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1 tion factor, epithiospecifier protein and an unknown protein.
2 ction from a protein of known function to an unknown protein.
3 crease the accuracy of the assignment of the unknown protein.
4 mal growth factor-related receptor]), and an unknown protein.
5  available protein spectra to match with the unknown protein.
6 amic, suggesting their stabilization by some unknown protein.
7 r1), a trypsin-like protein (Lltryp2) and an unknown protein.
8 psin like proteins (LuloChym1A and 2) and an unknown protein.
9 may interact with or be phosphorylated by an unknown protein.
10 rotein, NADH dehydrogenase subunit 2, and an unknown protein.
11 to the modeling of structure and function of unknown proteins.
12 n data allows the prediction of function for unknown proteins.
13 e of ESTs encoding novel and/or functionally unknown proteins.
14 igned putative functions, whereas 123 encode unknown proteins.
15 ilies representing these 48% of structurally unknown proteins.
16 t to result from a prion form of one or more unknown proteins.
17 genes in Leishmania, of which 40% may encode unknown proteins.
18 for the automatic annotation of a testset of unknown proteins.
19 eviridae members, such as its high number of unknown proteins.
20   The main use is to predict the function of unknown proteins.
21 duced by BMP rather than amelogenin or other unknown proteins.
22 ify new functions for several unannotated or unknown proteins.
23 ort system, (2) immunity, and (3) previously unknown proteins.
24 bers of apparently nonspecific contacts with unknown proteins.
25 ng both known ribosomal assembly factors and unknown proteins.
26 jor capsid proteins VP1 and VP2 and smaller, unknown proteins.
27                     The contribution of the "unknown" protein allergens is apparent in phylogenetical
28  In the current study, we characterized this unknown protein and tested its potential targeting roles
29  isotope labeling, which impedes analysis of unknown proteins and complex mixtures and exponentially
30 the utility of HiFun, we annotated 2 212 663 unknown proteins and discovered novel motifs in the UHGP
31                      Regions III and V bound unknown proteins and exerted strong enhancer-like activi
32 dentification of the biochemical function of unknown proteins and improves the quality of reconstruct
33  this response could invoke known as well as unknown proteins and pathways.
34 c stem cells to classify a set of previously unknown proteins, and validate our findings against a re
35                                Some of these unknown proteins are likely to be involved in uncharacte
36               Two functional predictions for unknown proteins are made based on integrating other dat
37                   However, capturing labile, unknown protein assemblies directly from cells remains a
38 listic framework for predicting functions of unknown proteins based on the functional similarity.
39 ther, FragFold is able to predict previously unknown protein binding modes, explaining prior genetic
40  level is crucial for discovering previously unknown protein biomarkers for cancer diagnosis and drug
41 g pathway involves the phosphorylation of an unknown protein by polo-like kinase 1/Xenopus laevis pol
42 binding activity of DEF-A, we identified the unknown protein by using conventional purification metho
43                Finally, using in-line LC-MS, unknown proteins can be identified from solubilized Esch
44                    Often functional clues of unknown proteins can be obtained by predicting small lig
45  functional analysis because the function of unknown proteins can be postulated on the basis of their
46 inciples of proteome organization and enable unknown protein characterization.
47 rithms, constitute a significant fraction of unknown protein-coding genes.
48 ngs provide novel insights into a previously unknown protein complex that can regulate EGFR traffic a
49 free methods for the discovery of previously unknown protein complexes in cryo electron tomograms.
50  genes, which may interact within shared but unknown protein complexes.
51 robably consisting of xnf7 and several other unknown protein components.
52 , respectively, of which 522 were previously unknown protein constituents.
53  by Plk1/Plx1-mediated phosphorylation of an unknown protein, correlates with the activation of the t
54 ensemble averaging" procedure to account for unknown protein costs.
55 ctor-2, Grb2-associated protein 2, and other unknown proteins could distinguish DCIS from IDC of the
56  contain a rich repertoire of both known and unknown protein-encoding and non-coding RNAs.
57 protocol could identify known and previously unknown proteins expressed selectively in AFD.
58 laments [7, 8], but it is plausible that yet-unknown proteins facilitate anchoring of the ER membrane
59 ructure of the Fkh1-DBD reveals a previously unknown protein fold among all known Forkhead proteins.
60      The RGMB structure reveals a previously unknown protein fold and a functionally important autoca
61                    Here we show a previously unknown protein fold, and the design and interpretation
62 s of protein interfacial interactions within unknown proteins following appropriate calibration.
63 d is demonstrated for a peptide standard and unknown proteins from a yeast lysate using all 6118 poss
64 ntification and characterization of a priori unknown proteins from an Escherichia coli (E. coli) solu
65  machine learning to enable the discovery of unknown protein functions and uncover the relationship b
66 rated in the bait toward a target residue of unknown proteins, here we genetically encode chemical cr
67 sequences is a common method for identifying unknown proteins; however, the processing of MSMS by cur
68                   Sixteen HYPOXIA-RESPONSIVE UNKNOWN PROTEIN (HUP) genes, including four that are Ara
69 nd structural similarity with PMI15, another unknown protein in Arabidopsis that, when mutated, cause
70  the Hv channel VSD assembles with an as yet unknown protein in the cell membrane as a requirement fo
71 o model potential binding sites for known or unknown proteins in DNA sequences.
72 e predicted interactions for many previously unknown proteins in known pathways and complexes.
73 the potential importance of these previously unknown proteins in microbial metabolism.
74 quire specific interactions between CFTR and unknown proteins in the apical compartment of epithelial
75 fication of RanGAP1 in vitro and of multiple unknown proteins in vivo.
76                The screen yielded previously unknown proteins including one we named COPR1, for comod
77  with filamentous CAZ structures via largely unknown protein interactions.
78                  Our data suggest previously unknown protein interfaces across Y complexes and to inn
79          An open reading frame coding for an unknown protein is identified in the promoter of IRXA2 o
80  co-occurrence data, the neighborhood around unknown proteins is quickly connected to well-characteri
81  to chemical labeling, as well as previously unknown protein isoforms including pSPs.
82 KCC1, which is directly phosphorylated by an unknown protein kinase in response to various secretagog
83 ated protein kinases (MAPKs), but also by an unknown protein kinase(s).
84 phosphorylation occurs by multiple known and unknown protein kinases.
85 hrocyte invasion, while identifying numerous unknown proteins likely to be involved in invasion.
86  neurons by using a host of known and as yet unknown protein machinery.
87 mon poxvirus carries numerous genes encoding unknown proteins, many of which have low sequence comple
88  are required for POK1 localization, and yet unknown proteins may stabilize TAN1-POK1 interactions.
89     The mechanistic details of this hitherto unknown protein-mediated entry are not understood.
90 ccumulation, and uncover multiple previously unknown proteins modulated by short-term -N in green alg
91     Our results indicate that the previously unknown protein NPX1 acts as a negative regulator in pla
92                          Notably, a hitherto-unknown protein (NUQM) completes an interdomain bridge i
93 ht to be involved in membrane fusion, and an unknown protein of 40 kDa.
94 er microarray, we found that thrombin and an unknown protein of E. coli (protein X) formed a complex
95 so allow the identification of the remaining unknown proteins of this FMRP-associated mRNP as well as
96 rresponding to fibronectin, vitronectin, and unknown proteins, one of which was identical to the size
97 relevant Cys residues were sequestered by an unknown protein or that a significant portion of the Fep
98 istically 'unusual' in the composition of an unknown protein, or to automatically cluster proteins in
99 s a regulatory domain that interacts with an unknown protein partner to modulate the autokinase activ
100 A-IV interacts with lipids and possibly with unknown protein partners.
101 ach to human beta-cells to define previously unknown protein/peptide products.
102 rast, HRD1 and HRD3 genes encoded previously unknown proteins predicted to be membrane bound.
103 ng methods for modeling the 3D structures of unknown protein-protein complexes.
104 rary will be useful to predict structures of unknown protein-protein interactions.
105 MDP-1 is most likely a phosphotyrosine in an unknown protein rather than a small sugar-based substrat
106 mall proline-rich superfamily, loricrin, and unknown proteins related to the desmoplakin family.
107    The most common method for determining an unknown protein's structural class is to perform expensi
108 st-genomic age, it is possible to predict an unknown protein's structural class using machine learnin
109 pathway and the O-linked glycosylation of an unknown protein(s) by UDP-N-acetylglucosaminyl transfera
110 at the SH2 domain is binding to a heretofore unknown protein(s) necessary for proper EGFR function.
111 l site can also bind NF-kappaB as well as an unknown protein(s) of approximately 40 kDa.
112 Kgamma, and induces polyubiquitination of an unknown protein(s) that associates with NEMO, likely by
113 in RING E3 ligase complex to ubiquitylate an unknown protein(s) to limit error-prone repair during V(
114 stitutive occupancy of a binding site for an unknown protein(s); however, we detect no protein-DNA in
115 s, has been successfully used to identify 52 unknown protein samples (seven different proteins) with
116 ion across gestation and discover previously unknown proteins secreted by the human placenta that reg
117 on at subpicomole levels and for identifying unknown proteins separated by 2-dimensional gel electrop
118 ical was suggested to take an H atom from an unknown protein source, most likely cysteine 141.
119 ingle template, inter-atomic distances of an unknown protein structure are assumed to be distributed
120                                 A relatively unknown protein structure motif forms stable isolated si
121 es that this method can determine previously unknown protein structures and here yields, to our knowl
122 tational methods can be used to both predict unknown protein structures and model ligand interactions
123 lex structures or direct de novo modeling of unknown protein structures.
124                          The accumulation of unknown proteins, sucrose transport and cleavage enzymes
125 es, our new method reveals a large number of unknown proteins, supporting the notion that there are m
126 cts of which we recommend before applying to unknown protein systems.
127  therefore postulate that HtrA may act on an unknown protein target that potentiates the activation o
128                    We show that a previously unknown protein, termed as Charon, functions as a regula
129 onnection to IKK and SAPK/JNK), a previously unknown protein that directly interacts with NEMO/IKKgam
130 example of the identification of an a priori unknown protein that is not present in an annotated prot
131               This gene encodes a previously unknown protein that is predicted to function as a carbo
132 we identified a QTL, YIGE1, which encodes an unknown protein that regulates EL by affecting pistillat
133  and functionally characterized a previously unknown protein that we called ASTROPRINCIN (APCN) due t
134     The TFF1 protein partner is a previously unknown protein that we have called TFIZ1 for trefoil fa
135                Here we identify a heretofore unknown protein that we name GROWTH POLE RING (GPR) due
136 ic subunits: Dicer-2(DCR-2) and a previously unknown protein that we named R2D2.
137 lobiose and glucose include Lam81A and three unknown proteins that are homologous to aminopeptidases
138 scription factors, signaling components, and unknown proteins that are rapidly and robustly induced b
139 methyltransferase activity and on additional unknown proteins that bind to CARM1.
140 el-purified apomyoglobin and BSA, as well as unknown proteins that cofractionate with Tyl-virus-like
141 a: a mixture of known proteins, a mixture of unknown proteins that commonly contain sequence variatio
142 unctionally diverse assemblage of previously unknown proteins that regulate postsynaptic inhibition a
143 ogy of this element, we found binding of two unknown proteins that were antigenically distinct from G
144 aradigm to perform quantitative analysis of "unknown" proteins that differ in accurate mass.
145 gh both techniques were able to identify the unknown protein, the VHPLC method gave twice as many seq
146 llobiose include a xylanase (Xyl10A) and two unknown proteins, the C-terminal regions of which are ho
147 calization and the prediction of the role of unknown proteins, the confirmation of bioinformatic pred
148 d xenograft (PDX), and identified a function unknown protein, transmembrane and coiled-coil domain fa
149  the nucleus is accomplished by a previously unknown protein tyrosine phosphatase (PTP).
150  and vesicular datasets identified known and unknown proteins ubiquitous to AV calcification.
151 plex containing NALCN and a large previously unknown protein UNC-80.
152       We identified PhoX, and the previously unknown proteins UshA and CpdB as the major phosphatases
153              The in vivo importance of these unknown proteins was validated in invertebrate (fruit fl
154  one approach to characterizing functions of unknown proteins, we now present in GenProtEC some level
155  provide on the structural preferences of an unknown protein?" We have selected 20 different proteins
156                                Many of these unknown proteins were abundant in both corn and prairie
157 , lipopolysaccharide biosynthesis, and other unknown proteins were confirmed for attenuation.
158 -like protein, a peptide transporter and two unknown proteins, which may represent components require
159             Here, we identify two previously unknown proteins, which we have named "TRP channel-assoc
160  include a mixture of well-characterized and unknown proteins whose biological roles and importance a
161 nes encoding human (h) Grb7 and a previously unknown protein with high homology to hGrb-IR and mGrb10
162                        We assign function to unknown proteins with a probability representing the con
163  rendered their surface capable of detecting unknown proteins with cognizance not seen with conventio
164 eins for effectively predicting function for unknown proteins with high reliability.
165 acterization of both modified and unmodified unknown proteins with masses up to approximately 28 kDa.
166 e that the human genome codes for previously unknown proteins with unrelated functions that can augme

 
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