Structure of PDB 2fxf Chain B Binding Site BS02
Receptor Information
>2fxf Chain B (length=164) Species:
9606
(Homo sapiens) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
AKFVIRPATAADCSDILRLIKELAKYEYQVILTEKDLLEDGFGEHPFYHC
LVAEVPKEHWTPEGHSIVGFAMYYFTYDPWIGKLLYLEDFFVMSDYRGFG
IGSEILKNLSQVAMRCRCSSMHFLVAEWNEPSINFYKRRGASDLEGWRLF
KIDKEYLLKMATEE
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
2fxf Chain B Residue 2000 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
2fxf
The Crystal Structure of Human spermidine/spermine N1-acetyltransferase
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
Y27 D93 F94 F95 V96 R101 G102 F103 G104 G106 S107 L128 S136 F139 Y140 R142 R143
Binding residue
(residue number reindexed from 1)
Y26 D89 F90 F91 V92 R97 G98 F99 G100 G102 S103 L124 S132 F135 Y136 R138 R139
Annotation score
4
Enzymatic activity
Enzyme Commision number
2.3.1.57
: diamine N-acetyltransferase.
Gene Ontology
Molecular Function
GO:0004145
diamine N-acetyltransferase activity
GO:0005515
protein binding
GO:0008080
N-acetyltransferase activity
GO:0016746
acyltransferase activity
GO:0016747
acyltransferase activity, transferring groups other than amino-acyl groups
GO:0019809
spermidine binding
GO:0042802
identical protein binding
Biological Process
GO:0001525
angiogenesis
GO:0006596
polyamine biosynthetic process
GO:0009447
putrescine catabolic process
GO:0032918
spermidine acetylation
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:2fxf
,
PDBe:2fxf
,
PDBj:2fxf
PDBsum
2fxf
PubMed
UniProt
P21673
|SAT1_HUMAN Diamine acetyltransferase 1 (Gene Name=SAT1)
[
Back to BioLiP
]