Structure of PDB 1q9i Chain A Binding Site BS04
Receptor Information
>1q9i Chain A (length=568) Species:
56812
(Shewanella frigidimarina) [
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ADNLAEFHVQNQECDSCHTPDGELSNDSLTYENTQCVSCHGTLAEVAETT
KHEHYNAHASHFPGEVACTSCHSAHEKSMVYCDSCHSFDFNMPYAKKWLR
DEPTIAELAKDKSERQAALASAPHDTVDVVVVGSGGAGFSAAISATDSGA
KVILIEKEPVIGGNAKLAAGGMNAAWTDQQKAKKITDSPELMFEDTMKGG
QNINDPALVKVLSSHSKDSVDWMTAMGADLTDVGMMGGASVNRAHRPTGG
CGVGAHVVQVLYDNAVKRNIDLRMNTRGIEVLKDDKGTVKGILVKGMYKG
YYWVKADAVILATGGFAKNNERVAKLDPSLKGFISTNQPGAVGDGLDVAE
NAGGALKDMQYIQAHPTLSVKGGVMVTEAVRGNGAILVNREGKRFVNEIT
TRDKASAAILAQTGKSAYLIFDDSVRKSLCKIDKYIGLGVAPTADSLVKL
GKMEGIDGKALTETVARYNSLVSSGKDTDFERPNLPRALNEGNYYAIEVT
PGVHHTMGGVMIDTKAEVMNAKKQVIPGLYGAGEVTGGVHGANRLGGNAI
SDIITFGRLAGEEAAKYS
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
1q9i Chain A Residue 804 [
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Receptor-Ligand Complex Structure
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PDB
1q9i
Probing Domain Mobility in a Flavocytochrome
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
Y55 S60 H61 F62 C82 C85 H86 F88 Q338 V374 K431 K434 Y435
Binding residue
(residue number reindexed from 1)
Y55 S60 H61 F62 C82 C85 H86 F88 Q338 V374 K431 K434 Y435
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
M236 Q363 H365 M375 E378 R381 R402 H504 H505 R544
Catalytic site (residue number reindexed from 1)
M236 Q363 H365 M375 E378 R381 R402 H504 H505 R544
Enzyme Commision number
1.3.2.4
: fumarate reductase (cytochrome).
Gene Ontology
Molecular Function
GO:0010181
FMN binding
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
Biological Process
GO:0008202
steroid metabolic process
Cellular Component
GO:0042597
periplasmic space
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1q9i
,
PDBe:1q9i
,
PDBj:1q9i
PDBsum
1q9i
PubMed
15109257
UniProt
Q07WU7
|FCCA_SHEFN Fumarate reductase (cytochrome) (Gene Name=fccA)
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