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1 xtended by a 70-residue linker to the RPA70N protein interaction domain).
2 evelopmental control and requires the FCA WW protein interaction domain.
3 nal repeat structure suggestive of a protein-protein interaction domain.
4 inases (MAGUKs) that contain the PDZ protein-protein interaction domain.
5 o profile the binding sites for any class of protein interaction domain.
6 t Cry3 lacks both an NLS motif and a protein-protein interaction domain.
7 as well as the FIP3-Fas receptor-interacting protein interaction domain.
8 large to be a membrane spanning or a protein/protein interaction domain.
9 , in this case, serves as autonomous protein-protein interaction domain.
10 hat the C-terminal half of VirB11 contains a protein interaction domain.
11 c ring finger functioning as a major protein-protein interaction domain.
12 des a homeodomain protein with a SIX protein-protein interaction domain.
13 tylated histones, and the C-terminal protein-protein interaction domain.
14 rminal ssDNA-binding domain and a C-terminal protein interaction domain.
15 potent, protease-resistant ligands to a PDZ protein-interaction domain.
16 a-grasp motif most commonly found in protein-protein interaction domains.
17 th Pkn4 and each contains well-known protein-protein interaction domains.
18 complexes created via a multitude of protein-protein interaction domains.
19 that contains a calmodulin binding site and protein interaction domains.
20 e-activated deoxyribonuclease superfamily of protein interaction domains.
21 ding pathway through a unique combination of protein interaction domains.
22 otif, sequences that act as specific protein-protein interaction domains.
23 with similarity to the PDZ family of protein-protein interaction domains.
24 and substrates by means of carboxy-terminal protein interaction domains.
25 pecialized proteins that often carry protein/protein interaction domains.
26 ty of targeting proteins via its TPR protein-protein interaction domains.
27 ter association of the CREB and CREB binding protein interaction domains.
28 ts of MAGUK proteins have additional protein-protein interaction domains.
29 iation (RA) and Src homology 3 (SH3) protein-protein interaction domains.
30 TPR motifs function as protein-protein interaction domains.
31 urs via both extracellular and intracellular protein interaction domains.
32 not require amino- or carboxy-terminal E2F1 protein interaction domains.
33 ed perhaps as modular "polar zipper" protein-protein interaction domains.
34 nd substrates through their variable protein-protein interaction domains.
35 Leupaxin possesses two types of protein interaction domains.
36 mino acid sequence contains multiple DNA and protein interaction domains.
37 ors based on targeting by eukaryotic protein-protein interaction domains.
38 ther bHLH factors, R harbors several protein-protein interaction domains.
39 e residues, they provide regulatable protein-protein interaction domains.
40 ssed scaffold protein that contains multiple protein interaction domains.
41 GTPase, protein kinase, and multiple protein-protein interaction domains.
42 ese problems, we have focused on families of protein interaction domains.
43 e in the category of multifunctional modular protein interaction domains.
44 ospholipid-binding domains and/or as protein-protein interaction domains.
45 d in deletion mutants lacking several of the protein interaction domains.
46 ecreted protein containing a large number of protein interaction domains.
47 ibose) polymerases that have SAM and ankyrin protein-interaction domains.
48 cellular signalling networks contain modular protein-interaction domains.
49 iously discovered role in regulating protein-protein interactions, domain 4 is an autoinhibitory doma
52 C-terminal, winged helix-loop-helix, protein-protein interaction domain adopts several conformations
53 essive because it lacks an effective protein-protein interaction domain although it does possess a nu
54 olymerase catalytic domain and a WWE protein-protein interaction domain, although similar proteins ha
55 erminus is composed of two potential protein-protein interaction domains: an "MAM" domain (named afte
56 analysis indicates an N-terminal POZ protein-protein interaction domain and a C-terminal kelch repeat
58 a novel protein that contains a GYF protein-protein interaction domain and interacts specifically wi
60 re examined: rfa1-M2 which is mutated in the protein interaction domain and rfa1-M4 which is mutated
61 human Bright through amino acids in Bright's protein interaction domain and that specific tyrosine re
62 ontaining a conserved amino terminal BTB/POZ protein interaction domain and three C-terminal Kruppel-
63 e revealed an amino-terminal BTB/POZ protein-protein interaction domain and three carboxy-terminal zi
64 racterized by the presence of two tandem PDZ protein interaction domains and a C-terminal domain that
65 ree consecutive Src homology 3 (SH3) protein-protein interaction domains and a C-terminal SH2 domain.
66 contain three carboxyl-terminal LIM protein-protein interaction domains and a proline-rich, pre-LIM
67 each scaffold protein has a different set of protein interaction domains and a unique set of interact
68 DZ proteins usually contain multiple protein-protein interaction domains and act as molecular scaffol
69 pears to have distinct enzymatic and protein-protein interaction domains and functions as a homodimer
70 The adapter protein FADD consists of two protein interaction domains and is an essential componen
72 tial extracellular and intracellular protein-protein interaction domains and its wide mRNA expression
73 f (beta)APP identifies PI domains as general protein interaction domains and may have important impli
74 ly, by overlapping the sequences of pairs of protein interaction domains and peptides, we have been a
75 evance for understanding the large family of protein interaction domains and the modular organization
76 copeptide repeat region, likely serving as a protein interaction domain, and a novel C-terminal regio
78 that this activity is due to a novel protein-protein interaction domain, and that homotypic interacti
79 of MG200, previously described as a protein-protein interaction domain, and to a 25-residue-long pep
80 target a conserved cysteine within the NR0B1 protein interaction domain, and we demonstrate that thes
81 n amino-terminal C2 domain, three WW protein-protein interaction domains, and a carboxy-terminal hect
82 series of spectrin repeats, two GEF domains, protein interaction domains, and a putative kinase domai
84 Many signaling proteins contain multiple protein interaction domains, and the decoy mechanism may
85 motifs indicative of protein-protein or RNA-protein interaction domains are discernible in the predi
87 lin-10 gene activity, suggesting that these protein interaction domains are not essential for LIN-10
89 rmining potential ligand binding and protein-protein interaction domains, as well as providing new in
91 nation machinery, while a C-terminal protein-protein interaction domain binds a specific substrate fo
92 basic helix-loop-helix/Per-ARNT-Sim protein-protein interaction domain, binds the C-terminal activat
94 region does not show any homology with known protein interaction domains but has been suggested to be
95 bear any obvious resemblance to other known protein interaction domains but is highly conserved amon
96 ding E2f, interact through carboxyl-terminal protein interaction domains, but genetic evidence sugges
98 e characterized by the presence of a protein-protein interaction domain called the POZ or BTB domain
101 es show that PDZ domains (like other protein-protein interaction domains) can engage in a variety of
102 The N terminus of SPY contains a protein-protein interaction domain consisting of 10 tetratricope
103 ne (GlcNAc) transferase (OGT) with a protein-protein interaction domain consisting of 10 tetratricope
105 kstrin homology (PHn) domain and an adjacent protein interaction domain designated as PHn-CC-Ex, amin
106 us, this study characterizes a novel protein/protein interaction domain disrupted in a KLF gene varia
107 ns that converted the GK from an enzyme to a protein interaction domain dramatically reduce flexibili
108 rge and complex, with multiple enzymatic and protein-interaction domains, each of which is targeted b
109 S arises from its more general function as a protein interaction domain, enabling TFIIS to bind a car
110 mot80, but not a mutant lacking its polarity protein interaction domain, enhances ERK1/2-dependent pr
111 amphipathic helix that may encode a protein-protein interaction domain essential for targeting the p
112 n of these complexes and, along with protein-protein interaction domains, form the core of AKAP funct
113 lar to the SAM (sterile alpha motif) protein-protein interaction domain, found in several ETS transcr
115 sequence (DSLL) comprising the core of this protein interaction domain functions as a transplantable
116 e guanylate kinase as it evolved into the GK protein interaction domain (GKPID) to investigate the ro
117 A molecular complex scaffolded by the GK protein-interaction domain (GKPID) mediates spindle orie
118 alpha-SynDelta6, missing part of the protein-protein interaction domain, had reduced toxicity but no
119 is data showed that CMF1 has crucial protein-protein interaction domains, has a retinoblastoma protei
121 rmore, mutations within two highly conserved protein interaction domains have a dominant-negative eff
122 iological functions of many distinct protein-protein interaction domains have been dissected through
123 oplasm, a process which requires the protein-protein interaction domain (I) in NCp7; subsequently, th
124 eucine residue within the first helix of the protein interaction domain impairs its function in BR si
126 of the enhanceosome, requires a new protein-protein interaction domain in the p65 subunit of NF-kapp
127 de protocols for constructing microarrays of protein interaction domains in individual wells of 96-we
128 g mutational analyses, we mapped the protein-protein interaction domains in JMJ, Nkx2.5, and GATA4.
129 ent binding of ubiquitin ligases to multiple protein interaction domains in LIM-HD recruited protein
130 ar to those of B-boxes, which act as protein-protein interaction domains in several transcription fac
131 binding specificity and organization of the protein interaction domains in wheat PABP was investigat
132 our proteins, each with well defined protein-protein interaction domains, include three 'scaffolds' (
134 s implicated both the BRCT and Myb domain as protein interaction domains involved in telomere length
136 nalysis and GST pull-down assay, the protein-protein interaction domain is defined as a coiled-coil d
139 suggesting that intact function of this BRCT protein-interaction domain is required both for coordina
140 Ralpha(DeltaRIIa) demonstrated that the RIIa protein interaction domain located within R1A was respon
141 taCC) demonstrated that the coiled-coil (CC) protein interaction domain located within the PML moiety
142 myosins form heavy chain dimers and contain protein interaction domains located at their unique N-te
145 ta suggest that the presence of two distinct protein interaction domains may help to determine the sp
147 n as the leucine rich region, functions as a protein interaction domain, mediating self-association o
148 expression of its N-terminal, TPR-containing protein interaction domains mimics the effects of LGN in
149 tein interactions and an increasing focus on protein-interaction domains: most frequently, pull-down
151 he organ of Corti, and carry several protein-protein interaction domains, no functional connection be
152 not map to any of the previously identified protein interaction domains, nor, with one exception, to
153 , constructed without the C-terminal protein-protein interaction domain of alpha, bound DNA with 200-
154 The enhancement requires the presence of the protein interaction domain of gp32 (the acidic carboxy-t
155 iptional activator and that mutations in the protein interaction domain of IRF6 disrupt this activity
156 l analysis of JMJ indicates that the protein-protein interaction domain of JMJ mediates the repressio
158 with a selective mutation in the N-terminal protein interaction domain of PKGIalpha display inherite
159 eins that interact with PKGI, the N-terminal protein interaction domain of PKGIalpha was used to scre
163 les and the DNA methyltransferase-associated protein interaction domain of the alpha subunit are key
168 ology 3 (SH3) and guanylate kinase-like (GK) protein interaction domains of Dlg, whereas an intramole
169 The in vivo significance of these protein-protein interaction domains of PCDH15 in hair cells has
170 ) and caspase recruitment domains, which are protein interaction domains of the death fold superfamil
171 rminal caspase recruitment domain, which are protein interaction domains of the death fold superfamil
172 ne/histidine-rich region (CH1 domain) of the protein interaction domains of the transcriptional coreg
176 ain of Elk-3, but not the C-terminal-binding protein interaction domain, partially alleviated this re
180 -shaped structure, with two pairs of protein-protein interaction domains positioned approximately 10
181 In particular, SH3, WW, and several new protein-interaction domains prefer ligand sequences that
182 et of four zinc fingers and a likely protein-protein interaction domain provided by the C-terminal pa
184 and ARF7 C-terminal domains (i.e., a protein-protein interaction domain referred to as domain III/IV
185 inclusion or exclusion of exons that encode protein interaction domains, regulatory signals, or tran
186 sized that this region constitutes a protein-protein interaction domain required for cooperative asse
187 e that the Nse1 RING-like motif is a protein-protein interaction domain required for Smc5-Smc6 holoco
188 pose that amino acids 91-97 of ATM contain a protein interaction domain required for the DNA damage-i
189 n to associate with two proteins through the protein interaction domain retained in POT1(DeltaOB)-the
190 a nucleic acid-binding domain and a protein-protein interaction domain separated by a flexible serin
191 f the E2F1 transcription factor is a protein-protein interaction domain since it associates with cycl
192 , Cul3 binds a BTB domain, and an associated protein-interaction domain such as MATH recruits substra
193 reted proteins that contain specific protein-protein interaction domains, such as von Willebrand A, Y
194 encodes a protein containing several protein-protein interaction domains, suggesting that it brings d
195 the C terminus of Bre2 as a critical protein-protein interaction domain that binds to the Dpy-30 doma
197 YRIN domain is a recently identified protein-protein interaction domain that is found at the N termin
198 ant was isolated that abolishes a WW protein-protein interaction domain that may be important for REF
199 data provide evidence that the SCAN box is a protein interaction domain that mediates both hetero- an
200 he death-effector domain (DED) is a critical protein interaction domain that recruits caspases into c
201 valis to streptococci is driven by a protein-protein interaction domain that resembles the eukaryotic
202 ion to its catalytic domain, several protein-protein interaction domains that allow it to interface w
203 ve a large number and typically a variety of protein interaction domains that allow many different pr
204 he coactivators CBP and p300 through protein-protein interaction domains that are evolutionarily cons
206 endent DNA-based motor is coupled to protein-protein interaction domains that can attach the motor to
208 latory proteins, consists of two LIM protein-protein interaction domains that enable it to function a
209 series of putative nucleic acid and protein-protein interaction domains that fold into an elongated
210 tivation domain had homology to "PQ" protein-protein interaction domains that have been described pre
211 Bromodomains are acetyl-lysine specific protein interaction domains that have recently emerged a
213 ta identify evolutionarily conserved protein-protein interaction domains that link mLin-2/CASK to SAP
214 e protein kinase interaction domain as novel protein interaction domains that mediate the binding bet
216 in a PDZ domain and one or more LIM domains, protein interaction domains that participate in a wide v
217 e-associated recruitment domains (CARDs) are protein interaction domains that participate in activati
218 ic acid-binding domains and adaptor (protein-protein interaction) domains that comprise the repair ma
219 (e.g., localization and/or specific protein-protein interaction domains) that allow it to efficientl
220 amily of proteins containing a novel protein/protein interaction domain, the EH domain, of as yet unk
222 t the homeodomain of PDX-1 acts as a protein-protein interaction domain to recruit multiple proteins,
224 the liver or intestine and may be a general protein interaction domain utilized by fatty acid-bindin
232 mal subunit interaction domain and a protein-protein interaction domain which mediates homomer and he
233 ition by Cyp-40 required both its C-terminal protein-interaction domain, which bound specifically to
234 interaction domain, and a number of protein-protein interaction domains (with receptors, other trans
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