Structure of PDB 7dyw Chain A Binding Site BS02
Receptor Information
>7dyw Chain A (length=236) Species:
9606
(Homo sapiens) [
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QSTVPRLHRPSLQHFREQFLVPGRPVILKGVADHWPCMQKWSLEYIQEIA
GCRTVPVEVGSRYTDEEWSQTLMTVNEFISKYIVNEPRDVGYLAQHQLFD
QIPELKQDISIPDYCSLGDGEEEEITINAWFGPQGTISPLHQDPQQNFLV
QVMGRKYIRLYSPQESGALYPHDTHLLHNTSQVDVENPDLEKFPKFAKAP
FLSCILSPGEILFIPVKYWHYVRALDLSFSVSFWWS
Ligand information
Ligand ID
MN
InChI
InChI=1S/Mn/q+2
InChIKey
WAEMQWOKJMHJLA-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mn+2]
CACTVS 3.341
[Mn++]
Formula
Mn
Name
MANGANESE (II) ION
ChEMBL
DrugBank
DB06757
ZINC
PDB chain
7dyw Chain A Residue 602 [
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Receptor-Ligand Complex Structure
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PDB
7dyw
5-Substituted Pyridine-2,4-dicarboxylate Derivatives Have Potential for Selective Inhibition of Human Jumonji-C Domain-Containing Protein 5.
Resolution
2.13 Å
Binding residue
(original residue number in PDB)
H321 D323 H400
Binding residue
(residue number reindexed from 1)
H141 D143 H220
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.14.11.73
: [protein]-arginine 3-hydroxylase.
3.4.-.-
External links
PDB
RCSB:7dyw
,
PDBe:7dyw
,
PDBj:7dyw
PDBsum
7dyw
PubMed
37527664
UniProt
Q8N371
|KDM8_HUMAN Bifunctional peptidase and arginyl-hydroxylase JMJD5 (Gene Name=KDM8)
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