ライフサイエンスコーパス: Arabidopsis protein

1 fic transcription factor, p24, and a related Arabidopsis protein.

2 psis immune system proteins, and ~8000 other Arabidopsis proteins.

3 ractions were identified for 3,617 conserved Arabidopsis proteins.

4 cating a difference between the rice and the Arabidopsis proteins.

5 The Arabidopsis protein AINTEGUMENTA (ANT) is a member of a

6 The Arabidopsis protein AINTEGUMENTA (ANT) is an important r

7 eals previously unknown hormone functions of Arabidopsis proteins and direct beneficial activities me

8 (the LOB domain) that is present in 42 other Arabidopsis proteins and in proteins from a variety of o

9 in, is similar in sequence to domains in two Arabidopsis proteins and one Oryza protein.

10 -binding motif of about 60 aa present in the Arabidopsis proteins APETALA2, AINTEGUMENTA, and TINY; t

11 oteins that are most similar to hypothetical Arabidopsis proteins, appeared to be present exclusively

12 ive orthologs, indicating that the yeast and Arabidopsis proteins are functionally equivalent.

13 ht Yellow-2 cells, showed that the maize and Arabidopsis proteins are targeted to mitochondria.

14 GFP-fusion experiments demonstrated that the Arabidopsis proteins are targeted to peroxisomes, and su

15 The Arabidopsis protein At5g01750 from the DUF567 family was

16 We named this Arabidopsis protein AtDTX1 (for Arabidopsis thaliana Det

17 and Sar proteins, as well as a novel 22 kDa Arabidopsis protein (ATG81).

18 NIP subgroup II, which is represented by the Arabidopsis protein AtNIP6;1.

19 We have identified a novel Arabidopsis protein, AtNSI, that interacts with NSP.

20 In this report we show that an Arabidopsis protein called RCE1 functions as a RUB-conju

21 In addition, we identified an Arabidopsis protein called RCE1 that is a likely RUB-con

22 all, DNA elements tested indicates that the Arabidopsis proteins can form functional interactions wi

23 Therefore, it is likely that the Arabidopsis proteins can function similarly to the yeast

24 cated that PATL1 is one of a small family of Arabidopsis proteins, characterized by a variable N-term

25 The chain consists of GCR1 (the sole Arabidopsis protein coding for a potential G-protein-cou

26 st 610 members that represent nearly 2.5% of Arabidopsis protein coding genes.

27 zation of SET DOMAIN GROUP 2 (SDG2), a large Arabidopsis protein containing a histone lysine methyltr

28 h the RING protein AtRBX1 and representative Arabidopsis proteins containing a BTB domain in vitro, w

29 l-anchored protein 1 (WIT1) and WIT2 are two Arabidopsis proteins containing a coiled-coil domain and

30 enome, although multiple copies are found in Arabidopsis proteins containing members of the Royal fam

31 Bioinformatics analysis identified putative Arabidopsis proteins containing sequences similar to the

32 h mutants in transgenic plants show that the Arabidopsis protein CORYNE, currently thought to be a ki

33 About 11% of BESs have homology to the Arabidopsis protein database.

34 The partially purified recombinant Arabidopsis protein did not produce PABA unless the E. c

35 was obtained using several randomly selected Arabidopsis proteins displaying a MYR site only.

36 omain that defines a superfamily of thirteen Arabidopsis proteins divided into four distinct phylogen

37 The Arabidopsis protein expressed in, and purified from, Esc

38 specific signature sequence found in a small Arabidopsis protein family that may be additional target

39 of the Snakin/Gibberellic Acid Stimulated in Arabidopsis protein family.

40 As in Arabidopsis, protein farnesyltransferase and protein ger

41 The 205-kDa immunoaffinity-purified Arabidopsis protein had PI 4-kinase activity.

42 We show that Arabidopsis protein half-lives vary from several hours t

43 d information and literature, more than 1500 Arabidopsis proteins have a manually assigned subcellula

44 Like psTic20, all four Arabidopsis proteins have a predicted transit peptide co

45 t belong to a family of five closely related Arabidopsis proteins having no known homologues amongst

46 epresented by some cDNAs revealed five novel Arabidopsis proteins important for Agrobacterium-mediate

47 vrRpt2 protease activity eliminates multiple Arabidopsis proteins in a transient expression system.

48 ed with pathogens and exclusive targeting of Arabidopsis proteins in the phytohormone signalling netw

49 Copper (Cu) is a cofactor of around 300 Arabidopsis proteins, including photosynthetic and mitoc

50 lysis using an antibody against a homologous Arabidopsis protein indicates that this soybean protein

51 Arabidopsis proteins interacted specifically with a prob

52 ological communities from partially observed Arabidopsis protein interaction datasets better than the

53 rity to AtCTR1 and also to EDR1, a CTR1-like Arabidopsis protein involved in defence and stress respo

54 with another previously identified group of Arabidopsis proteins involved in general wall O-acetylat

55 erm, consistent with the hypothesis that the Arabidopsis protein is resident in a nuclear polyadenyla

56 We report three Arabidopsis proteins isolated by ATP-affinity: PEROXIDAS

57 ptor-like cytoplasmic kinases, including the Arabidopsis protein kinase AVRPPHB Susceptible1 (PBS1).

58 haScreen) to profile interactions against an Arabidopsis protein kinase library.

59 stream of phosphatidic acid and involves the Arabidopsis protein kinase, AGC2-1, regulated by the 3'-

60 ed two endoplasmic reticulum (ER)-associated Arabidopsis proteins, KMS1 and KMS2, which are conserved

61 ree of which appear to be closely related to Arabidopsis proteins known to associate with the PRC2.

62 osol of plant cells and that the avocado and Arabidopsis protein members reveal a new aspect of the c

63 We probed the Arabidopsis protein microarray AtPMA-5000 with the N-ter

64 ellular activities targeted by SA, we probed Arabidopsis protein microarrays with a functional analog

65 Ruthenium Red and Gd(3+), as well as to the Arabidopsis protein MICU, a regulatory MCUC component.

66 e ESV1 protein and a similar uncharacterized Arabidopsis protein (named Like ESV1 [LESV]) are located

67 Among them, the plasma membrane-associated Arabidopsis proteins OCTOPUS (OPS) and BREVIS RADIX (BRX

68 AR sequence shows significant homology to an Arabidopsis protein of unknown function that is essentia

69 APT1 protein is homologous to SABRE and KIP, Arabidopsis proteins of unknown function involved in the

70 etide cyclase family comprising 37 annotated Arabidopsis proteins of unknown function.

71 y when coexpressed with AvrPphB and a second Arabidopsis protein, PBS1, which is a specific substrate

72 me, interacts with a previously unidentified Arabidopsis protein, PEX22.

73 Here, all Arabidopsis proteins predicted to contain long stretches

74 ay help to explain some of the phenotypes of Arabidopsis protein prenyltransferase mutants.

75 ants tested failed to interact with RIN4, an Arabidopsis protein previously shown to be required for

76 One such cellular factor is VIP1, an Arabidopsis protein proposed to interact with and facili

77 Here we report two closely-related Arabidopsis proteins, Protein Associated With Hrd1-1 (PA

78 In particular, our analysis of an Arabidopsis protein-protein interaction network revealed

79 tics very similar to one another, and to the Arabidopsis protein purified from leaves.

80 The TUG C terminus resembled the Arabidopsis protein PUX1.

81 The Arabidopsis proteins RAR1 and SGT1 are required for the

82 Antibodies raised against the Arabidopsis protein recognized distinctive polypeptides

83 e ITB1 gene showed that it encodes SCAR2, an Arabidopsis protein related to Scar/WAVE.

84 he Tobacco mosaic virus movement protein and Arabidopsis protein RGP2 was not affected by myosin VIII

85 tease that results in the elimination of the Arabidopsis protein RIN4.

86 The Arabidopsis protein RPM1 activates disease resistance in

87 ULICOLA1 (RPM1) via modification of a second Arabidopsis protein, RPM1-INTERACTING PROTEIN4 (AtRIN4).

88 ain near the N terminus was predicted in the Arabidopsis protein sequence, similar to that of the rat

89 Both the maize and the Arabidopsis proteins show preferential localization to m

90 (GRMZM2G438524), which is orthologous to the Arabidopsis protein SOT1 (AT5G46580).

91 ow that BONCAT is sensitive enough to detect Arabidopsis proteins synthesized within a 30-min interva

92 RIN4 is an Arabidopsis protein targeted by AvrRpt2 and AvrRpm1 for

93 All five C-terminally tagged Arabidopsis proteins tested, including four PM proteins,

94 reening with OBF4 we have isolated AtEBP, an Arabidopsis protein that contains a novel DNA-binding do

95 hese results are discussed in the context of Arabidopsis proteins that are putative substrates of PGG

96 ons in an SCF complex, we have characterized Arabidopsis proteins that bind to COI1.

97 /Chip each show structural similarity to two Arabidopsis proteins that cooperate with one another to

98 ork, we used cryptochrome 2 (CRY2) and CIB1, Arabidopsis proteins that interact upon light illuminati

99 We identify and characterize two novel Arabidopsis proteins that show homology to an orphan ver

100 This complex contains AtPEP12p, an Arabidopsis protein thought to be involved in protein tr

101 used to assign the complete set of candidate Arabidopsis proteins to one of these fold classes.

102 ertion position and primer sequences for all Arabidopsis proteins to study their subcellular localiza

103 ns-activation of gene expression by the four Arabidopsis proteins via some, but not all, DNA elements

104 An Arabidopsis protein was found to interact specifically w

105 ters and inhibition data for the recombinant Arabidopsis protein were consistent with these propertie

106 Expression of an Arabidopsis protein with homology to vertebrate retinoid

107 plants we have cloned several genes encoding Arabidopsis proteins with high homology to animal villin

108 We have collected a set of 44 Arabidopsis proteins with similarity to the USPA (univer