Structure of PDB 6qfb Chain D Binding Site BS03
Receptor Information
>6qfb Chain D (length=1025) Species:
9606
(Homo sapiens) [
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SAKAISEQTGKELLYKFICTTSAIQNRFKYARVTPDTDWARLLQDHPWLL
SQNLVVKPDQLIKRRGKLGLVGVNLTLDGVKSWLKPRLGQEATVGKATGF
LKNFLIEPFVPHSQAEEFYVCIYATREGDYVLFHHEGGVDVGDVDAKAQK
LLVGVDEKLNPEDIKKHLLVHAPEDKKEILASFISGLFNFYEDLYFTYLE
INPLVVTKDGVYVLDLAAKVDATADYICKVKWGDIEFPPPFGREAYPEEA
YIADLDAKSGASLKLTLLNPKGRIWTMVAGGGASVVYSDTICDLGGVNEL
ANYGEYSGAPSEQQTYDYAKTILSLMTREKHPDGKILIIGGSIANFTNVA
ATFKGIVRAIRDYQGPLKEHEVTIFVRRGGPNYQEGLRVMGEVGKTTGIP
IHVFGTETHMTAIVGMALGHRPIPKSTTLFSRHTKAIVWGMQTRAVQGML
DFDYVCSRDEPSVAAMVYPFTGDHKQKFYWGHKEILIPVFKNMADAMRKH
PEVDVLINFASLRSAYDSTMETMNYAQIRTIAIIAEGIPEALTRKLIKKA
DQKGVTIIGPATVGGIKPGCFKIGNTGGMLDNILASKLYRPGSVAYVSRS
GGMSNELNNIISRTTDGVYEGVAIGGDRYPGSTFMDHVLRYQDTPGVKMI
VVLGEIGGTEEYKICRGIKEGRLTKPIVCWCIGTCATMFSQASETAVAKN
QALKEAGVFVPRSFDELGEIIQSVYEDLVANGVIVPAQEVPPPTVPMDYS
WARELGLIRKPASFMTSICDERGQELIYAGMPITEVFKEEMGIGGVLGLL
WFQKRLPKYSCQFIEMCLMVTADHGPAVSGAHNTIICARAGKDLVSSLTS
GLLTIGDRFGGALDAAAKMFSKAFDSGIIPMEFVNKMKKEGKLIMGIGHR
VKSINNPDMRVQILKDYVRQHFPATPLLDYALEVEKITTSKKPNLILNVD
GLIGVAFVDMLRNCGSFTREEADEYIDIGALNGIFVLGRSMGFIGHYLDQ
KRLKQGLYRHPWDDISYVLPEHMSM
Ligand information
Ligand ID
ADP
InChI
InChI=1S/C10H15N5O10P2/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(24-10)1-23-27(21,22)25-26(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
XTWYTFMLZFPYCI-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)O)O)O)N
Formula
C10 H15 N5 O10 P2
Name
ADENOSINE-5'-DIPHOSPHATE
ChEMBL
CHEMBL14830
DrugBank
DB16833
ZINC
ZINC000012360703
PDB chain
6qfb Chain D Residue 1203 [
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Receptor-Ligand Complex Structure
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PDB
6qfb
Structure of ATP citrate lyase and the origin of citrate synthase in the Krebs cycle.
Resolution
3.25 Å
Binding residue
(original residue number in PDB)
V56 K58 R65 R66 G67 F110 V111 H113 E118 P204 L215 D216
Binding residue
(residue number reindexed from 1)
V55 K57 R64 R65 G66 F109 V110 H112 E117 P203 L214 D215
Annotation score
5
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
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6qfb
,
PDBe:6qfb
,
PDBj:6qfb
PDBsum
6qfb
PubMed
30944476
UniProt
P53396
|ACLY_HUMAN ATP-citrate synthase (Gene Name=ACLY)
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