Structure of PDB 5wpk Chain B Binding Site BS01
Receptor Information
>5wpk Chain B (length=422) Species:
1313
(Streptococcus pneumoniae) [
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ISWNGFSKKSYQERLELLKAQALLSPERQASLEKDEQMSVTVADQLSENV
VGTFSLPYSLVPEVLVNGQEYTVPYVTEEPSVVAAASYASKIIKRAGGFT
AQVHQRQMIGQVALYQVANPKLAQEKIASKKAELLELANQAYPSIVKRGG
GARDLHVEQIKGEPDFLVVYIHVDTQEAMGANMLNTMLEALKPVLEELSQ
GQSLMGILSNYATDSLVTASCRIAFRYLSRQKDQGREIAEKIALASQFAQ
ADPYRAATHNKGIFNGIDAILIATGNDWRAIEAGAHAFASRDGRYQGLSC
WTLDLEREELVGEMTLPMPVATKGGSIGLNPRVALSHDLLGNPSARELAQ
IIESIGLAQNFAALKALVSTGIQQGHMKLQAKSLALLAGASESEVAPLVE
RLISDKTFNLETAQRYLENLRS
Ligand information
Ligand ID
HMG
InChI
InChI=1S/C27H44N7O20P3S/c1-26(2,21(40)24(41)30-5-4-15(35)29-6-7-58-17(38)9-27(3,42)8-16(36)37)11-51-57(48,49)54-56(46,47)50-10-14-20(53-55(43,44)45)19(39)25(52-14)34-13-33-18-22(28)31-12-32-23(18)34/h12-14,19-21,25,39-40,42H,4-11H2,1-3H3,(H,29,35)(H,30,41)(H,36,37)(H,46,47)(H,48,49)(H2,28,31,32)(H2,43,44,45)/p-5/t14-,19-,20-,21+,25-,27+/m1/s1
InChIKey
CABVTRNMFUVUDM-VRHQGPGLSA-I
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.5
C[C@](CC(=O)[O-])(CC(=O)SCCNC(=O)CCNC(=O)[C@@H](C(C)(C)COP(=O)([O-])OP(=O)([O-])OC[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)OP(=O)([O-])[O-])O)O
CACTVS 3.385
C[C@](O)(CC([O-])=O)CC(=O)SCCNC(=O)CCNC(=O)[C@H](O)C(C)(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
CACTVS 3.385
C[C](O)(CC([O-])=O)CC(=O)SCCNC(=O)CCNC(=O)[CH](O)C(C)(C)CO[P]([O-])(=O)O[P]([O-])(=O)OC[CH]1O[CH]([CH](O)[CH]1O[P]([O-])([O-])=O)n2cnc3c(N)ncnc23
ACDLabs 12.01
[O-]C(=O)CC(O)(C)CC(=O)SCCNC(=O)CCNC(=O)C(O)C(C)(C)COP([O-])(=O)OP([O-])(=O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3OP([O-])([O-])=O
OpenEye OEToolkits 1.7.5
CC(C)(COP(=O)([O-])OP(=O)([O-])OCC1C(C(C(O1)n2cnc3c2ncnc3N)O)OP(=O)([O-])[O-])C(C(=O)NCCC(=O)NCCSC(=O)CC(C)(CC(=O)[O-])O)O
Formula
C27 H39 N7 O20 P3 S
Name
3-HYDROXY-3-METHYLGLUTARYL-COENZYME A;
(S)-HMG-COA
ChEMBL
DrugBank
DB03169
ZINC
PDB chain
5wpk Chain A Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
5wpk
Structural Features and Domain Movements Controlling Substrate Binding and Cofactor Specificity in Class II HMG-CoA Reductase.
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
E50 N51
Binding residue
(residue number reindexed from 1)
E48 N49
Annotation score
5
Enzymatic activity
Enzyme Commision number
1.1.1.88
: hydroxymethylglutaryl-CoA reductase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004420
hydroxymethylglutaryl-CoA reductase (NADPH) activity
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0140643
hydroxymethylglutaryl-CoA reductase (NADH) activity
Biological Process
GO:0015936
coenzyme A metabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:5wpk
,
PDBe:5wpk
,
PDBj:5wpk
PDBsum
5wpk
PubMed
29224355
UniProt
Q8DNS5
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