MDH1

مالات دهیدروژناز سیتوپلاسمی یا مالات دهیدروژناز ۱ (انگلیسی: Malate dehydrogenase 1) یک آنزیم است که در انسان توسط ژن «MDH1» کُدگذاری می‌شود.[4]

MDH1
معین‌کننده‌ها
نام‌های دیگرMDH1, HEL-S-32, MDH-s, MDHA, MGC:1375, MOR2, malate dehydrogenase 1, EIEE88, DEE88, KAR
شناسه‌های بیرونیOMIM: 154200 MGI: 97051 HomoloGene: 4324 GeneCards: MDH1
EC number1.1.1.96
هم‌ساخت‌شناسی
گونه‌هاانسانموش
Entrez

4190

17449

آنسامبل

ENSG00000014641

ENSMUSG00000020321

یونی‌پروت

P40925

P14152

RefSeq (mRNA)

NM_001199111، NM_001199112، NM_001316374 NM_005917، NM_001199111، NM_001199112، NM_001316374

NM_001316675 NM_008618، NM_001316675

RefSeq (پروتئین)

NP_001186041، NP_001303303، NP_005908 NP_001186040، NP_001186041، NP_001303303، NP_005908

NP_032644 NP_001303604، NP_032644

موقعیت (UCSC)n/aChr : 21.56 – 21.57 Mb
جستجوی PubMed[2][3]
ویکی‌داده
مشاهده/ویرایش HumanView/Edit Mouse

این آنزیم، اکسیداسیون برگشت‌پذیر مالات به اگزالواستات را با استفاده از کوفاکتور نیکوتین‌آمید آدنین دی‌نوکلئوتید کاتالیزه می‌کند و نقش محوری در حمل‌ونقل مالات-آسپارتات مابین میتوکندری و سیتوزول دارد.

منابع

  1. GRCm38: Ensembl release 89: ENSMUSG00000020321 - Ensembl, May 2017
  2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Entrez Gene: Malate dehydrogenase 1, NAD (soluble)".

بیشتر بخوانید

  • Fahien LA, Laboy JI, Din ZZ, Prabhakar P, Budker T, Chobanian M (Apr 1999). "Ability of cytosolic malate dehydrogenase and lactate dehydrogenase to increase the ratio of NADPH to NADH oxidation by cytosolic glycerol-3-phosphate dehydrogenase". Archives of Biochemistry and Biophysics. 364 (2): 185–94. doi:10.1006/abbi.1999.1117. PMID 10190973.
  • Kaltenbach LS, Romero E, Becklin RR, Chettier R, Bell R, Phansalkar A, Strand A, Torcassi C, Savage J, Hurlburt A, Cha GH, Ukani L, Chepanoske CL, Zhen Y, Sahasrabudhe S, Olson J, Kurschner C, Ellerby LM, Peltier JM, Botas J, Hughes RE (May 2007). "Huntingtin interacting proteins are genetic modifiers of neurodegeneration". PLoS Genetics. 3 (5): e82. doi:10.1371/journal.pgen.0030082. PMC 1866352. PMID 17500595.
  • Rio Frio T, Panek S, Iseli C, Di Gioia SA, Kumar A, Gal A, Rivolta C (2009). "Ultra high throughput sequencing excludes MDH1 as candidate gene for RP28-linked retinitis pigmentosa". Molecular Vision. 15: 2627–33. PMC 2790479. PMID 20011630.
  • Tanaka T, Inazawa J, Nakamura Y (Feb 1996). "Molecular cloning and mapping of a human cDNA for cytosolic malate dehydrogenase (MDH1)". Genomics. 32 (1): 128–30. doi:10.1006/geno.1996.0087. PMID 8786100.
  • Friedrich CA, Ferrell RE, Siciliano MJ, Kitto GB (Jan 1988). "Biochemical and genetic identity of alpha-keto acid reductase and cytoplasmic malate dehydrogenase from human erythrocytes". Annals of Human Genetics. 52 (Pt 1): 25–37. doi:10.1111/j.1469-1809.1988.tb01075.x. PMID 3052244.
  • Chapman AD, Cortés A, Dafforn TR, Clarke AR, Brady RL (Jan 1999). "Structural basis of substrate specificity in malate dehydrogenases: crystal structure of a ternary complex of porcine cytoplasmic malate dehydrogenase, alpha-ketomalonate and tetrahydoNAD". Journal of Molecular Biology. 285 (2): 703–12. doi:10.1006/jmbi.1998.2357. PMID 10075524.
  • Martins-de-Souza D, Gattaz WF, Schmitt A, Maccarrone G, Hunyadi-Gulyás E, Eberlin MN, Souza GH, Marangoni S, Novello JC, Turck CW, Dias-Neto E (Jul 2009). "Proteomic analysis of dorsolateral prefrontal cortex indicates the involvement of cytoskeleton, oligodendrocyte, energy metabolism and new potential markers in schizophrenia". Journal of Psychiatric Research. 43 (11): 978–86. doi:10.1016/j.jpsychires.2008.11.006. PMID 19110265.
  • Corbett JM, Wheeler CH, Baker CS, Yacoub MH, Dunn MJ (Nov 1994). "The human myocardial two-dimensional gel protein database: update 1994". Electrophoresis. 15 (11): 1459–65. doi:10.1002/elps.11501501209. PMID 7895732.
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