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1 rotation is mostly uncoupled from the motor domain.
2 fold and a Holliday junction resolvase-like domain.
3 high-resolution structure exists for the TP domain.
4 a small peptide motif within its MT-binding domain.
5 ls, but not the DNA methylation, of the Peg3 domain.
6 tional Src inhibitors that target the kinase domain.
7 ces stem from the orientations of the apical domain.
8 iled-coil 2-leucine zipper ubiquitin binding domain.
9 , they become inapplicable in the low-energy domain.
10 and a beta-hairpin turn of the Phy-specific domain.
11 minal hydroxyphenylpyruvate dioxygenase-like domain.
12 Sso7d binding module and a cellulose-binding domain.
13 binding specificity of the overexpressed SH2 domain.
14 the hormone binding signal to the catalytic domain.
15 sequence similarity and different auxiliary domains.
16 omain and the HCN C terminus through the TPR domains.
17 phatidylinositol (4,5)-bisphosphate-enriched domains.
18 of mitochondria to maintain distinct Ca(2+) domains.
19 are notably more impactful within their own domains.
20 atic stripes and locally aligned focal conic domains.
21 structures reveals propagating polarization domains.
22 insically disordered regions and coiled coil domains.
23 ns with moderately hydrophobic transmembrane domains.
24 which connects the HIRAN and ATPase/helicase domains.
25 ted CARD8 protein lacking the FIIND and CARD domains.
26 zing auxin response between their expression domains.
27 acement between the VAMP721 SNARE and longin domains.
28 re leads to the formation of distinct margin domains.
31 ortion of CD23, including the stalk and head domain; 1 variant was identical with the first, except f
38 llular matrix protein, the fibronectin extra domain A isoform (FnEDA), which is relatively restricted
39 The structure shows that POT1C contains two domains, a third OB fold and a Holliday junction resolva
40 lapse repeatability of about 2% in the model domain-a threshold that is low enough for observing subt
41 5 (SCA5) L253P mutation in the actin-binding domain (ABD) of beta-III-spectrin causes high-affinity a
44 introduction of new rAb fragments and single-domain Abs have reinvigorated the concept of passive imm
48 structure revealed that DddY contains a cap domain and a catalytic domain with a Zn(2+) bound at its
49 terminal extension containing a proline-rich domain and an actin-binding Wiskott-Aldrich syndrome pro
50 s that bind to the interface between TAM Ig1 domain and Gas6 Lg1 domain can inhibit TAM activation, a
52 his study, we identified pleckstrin homology domain and leucine-rich repeat protein phosphatase 1 (PH
53 cleotide-binding domain through a 37-residue domain and the HCN C terminus through the TPR domains.
54 ion causes structural perturbation in the A2 domain and thereby destabilizes the domain by approximat
56 static forces on individual atoms, residues, domains and molecules, and generates an output that can
57 proach to control the buckling of individual domains and thus the outcome configurations of planar-pa
58 hesis) and StoA (apical sterol-rich membrane domains), and its essentiality in polar deposition of ch
59 s, such as AR-V7, at their conserved SET/NAP domain, and exacerbate and repress the transactivation o
60 NLS and the neighboring microtubule-binding domain, and RhoA-GTP binding may relieve this inhibition
61 ng insertion of its N-proximal transmembrane domain, and subsequently, COX18 transiently interacts wi
62 r correlation describing the size of genetic domains; and (3) a dimensionless constant quantifying th
64 The polyglutamine-proximal portions of these domains are immobilized and clustered, limiting access t
68 an N-terminal sugar phosphate isomerase-like domain associated with DSD activity and a novel C-termin
69 ns while enhancing network-based analyses of domain associations, subcellular localization, and co-co
70 s developed to show that a unique, conserved domain at the C-terminus of Swc5, called Bucentaur (BCNT
75 P) sequencing (ChIP-Seq) data shows that the domain boundaries identified by ClusterTAD have a high e
76 at the dimer interface of the catalytic core domain but at the same time markedly impair HIV-1 replic
77 n the A2 domain and thereby destabilizes the domain by approximately 10 kJ/mol, promoting its unfoldi
78 nterface between TAM Ig1 domain and Gas6 Lg1 domain can inhibit TAM activation, and support the furth
79 N-terminal fragment comprising the catalytic domain can interact both with itself and with a C-termin
81 rt from trivial 180(o) commensurate magnetic domains, can be described by ferromagnetic and ferroelec
84 how that there is a rearrangement in the eag domain-CNBHD interaction with the kinetics, voltage-depe
85 ry mediate de novo formation of a 3D contact domain comprising IGF2 and a lineage-specific super-enha
86 zation domain, leucine rich repeat and pyrin domain containing 1 (NLRP1), NLRP3, and nucleotide-bindi
88 y protein nucleotide-binding oligomerization domain-containing 2 (NOD2); however, the reported effect
90 ndent mechanism involving Toll-IL-1-receptor domain-containing adapter-inducing IFN-alpha (TRIF) and
91 rine/threonine-protein kinase 3 (RIPK3), TIR-domain-containing adapter-inducing interferon-beta (TRIF
92 essor genes, including Src homology region 2 domain-containing phosphatase-1 (SHP-1) and TXNIP (thior
95 We show that upon citrate binding, the PAS domain contracts, resulting in a shortening of the C-ter
96 conjugated unimNPs with the cholera toxin B domain (CTB) for RGC-targeting and with Cy5.5 for unimNP
97 ifferences in how the Rb and p107 C-terminal domains (CTDs) associate with the coiled-coil and marked
98 pha), and phosphorylation of the DNA-binding domain (DBD) at Thr-38 in CAR regulates this conversion.
99 a serine-rich motif immediately after the PH domain decreases both PtdIns(4)P binding and ceramide tr
102 identified single-point mutations in the Fc domain (e.g., E345K or E430G) enhancing Fc:Fc interactio
103 s model, a loop defined by the SCI's B and C domains encircles the C-terminal segment of the IR alpha
107 atic hydroxylation reactions represent a new domain for high-valent bis(mu-oxido)dimetal reactivity.
108 tide that reconstitutes the collagen-binding domain for integrins GFOGER reverted the assembly of FN
109 tive research was used to identify important domains for the Population, Intervention, Comparison, Ou
110 opeller-shaped structure, where the two Cas2 domains form a central hub (twofold axis of symmetry) fl
112 In this study, we demonstrate that binding domains from autolysins and lysins can be fused to the F
117 play key residues of the p53 transactivation domain have emerged as bona fide clinical candidates for
118 ked to palmitoylation of the cysteine-string domain, however the regions of the mutant proteins that
120 nd loaded with plasmid DNA encoding perlecan domain I and VEGF189 and analyzed in vivo for their abil
121 ng plasmid DNA encoding VEGF189 and perlecan domain I have the potential to induce angiogenesis and w
122 separase (also known as Esp1) contains four domains (I-IV), and a substrate-binding domain immediate
124 However, most evidence suggests that the domain immediately downstream of the S2' cleavage site i
125 four domains (I-IV), and a substrate-binding domain immediately precedes the catalytic domain and has
126 omain from the C-terminal growth factor (GF) domain in each monomer, pro-TGF-beta is secreted and sto
127 found that the RING B-box coiled-coil (RBCC) domain in KAP1 and the proximal coupling of ubiquitin co
128 biquitin conjugation to ER degradation (CUE) domain in SMARCAD1 mediate their direct interaction.
131 slocation could be restored by alpha-helical domains in a position- and organism-dependent manner.
133 Recent observations of switching of magnetic domains in ferromagnetic metals by circularly polarized
134 viours of heterochromatin, and how chromatin domains in general regulate essential nuclear functions.
135 Here, the authors identify two pseudoGTPase domains in p190RhoGAP, characterize them biochemically a
136 examined associations between the 12 symptom domains in the Neuropsychiatric Inventory (NPI) and rela
138 advancements in a number of crucial sensing domains, including biomolecules, environmental toxins, e
141 ne protein with a single immunoglobulin (Ig) domain, instructs the distinct, neuron-type-specific ela
142 lular protein, and it suggests that the SLII domain is a potential target for antiviral therapy.
143 show here that while the central DNA binding domain is essential for anchoring at parS, this interact
144 So far, it has been assumed that the pilin domain is essential for the allosteric propagation withi
146 ediately upstream of the SNARE heptad-repeat domain, is required for normal fusion activity with HOPS
147 vertebrate thalamus, pretectum, and midbrain domains jointly correspond to a single amphioxus region,
148 indicates how tension between the two motor domains keeps their cycles out of phase in order to stim
149 cs are regulated by kinases, such as the LIM domain kinase (LIMK), which regulates actin activity thr
151 tween GK and the nearby Src homology 3 (SH3) domain, leading to a closed conformation, whereas a non-
152 proteins nucleotide-binding oligomerization domain, leucine rich repeat and pyrin domain containing
153 sis, is executed by the mixed lineage kinase domain-like (MLKL) protein, which is triggered by recept
154 PK3) phosphorylation of mixed-lineage kinase domain-like protein (MLKL), which results in disruption
159 ted by its conserved mitochondrial targeting domain (MTD), which, in unstressed conditions, is inhibi
163 cted that a region in the nucleotide-binding domain (NBD) of DnaK interacted with a region in the mid
164 inding site of NRP1 and the NRP1 cytoplasmic domain (NCD), but not the known NCD interactor GIPC1.
165 LRP3, and nucleotide-binding oligomerization domain (NOD)-like receptor C4 (NLRC4) were associated wi
169 e, we report that the hydrophilic N-terminal domain of Brassica napus DGAT1 (BnaDGAT11-113) regulates
171 with a novel binding motif in the N-terminal domain of CaV1 LTCC alpha1 subunits that is not conserve
172 ver, replacement of TM2 by the transmembrane domain of CD4, the asialoglycoprotein receptor, or the t
175 ranslation and show that the functional core domain of eIF4G plus an adjacent probable RNA-binding do
177 inding of the S339D/S340D mutant to the FERM domain of Ezrin is sensitive to buffer salt concentratio
183 Conversely, receptors with the intracellular domain of IR display higher IRS-1 phosphorylation, stron
184 NA is found throughout much of the bacterial domain of life, where it commonly controls the expressio
185 show that TIGIT bound to the immunoglobulin domain of nectin-2 that is most distal from the membrane
186 nt polypeptide chains, also binds to the TPR domain of Sec72, even though it lacks the TPR-binding C-
187 tab and HAP1-DeltaOSCP, lacking the membrane domain of subunit b or the OSCP, respectively, in which
189 ha13 protein from binding to the cytoplasmic domain of the beta3 integrin prevents outside-in signali
191 system, the phosphorylation of the receiver domain of the histidine kinase CYTOKININ-INDEPENDENT 1 (
193 otaxis protein CheY, the N-terminal receiver domain of the nitrogen regulation protein NT-NtrC, and t
194 the unfolded protein stress-sensing luminal domain of the UPR transducers PERK and IRE1alpha does no
198 tive cost-benefit valuation across different domains of effort and provide insight into the multidime
199 was utilized to demonstrate that isolated TM domains of Hendra virus F protein associate in a monomer
201 for ten core proteins, nearly all essential domains of its RNA, and five stably associated auxiliary
203 ame unimodal core coalignment but form local domains of microtubules polymerizing in the same directi
204 lve the crystal structures of the N-terminal domains of PHF1 and MTF2 with bound CpG-containing DNAs
206 Cerebellar systems are implicated in diverse domains of sex-biased behavior and pathology, but we lac
207 t mobile small RNAs generate sharply defined domains of target gene expression through an intrinsic a
208 physical-impairment and everyday-activities domains of the Migraine Physical Function Impact Diary (
209 We find that both the N- and C-terminal domains of TTP are involved in an interaction with CNOT9
213 study identified LMO1, which encodes an LIM-domain-only transcriptional cofactor, as a neuroblastoma
214 eld fluorescein angiography (UWFA), spectral-domain optical coherence tomography (SD-OCT), and optica
215 erent redox states have a profound effect on domain orientation in the enzyme and we analyse the data
216 y, we demonstrate that only three of the six domain orientations are present in solution, where Dcp2
217 exchange between the TCR alpha/beta constant domain pair and the IgG1 CH3 homodimer was evidenced by
218 tramers composed of a stable oligomerization domain (Pcore) flanked by large intrinsically disordered
220 of sporozoite factors reveals the 6-cysteine domain protein P36 as a major parasite determinant of ho
222 members of a small family of immunoglobulin domain proteins, we found that OIG-8, a previously uncha
224 rcome such limitations, protein transduction domains (PTDs) have been used as protein carriers, howev
225 pathway, including RNA POLYMERASE V (POL V), DOMAINS REARRANGED METHYLTRANSFERASE 2 (DRM2) and SAWADE
227 as pRNA acceptors indicated that the PRNTase domain recognizes the C-2-amino group, but not the C-6-o
228 onnection to extensive annotation of several domain-relevant semantic classes, and connection to comp
231 obular, cofactor-containing extracytoplasmic domains requiring the dual action of the co-translationa
232 al cysteine pairs in the CSF3R extracellular domain resulted in either gain- or loss-of-function chan
234 of 40 CBMs, in fusion with an N-terminal GFP domain, revealed that type A CBMs possess the ability to
242 ing to account for the separation of the two domains starting from a homogeneous array of cells, and
246 be associated with topologically associating domain (TAD) borders, while dCP enhancers are more often
248 n through transcriptional enhancer associate domain (TEAD) and runt-related transcription factor 2 (R
249 n mice with a mutation in the TR DNA-binding domain that abrogates binding to DNA and leads to comple
250 i by targeting cellular ligases through a sT domain that also inhibits MCV large T oncoprotein turnov
251 fication of cysteine residues within the RGS domain that are located distal to the Galpha-binding int
252 NEMO (residues 112-150) in its coiled-coil 1 domain that impedes the binding of linear (M1-linked) di
253 We also showed that YeeJ contains a LysM domain that interacts with peptidoglycan and thus assist
255 e Xist locus is coated with a broad H3K27me3 domain that is established during oocyte growth and pers
256 pecific NLS sequence in the N-terminal lyase domain that promotes transport of the protein independen
257 the allosteric propagation within the lectin domain that would otherwise be conformationally rigid.
258 mber of redox-inactive ketoreductase (KR(0)) domains that are implicated in the generation of C2-epim
259 mational changes within the Uba1 adenylation domains that effectively disassemble the adenylation act
260 ditors containing mutated cytidine deaminase domains that narrow the width of the editing window from
261 a membrane, respectively, to create membrane domains that partition upstream regulators of the TORC1
263 Lon to bind DNA is determined by its ATPase domain, that this binding is required for processing pro
264 1 localization at CME sites are the third EH domain, the proline-rich region, and the coiled-coil reg
265 Although EPFR formation occurs on the metal domains, these differences were correlated with the alte
266 ment with an absence of predicted structural domains, these were characterized as intrinsically disor
267 surface uniformity and conserved fold of SH3 domains, they display different binding mechanisms and a
268 IP8b binds the HCN cyclic nucleotide-binding domain through a 37-residue domain and the HCN C terminu
269 e linker dictates the rotation of the lectin domain, thus modulating the GalNAc-Ts' long-range prefer
270 eterodimers further dimerize through SAV1 WW domains to form a heterotetramer, in which MST2 undergoe
274 irreversible phase transition to cylindrical domains under the electric field, accompanied by a trans
275 are the best-studied von Willebrand factor A domains undergoing significant conformational changes fo
276 both N-domain twisting and rotation of the C domain (up to 30 degrees ) at the end of the relatively
277 racts also demarcate seven columnar neuropil domains (ventromedial, ventro-lateral, centromedial, cen
279 otentially related to the controllability of domain wall electronic properties.The electronic states
282 eversal curve measurements indicate a strong domain wall pinning along the direction orthogonal to th
283 eal that the higher coercive field is due to domain wall pinning in deeper defects and hence a higher
284 y to present phase co-existence separated by domain walls (DWs) above room temperature provides immen
285 energy in well-defined train of polarization domain walls allows undistorted propagation of polarizat
287 onic properties.The electronic states within domain walls in an interacting electronic system remain
289 The possibility of controlling magnetic domain walls using voltages offers an energy efficient r
290 P-D, containing homotrimeric neck and lectin domains, was expressed in Escherichia coli BL21(lambdaDE
297 possesses an ubiquitin (Ub) E2 variant (UEV) domain with a pocket that can bind PT/SAP motifs and ano
300 nalysis, highly conserved protein motifs and domains within each of the AARS loci were identified and
301 we define the Xist RNA Polycomb Interaction Domain (XR-PID), a 600 nt sequence encompassing the Xist
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