Structure of PDB 6uuw Chain D Binding Site BS03
Receptor Information
>6uuw Chain D (length=1034) Species:
9606
(Homo sapiens) [
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SAKAISEQTGKELLYKFICTTSAIQNRFKYARVTPDTDWARLLQDHPWLL
SQNLVVKPDQLIKRRGKLGLVGVNLTLDGVKSWLKPRLGQEATVGKATGF
LKNFLIEPFVPHSQAEEFYVCIYATREGDYVLFHHEGGAQKLLVGVDEKL
NPEDIKKHLLVHAPEDKKEILASFISGLFNFYEDLYFTYLEINPLVVTKD
GVYVLDLAAKVDATADYICKVKWGDIEFPPPFGREAYPEEAYIADLDAKS
GASLKLTLLNPKGRIWTMVAGGGASVVYSDTICDLGGVNELANYGEYSGA
PSEQQTYDYAKTILSLMTREKHPDGKILIIGGSIANFTNVAATFKGIVRA
IRDYQGPLKEHEVTIFVRRGGPNYQEGLRVMGEVGKTTGIPIHVFGTETH
MTAIVGMALGHRPIPNQPPTAGKSTTLFSRHTKAIVWGMQTRAVQGMLDF
DYVCSRDEPSVAAMVYPFTGDHKQKFYWGHKEILIPVFKNMADAMRKHPE
VDVLINFASLRSAYDSTMETMNYAQIRTIAIIAQGIPEALTRKLIKKADQ
KGVTIIGPATVGGIKPGCFKIGNTGGMLDNILASKLYRPGSVAYVSRSGG
MSNELNNIISRTTDGVYEGVAIGGDRYPGSTFMDHVLRYQDTPGVKMIVV
LGEIGGTEEYKICRGIKEGRLTKPIVCWCIGTCATMFSSEVQFGHAGACA
NQASETAVAKNQALKEAGVFVPRSFDELGEIIQSVYEDLVANGVIVPAQE
VPPPTVPMDYSWARELGLIRKPASFMTSICDERGQELIYAGMPITEVFKE
EMGIGGVLGLLWFQKRLPKYSCQFIEMCLMVTADHGPAVSGAHNTIICAR
AGKDLVSSLTSGLLTIGDRFGGALDAAAKMFSKAFDSGIIPMEFVNKMKK
EGKLIMGIGHRVKSINNPDMRVQILKDYVRQHFPATPLLDYALEVEKITT
SKKPNLILNVDGLIGVAFVDMLRNCGSFTREEADEYIDIGALNGIFVLGR
SMGFIGHYLDQKRLKQGLYRHPWDDISYVLPEHM
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
6uuw Chain D Residue 1202 [
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Receptor-Ligand Complex Structure
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PDB
6uuw
Molecular basis for acetyl-CoA production by ATP-citrate lyase
Resolution
2.85 Å
Binding residue
(original residue number in PDB)
F347 F572 S574 R576 I597 Q599 A624 T625 V626
Binding residue
(residue number reindexed from 1)
F337 F507 S509 R511 I532 Q534 A559 T560 V561
Annotation score
3
Enzymatic activity
Enzyme Commision number
2.3.3.8
: ATP citrate synthase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0003878
ATP citrate synthase activity
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016740
transferase activity
GO:0046872
metal ion binding
GO:0046912
acyltransferase activity, acyl groups converted into alkyl on transfer
Biological Process
GO:0006085
acetyl-CoA biosynthetic process
GO:0006101
citrate metabolic process
GO:0006107
oxaloacetate metabolic process
GO:0006629
lipid metabolic process
GO:0006633
fatty acid biosynthetic process
GO:0006695
cholesterol biosynthetic process
GO:0008610
lipid biosynthetic process
GO:0015936
coenzyme A metabolic process
Cellular Component
GO:0005576
extracellular region
GO:0005654
nucleoplasm
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0016020
membrane
GO:0035578
azurophil granule lumen
GO:0070062
extracellular exosome
GO:1904813
ficolin-1-rich granule lumen
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:6uuw
,
PDBe:6uuw
,
PDBj:6uuw
PDBsum
6uuw
PubMed
31873304
UniProt
P53396
|ACLY_HUMAN ATP-citrate synthase (Gene Name=ACLY)
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