P43355
PR
Gene name |
MAGEA1 (MAGE1, MAGE1A) |
Protein name |
Melanoma-associated antigen 1 |
Names |
Antigen MZ2-E, Cancer/testis antigen 1.1, CT1.1, MAGE-1 antigen |
Species |
Homo sapiens (Human) |
KEGG Pathway |
hsa:4100 |
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
3 structures for P43355
| Entry ID | Method | Resolution | Chain | Position | Source |
|---|---|---|---|---|---|
| 1W72 | X-ray | 215 A | C/F | 161-169 | PDB |
| 3BO8 | X-ray | 180 A | C | 161-169 | PDB |
| AF-P43355-F1 | Predicted | AlphaFoldDB |
170 variants for P43355
| Variant ID(s) | Position | Change | Description | Diseaes Association | Provenance |
|---|---|---|---|---|---|
|
CA415290646 rs1389171390 |
6 | R>K | No |
ClinGen TOPMed gnomAD |
|
|
rs781891821 CA10546058 |
7 | S>R | No |
ClinGen ExAC TOPMed gnomAD |
|
| TCGA novel | 12 | P>S | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA415290682 rs1556944064 |
12 | P>T | No |
ClinGen gnomAD |
|
|
rs781874892 CA10546055 |
13 | E>K | No |
ClinGen ExAC gnomAD |
|
|
CA415290701 rs1444089551 |
14 | E>D | No |
ClinGen TOPMed |
|
|
CA10546054 rs782796633 |
15 | A>D | No |
ClinGen 1000Genomes ExAC gnomAD |
|
|
CA415290734 rs1556944071 |
20 | Q>K | No |
ClinGen gnomAD |
|
| TCGA novel | 22 | A>D | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA10546052 rs781934369 |
27 | C>Y | No |
ClinGen ExAC gnomAD |
|
| TCGA novel | 28 | V>E | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1191077612 CA415290805 |
31 | A>T | No |
ClinGen TOPMed |
|
|
rs2008160 VAR_004283 CA10546050 |
32 | T>A | No |
ClinGen UniProt 1000Genomes ESP ExAC TOPMed dbSNP gnomAD |
|
| TCGA novel | 32 | T>I | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs781981187 CA10546049 |
33 | S>A | No |
ClinGen ExAC gnomAD |
|
|
rs1203743166 CA415290827 |
34 | S>F | No |
ClinGen TOPMed gnomAD |
|
| TCGA novel | 35 | S>F | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA10546046 rs151247964 |
37 | P>L | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
|
rs1266852633 CA415290860 |
40 | L>P | No |
ClinGen TOPMed gnomAD |
|
|
rs1266852633 CA415290861 |
40 | L>R | No |
ClinGen TOPMed gnomAD |
|
|
rs782207325 CA10546044 |
41 | G>D | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs782306002 CA10546045 |
41 | G>S | No |
ClinGen ExAC gnomAD |
|
|
rs782098342 CA10546043 |
45 | E>D | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
CA337641252 rs782559268 |
46 | V>L | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA10546042 rs782559268 |
46 | V>M | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA10546040 rs782643679 |
48 | T>P | No |
ClinGen ExAC gnomAD |
|
|
rs1365830109 CA415290902 |
49 | A>S | No |
ClinGen TOPMed |
|
|
CA10546038 rs781985915 |
50 | G>E | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
CA10546039 rs782483613 |
50 | G>R | No |
ClinGen ExAC TOPMed gnomAD |
|
| TCGA novel | 51 | S>* | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1392532041 CA415290911 |
51 | S>P | No |
ClinGen TOPMed gnomAD |
|
|
CA10546036 rs111525045 |
53 | D>H | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
|
rs1556944096 CA415290928 |
53 | D>V | No |
ClinGen gnomAD |
|
|
CA415290942 rs1383519941 |
55 | P>L | No |
ClinGen TOPMed |
|
|
CA415290947 rs1170562291 |
56 | Q>R | No |
ClinGen TOPMed |
|
|
rs781905272 CA10546035 |
57 | S>G | No |
ClinGen ExAC gnomAD |
|
|
CA10546034 rs782761428 |
58 | P>L | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA337641261 rs144650259 |
61 | A>G | No |
ClinGen ESP gnomAD |
|
|
VAR_053491 rs2233044 COSM1466466 CA10546032 |
63 | A>T | large_intestine [Cosmic] | No |
ClinGen cosmic curated UniProt 1000Genomes ESP ExAC TOPMed dbSNP gnomAD |
|
CA10546030 rs782043198 |
65 | P>L | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA TOPMed gnomAD |
|
rs782733251 CA10546031 |
65 | P>S | No |
ClinGen ExAC gnomAD |
|
| TCGA novel | 66 | T>N | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs781929533 CA10546029 |
67 | T>I | No |
ClinGen ExAC gnomAD |
|
|
rs782414241 CA10546028 |
68 | I>T | No |
ClinGen ExAC gnomAD |
|
|
rs782303860 CA10546027 |
69 | N>S | No |
ClinGen ExAC TOPMed gnomAD |
|
|
COSM1117249 CA337641272 rs781993726 |
72 | R>* | Variant assessed as Somatic; 0.0 impact. endometrium [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated ExAC NCI-TCGA TOPMed gnomAD |
|
VAR_011737 rs2008144 CA10546025 |
72 | R>Q | No |
ClinGen UniProt 1000Genomes ESP ExAC TOPMed dbSNP gnomAD |
|
|
CA10546024 rs782211531 |
75 | Q>* | No |
ClinGen ExAC gnomAD |
|
|
rs940562569 CA337641276 |
76 | P>A | No |
ClinGen Ensembl |
|
|
rs1556944112 CA415291063 |
77 | S>G | No |
ClinGen gnomAD |
|
|
CA10546023 rs782627136 |
77 | S>I | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs143755053 CA415291069 |
78 | E>K | No |
ClinGen ESP TOPMed |
|
| TCGA novel | 80 | S>A | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA415291105 rs1225102165 |
83 | R>C | No |
ClinGen TOPMed gnomAD |
|
|
rs782432961 CA10546020 |
83 | R>H | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs1556944117 CA415291125 |
86 | E>A | No |
ClinGen gnomAD |
|
|
rs782207286 CA10546019 |
87 | G>E | No |
ClinGen 1000Genomes ExAC gnomAD |
|
|
CA415291130 rs1556944118 |
87 | G>R | No |
ClinGen gnomAD |
|
|
rs782683172 CA10546018 |
88 | P>L | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA gnomAD |
|
rs1283658297 CA415291141 |
89 | S>N | No |
ClinGen TOPMed |
|
|
rs781872243 CA10546016 |
90 | T>I | No |
ClinGen ExAC gnomAD |
|
|
rs1404608153 CA415291157 |
92 | C>S | No |
ClinGen TOPMed |
|
|
rs782726763 CA10546015 |
93 | I>F | No |
ClinGen ExAC gnomAD |
|
|
rs782491782 CA10546014 COSM1466465 |
96 | S>P | large_intestine [Cosmic] | No |
ClinGen cosmic curated ExAC gnomAD |
|
CA415291184 rs1602751635 |
97 | L>V | No |
ClinGen Ensembl |
|
|
rs1556944129 CA415291193 |
98 | F>Y | No |
ClinGen gnomAD |
|
|
rs1363932326 CA415291199 |
99 | R>* | No |
ClinGen TOPMed gnomAD |
|
|
rs1556944132 CA415291200 |
99 | R>Q | No |
ClinGen gnomAD |
|
|
CA10546013 rs61737513 |
100 | A>V | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
|
CA415291231 rs1556944136 |
104 | K>R | No |
ClinGen gnomAD |
|
| TCGA novel | 108 | D>A | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1556944143 CA415291306 |
115 | L>R | No |
ClinGen gnomAD |
|
|
CA10546012 rs373351745 |
118 | R>Q | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
| TCGA novel | 123 | V>I | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA415291407 rs1556944145 |
130 | E>D | No |
ClinGen gnomAD |
|
|
rs146942997 CA10546008 |
134 | K>N | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
| TCGA novel | 136 | Y>C | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs781959861 CA10546007 |
137 | K>N | No |
ClinGen ExAC gnomAD |
|
|
CA415291493 rs1569525184 |
142 | E>* | No |
ClinGen Ensembl |
|
|
rs1556944151 CA415291514 |
145 | G>S | No |
ClinGen gnomAD |
|
|
rs782053099 CA10546005 |
148 | S>F | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA TOPMed gnomAD |
| TCGA novel | 150 | S>P | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1271618549 CA415291565 |
152 | Q>R | No |
ClinGen TOPMed |
|
| TCGA novel | 156 | G>V | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA337641297 rs782245100 |
158 | D>E | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA415291610 rs782650488 |
159 | V>L | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA10546001 rs782650488 |
159 | V>M | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA415291627 rs1556944158 |
161 | E>A | No |
ClinGen gnomAD |
|
| TCGA novel | 161 | E>D | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA415291641 rs1556944160 |
163 | D>A | No |
ClinGen gnomAD |
|
|
rs782661974 CA10546000 |
163 | D>E | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
rs1556944159 CA415291639 |
163 | D>H | No |
ClinGen gnomAD |
|
|
rs1010428087 CA337641299 |
164 | P>A | No |
ClinGen Ensembl |
|
|
rs782563036 CA10545999 |
165 | T>A | No |
ClinGen ExAC gnomAD |
|
|
rs782563036 CA10545998 |
165 | T>P | No |
ClinGen ExAC gnomAD |
|
|
CA415291653 rs1290477231 |
166 | G>S | No |
ClinGen TOPMed gnomAD |
|
| TCGA novel | 168 | S>F | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
| TCGA novel | 169 | Y>C | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA10545995 rs782682055 |
176 | G>C | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs782682055 CA337641308 |
176 | G>R | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA415291743 rs1556944169 |
177 | L>I | No |
ClinGen gnomAD |
|
|
rs144596051 CA415291758 |
178 | S>F | No |
ClinGen ESP TOPMed |
|
|
rs782519489 CA10545994 |
179 | Y>C | No |
ClinGen ExAC gnomAD |
|
|
rs782734083 CA10545992 |
184 | G>A | No |
ClinGen ExAC |
|
|
CA10545991 rs782105925 |
185 | D>A | No |
ClinGen ExAC gnomAD |
|
|
rs1556944175 CA415291892 |
190 | P>L | No |
ClinGen gnomAD |
|
|
rs781792706 CA10545990 |
197 | I>V | No |
ClinGen ExAC gnomAD |
|
|
rs1556944178 CA415291965 |
198 | V>I | No |
ClinGen gnomAD |
|
| TCGA novel | 201 | M>I | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA10545989 rs782728367 |
204 | M>V | No |
ClinGen ExAC gnomAD |
|
|
CA415292062 rs1556944186 |
206 | G>D | No |
ClinGen gnomAD |
|
| TCGA novel | 210 | P>S | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs782555287 CA415292213 |
219 | S>G | No |
ClinGen 1000Genomes |
|
|
rs781984291 CA10545987 |
221 | M>T | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs782169023 CA415292257 |
222 | E>G | No |
ClinGen 1000Genomes |
|
|
CA337641326 rs1034431294 |
222 | E>K | Variant assessed as Somatic; impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA TOPMed |
|
rs952057687 CA337641329 |
223 | V>M | No |
ClinGen Ensembl |
|
|
rs1470295473 CA415292277 |
224 | Y>F | No |
ClinGen TOPMed |
|
|
rs782381592 CA10545986 |
225 | D>V | No |
ClinGen ExAC TOPMed gnomAD |
|
|
rs373257494 CA10545984 |
229 | H>N | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
CA10545983 rs782306135 |
229 | H>Q | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA415292371 rs1263687818 |
231 | A>T | No |
ClinGen TOPMed gnomAD |
|
|
CA415292406 rs1556944207 |
234 | E>* | No |
ClinGen gnomAD |
|
|
CA10545981 rs369289180 |
238 | L>P | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
CA415292546 rs1556944213 |
245 | Q>R | No |
ClinGen gnomAD |
|
|
rs782441595 CA10545980 |
247 | K>E | No |
ClinGen ExAC |
|
|
rs1269766512 CA415292567 |
247 | K>M | No |
ClinGen TOPMed |
|
|
CA415292569 rs1556944216 |
247 | K>N | No |
ClinGen gnomAD |
|
| TCGA novel | 249 | L>Q | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA337641338 rs962244158 |
252 | R>L | No |
ClinGen gnomAD |
|
|
CA415292650 rs962244158 |
252 | R>Q | No |
ClinGen gnomAD |
|
|
CA10545979 rs202173682 |
254 | V>G | No |
ClinGen ExAC gnomAD |
|
|
rs782477850 CA10545978 |
255 | P>A | No |
ClinGen ExAC |
|
|
rs781843123 CA10545976 |
255 | P>L | No |
ClinGen ExAC gnomAD |
|
|
rs782477850 CA10545977 |
255 | P>T | No |
ClinGen ExAC |
|
|
rs782457391 CA10545974 |
256 | D>G | No |
ClinGen ExAC |
|
|
rs781888492 CA10545973 |
257 | S>R | No |
ClinGen ExAC |
|
|
CA10545972 rs142315436 |
258 | D>A | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
rs1450308862 CA415292739 |
260 | A>P | No |
ClinGen TOPMed gnomAD |
|
|
rs1450308862 CA415292738 |
260 | A>T | No |
ClinGen TOPMed gnomAD |
|
|
rs781817941 CA10545970 |
260 | A>V | No |
ClinGen ExAC gnomAD |
|
|
CA10545969 rs376229047 |
261 | R>C | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ESP ExAC NCI-TCGA TOPMed gnomAD |
|
CA10545968 rs782046671 |
264 | F>I | No |
ClinGen ExAC gnomAD |
|
| TCGA novel | 268 | P>T | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
| TCGA novel | 269 | R>S | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs782464959 CA337641360 |
272 | A>G | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
|
rs782788272 CA337641358 |
272 | A>S | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA10545966 rs782788272 |
272 | A>T | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen ExAC NCI-TCGA TOPMed gnomAD |
|
rs782464959 CA10545965 |
272 | A>V | No |
ClinGen 1000Genomes ExAC TOPMed gnomAD |
|
| TCGA novel | 274 | T>P | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
COSM1466458 rs781992458 CA337641363 |
278 | K>E | large_intestine [Cosmic] | No |
ClinGen cosmic curated ExAC gnomAD |
|
rs781992458 CA10545964 |
278 | K>Q | No |
ClinGen ExAC gnomAD |
|
| VAR_036581 | 278 | K>T | a breast cancer sample; somatic mutation [UniProt] | No | UniProt |
|
CA415292982 rs782202233 |
280 | L>F | No |
ClinGen Ensembl |
|
|
rs1156384241 CA415293011 |
282 | Y>F | No |
ClinGen TOPMed |
|
| TCGA novel | 283 | V>A | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1556944244 CA415293019 |
283 | V>M | No |
ClinGen gnomAD |
|
|
rs1182968785 CA415293049 |
285 | K>E | No |
ClinGen TOPMed |
|
| TCGA novel | 285 | K>R | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
| TCGA novel | 286 | V>A | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
rs1459904286 CA415293081 |
288 | A>P | No |
ClinGen TOPMed |
|
| TCGA novel | 289 | R>I | Variant assessed as Somatic; impact. [NCI-TCGA] | No | NCI-TCGA |
|
CA10545961 rs782387656 |
290 | V>A | No |
ClinGen ExAC TOPMed gnomAD |
|
|
CA415293118 COSM3235161 rs1216226226 |
291 | R>C | Variant assessed as Somatic; 0.0 impact. large_intestine [NCI-TCGA, Cosmic] | No |
ClinGen cosmic curated NCI-TCGA TOPMed gnomAD |
|
CA10545960 rs369028108 |
296 | S>T | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
rs61737511 CA10545958 |
298 | R>C | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
|
rs61737511 CA10545957 |
298 | R>G | No |
ClinGen 1000Genomes ESP ExAC TOPMed gnomAD |
|
|
CA10545956 rs376635182 |
298 | R>H | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
CA415293202 rs376635182 |
298 | R>L | No |
ClinGen ESP ExAC TOPMed gnomAD |
|
|
rs1556944256 CA415293347 |
308 | G>E | Variant assessed as Somatic; 0.0 impact. [NCI-TCGA] | No |
ClinGen NCI-TCGA gnomAD |
No associated diseases with P43355
3 GO annotations of cellular component
| Name | Definition |
|---|---|
| cytoplasm | The contents of a cell excluding the plasma membrane and nucleus, but including other subcellular structures. |
| 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. |
1 GO annotations of molecular function
| Name | Definition |
|---|---|
| histone deacetylase binding | Binding to histone deacetylase. |
2 GO annotations of biological process
| Name | Definition |
|---|---|
| negative regulation of Notch signaling pathway | Any process that stops, prevents, or reduces the frequency, rate or extent of the Notch signaling pathway. |
| negative regulation of transcription by RNA polymerase II | Any process that stops, prevents, or reduces the frequency, rate or extent of transcription mediated by RNA polymerase II. |
17 homologous proteins in AiPD
| UniProt AC | Gene Name | Protein Name | Species | Evidence Code |
|---|---|---|---|---|
| P43356 | MAGEA2B | Melanoma-associated antigen 2 | Homo sapiens (Human) | PR |
| O15479 | MAGEB2 | Melanoma-associated antigen B2 | Homo sapiens (Human) | PR |
| O15480 | MAGEB3 | Melanoma-associated antigen B3 | Homo sapiens (Human) | PR |
| P43357 | MAGEA3 | Melanoma-associated antigen 3 | Homo sapiens (Human) | PR |
| P43358 | MAGEA4 | Melanoma-associated antigen 4 | Homo sapiens (Human) | PR |
| P43360 | MAGEA6 | Melanoma-associated antigen 6 | Homo sapiens (Human) | PR |
| P43361 | MAGEA8 | Melanoma-associated antigen 8 | Homo sapiens (Human) | PR |
| P43363 | MAGEA10 | Melanoma-associated antigen 10 | Homo sapiens (Human) | PR |
| P43365 | MAGEA12 | Melanoma-associated antigen 12 | Homo sapiens (Human) | PR |
| Q8TD90 | MAGEE2 | Melanoma-associated antigen E2 | Homo sapiens (Human) | PR |
| Q96MG7 | NSMCE3 | Non-structural maintenance of chromosomes element 3 homolog | Homo sapiens (Human) | PR |
| Q9BZ81 | MAGEB5 | Melanoma-associated antigen B5 | Homo sapiens (Human) | PR |
| Q9HAY2 | MAGEF1 | Melanoma-associated antigen F1 | Homo sapiens (Human) | PR |
| P43364 | MAGEA11 | Melanoma-associated antigen 11 | Homo sapiens (Human) | PR |
| Q9UNF1 | MAGED2 | Melanoma-associated antigen D2 | Homo sapiens (Human) | PR |
| Q9Y5V3 | MAGED1 | Melanoma-associated antigen D1 | Homo sapiens (Human) | PR |
| Q96JG8 | MAGED4B | Melanoma-associated antigen D4 | Homo sapiens (Human) | PR |
| 10 | 20 | 30 | 40 | 50 | 60 |
| MSLEQRSLHC | KPEEALEAQQ | EALGLVCVQA | ATSSSSPLVL | GTLEEVPTAG | STDPPQSPQG |
| 70 | 80 | 90 | 100 | 110 | 120 |
| ASAFPTTINF | TRQRQPSEGS | SSREEEGPST | SCILESLFRA | VITKKVADLV | GFLLLKYRAR |
| 130 | 140 | 150 | 160 | 170 | 180 |
| EPVTKAEMLE | SVIKNYKHCF | PEIFGKASES | LQLVFGIDVK | EADPTGHSYV | LVTCLGLSYD |
| 190 | 200 | 210 | 220 | 230 | 240 |
| GLLGDNQIMP | KTGFLIIVLV | MIAMEGGHAP | EEEIWEELSV | MEVYDGREHS | AYGEPRKLLT |
| 250 | 260 | 270 | 280 | 290 | 300 |
| QDLVQEKYLE | YRQVPDSDPA | RYEFLWGPRA | LAETSYVKVL | EYVIKVSARV | RFFFPSLREA |
| ALREEEEGV |