Structure of PDB 5cjh Chain B Binding Site BS01
Receptor Information
>5cjh Chain B (length=733) Species:
242507
(Pyricularia oryzae 70-15) [
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TFGRCAVKSNQAGGGTRSHDWWPCQLRLDVLRQFQPSQNPLGGDFDYAEA
FQSLDYEAVKKDIAALMTESQDWWPADFGNYGGLFVRMAWHSAGTYRAMD
GRGGGGMGQQRFAPLNSWPDNQNLDKARRLIWPIKQKYGNKISWADLMLL
TGNVALENMGFKTLGFGGGRADTWQSDEAVYWGAETTFVPQGNDVRYNNS
VDINARADKLEKPLAATHMGLIYVNPEGPNGTPDPAASAKDIREAFGRMG
MNDTETVALIAGGHAFGKTHGAVKGSNIGPAPEAADLGMQGLGWHNSVGD
GNGPNQMTSGLEVIWTKTPTKWSNGYLESLINNNWTLVESPAGAHQWEAV
NGTVDYPDPFDKTKFRKATMLTSDLALINDPEYLKISQRWLEHPEELADA
FAKAWFKLLHRDLGPTTRYLGPEVPKESFIWQDPLPAREGDLIDDADVDK
LKAAILSTDGLDVSKLASTAMACATTYRNSDKRGGCNGARIALEPQRNWV
SNNPTQLSAVLDALKKVQSDFNGSNGNKKVSLADLIVLGGTAAVEKAAKD
AGVDIKVPFSAGRVDATQEQTDVTQFSYLEPQADGFRNYGRGTARARTEE
IMVDKASQLTLTPPELTVLVGGMRALGANYDGSDVGVFTANKGKLTPDFF
VNLVDMNIAWTASGADGESWVGTDRKSRSEKYKGSRADLVFGSHAELRAI
AEVYAENGNQEKFVKDFVAAWTKVMNLDRFDLK
Ligand information
Ligand ID
522
InChI
InChI=1S/C34H36N4O6.Fe/c1-7-21-16(2)26-14-31-34(20(6)44-43)19(5)27(38-31)12-24-17(3)22(8-10-32(39)40)29(36-24)15-30-23(9-11-33(41)42)18(4)25(37-30)13-28(21)35-26;/h7,12-15,20H,1,8-11H2,2-6H3,(H5,35,36,37,38,39,40,41,42,43);/q;+2/p-2/b24-12-,25-13-,26-14-,27-12-,28-13-,29-15-,30-15-,31-14-;/t20-;/m0./s1
InChIKey
OKPCXGMPQJNPGA-HGMAEFONSA-L
SMILES
Software
SMILES
OpenEye OEToolkits 1.9.2
Cc1c2n3c(c1C=C)C=C4C(=C(C5=[N]4[Fe]36[N]7=C(C=C8N6C(=C5)C(=C8C)CCC(=O)O)C(=C(C7=C2)[C@H](C)OO)C)CCC(=O)O)C
ACDLabs 12.01
O=C(O)CCC=2C1=CC8=N7[Fe]53N1C(C=2C)=CC4=N3C(C(=C4C)C(OO)C)=Cc6n5c(c(c6C)[C@H]=C)C=C7C(C)=C8CCC(=O)O
CACTVS 3.385
C[CH](OO)C1=C(C)C2=NC1=Cc3n4[Fe][N]5C(=C2)C(=C(CCC(O)=O)C5=CC6=NC(=Cc4c(C=C)c3C)C(=C6CCC(O)=O)C)C
OpenEye OEToolkits 1.9.2
Cc1c2n3c(c1C=C)C=C4C(=C(C5=[N]4[Fe]36[N]7=C(C=C8N6C(=C5)C(=C8C)CCC(=O)O)C(=C(C7=C2)C(C)OO)C)CCC(=O)O)C
CACTVS 3.385
C[C@H](OO)C1=C(C)C2=NC1=Cc3n4[Fe][N@@]5C(=C2)C(=C(CCC(O)=O)C5=CC6=NC(=Cc4c(C=C)c3C)C(=C6CCC(O)=O)C)C
Formula
C34 H34 Fe N4 O6
Name
Peroxidized Heme
ChEMBL
DrugBank
ZINC
PDB chain
5cjh Chain B Residue 801 [
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Receptor-Ligand Complex Structure
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PDB
5cjh
Eukaryotic Catalase-Peroxidase: The Role of the Trp-Tyr-Met Adduct in Protein Stability, Substrate Accessibility, and Catalysis of Hydrogen Peroxide Dismutation.
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
G133 L134 V136 R137 W140 Y273 V274 P276 F296 L309 I310 G313 H314 G317 K318 T319 H320 T358 S359 W365 W455
Binding residue
(residue number reindexed from 1)
G83 L84 V86 R87 W90 Y223 V224 P226 F246 L259 I260 G263 H264 G267 K268 T269 H270 T308 S309 W315 W405
Annotation score
1
Binding affinity
MOAD
: Kd=14.4uM
Enzymatic activity
Catalytic site (original residue number in PDB)
R137 H141 H314 W365 D424
Catalytic site (residue number reindexed from 1)
R87 H91 H264 W315 D374
Enzyme Commision number
1.11.1.21
: catalase peroxidase.
Gene Ontology
Molecular Function
GO:0004096
catalase activity
GO:0004601
peroxidase activity
GO:0020037
heme binding
GO:0046872
metal ion binding
Biological Process
GO:0006979
response to oxidative stress
GO:0042744
hydrogen peroxide catabolic process
GO:0070301
cellular response to hydrogen peroxide
GO:0098869
cellular oxidant detoxification
Cellular Component
GO:0005575
cellular_component
GO:0005576
extracellular region
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5cjh
,
PDBe:5cjh
,
PDBj:5cjh
PDBsum
5cjh
PubMed
26290940
UniProt
A4QUT2
|KATG2_PYRO7 Catalase-peroxidase 2 (Gene Name=KATG2)
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