Structure of PDB 1mj9 Chain A Binding Site BS01
Receptor Information
>1mj9 Chain A (length=273) Species:
4932
(Saccharomyces cerevisiae) [
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ARVRNLNRIIMGKYEIEPWYFSPYPIELTDEDFIYIDDFTLQYFGSKKQY
ERYRKKCTLRHPPGNEIYRDDYVSFFEIDGRKQRTWCRNLCLLSKLFLDH
KTLYYDVDPFLFYCMTRRDELGHHLVGYFSKEKESADGYNVASILTLPQY
QRMGYGKLLIEFSYELSKKENKVGSPEKPLSDLGLLSYRAYWSDTLITLL
VEHQKEITIDEISSMTSMTTTDILHTAKTLNILRYYKGQHIIFLNEDILD
RYNRLKAKKRRTIDPNRLIWKPP
Ligand information
Ligand ID
COA
InChI
InChI=1S/C21H36N7O16P3S/c1-21(2,16(31)19(32)24-4-3-12(29)23-5-6-48)8-41-47(38,39)44-46(36,37)40-7-11-15(43-45(33,34)35)14(30)20(42-11)28-10-27-13-17(22)25-9-26-18(13)28/h9-11,14-16,20,30-31,48H,3-8H2,1-2H3,(H,23,29)(H,24,32)(H,36,37)(H,38,39)(H2,22,25,26)(H2,33,34,35)/t11-,14-,15-,16+,20-/m1/s1
InChIKey
RGJOEKWQDUBAIZ-IBOSZNHHSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC(C)(COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)C(C(=O)NCCC(=O)NCCS)O
CACTVS 3.341
CC(C)(CO[P@@](O)(=O)O[P@](O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O[P](O)(O)=O)n2cnc3c(N)ncnc23)[C@@H](O)C(=O)NCCC(=O)NCCS
OpenEye OEToolkits 1.5.0
CC(C)(CO[P@](=O)(O)O[P@@](=O)(O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)[C@H](C(=O)NCCC(=O)NCCS)O
CACTVS 3.341
CC(C)(CO[P](O)(=O)O[P](O)(=O)OC[CH]1O[CH]([CH](O)[CH]1O[P](O)(O)=O)n2cnc3c(N)ncnc23)[CH](O)C(=O)NCCC(=O)NCCS
ACDLabs 10.04
O=C(NCCS)CCNC(=O)C(O)C(C)(C)COP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3OP(=O)(O)O
Formula
C21 H36 N7 O16 P3 S
Name
COENZYME A
ChEMBL
CHEMBL1213327
DrugBank
DB01992
ZINC
ZINC000008551087
PDB chain
1mj9 Chain A Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
1mj9
The catalytic mechanism of the ESA1 histone acetyltransferase involves a self-acetylated intermediate.
Resolution
2.5 Å
Binding residue
(original residue number in PDB)
F258 L259 I305 L306 T307 Q312 R313 M314 G315 G317 K318 S342 L344 G345 S348 R421
Binding residue
(residue number reindexed from 1)
F97 L98 I144 L145 T146 Q151 R152 M153 G154 G156 K157 S181 L183 G184 S187 R260
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
S304 E338
Catalytic site (residue number reindexed from 1)
S143 E177
Enzyme Commision number
2.3.1.-
2.3.1.48
: histone acetyltransferase.
Gene Ontology
Molecular Function
GO:0004402
histone acetyltransferase activity
Biological Process
GO:0006355
regulation of DNA-templated transcription
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1mj9
,
PDBe:1mj9
,
PDBj:1mj9
PDBsum
1mj9
PubMed
12368900
UniProt
Q08649
|ESA1_YEAST Histone acetyltransferase ESA1 (Gene Name=ESA1)
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