Structure of PDB 5a3t Chain A Binding Site BS01
Receptor Information
>5a3t Chain A (length=454) Species:
9606
(Homo sapiens) [
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SMFLPPPECPVFEPSWEEFADPFAFIHKIRPIAEQTGICKVRPPPDWQPP
FACDVDKLHFTPRIQRLNELEAQTRVKRDYTLRTFGEMADAFKSDYFNMP
VHMVPTELVEKEFWRLVSTIEEDVTVEYGADIASKEFGSGFPVRDIKLSP
EEEEYLDSGWNLNNMPVMEQSVLAHITADICGMKLPWLYVGMCFSSFCWH
IEDHWSYSINYLHWGEPKTWYGVPGYAAEQLENVMKKLAPELFVSQPDLL
HQLVTIMNPNTLMTHEVPVYRTNQCAGEFVITFPRAYHSGFNQGFNFAEA
VNFCTVDWLPLGRQCVEHYRLLHRYCVFSHDEMICKMASKADVLDVVVAS
TVQKDMAIMIEDEKALRETVRKLGVIDSERMDFELLPDDERQCVKCKTTC
FMSAISCSCKPGLLVCLHHVKELCSCPPYKYKLRYRYTLDDLYPMMNALK
LRAE
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
5a3t Chain A Residue 1754 [
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Receptor-Ligand Complex Structure
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PDB
5a3t
Structural Analysis of Human Kdm5B Guides Histone Demethylase Inhibitor Development.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
C692 C695 C715 H718
Binding residue
(residue number reindexed from 1)
C393 C396 C416 H419
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)
G182 Y189 H200 E202 H288 A300
Enzyme Commision number
1.14.11.67
: [histone H3]-trimethyl-L-lysine(4) demethylase.
External links
PDB
RCSB:5a3t
,
PDBe:5a3t
,
PDBj:5a3t
PDBsum
5a3t
PubMed
27214403
UniProt
Q9UGL1
|KDM5B_HUMAN Lysine-specific demethylase 5B (Gene Name=KDM5B)
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