PDB ID 1B3U     CHAIN A
Protein name PROTEIN (PROTEIN PHOSPHATASE PP2A)
Uniprot Accession P30153
The number of similar proteins 16
The number of binding states 7
The number of binding partners 6

Coloring

Unicolor (beige)

The number of binding partners

Group

Binding
state
Binding partners
1B3U (CHAIN: A)
1 Monomeric state
2 P67775  
3 Q9W9P1  
4 P67775   Q13362  
5 P67775   Q9Y5P8  
6 P67775   P63151  
7 P67775   Q8BH58  

Downdload

Format:

Molecule viewer

#binding
partners
  5
  4
  3
  2
  1
  0

Sequence information

1   AAADGDDSLY   PIAVLIDELR   NEDVQLRLNS   IKKLSTIALA   LGVERTRSEL   50
51   LPFLTDTIYD   EDEVLLALAE   QLGTFTTLVG   GPEYVHCLLP   PLESLATVEE   100
101   TVVRDKAVES   LRAISHEHSP   SDLEAHFVPL   VKRLAGGDWF   TSRTSACGLF   150
151   SVCYPRVSSA   VKAELRQYFR   NLCSDDTPMV   RRAAASKLGE   FAKVLELDNV   200
201   KSEIIPMFSN   LASDEQDSVR   LLAVEACVNI   AQLLPQEDLE   ALVMPTLRQA   250
251   AEDKSWRVRY   MVADKFTELQ   KAVGPEITKT   DLVPAFQNLM   KDCEAEVRAA   300
301   ASHKVKEFCE   NLSADCRENV   IMSQILPCIK   ELVSDANQHV   KSALASVIMG   350
351   LSPILGKDNT   IEHLLPLFLA   QLKDECPEVR   LNIISNLDCV   NEVIGIRQLS   400
401   QSLLPAIVEL   AEDAKWRVRL   AIIEYMPLLA   GQLGVEFFDE   KLNSLCMAWL   450
451   VDHVYAIREA   ATSNLKKLVE   KFGKEWAHAT   IIPKVLAMSG   DPNYLHRMTT   500
501   LFCINVLSEV   CGQDITTKHM   LPTVLRMAGD   PVANVRFNVA   KSLQKIGPIL   550
551   DNSTLQSEVK   PILEKLTQDQ   DVDVKYFAQE   ALTVLSLA     600

Variants

Residue AA Source dbSNP Clinical
Significance
Allele
Frequency
(4.7kJPN)
Disease name
3_GLY ARG 4.7kJPN
chr11:111637040
rs1555053169
- 0.0002 -
9_LEU VAL 4.7kJPN
chr19:52693377
rs1298006628
- 0.0001 -
25_GLN ARG 4.7kJPN
chr11:111636973
-
- 0.0001 -
48_SER THR 4.7kJPN
chr19:52705264
-
- 0.0001 -
50_LEU PHE 4.7kJPN
chr19:52705269
-
- 0.0001 -
74_THR ASN 4.7kJPN
chr19:52709270
-
- 0.0001 -
76_THR ALA 4.7kJPN
chr19:52709275
-
- 0.0001 -
77_GLY ASP ClinVar
chr11:111635566
rs1805076
Pathogenic - Lung cancer [MedGen:C0684249,OMIM:211980,SNOMED CT:187875007]
77_THR ILE 4.7kJPN
chr19:52709279
-
- 0.0001 -
104_ARG CYS 4.7kJPN
chr11:111631733
rs782083920
- 0.0006 -
117_GLU ASP 4.7kJPN
chr11:111631692
-
- 0.0003 -
131_VAL LEU VAR_073718 -
Disease - Mental retardation, autosomal dominant 36 (MRD36) [MIM:616362]
134_LEU SER 4.7kJPN
chr11:111631642
-
- 0.0001 -
144_THR LYS 4.7kJPN
chr11:111631612
rs115633648
- 0.0027 -
163_ALA VAL 4.7kJPN
chr19:52714733
rs749322788
- 0.0001 -
178_PRO LEU VAR_074488 rs786205228
Disease - Mental retardation, autosomal dominant 36 (MRD36) [MIM:616362]
178_PRO LEU ClinVar
chr19:52715971
rs786205228
Pathogenic - Malignant neoplasm of body of uterus [MedGen:C0153574,Orphanet:ORPHA213569]; Mental retardation, autosomal dominant 36 [MedGen:C4225352,OMIM:616362,Orphanet:ORPHA457284]; Uterine Carcinosarcoma [MedGen:C0280630]; not provided [MedGen:CN517202]
178_PRO ARG ClinVar
chr19:52715971
rs786205228
Likely pathogenic - Malignant neoplasm of body of uterus [MedGen:C0153574,Orphanet:ORPHA213569]; Uterine Carcinosarcoma [MedGen:C0280630]
181_ARG TRP VAR_074489 rs786205227
Disease - Mental retardation, autosomal dominant 36 (MRD36) [MIM:616362]
181_ARG TRP ClinVar
chr19:52715979
rs786205227
Pathogenic - Mental retardation, autosomal dominant 36 [MedGen:C4225352,OMIM:616362,Orphanet:ORPHA457284]; not provided [MedGen:CN517202]
182_ARG TRP ClinVar
chr19:52715982
rs1057519946
Likely pathogenic - Adenocarcinoma of prostate [MedGen:C0007112]; Adenocarcinoma of stomach [MedGen:C0278701]; Lung adenocarcinoma [Human Phenotype Ontology:HP:0030078,MeSH:C538231,MedGen:C0152013]; Malignant neoplasm of body of uterus [MedGen:C0153574,Orphanet:ORPHA213569]; Neoplasm of the breast [Human Phenotype Ontology:HP:0100013,MeSH:D001943,MedGen:C1458155,Orphanet:ORPHA180250,SNOMED CT:126926005]; Neoplasm of the large intestine [Human Phenotype Ontology:HP:0100834,MeSH:D015179,MedGen:C0009404,SNOMED CT:126837005]; Ovarian Serous Cystadenocarcinoma [MedGen:C0279663]; Squamous cell carcinoma of the head and neck [MeSH:C535575,MedGen:C1168401,OMIM:275355,Orphanet:ORPHA67037]; Uterine Carcinosarcoma [MedGen:C0280630]
182_ARG GLN ClinVar
chr19:52715983
rs1057519947
Likely pathogenic - Adenocarcinoma of prostate [MedGen:C0007112]; Adenocarcinoma of stomach [MedGen:C0278701]; Lung adenocarcinoma [Human Phenotype Ontology:HP:0030078,MeSH:C538231,MedGen:C0152013]; Malignant neoplasm of body of uterus [MedGen:C0153574,Orphanet:ORPHA213569]; Neoplasm of the breast [Human Phenotype Ontology:HP:0100013,MeSH:D001943,MedGen:C1458155,Orphanet:ORPHA180250,SNOMED CT:126926005]; Neoplasm of the large intestine [Human Phenotype Ontology:HP:0100834,MeSH:D015179,MedGen:C0009404,SNOMED CT:126837005]; Ovarian Serous Cystadenocarcinoma [MedGen:C0279663]; Squamous cell carcinoma of the head and neck [MeSH:C535575,MedGen:C1168401,OMIM:275355,Orphanet:ORPHA67037]; Uterine Carcinosarcoma [MedGen:C0280630]; not provided [MedGen:CN517202]
182_ARG GLY ClinVar
chr19:52715982
rs1057519946
Likely pathogenic - Adenocarcinoma of prostate [MedGen:C0007112]; Adenocarcinoma of stomach [MedGen:C0278701]; Lung adenocarcinoma [Human Phenotype Ontology:HP:0030078,MeSH:C538231,MedGen:C0152013]; Malignant neoplasm of body of uterus [MedGen:C0153574,Orphanet:ORPHA213569]; Neoplasm of the breast [Human Phenotype Ontology:HP:0100013,MeSH:D001943,MedGen:C1458155,Orphanet:ORPHA180250,SNOMED CT:126926005]; Neoplasm of the large intestine [Human Phenotype Ontology:HP:0100834,MeSH:D015179,MedGen:C0009404,SNOMED CT:126837005]; Ovarian Serous Cystadenocarcinoma [MedGen:C0279663]; Squamous cell carcinoma of the head and neck [MeSH:C535575,MedGen:C1168401,OMIM:275355,Orphanet:ORPHA67037]; Uterine Carcinosarcoma [MedGen:C0280630]
229_ASN SER 4.7kJPN
chr19:52716245
-
- 0.0001 -
240_GLU ASP 4.7kJPN
chr11:111626103
-
- 0.0001 -
241_ALA THR 4.7kJPN
chr19:52716280
-
- 0.0001 -
257_ARG HIS VAR_074490 rs863225094
Disease - Mental retardation, autosomal dominant 36 (MRD36) [MIM:616362]
257_ARG HIS ClinVar
chr19:52716329
rs863225094
Pathogenic - Abnormal facial shape [Human Phenotype Ontology:HP:0001999,MedGen:C0424503]; Autistic behavior [Human Phenotype Ontology:HP:0000729,MedGen:C0856975]; Brachydactyly [Human Phenotype Ontology:HP:0001156,MedGen:C0221357,Orphanet:ORPHA294937,SNOMED CT:43476002]; Generalized hypotonia [Human Phenotype Ontology:HP:0001290,MedGen:C1858120]; Impaired use of nonverbal behaviors [Human Phenotype Ontology:HP:0000758,MedGen:C4021798]; Mental retardation, autosomal dominant 36 [MedGen:C4225352,OMIM:616362,Orphanet:ORPHA457284]; Microcephaly [Human Phenotype Ontology:HP:0000252,MedGen:C4551563]; Profound global developmental delay [Human Phenotype Ontology:HP:0012736,MedGen:C3553450]; Stereotypy [Human Phenotype Ontology:HP:0000733,MedGen:C0038273]; Synophrys [Human Phenotype Ontology:HP:0000664,MedGen:C0431447]; not provided [MedGen:CN517202]
257_ARG CYS 4.7kJPN
chr11:111626054
rs1283934812
- 0.0001 -
257_ARG SER 4.7kJPN
chr19:52716328
-
- 0.0001 -
294_GLU ASP 4.7kJPN
chr11:111625741
rs1347203213
- 0.0016 -
317_ARG GLY 4.7kJPN
chr11:111625264
rs782527776
- 0.0004 -
318_GLU TER 4.7kJPN
chr11:111625261
-
- 0.0001 -
341_LYS ARG 4.7kJPN
chr11:111624270
rs115165302
- 0.0001 -
375_GLU ASP 4.7kJPN
chr11:111624167
-
- 0.0002 -
388_ASP GLY 4.7kJPN
chr11:111623019
-
- 0.0002 -
427_PRO LEU 4.7kJPN
chr11:111622902
rs1555048136
- 0.0001 -
477_ALA VAL 4.7kJPN
chr19:52724301
-
- 0.0001 -
490_GLY ARG 4.7kJPN
chr19:52724339
rs969720045
- 0.0003 -
500_THR MET 4.7kJPN
chr19:52724370
-
- 0.0001 -
512_GLY ARG 4.7kJPN
chr19:52725370
rs770604606
- 0.0001 -
523_THR MET 4.7kJPN
chr19:52725404
rs747537922
- 0.0001 -
526_ARG CYS 4.7kJPN
chr19:52725412
rs770194852
- 0.0001 -
528_ALA THR 4.7kJPN
chr19:52725418
-
- 0.0001 -
573_ASP GLU 4.7kJPN
chr11:111612808
rs143440908
- 0.0003 -
574_VAL ILE 4.7kJPN
chr19:52729031
rs1158328586
- 0.0001 -
(Powered by wupsivus)

Reference

PiSite: a database of protein interaction sites using multiple binding states in the PDB, Miho Higurashi, Takashi Ishida and Kengo Kinoshita, Nucleic Acids Research 2009 37(Database issue):D360-D364

COPYRIGHTc2008-2019 Miho Higurashi, Takashi Ishida and Kengo Kinoshita. All rights reserved.