Structure of PDB 6qcl Chain H Binding Site BS01
Receptor Information
>6qcl Chain H (length=261) Species:
1092
(Chlorobium limicola) [
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GSHMVEPLIRTTISDDRGEEPRYAGYAASELCSKGYGIEDVIGLLWNKKL
PTREESEIIKRIVMISADHGPAVSGAFGSILAACAGIDMPQAVSAGMTMI
GPRFGGAVTNAGKYFKMAVEDYPNDIPGFLSWMKKNVGPVPGIGHRVKSV
KNPDQRVKYLVSYIKNETSLHTPCLDYALEVEKVTTAKKGNLILNVDGTI
GCILMDLDFPVHSLNGFFVLARTIGMIGHWIDQNNQNSRLIRLYDYLINY
AVKPEQEVPEK
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
6qcl Chain H Residue 1001 [
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Receptor-Ligand Complex Structure
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PDB
6qcl
Structure of ATP citrate lyase and the origin of citrate synthase in the Krebs cycle.
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
R449 G451 A453 P485 V486 G488 I489 G490 R492 K535 L538 N541
Binding residue
(residue number reindexed from 1)
R103 G105 A107 P139 V140 G142 I143 G144 R146 K189 L192 N195
Annotation score
4
Enzymatic activity
Enzyme Commision number
2.3.3.16
: citrate synthase (unknown stereospecificity).
Gene Ontology
Molecular Function
GO:0046912
acyltransferase activity, acyl groups converted into alkyl on transfer
View graph for
Molecular Function
External links
PDB
RCSB:6qcl
,
PDBe:6qcl
,
PDBj:6qcl
PDBsum
6qcl
PubMed
30944476
UniProt
Q9AJC4
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