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

1 structures for Q99578

Entry ID Method Resolution Chain Position Source
AF-Q99578-F1 Predicted AlphaFoldDB

174 variants for Q99578

Variant ID(s) Position Change Description Diseaes Association Provenance
CA299517517
rs772590756
2 E>K No ClinGen
ExAC
gnomAD
CA8945014
rs772590756
2 E>Q No ClinGen
ExAC
gnomAD
rs1161813272
CA402478246
3 V>A No ClinGen
gnomAD
CA299517516
COSM226807
rs867661849
4 E>K Variant assessed as Somatic; impact. skin [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
Ensembl
NCI-TCGA
rs1002961408
CA299517515
6 E>K Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
Ensembl
NCI-TCGA
CA402478219
rs1381154303
7 A>G No ClinGen
gnomAD
rs907330766
CA299517514
7 A>T No ClinGen
gnomAD
TCGA novel 8 S>T Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA402478205
rs1417724027
9 C>S No ClinGen
gnomAD
CA8945013
rs140593847
10 S>F No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs140593847
CA8945012
10 S>Y No ClinGen
ESP
ExAC
TOPMed
gnomAD
CA299517512
rs959230566
11 P>L No ClinGen
TOPMed
gnomAD
CA8945010
rs749608210
11 P>S No ClinGen
ExAC
gnomAD
CA299517511
rs201814254
12 G>D No ClinGen
1000Genomes
rs756364776
CA8945008
14 A>S No ClinGen
ExAC
TOPMed
gnomAD
rs745967365
CA8945007
14 A>V No ClinGen
ExAC
gnomAD
rs1233900623
CA402478174
15 S>* Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
CA8945004
rs752640941
15 S>A No ClinGen
ExAC
gnomAD
rs752640941
CA8945005
15 S>T No ClinGen
ExAC
gnomAD
rs142911081
CA8945003
16 G>A No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
CA8945002
rs199603585
17 G>R No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
TCGA novel 17 G>V Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA8945001
rs753566491
18 S>P No ClinGen
ExAC
TOPMed
gnomAD
rs1401934850
CA402478155
19 R>K Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA402478121
rs1598791448
23 V>G No ClinGen
Ensembl
CA402478126
rs1361352728
23 V>M No ClinGen
gnomAD
TCGA novel 24 V>A Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA8945000
rs766054548
25 M>V No ClinGen
ExAC
TOPMed
gnomAD
CA8944999
rs760273264
29 G>E Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
TCGA novel 29 G>W Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1177337094
CA402478080
30 G>A No ClinGen
gnomAD
TCGA novel 30 G>E Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs765499217 31 V>S Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No NCI-TCGA
CA8944996
rs766978653
35 A>S No ClinGen
ExAC
TOPMed
CA8944970
rs143764572
36 M>I No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1380040475
CA402478024
37 T>A No ClinGen
TOPMed
TCGA novel 37 T>I Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA402478012
rs1338746593
38 M>I No ClinGen
gnomAD
rs770344980
CA402478008
39 Q>* No ClinGen
ExAC
TOPMed
gnomAD
rs770344980
CA8944969
39 Q>K No ClinGen
ExAC
TOPMed
gnomAD
rs759963635
CA8944968
39 Q>R No ClinGen
ExAC
TOPMed
gnomAD
rs776728832
CA8944967
40 F>L No ClinGen
ExAC
gnomAD
rs1313744392
CA402477989
42 S>R No ClinGen
gnomAD
rs771120789
CA8944966
43 H>Y No ClinGen
ExAC
gnomAD
rs1404336385
CA402477958
46 P>T No ClinGen
gnomAD
rs1335325861
CA402477932
49 H>R No ClinGen
TOPMed
rs1430955035
CA402477914
52 T>A No ClinGen
TOPMed
gnomAD
rs777863748
CA8944964
53 I>V No ClinGen
ExAC
TOPMed
gnomAD
CA402476643
rs1328954282
62 R>M No ClinGen
TOPMed
CA402476636
rs1469467859
63 I>S No ClinGen
TOPMed
gnomAD
CA402476637
rs1469467859
63 I>T No ClinGen
TOPMed
gnomAD
rs748213647
CA8944944
63 I>V No ClinGen
ExAC
gnomAD
rs1280601502
CA402476628
64 D>E No ClinGen
TOPMed
TCGA novel 64 D>G Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA402476620
rs1200887243
65 N>K No ClinGen
gnomAD
rs1452167530
CA402476610
67 P>T No ClinGen
gnomAD
rs1376207709
CA402476604
68 A>T No ClinGen
TOPMed
TCGA novel 70 L>F Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs1262882444
CA402476583
71 D>N No ClinGen
TOPMed
rs1568043990
CA402476572
72 I>N No ClinGen
Ensembl
rs745671453
CA8944941
75 T>A No ClinGen
ExAC
TOPMed
gnomAD
rs1182646862
CA402476542
77 G>S Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
TCGA novel 78 Q>= Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs201719862
CA299495078
79 A>E No ClinGen
Ensembl
CA402477344
rs1425850088
79 A>T No ClinGen
gnomAD
CA402477331
rs1339861578
80 E>D No ClinGen
TOPMed
rs1475177444
CA402477312
83 A>T No ClinGen
gnomAD
CA8944913
rs746721549
84 M>I No ClinGen
ExAC
gnomAD
rs868710992
CA299495076
85 R>Q No ClinGen
TOPMed
TCGA novel 86 E>* Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA402477278
rs1598716561
87 Q>* No ClinGen
Ensembl
CA402477267
rs1295593277
88 Y>C No ClinGen
gnomAD
rs1213491100
CA402477258
89 M>K No ClinGen
gnomAD
rs1221826475
CA402477262
89 M>L No ClinGen
TOPMed
CA402477259
rs1213491100
89 M>T No ClinGen
gnomAD
COSM1388691
CA402477251
rs1359368764
90 R>* Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
CA402477240
rs1285624121
91 G>D No ClinGen
gnomAD
CA8944911
rs758087210
92 G>E No ClinGen
ExAC
gnomAD
CA402477235
rs1452965453
92 G>R No ClinGen
gnomAD
CA402477190
rs1334507038
97 I>V No ClinGen
gnomAD
rs778619263
CA8944909
101 V>I No ClinGen
ExAC
TOPMed
gnomAD
rs962872061
COSM1223834
CA299495074
104 R>C large_intestine [Cosmic] No ClinGen
cosmic curated
TOPMed
gnomAD
rs754435765
CA8944907
104 R>H Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs754435765
CA299495073
104 R>L No ClinGen
ExAC
gnomAD
rs754435765
CA402477129
104 R>P No ClinGen
ExAC
gnomAD
CA402477131
rs962872061
104 R>S Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
rs1169941643
CA779483041
105 Q>H No ClinGen
TOPMed
rs1242915978
CA402477100
107 F>L No ClinGen
gnomAD
COSM393347
rs1182138488
CA402477094
108 Q>L lung [Cosmic] No ClinGen
cosmic curated
gnomAD
rs756516595
CA8944905
113 F>L No ClinGen
ExAC
CA8944904
rs750689156
115 E>D No ClinGen
ExAC
TOPMed
gnomAD
rs1432933021
CA402477037
115 E>G No ClinGen
TOPMed
rs867935451
CA299495069
115 E>K No ClinGen
Ensembl
CA402477029
rs1432650081
116 L>P No ClinGen
TOPMed
rs1334488835
CA402477000
119 Q>H No ClinGen
gnomAD
CA402476997
rs1203158376
120 V>I No ClinGen
gnomAD
rs767747736
CA8944903
121 R>C No ClinGen
ExAC
gnomAD
TCGA novel 122 H>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA402476969
rs1282267927
123 T>I No ClinGen
TOPMed
CA402476956
rs1381670092
124 Y>* No ClinGen
gnomAD
rs774524808
CA8944901
124 Y>C No ClinGen
ExAC
TOPMed
gnomAD
rs267605184
CA299495068
COSM1711220
127 P>S Variant assessed as Somatic; impact. skin [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
NCI-TCGA
gnomAD
rs267605184
CA402476936
127 P>T No ClinGen
gnomAD
TCGA novel 128 L>P Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA8944898
rs762925413
129 V>A No ClinGen
ExAC
TOPMed
gnomAD
CA8944899
rs764225175
129 V>M No ClinGen
ExAC
gnomAD
TCGA novel 131 V>W Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA299495067
rs960651232
138 E>* No ClinGen
Ensembl
CA402476841
rs1352826050
138 E>G No ClinGen
gnomAD
rs776641218
CA8944897
139 Q>E No ClinGen
ExAC
gnomAD
CA402476832
rs1274638935
139 Q>L No ClinGen
TOPMed
rs760547840
CA8944895
COSM1611231
141 R>C liver [Cosmic] No ClinGen
cosmic curated
ExAC
TOPMed
gnomAD
COSM1523030
CA402476816
rs1162004248
141 R>H lung Variant assessed as Somatic; 0.0 impact. [Cosmic, NCI-TCGA] No ClinGen
cosmic curated
NCI-TCGA
TOPMed
gnomAD
CA402476818
rs1162004248
141 R>L No ClinGen
TOPMed
gnomAD
CA8944894
rs773095164
142 Q>* No ClinGen
ExAC
gnomAD
rs1446142878
CA402477885
143 V>A No ClinGen
gnomAD
CA8944852
rs763924692
143 V>L No ClinGen
ExAC
gnomAD
CA402477871
rs1452680761
145 T>S No ClinGen
TOPMed
rs1196354609
CA402477819
151 L>F No ClinGen
gnomAD
TCGA novel 151 L>I Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA8944846
rs777127147
154 E>* Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
TOPMed
gnomAD
CA8944845
rs771385813
155 Y>N No ClinGen
ExAC
TOPMed
gnomAD
COSM3422179
rs199574261
CA8944843
158 G>V Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
1000Genomes
ExAC
NCI-TCGA
TOPMed
gnomAD
CA402477754
rs1392527593
160 F>S No ClinGen
gnomAD
rs754174204 161 E>* Variant assessed as Somatic; 4.624e-05 impact. [NCI-TCGA] No NCI-TCGA
CA402477730
rs1426086448
164 A>T No ClinGen
gnomAD
rs758760009
CA8944841
167 R>G Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs748387427
CA8944840
168 F>L No ClinGen
ExAC
TOPMed
gnomAD
CA402477695
rs1442574006
169 C>Y No ClinGen
gnomAD
rs939233556
CA299474747
170 I>T No ClinGen
Ensembl
rs367551216
CA8944839
171 D>V No ClinGen
ESP
ExAC
TOPMed
gnomAD
rs1182424588
CA402477669
173 A>T No ClinGen
gnomAD
rs1249827726
CA402477651
175 H>R Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA402477628
rs944213504
179 R>G No ClinGen
TOPMed
gnomAD
CA299474744
rs944213504
179 R>W No ClinGen
TOPMed
gnomAD
CA8944837
rs753906491
180 E>* No ClinGen
ExAC
gnomAD
CA8944835
rs757214621
COSM988349
182 R>C Variant assessed as Somatic; 0.0 impact. large_intestine endometrium [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
gnomAD
rs148544378
CA8944834
182 R>H No ClinGen
1000Genomes
ESP
ExAC
TOPMed
gnomAD
COSM1680344
CA299474742
rs148544378
182 R>L ovary [Cosmic] No ClinGen
cosmic curated
1000Genomes
ESP
ExAC
TOPMed
gnomAD
rs757214621
CA8944836
182 R>S No ClinGen
ExAC
gnomAD
rs1354660050
CA402477605
183 K>Q No ClinGen
gnomAD
rs1281697567
CA402477594
184 K>R No ClinGen
gnomAD
CA402477587
rs1335690802
185 E>G No ClinGen
gnomAD
CA402477590
rs1377643588
185 E>K No ClinGen
Ensembl
CA8944830
rs775014461
187 M>I No ClinGen
ExAC
gnomAD
rs144676190
CA8944831
187 M>T No ClinGen
ESP
ExAC
TOPMed
rs1406264401
CA402477575
187 M>V No ClinGen
gnomAD
CA402477569
rs1164384600
188 P>T No ClinGen
TOPMed
gnomAD
rs1422428322
CA402477539
192 E>K Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
CA402477532
rs1275765276
193 K>E No ClinGen
TOPMed
CA8944828
rs759077601
193 K>N No ClinGen
ExAC
TOPMed
gnomAD
rs776068581
CA8944827
CA299474740
194 K>N No ClinGen
ExAC
TOPMed
gnomAD
rs77976328
CA299474739
197 R>K Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
ExAC
NCI-TCGA
gnomAD
rs1443653628
CA402477504
197 R>S No ClinGen
TOPMed
rs77976328
COSM417843
CA8944825
197 R>T Variant assessed as Somatic; impact. urinary_tract [NCI-TCGA, Cosmic] No ClinGen
cosmic curated
ExAC
NCI-TCGA
gnomAD
rs1472673491 198 K>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA402477502
rs1180058008
198 K>Q No ClinGen
gnomAD
rs17851608
CA299474738
200 S>C No ClinGen
Ensembl
TCGA novel 200 S>N Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
CA402477480
rs1269751965
200 S>R No ClinGen
gnomAD
CA8944823
rs559678016
201 L>M No ClinGen
ExAC
gnomAD
TCGA novel 201 L>Q Variant assessed as Somatic; impact. [NCI-TCGA] No NCI-TCGA
rs200268352
CA299474737
203 K>E No ClinGen
gnomAD
CA8944821
rs531935933
203 K>N No ClinGen
1000Genomes
ExAC
TOPMed
gnomAD
rs1262780804
CA402477450
205 L>F Variant assessed as Somatic; impact. [NCI-TCGA] No ClinGen
NCI-TCGA
TOPMed
gnomAD
rs190327842
CA299474736
207 G>C No ClinGen
1000Genomes
ExAC
gnomAD
rs190327842
CA8944819
207 G>S No ClinGen
1000Genomes
ExAC
gnomAD
rs1345583352
CA402477419
210 K>* No ClinGen
gnomAD
rs1428795230
CA402477402
212 K>R No ClinGen
TOPMed
CA299474734
rs746661774
213 R>G No ClinGen
TOPMed
gnomAD
rs1346617687
CA402477389
214 E>* Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] No ClinGen
NCI-TCGA
gnomAD
rs1290464123
CA402477388
214 E>A No ClinGen
gnomAD
rs749404972
CA8944816
215 N>D No ClinGen
ExAC
gnomAD
CA402477359
rs1386237332
218 T>R No ClinGen
TOPMed
gnomAD

No associated diseases with Q99578

1 regional properties for Q99578

Type Name Position InterPro Accession
domain Small GTP-binding protein domain 19 - 174 IPR005225

Functions

Description
EC Number 3.6.5.2 Acting on GTP; involved in cellular and subcellular movement
Subcellular Localization
  • Nucleus
  • Cell membrane
  • Colocalizes with PLXNB3 at the plasma membrane (PubMed:16122393)
PANTHER Family
PANTHER Subfamily
PANTHER Protein Class
PANTHER Pathway Category No pathway information available

11 GO annotations of cellular component

Name Definition
cell body The portion of a cell bearing surface projections such as axons, dendrites, cilia, or flagella that includes the nucleus, but excludes all cell projections.
cytoplasm The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures.
cytosol The part of the cytoplasm that does not contain organelles but which does contain other particulate matter, such as protein complexes.
dendritic tree The entire complement of dendrites for a neuron, consisting of each primary dendrite and all its branches.
Golgi apparatus A membrane-bound cytoplasmic organelle of the endomembrane system that further processes the core oligosaccharides (e.g. N-glycans) added to proteins in the endoplasmic reticulum and packages them into membrane-bound vesicles. The Golgi apparatus operates at the intersection of the secretory, lysosomal, and endocytic pathways.
membrane raft Any of the small (10-200 nm), heterogeneous, highly dynamic, sterol- and sphingolipid-enriched membrane domains that compartmentalize cellular processes. Small rafts can sometimes be stabilized to form larger platforms through protein-protein and protein-lipid interactions.
neuron projection A prolongation or process extending from a nerve cell, e.g. an axon or dendrite.
nucleoplasm That part of the nuclear content other than the chromosomes or the nucleolus.
nucleus A membrane-bounded organelle of eukaryotic cells in which chromosomes are housed and replicated. In most cells, the nucleus contains all of the cell's chromosomes except the organellar chromosomes, and is the site of RNA synthesis and processing. In some species, or in specialized cell types, RNA metabolism or DNA replication may be absent.
plasma membrane The membrane surrounding a cell that separates the cell from its external environment. It consists of a phospholipid bilayer and associated proteins.
synapse The junction between an axon of one neuron and a dendrite of another neuron, a muscle fiber or a glial cell. As the axon approaches the synapse it enlarges into a specialized structure, the presynaptic terminal bouton, which contains mitochondria and synaptic vesicles. At the tip of the terminal bouton is the presynaptic membrane; facing it, and separated from it by a minute cleft (the synaptic cleft) is a specialized area of membrane on the receiving cell, known as the postsynaptic membrane. In response to the arrival of nerve impulses, the presynaptic terminal bouton secretes molecules of neurotransmitters into the synaptic cleft. These diffuse across the cleft and transmit the signal to the postsynaptic membrane.

7 GO annotations of molecular function

Name Definition
calmodulin binding Binding to calmodulin, a calcium-binding protein with many roles, both in the calcium-bound and calcium-free states.
chromatin binding Binding to chromatin, the network of fibers of DNA, protein, and sometimes RNA, that make up the chromosomes of the eukaryotic nucleus during interphase.
G protein activity A molecular function regulator that cycles between active GTP-bound and inactive GDP-bound states. In its active state, binds to a variety of effector proteins to regulate cellular processes. Intrinsic GTPase activity returns the G protein to its GDP-bound state. The return to the GDP-bound state can be accelerated by the action of a GTPase-activating protein (GAP).
GDP binding Binding to GDP, guanosine 5'-diphosphate.
GTP binding Binding to GTP, guanosine triphosphate.
GTPase activity Catalysis of the reaction: GTP + H2O = GDP + H+ + phosphate.
semaphorin receptor binding Binding to a semaphorin receptor.

14 GO annotations of biological process

Name Definition
adenylate cyclase-activating G protein-coupled receptor signaling pathway A G protein-coupled receptor signaling pathway in which the signal is transmitted via the activation of adenylyl cyclase activity and a subsequent increase in the intracellular concentration of cyclic AMP (cAMP).
chemical synaptic transmission The vesicular release of classical neurotransmitter molecules from a presynapse, across a chemical synapse, the subsequent activation of neurotransmitter receptors at the postsynapse of a target cell (neuron, muscle, or secretory cell) and the effects of this activation on the postsynaptic membrane potential and ionic composition of the postsynaptic cytosol. This process encompasses both spontaneous and evoked release of neurotransmitter and all parts of synaptic vesicle exocytosis. Evoked transmission starts with the arrival of an action potential at the presynapse.
intracellular signal transduction The process in which a signal is passed on to downstream components within the cell, which become activated themselves to further propagate the signal and finally trigger a change in the function or state of the cell.
maintenance of protein location in cell Any process in which a protein is maintained in a specific location within, or in the membrane of, a cell, and is prevented from moving elsewhere.
negative regulation of neuron projection development Any process that decreases the rate, frequency or extent of neuron projection development. Neuron projection development is the process whose specific outcome is the progression of a neuron projection over time, from its formation to the mature structure. A neuron projection is any process extending from a neural cell, such as axons or dendrites (collectively called neurites).
positive regulation of MAPK cascade Any process that activates or increases the frequency, rate or extent of signal transduction mediated by the MAPK cascade.
positive regulation of neuron projection development Any process that increases the rate, frequency or extent of neuron projection development. Neuron projection development is the process whose specific outcome is the progression of a neuron projection over time, from its formation to the mature structure. A neuron projection is any process extending from a neural cell, such as axons or dendrites (collectively called neurites).
positive regulation of transcription by RNA polymerase II Any process that activates or increases the frequency, rate or extent of transcription from an RNA polymerase II promoter.
Ras protein signal transduction The series of molecular signals within the cell that are mediated by a member of the Ras superfamily of proteins switching to a GTP-bound active state.
regulation of calcium-mediated signaling Any process that modulates the frequency, rate or extent of calcium-mediated signaling, the process in which a cell uses calcium ions to convert an extracellular signal into a response.
regulation of Cdc42 protein signal transduction Any process that modulates the frequency, rate or extent of Cdc42 protein signal transduction.
regulation of endocytosis Any process that modulates the frequency, rate or extent of endocytosis.
regulation of protein phosphorylation Any process that modulates the frequency, rate or extent of addition of phosphate groups into an amino acid in a protein.
small GTPase mediated signal transduction The series of molecular signals in which a small monomeric GTPase relays a signal.

34 homologous proteins in AiPD

UniProt AC Gene Name Protein Name Species Evidence Code
P08642 HRAS GTPase HRas Gallus gallus (Chicken) SS
Q6T310 RASL11A Ras-like protein family member 11A Homo sapiens (Human) PR
Q8IYK8 REM2 GTP-binding protein REM 2 Homo sapiens (Human) PR
P55040 GEM GTP-binding protein GEM Homo sapiens (Human) PR
Q6IQ22 RAB12 Ras-related protein Rab-12 Homo sapiens (Human) PR
Q9BU20 CPLANE2 Ciliogenesis and planar polarity effector 2 Homo sapiens (Human) PR
Q96HU8 DIRAS2 GTP-binding protein Di-Ras2 Homo sapiens (Human) PR
P62070 RRAS2 Ras-related protein R-Ras2 Homo sapiens (Human) PR
P11234 RALB Ras-related protein Ral-B Homo sapiens (Human) PR
P11233 RALA Ras-related protein Ral-A Homo sapiens (Human) PR
P01116 KRAS GTPase KRas Homo sapiens (Human) EV
P01112 HRAS GTPase HRas Homo sapiens (Human) SS
Q9JIW9 Ralb Ras-related protein Ral-B Mus musculus (Mouse) PR
Q61411 Hras GTPase HRas Mus musculus (Mouse) SS
P32883 Kras GTPase KRas Mus musculus (Mouse) SS
O08989 Mras Ras-related protein M-Ras Mus musculus (Mouse) PR
Q5PR73 Diras2 GTP-binding protein Di-Ras2 Mus musculus (Mouse) PR
Q91Z61 Diras1 GTP-binding protein Di-Ras1 Mus musculus (Mouse) PR
P62071 Rras2 Ras-related protein R-Ras2 Mus musculus (Mouse) PR
P35283 Rab12 Ras-related protein Rab-12 Mus musculus (Mouse) PR
Q08AT1 Rasl12 Ras-like protein family member 12 Mus musculus (Mouse) PR
A2A825 Cplane2 Ciliogenesis and planar polarity effector 2 Mus musculus (Mouse) PR
P55041 Gem GTP-binding protein GEM Mus musculus (Mouse) PR
Q8VEL9 Rem2 GTP-binding protein REM 2 Mus musculus (Mouse) PR
P70425 Rit2 GTP-binding protein Rit2 Mus musculus (Mouse) PR
P36860 Ralb Ras-related protein Ral-B Rattus norvegicus (Rat) PR
P08644 Kras GTPase KRas Rattus norvegicus (Rat) SS
Q9WTY2 Rem2 GTP-binding protein REM 2 Rattus norvegicus (Rat) PR
P20171 Hras GTPase HRas Rattus norvegicus (Rat) SS
P97538 Mras Ras-related protein M-Ras Rattus norvegicus (Rat) PR
Q5BJQ5 Rit2 GTP-binding protein Rit2 Rattus norvegicus (Rat) PR
B7ZTR0 cplane2 Ciliogenesis and planar polarity effector 2 Xenopus tropicalis (Western clawed frog) (Silurana tropicalis) PR
P79737 nras GTPase NRas Danio rerio (Zebrafish) (Brachydanio rerio) SS
A1DZY4 zgc:110179 Ras-like protein family member 11A-like Danio rerio (Zebrafish) (Brachydanio rerio) PR
10 20 30 40 50 60
MEVENEASCS PGSASGGSRE YKVVMLGAGG VGKSAMTMQF ISHQFPDYHD PTIEDAYKTQ
70 80 90 100 110 120
VRIDNEPAYL DILDTAGQAE FTAMREQYMR GGEGFIICYS VTDRQSFQEA AKFKELIFQV
130 140 150 160 170 180
RHTYEIPLVL VGNKIDLEQF RQVSTEEGLS LAQEYNCGFF ETSAALRFCI DDAFHGLVRE
190 200 210
IRKKESMPSL MEKKLKRKDS LWKKLKGSLK KKRENMT