PDB ID 1Z8J     CHAIN A
Protein name Thrombin light chain
Uniprot Accession P00734
The number of similar proteins 351
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
1Z8J (CHAIN: A)
1 P00734  
2 Monomeric state
3 P00734   P01008  
4 P00734   P00734  
5 P00734   P00734  
6 P00734   P00734   P00734  
7 P00734   P00734   P00734  

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Format:

Molecule viewer


Only interaction residues
#binding
partners
  4
  3
  2
  1
  0

Sequence information

1   TFFNPRTFGS   GEADCGLRPL   FEKKSLEDKT   ERELLESYID     50

Variants

Residue AA Source dbSNP Clinical
Significance
Allele
Frequency
(> 0.0001)
Disease name
1D_GLY ALA ClinVar
chr11:46748168
rs2134532862
Likely pathogenic - Congenital prothrombin deficiency [MONDO:MONDO:0013361,MedGen:C0272317,OMIM:613679,Orphanet:325]
1E_SER LEU 8.3kJPN
chr11:46748165
rs200812621
- 0.0004 -
4_ARG TER ClinVar
chr11:46748272
-
Pathogenic - Congenital prothrombin deficiency [MONDO:MONDO:0013361,MedGen:C0272317,OMIM:613679,Orphanet:325]
8_GLU LYS ClinVar
chr11:46748284
rs121918483
Pathogenic - Congenital prothrombin deficiency [MONDO:MONDO:0013361,MedGen:C0272317,OMIM:613679,Orphanet:325]
14C_GLU LYS ClinVar
chr11:46748311
rs121918484
Pathogenic - Congenital prothrombin deficiency [MONDO:MONDO:0013361,MedGen:C0272317,OMIM:613679,Orphanet:325]
14H_GLU GLY ClinVar
chr11:46748327
rs2134533215
Likely pathogenic - Congenital prothrombin deficiency [MONDO:MONDO:0013361,MedGen:C0272317,OMIM:613679,Orphanet:325]
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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.