Structure of PDB 2h2j Chain C Binding Site BS02
Receptor Information
>2h2j Chain C (length=438) Species:
3888
(Pisum sativum) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
LSPAVQTFWKWLQEEGVITAKTPVKASVVTEGLGLVALKDISRNDVILQV
PKRLWINPDAVAASEIGRVCSELKPWLSVILFLIRERSREDSVWKHYFGI
LPQETDSTIYWSEEELQELQGSQLLKTTVSVKEYVKNECLKLEQEIILPN
KRLFPDPVTLDDFFWAFGILRSRAFSRLRNENLVVVPMADLINHSAGVTT
EDHAYEVKGAAGLFSWDYLFSLKSPLSVKAGEQVYIQYDLNKSNAELALD
YGFIEPNENRHAYTLTLEISESDPFFDDKLDVAESNGFAQTAYFDIFYNR
TLPPGLLPYLRLVALGGTDAFLLESLFRDTIWGHLELSVSRDNEELLCKA
VREACKSALAGYHTTIEQDRELKEGNLDSRLAIAVGIREGEKMVLQQIDG
IFEQKELELDQLEYYQERRLKDLGLCGENGDILENLYF
Ligand information
Ligand ID
MLZ
InChI
InChI=1S/C7H16N2O2/c1-9-5-3-2-4-6(8)7(10)11/h6,9H,2-5,8H2,1H3,(H,10,11)/t6-/m0/s1
InChIKey
PQNASZJZHFPQLE-LURJTMIESA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CNCCCCC(C(=O)O)N
OpenEye OEToolkits 1.5.0
CNCCCC[C@@H](C(=O)O)N
CACTVS 3.341
CNCCCC[CH](N)C(O)=O
CACTVS 3.341
CNCCCC[C@H](N)C(O)=O
ACDLabs 10.04
O=C(O)C(N)CCCCNC
Formula
C7 H16 N2 O2
Name
N-METHYL-LYSINE
ChEMBL
DrugBank
DB01714
ZINC
ZINC000001529511
PDB chain
2h2j Chain C Residue 902 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
2h2j
Catalytic Roles for Carbon-Oxygen Hydrogen Bonding in SET Domain Lysine Methyltransferases.
Resolution
2.45 Å
Binding residue
(original residue number in PDB)
R222 F224 S225 R226 D239 I241 Y254 Y287 Y300
Binding residue
(residue number reindexed from 1)
R173 F175 S176 R177 D190 I192 Y205 Y238 Y251
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y287
Catalytic site (residue number reindexed from 1)
Y238
Enzyme Commision number
2.1.1.127
: [ribulose-bisphosphate carboxylase]-lysine N-methyltransferase.
2.1.1.259
: [fructose-bisphosphate aldolase]-lysine N-methyltransferase.
Gene Ontology
Molecular Function
GO:0016279
protein-lysine N-methyltransferase activity
GO:0030785
[ribulose-bisphosphate carboxylase]-lysine N-methyltransferase activity
Biological Process
GO:0018022
peptidyl-lysine methylation
Cellular Component
GO:0009507
chloroplast
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:2h2j
,
PDBe:2h2j
,
PDBj:2h2j
PDBsum
2h2j
PubMed
16682405
UniProt
Q43088
|RBCMT_PEA Ribulose-1,5 bisphosphate carboxylase/oxygenase large subunit N-methyltransferase, chloroplastic (Gene Name=RBCMT)
[
Back to BioLiP
]