ライフサイエンスコーパス: protein interaction motif

1 nal ankyrin repeat domain (ARD), a prevalent protein interaction motif.

2 f APP, including the highly conserved YENPTY protein interaction motif.

3 and suggest a new role for PEST domains as a protein interaction motif.

4 even in the absence of binding to the major protein interaction motif.

5 fines the amino-terminal A helix of PKA as a protein interaction motif.

6 nzymatic activity and functions as a protein-protein interaction motif.

7 agy by mimicking a host short linear protein-protein interaction motif.

8 omain is an evolutionarily conserved protein-protein interaction motif.

9 A) domain, which may represent a new protein-protein interaction motif.

10 domain that folds as a four-helix bundle, a protein-interaction motif.

11 CUB and epidermal growth factor-like protein-protein interaction motifs.

12 mbly intermediates that contain WD40 protein-protein interaction motifs.

13 mbrane and four different classes of protein-protein interaction motifs.

14 rally related proteins that contain multiple protein interaction motifs.

15 esion targeting domains, and several protein-protein interaction motifs.

16 ntaining leucine zipper and helix-loop-helix protein interaction motifs.

17 central region of CAN that contains several protein interaction motifs.

18 gion (Cbl-N) lacks recognizable catalytic or protein interaction motifs.

19 e C-terminal periplasmic domain with protein-protein interaction motifs.

20 s two eps15 homology (EH) domains, a protein-protein interaction motif also present in other proteins

21 alpha helices (PAH1 to -4) that are protein-protein interaction motifs and is the scaffold upon whic

22 of which more than 40 are now known, act as protein interaction motifs and that the MoMOD1 protein a

23 ed C terminus that conforms to a type II PDZ protein interaction motif, and by screening PDZ domain p

24 modular PDZ domains that are modular protein-protein interaction motifs, and a C-terminal domain.

25 ific DNA binding domain (the SBP box), and a protein interaction motif (ankyrin repeats).

26 c amino acid residue properties, rather than protein interaction motifs, are more critical for Pol th

27 Omi has several novel putative protein-protein interaction motifs, as well as a PDZ domain and

28 A-PK holo-enzyme by acquisition of a protein-protein interaction motif at the C-terminus of Ku80.

29 talytic domain but lacks some of the protein-protein interaction motifs at the C terminus.

30 These findings highlight a new protein-protein interaction motif based on Y-X-X-X-Y and provide

31 suggest that chromo domains may function as protein interaction motifs, bringing together different

32 and a cytoplasmic part with various protein-protein interaction motifs but lacking any enzymatic act

33 an obligate homodimer via an essential GxxxG protein-interaction motif, but its ssRNA-binding mechani

34 vealed that BE6 binds paxillin through small protein interaction motifs called LD motifs that have be

35 LIM domains are protein-protein interaction motifs, can inhibit binding of LIM-H

36 Deletion of the protein interaction motif DED from pro-caspase-8 greatly

37 other splicing factors may serve as protein-protein interaction motifs elsewhere during spliceosome

38 This unique protein-protein interaction motif expands the regulatory potenti

39 is an integral membrane protein with protein-protein interaction motifs facing the extracellular matr

40 ase recruitment domain, a recently described protein interaction motif found in apoptotic signaling m

41 lity of our results to similar short protein-protein interaction motifs found in other transcription

42 D95/Discs large/ZO-1) domains are ubiquitous protein interaction motifs found in scaffolding proteins

43 arallel alpha-helices containing the protein-protein interaction motif GXXXG.

44 l sorting motif and several possible protein-protein interaction motifs had no discernible effect on

45 Taken together, we show that Homer1 and its protein interaction motif have broad global functions wi

46 on, two predicted B-Boxes, and a coiled-coil protein interaction motif immediately preceding an ADP-r

47 yrin repeat (ANK) is the most common protein-protein interaction motif in nature, and is predominantl

48 terminal (BRCT) domains are a common protein-protein interaction motif in proteins involved in the DN

49 xy terminal) was noted as a putative protein-protein interaction motif in the breast cancer suppresso

50 Finally, we show that an RGD protein-protein interaction motif in the LON-2 N-terminal domain

51 n repeat is one of the most abundant protein-protein interaction motifs in eukaryotes yet occurs in o

52 Two highly conserved protein:protein interaction motifs in FANCM, designated MM1 and

53 t extracellular loop (EL1) of CLDN1, but not protein interaction motifs in intracellular domains, are

54 is one of the most common, modular, protein-protein interaction motifs in nature.

55 lysis to determine how previously identified protein interaction motifs in the C terminus of mGluR1a

56 g and activity, we have examined two protein-protein interaction motifs in the cytoplasmic domain of

57 Protein interaction motifs in the cytosolic sequence are

58 omputational methods can frequently identify protein-interaction motifs in otherwise uncharacterized

59 MAGUKs are composed of modular protein-protein interaction motifs including L27, PDZ, Src homol

60 ing proteins contain a common set of modular protein interaction motifs including PDZ (postsynaptic d

61 MAGUKs comprise multiple protein-protein interaction motifs including PDZ, SH3 and guanyl

62 The molecule consists of multiple protein-protein interaction motifs, including a serine-rich regi

63 Neither of these protein interaction motifs is important for trafficking

64 gnaling complex is INAD, a protein with five protein-interaction motifs known as PDZ domains.

65 is C-terminal region harbors several protein-protein interaction motifs, likely relevant for signal t

66 However, mutation of a putative protein-protein interaction motif, LXXLL, in the ETS domain of E

67 questers it at postsynaptic sites; different protein interactions motifs mediate each step.

68 The POZ domain is a conserved protein-protein interaction motif present in a variety of transc

69 PDZ and LIM domains are modular protein interaction motifs present in proteins with dive

70 ith canonical DNA-binding zinc fingers, with protein interaction motifs such as FOG zinc fingers, and

71 ed by adaptor molecules that contain protein-protein interaction motifs such as the death domain.

72 is characterized by several putative protein-protein interaction motifs, suggesting that GRASP may be

73 ronal NO synthase contains a modular protein-protein interaction motif, termed the PDZ domain, that l

74 suggest that PIP motifs are a more versatile protein interaction motif than previously believed.

75 id binding and hydrolysis coupled to protein-protein interaction motifs that could allow for efficien

76 ultiple PDZ domains as well as other protein-protein interaction motifs that help to form large macro

77 PDZ domains are multifunctional protein-interaction motifs that often bind to the C-term

78 IQGAP1 possesses multiple protein interaction motifs to achieve its scaffolding fu

79 roperties will likely reveal further protein-protein interaction motifs to enrich our mechanistic mod

80 the autoinhibited state has shown that these protein interaction motifs turn inward and lock the kina

81 e/threonine kinase pathways may also require protein interaction motifs which are capable of recogniz

82 We have identified a conserved protein-protein interaction motif within the CBP-binding domains