Structure of PDB 3sqz Chain A Binding Site BS01
Receptor Information
>3sqz Chain A (length=388) Species:
1309
(Streptococcus mutans) [
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MRIGIDKIGFTSSQYVLNMKDLAEARGEDPQKFSKGLLLNALSIAPITDD
VVTLAAGSANEILTAEDKEKIDMVILATESSVDQSKAGAVYVHSLLGIQP
FARSFEMKEACYSATAALNYAKLHVEKHPDTRVLVLASDIAKYGIGTPGE
STQGAGSIAMLVKKDPRILILHDETLAQTRDIMDFWRPNYTTTPYVNGMY
STKQYLDMLKTTWAEYQKRFDVSLTDFAAFCFHLPFPKLALKGFNKIMDK
QVPSDLQEKLKVNFEASILYSKQIGNIYTGSLFLGLLSLLENSQNLVAGD
KIALFSYGSGAVAEIFTGTLVKGFKEQLQTNRLDKLKRRTPLSVENYEKI
FFEEAQLDDKGNASFKEYQTGPFALKEILEHQRIYGKV
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
3sqz Chain A Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
3sqz
Crystal structure of HMG-CoA synthase from Streptococcus mutans
Resolution
1.2 Å
Binding residue
(original residue number in PDB)
D29 K32 G36 Y143 P148 G149 T152 F185 G198 S201 F236 K238 K242
Binding residue
(residue number reindexed from 1)
D29 K32 G36 Y143 P148 G149 T152 F185 G198 S201 F236 K238 K242
Annotation score
3
Enzymatic activity
Enzyme Commision number
2.3.3.10
: hydroxymethylglutaryl-CoA synthase.
Gene Ontology
Molecular Function
GO:0004421
hydroxymethylglutaryl-CoA synthase activity
GO:0016746
acyltransferase activity
Biological Process
GO:0006084
acetyl-CoA metabolic process
GO:0010142
farnesyl diphosphate biosynthetic process, mevalonate pathway
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3sqz
,
PDBe:3sqz
,
PDBj:3sqz
PDBsum
3sqz
PubMed
UniProt
Q8DUI5
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