Structure of PDB 6are Chain C Binding Site BS01
Receptor Information
>6are Chain C (length=394) Species:
330879
(Aspergillus fumigatus Af293) [
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MSSLPAVYIVSSARTPVGSFLGSLSSLTAPQLGAHAIKAALAKVDGLKPS
DVQEVFFGNVISANVGQNPARQCALGAGLEESTICTTVNKVCASGLKAII
LGAQTIMTGNADVVVAGGTESMSNAPHYLPNLRTGAKYGHQSLVDGIMKD
GLTDAGKQELMGLQAEECAQDHGFSREQQDEYAIRTYEKAQAAQKAGLFD
EEIAPIQLPGPDVTVTQDEEPKNLNPEKLRAIKPAFIPGSGTVTAPNSSP
LNDGAAAVVLVSEAKLKELNLKPVAKILGWGDAAQQPSKFTTAPALAIPK
ALKHAGVGQDAIDAFEINEAFSVVALANMKLLGIPEEKVNLHGGAVAIGH
PIGASGARILTTLLGVLKAKKGKLGCAGICNGGGGASALVVELL
Ligand information
Ligand ID
ACO
InChI
InChI=1S/C23H38N7O17P3S/c1-12(31)51-7-6-25-14(32)4-5-26-21(35)18(34)23(2,3)9-44-50(41,42)47-49(39,40)43-8-13-17(46-48(36,37)38)16(33)22(45-13)30-11-29-15-19(24)27-10-28-20(15)30/h10-11,13,16-18,22,33-34H,4-9H2,1-3H3,(H,25,32)(H,26,35)(H,39,40)(H,41,42)(H2,24,27,28)(H2,36,37,38)/t13-,16-,17-,18+,22-/m1/s1
InChIKey
ZSLZBFCDCINBPY-ZSJPKINUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC(=O)SCCNC(=O)CCNC(=O)[C@@H](C(C)(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)O
CACTVS 3.341
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
ACDLabs 10.04
O=C(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)C
CACTVS 3.341
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
OpenEye OEToolkits 1.5.0
CC(=O)SCCNC(=O)CCNC(=O)C(C(C)(C)COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)O
Formula
C23 H38 N7 O17 P3 S
Name
ACETYL COENZYME *A
ChEMBL
CHEMBL1230809
DrugBank
ZINC
ZINC000008551095
PDB chain
6are Chain C Residue 406 [
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Receptor-Ligand Complex Structure
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PDB
6are
Structure of Aspergillus fumigatus Cytosolic Thiolase: Trapped Tetrahedral Reaction Intermediates and Activation by Monovalent Cations
Resolution
1.75 Å
Binding residue
(original residue number in PDB)
C92 L152 M161 Y187 N227 N229 I236 A249 P250 S253 A324 F325 H354 C384 N385
Binding residue
(residue number reindexed from 1)
C92 L152 M161 Y187 N223 N225 I232 A245 P246 S249 A320 F321 H350 C380 N381
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
C92 H354 C384 G386
Catalytic site (residue number reindexed from 1)
C92 H350 C380 G382
Enzyme Commision number
2.3.1.9
: acetyl-CoA C-acetyltransferase.
Gene Ontology
Molecular Function
GO:0003985
acetyl-CoA C-acetyltransferase activity
GO:0016746
acyltransferase activity
GO:0016747
acyltransferase activity, transferring groups other than amino-acyl groups
GO:0046872
metal ion binding
Biological Process
GO:0006635
fatty acid beta-oxidation
GO:0006696
ergosterol biosynthetic process
GO:0016126
sterol biosynthetic process
Cellular Component
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6are
,
PDBe:6are
,
PDBj:6are
PDBsum
6are
PubMed
UniProt
Q4WCL5
|ER10B_ASPFU Acetyl-CoA acetyltransferase erg10B, cytosolic (Gene Name=erg10B)
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