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

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

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

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

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

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

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

14 The Arabidopsis protein At5g01750 from the DUF567 family was

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

39 As in Arabidopsis, protein farnesyltransferase and protein ger

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

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

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

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

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

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

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

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

48 Arabidopsis proteins interacted specifically with a prob

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

67 Here, all Arabidopsis proteins predicted to contain long stretches

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

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

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

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

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

73 The TUG C terminus resembled the Arabidopsis protein PUX1.

74 The Arabidopsis proteins RAR1 and SGT1 are required for the

75 Antibodies raised against the Arabidopsis protein recognized distinctive polypeptides

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

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

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

79 The Arabidopsis protein RPM1 activates disease resistance in

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

96 An Arabidopsis protein was found to interact specifically w

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

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

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