Mechanism of inducible nitric-oxide synthase dimerization inhibition by novel pyrimidine imidazoles. - Wikidata - awgldk - TriplyDB

Mechanism of inducible nitric-oxide synthase dimerization inhibition by novel pyrimidine imidazoles.

Mechanism of inducible nitric-oxide synthase dimerization inhibition by novel pyrimidine imidazoles.

http://www.wikidata.org/entity/Q37000579

about

Characterization of calmodulin-free murine inducible nitric-oxide synthase Protein-protein interactions as drug targets.Escherichia coli K1 induces pterin production for enhanced expression of Fcγ receptor I to invade RAW 264.7 macrophages.Nitric oxide synthase and structure-based inhibitor design.Computational Structural Biology of -nitrosylation of Cancer Targets

P2860

Q28545170-56B50EF5-F6F9-4E94-A7D5-C7BFCFEF28C2 Q35824701-E76161C8-8628-4542-A2C6-D2797855BE69 Q37624700-C56A80F2-07EF-4697-AC81-056A56C9AEF2 Q39021613-15D4E042-3B9B-4074-9FC1-128D7B3E7EF3 Q58781601-A9DEAEA6-A2D8-45B0-A4EB-B3A6EF8069B8

P2860

Mechanism of inducible nitric-oxide synthase dimerization inhibition by novel pyrimidine imidazoles.

http://www.wikidata.org/entity/Q37000579

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 21 May 2013

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Mechanism of inducible nitric- ...... y novel pyrimidine imidazoles.

@en

Mechanism of inducible nitric- ...... y novel pyrimidine imidazoles.

@nl

type

label

Mechanism of inducible nitric- ...... y novel pyrimidine imidazoles.

@en

Mechanism of inducible nitric- ...... y novel pyrimidine imidazoles.

@nl

prefLabel

Mechanism of inducible nitric- ...... y novel pyrimidine imidazoles.

@en

Mechanism of inducible nitric- ...... y novel pyrimidine imidazoles.

@nl

P1433

Q37000579-C1EC036C-93E1-4D21-9871-1CB39EB7B83D

P1476

Q37000579-C4FDD67B-8229-461D-92F9-4ACF2BB58281

P2093

Q37000579-00AA2351-68DA-43F8-BE3D-6B44A900A3FB

Q37000579-14B8BECB-2971-4A0F-92AE-239CC96DB74D

Q37000579-8A2325F0-2ED2-43E8-A453-20880F20E0A3

Q37000579-AEAD841C-15C0-423C-AA57-A0A1EBCEAB5E

Q37000579-B7CED5EE-33EC-4598-8C59-0DB9136CF42B

Q37000579-C8B8E2BC-5523-4413-9792-6209F561D883

Q37000579-E37938B5-BDF8-44B9-BE0E-69DE9A64475A

Q37000579-F9B31051-1412-4A53-98F0-312CFE9E8FCE

P2860

Q37000579-04CB99CC-F6F7-4EEA-9F8A-6577257757B1

Q37000579-07837660-646F-4219-8F16-1EB509F8735F

Q37000579-09CC760D-6381-41E7-AE94-F0BCCAEB8CEB

Q37000579-12A893B5-B607-4A7B-A3AC-2C5E5BAC34ED

Q37000579-16D4EE38-F4ED-440C-B804-5AC4C2570606

Q37000579-1E5DDD73-5512-4C61-94D7-19DB06BAF91F

Q37000579-22D6B7D9-546E-46D1-B26A-39DF10DA24CC

Q37000579-248262E0-698D-4DF9-8FE5-3C112692EBAA

Q37000579-25E61DCB-DB2E-4D6E-A326-FC7D573296F7

Q37000579-2B35C881-D188-4AA9-B8DE-7E671B39205E

P304

Q37000579-6E1B3643-27B8-424A-A3AD-7D970EC41211

P31

Q37000579-1CDB5224-6F47-478A-984A-6B148223B809

P356

Q37000579-963A459F-1458-431B-87FB-9D576752B474

P407

Q37000579-1C0E10D4-3AC4-4D26-B191-714F0361C46F

P433

Q37000579-108CA4E3-C41A-4913-AD93-E313A21D71E7

P478

Q37000579-5F132F75-9AF7-4F2E-A845-E079D4F78B19

P577

Q37000579-17EF47AD-63A9-4281-9BF3-095CA74188EC

P5875

Q37000579-E8B2E900-2CD2-4BEB-848F-9ED6E9A75E16

P698

Q37000579-F969F568-F95E-4672-834B-EDF0779C1721

P932

Q37000579-5C1F3B5A-5C18-49FA-8D03-D9416AFF127C

P356

JBC.M112.446542

P1433

Journal of Biological Chemistry

P1476

Mechanism of inducible nitric- ...... y novel pyrimidine imidazoles.

@en

P2093

Amit Saha

http://www.w3.org/2001/XMLSchema#string

Arnab Ghosh

http://www.w3.org/2001/XMLSchema#string

Brindaban C Ranu

http://www.w3.org/2001/XMLSchema#string

Dennis J Stuehr

http://www.w3.org/2001/XMLSchema#string

Koustubh Panda

http://www.w3.org/2001/XMLSchema#string

Latika Nagpal

http://www.w3.org/2001/XMLSchema#string

Mohammad M Haque

http://www.w3.org/2001/XMLSchema#string

Nirmalya Mukherjee

http://www.w3.org/2001/XMLSchema#string

P2860

Allosteric inhibitors of inducible nitric oxide synthase dimerization discovered via combinatorial chemistry

Structure of a nitric oxide synthase heme protein from Bacillus subtilis

Design, synthesis, and activity of 2-imidazol-1-ylpyrimidine derived inducible nitric oxide synthase dimerization inhibitors

The structure of nitric oxide synthase oxygenase domain and inhibitor complexes

Structure of nitric oxide synthase oxygenase dimer with pterin and substrate

Nitric oxide synthases: structure, function and inhibition

Characterization of the inducible nitric oxide synthase oxygenase domain identifies a 49 amino acid segment required for subunit dimerization and tetrahydrobiopterin interaction

Characterization of heme-deficient neuronal nitric-oxide synthase reveals a role for heme in subunit dimerization and binding of the amino acid substrate and tetrahydrobiopterin.

Mammalian nitric oxide synthases.

Visualizing inducible nitric-oxide synthase in living cells with a heme-binding fluorescent inhibitor.

P304

19685-19697

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1074/JBC.M112.446542

http://www.w3.org/2001/XMLSchema#string

P407

P433

27

http://www.w3.org/2001/XMLSchema#string

P478

288

http://www.w3.org/2001/XMLSchema#string

P577

2013-05-21T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

236930581

http://www.w3.org/2001/XMLSchema#string

P698

23696643

http://www.w3.org/2001/XMLSchema#string

P932

3707674

http://www.w3.org/2001/XMLSchema#string