Structure of PDB 1kbp Chain D Binding Site BS02
Receptor Information
>1kbp Chain D (length=424) Species:
3885
(Phaseolus vulgaris) [
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RDMPLDSDVFRVPPGYNAPQQVHITQGDLVGRAMIISWVTMDEPGSSAVR
YWSEKNGRKRIAKGKMSTYRFFNYSSGFIHHTTIRKLKYNTKYYYEVGLR
NTTRRFSFITPPQTGLDVPYTFGLIGDLGQSFDSNTTLSHYELSPKKGQT
VLFVGDLSYADRYPNHDNVRWDTWGRFTERSVAYQPWIWTAGNHEIEFAP
EINETEPFKPFSYRYHVPYEASQSTSPFWYSIKRASAHIIVLSSYSAYGR
GTPQYTWLKKELRKVKRSETPWLIVLMHSPLYNSYNHHFMEGEAMRTKFE
AWFVKYKVDVVFAGHVHAYERSERVSNIAYKITDGLCTPVKDQSAPVYIT
IGDAGNYGVIDSNMIQPQPEYSAFREASFGHGMFDIKNRTHAHFSWNRNQ
DGVAVEADSVWFFNRHWYPVDDST
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
1kbp Chain D Residue 439 [
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Receptor-Ligand Complex Structure
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PDB
1kbp
Mechanism of Fe(III)-Zn(II) purple acid phosphatase based on crystal structures.
Resolution
2.65 Å
Binding residue
(original residue number in PDB)
D164 N201 H286 H323
Binding residue
(residue number reindexed from 1)
D156 N193 H278 H315
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
D135 D164 Y167 N201 H202 H286 H295 H296 H323 H325
Catalytic site (residue number reindexed from 1)
D127 D156 Y159 N193 H194 H278 H287 H288 H315 H317
Enzyme Commision number
3.1.3.2
: acid phosphatase.
Gene Ontology
Molecular Function
GO:0003993
acid phosphatase activity
GO:0008199
ferric iron binding
GO:0008270
zinc ion binding
GO:0016787
hydrolase activity
GO:0046872
metal ion binding
Cellular Component
GO:0005576
extracellular region
View graph for
Molecular Function
View graph for
Cellular Component
External links
PDB
RCSB:1kbp
,
PDBe:1kbp
,
PDBj:1kbp
PDBsum
1kbp
PubMed
8683579
UniProt
P80366
|PPAF_PHAVU Fe(3+)-Zn(2+) purple acid phosphatase
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