Performance Enhancement in Active Power Filter (APF) by FPGA Implementation

The generated electrical power in present days is not able to meet its end-user requirement as power demand is gradually increasing and expected to be increasing more in future days. In the power quality management, the parameters/factors like harmonic currents (HC) and reactive power (RP) yields the major issues in the power distribution units causing transformer heating, line losses, and machine vibration. To overcome these issues, several control mechanisms have been presented and implemented in recent past. The control algorithm based on synchronous reference frame (SRF) offers a better response by dividing the HC and RP. But the SRF based control algorithm requires better synchronization among the utility voltage and input current. To achieve this, the existing researches have used digital signal processing (DSP) and microcontroller, but these systems fail to provide better performance as they face issues like limited sampling time, less accuracy, and high computational complexity. Thus, to enhance the performance of active power filter (APF), we present an FPGA based approach. Also, to validate the performance of the proposed approach, we have used Xilinx 14.7 and Modelsim (6.3f) simulator and compared with other previous work. From the results analysis, it is found that the approach has good performance

Antigenic relationship between reactivity to hepatitis B e antigen and 19 kDa protein of Mycobacterium tuberculosis among the Tibetan settlers in Karnataka

McGlynn and her co-workers have reported that among the Vietnamese refugees in Philadelphia and among Alaskan natives who are hepatitis B carriers, there is a statistically significant association between anegative tuberculin test and the presence of hepatitis B e antigen. A repetition of this work among the population of Bangalore did not yield any significant results because of the very low incidence of hepatitis found among this population. However, on the basis of available data that hepatitis B infection is more prevalent among the Mongolian population than among people of other populations, the work was repeated among Tibetans who had settled down in Karnataka. This set of experiments showed that, contrary to the report of McGlynnet al, there is a statistically significant association between apositive tuberculin test and the presence of hepatitis B e antigen and that those individuals who showed the presence of hepatitis B e antigen exhibited less severe form of the disease than those who were negative to this antigen. These findings suggested that immunity to tuberculosis and hepatitis B infections may have a common underlying principle. Data bank search revealed a stretch of amino acid sequences which is common to hepatitis B e antigen and 19 kDa antigen ofMycobacterium tuberculosis. The significance of these results is discussed

Structure of 4,​6-​diacetylresorcinol

The title compd. is monoclinic, space group P21/c, with a 7.089(1)​, b 11.361(1)​, c 11.656(1) Å, and β 100.45(3)​°; Z = 4, dm = 1.410(5)​, dc = 1.397; T = 300 K; final R = 0.057 for 1701 reflections. At. coordinates are given. The mol. is almost planar, with O(9) and O(12) of the acetyl groups deviating by 0.074(1) and 0.071(2) Å from the mean plane of the benzene ring. The bond lengths and bond angles of the benzene ring are normal. There are intramol. H bonds between O(9) and H(14) and between O(12) and H(13)​; there are no intermol. H bonds. The mols. are packed in layers parallel to the ac plane and are held together essentially by van der Waals interactions

Structural analysis of peptide helices containing centrally positioned lactic acid residues

The effect of insertion of lactic acid (Lac) residues into peptide helices has been probed using specifically designed sequences. The crystal structures of 11-residue and 14-residue depsipeptides Boc-Val-Val-Ala-Leu-Val-Lac-Leu-Aib-Val-Ala-Leu-OMe (1) and Boc-Val-Ala-Leu-Aib-Val-Ala-Leu-Val-Lac-Leu-Aib-Val-Ala-Leu-OMe (3), containing centrally positioned Lac residues, have been determined. The structure of an 11-residue peptide Boc-Val-Ala-Leu-Aib-Val-Ala-Leu-Aib-Val-Ala-Leu-OMe (2), analog of a which is an amide previously determined Lac-containing depsipeptide, Boc-Val-Ala-Leu-Aib-Val-Lac-Leu-Aib-Val-Ala-Leu-OMe I. L. Karle, C. Das, and P. Balaram, Biopolymers, Vol. 59, (2001) pp. 276-289], is also reported. Peptide 1 adopts a helical fold, which is stabilized by mixture of 4→1 and 5→1 hydrogen bonds. Peptide 2 adopts a completely α-helical conformation stabilized by eight successive 5→1 hydrogen bonds. Peptide 3 appears to be predominately α-helical, with seven 5→1 hydrogen bonds and three 4→1 interaction interspersed in the sequence. In the structure of peptide 3 in addition to water molecules in the head-to-tail region, hydration at an internal segment of the helix is also observed. A comparison of five related peptide helices, containing a single Lac residue, reveals that the hydroxy acid can be comfortably accommodated at interior positions in the helix, with the closest C=O...O distances lying between 2.8 and 3.3 Å

Aromatic interactions in tryptophan-containing peptides: crystal structures of model tryptophan peptides and phenylalanine analogs

The crystal structures of the peptides, Boc-Leu-Trp-Val-OMe (1), Ac-Leu-Trp-Val-OMe (2a and 2b), Boc-Leu-Phe-Val-OMe (3), Ac-Leu-Phe-Val-OMe (4), and Boc-Ala-Aib-Leu-Trp-Val-OMe (5) have been determined by X-ray diffraction in order to explore the nature of interactions between aromatic rings, specifically the indole side chain of Trp residues. Peptide 1 adopts a type I β-turn conformation stabilized by an intramolecular 4→1 hydrogen bond. Molecules of 1 pack into helical columns stabilized by two intermolecular hydrogen bonds, Leu(1)NH...O(2)Trp(2) and IndoleNH...O(1)Leu(1). The superhelical columns further pack into the tetragonal space group P43 by means of a continuous network of indole-indole interactions. Peptide 2 crystallizes in two polymorphic forms, P21 (2a) and P212121 (2b). In both forms, the peptide backbone is extended, with antiparallel β-sheet association being observed in crystals. Extended strand conformations and antiparallel β-sheet formation are also observed in the Phe-containing analogs, Boc-Leu-Phe-Val-OMe (3) and Ac-Leu-Phe-Val-OMe (4). Peptide 5 forms a short stretch of 310-helix. Analysis of aromatic-aromatic and aromatic-amide interactions in the structures of peptides, 1, 2a, 2b are reported along with the examples of 14 Trp-containing peptides from the Cambridge Crystallographic Database. The results suggest that there is no dramatic preference for a preferred orientation of two proximal indole rings. In Trp-containing peptides specific orientations of the indole ring, with respect to the preceding and succeeding peptide units, appear to be preferred in β-turns and extended structures

Stereochemistry of Schellman motifs in peptides: crystal structure of a hexapeptide with a C-terminus 6 →1 hydrogen bond

The Schellman motif is a widely observed helix terminating structural motif in proteins, which is generated when the C-terminus residue adopts a left-handed helical (αL) conformation. The resulting hydrogen-bonding pattern involves the formation of an intramolecular 6→1 interaction. This helix terminating motif is readily mimicked in synthetic helical peptides by placing an achiral residue at the penultimate position of the sequence. Thus far, the Schellman motif has been characterized crystallographically only in peptide helices of length 7 residues or greater. The structure of the hexapeptide Boc-Pro-Aib-Gly-Leu-Aib-Leu-OMe in crystals reveal a short helical stretch terminated by a Schellman motif, with the formation of 6 → 1 C-terminus hydrogen bond. The crystals are in the space group P212121 with a = 18.155(3) Å, b = 18.864(8) Å, c = 11.834(4) Å, and Z = 4 . The final R1 and wR2 values are 7.68 and 14.6%, respectively , for 1524 observed reflections [Fo ≥ 3ς(Fo)]. A 6 →1 hydrogen bond between Pro(1)CO · · · Leu(6)NH and a 5 →2 hydrogen bond between Aib(2)CO · · · Aib(5)NH are observed. An analysis of the available oligopeptides having an achiral Aib residue at the penultimate position suggests that chain length and sequence effects may be the other determining factors in formation of Schellman motifs

The crystal structure of benzyloxycarbonyl-(α-aminoisobutyryl)-L-alanyl methyl ester

Crystals of the title compound, C20,H29,N3,O6, are monoclinic, space group P2, with a = 8-839 (3), b = f10.818 (3), c = 11.414 (2) A, β = 95.69 (2)° Z = 2; final R = 0.053. The molecular conformation is defined by the following angles (φ, ψ): Aib-1 58- 1, 36.8; Aib-2 68.3, 18.6; Ala-3 (φ) -136.2°. The molecule adopts a type 111 β -turn conformation stabilized by an intramolecular hydrogen bond between the CO of the benzyloxycarbonyl group and the NH of the alanyl residue. The hydrogen-bond parameters are N···O 2-904 Å and ∠NH···O 156.9°

Tryptophan-containing peptide helices: Interactions involving the indole side chain

Two designed peptide sequences containing Trp residues at positions i and i + 5 (Boc-Leu-Trp-Val-Ala-Aib-Leu-Trp-Val-OMe, 1) as well as i and i + 6 (Boc-Leu-Trp-Val-Aib-Ala-Aib-Leu-Trp-Val-OMe, 2) containing one and two centrally positioned Aib residues, respectively, for helix nucleation, have been shown to form stable helices in chloroform solutions. Structures derived from nuclear magnetic resonance (NMR) data reveal six and seven intramolecularly hydrogen-bonded NH groups in peptides 1 and 2, respectively. The helical conformation of octapeptide 1 has also been established in the solid state by X-ray diffraction. The crystal structure reveals an interesting packing motif in which helical columns are stabilized by side chain-backbone hydrogen bonding involving the indole Nε1H of Trp(2) as donor, and an acceptor C=O group from Leu(6) of a neighboring molecule. Helical columns also associate laterally, and strong interactions are observed between the Trp(2) and Trp(7) residues on neighboring molecules. The edge-to-face aromatic interactions between the indoles suggest a potential C-H…π interaction involving the Cζ3H of Trp(2). Concentration dependence of NMR chemical shifts provides evidence for peptide association in solution involving the Trp(2) Nε1H protons, presumably in a manner similar to that observed in the crystal

Stereochemistry of linking segments in the design of helix-helix motifs in peptides. Crystallographic comparison of a glycyl- dipropylglycyl-glycyl segment in a tripeptide and a 14-residue peptide

As part of a program to develop synthetic helix–linker–helix peptides the conformational properties of various linking segments are currently being investigated. The propensity of α,α-di-n-propylglycine (Dpg) residues to adopt backbone conformations in the extended region of the Ramachandran map, suggested by theoretical calculations and supported by experimental observations, prompted us to investigate the utility of the Gly-Dpg-Gly segment as a rigid linking motif. The crystal structure of the achiral tripeptide Boc-Gly-Dpg-Gly-OH 1 revealed a fully extended conformation (ϕ = ±178°, ψ = ±171°) at Dpg(2), with Gly(1) adopting a helical conformation (ϕ = +-72 °, ψ = +-32 °). The addition of flanking helical segments in the 14 residue peptide Boc-Val-Val-Ala-Leu-Gly-Dpg-Gly-Val-Ala-Leu-Aib-Val-Ala-Leu-OMe 2 resulted in the crystallographic characterization of a continuous helix over the entire length of the peptide. Peptide 1 crystallized in the centrosymmetric space group P21/c with a = 9.505(2) Å, b = 11.025(2) Å, c = 20.075(4) Å, β = 90.19° and Z = 4. Peptide 2 crystallized in space group P212121 with a = 10.172(1) Å, b = 17.521(4) Å, c = 46.438(12) Å and Z = 4. A comparative analysis of Gly-Dpg-Gly segments from available crystal structures indicates a high conformational variability of this segment. This analysis suggests that context and environment may be strong conformational determinants for the Gly-Dpg-Gly segment