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

1 er motif, in this case, serves as autonomous protein-protein interaction domain.

2 the zinc ring finger functioning as a major protein-protein interaction domain.

3 te, encodes a homeodomain protein with a SIX protein-protein interaction domain.

4 nize acetylated histones, and the C-terminal protein-protein interaction domain.

5 f, whilst Cry3 lacks both an NLS motif and a protein-protein interaction domain.

6 C-terminal repeat structure suggestive of a protein-protein interaction domain.

7 nylate kinases (MAGUKs) that contain the PDZ protein-protein interaction domain.

8 ciently large to be a membrane spanning or a protein/protein interaction domain.

9 icted WD40 propellers on TOPLESS function as protein-protein interaction domains.

10 to understand the functional intricacies of protein-protein interaction domains.

11 regulators based on targeting by eukaryotic protein-protein interaction domains.

12 se for other bHLH factors, R harbors several protein-protein interaction domains.

13 otyrosine residues, they provide regulatable protein-protein interaction domains.

14 g a Roc-GTPase, protein kinase, and multiple protein-protein interaction domains.

15 - and phospholipid-binding domains and/or as protein-protein interaction domains.

16 of a beta-grasp motif most commonly found in protein-protein interaction domains.

17 eract with Pkn4 and each contains well-known protein-protein interaction domains.

18 protein complexes created via a multitude of protein-protein interaction domains.

19 LXXLL motif, sequences that act as specific protein-protein interaction domains.

20 region with similarity to the PDZ family of protein-protein interaction domains.

21 a variety of targeting proteins via its TPR protein-protein interaction domains.

22 Subsets of MAGUK proteins have additional protein-protein interaction domains.

23 as Association (RA) and Src homology 3 (SH3) protein-protein interaction domains.

24 TPR motifs function as protein-protein interaction domains.

25 y selected perhaps as modular "polar zipper" protein-protein interaction domains.

26 they bind substrates through their variable protein-protein interaction domains.

27 ted by specialized proteins that often carry protein/protein interaction domains.

28 its previously discovered role in regulating protein-protein interactions, domain 4 is an autoinhibit

29 X11alpha/Mint-1 has multiple protein-protein interaction domains, a Munc-18 interacti

30 The C-terminal, winged helix-loop-helix, protein-protein interaction domain adopts several confor

31 non-repressive because it lacks an effective protein-protein interaction domain although it does poss

32 ibose) polymerase catalytic domain and a WWE protein-protein interaction domain, although similar pro

33 s COOH terminus is composed of two potential protein-protein interaction domains: an "MAM" domain (na

34 equence analysis indicates an N-terminal POZ protein-protein interaction domain and a C-terminal kelc

35 suggests that this structure functions as a protein-protein interaction domain and a signaling eleme

36 encodes a novel protein that contains a GYF protein-protein interaction domain and interacts specifi

37 sequence revealed an amino-terminal BTB/POZ protein-protein interaction domain and three carboxy-ter

38 ed of three consecutive Src homology 3 (SH3) protein-protein interaction domains and a C-terminal SH2

39 s, which contain three carboxyl-terminal LIM protein-protein interaction domains and a proline-rich,

40 PDZ proteins usually contain multiple protein-protein interaction domains and act as molecular

41 APM1 appears to have distinct enzymatic and protein-protein interaction domains and functions as a h

42 MAGI-2 contains eight potential protein-protein interaction domains and is localized to

43 ts potential extracellular and intracellular protein-protein interaction domains and its wide mRNA ex

44 Slower allosteric changes transpire in the protein-protein interaction domains and linker regions,

45 vitro, that this activity is due to a novel protein-protein interaction domain, and that homotypic i

46 AGR) box of MG200, previously described as a protein-protein interaction domain, and to a 25-residue-

47 aining an amino-terminal C2 domain, three WW protein-protein interaction domains, and a carboxy-termi

48 hCNK1 contains several protein-protein interaction domains, and Rho interacts w

49 e of these, coined dAnk1-3, contain a common protein-protein interaction domain (ankyrin repeats), in

50 Catalytic centers or protein-protein interaction domains are in close relatio

51 in determining potential ligand binding and protein-protein interaction domains, as well as providin

52 g ubiquination machinery, while a C-terminal protein-protein interaction domain binds a specific subs

53 ntains a basic helix-loop-helix/Per-ARNT-Sim protein-protein interaction domain, binds the C-terminal

54 ctors are characterized by the presence of a protein-protein interaction domain called the POZ or BTB

55 We recently identified a new protein-protein interaction domain, called the L27 domai

56 al studies show that PDZ domains (like other protein-protein interaction domains) can engage in a var

57 lucosamine (GlcNAc) transferase (OGT) with a protein-protein interaction domain consisting of 10 tetr

58 The N terminus of SPY contains a protein-protein interaction domain consisting of 10 tetr

59 Thus, this study characterizes a novel protein/protein interaction domain disrupted in a KLF ge

60 form an amphipathic helix that may encode a protein-protein interaction domain essential for targeti

61 alization of these complexes and, along with protein-protein interaction domains, form the core of AK

62 ck, and broad complex) is a diverse group of protein-protein interaction domains found within metazoa

63 lly similar to the SAM (sterile alpha motif) protein-protein interaction domain, found in several ETS

64 alpha-SynDelta6, missing part of the protein-protein interaction domain, had reduced toxicity

65 e analysis data showed that CMF1 has crucial protein-protein interaction domains, has a retinoblastom

66 The biological functions of many distinct protein-protein interaction domains have been dissected

67 the cytoplasm, a process which requires the protein-protein interaction domain (I) in NCp7; subseque

68 Furthermore, DOZ reduces the flexibility of protein-protein interaction domains important for recept

69 context of the enhanceosome, requires a new protein-protein interaction domain in the p65 subunit of

70 Using mutational analyses, we mapped the protein-protein interaction domains in JMJ, Nkx2.5, and

71 st similar to those of B-boxes, which act as protein-protein interaction domains in several transcrip

72 These four proteins, each with well defined protein-protein interaction domains, include three 'scaf

73 This GEF contains several protein-protein interaction domains, including a PDZ dom

74 hybrid analysis and GST pull-down assay, the protein-protein interaction domain is defined as a coile

75 This protein-protein interaction domain is important for the

76 sed in the organ of Corti, and carry several protein-protein interaction domains, no functional conne

77 protein, constructed without the C-terminal protein-protein interaction domain of alpha, bound DNA w

78 utational analysis of JMJ indicates that the protein-protein interaction domain of JMJ mediates the r

79 ophobic residues of SKIP thus defining a new protein-protein interaction domain of SKIP.

80 se mutation of a critical residue in the NHL protein-protein interaction domain of the protein.

81 suggest that the CRD may function as a major protein-protein interaction domain of these kinases.

82 The in vivo significance of these protein-protein interaction domains of PCDH15 in hair ce

83 Novel protein-protein interaction domains on acetylated Tat ar

84 Like other protein-protein interaction domains, PDZ domains are inv

85 NHERF1 begins with two modular protein-protein interaction domains-PDZ1 and PDZ2-and en

86 nctive V-shaped structure, with two pairs of protein-protein interaction domains positioned approxima

87 rminal set of four zinc fingers and a likely protein-protein interaction domain provided by the C-ter

88 R domains function simply as general purpose protein-protein interaction domains put to diverse uses.

89 on ARF5 and ARF7 C-terminal domains (i.e., a protein-protein interaction domain referred to as domain

90 hypothesized that this region constitutes a protein-protein interaction domain required for cooperat

91 e propose that the Nse1 RING-like motif is a protein-protein interaction domain required for Smc5-Smc

92 sists of a nucleic acid-binding domain and a protein-protein interaction domain separated by a flexib

93 rminus of the E2F1 transcription factor is a protein-protein interaction domain since it associates w

94 ding secreted proteins that contain specific protein-protein interaction domains, such as von Willebr

95 cnk encodes a protein containing several protein-protein interaction domains, suggesting that it

96 , among which, the TAZ2 domain is known as a protein-protein interaction domain that binds to E1A and

97 ntified the C terminus of Bre2 as a critical protein-protein interaction domain that binds to the Dpy

98 The PYRIN domain is a recently identified protein-protein interaction domain that is found at the

99 ssor mutant was isolated that abolishes a WW protein-protein interaction domain that may be important

100 P. gingivalis to streptococci is driven by a protein-protein interaction domain that resembles the eu

101 in addition to its catalytic domain, several protein-protein interaction domains that allow it to int

102 y with the coactivators CBP and p300 through protein-protein interaction domains that are evolutionar

103 ATP-dependent DNA-based motor is coupled to protein-protein interaction domains that can attach the

104 l coregulatory proteins, consists of two LIM protein-protein interaction domains that enable it to fu

105 reveal a series of putative nucleic acid and protein-protein interaction domains that fold into an el

106 oxA10 activation domain had homology to "PQ" protein-protein interaction domains that have been descr

107 Our data identify evolutionarily conserved protein-protein interaction domains that link mLin-2/CAS

108 PDZ motifs are protein-protein interaction domains that often bind to C

109 s, nucleic acid-binding domains and adaptor (protein-protein interaction) domains that comprise the r

110 in Vam3p (e.g., localization and/or specific protein-protein interaction domains) that allow it to ef

111 erging family of proteins containing a novel protein/protein interaction domain, the EH domain, of as

112 ence that the homeodomain of PDX-1 acts as a protein-protein interaction domain to recruit multiple p

113 A second protein-protein interaction domain was identified at ami

114 Three protein-protein interaction domains were identified in e

115 Several characterized protein-protein interaction domains were identified, as

116 S ribosomal subunit interaction domain and a protein-protein interaction domain which mediates homome

117 n, a DNA interaction domain, and a number of protein-protein interaction domains (with receptors, oth

118 We identified a protein-protein interaction domain within the amino-term

119 oteins and are recruited by the 4-amino acid protein-protein interaction domain, WRPW.