Structure of PDB 3n5x Chain B

Receptor sequence
>3n5xB (length=411) Species: 10116 (Rattus norvegicus) [Search protein sequence]
RFLKVKNWETDVVLTDTLHLKSTLETGCTEHICMGSIMLPVRTKDQLFPL
AKEFLDQYYSSIKRFGSKAHMDRLEEVNKEIESTSTYQLKDTELIYGAKH
AWRNASRCVGRIQWSKLQVFDARDCTTAHGMFNYICNHVKYATNKGNLRS
AITIFPQRTDGKHDFRVWNSQLIRYAGYKQPDGSTLGDPANVQFTEICIQ
QGWKAPRGRFDVLPLLLQANGNDPELFQIPPELVLEVPIRHPKFDWFKDL
GLKWYGLPAVSNMLLEIGGLEFSACPFSGWYMGTEIGVRDYCDNSRYNIL
EEVAKKMDLDMRKTSSLWKDQALVEINIAVLYSFQSDKVTIVDHHSATES
FIKHMENEYRCRGGCPADWVWIVPPMSGSITPVFHQEMLNYRLTPSFEYQ
PDPWNTHVWKG
3D structure
PDB3n5x Role of zinc in isoform-selective inhibitor binding to neuronal nitric oxide synthase .
ChainB
Resolution1.8 Å
3D
structure
Catalytic site residues are labeled in the structure
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Enzymatic activity
Catalytic site (original residue number in PDB) C415 R418 W587 E592
Catalytic site (residue number reindexed from 1) C108 R111 W280 E285
Enzyme Commision number 1.14.13.39: nitric-oxide synthase (NADPH).
Interaction with ligand
Site
#
Ligand Ligand
chain
Binding residues on receptor
(original residue number in PDB)
Binding residues on receptor
(residue number reindexed from 1)
Binding affinity
BS01 XFK B W306 F691 H692 W8 F384 H385 MOAD: Ki=103nM
BindingDB: Ki=103nM
BS02 ZN B C326 C331 C28 C33
BS03 HEM B W409 C415 M570 F584 W587 E592 R596 W678 F704 W102 C108 M263 F277 W280 E285 R289 W371 F397
BS04 XFK B M336 V567 F584 W587 E592 R596 W678 M38 V260 F277 W280 E285 R289 W371 MOAD: Ki=103nM
BindingDB: Ki=103nM
BS05 XFK B R596 D600 V677 W678 R289 D293 V370 W371 MOAD: Ki=103nM
BindingDB: Ki=103nM
BS06 CL B R596 D600 R289 D293
Gene Ontology
Molecular Function
GO:0004517 nitric-oxide synthase activity
Biological Process
GO:0006809 nitric oxide biosynthetic process

View graph for
Molecular Function

View graph for
Biological Process
External links
PDB RCSB:3n5x, PDBe:3n5x, PDBj:3n5x
PDBsum3n5x
PubMed21138269
UniProtP29476|NOS1_RAT Nitric oxide synthase 1 (Gene Name=Nos1)

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