PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 19074821-1 2009 Vitamin B(6) is essential in all organisms, due to its requirement as a cofactor in the form of pyridoxal 5"-phosphate (PLP) for key metabolic enzymes. Niacinamide 0-9 pyridoxal phosphatase Homo sapiens 120-123 25972531-1 2015 BACKGROUND: Vitamin B-6 interconversion enzymes are important for supplying pyridoxal 5"-phosphate (PLP), the co-enzyme form, to tissues. Niacinamide 12-21 pyridoxal phosphatase Homo sapiens 100-103 23444286-3 2013 The apparent clearances (CL) of doxylamine and pyridoxal 5"-phosphate (PLP; the active metabolite of vitamin B(6) ) during the first-trimester pregnancy in women who participated in a Diclectin randomized trial were compared with those of healthy, adult, nonpregnant women who participated in a voluntary PK trial. Niacinamide 101-110 pyridoxal phosphatase Homo sapiens 71-74 20233826-2 2010 OBJECTIVE: To conduct a systematic review with meta-analysis of prospective studies assessing the association of vitamin B(6) intake or blood levels of pyridoxal 5"-phosphate (PLP; the active form of vitamin B(6)) with risk of colorectal cancer. Niacinamide 200-209 pyridoxal phosphatase Homo sapiens 176-179 23185966-1 2012 Pyridoxal-5"-phosphate (PLP) represents an active form of Vitamin B(6) that shows relatively fast imine formation with hydrazines under physiological conditions without the need of a catalyst. Niacinamide 58-67 pyridoxal phosphatase Homo sapiens 24-27 21349613-14 2011 However, erythrocyte PLP concentration was positively associated with blood glucose level (r(s) = 0.88, p = 0.002) at admission in the deficient vitamin B-6 group after adjusting for age, gender, APACHE II score, diabetic history and insulin therapy. Niacinamide 145-154 pyridoxal phosphatase Homo sapiens 21-24 17851041-2 2007 We hypothesized that the gene PNPO (pyridoxine 5"-phosphatase oxidase gene) might be a candidate for susceptibility to schizophrenia because PNPO encodes pyridoxamine 5"-phosphate oxidase (EC 1.4.3.5), a rate-limiting enzyme in pyridoxal 5"-phosphate (PLP, vitamin B(6)) synthesis. Niacinamide 257-266 pyridoxal phosphatase Homo sapiens 252-255 18510874-4 2008 Once inside the cells, the transduced PEP-1-PLPP fusion protein was stable for 36 h. The concentration of PLP was markedly decreased by the addition of exogenous PEP-1-PLPP to media pretreated with the vitamin B(6) precursors; pyridoxine, pyridoxal kinase and pyridoxine-5"-phosphate oxidase into cells. Niacinamide 202-211 pyridoxal phosphatase Homo sapiens 44-47 18510874-5 2008 The results suggest that the transduction of the PEP-1-PLPP fusion protein can be one mode of PLP level regulation, and to replenish this enzyme in the various neurological disorders related to vitamin B(6). Niacinamide 194-203 pyridoxal phosphatase Homo sapiens 55-58 17851041-3 2007 PLP is a metabolically-active form of vitamin B(6) and thus, is required as a co-factor for enzymes involved in both homocysteine metabolism and synthesis of neurotransmitters such as catecholamine. Niacinamide 38-47 pyridoxal phosphatase Homo sapiens 0-3 12194934-1 2002 BACKGROUND: Pyridoxal 5"-phosphate (PLP) is the biologically active form of vitamin B(6). Niacinamide 76-85 pyridoxal phosphatase Homo sapiens 36-39 12662064-1 2003 The tautomeric equilibria of a series of 3-hydroxypyridine derivatives including pyridoxal-5"-phosphate (PLP), the active form of vitamin B(6), have been studied using density functional calculations (B3LYP/6-311+G//B3LYP/6-31G) in the gas phase and in different solvents. Niacinamide 130-139 pyridoxal phosphatase Homo sapiens 105-108 12194934-14 2002 CONCLUSIONS: This new PLP assay is the first homogeneous, nonradioactive, vitamin B(6) diagnostic method. Niacinamide 74-83 pyridoxal phosphatase Homo sapiens 22-25