Structure of PDB 5fup Chain A Binding Site BS03
Receptor Information
>5fup Chain A (length=454) Species:
9606
(Homo sapiens) [
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SMFLPPPECPVFEPSWEEFADPFAFIHKIRPIAEQTGICKVRPPPDWQPP
FACDVDKLHFTPRIQRLNELEAQTRVRDYTLRTFGEMADAFKSDYFNMPV
HMVPTELVEKEFWRLVSTIEEDVTVEYGADIASKEFGSGFPVRDIKLSPE
EEEYLDSGWNLNNMPVMEQSVLAHITADICGMKLPWLYVGMCFSSFCWHI
EDHWSYSINYLHWGEPKTWYGVPGYAAEQLENVMKKLAPELFVSQPDLLH
QLVTIMNPNTLMTHEVPVYRTNQCAGEFVITFPRAYHSGFNQGFNFAEAV
NFCTVDWLPLGRQCVEHYRLLHRYCVFSHDEMICKMASKADVLDVVVAST
VQKDMAIMIEDEKALRETVRKLGVIDSERMDFELLPDDERQCVKCKTTCF
MSAISCSCKPGLLVCLHHVKELCSCPPYKYKLRYRYTLDDLYPMMNALKL
RAES
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
5fup Chain A Residue 1757 [
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Receptor-Ligand Complex Structure
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PDB
5fup
Structural Analysis of Human Kdm5B Guides Histone Demethylase Inhibitor Development.
Resolution
2.15 Å
Binding residue
(original residue number in PDB)
H499 E501 H587
Binding residue
(residue number reindexed from 1)
H199 E201 H287
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
G481 Y488 H499 E501 H587 A599
Catalytic site (residue number reindexed from 1)
G181 Y188 H199 E201 H287 A299
Enzyme Commision number
1.14.11.67
: [histone H3]-trimethyl-L-lysine(4) demethylase.
External links
PDB
RCSB:5fup
,
PDBe:5fup
,
PDBj:5fup
PDBsum
5fup
PubMed
27214403
UniProt
Q9UGL1
|KDM5B_HUMAN Lysine-specific demethylase 5B (Gene Name=KDM5B)
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