PDB ID 3FX0     CHAIN A
Protein name NF-kappa-B essential modulator
Uniprot Accession Q9Y6K9
The number of similar proteins 18
The number of binding states 6
The number of binding partners 4

Coloring

Unicolor (beige)

The number of binding partners

Group

Binding
state
Binding partners
3FX0 (CHAIN: A)
1 Q9Y6K9  
2 O88522   P62988  
3 O88522   Q96EP0  
4 D3DWY0   6XX0   6XX0  
5 O88522   Q96C32   Q96C32  
6 Q9Y6K9   Q96EP0   P0CG48   P0CG48  

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Format:

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Only interaction residues
#binding
partners
  4
  3
  2
  1
  0

Sequence information

1   GSHMKSSVVG   SERKRGMQLE   DLKQQLQQAE   EALVAKQEVI   DKLKEEAEQH   50
51   KIVMETVPVL   KAQADIYKAD   FQAERQAREK   LAEKKELLQE   QLEQLQ   100

Variants

Residue AA Source dbSNP Clinical
Significance
Allele
Frequency
(> 0.0001)
Disease name
288_ALA GLY VAR_011322 rs137853330
LP/P - Ectodermal dysplasia and immunodeficiency 1 (EDAID1) [MIM:300291]
288_ALA GLY ClinVar
chrX:153791119
rs137853330
Pathogenic - Ectodermal dysplasia and immunodeficiency 1 [MONDO:MONDO:0020740,MedGen:C1846008,OMIM:300291,Orphanet:238468,Orphanet:98813]
290_GLN TER ClinVar
chrX:153791124
rs1156900338
Pathogenic - not provided [MedGen:CN517202]
311_ASP ASN VAR_011323 rs179363867
LP/P - Ectodermal dysplasia and immunodeficiency 1 (EDAID1) [MIM:300291]
311_ASP ASN ClinVar
chrX:153791792
rs179363867
Likely pathogenic - not provided|Ectodermal dysplasia and immunodeficiency 1 [MedGen:CN517202|MONDO:MONDO:0020740,MedGen:C1846008,OMIM:300291,Orphanet:238468,Orphanet:98813]
312_PHE LEU ClinVar
chrX:153791797
rs2148385082
Likely pathogenic - not provided [MedGen:C3661900]
314_ALA PRO VAR_072606 -
LP/P - Incontinentia pigmenti (IP) [MIM:308300]
315_GLU ALA VAR_031959 rs137853331
LP/P - Immunodeficiency 33 (IMD33) [MIM:300636]
315_GLU ALA ClinVar
chrX:153791805
rs137853331
Pathogenic - Immunodeficiency 33 [MONDO:MONDO:0010386,MedGen:C1970879,OMIM:300636,Orphanet:319605,Orphanet:319612]
319_ARG GLN VAR_031960 rs137853332
LP/P - Immunodeficiency 33 (IMD33) [MIM:300636]
319_ARG GLN ClinVar
chrX:153791817
rs137853332
Pathogenic - Immunodeficiency 33 [MONDO:MONDO:0010386,MedGen:C1970879,OMIM:300636,Orphanet:319605,Orphanet:319612]
322_LEU PRO VAR_072607 -
LP/P - Incontinentia pigmenti (IP) [MIM:308300]
323_ALA PRO VAR_042666 rs179363865
LP/P - Incontinentia pigmenti (IP) [MIM:308300]
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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.