Structure of PDB 4pip Chain A Binding Site BS02
Receptor Information
>4pip Chain A (length=316) Species:
1772
(Mycolicibacterium smegmatis) [
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LSLANYLAAAAEALRRDVRAGLTATQKSLPPKWFYDAVGSDLFDQITRLP
EYYPTRTEAQILRTRSAEIISAAGADTLVELGSGTSEKTRMLLDAMRDAE
LLRRFIPFDVDAGVLRSAGAAIGAEYPGIEIDAVCGDFEEHLGKIPHVGR
RLVVFLGSTIGNLTPAPRAEFLSTLADTLQPGDSLLLGTDLVKDTGRLVR
AYDDAAGVTAAFNRNVLAVVNRELSADFDLDAFEHVAKWNSDEERIEVWL
RARTAQHVRVAALDLEVDFAAGEEMLTAVSCKFRPENVVAELAEAGLRQT
HWWTDPAGDFGLSLAV
Ligand information
Ligand ID
SAH
InChI
InChI=1S/C14H20N6O5S/c15-6(14(23)24)1-2-26-3-7-9(21)10(22)13(25-7)20-5-19-8-11(16)17-4-18-12(8)20/h4-7,9-10,13,21-22H,1-3,15H2,(H,23,24)(H2,16,17,18)/t6-,7+,9+,10+,13+/m0/s1
InChIKey
ZJUKTBDSGOFHSH-WFMPWKQPSA-N
SMILES
Software
SMILES
CACTVS 3.341
N[CH](CCSC[CH]1O[CH]([CH](O)[CH]1O)n2cnc3c(N)ncnc23)C(O)=O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)CSCCC(C(=O)O)N)O)O)N
CACTVS 3.341
N[C@@H](CCSC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3c(N)ncnc23)C(O)=O
ACDLabs 10.04
O=C(O)C(N)CCSCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CSCC[C@@H](C(=O)O)N)O)O)N
Formula
C14 H20 N6 O5 S
Name
S-ADENOSYL-L-HOMOCYSTEINE
ChEMBL
CHEMBL418052
DrugBank
DB01752
ZINC
ZINC000004228232
PDB chain
4pip Chain A Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
4pip
Ergothioneine Biosynthetic Methyltransferase EgtD Reveals the Structural Basis of Aromatic Amino Acid Betaine Biosynthesis.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
K36 Y39 F47 G86 S87 T89 K92 D113 V114 D141 F142 G161
Binding residue
(residue number reindexed from 1)
K32 Y35 F43 G82 S83 T85 K88 D109 V110 D137 F138 G157
Annotation score
5
Enzymatic activity
Enzyme Commision number
2.1.1.44
: L-histidine N(alpha)-methyltransferase.
Gene Ontology
Molecular Function
GO:0008168
methyltransferase activity
GO:0008276
protein methyltransferase activity
GO:0052706
L-histidine N(alpha)-methyltransferase activity
Biological Process
GO:0032259
methylation
GO:0052699
ergothioneine biosynthetic process
GO:0052704
ergothioneine biosynthesis from histidine via gamma-glutamyl-hercynylcysteine sulfoxide
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:4pip
,
PDBe:4pip
,
PDBj:4pip
PDBsum
4pip
PubMed
25404173
UniProt
A0R5M8
|EGTD_MYCS2 Histidine N-alpha-methyltransferase (Gene Name=egtD)
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