Structure of PDB 2yap Chain A Binding Site BS03
Receptor Information
>2yap Chain A (length=439) Species:
262724
(Thermus thermophilus HB27) [
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GPSFPEPKVVRSQGGLLSLKLSATPTPLAIAGQRATLLTYGGSFPGPTLR
VRPRDTVRLTLENRLPEPTNLHWHGLPISPKVDDPFLEIPPGESWTYEFT
VPKELAGTFWYHPHLHGRVAPQLFAGLLGALVVESSLDAIPELREAEEHL
LVLKDLALQGGRPAPHTPMDWMNGKEGDLVLVNGALRPTLVAQKATLRLR
LLNASNARYYRLALQDHPLYLIAADGGFLEEPLEVSELLLAPGERAEVLV
RLRKEGRFLLQALPYDRGAMGMMDMGGMAHAMPQGPSRPETLLYLIAPKN
PKPLPLPKALSPFPTLPAPVVTRRLVLTEDMMAARFFINGQVFDHRRVDL
KGQAQTVEVWEVENQGDMDHPFHLHVHPFQVLSVGGRPFPYRAWKDVVNL
KAGEVARLLVPLREKGRTVFHCHIVEHEDRGMMGVLEVG
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
2yap Chain A Residue 1465 [
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Receptor-Ligand Complex Structure
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PDB
2yap
X-Ray-Induced Catalytic Active-Site Reduction of a Multicopper Oxidase: Structural Insights Into the Proton-Relay Mechanism and O2-Reduction States.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
H137 H398 H444
Binding residue
(residue number reindexed from 1)
H114 H375 H421
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H95 H97 H135 H137 H393 H396 H398 H444 C445 H446 I447 H450 M455
Catalytic site (residue number reindexed from 1)
H72 H74 H112 H114 H370 H373 H375 H421 C422 H423 I424 H427 M432
Enzyme Commision number
1.10.3.2
: laccase.
Gene Ontology
Molecular Function
GO:0005507
copper ion binding
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
GO:0052716
hydroquinone:oxygen oxidoreductase activity
Cellular Component
GO:0030288
outer membrane-bounded periplasmic space
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Molecular Function
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Cellular Component
External links
PDB
RCSB:2yap
,
PDBe:2yap
,
PDBj:2yap
PDBsum
2yap
PubMed
26627648
UniProt
Q72HW2
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