A6NCK2
PR
Gene name |
TRIM43B |
Protein name |
Tripartite motif-containing protein 43B |
Names |
|
Species |
Homo sapiens (Human) |
KEGG Pathway |
hsa:653192 |
EC number |
|
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 A6NCK2
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| AF-A6NCK2-F1 | Predicted | AlphaFoldDB |
182 variants for A6NCK2
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
|
CA1772921 rs536256473 |
2 | D>N | No |
ClinGen 1000Genomes ExAC gnomAD |
|
|
rs376058095 CA1772920 |
6 | S>P | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
CA1772918 rs752660513 |
8 | A>D | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA427623420 rs752660513 |
8 | A>V | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs199943409 CA52234851 |
14 | T>I | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs199943409 CA1772915 |
14 | T>S | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA427623240 rs1862895 |
15 | C>W | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs1327721229 CA427623253 |
15 | C>Y | No |
ClinGen TOPMed gnomAD |
|
|
CA1772912 rs375271552 |
17 | I>F | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
CA1772911 rs375271552 |
17 | I>V | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
rs1415564699 CA427623140 |
19 | L>F | No |
ClinGen gnomAD |
|
|
CA427623051 rs1480818131 |
23 | V>E | No |
ClinGen gnomAD |
|
|
CA1772908 rs769206493 |
25 | P>A | No |
ClinGen ExAC gnomAD |
|
|
CA427622996 rs1208542086 |
25 | P>L | No |
ClinGen TOPMed |
|
|
CA1772907 rs769206493 |
25 | P>S | No |
ClinGen ExAC gnomAD |
|
|
rs13000235 CA52234839 |
30 | C>W | No |
ClinGen Ensembl |
|
|
CA427622834 rs756253345 |
32 | H>P | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA1772904 rs756253345 |
32 | H>R | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs1213131669 CA427622811 |
33 | S>N | No |
ClinGen TOPMed gnomAD |
|
|
rs746128185 CA1772903 |
35 | C>Y | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs1469203496 CA427622729 |
36 | R>K | No |
ClinGen TOPMed |
|
|
CA1772902 rs781322919 |
36 | R>W | No |
ClinGen ExAC gnomAD |
|
|
rs752607296 CA1772900 |
37 | P>H | No |
ClinGen ExAC gnomAD |
|
|
CA427622705 rs752607296 |
37 | P>L | No |
ClinGen ExAC gnomAD |
|
|
rs758238462 CA1772901 |
37 | P>S | No |
ClinGen ExAC gnomAD |
|
|
rs917384450 CA52234831 |
39 | L>R | No |
ClinGen TOPMed |
|
|
CA1772898 rs1205005952 |
40 | C>F | No |
ClinGen gnomAD |
|
|
rs1439489276 CA427622615 |
41 | L>V | No |
ClinGen gnomAD |
|
|
CA1772896 rs369206903 |
42 | S>* | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
rs369206903 CA1772895 |
42 | S>L | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
CA427622546 rs1460443980 |
43 | W>C | No |
ClinGen TOPMed gnomAD |
|
|
CA427622490 rs1161147932 |
46 | A>T | No |
ClinGen gnomAD |
|
|
CA427622478 rs1419474526 |
46 | A>V | No |
ClinGen gnomAD |
|
|
CA1772893 rs551182192 |
49 | P>L | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
CA427622393 rs1455793825 |
50 | A>T | No |
ClinGen gnomAD |
|
|
rs984809358 CA52234819 |
53 | P>S | No |
ClinGen TOPMed |
|
|
rs1437332018 CA427622298 |
54 | A>T | No |
ClinGen TOPMed |
|
|
CA52234814 rs1028681429 |
54 | A>V | No |
ClinGen TOPMed gnomAD |
|
|
rs1283235465 CA427622271 |
55 | C>G | No |
ClinGen gnomAD |
|
|
CA427622268 rs1233858346 |
55 | C>Y | No |
ClinGen TOPMed |
|
|
CA427622227 rs772886426 |
57 | E>K | No |
ClinGen ExAC gnomAD |
|
|
rs772886426 CA1772892 |
57 | E>Q | No |
ClinGen ExAC gnomAD |
|
|
rs1445551621 CA427622192 |
58 | P>L | No |
ClinGen TOPMed gnomAD |
|
|
rs1270859796 CA427622173 |
59 | S>L | No |
ClinGen TOPMed |
|
|
rs774708680 CA1772889 |
60 | P>L | No |
ClinGen ExAC gnomAD |
|
|
CA427622157 rs1316703340 |
60 | P>S | No |
ClinGen gnomAD |
|
|
CA1772888 rs769087749 |
62 | M>T | No |
ClinGen ExAC gnomAD |
|
| TCGA novel | 67 | N>Y | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA427621935 rs1303651395 |
69 | L>I | No |
ClinGen gnomAD |
|
|
rs1368082864 CA427621896 |
70 | L>P | No |
ClinGen gnomAD |
|
|
rs528245128 CA1772887 |
71 | K>M | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
| TCGA novel | 73 | L>V | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs775387040 CA427621764 |
75 | T>I | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs775387040 CA1772886 |
75 | T>N | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA1772885 rs769898750 |
77 | A>T | No |
ClinGen ExAC gnomAD |
|
|
rs1436323582 CA427621712 |
77 | A>V | No |
ClinGen TOPMed gnomAD |
|
|
CA52234803 rs901585249 |
80 | A>V | No |
ClinGen TOPMed |
|
|
CA427621584 rs1161536023 |
82 | L>P | No |
ClinGen TOPMed gnomAD |
|
|
rs1019149050 CA52234801 |
83 | W>R | No |
ClinGen TOPMed |
|
|
CA427621402 rs1413351582 |
91 | Q>E | No |
ClinGen gnomAD |
|
|
rs1240839834 CA427621377 |
92 | I>T | No |
ClinGen gnomAD |
|
|
CA1772881 rs542608231 |
93 | C>G | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
rs542608231 CA427621360 |
93 | C>R | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
rs542608231 CA427621358 |
93 | C>S | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
rs1473989778 CA427621354 |
93 | C>Y | No |
ClinGen gnomAD |
|
|
rs200840140 CA1772880 |
94 | G>W | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs1463971224 CA427621211 |
99 | T>I | No |
ClinGen gnomAD |
|
|
rs1297179014 CA427621188 |
100 | K>R | No |
ClinGen gnomAD |
|
|
rs1382279215 CA427621156 |
101 | K>N | No |
ClinGen gnomAD |
|
|
rs1365637524 CA427621054 |
106 | M>V | No |
ClinGen TOPMed |
|
|
CA1772876 rs753791053 |
107 | D>N | No |
ClinGen ExAC gnomAD |
|
|
CA427620956 rs1173254528 |
110 | L>I | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA gnomAD |
|
rs561398896 CA1772874 |
112 | C>R | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
CA52234788 rs905830016 |
112 | C>Y | No |
ClinGen TOPMed |
|
|
rs1291321331 CA427620919 |
113 | L>F | No |
ClinGen TOPMed |
|
|
CA427620915 rs1374990958 |
114 | L>V | No |
ClinGen gnomAD |
|
|
rs1210128649 CA427620884 |
115 | C>Y | No |
ClinGen gnomAD |
|
|
CA427620839 rs1427958437 |
117 | N>K | No |
ClinGen gnomAD |
|
|
CA427620834 rs1418030523 |
118 | S>Y | No |
ClinGen gnomAD |
|
|
CA427620816 rs1190636376 |
120 | E>* | No |
ClinGen gnomAD |
|
| TCGA novel | 120 | E>D | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1486209072 CA427620809 |
121 | H>Y | No |
ClinGen gnomAD |
|
|
CA1772873 rs755640959 CA427620800 |
122 | G>R | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA427620792 rs1482103113 |
123 | A>T | No |
ClinGen gnomAD |
|
|
CA1772871 rs544922225 |
125 | K>E | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
CA1772870 rs767095882 |
127 | Y>H | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA1772868 rs371134371 |
128 | P>A | No |
ClinGen ExAC gnomAD |
|
|
CA1772867 rs764468196 |
128 | P>L | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs371134371 CA1772869 |
128 | P>S | No |
ClinGen ExAC gnomAD |
|
|
rs763279378 CA427620737 |
129 | I>M | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs1398957418 CA427620742 |
129 | I>V | No |
ClinGen gnomAD |
|
|
rs575739368 CA1772864 |
130 | E>K | No |
ClinGen 1000Genomes ExAC gnomAD |
|
|
rs575739368 CA1772865 |
130 | E>Q | No |
ClinGen 1000Genomes ExAC gnomAD |
|
|
CA1772862 rs559151097 |
131 | E>G | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
CA1772863 rs759648985 |
131 | E>K | No |
ClinGen ExAC gnomAD |
|
|
rs771213408 CA1772861 |
132 | A>T | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs1363028068 CA427620694 |
135 | E>K | No |
ClinGen gnomAD |
|
|
CA427620691 rs1421211052 |
135 | E>V | No |
ClinGen gnomAD |
|
|
CA1772859 rs778188224 |
136 | D>G | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA427620686 rs1252264106 |
136 | D>H | No |
ClinGen TOPMed gnomAD |
|
|
CA427620677 rs114549087 |
137 | R>P | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
|
CA1772858 rs114549087 |
137 | R>Q | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
|
rs545199654 CA52234774 |
137 | R>W | No |
ClinGen 1000Genomes TOPMed gnomAD |
|
|
CA1772827 rs765554119 |
140 | L>F | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA427620615 rs1262313218 |
140 | L>H | No |
ClinGen TOPMed gnomAD |
|
|
rs932792632 CA52234645 |
143 | Q>* | No |
ClinGen TOPMed |
|
| TCGA novel | 144 | M>I | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs921443630 CA52234643 |
148 | W>R | No |
ClinGen TOPMed |
|
|
CA427620506 rs1303820414 |
150 | K>E | No |
ClinGen TOPMed |
|
|
rs1235217499 CA427620490 |
151 | I>F | No |
ClinGen TOPMed gnomAD |
|
|
CA1772826 rs574055938 |
151 | I>S | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA1772825 rs368669319 |
153 | E>K | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
|
rs767059540 CA1772824 |
154 | N>D | No |
ClinGen ExAC TOPMed gnomAD |
|
| TCGA novel | 155 | Q>* | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1229001438 CA427620433 |
156 | R>I | No |
ClinGen gnomAD |
|
|
CA1772822 rs773434974 |
159 | Y>H | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs761970818 CA1772820 |
161 | E>V | No |
ClinGen ExAC gnomAD |
|
|
rs769456796 CA1772818 |
162 | R>G | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs373596756 CA1772816 |
163 | R>K | No |
ClinGen ESP ExAC gnomAD |
|
|
CA52234628 rs911525586 |
164 | T>K | No |
ClinGen TOPMed |
|
|
rs911525586 CA427620367 |
164 | T>R | No |
ClinGen TOPMed |
|
|
CA1772814 rs776550245 |
165 | A>T | No |
ClinGen ExAC gnomAD |
|
|
CA1772813 rs770913548 |
166 | F>C | No |
ClinGen ExAC gnomAD |
|
|
CA1772811 rs199682241 |
166 | F>L | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs747731168 CA427620334 |
168 | L>F | No |
ClinGen ExAC gnomAD |
|
|
rs201662353 CA1772810 |
168 | L>W | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
| rs549632893 | 170 | G>= | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs750875154 CA1772785 |
171 | D>N | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs1469847259 CA427620311 |
171 | D>V | No |
ClinGen gnomAD |
|
|
rs1274373666 CA427620303 |
172 | V>A | No |
ClinGen gnomAD |
|
|
rs1213544565 CA427620298 |
173 | V>I | No |
ClinGen gnomAD |
|
|
CA1772782 rs1481967811 |
174 | L>F | No |
ClinGen TOPMed gnomAD |
|
|
rs781744171 CA427620243 |
175 | R>G | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA427620236 rs539398172 |
175 | R>P | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
rs539398172 CA1772780 |
175 | R>Q | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
rs781744171 CA1772781 |
175 | R>W | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA427620214 rs1373663525 |
176 | A>E | No |
ClinGen gnomAD |
|
|
rs1224663887 CA427620222 |
176 | A>T | No |
ClinGen gnomAD |
|
|
rs570148739 CA1772779 |
178 | M>I | No |
ClinGen 1000Genomes ExAC gnomAD |
|
|
rs763170442 CA1772777 |
180 | R>G | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs1276407401 CA427620098 |
181 | N>S | No |
ClinGen TOPMed gnomAD |
|
|
CA1772776 rs753593295 |
182 | E>* | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA427620084 rs753593295 |
182 | E>Q | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA52234452 rs528807377 |
184 | R>G | No |
ClinGen 1000Genomes gnomAD |
|
|
CA1772775 rs559624347 |
188 | P>L | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
CA427619947 rs1348031347 |
188 | P>S | No |
ClinGen gnomAD |
|
|
rs761165896 CA1772771 |
200 | R>T | No |
ClinGen ExAC |
|
|
rs1326284738 CA427619550 |
205 | Y>C | No |
ClinGen TOPMed |
|
|
CA427619558 rs1408192244 |
205 | Y>H | No |
ClinGen TOPMed gnomAD |
|
|
rs1434181201 CA427619533 |
206 | Q>E | No |
ClinGen TOPMed |
|
|
CA427619489 rs1274224980 |
207 | E>D | No |
ClinGen TOPMed |
|
|
CA52234444 rs549517427 |
207 | E>K | No |
ClinGen 1000Genomes |
|
|
CA427619479 rs1487820476 |
208 | I>F | No |
ClinGen gnomAD |
|
|
rs1362033612 CA427619473 |
208 | I>T | No |
ClinGen TOPMed |
|
|
CA1772769 rs529482281 |
209 | F>C | No |
ClinGen 1000Genomes ExAC gnomAD |
|
|
rs773916265 CA1772770 |
209 | F>L | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA1772768 rs748970463 |
210 | Q>* | No |
ClinGen ExAC gnomAD |
|
|
rs1255622485 CA427619380 |
212 | L>F | No |
ClinGen TOPMed |
|
|
CA1772766 rs563777718 |
215 | S>N | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
rs1275389887 CA427619270 |
216 | W>C | No |
ClinGen TOPMed |
|
|
rs1218104095 CA427619208 |
219 | M>T | No |
ClinGen gnomAD |
|
| TCGA novel | 221 | Q>E | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1558813563 CA427619151 |
222 | K>N | No |
ClinGen Ensembl |
|
| TCGA novel | 224 | K>T | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs781537876 CA1772760 |
225 | H>R | No |
ClinGen ExAC gnomAD |
|
|
CA427619128 rs1359595461 |
225 | H>Y | No |
ClinGen gnomAD |
|
|
CA1772759 rs543584416 |
227 | K>* | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
CA427619102 rs1395898279 |
228 | E>* | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA gnomAD |
|
CA427619104 rs1395898279 |
228 | E>K | No |
ClinGen gnomAD |
|
|
rs1175502009 CA427619057 |
230 | Y>C | No |
ClinGen TOPMed gnomAD |
|
|
rs1431474302 CA427619015 |
232 | E>Q | No |
ClinGen gnomAD |
|
|
CA1772758 rs751531671 |
233 | L>V | No |
ClinGen ExAC gnomAD |
|
|
CA1772757 rs577958837 |
236 | M>V | No |
ClinGen 1000Genomes ExAC gnomAD |
|
|
CA1772756 rs758572985 |
237 | C>* | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs370477305 CA1772755 |
238 | H>R | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
|
rs765508068 CA1772754 |
240 | P>Q | No |
ClinGen ExAC gnomAD |
|
|
CA427618835 rs1213444592 |
240 | P>S | No |
ClinGen gnomAD |
|
|
CA1772753 rs370698848 |
241 | E>D | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA427618790 rs750242500 |
242 | V>L | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA1772752 rs750242500 |
242 | V>M | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs1403462390 CA427618738 |
244 | L>P | No |
ClinGen TOPMed |
|
|
CA427618726 rs1309883091 |
245 | L>F | No |
ClinGen gnomAD |
No associated diseases with A6NCK2
9 regional properties for A6NCK2
| Type | Name | Position | InterPro Accession |
|---|---|---|---|
| domain | B-box-type zinc finger | 88 - 129 | IPR000315 |
| domain | Zinc finger, RING-type | 15 - 56 | IPR001841 |
| domain | B30.2/SPRY domain | 269 - 446 | IPR001870 |
| domain | SPRY domain | 334 - 446 | IPR003877 |
| domain | Butyrophylin-like, SPRY domain | 319 - 343 | IPR003879-1 |
| domain | Butyrophylin-like, SPRY domain | 349 - 362 | IPR003879-2 |
| domain | Butyrophylin-like, SPRY domain | 394 - 418 | IPR003879-3 |
| domain | Butyrophylin-like, SPRY domain | 425 - 443 | IPR003879-4 |
| conserved_site | Zinc finger, RING-type, conserved site | 30 - 39 | IPR017907 |
1 GO annotations of cellular component
| Name | Definition |
|---|---|
| cytoplasm | The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures. |
2 GO annotations of molecular function
| Name | Definition |
|---|---|
| ubiquitin protein ligase activity | Catalysis of the transfer of ubiquitin to a substrate protein via the reaction X-ubiquitin + S -> X + S-ubiquitin, where X is either an E2 or E3 enzyme, the X-ubiquitin linkage is a thioester bond, and the S-ubiquitin linkage is an amide bond: an isopeptide bond between the C-terminal glycine of ubiquitin and the epsilon-amino group of lysine residues in the substrate or, in the linear extension of ubiquitin chains, a peptide bond the between the C-terminal glycine and N-terminal methionine of ubiquitin residues. |
| zinc ion binding | Binding to a zinc ion (Zn). |
3 GO annotations of biological process
| Name | Definition |
|---|---|
| innate immune response | Innate immune responses are defense responses mediated by germline encoded components that directly recognize components of potential pathogens. |
| protein ubiquitination | The process in which one or more ubiquitin groups are added to a protein. |
| regulation of gene expression | Any process that modulates the frequency, rate or extent of gene expression. Gene expression is the process in which a gene's coding sequence is converted into a mature gene product (protein or RNA). |
15 homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| Q9H2S5 | RNF39 | RING finger protein 39 | Homo sapiens (Human) | PR |
| Q86UV7 | TRIM73 | Tripartite motif-containing protein 73 | Homo sapiens (Human) | PR |
| Q86XT4 | TRIM50 | E3 ubiquitin-protein ligase TRIM50 | Homo sapiens (Human) | PR |
| Q6ZMU5 | TRIM72 | Tripartite motif-containing protein 72 | Homo sapiens (Human) | PR |
| Q9UPQ4 | TRIM35 | E3 ubiquitin-protein ligase TRIM35 | Homo sapiens (Human) | PR |
| Q9BZY9 | TRIM31 | E3 ubiquitin-protein ligase TRIM31 | Homo sapiens (Human) | PR |
| Q9C029 | TRIM7 | E3 ubiquitin-protein ligase TRIM7 | Homo sapiens (Human) | PR |
| O15553 | MEFV | Pyrin | Homo sapiens (Human) | SS |
| Q8N9V2 | TRIML1 | Probable E3 ubiquitin-protein ligase TRIML1 | Homo sapiens (Human) | PR |
| P19474 | TRIM21 | E3 ubiquitin-protein ligase TRIM21 | Homo sapiens (Human) | PR |
| Q14142 | TRIM14 | Tripartite motif-containing protein 14 | Homo sapiens (Human) | PR |
| A6NK02 | TRIM75 | Tripartite motif-containing protein 75 | Homo sapiens (Human) | PR |
| Q5EBN2 | TRIM61 | Putative tripartite motif-containing protein 61 | Homo sapiens (Human) | PR |
| Q3TL54 | Trim43a | Tripartite motif-containing protein 43A | Mus musculus (Mouse) | PR |
| P86449 | Trim43c | Tripartite motif-containing protein 43C | Mus musculus (Mouse) | PR |
| 10 | 20 | 30 | 40 | 50 | 60 |
| MDSDFSHAFQ | KELTCVICLN | YLVDPVTICC | GHSFCRPCLC | LSWEEAQSPA | NCPACREPSP |
| 70 | 80 | 90 | 100 | 110 | 120 |
| KMDFKTNILL | KNLVTIARKA | SLWQFLSSEK | QICGTHRQTK | KMFCDMDKSL | LCLLCSNSQE |
| 130 | 140 | 150 | 160 | 170 | 180 |
| HGAHKHYPIE | EAAEEDREKL | LKQMRILWKK | IQENQRNLYE | ERRTAFLLRG | DVVLRAQMIR |
| 190 | 200 | 210 | 220 | 230 | 240 |
| NEYRKLHPVL | HKEEKQHLER | LNKEYQEIFQ | QLQRSWVKMD | QKSKHLKEMY | QELMEMCHKP |
| 250 | 260 | 270 | 280 | 290 | 300 |
| EVELLQDLGD | IVARSESVLL | HMPQPVNPEL | TAGPITGLVY | RLNRFRVEIS | FHFEVTNHNI |
| 310 | 320 | 330 | 340 | 350 | 360 |
| RLFEDVRSWM | FRRGPLNSDR | SDYFAAWGAR | VFSFGKHYWE | LDVDNSCDWA | LGVCNNSWIR |
| 370 | 380 | 390 | 400 | 410 | 420 |
| KNSTMVNSED | IFLLLCLKVD | NHFNLLTTSP | VFPHYIEKPL | GRVGVFLDFE | SGSVSFLNVT |
| 430 | 440 | ||||
| KSSLIWSYPA | GSLTFPVRPF | FYTGHR |