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PDBsum entry 6yf3

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protein ligands metals links
Isomerase PDB id
6yf3

 

 

 

 

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Contents
Protein chain
108 a.a.
Ligands
OOZ
Metals
_NA
_CD
_CL ×2
Waters ×142
PDB id:
6yf3
Name: Isomerase
Title: Fkbp12 in complex with the bmp potentiator compound 10 at 1.00a resolution
Structure: Peptidyl-prolyl cis-trans isomerase fkbp1a. Chain: a. Synonym: ppiase fkbp1a,12 kda fk506-binding protein,fkbp-12, calstabin-1,fk506-binding protein 1a,fkbp-1a,immunophilin fkbp12, rotamase. Engineered: yes
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: fkbp1a, fkbp1, fkbp12. Expressed in: escherichia coli bl21. Expression_system_taxid: 511693.
Resolution:
1.00Å     R-factor:   0.157     R-free:   0.158
Authors: J.Kallen
Key ref: m.h.larraufie et al. (2021). Phenotypic screen identifies calcineurin-sparing FK506 analogs as BMP potentiators for treatment of acute kidney injury. Cell Chem Biol, 0, . PubMed id: 33894161
Date:
25-Mar-20     Release date:   10-Mar-21    
PROCHECK
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 Headers
 References

Protein chain
Pfam   ArchSchema ?
P62942  (FKB1A_HUMAN) -  Peptidyl-prolyl cis-trans isomerase FKBP1A from Homo sapiens
Seq:
Struc:
108 a.a.
108 a.a.*
Key:    PfamA domain  Secondary structure
* PDB and UniProt seqs differ at 1 residue position (black cross)

 Enzyme reactions 
   Enzyme class: E.C.5.2.1.8  - peptidylprolyl isomerase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]
      Reaction: [protein]-peptidylproline (omega=180) = [protein]-peptidylproline (omega=0)
Peptidylproline (omega=180)
= peptidylproline (omega=0)
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

 
    Added reference    
 
 
Cell Chem Biol 0: (2021)
PubMed id: 33894161  
 
 
Phenotypic screen identifies calcineurin-sparing FK506 analogs as BMP potentiators for treatment of acute kidney injury.
m.h.larraufie, x.gao, x.xia, p.j.devine, d.liu, a.harsch, j.kallen, n.savage, j.ding, k.tan, m.mihalic, p.krastel, g.michaud, m.salcius, a.izaac, j.gao, f.harbinski, s.roggos.canham, s.bushell, e.altinoglu, p.lustenberger, e.willic.fryer, f.cong, l.klickstein, j.tallarico, r.jain, d.m.ros.wang.
 
  ABSTRACT  
 
No abstract given.

 

 

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