Structure of PDB 5lwz Chain B Binding Site BS02
Receptor Information
>5lwz Chain B (length=381) Species:
330879
(Aspergillus fumigatus Af293) [
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SPIEEQATRLLKEVPLIDGHNDFPYMIRGWFRNDINGQDAHLYDMPIGQT
DLQRLQKGLLGGQFWSAFVPCPKNPDKEVGSLEALRQTLQQLDVIHRLIE
RHPTILQFADSAASIWSSFRAGRVASLIGIEGLHQIADSVSALRMLHRLG
VRYVTLTHNCHNAFADAATVSPELHGGLSRKGERLIRELNRMGMMIDLSH
TSHEAQTQALRLSRAPVIYSHSSIYSLRAHARNVTDENLHLLHRNRGVVM
ICFLRELLASEADQATLAHVIDHIIYAGTRIGYEHVGIGSDFDGMLRGPD
GLHDVSCYPALVAGLLERGVSEEDVKRVMGLNVIRVLEEVERVAAELQGA
GEECLCDELDEVWNEDIKEQLTRERERVRKL
Ligand information
Ligand ID
FE
InChI
InChI=1S/Fe/q+3
InChIKey
VTLYFUHAOXGGBS-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Fe+3]
Formula
Fe
Name
FE (III) ION
ChEMBL
DrugBank
DB13949
ZINC
PDB chain
5lwz Chain B Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
5lwz
Gliotoxin Biosynthesis: Structure, Mechanism, and Metal Promiscuity of Carboxypeptidase GliJ.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
H23 D25 E134
Binding residue
(residue number reindexed from 1)
H20 D22 E131
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H23 D25 E134 H161 H203 H224 D294
Catalytic site (residue number reindexed from 1)
H20 D22 E131 H158 H200 H221 D291
Enzyme Commision number
3.4.13.19
: membrane dipeptidase.
Gene Ontology
Molecular Function
GO:0008237
metallopeptidase activity
GO:0016805
dipeptidase activity
GO:0046872
metal ion binding
GO:0070573
metallodipeptidase activity
Biological Process
GO:0006508
proteolysis
GO:0043386
mycotoxin biosynthetic process
GO:0052562
symbiont-mediated suppression of host immune response
GO:2001310
gliotoxin biosynthetic process
Cellular Component
GO:0005575
cellular_component
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5lwz
,
PDBe:5lwz
,
PDBj:5lwz
PDBsum
5lwz
PubMed
28525266
UniProt
Q4WMJ8
|GLIJ_ASPFU Dipeptidase gliJ (Gene Name=gliJ)
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