Structure of PDB 6hsp Chain B Binding Site BS02
Receptor Information
>6hsp Chain B (length=389) Species:
7955
(Danio rerio) [
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NRVFVIGVGMTKFEKPGARDIDYPDMAKEAGQRALADAGIKYSAIQQACV
GYVYGDSTCGQRAIYHSLGLSGIPIINVNNNCSTGSTALFMGRQLIQGGL
ADCVLALGFEKMEYMDRTNPMDKHMEVMINRYGLAAVPAAPQMFGNAGRE
HMEKYGTKPEHFAKVAWKNHKHSTNNPYSQFQDEYSLEQVIDSRKVFEFL
TLLQCCPTSDGAGAAVLASESFVRRNGLEKKAVEIVAQEMVTDLSTTFEE
NSCMKMVGYDMTRLAAERCYDTAGVKPSDVDVIELHDCFSANELITYEAL
GLCPEGKAGELIDRGDNTYGGKWVINPSGGLISKGHPLGATGLAQCAELC
WQLRAEAGPRQVPGAKLALQHNIGLGGAVVVTLYKMGFP
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
6hsp Chain B Residue 503 [
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Receptor-Ligand Complex Structure
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PDB
6hsp
The peroxisomal zebrafish SCP2-thiolase (type-1) is a weak transient dimer as revealed by crystal structures and native mass spectrometry.
Resolution
1.73 Å
Binding residue
(original residue number in PDB)
K20 C87 F193 R206 L214 C217 C218 P219 F301
Binding residue
(residue number reindexed from 1)
K15 C82 F181 R194 L202 C205 C206 P207 F289
Annotation score
3
Enzymatic activity
Enzyme Commision number
2.3.1.155
: acetyl-CoA C-myristoyltransferase.
2.3.1.16
: acetyl-CoA C-acyltransferase.
2.3.1.176
: propanoyl-CoA C-acyltransferase.
Gene Ontology
Molecular Function
GO:0016746
acyltransferase activity
GO:0016747
acyltransferase activity, transferring groups other than amino-acyl groups
View graph for
Molecular Function
External links
PDB
RCSB:6hsp
,
PDBe:6hsp
,
PDBj:6hsp
PDBsum
6hsp
PubMed
30573650
UniProt
Q6P4V5
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