Raster3D Version 2.0. A program for photorealistic molecular graphics - PubMed (original) (raw)
Raster3D Version 2.0. A program for photorealistic molecular graphics
E A Merritt et al. Acta Crystallogr D Biol Crystallogr. 1994.
Abstract
Raster3D Version 2.0 is a program suite for the production of photorealistic molecular graphics images. The code is hardware independent, and is particularly suited for use in producing large raster images of macromolecules for output to a film recorder or high-quality color printer. The Raster3D suite contains programs for composing illustrations of space-filling models, ball-and-stick models and ribbon-and-cylinder representations. It may also be used to render figures composed using other graphics tools, notably the widely used program Molscript [Kraulis (1991). J. Appl. Cryst. 24, 946-950].
Similar articles
- An extensively modified version of MolScript that includes greatly enhanced coloring capabilities.
Esnouf RM. Esnouf RM. J Mol Graph Model. 1997 Apr;15(2):132-4, 112-3. doi: 10.1016/S1093-3263(97)00021-1. J Mol Graph Model. 1997. PMID: 9385560 - Raster3D: photorealistic molecular graphics.
Merritt EA, Bacon DJ. Merritt EA, et al. Methods Enzymol. 1997;277:505-24. doi: 10.1016/s0076-6879(97)77028-9. Methods Enzymol. 1997. PMID: 18488322 No abstract available. - SETOR: hardware-lighted three-dimensional solid model representations of macromolecules.
Evans SV. Evans SV. J Mol Graph. 1993 Jun;11(2):134-8, 127-8. doi: 10.1016/0263-7855(93)87009-t. J Mol Graph. 1993. PMID: 8347566 - Further additions to MolScript version 1.4, including reading and contouring of electron-density maps.
Esnouf RM. Esnouf RM. Acta Crystallogr D Biol Crystallogr. 1999 Apr;55(Pt 4):938-40. doi: 10.1107/s0907444998017363. Acta Crystallogr D Biol Crystallogr. 1999. PMID: 10089341 - Visual methods from atoms to cells.
Goodsell DS. Goodsell DS. Structure. 2005 Mar;13(3):347-54. doi: 10.1016/j.str.2005.01.012. Structure. 2005. PMID: 15766535 Review.
Cited by
- Expanding the genetic and phenotypic landscape of replication factor C complex-related disorders: RFC4 deficiency is linked to a multisystemic disorder.
Morimoto M, Ryu E, Steger BJ, Dixit A, Saito Y, Yoo J, van der Ven AT, Hauser N, Steinbach PJ, Oura K, Huang AY, Kortüm F, Ninomiya S, Rosenthal EA, Robinson HK, Guegan K, Denecke J, Subramony SH, Diamonstein CJ, Ping J, Fenner M, Balton EV, Strohbehn S, Allworth A, Bamshad MJ, Gandhi M, Dipple KM, Blue EE, Jarvik GP; University of Washington Center for Rare Disease Research; Lau CC, Holm IA, Weisz-Hubshman M, Solomon BD; Undiagnosed Diseases Network; Nelson SF, Nishino I, Adams DR, Kang S, Gahl WA, Toro C, Myung K, Malicdan MCV. Morimoto M, et al. Am J Hum Genet. 2024 Sep 5;111(9):1970-1993. doi: 10.1016/j.ajhg.2024.07.008. Epub 2024 Aug 5. Am J Hum Genet. 2024. PMID: 39106866 - Macrocephaly and developmental delay caused by missense variants in RAB5C.
Koop K, Yuan W, Tessadori F, Rodriguez-Polanco WR, Grubbs J, Zhang B, Osmond M, Graham G, Sawyer S, Conboy E, Vetrini F, Treat K, Płoski R, Pienkowski VM, Kłosowska A, Fieg E, Krier J, Mallebranche C, Alban Z, Aldinger KA, Ritter D, Macnamara E, Sullivan B, Herriges J, Alaimo JT, Helbig C, Ellis CA, van Eyk C, Gecz J, Farrugia D, Osei-Owusu I, Adès L, van den Boogaard MJ, Fuchs S, Bakker J, Duran K, Dawson ZD, Lindsey A, Huang H, Baldridge D, Silverman GA, Grant BD, Raizen D; Undiagnosed Diseases Network; van Haaften G, Pak SC, Rehmann H, Schedl T, van Hasselt P. Koop K, et al. Hum Mol Genet. 2023 Oct 17;32(21):3063-3077. doi: 10.1093/hmg/ddad130. Hum Mol Genet. 2023. PMID: 37552066 Free PMC article. - A brief history of visualizing membrane systems in molecular dynamics simulations.
Corey RA, Baaden M, Chavent M. Corey RA, et al. Front Bioinform. 2023 May 5;3:1149744. doi: 10.3389/fbinf.2023.1149744. eCollection 2023. Front Bioinform. 2023. PMID: 37213533 Free PMC article. - A second case of glutaminase hyperactivity: Expanding the phenotype with epilepsy.
Rumping L, Pouwels PJW, Wolf NI, Rehmann H, Wamelink MMC, Waisfisz Q, Jans JJM, Prinsen HCMT, van de Kamp JM, van Hasselt PM. Rumping L, et al. JIMD Rep. 2023 Feb 24;64(3):217-222. doi: 10.1002/jmd2.12359. eCollection 2023 May. JIMD Rep. 2023. PMID: 37151363 Free PMC article. - Bi-allelic variants in NAE1 cause intellectual disability, ischiopubic hypoplasia, stress-mediated lymphopenia and neurodegeneration.
Muffels IJJ, Schene IF, Rehmann H, Massink MPG, van der Wal MM, Bauder C, Labeur M, Armando NG, Lequin MH, Houben ML, Giltay JC, Haitjema S, Huisman A, Vansenne F, Bluvstein J, Pappas J, Shailee LV, Zarate YA, Mokry M, van Haaften GW, Nieuwenhuis EES, Refojo D, van Wijk F, Fuchs SA, van Hasselt PM. Muffels IJJ, et al. Am J Hum Genet. 2023 Jan 5;110(1):146-160. doi: 10.1016/j.ajhg.2022.12.003. Am J Hum Genet. 2023. PMID: 36608681 Free PMC article.
LinkOut - more resources
Other Literature Sources