Descriptions

The autoinhibited protein was predicted that may have potential autoinhibitory elements via cis-regPred.

Autoinhibitory domains (AIDs)

Target domain

Relief mechanism

Assay

cis-regPred

Accessory elements

No accessory elements

Autoinhibited structure

Activated structure

3 structures for P26378

Entry ID Method Resolution Chain Position Source
1FXL X-ray 180 A A 49-215 PDB
1G2E X-ray 230 A A 49-215 PDB
AF-P26378-F1 Predicted AlphaFoldDB

174 variants for P26378

Variant ID(s) Position Change Description Diseaes Association Provenance
rs747098973
CA845313
2 E>Q No ClinGen
ExAC
TOPMed
gnomAD
rs1400983164
CA340298966
4 N>S No ClinGen
gnomAD
CA340298971
rs1160252807
5 G>S No ClinGen
gnomAD
CA845315
rs781296512
8 M>T No ClinGen
ExAC
gnomAD
CA22467493
rs902567011
9 I>V No ClinGen
gnomAD
CA340297704
rs1328238654
11 S>N No ClinGen
TOPMed
rs761863819
CA845359
13 M>T No ClinGen
ExAC
gnomAD
CA340297729
rs750517639
14 E>D Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs555445078
CA845360
14 E>K No ClinGen
1000Genomes
ExAC
gnomAD
rs756230853
CA845362
15 P>S No ClinGen
ExAC
gnomAD
rs150277981
CA845366
21 P>L No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs755433268
CA845365
21 P>S No ClinGen
ExAC
gnomAD
rs1251084845
CA340297774
22 T>A No ClinGen
gnomAD
rs1251084845
CA340297773
22 T>P No ClinGen
gnomAD
rs770471086
CA845368
24 N>S No ClinGen
ExAC
TOPMed
gnomAD
CA845369
rs780502540
26 S>N No ClinGen
ExAC
gnomAD
CA340297810
rs1356152656
27 N>K No ClinGen
TOPMed
rs747257950
CA22467494
27 N>S No ClinGen
gnomAD
CA22467495
rs1053672972
28 G>E No ClinGen
gnomAD
rs1351649500
CA340297831
31 S>C No ClinGen
gnomAD
rs1050931177
CA22467496
32 N>K No ClinGen
TOPMed
gnomAD
rs541366902
CA845370
32 N>S No ClinGen
1000Genomes
ExAC
gnomAD
CA340297853
rs1446048734
34 R>K No ClinGen
TOPMed
CA340297858
rs1369439606
35 N>H No ClinGen
gnomAD
CA845371
rs769284873
35 N>S No ClinGen
ExAC
TOPMed
gnomAD
rs150394218
CA845373
37 P>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs1012234646
CA22467498
39 P>H No ClinGen
gnomAD
rs774263808
CA845375
40 M>T No ClinGen
ExAC
gnomAD
rs577777036
CA845376
42 T>I No ClinGen
1000Genomes
ExAC
gnomAD
rs752000055
CA22467499
44 A>T No ClinGen
Ensembl
CA340297928
rs1321742053
46 T>A No ClinGen
gnomAD
rs767501506
CA845377
47 D>G No ClinGen
ExAC
gnomAD
COSM3400862
CA845378
RCV000785703
rs116391279
55 V>I central_nervous_system [Cosmic] No ClinGen
cosmic curated
ClinVar
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
CA340298025
rs1241348846
60 Q>K No ClinGen
gnomAD
rs1474322779
CA340298029
60 Q>R No ClinGen
gnomAD
CA22467500
rs971417184
61 N>S No ClinGen
Ensembl
CA845380
rs766676470
62 M>I No ClinGen
ExAC
gnomAD
rs1459326800
COSM302125
CA340298115
72 G>R central_nervous_system [Cosmic] No ClinGen
cosmic curated
gnomAD
rs765764372
CA845383
74 I>T No ClinGen
ExAC
TOPMed
gnomAD
CA845382
rs755382094
74 I>V No ClinGen
ExAC
TOPMed
CA845384
rs753118324
76 E>G No ClinGen
ExAC
gnomAD
rs1232144655
CA340298223
87 I>T No ClinGen
gnomAD
CA22467502
rs759928291
87 I>V No ClinGen
Ensembl
CA845404
rs374811070
95 G>A No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA340299113
rs752957527
103 K>N Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs1278816516
CA340299125
105 A>S No ClinGen
gnomAD
CA340299149
rs1220729294
108 A>G No ClinGen
gnomAD
rs1337978854
CA340299167
111 T>A No ClinGen
TOPMed
CA845407
rs758825213
COSM3671790
111 T>I Variant assessed as Somatic; 0.0 impact. prostate [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
TOPMed
gnomAD
rs940845628
CA22471041
112 L>S No ClinGen
TOPMed
CA845411
rs199634128
119 T>N No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1469105007
CA340299238
122 I>V No ClinGen
TOPMed
gnomAD
CA340299318
rs1572620166
124 V>I No ClinGen
Ensembl
CA340299330
rs1370157409
126 Y>H No ClinGen
gnomAD
rs868813722
CA22472845
129 P>L Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
Ensembl
NCI-TCGA
CA22472846
rs989472197
130 S>R No ClinGen
TOPMed
CA845436
rs758122922
133 S>L No ClinGen
ExAC
gnomAD
CA22472848
rs267598638
136 D>N No ClinGen
Ensembl
CA340299401
rs1433948845
137 A>S No ClinGen
TOPMed
rs374149997
CA845439
142 S>R No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA845440
rs199932597
143 G>S Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
1000Genomes
ExAC
NCI-TCGA
TOPMed
gnomAD
rs775564920
CA845443
148 M>V No ClinGen
ExAC
gnomAD
rs763306293
CA845444
149 T>I No ClinGen
ExAC
gnomAD
rs1250338534
CA340299489
150 Q>L No ClinGen
gnomAD
rs774725609
CA845446
156 L>F No ClinGen
ExAC
gnomAD
CA340299533
rs1368838245
156 L>R No ClinGen
TOPMed
rs1175579240
CA340299547
158 S>L Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
CA340299552
rs1458930048
159 Q>R No ClinGen
gnomAD
rs750975848
CA845449
161 G>S No ClinGen
ExAC
gnomAD
CA22472851
rs138779266
162 R>C Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ESP
NCI-TCGA
TOPMed
gnomAD
CA845450
rs200396874
162 R>H Variant assessed as Somatic; 4.619e-05 impact. [NCI-TCGA] No ClinGen
1000Genomes
ExAC
NCI-TCGA
gnomAD
rs1572620923
CA340299587
165 T>A No ClinGen
Ensembl
CA845451
rs369875371
166 S>L No ClinGen
ESP
ExAC
gnomAD
CA845453
rs370062289
168 I>V No ClinGen
ESP
ExAC
gnomAD
rs962063964
CA22472852
170 V>F No ClinGen
gnomAD
CA22472853
rs17853533
VAR_058091
171 D>G No ClinGen
UniProt
Ensembl
dbSNP
CA22472854
rs929829288
172 Q>P No ClinGen
TOPMed
rs751438360
CA845455
173 V>D No ClinGen
ExAC
rs1427053388
CA340299661
175 G>V No ClinGen
TOPMed
CA340299681
rs1231539470
179 G>R No ClinGen
gnomAD
rs1169691831
CA340299715
184 R>C Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA22473025
rs749270666
186 D>E No ClinGen
Ensembl
rs751205371
CA845472
196 K>R No ClinGen
ExAC
TOPMed
gnomAD
CA340299807
rs1259386502
197 G>R Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
CA22473026
rs267598639
200 G>D No ClinGen
Ensembl
rs866002286
CA22473027
201 Q>* No ClinGen
Ensembl
rs1211106652
CA340299856
204 S>T No ClinGen
gnomAD
CA340299860
rs1484366574
205 G>S No ClinGen
TOPMed
gnomAD
CA340299870
rs1203348000
206 A>G No ClinGen
TOPMed
rs767350030
CA340299876
207 T>K Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
CA845474
rs767350030
207 T>M No ClinGen
ExAC
gnomAD
rs756130254
CA845476
209 P>L No ClinGen
ExAC
TOPMed
gnomAD
CA340299891
rs1379114396
210 I>V No ClinGen
TOPMed
gnomAD
rs1350636054
CA340299902
211 T>N No ClinGen
TOPMed
CA340299930
rs1174438397
215 A>V No ClinGen
gnomAD
CA340299945
rs370446022
217 N>K No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1572628359
CA340299942
217 N>T No ClinGen
Ensembl
rs772277106
CA845482
218 P>S No ClinGen
ExAC
gnomAD
CA22473029
rs371102695
222 S>C No ClinGen
ESP
rs773624398
CA845483
223 S>T No ClinGen
ExAC
gnomAD
CA340299996
rs1572628509
225 A>T No ClinGen
Ensembl
rs144250728
CA845485
230 L>I No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA340300027
rs144250728
230 L>V No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA845487
COSM357151
rs762544492
235 N>D lung [Cosmic] No ClinGen
cosmic curated
ExAC
gnomAD
CA22473030
rs1039135672
235 N>K No ClinGen
Ensembl
CA340300068
rs1345370346
236 R>Q Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
rs763451875
CA340300066
236 R>W Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
rs763739803
CA845489
237 R>C Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA845491
rs761620230
237 R>H No ClinGen
ExAC
TOPMed
gnomAD
rs761620230
CA845490
237 R>L Variant assessed as Somatic; 9.243e-05 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
rs997892423
CA22473031
238 Y>H No ClinGen
Ensembl
CA340300082
rs1460314684
239 P>A No ClinGen
TOPMed
CA22473032
rs774540893
239 P>L No ClinGen
Ensembl
rs969828287
CA22473033
241 P>S No ClinGen
TOPMed
gnomAD
rs1175366786
CA340300132
246 A>V No ClinGen
gnomAD
CA845493
rs569206522
248 R>K No ClinGen
1000Genomes
ExAC
gnomAD
rs1188457168
CA340300219
257 M>L No ClinGen
gnomAD
CA340300221
rs1420508897
257 M>T No ClinGen
TOPMed
gnomAD
CA340300246
rs1325738088
261 V>I No ClinGen
TOPMed
rs781472470
CA845520
265 M>T No ClinGen
ExAC
gnomAD
CA340300314
rs1416346938
269 V>D No ClinGen
gnomAD
CA845522
rs770467595
270 P>R No ClinGen
ExAC
gnomAD
CA845525
rs116030028
271 P>A No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA340300322
rs116030028
271 P>S No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA845524
rs116030028
271 P>T Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
1000Genomes
ESP
ExAC
NCI-TCGA
TOPMed
gnomAD
rs772924325
CA845526
272 S>P No ClinGen
ExAC
gnomAD
rs760313718
CA845527
273 A>G No ClinGen
ExAC
gnomAD
rs1355484430
CA340300332
273 A>P No ClinGen
TOPMed
gnomAD
rs1355484430
CA340300333
273 A>S Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
CA340300341
rs1352823026
274 C>F No ClinGen
gnomAD
CA340300347
rs1283346959
275 P>R No ClinGen
TOPMed
gnomAD
VAR_052204
CA845528
rs2494876
275 P>S No ClinGen
UniProt
1000Genomes
ESP
ExAC
TOPMed
dbSNP
gnomAD
CA845529
rs776339902
276 P>L No ClinGen
ExAC
TOPMed
gnomAD
CA845530
rs199787012
281 I>V No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
CA845531
rs765189019
283 I>T Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs763032801
COSM910495
CA845533
285 G>E Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
gnomAD
COSM3689751
rs1236212349
CA340300431
288 S>N Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
rs764091821
CA845534
289 L>F No ClinGen
ExAC
gnomAD
CA340300438
rs1159474949
289 L>H No ClinGen
gnomAD
CA340300447
rs1407663589
291 G>R No ClinGen
TOPMed
gnomAD
CA340300461
rs1399342049
292 M>I No ClinGen
gnomAD
CA845538
rs781450709
295 P>S No ClinGen
ExAC
gnomAD
rs1572647481
CA340300501
298 T>I No ClinGen
Ensembl
rs750789231
CA845540
299 G>R No ClinGen
ExAC
gnomAD
rs368200868
CA340300511
300 T>I No ClinGen
ESP
TOPMed
gnomAD
rs368200868
CA22473529
300 T>S No ClinGen
ESP
TOPMed
gnomAD
rs756501874
CA845541
305 F>V No ClinGen
ExAC
gnomAD
rs1348209023
CA340300567
308 N>S No ClinGen
gnomAD
CA340300580
rs1282739153
310 S>C No ClinGen
TOPMed
gnomAD
COSM1687655
rs755538583
CA845544
312 D>N upper_aerodigestive_tract Variant assessed as Somatic; 0.0 impact. skin [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
ExAC
NCI-TCGA
gnomAD
rs746506386
CA845546
COSM3386225
314 D>N pancreas [Cosmic] No ClinGen
cosmic curated
ExAC
TOPMed
gnomAD
rs776306356
CA845548
317 V>A Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs775408177
CA845551
334 I>T No ClinGen
ExAC
gnomAD
CA845553
rs762942843
342 C>W No ClinGen
ExAC
TOPMed
gnomAD
CA340300828
rs1303937161
346 G>S No ClinGen
gnomAD
CA22473531
rs868045736
349 T>I Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
Ensembl
NCI-TCGA
CA340300847
rs1572648072
349 T>P No ClinGen
Ensembl
rs1048552996
CA22473532
353 Y>C No ClinGen
TOPMed
rs1572648137
CA340300889
354 D>E No ClinGen
Ensembl
CA340300903
rs1341487754
356 A>V Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA340300911
rs1377921361
358 M>V No ClinGen
TOPMed
rs17853531
VAR_058092
CA845559
361 A>T No ClinGen
UniProt
ExAC
TOPMed
dbSNP
gnomAD
CA22473534
rs941061407
365 G>E No ClinGen
TOPMed
CA340300974
rs1437298847
367 R>C No ClinGen
TOPMed
rs377132231
CA845561
COSM77643
367 R>H ovary large_intestine Variant assessed as Somatic; 4.636e-05 impact. [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
ESP
ExAC
NCI-TCGA
TOPMed
CA340300978
rs1196239051
368 L>V No ClinGen
gnomAD
CA845562
rs150762056
372 V>M No ClinGen
ESP
ExAC
gnomAD
CA22473535
rs867053382
376 S>Y No ClinGen
Ensembl
CA340301034
rs1271862494
377 F>L No ClinGen
gnomAD
rs756742405
CA845565
380 N>S No ClinGen
ExAC
gnomAD
rs1279993985
CA340301069
381 K>N No ClinGen
TOPMed
rs745455583
CA845567
383 H>P No ClinGen
ExAC
gnomAD
rs745455583
CA340301080
383 H>R No ClinGen
ExAC
gnomAD
CA845568
rs769429049
385 S>F No ClinGen
ExAC
gnomAD

No associated diseases with P26378

4 regional properties for P26378

Type Name Position InterPro Accession
domain RNA recognition motif domain 51 - 129 IPR000504-1
domain RNA recognition motif domain 137 - 217 IPR000504-2
domain RNA recognition motif domain 302 - 380 IPR000504-3
domain HuD, RNA recognition motif 3 299 - 384 IPR034918

Functions

Description
EC Number
Subcellular Localization
  • Cytoplasm
  • Perikaryon
  • Cell projection, dendrite
  • Cell projection, axon
  • Cell projection, growth cone
  • Co-localizes with ribosomal RNA in polysomes
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

11 GO annotations of cellular component

Name Definition
axon The long process of a neuron that conducts nerve impulses, usually away from the cell body to the terminals and varicosities, which are sites of storage and release of neurotransmitter.
cytoplasm The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures.
cytoskeleton A cellular structure that forms the internal framework of eukaryotic and prokaryotic cells. The cytoskeleton includes intermediate filaments, microfilaments, microtubules, the microtrabecular lattice, and other structures characterized by a polymeric filamentous nature and long-range order within the cell. The various elements of the cytoskeleton not only serve in the maintenance of cellular shape but also have roles in other cellular functions, including cellular movement, cell division, endocytosis, and movement of organelles.
cytosol The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes.
dendrite A neuron projection that has a short, tapering, morphology. Dendrites receive and integrate signals from other neurons or from sensory stimuli, and conduct nerve impulses towards the axon or the cell body. In most neurons, the impulse is conveyed from dendrites to axon via the cell body, but in some types of unipolar neuron, the impulse does not travel via the cell body.
glutamatergic synapse A synapse that uses glutamate as a neurotransmitter.
growth cone The migrating motile tip of a growing neuron projection, where actin accumulates, and the actin cytoskeleton is the most dynamic.
membrane A lipid bilayer along with all the proteins and protein complexes embedded in it an attached to it.
nuclear envelope The double lipid bilayer enclosing the nucleus and separating its contents from the rest of the cytoplasm; includes the intermembrane space, a gap of width 20-40 nm (also called the perinuclear space).
perikaryon The portion of the cell soma (neuronal cell body) that excludes the nucleus.
polysomal ribosome A ribosome bound to mRNA that forms part of a polysome.

5 GO annotations of molecular function

Name Definition
mRNA 3'-UTR AU-rich region binding Binding to a region containing frequent adenine and uridine bases within the 3' untranslated region of a mRNA molecule or in pre-mRNA intron. The ARE-binding element consensus is UUAUUUAUU. ARE-binding proteins control the stability and/or translation of mRNAs.
mRNA 3'-UTR binding Binding to a 3' untranslated region of an mRNA molecule.
poly(A) binding Binding to a sequence of adenylyl residues in an RNA molecule, such as the poly(A) tail, a sequence of adenylyl residues at the 3' end of eukaryotic mRNA.
pre-mRNA intronic pyrimidine-rich binding Binding to a pyrimidine-rich (CU-rich) intronic sequence of a pre-messenger RNA (pre-mRNA).
translation regulator activity Any molecular function involved in the initiation, activation, perpetuation, repression or termination of polypeptide synthesis at the ribosome.

16 GO annotations of biological process

Name Definition
3'-UTR-mediated mRNA stabilization An mRNA stabilization process in which one or more RNA-binding proteins associate with the 3'-untranslated region (UTR) of an mRNA.
aging A developmental process that is a deterioration and loss of function over time. Aging includes loss of functions such as resistance to disease, homeostasis, and fertility, as well as wear and tear. Aging includes cellular senescence, but is more inclusive. May precede death and may succeed developmental maturation (GO:0021700).
associative learning Learning by associating a stimulus (the cause) with a particular outcome (the effect).
cellular response to nerve growth factor stimulus A process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a nerve growth factor stimulus.
cerebral cortex neuron differentiation The process in which a relatively unspecialized cell acquires specialized features of a neuron residing in the cerebral cortex.
dendrite morphogenesis The process in which the anatomical structures of a dendrite are generated and organized.
locomotory behavior The specific movement from place to place of an organism in response to external or internal stimuli. Locomotion of a whole organism in a manner dependent upon some combination of that organism's internal state and external conditions.
mRNA processing Any process involved in the conversion of a primary mRNA transcript into one or more mature mRNA(s) prior to translation into polypeptide.
positive regulation of 3'-UTR-mediated mRNA stabilization Any process that activates or increases the frequency, rate or extent of 3'-UTR-mediated mRNA stabilization.
positive regulation of dendrite development Any process that activates or increases the frequency, rate or extent of dendrite development.
regeneration The regrowth of a lost or destroyed body part, such as an organ or tissue. This process may occur via renewal, repair, and/or growth alone (i.e. increase in size or mass).
regulation of translation at synapse, modulating synaptic transmission Any process that modulates synaptic transmission by regulating translation occurring at the synapse.
response to cocaine Any process that results in a change in state or activity of a cell or an organism (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a cocaine stimulus. Cocaine is a crystalline alkaloid obtained from the leaves of the coca plant.
response to endoplasmic reticulum stress Any process that results in a change in state or activity of a cell (in terms of movement, secretion, enzyme production, gene expression, etc.) as a result of a stress acting at the endoplasmic reticulum. ER stress usually results from the accumulation of unfolded or misfolded proteins in the ER lumen.
RNA processing Any process involved in the conversion of one or more primary RNA transcripts into one or more mature RNA molecules.
RNA splicing The process of removing sections of the primary RNA transcript to remove sequences not present in the mature form of the RNA and joining the remaining sections to form the mature form of the RNA.

12 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
Q14576 ELAVL3 ELAV-like protein 3 Homo sapiens (Human) PR
Q12926 ELAVL2 ELAV-like protein 2 Homo sapiens (Human) PR
O75821 EIF3G Eukaryotic translation initiation factor 3 subunit G Homo sapiens (Human) PR
Q60900 Elavl3 ELAV-like protein 3 Mus musculus (Mouse) PR
Q7TPD6 Raver2 Ribonucleoprotein PTB-binding 2 Mus musculus (Mouse) PR
Q60899 Elavl2 ELAV-like protein 2 Mus musculus (Mouse) PR
Q61701 Elavl4 ELAV-like protein 4 Mus musculus (Mouse) PR
Q8CH84 Elavl2 ELAV-like protein 2 Rattus norvegicus (Rat) PR
O09032 Elavl4 ELAV-like protein 4 Rattus norvegicus (Rat) PR
Q28FX0 elavl3 ELAV-like protein 3 Xenopus tropicalis (Western clawed frog) (Silurana tropicalis) PR
Q28GD4 elavl2 ELAV-like protein 2 Xenopus tropicalis (Western clawed frog) (Silurana tropicalis) PR
A4QNI8 elavl4 ELAV-like protein 4 Xenopus tropicalis (Western clawed frog) (Silurana tropicalis) PR
10 20 30 40 50 60
MEWNGLKMII STMEPQVSNG PTSNTSNGPS SNNRNCPSPM QTGATTDDSK TNLIVNYLPQ
70 80 90 100 110 120
NMTQEEFRSL FGSIGEIESC KLVRDKITGQ SLGYGFVNYI DPKDAEKAIN TLNGLRLQTK
130 140 150 160 170 180
TIKVSYARPS SASIRDANLY VSGLPKTMTQ KELEQLFSQY GRIITSRILV DQVTGVSRGV
190 200 210 220 230 240
GFIRFDKRIE AEEAIKGLNG QKPSGATEPI TVKFANNPSQ KSSQALLSQL YQSPNRRYPG
250 260 270 280 290 300
PLHHQAQRFR LDNLLNMAYG VKRLMSGPVP PSACPPRFSP ITIDGMTSLV GMNIPGHTGT
310 320 330 340 350 360
GWCIFVYNLS PDSDESVLWQ LFGPFGAVNN VKVIRDFNTN KCKGFGFVTM TNYDEAAMAI
370 380
ASLNGYRLGD RVLQVSFKTN KAHKS