Structure of PDB 5a3p Chain A Binding Site BS03
Receptor Information
>5a3p Chain A (length=455) Species:
9606
(Homo sapiens) [
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SMFLPPPECPVFEPSWEEFADPFAFIHKIRPIAEQTGICKVRPPPDWQPP
FACDVDKLHFTPRIQRLNELEAQTRVKRDYTLRTFGEMADAFKSDYFNMP
VHMVPTELVEKEFWRLVSTIEEDVTVEYGADIASKEFGSGFPVRDIKLSP
EEEEYLDSGWNLNNMPVMEQSVLAHITADICGMKLPWLYVGMCFSSFCWH
IEDHWSYSINYLHWGEPKTWYGVPGYAAEQLENVMKKLAPELFVSQPDLL
HQLVTIMNPNTLMTHEVPVYRTNQCAGEFVITFPRAYHSGFNQGFNFAEA
VNFCTVDWLPLGRQCVEHYRLLHRYCVFSHDEMICKMASKADVLDVVVAS
TVQKDMAIMIEDEKALRETVRKLGVIDSERMDFELLPDDERQCVKCKTTC
FMSAISCSCKPGLLVCLHHVKELCSCPPYKYKLRYRYTLDDLYPMMNALK
LRAES
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
5a3p Chain A Residue 1757 [
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Receptor-Ligand Complex Structure
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PDB
5a3p
Structural Analysis of Human Kdm5B Guides Histone Demethylase Inhibitor Development.
Resolution
2.008 Å
Binding residue
(original residue number in PDB)
N91 L413 V414 T416 E419
Binding residue
(residue number reindexed from 1)
N68 L116 V117 T119 E122
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:5a3p
,
PDBe:5a3p
,
PDBj:5a3p
PDBsum
5a3p
PubMed
27214403
UniProt
Q9UGL1
|KDM5B_HUMAN Lysine-specific demethylase 5B (Gene Name=KDM5B)
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