PDB ID 5CBX     CHAIN A
Protein name AncGR DNA Binding Domain
PDB 5CBX
The number of similar proteins 26
The number of binding states 2
The number of binding partners 1

Coloring

Unicolor (beige)

The number of binding partners

Group

Binding
state
Binding partners
5CBX (CHAIN: A)
1 5CBX  
2 Monomeric state

Downdload

Format:

Molecule viewer


Only interaction residues
#binding
partners
  1
  0

Sequence information

1   MHHHHHHSSG   VDLGTENLYF   QSNAGPPPKI   CLVCGDEASG   CHYGVLTCGS   50
51   CKVFFKRAVE   GQHNYLCAGR   NDCIIDKIRR   KNCPACRFRK   CLQAGMNLEA   100
101   RKTKK           150

Variants

Residue AA Source dbSNP Clinical
Significance
Allele
Frequency
(> 0.0001)
Disease name
451_GLY ARG ClinVar
chr4:149181130
rs121912566
Pathogenic - Autosomal dominant pseudohypoaldosteronism type 1 [MONDO:MONDO:0008329,MedGen:C1449842,OMIM:177735,Orphanet:171871,Orphanet:756]
463_CYS TER ClinVar
chr4:149115976
rs121912564
Pathogenic - Autosomal dominant pseudohypoaldosteronism type 1 [MONDO:MONDO:0008329,MedGen:C1449842,OMIM:177735,Orphanet:171871,Orphanet:756]
469_ARG TER ClinVar
chr4:149115960
rs1131691921
Pathogenic/Likely pathogenic - not provided|Autosomal dominant pseudohypoaldosteronism type 1|Pseudohyperaldosteronism type 2 [MedGen:C3661900|MONDO:MONDO:0008329,MedGen:C1449842,OMIM:177735,Orphanet:171871,Orphanet:756|MONDO:MONDO:0011517,MedGen:C1854631,OMIM:605115,Orphanet:88660]; Autosomal dominant pseudohypoaldosteronism type 1|NR3C2-related condition [MONDO:MONDO:0008329,MedGen:C1449842,OMIM:177735,Orphanet:171871,Orphanet:756|]
479_ARG TER ClinVar
chr5:142689695
rs1658915833
Pathogenic - not provided [MedGen:C3661900]
479_ARG GLN 8.3kJPN
chr5:142689694
rs1400646165
- 0.0001 -
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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.