P04637

PTMD Annotation Information


※ Protein Information

Tag Content
UniProt Accession P53_HUMAN; P04637;
Entrez ID 7157
GenBank Protein ID NM_000546.5; NM_001126112.2; NM_001126113.2; NM_001126114.2; NM_001126115.1; NM_001126116.1; NM_001126117.1; NM_001126118.1; NM_001276695.1; NM_001276696.1; NM_001276697.1; NM_001276698.1; NM_001276699.1; NM_001276760.1; NM_001276761.1;
GenBank Nucleotide ID NP_000537.3; NP_001119584.1; NP_001119585.1; NP_001119586.1; NP_001119587.1; NP_001119588.1; NP_001119589.1; NP_001119590.1; NP_001263624.1; NP_001263625.1; NP_001263626.1; NP_001263627.1; NP_001263628.1; NP_001263689.1; NP_001263690.1;
Protein Name Cellular tumor antigen p53 (Antigen NY-CO-13) (Phosphoprotein p53) (Tumor suppressor p53)
Gene Name TP53; P53
Organism Homo sapiens
NCBI Taxa ID 9606
Functional DescriptionActs as a tumor suppressor in many tumor types; induces growth arrest or apoptosis depending on the physiological circumstances and cell type. Involved in cell cycle regulation as a trans-activator that acts to negatively regulate cell division by controlling a set of genes required for this process. One of the activated genes is an inhibitor of cyclin-dependent kinases. Apoptosis induction seems to be mediated either by stimulation of BAX and FAS antigen expression, or by repression of Bcl-2 expression. In cooperation with mitochondrial PPIF i(view all)
Sequence
(Fasta)
MEEPQSDPSV EPPLSQETFS DLWKLLPENN VLSPLPSQAM DDLMLSPDDI EQWFTEDPGP 60
DEAPRMPEAA PPVAPAPAAP TPAAPAPAPS WPLSSSVPSQ KTYQGSYGFR LGFLHSGTAK 120
SVTCTYSPAL NKMFCQLAKT CPVQLWVDST PPPGTRVRAM AIYKQSQHMT EVVRRCPHHE 180
RCSDSDGLAP PQHLIRVEGN LRVEYLDDRN TFRHSVVVPY EPPEVGSDCT TIHYNYMCNS 240
SCMGGMNRRP ILTIITLEDS SGNLLGRNSF EVRVCACPGR DRRTEEENLR KKGEPHHELP 300
PGSTKRALPN NTSSSPQPKK KPLDGEYFTL QIRGRERFEM FRELNEALEL KDAQAGKEPG 360
GSRAHSSHLK SKKGQSTSRH KKLMFKTEGP DSD 394

※ PTM-Disease Association

NumPTMDiseaseCell TypeTypePTM SitePMID
1AcetylationBreast cancer/tumor/carcinomaD24920214
[Reference]: Our results provide evidence that melatonin enhances p53 acetylation by modulating the MDM2/MDMX/p300 pathway, disclosing new insights for understanding its anticancer effect.
2UbiquitinationGastric cancerP24240108
[Reference]: Collectively, our novel findings indicate that AURKA promotes tumor growth and cell survival through regulation of HDM2-induced ubiquitination and inhibition of P53
3PhosphorylationPancreatic cancer/carcinoma/adenocarcinomaP23845906
[Reference]: Here, we found that cisplatin mainly induced non-apoptotic death of the pancreatic cancer cells (AsPC-1 and Capan-2), which was associated with a significant p53 activation (phosphorylation and accumulation).
4PhosphorylationHead and neck squamous cell carcinomaP23414419
[Reference]: P276-00 treatment suppressed cell proliferation through inhibition of CCND1 expression, reduced phosphorylation of retinoblastoma protein and abrogative transcription of E2F1 gene targets
5PhosphorylationMelanomaA375 cell lineP22968364
[Reference]: Ruthenium complexes containing 2,6-bis(benzimidazolyl)pyridine derivatives induce cancer cell apoptosis by triggering DNA damage-mediated p53 phosphorylation
6UbiquitinationHepatocellular carcinoma/Hepatocarcinoma/HepatomaU16581249
[Reference]: Gankyrin regulates the phosphorylation of the retinoblastoma protein (pRb) by CDK4 and enhances the ubiquitylation of p53 by the RING ubiquitin ligase MDM3.
7Serine PhosphorylationBreast cancer/tumor/carcinomaMCF7AS1515958581; 23798621
[Reference]: DACH1 phosphorylation at serine residue (S439) inhibited p53 binding and phosphorylation at p53 amino-terminal sites (S15, S20) enhanced DACH1 binding. DACH1 binding to p53 was inhibited by NAD-dependent deacetylation via DACH1 K628. DACH1 repressed p21CIP1 and induced RAD51, an association found in basal breast cancer. DACH1 inhibits breast cancer cellular growth in an NAD and p53-dependent manner through direct protein-protein association.
8Serine PhosphorylationAtaxia-telangiectasic cancerDS159733515
[Reference]: Ionizing radiation, but not ultraviolet radiation, rapidly enhanced this p53-directed kinase activity of endogenous ATM. These observations, along with the fact that phosphorylation of p53 on serine-15 in response to ionizing radiation is reduced in ataxia telangiectasia cells, suggest that ATM is a protein kinase that phosphorylates p53 in vivo.
9Serine PhosphorylationBrain cancer/tumorGBM8401 cell lineDS1523268709
[Reference]: P. indica root aqueous extracts suppress cancer cell proliferation and migration through the phosphorylated-p53 and p21 pathways
10Serine PhosphorylationProstate cancer/carcinoma/adenocarcinomacell linePS1523359208
[Reference]: AA can activate p53 through increasing the phosphorylation of p53 on Ser15 in LNCaP cells
11Serine PhosphorylationDown syndromeUS1520696760
[Reference]: Accordingly, brains from embryonic DYRK1A transgenic mice exhibited elevated levels of Dyrk1A, Ser-15 (mouse Ser-18)-phosphorylated p53, and p21(CIP1) as well as impaired neuronal proliferation.
12Serine PhosphorylationColon cancer/carcinomacell lineUS1525860929
[Reference]: FBXW7-mutated colorectal cancer cells exhibit aberrant expression of phosphorylated-p53 at Serine-15.
13Serine PhosphorylationNeuroblastomaUS1523824039
[Reference]: MPTQ-mediated apoptosis is associated with increased phosphorylation of p53 at Ser15 and Ser20 which correlates with the hyperphosphorylation of Ataxia-Telangiectasia mutated protein (ATM)
14Serine PhosphorylationBreast cancer/tumor/carcinomaMCF7AS2023798621
[Reference]: DACH1 phosphorylation at serine residue (S439) inhibited p53 binding and phosphorylation at p53 amino-terminal sites (S15, S20) enhanced DACH1 binding. DACH1 binding to p53 was inhibited by NAD-dependent deacetylation via DACH1 K628. DACH1 repressed p21CIP1 and induced RAD51, an association found in basal breast cancer. DACH1 inhibits breast cancer cellular growth in an NAD and p53-dependent manner through direct protein-protein association.
15Serine PhosphorylationOvarian cancer/carcinomaUS2020009884
[Reference]: In p53-positive ovarian carinomas, S392 phosphorylation was associated with advanced tumor stage and high tumor grade. S20 phosphorylation was associated with low tumor grade in p53-positive, and high tumor grade in p53-negative, ovarian carcinomas.
16Serine PhosphorylationNeuroblastomaUS2023824039
[Reference]: MPTQ-mediated apoptosis is associated with increased phosphorylation of p53 at Ser15 and Ser20 which correlates with the hyperphosphorylation of Ataxia-Telangiectasia mutated protein (ATM)
17Serine PhosphorylationB-cell tumorAS2315343266
[Reference]: Our finding that S23A/S23A animals are tumor prone suggests that Ser23 phosphorylation is important for the tumor suppressor function of p53.
18Serine PhosphorylationT cell lymphomaNS3711042698
[Reference]: A serine 37 mutation associated with two missense mutations at highly conserved regions of p53 affect pro-apoptotic genes expression in a T-lymphoblastoid drug resistant cell line.
19Serine PhosphorylationBreast cancer/tumor/carcinomaMCF7DS4617404016
[Reference]: Effect of distinct anticancer drugs on the phosphorylation of p53 protein at serine 46 in human MCF-7 breast cancer cells
20Serine PhosphorylationAcute lymphoblastic leukaemiaDS4623717325; 16377624
[Reference]: TP53INP1 Functions as a Tumor Suppressor and Induces Apoptosis through Phosphorylating p53 at Serine-46
21Serine PhosphorylationHuntington's diseaseUS4622011578
[Reference]: Mass spectrometry analysis of the post-translational modifications of alpha-enolase from pancreatic ductal adenocarcinoma cells.
22Arginine MethylationLung cancer/carcinomaH1299 cell linePR21324384472
[Reference]: It has been reported that p53 with R213Q mutation is exist in certain tumor cell lines and its methylation on R213 as well
23Serine PhosphorylationLymphomaDS31224173284
[Reference]: Our study shows that in addition to protecting against tumours caused by ionising radiation, phosphorylation of p53 on Ser312 also contributes to the suppression of carcinogen-mediated tumourigenesis
24Lysine MethylationGlioblastomaPK37022864287
[Reference]: We also found that endogenous full-length PHF20 interacted with endogenous p53 in cell lines U87 (glioblastoma) and MCF7 (breast cancer), which both express wild-type p53; PHF20 is an effector protein of p53 double lysine methylation that stabilizes and activates p53.
25Lysine MethylationBreast cancer/tumor/carcinomaMCF7PK37022864287
[Reference]: We also found that endogenous full-length PHF20 interacted with endogenous p53 in cell lines U87 (glioblastoma) and MCF7 (breast cancer), which both express wild-type p53; PHF20 is an effector protein of p53 double lysine methylation that stabilizes and activates p53.
26Lysine MethylationLymphomaDK37224189068
[Reference]: We also show that reduced PRMT5 expression leads to cyclin D1 transcriptional repression via loss of TP53K372 methylation, which results in decreased BCL3 expression and enhanced recruitment of NF-B p52-HDAC1 repressor complexes to the cyclin D1 promoter.
27Serine PhosphorylationBreast cancer/tumor/carcinomaMCF7AS39221084272
[Reference]: lack of phosphorylation at Ser392 may be important in breast cancer pathogenesis and inability to phosphorylate p53 at this site has been related to treatment response
28Serine PhosphorylationVestibular schwannomasPS39216299809
[Reference]: Our results suggest that age dependent phosphorylation of p53 protein and deregulation of p53 gene has a role in the development of human vestibular schwannomas.
29Serine PhosphorylationOvarian cancer/carcinomaUS39220009884
[Reference]: Expression of p53 protein phosphorylated at serine 20 and serine 392 in malignant and benign ovarian neoplasms: correlation with clinicopathological parameters of tumors.
30Serine PhosphorylationHepatocellular carcinoma/Hepatocarcinoma/HepatomaUS39221455220
[Reference]: Met ensures cell survival through a new path in which c-Abl and p38-MAPK are employed to elicit p53 phosphorylation on Ser(392) and Mdm2 upregulation. We found a clinical correlation between activated Met, phospho-p53, and Mdm2 levels in human tumors, supporting the role of this path in tumorigenesis.

※ Disease Cross-ref Annotation

DatabaseAnnotation
Cancer Gene Census
breast, colorectal, lung, sarcoma, adrenocortical, glioma, Spitzoid tumour, multiple other tumour types breast, sarcoma, adrenocortical carcinoma, glioma, multiple other tumour types Li-Fraumeni syndrome
CTD (Curated)
(count: 83)
(view all)
MESH:D058186 ; Acute Kidney Injury
MESH:D000230 ; Adenocarcinoma
MESH:D018262 ; Adenocarcinoma, Clear Cell
MESH:C562730 ; Adenocarcinoma Of Esophagus
MESH:D000236 ; Adenoma
MESH:D000310 ; Adrenal Gland Neoplasms
HGMD
(count: 201)
(view all)
CP035472; Li-Fraumeni syndrome; Complex rearrangements
CD011205; Li-Fraumeni syndrome; Small deletions
CD983489; Li-Fraumeni syndrome; Small deletions
CD941800; Li-Fraumeni syndrome; Small deletions
CD002536; Li-Fraumeni syndrome; Small deletions
CD920913; Adrenocortical carcinoma; Small deletions
GWASdb
(count: 8)
(view all)
rs78378222; Skin cancer (cutaneous basal cell carcinoma); pigmented basal cell carcinoma
rs78378222; Basal cell carcinoma; basal cell carcinoma
rs12951053; Hematology traits; myocardial infarction|nephrotic syndrome|hypersensitivity reaction type II disease|hematopoietic system disease
rs1625895; Sex hormone-binding globulin levels; breast cancer
rs1042522; Drug response to Fluorouracil; Null
rs1042522; Drug response to Cisplatin; Null

※ PTM Sites

PTM Modification Sites
Phosphorylation
(count: 35)
(view all)
106       SQKTYQGSYGFRLGF     dbPAF
126       AKSVTCTYSPALNKM     dbPAF
149       PVQLWVDSTPPPGTR     dbPAF
15        PSVEPPLSQETFSDL     dbPAF
150       VQLWVDSTPPPGTRV     dbPAF
155       DSTPPPGTRVRAMAI     dbPAF
Acetylation
(count: 14)
(view all)
120       FLHSGTAKSVTCTYS     PLMD
164       VRAMAIYKQSQHMTE     PLMD
292       EEENLRKKGEPHHEL     PLMD
305       ELPPGSTKRALPNNT     PLMD
319       TSSSPQPKKKPLDGE     PLMD
320       SSSPQPKKKPLDGEY     PLMD
Ubiquitination
(count: 14)
(view all)
101       SSSVPSQKTYQGSYG     PLMD
120       FLHSGTAKSVTCTYS     PLMD
132       TYSPALNKMFCQLAK     PLMD
139       KMFCQLAKTCPVQLW     PLMD
164       VRAMAIYKQSQHMTE     PLMD
291       TEEENLRKKGEPHHE     PLMD
Sumoylation
(count: 1)
386       RHKKLMFKTEGPDSD     PLMD
Butyrylation
(count: 5)
319       TSSSPQPKKKPLDGE     PLMD
320       SSSPQPKKKPLDGEY     PLMD
372       HSSHLKSKKGQSTSR     PLMD
373       SSHLKSKKGQSTSRH     PLMD
382       QSTSRHKKLMFKTEG     PLMD
Methylation
(count: 5)
370       RAHSSHLKSKKGQST     PLMD
372       HSSHLKSKKGQSTSR     PLMD
373       SSHLKSKKGQSTSRH     PLMD
382       QSTSRHKKLMFKTEG     PLMD
386       RHKKLMFKTEGPDSD     PLMD
Propionylation
(count: 3)
292       EEENLRKKGEPHHEL     PLMD
319       TSSSPQPKKKPLDGE     PLMD
320       SSSPQPKKKPLDGEY     PLMD
Neddylation
(count: 5)
320       SSSPQPKKKPLDGEY     PLMD
321       SSPQPKKKPLDGEYF     PLMD
370       RAHSSHLKSKKGQST     PLMD
372       HSSHLKSKKGQSTSR     PLMD
373       SSHLKSKKGQSTSRH     PLMD

※ Protein-Protein Interaction

NetworkInteraction
ABSource
A8MT69P04637HPRD
A9UF04P04637MINT
B1AJR8P04637BioGRID
B7Z4V2P04637MINT
C9JP52P04637BioGRID
E7ESA6P04637HPRD; IntAct; MINT
E7EX81P04637HPRD; MINT
E9PAT7P04637HPRD
E9PFC7P04637HPRD
E9PG89P04637HPRD
E9PHZ3P04637HPRD
E9PMS4P04637BioGRID
F5GXF0P04637HPRD; MINT
F5HB16P04637BioGRID
F8WEU1P04637MINT
G3V1P6P04637HPRD
G3V1V9P04637IntAct
H0Y7U1P04637BioGRID
H0YBT0P04637IntAct
H0YG33P04637HPRD
H3BSF1P04637MINT
H7C2I1P04637HPRD
O00231P04637HPRD; IntAct; MINT
O00255P04637IntAct
O14503P04637MINT
O14576P04637MINT
O14641P04637HPRD; IntAct; MINT
O14757P04637HPRD; MINT
O14920P04637DIP; MINT
O14965P04637HPRD
O14980P04637DIP; MINT
O15111P04637HPRD
O15126P04637HPRD; IntAct; MINT
O15151P04637HPRD; DIP; IntAct; MINT
O15169P04637IntAct
O15297P04637HPRD
O15350P04637HPRD
O15379P04637HPRD; IntAct
O43257P04637HPRD
O43261P04637HPRD; IntAct; MINT
O43474P04637HPRD
O43524P04637IntAct
O43715P04637HPRD
O60285P04637IntAct
O60551P04637HPRD; MINT
O60729P04637HPRD
O60936P04637DIP
O75150P04637IntAct
O75528P04637HPRD
O75569P04637HPRD
O75925P04637HPRD; IntAct
O75928P04637IntAct
O95376P04637HPRD; IntAct; MINT
O95863P04637MINT
O95967P04637HPRD
O95997P04637HPRD
O96017P04637MINT;HPRD
P00374P04637HPRD
P00480P04637BioGRID
P00491P04637HPRD; IntAct; MINT
P00519P04637HPRD
P02749P04637IntAct
P03120P04637MINT
P03372P04637HPRD
P04019P04637MINT
P04150P04637HPRD
P04183P04637HPRD; IntAct; MINT
P04271P04637HPRD
P04637P04637HPRD; DIP; IntAct; MINT
P04637P04792HPRD; IntAct; MINT
P04637P05109HPRD; IntAct; MINT
P04637P05112BioGRID
P04637P05387BioGRID
P04637P05549HPRD
P04637P06400IntAct
P04637P06493HPRD; DIP
P04637P06748HPRD; IntAct; MINT;IntAct
P04637P07384HPRD
P04637P07900HPRD; DIP
P04637P08047HPRD; MINT
P04637P08238HPRD
P04637P09429HPRD; DIP; IntAct
P04637P09529BioGRID
P04637P09874HPRD; DIP; IntAct; MINT
P04637P09884HPRD
P04637P0CG47HPRD; IntAct
P04637P0CG48MINT
P04637P10275MINT
P04637P10415HPRD; DIP; IntAct; MINT
P04637P10828HPRD; DIP
P04637P11021MINT
P04637P11274HPRD; IntAct
P04637P11387HPRD
P04637P11388HPRD
P04637P12004BioGRID
P04637P12429HPRD; IntAct; MINT
P04637P12956HPRD; IntAct
P04637P13497IntAct
P04637P13639HPRD
P04637P13693MINT
P04637P14174HPRD
P04637P15559HPRD; DIP
P04637P17028HPRD; IntAct; MINT
P04637P17252HPRD
P04637P17676IntAct
P04637P17844HPRD; IntAct;IntAct
P04637P18146HPRD
P04637P18283IntAct
P04637P18754MINT
P04637P18847HPRD; IntAct
P04637P18887IntAct
P04637P19447HPRD
P04637P19525HPRD
P04637P19544HPRD
P04637P20023HPRD
P04637P20042HPRD; IntAct; MINT
P04637P20073MINT
P04637P20226HPRD; IntAct
P04637P20248HPRD
P04637P20338HPRD; IntAct; MINT
P04637P21673HPRD; IntAct; MINT
P04637P23511IntAct;HPRD
P04637P24522MINT
P04637P24941HPRD
P04637P25208HPRD; IntAct
P04637P25963HPRD
P04637P26447HPRD; MINT
P04637P26583HPRD
P04637P27361HPRD
P04637P27694HPRD; DIP; IntAct
P04637P27695HPRD
P04637P28360HPRD
P04637P28482HPRD
P04637P29034HPRD
P04637P29320HPRD
P04637P29590HPRD; IntAct; MINT;IntAct
P04637P29965HPRD
P04637P30153MINT
P04637P30419HPRD; MINT
P04637P31350HPRD; DIP
P04637P31947IntAct
P04637P32745HPRD
P04637P32780HPRD; MINT
P04637P34931MINT
P04637P35232HPRD; IntAct; MINT
P04637P35354HPRD
P04637P36405HPRD; IntAct; MINT
P04637P36873HPRD;IntAct
P04637P36956IntAct
P04637P38398DIP; MINT
P04637P38646HPRD; MINT
P04637P38936MINT
P04637P41218HPRD; MINT
P04637P41235HPRD
P04637P42345MINT
P04637P42680HPRD
P04637P42694MINT
P04637P42773HPRD; IntAct; MINT
P04637P42858HPRD; IntAct
P04637P43356IntAct
P04637P45983HPRD; MINT
P04637P45984HPRD
P04637P46821MINT
P04637P48643HPRD; IntAct; MINT
P04637P48729HPRD
P04637P48730HPRD; MINT
P04637P49459HPRD; DIP
P04637P49642HPRD
P04637P49841MINT;HPRD
P04637P49848DIP
P04637P49888HPRD; IntAct; MINT
P04637P50453HPRD; IntAct; MINT
P04637P50748BioGRID
P04637P50750HPRD
P04637P51532IntAct
P04637P51587HPRD; DIP
P04637P51784IntAct
P04637P51813IntAct; MINT
P04637P51946HPRD
P04637P51948HPRD
P04637P51959HPRD
P04637P52292HPRD
P04637P53350HPRD; MINT
P04637P53779HPRD
P04637P54132HPRD
P04637P55060IntAct
P04637P55199HPRD
P04637P55209HPRD
P04637P55774HPRD; IntAct; MINT
P04637P60484HPRD
P04637P60568BioGRID
P04637P60953HPRD; IntAct; MINT
P04637P61086HPRD
P04637P61201HPRD
P04637P61224MINT
P04637P61289MINT;HPRD
P04637P61964IntAct
P04637P61978MINT
P04637P61981HPRD
P04637P62081IntAct
P04637P62136MINT;HPRD
P04637P62328IntAct
P04637P62988DIP
P04637P63104HPRD; MINT
P04637P63151MINT
P04637P63162HPRD; IntAct
P04637P63165HPRD; DIP
P04637P63279HPRD; DIP; IntAct; MINT
P04637P67775HPRD
P04637P67809HPRD
P04637P68133HPRD
P04637P68400HPRD
P04637P78527HPRD
P04637P84022HPRD
P04637P84090HPRD; IntAct; MINT
P04637Q00005HPRD
P04637Q00535HPRD
P04637Q00987HPRD; DIP; IntAct; MINT
P04637Q01094HPRD
P04637Q01484IntAct
P04637Q02447HPRD
P04637Q02880HPRD
P04637Q03013HPRD; IntAct; MINT
P04637Q03164IntAct
P04637Q03468HPRD
P04637Q03701HPRD; MINT
P04637Q05086HPRD; IntAct; MINT
P04637Q06187HPRD
P04637Q06609IntAct;HPRD
P04637Q06945DIP
P04637Q07817HPRD; MINT;IntAct
P04637Q09472HPRD; DIP; IntAct; MINT
P04637Q12772IntAct
P04637Q12824HPRD
P04637Q12873MINT
P04637Q12888HPRD; DIP; IntAct
P04637Q13043HPRD
P04637Q13098HPRD
P04637Q13155DIP
P04637Q13190HPRD; IntAct; MINT
P04637Q13227HPRD
P04637Q13263IntAct
P04637Q13315HPRD; MINT
P04637Q13330HPRD
P04637Q13362MINT
P04637Q13526HPRD; IntAct; MINT
P04637Q13535HPRD; IntAct
P04637Q13547HPRD; IntAct; MINT
P04637Q13625DIP; IntAct; MINT;HPRD
P04637Q13972MINT
P04637Q14061HPRD; IntAct; MINT
P04637Q14151MINT
P04637Q14186HPRD
P04637Q14191HPRD; IntAct
P04637Q14676HPRD
P04637Q14695IntAct; MINT
P04637Q14974HPRD
P04637Q14999IntAct
P04637Q15013IntAct; MINT
P04637Q15102HPRD; IntAct; MINT
P04637Q15181HPRD; IntAct
P04637Q15291IntAct
P04637Q15392HPRD
P04637Q15424MINT
P04637Q15486HPRD; IntAct; MINT
P04637Q15572HPRD
P04637Q15573HPRD
P04637Q15596IntAct
P04637Q15648HPRD; DIP; MINT
P04637Q15672IntAct
P04637Q15759IntAct
P04637Q15796HPRD; IntAct
P04637Q15831HPRD; IntAct
P04637Q15843HPRD
P04637Q16363HPRD; IntAct
P04637Q16539MINT
P04637Q16594HPRD; DIP
P04637Q16611HPRD
P04637Q16637HPRD; MINT
P04637Q16665HPRD
P04637Q16666DIP;HPRD
P04637Q2KN33MINT
P04637Q4LE28HPRD; DIP; MINT
P04637Q53GS9IntAct
P04637Q53T94HPRD
P04637Q5JVS0HPRD
P04637Q5SRQ6HPRD
P04637Q5VTR2IntAct
P04637Q66K89HPRD
P04637Q6LET9MINT
P04637Q6NUQ0MINT
P04637Q6UW56MINT
P04637Q6ZSW6MINT
P04637Q7L1I2BioGRID
P04637Q7L5N1HPRD
P04637Q7LG56HPRD; DIP
P04637Q7Z2E3IntAct
P04637Q7Z566MINT
P04637Q7Z6Z7IntAct;HPRD
P04637Q86TM6HPRD; MINT
P04637Q86WX3IntAct
P04637Q86XK2HPRD; IntAct
P04637Q86Z02HPRD; IntAct
P04637Q8IW41HPRD; IntAct
P04637Q8IWT3HPRD; IntAct
P04637Q8IZD2IntAct
P04637Q8N114HPRD
P04637Q8N2W9HPRD; IntAct; MINT
P04637Q8N488MINT
P04637Q8N726DIP; IntAct
P04637Q8N9B5IntAct
P04637Q8N9N5MINT;HPRD
P04637Q8NA92HPRD; IntAct; MINT
P04637Q8NHY2HPRD; IntAct; MINT
P04637Q8TAF3IntAct
P04637Q8TAQ5MINT
P04637Q8TBK6IntAct; MINT;HPRD
P04637Q8TDN4HPRD; IntAct
P04637Q8TDT2BioGRID
P04637Q8TDY2IntAct
P04637Q8WTS6HPRD; DIP; IntAct
P04637Q8WUF5HPRD; DIP; MINT
P04637Q8WWV6IntAct
P04637Q8WYH8HPRD
P04637Q92754HPRD
P04637Q92769HPRD
P04637Q92793IntAct
P04637Q92831HPRD; IntAct
P04637Q92841IntAct
P04637Q92890MINT
P04637Q92905HPRD
P04637Q92922IntAct
P04637Q92993IntAct;HPRD
P04637Q92994HPRD
P04637Q93009HPRD; DIP; IntAct; MINT
P04637Q96A56HPRD
P04637Q96EB6HPRD; IntAct
P04637Q96G74IntAct
P04637Q96GM5HPRD
P04637Q96GM8MINT
P04637Q96KB5HPRD; IntAct
P04637Q96KQ4MINT
P04637Q96M61HPRD; IntAct; MINT
P04637Q96PM5HPRD; DIP; IntAct; MINT
P04637Q96PM9IntAct
P04637Q96PU4IntAct
P04637Q96S44HPRD
P04637Q96SB4MINT
P04637Q96ST3HPRD; IntAct
P04637Q99547HPRD; IntAct; MINT
P04637Q99608HPRD
P04637Q99612HPRD
P04637Q99627HPRD
P04637Q99728HPRD; IntAct
P04637Q99816HPRD
P04637Q99856HPRD
P04637Q99966IntAct
P04637Q99973HPRD
P04637Q99986HPRD; IntAct
P04637Q9BQD7HPRD; IntAct
P04637Q9BT78HPRD
P04637Q9BTK6MINT
P04637Q9BTV7HPRD
P04637Q9BUJ2IntAct;HPRD; MINT
P04637Q9BV47IntAct
P04637Q9BVP2HPRD; IntAct
P04637Q9BWC9HPRD; IntAct; MINT
P04637Q9BX70HPRD; IntAct; MINT
P04637Q9C0J8HPRD; IntAct
P04637Q9GZV1HPRD
P04637Q9H0Q3IntAct; MINT
P04637Q9H2X6HPRD; IntAct; MINT
P04637Q9H3D4HPRD; IntAct
P04637Q9H3E2BioGRID
P04637Q9H4B4HPRD
P04637Q9H7Z6IntAct; MINT
P04637Q9H9J4MINT
P04637Q9HBD4HPRD
P04637Q9HBJ7MINT
P04637Q9HBM6HPRD
P04637Q9NPI1DIP; IntAct
P04637Q9NRG4HPRD; DIP
P04637Q9NS56HPRD; MINT
P04637Q9NTD8DIP
P04637Q9NVC6HPRD
P04637Q9NVN8IntAct
P04637Q9NZB8MINT
P04637Q9NZC7HPRD; MINT
P04637Q9UBE0MINT
P04637Q9UBF1IntAct
P04637Q9UBW8HPRD
P04637Q9UER7HPRD; DIP; IntAct
P04637Q9UHC7MINT
P04637Q9UK53HPRD
P04637Q9UKY1HPRD; MINT
P04637Q9UM63HPRD
P04637Q9UN74HPRD; IntAct; MINT
P04637Q9UNH5HPRD
P04637Q9UNL4MINT;HPRD
P04637Q9UNS2HPRD
P04637Q9UQR1HPRD
P04637Q9Y276MINT
P04637Q9Y297DIP
P04637Q9Y2A0IntAct
P04637Q9Y3T9IntAct
P04637Q9Y675MINT
P04637RTDDIP