Structure of PDB 4ih3 Chain E Binding Site BS01
Receptor Information
>4ih3 Chain E (length=332) Species:
9606
(Homo sapiens) [
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MKIDIHSHILPKEWPDLKKRFGYGGWVQLQHHSKGEAKLLKDGKVFRVVR
ENCWDPEVRIREMDQKGVTVQALSTVPVMFSYWAKPEDTLNLCQLLNNDL
ASTVVSYPRRFVGLGTLPMQAPELAVKEMERCVKELGFPGVQIGTHVNEW
DLNAQELFPVYAAAERLKCSLFVHPWDMQMDGRMAKYWLPWLVGMPAETT
IAICSMIMGGVFEKFPKLKVCFAHGGGAFPFTVGRISHGFSMRPDLCAQD
NPMNPKKYLGSFYTDALVHDPLSLKLLTDVIGKDKVILGTDYPFPLGELE
PGKLIESMEEFDEETKNKLKAGNALAFLGLER
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
4ih3 Chain E Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
4ih3
Human alpha-amino-beta-carboxymuconate-epsilon-semialdehyde decarboxylase (ACMSD): A structural and mechanistic unveiling.
Resolution
2.493 Å
Binding residue
(original residue number in PDB)
H6 H8 H174 D291
Binding residue
(residue number reindexed from 1)
H6 H8 H174 D291
Annotation score
1
Enzymatic activity
Enzyme Commision number
4.1.1.45
: aminocarboxymuconate-semialdehyde decarboxylase.
Gene Ontology
Molecular Function
GO:0001760
aminocarboxymuconate-semialdehyde decarboxylase activity
GO:0005515
protein binding
GO:0008270
zinc ion binding
GO:0016787
hydrolase activity
GO:0016831
carboxy-lyase activity
GO:0046872
metal ion binding
Biological Process
GO:0006569
tryptophan catabolic process
GO:0019748
secondary metabolic process
GO:1904985
negative regulation of quinolinate biosynthetic process
GO:1905004
picolinic acid biosynthetic process
GO:1905012
regulation of 'de novo' NAD biosynthetic process from tryptophan
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4ih3
,
PDBe:4ih3
,
PDBj:4ih3
PDBsum
4ih3
PubMed
25392945
UniProt
Q8TDX5
|ACMSD_HUMAN 2-amino-3-carboxymuconate-6-semialdehyde decarboxylase (Gene Name=ACMSD)
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