Structure of PDB 4l1f Chain B Binding Site BS03
Receptor Information
>4l1f Chain B (length=380) Species:
591001
(Acidaminococcus fermentans DSM 20731) [
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MDFNLTEDQQMIKDMAAEFAEKFLAPTVEERDKAHIWDRKLIDKMGEAGF
CGICFPEEYGGMGLDVLSYILAVEELSKVDDGTGITLSANVSLCATPIYM
FGTEEQKQKYLAPIAEGTHVGAFGLTEPSAGTDASAQQTTAVLKGDKYIL
NGSKIFITNGKEADTYVVFAMTDKSQGVHGISAFILEKGMPGFRFGKIED
KMGGHTSITAELIFEDCEVPKENLLGKEGEGFKIAMETLDGGRIGVAAQA
LGIAEGALAAAVKYSKEREQFGRSISKFQALQFMMADMATKIEAARYLVY
HAAMLKNEGKPYSEAAAMAKCFASDVAMEVTTDAVQIFGGYGYTVDYPAE
RYMRNAKITQIYEGTNQVMRIVTSRALLRD
Ligand information
Ligand ID
COS
InChI
InChI=1S/C21H36N7O16P3S2/c1-21(2,16(31)19(32)24-4-3-12(29)23-5-6-49-48)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
REVPHPVBPSIEKM-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)NCCSS)O
ACDLabs 10.04
O=C(NCCSS)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 1.5.0
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)NCCSS)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)NCCSS
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)NCCSS
Formula
C21 H36 N7 O16 P3 S2
Name
COENZYME A PERSULFIDE
ChEMBL
DrugBank
DB04036
ZINC
ZINC000085432299
PDB chain
4l1f Chain B Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
4l1f
Studies on the Mechanism of Electron Bifurcation Catalyzed by Electron Transferring Flavoprotein (Etf) and Butyryl-CoA Dehydrogenase (Bcd) of Acidaminococcus fermentans.
Resolution
1.79 Å
Binding residue
(original residue number in PDB)
T132 H179 F232 M236 L239 D240 R243 Y362 E363 G364 R375
Binding residue
(residue number reindexed from 1)
T132 H179 F232 M236 L239 D240 R243 Y362 E363 G364 R375
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
L125 T126 G242 E363 R375
Catalytic site (residue number reindexed from 1)
L125 T126 G242 E363 R375
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0003995
acyl-CoA dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0016627
oxidoreductase activity, acting on the CH-CH group of donors
GO:0050660
flavin adenine dinucleotide binding
View graph for
Molecular Function
External links
PDB
RCSB:4l1f
,
PDBe:4l1f
,
PDBj:4l1f
PDBsum
4l1f
PubMed
24379410
UniProt
D2RL84
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