Structure of PDB 6t1t Chain A Binding Site BS02
Receptor Information
>6t1t Chain A (length=635) Species:
5482
(Candida tropicalis) [
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SRDVLSTLKKNNKNTLLLFGSQTGTAEDYANKLSRELHSRFGLKTMVADF
ADYDWDNFGDITEDILVFFIVATYGEGEPTDNADEFHTWLTEEADTLSTL
RYTVFGLGNSTYEFFNAIGRKFDRLLSEKGGDRFAEYAEGDDGTGTLDED
FMAWKDNVFDALKNDLNFEEKELKYEPNVKLTERDDLSAADSQVSLGEPN
KKYINSEGIDLTKGPFDHTHPYLARITETRELFSSKERHCIHVEFDISES
NLKYTTGDHLAIWPSNSDENIKQFAKCFGLEDKLDTVIELKALDSTYTIP
FPTPITYGAVIRHHLEISGPVSRQFFLSIAGFAPDEETKKTFTRLGGDKQ
EFATKVTRRKFNIADALLYSSNNTPWSDVPFEFLIENIQHLTPRYYSISS
SSLSEKQLINVTAVVEAEEEADGRPVTGVVTNLLKNIEIAQNKTGEKPLV
HYDLSGPRGKFNKFKLPVHVRRSNFKLPKNSTTPVILIGPGTGVAPLRGF
VRERVQQVKNGVNVGKTLLFYGCRNSNEDFLYKQEWAEYASVLGENFEMF
NAFSRQDPSKKVYVQDKILENSQLVHELLTEGAIIYVCGDASRMARDVQT
TISKIVAKSREISEDKAAELVKSWKVQNRYQEDVW
Ligand information
Ligand ID
FMN
InChI
InChI=1S/C17H21N4O9P/c1-7-3-9-10(4-8(7)2)21(15-13(18-9)16(25)20-17(26)19-15)5-11(22)14(24)12(23)6-30-31(27,28)29/h3-4,11-12,14,22-24H,5-6H2,1-2H3,(H,20,25,26)(H2,27,28,29)/t11-,12+,14-/m0/s1
InChIKey
FVTCRASFADXXNN-SCRDCRAPSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(COP(=O)(O)O)O)O)O
OpenEye OEToolkits 1.7.6
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)C[C@@H]([C@@H]([C@@H](COP(=O)(O)O)O)O)O
ACDLabs 12.01
N=2C(=O)NC(=O)C3=Nc1cc(C)c(C)cc1N(C=23)CC(O)C(O)C(O)COP(=O)(O)O
CACTVS 3.385
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[CH](O)[CH](O)[CH](O)CO[P](O)(O)=O)c2cc1C
CACTVS 3.385
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[C@H](O)[C@H](O)[C@H](O)CO[P](O)(O)=O)c2cc1C
Formula
C17 H21 N4 O9 P
Name
FLAVIN MONONUCLEOTIDE;
RIBOFLAVIN MONOPHOSPHATE
ChEMBL
CHEMBL1201794
DrugBank
DB03247
ZINC
ZINC000003831425
PDB chain
6t1t Chain A Residue 701 [
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Receptor-Ligand Complex Structure
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PDB
6t1t
Biochemical and structural insights into the cytochrome P450 reductase from Candida tropicalis.
Resolution
2.08 Å
Binding residue
(original residue number in PDB)
S65 Q66 T67 T69 A70 T117 Y118 G119 L151 G152 N153 Y156 F159
Binding residue
(residue number reindexed from 1)
S21 Q22 T23 T25 A26 T73 Y74 G75 L107 G108 N109 Y112 F115
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
S441 C632 D677 W679
Catalytic site (residue number reindexed from 1)
S397 C588 D633 W635
Enzyme Commision number
1.6.2.4
: NADPH--hemoprotein reductase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0003958
NADPH-hemoprotein reductase activity
GO:0003959
NADPH dehydrogenase activity
GO:0009055
electron transfer activity
GO:0010181
FMN binding
GO:0016491
oxidoreductase activity
GO:0050660
flavin adenine dinucleotide binding
GO:0050661
NADP binding
Biological Process
GO:0006696
ergosterol biosynthetic process
GO:0016126
sterol biosynthetic process
Cellular Component
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005741
mitochondrial outer membrane
GO:0005783
endoplasmic reticulum
GO:0005789
endoplasmic reticulum membrane
GO:0005829
cytosol
GO:0005886
plasma membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6t1t
,
PDBe:6t1t
,
PDBj:6t1t
PDBsum
6t1t
PubMed
31882753
UniProt
Q5PXH3
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