Structure of PDB 2blf Chain A Binding Site BS01
Receptor Information
>2blf Chain A (length=373) Species:
921
(Ancylobacter novellus) [
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ADTVTLPFANGERPLVMYPGKRPLIGLTARPPQLETPFSVFDEGLITPND
AFFVRYHLAGIPLEIDPDAFRLEIKGKVGTPLSLSLQDLKNDFPASEVVA
VNQCSGNSRGFVEPRVGGGQLANGAMGNARWRGVPLKAVLEKAGVQAGAK
QVTFGGLDGPVIPETPDFVKALSIDHATDGEVMLAYSMNGADLPWLNGYP
LRLVVPGYYGTYWVKHLNEITVIDKEFDGFWMKTAYRIPDNACACTEPGK
APTATIPINRFDVRSFITNVENGASVKAGEVPLRGIAFDGGYGITQVSVS
ADAGKSWTNATLDPGLGKYSFRGWKAVLPLTKGDHVLMCRATNARGETQP
MQATWNPAGYMRNVVEATRVIAA
Ligand information
Ligand ID
MSS
InChI
InChI=1S/C10H14N5O6PS2.Mo.O/c11-10-14-7-4(8(16)15-10)12-3-6(24)5(23)2(21-9(3)13-7)1-20-22(17,18)19;;/h2-3,9,12,23-24H,1H2,(H2,17,18,19)(H4,11,13,14,15,16);;/q;+2;/p-2/t2-,3+,9-;;/m1../s1
InChIKey
BDXDYZBRBRKVRM-MRZGRPIRSA-L
SMILES
Software
SMILES
CACTVS 3.341
NC1=NC2=C(N[CH]3[CH](N2)O[CH](CO[P](O)(O)=O)C4=C3S[Mo](=O)S4)C(=O)N1
CACTVS 3.341
NC1=NC2=C(N[C@@H]3[C@H](N2)O[C@H](CO[P](O)(O)=O)C4=C3S[Mo](=O)S4)C(=O)N1
OpenEye OEToolkits 1.5.0
C(C1C2=C(C3C(O1)NC4=C(N3)C(=O)NC(=N4)N)S[Mo](=O)S2)OP(=O)(O)O
OpenEye OEToolkits 1.5.0
C([C@@H]1C2=C([C@H]3[C@@H](O1)NC4=C(N3)C(=O)NC(=N4)N)S[Mo](=O)S2)OP(=O)(O)O
ACDLabs 10.04
O=P(O)(O)OCC2OC3NC=4N=C(N)NC(=O)C=4NC3C=1S[Mo](=O)SC=12
Formula
C10 H12 Mo N5 O7 P S2
Name
(MOLYBDOPTERIN-S,S)-OXO-MOLYBDENUM
ChEMBL
DrugBank
ZINC
PDB chain
2blf Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
2blf
Molecular Basis of Intramolecular Electron Transfer in Sulfite-Oxidizing Enzymes is Revealed by High Resolution Structure of a Heterodimeric Complex of the Catalytic Molybdopterin Subunit and a C-Type Cytochrome Subunit.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
F53 V54 R55 Y56 H57 N102 C104 S105 D158 F168 N197 R202 G210 T211 W213 V214 K215 Y236
Binding residue
(residue number reindexed from 1)
F53 V54 R55 Y56 H57 N102 C104 S105 D158 F168 N197 R202 G210 T211 W213 V214 K215 Y236
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R55 C104 A235 Y236
Catalytic site (residue number reindexed from 1)
R55 C104 A235 Y236
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0008482
sulfite oxidase activity
GO:0016491
oxidoreductase activity
GO:0020037
heme binding
GO:0030151
molybdenum ion binding
GO:0043546
molybdopterin cofactor binding
GO:0046872
metal ion binding
Biological Process
GO:0006790
sulfur compound metabolic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:2blf
,
PDBe:2blf
,
PDBj:2blf
PDBsum
2blf
PubMed
15863498
UniProt
Q9LA16
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