Structure of PDB 2d3m Chain A Binding Site BS01
Receptor Information
>2d3m Chain A (length=405) Species:
45385
(Aloe arborescens) [
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GPGMSSLSNSLPLMEDVQGIRKAQKADGTATVMAIGTAHPPHIFPQDTYA
DVYFRATNSEHKVELKKKFDHICKKTMIGKRYFNYDEEFLKKYPNITSYD
EPSLNDRQDICVPGVPALGTEAAVKAIEEWGRPKSEITHLVFCTSCGVDM
PSADFQCAKLLGLHANVNKYCIYMQGCYAGGTVMRYAKDLAENNRGARVL
VVCAELTIMMLRAPNETHLDNAIGISLFGDGAAALIIGSDPIIGVEKPMF
EIVCTKQTVIPNTEDVIHLHLRETGMMFYLSKGSPMTISNNVEACLIDVF
KSVGITPPEDWNSLFWIPHPGGRAILDQVEAKLKLRPEKFRAARTVLWDY
GNMVSASVGYILDEMRRKSAAKGLETYGEGLEWGVLLGFGPGITVETILL
HSLPL
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
2d3m Chain A Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
2d3m
Structural Insight into Chain-Length Control and Product Specificity of Pentaketide Chromone Synthase from Aloe arborescens
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
H71 K75 A177 I223 L227 F278 L280 S281 G321 G322 R323 A324 I325
Binding residue
(residue number reindexed from 1)
H71 K75 A177 I223 L227 F278 L280 S281 G321 G322 R323 A324 I325
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
C177 F228 H319 N352
Catalytic site (residue number reindexed from 1)
C177 F228 H319 N352
Enzyme Commision number
2.3.1.216
: 5,7-dihydroxy-2-methylchromone synthase.
Gene Ontology
Molecular Function
GO:0016746
acyltransferase activity
GO:0016747
acyltransferase activity, transferring groups other than amino-acyl groups
GO:0042803
protein homodimerization activity
Biological Process
GO:0009058
biosynthetic process
GO:0009813
flavonoid biosynthetic process
GO:0030639
polyketide biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2d3m
,
PDBe:2d3m
,
PDBj:2d3m
PDBsum
2d3m
PubMed
17462571
UniProt
Q58VP7
|PCS_ALOAR 5,7-dihydroxy-2-methylchromone synthase
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