Structure of PDB 6ttd Chain B Binding Site BS02
Receptor Information
>6ttd Chain B (length=457) Species:
63363
(Aquifex aeolicus) [
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SKQSLNIPGYSLFSDGQRVSITAKWTTLEVIPGKSTDMLVYEIDNEYNPV
IFLRKGQTFSADFVNNSGEDSIIHWHGFRAPWKSDGHPYYAVKDGETYSY
PDFTIIDRSGTYFYHPHPHGRTGYQVYYGLAGMIIIEDEDEDNLKQALDL
EYGVTDIPLIIQDKTFDSSGQLVYNPMGHMGFWGDTILVNLTPNPYMDVE
RKIYRFRILNGSNARPYRLALLRGNQRMRFWVIGVEGGLLDTPKEVNEIL
VAPGERIDILVDFRDASVNDVIKLYNFPHNLIMGMADNSEFEVMEFRVTK
DSAYDKSIPQRLSEVTPINTDGAQVQRITLGMRRMVFTINGETWEDGYAN
PQDINNPKVLFEQNNGDVVILEYVNNTGTYHPMHIHGFQFQVLERSLGPL
GATDLGWKDTVIVAPMETVRIAVDMSHPYNEHQIYLLHCHILEHHDEGMM
VNYRVNA
Ligand information
Ligand ID
CU
InChI
InChI=1S/Cu/q+2
InChIKey
JPVYNHNXODAKFH-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Cu+2]
CACTVS 3.341
[Cu++]
Formula
Cu
Name
COPPER (II) ION
ChEMBL
DrugBank
DB14552
ZINC
PDB chain
6ttd Chain B Residue 702 [
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Receptor-Ligand Complex Structure
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PDB
6ttd
Distal Mutations Shape Substrate-Binding Sites during Evolution of a Metallo-Oxidase into a Laccase
Resolution
1.801 Å
Binding residue
(original residue number in PDB)
H161 H456 H508
Binding residue
(residue number reindexed from 1)
H117 H386 H438
Annotation score
3
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005507
copper ion binding
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
Biological Process
GO:0051301
cell division
Cellular Component
GO:0030288
outer membrane-bounded periplasmic space
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6ttd
,
PDBe:6ttd
,
PDBj:6ttd
PDBsum
6ttd
PubMed
UniProt
O67206
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