Structure of PDB 8x2l Chain B Binding Site BS02
Receptor Information
>8x2l Chain B (length=525) Species:
9606
(Homo sapiens) [
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EGLSIFVILVWLGLNVFLFVWYYRVYDIPPKFFYTRKLLGSALALARAPA
ACLNFNCMLILLPVCRNLLSFLRGSSTRVRRQLDRNLTFHKMVAWMIALH
SAIHTIAHLFNVEWCVNARVNNSDPYSVALSELGDRQNESYLNFARKRIK
NPEGGLYLAVTLLAGITGVVITLCLILIITSSTKTIRRSYFEVFWYTHHL
FVIFFIGLAIHGAERIVRGQTAESLAVHNITVCEQKISEWGKIKECPIPQ
FAGNPPMTWKWIVGPMFLYLCERLVRFWRSQQKVVITKVVTHPFKTIELQ
MKKKGFKMEVGQYIFVKCPKVSKLEWHPFTLTSAPEEDFFSIHIRIVGDW
TEGLFNACGCDKLPKIAVDGPFGTASEDVFSYEVVMLVGAGIGVTPFASI
LKSVWYKYCNNATNLKLKKIYFYWLCRDTHAFEWFADLLQLLESQMQERN
NAGFLSYNIYLTGQKTLYGRPNWDNEFKTIASQHPNTRIGVFLCGPEALA
ETLSKQSISNSESGPRGVHFIFNKE
Ligand information
Ligand ID
HEM
InChI
InChI=1S/C34H34N4O4.Fe/c1-7-21-17(3)25-13-26-19(5)23(9-11-33(39)40)31(37-26)16-32-24(10-12-34(41)42)20(6)28(38-32)15-30-22(8-2)18(4)27(36-30)14-29(21)35-25;/h7-8,13-16H,1-2,9-12H2,3-6H3,(H4,35,36,37,38,39,40,41,42);/q;+2/p-2/b25-13-,26-13-,27-14-,28-15-,29-14-,30-15-,31-16-,32-16-;
InChIKey
KABFMIBPWCXCRK-RGGAHWMASA-L
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
Cc1c2n3c(c1CCC(=O)O)C=C4C(=C(C5=[N]4[Fe]36[N]7=C(C=C8N6C(=C5)C(=C8C)C=C)C(=C(C7=C2)C)C=C)C)CCC(=O)O
CACTVS 3.385
CC1=C(CCC(O)=O)C2=Cc3n4[Fe]5|6|N2=C1C=c7n5c(=CC8=N|6C(=Cc4c(C)c3CCC(O)=O)C(=C8C=C)C)c(C)c7C=C
ACDLabs 12.01
C=1c3c(c(c4C=C5C(=C(C=6C=C7C(=C(C8=CC=2C(=C(C=1N=2[Fe](n34)(N5=6)N78)CCC(=O)O)C)\C=C)C)\C=C)C)C)CCC(=O)O
Formula
C34 H32 Fe N4 O4
Name
PROTOPORPHYRIN IX CONTAINING FE;
HEME
ChEMBL
DrugBank
DB18267
ZINC
PDB chain
8x2l Chain B Residue 602 [
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Receptor-Ligand Complex Structure
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PDB
8x2l
Activation mechanism of phagocyte NADPH oxidase by cytosolic factors
Resolution
2.99 Å
Binding residue
(original residue number in PDB)
A57 L60 S112 H115 T116 H119 G179 I182 T183 F215 L219 H222 G223 R226 V228 P267 M268 T269
Binding residue
(residue number reindexed from 1)
A50 L53 S101 H104 T105 H108 G168 I171 T172 F204 L208 H211 G212 R215 V217 P256 M257 T258
Annotation score
4
Enzymatic activity
Enzyme Commision number
1.-.-.-
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0009055
electron transfer activity
GO:0016175
superoxide-generating NAD(P)H oxidase activity
GO:0016491
oxidoreductase activity
GO:0020037
heme binding
GO:0046872
metal ion binding
GO:0046982
protein heterodimerization activity
GO:0050660
flavin adenine dinucleotide binding
GO:0050664
oxidoreductase activity, acting on NAD(P)H, oxygen as acceptor
Biological Process
GO:0006801
superoxide metabolic process
GO:0006952
defense response
GO:0006954
inflammatory response
GO:0007584
response to nutrient
GO:0009410
response to xenobiotic stimulus
GO:0032760
positive regulation of tumor necrosis factor production
GO:0034220
monoatomic ion transmembrane transport
GO:0042554
superoxide anion generation
GO:0045087
innate immune response
GO:0045730
respiratory burst
GO:0045766
positive regulation of angiogenesis
GO:0050665
hydrogen peroxide biosynthetic process
GO:0071276
cellular response to cadmium ion
GO:0071361
cellular response to ethanol
GO:0071456
cellular response to hypoxia
GO:0097411
hypoxia-inducible factor-1alpha signaling pathway
GO:1904044
response to aldosterone
GO:1904845
cellular response to L-glutamine
GO:1990776
response to angiotensin
Cellular Component
GO:0005635
nuclear envelope
GO:0005737
cytoplasm
GO:0005789
endoplasmic reticulum membrane
GO:0005886
plasma membrane
GO:0016020
membrane
GO:0030425
dendrite
GO:0030670
phagocytic vesicle membrane
GO:0034702
monoatomic ion channel complex
GO:0035579
specific granule membrane
GO:0043020
NADPH oxidase complex
GO:0043025
neuronal cell body
GO:0045335
phagocytic vesicle
GO:0070821
tertiary granule membrane
GO:0097038
perinuclear endoplasmic reticulum
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:8x2l
,
PDBe:8x2l
,
PDBj:8x2l
PDBsum
8x2l
PubMed
38355798
UniProt
P04839
|CY24B_HUMAN Cytochrome b-245 heavy chain (Gene Name=CYBB)
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