Structure of PDB 1oah Chain B Binding Site BS02
Receptor Information
>1oah Chain B (length=482) Species:
876
(Desulfovibrio desulfuricans) [
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TGIAETETKMSAFKGQFPQQYASYMKNNEDRIMTDYKGSVPYHKNDNVNP
LPKGFKHAQPYLKNLWLGYPFMYEYNETRGHTYAIDDFLNIDRINRFAAD
GKGNLPATCWNCKTPKMMEWVSQYGDKFWSMDVNEFRAKDKINAHDETIG
CANCHDPATMELRLYSEPLKDWLKRSGKDWQKMSRNEKRTLVCAQCHVEY
YFTHKDNGPAAKPVFPWDNGFNPEDMYQYYKGHGAKGPDGKPGPFVDWVH
AASKVPMIKMQHPEYETFQDGPHGAAGVSCADCHMQYVREDGKKISSHWM
TSPMKDPEMRACRQCHADKTGEYLRQRVLYTQQKTFDQLLKAQEMSVKAH
EAVRLANAYEGHRAANYEALMAEAREMVRKGQLFWDYVSAENSVGFHNPA
KALDTLMTSMECSQKAVDLATEATDFGIAPALAGDIKKLVPPILTLSRKL
QQDPEFLKQNPWTRLLPALPKAEQVWEGQDRA
Ligand information
Ligand ID
HEC
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,9-12H2,1-6H3,(H,39,40)(H,41,42);/q-4;+4/b21-7?,22-8?,26-13-,29-14-,30-15-,31-16-;
InChIKey
HXQIYSLZKNYNMH-LJNAALQVSA-N
SMILES
Software
SMILES
ACDLabs 10.04
O=C(O)CCC1=C(C2=CC6=C(C(=C/C)\C5=CC4=C(C(\C3=Cc7c(c(c8C=C1N2[Fe](N34)(N56)n78)CCC(=O)O)C)=C/C)C)C)C
OpenEye OEToolkits 1.5.0
CC=C1C(=C2C=C3C(=CC)C(=C4N3[Fe]56N2C1=Cc7n5c(c(c7C)CCC(=O)O)C=C8N6C(=C4)C(=C8CCC(=O)O)C)C)C
CACTVS 3.341
C\C=C1/C(=C2C=C3N4C(=Cc5n6c(C=C7N8C(=C(C)\C7=C/C)C=C1N2[Fe@@]468)c(C)c5CCC(O)=O)C(=C3C)CCC(O)=O)C
CACTVS 3.341
CC=C1C(=C2C=C3N4C(=Cc5n6c(C=C7N8C(=C(C)C7=CC)C=C1N2[Fe]468)c(C)c5CCC(O)=O)C(=C3C)CCC(O)=O)C
Formula
C34 H34 Fe N4 O4
Name
HEME C
ChEMBL
DrugBank
ZINC
PDB chain
1oah Chain B Residue 1520 [
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Receptor-Ligand Complex Structure
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PDB
1oah
Cytochrome C Nitrite Reductase from Desulfovibrio Desulfuricans Atcc 27774. The Relevance of the Two Calcium Sites in the Structure of the Catalytic Subunit (Nrfa)
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
N113 T115 F125 I128 R130 C146 C149 K150 C233 H234 Y237 H299 N429
Binding residue
(residue number reindexed from 1)
N76 T78 F88 I91 R93 C109 C112 K113 C196 H197 Y200 H262 N392
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.7.2.2
: nitrite reductase (cytochrome; ammonia-forming).
Gene Ontology
Molecular Function
GO:0042279
nitrite reductase (cytochrome, ammonia-forming) activity
Cellular Component
GO:0042597
periplasmic space
View graph for
Molecular Function
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Cellular Component
External links
PDB
RCSB:1oah
,
PDBe:1oah
,
PDBj:1oah
PDBsum
1oah
PubMed
12618432
UniProt
Q8VNU2
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