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PDBsum entry 3ax0

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protein ligands metals Protein-protein interface(s) links
Oxidoreductase/metal transport PDB id
3ax0

 

 

 

 

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Contents
Protein chains
273 a.a.
78 a.a.
Ligands
NO3 ×5
Metals
_CU ×4
Waters ×338
PDB id:
3ax0
Name: Oxidoreductase/metal transport
Title: Crystal structure of streptomyces tyrosinase in a complex with caddie y98f mutant soaked in a cu(ii)-containing solution for 80 hr
Structure: Tyrosinase. Chain: a. Engineered: yes. Melc. Chain: b. Synonym: caddie protein orf378. Engineered: yes. Mutation: yes
Source: Streptomyces castaneoglobisporus. Organism_taxid: 79261. Strain: hut 6202. Gene: tyrc. Expressed in: escherichia coli. Expression_system_taxid: 562. Gene: orf378.
Resolution:
1.40Å     R-factor:   0.170     R-free:   0.195
Authors: Y.Matoba,M.Sugiyama
Key ref: Y.Matoba et al. (2011). A molecular mechanism for copper transportation to tyrosinase that is assisted by a metallochaperone, caddie protein. J Biol Chem, 286, 30219-30231. PubMed id: 21730070
Date:
26-Mar-11     Release date:   29-Jun-11    
PROCHECK
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 Headers
 References

Protein chain
Q83WS2  (Q83WS2_9ACTN) -  Tyrosinase from Streptomyces castaneoglobisporus
Seq:
Struc:
273 a.a.
273 a.a.*
Protein chain
Q83WS1  (Q83WS1_9ACTN) -  MelC from Streptomyces castaneoglobisporus
Seq:
Struc:
126 a.a.
78 a.a.*
Key:    Secondary structure  CATH domain
* PDB and UniProt seqs differ at 2 residue positions (black crosses)

 Enzyme reactions 
   Enzyme class: Chain A: E.C.1.14.18.1  - tyrosinase.
[IntEnz]   [ExPASy]   [KEGG]   [BRENDA]

      Pathway:
Melanin Biosynthesis
      Reaction:
1. L-tyrosine + O2 = L-dopaquinone + H2O
2. 2 L-dopa + O2 = 2 L-dopaquinone + 2 H2O
L-tyrosine
+ O2
= L-dopaquinone
+ H2O
2 × L-dopa
+ O2
= 2 × L-dopaquinone
+ 2 × H2O
      Cofactor: Cu cation
Molecule diagrams generated from .mol files obtained from the KEGG ftp site

 

 
    reference    
 
 
J Biol Chem 286:30219-30231 (2011)
PubMed id: 21730070  
 
 
A molecular mechanism for copper transportation to tyrosinase that is assisted by a metallochaperone, caddie protein.
Y.Matoba, N.Bando, K.Oda, M.Noda, F.Higashikawa, T.Kumagai, M.Sugiyama.
 
  ABSTRACT  
 
No abstract given.

 

 

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