1 with PDZ- and homeo-domain containing Drosophila protein Defective Proventriculus suggests tha

43 Here, we describe a novel Drosophila protein, Discs Lost (DLT), that plays a cruci

44 The Drosophila protein DSas-4 is related to the human microc

45 We show that the Drosophila protein DSP1, an HMG-1/2-like protein, binds

46 There are also sequence similarities to the Drosophila protein DVE.

47 sting of the Shroom targeting domain and the Drosophila protein elicits constriction.

48 the WRPW-bHLH proteins, which are similar to Drosophila proteins encoded by hairy and genes in the en

49 Three Drosophila proteins, ERCC1, MUS312, and MEI-9, function

50 er cells (BCs), identify the uncharacterized Drosophila protein Evi5 as an essential membrane traffic

51 ogs of Tribbles, an evolutionarily conserved Drosophila protein family that mediates protein degradat

52 The related Drosophila protein Fat interacts genetically and physica

53 plasmin-like domain (NPL) from the unrelated Drosophila protein, FKBP39, and we present evidence that

54 The Drosophila protein frequenin and its mammalian homolog n

55 ella, transcriptome was higher (28%) than to Drosophila proteins/genes (18%) in NCBI.

56 Both are related to the Drosophila protein Groucho, a transcriptional corepresso

57 t the EBNA-3 proteins act analogously to the Drosophila protein Hairless.

58 inal tetra-peptide in mature Smac and in the Drosophila proteins Hid/Grim/Reaper, defining a conserve

59 as the conserved N-terminal sequences in the Drosophila proteins Hid/Grim/Reaper.

60 The leonardo gene encodes a Drosophila protein highly homologous to the vertebrate 1

61 n of human DSCAM is highly homologous to the Drosophila protein; however, the intracellular domains o

62 ein 80 kDa subunit and the VHS domain of the Drosophila protein Hrs, though strict analysis of the st

63 Recent studies of mutations of Drosophila proteins implicated in synaptic transmission

64 We previously found that a Drosophila protein in the vanilloid receptor subfamily (

65 similar to the amino termini of proapoptotic Drosophila proteins in the Reaper/Hid/Grim family were i

66 graphy and mass spectroscopy to identify the Drosophila proteins in this complex.

67 rchitecture that is conserved in at least 14 Drosophila proteins, including Adf-1 and Stonewall.

68 ein interactions, led to the generation of a Drosophila protein interaction map (DPiM) encompassing 5

69 We describe a next-generation Drosophila protein interaction map-"DPIM2"-established f

70 We therefore propose the Drosophila protein is a member of the beta-subfamily of

71 revious results obtained with yeast HSF, the Drosophila protein is dispensable for general cell growt

72 essed in human cells, implying that no other Drosophila protein is necessary for inhibition.

73 The Drosophila protein is required for proper chromosome seg

74 cDNA sequences reveal that the Drosophila protein is similar to quaking (64% identity o

75 te that the average selection coefficient on Drosophila proteins is weakly positive.

76 The closest relative of mACF7 is the Drosophila protein Kakapo, which shares similar architec

77 repeats, a motif initially described in the Drosophila protein Kelch, and another domain predicted t

78 antibodies against the catalytic subunit of Drosophila protein kinase A (anti-DC0) label an unusual

79 Human PDK1 is homologous to the Drosophila protein kinase DSTPK61, which has been implic

80 The pathway takes its name from the Drosophila protein kinase, Hippo (STK4/MST1 and STK3/MST

81 Here we test the complement of Drosophila protein kinases (kinome) for cell cycle funct

82 y conserved linkers, first identified in the Drosophila protein Kruppel, that are found in many DNA b

83 Like the prototype Drosophila protein Mad, many members of the family play

84 The Drosophila protein MEI-S332, the founding member of a co

85 omain; this structure was conserved with the Drosophila protein Msp-300 and the mammalian Syne protei

86 The Drosophila protein Nanos encodes an evolutionarily conse

87 modular structure that can be traced to the Drosophila protein nervy.

88 The Drosophila protein O-glucosyltransferase (Poglut) Rumi r

89 We found that in Drosophila, Protein O-fucosyltransferase 1 (OFUT1), an e

90 Pellino is a Drosophila protein originally isolated in a two-hybrid s

91 LGN is closely related to a Drosophila protein, Partner of inscuteable (Pins), which

92 We identify Drosophila protein phosphatase 2A (PP2A) regulatory subu

93 Another Drosophila protein previously implicated in fat body spe

94 As in the Drosophila proteins Reaper, Grim and Hid, the amino-term

95 of these loci, located 3' to Psn, encodes a Drosophila protein related to the yeast 60S ribosomal pr

96 Here, we show that Cutoff (Cuff), a Drosophila protein related to the yeast transcription te

97 ment from model organisms indicates that the Drosophila protein resembles nonmuscle myosin-2s from me

98 l yeast two-hybrid (Y2H) screens of > 10,000 Drosophila proteins result in the 'FlyBi' dataset of 872

99 We searched the Drosophila protein sequences database using fully charac

100 Twenty-four Drosophila protein sequences were more similar to their

101 The Drosophila protein Sex Comb on Midleg (Scm) is a member

102 The Drosophila protein Sex-lethal (Sxl) contains two RNP con

103 The Drosophila protein Shaggy (Sgg, also known as Zeste-whit

104 In addition to the homology to yGCN5, the Drosophila protein shares sequencesimilarity with the N-

105 shut-down encodes a novel Drosophila protein similar to the heat-shock protein-bin

106 a yeast two-hybrid screen to isolate a novel Drosophila protein, SIN (SXL interactor), that interacts

107 h a newly cloned vertebrate homologue of the Drosophila protein Smoothened (vSmo), and that vSmo is c

108 to identify splicing events regulated by 56 Drosophila proteins, some previously unknown to regulate

109 Here we show that the Drosophila protein Spire represents a third class of act

110 y of the binding of a dsRBM derived from the Drosophila protein Staufen, indicates that dsRBMs can bi

111 th four transmembrane domains related to the Drosophila protein strabismus/van gogh (vang).

112 ral distinctions exist between the human and Drosophila proteins suggesting overlapping but not ident

113 An interaction between LC8 and the Drosophila protein swallow has been previously character

114 strulation (Sog) protein is another secreted Drosophila protein that contains a type-II signal and di

115 Thus, we have identified both a Drosophila protein that is directly associated with TBP

116 TLRs are mammalian homologues of Toll, a Drosophila protein that is essential for host defense ag

117 We report here a novel Drosophila protein that is homologous to Sina, named Sin

118 The latter is a Drosophila protein that is involved in transcriptional s

119 Drosophila proteins that confer apical membrane identity

120 We further identify a novel Drosophila protein, the six-banded (SBA), as an ortholog

121 ike receptor (TLR) proteins, homologs of the Drosophila protein Toll, have been found on the surface

122 la adapter protein, which interacts with the Drosophila protein-tyrosine phosphatase (PTP) dPTP61F.

123 the large cytosolic N-terminal region of the Drosophila protein V100, the neuron-specific V(0) subuni

124 The Drosophila protein Vein has structural similarities with

125 tigial-like 2 (Vgl-2) that is related to the Drosophila protein Vestigial.

126 We have identified a Drosophila protein with homology to vertebrate Crk, term

127 We describe a technique to tag Drosophila proteins with GFP at their native genomic loc

128 More than 80% of Drosophila proteins with multiple runs seem to function

129 in, a region of E(z) also conserved in other Drosophila proteins with roles in development and/or chr