Q99578
Gene name |
RIT2 (RIN, ROC2) |
Protein name |
GTP-binding protein Rit2 |
Names |
Ras-like protein expressed in neurons, Ras-like without CAAX protein 2 |
Species |
Homo sapiens (Human) |
KEGG Pathway |
hsa:6014 |
EC number |
3.6.5.2: Acting on GTP; involved in cellular and subcellular movement |
Protein Class |
|

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 |
|
|
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 |