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NDUFAF6

NDUFAF6 is a biology topic covered in the lgStudy science library. This page brings together a partial reference excerpt, illustrations, worked examples, real-world applications and a short study plan, so you can understand NDUFAF6 rather than just read about it. In short: NADH:ubiquinone oxidoreductase complex assembly factor 6 is a protein that in humans is encoded by the NDUFAF6 gene. The protein is involved in the assembly of complex I in the mitochondrial electron transport chain.

NDUFAF6 — main illustration
NDUFAF6 — illustration

Key takeaways

  • NDUFAF6 belongs to biology; place it in that map before memorising details.
  • Learn the definition first, then one example that makes the definition concrete.
  • Connect NDUFAF6 to a quantity you can measure, compute or draw — that is where exam questions come from.
  • Reproduce the core statement of NDUFAF6 from memory before moving on to harder problems.

Reference excerpt

NADH:ubiquinone oxidoreductase complex assembly factor 6 is a protein that in humans is encoded by the NDUFAF6 gene. The protein is involved in the assembly of complex I in the mitochondrial electron transport chain. Mutations in the NDUFAF6 gene have been shown to cause Complex I deficiency, Leigh syndrome, and Acadian variant Fanconi Syndrome.

Structure The NDUFAF6 gene is located on the q arm of chromosome 8 in position 22.1 and spans 222,728 base pairs. The gene produces a 38.2 kDa protein composed of 333 amino acids. The protein contains a predicted phytoene synthase domain.

Function The NDUFAF6 gene encodes a protein that localizes to mitochondria. The encoded protein plays an important role in the assembly of complex I (NADH-ubiquinone oxidoreductase) of the mitochondrial respiratory chain through regulation of subunit ND1 biogenesis.

Clinical Significance Mutations in the NDUFAF6 gene are associated with complex I enzymatic deficiency and lead to Leigh syndrome, which is characterized by lesions in the central nervous system and rapid deterioration of cognitive and motor functions. In Acadians, a non-coding mutation in NDUFAF6 has been shown to cause Acadian variant Fanconi Syndrome, symptoms of which include pulmonary interstitial fibrosis and proximal tubular dysfunction accompanied by slowly progressive kidney disease. Inheritance of mutations in the NDUFAF6 gene is autosomal recessive.

Interactions The protein encoded by NDUFAF6 interacts with RHOXF2, OTX1, GUCD1, and GALNT6 proteins.

References

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

Illustrations

NDUFAF6 illustration
NDUFAF6 illustration

Worked examples

Example 1 — a first encounter with NDUFAF6

Start with the simplest possible case. Write down what NDUFAF6 claims or describes in one sentence, then invent the smallest concrete situation in which that sentence is true. In biology, the smallest case is usually a single object, a single equation or a single measurement. Check that every symbol or term in your sentence has a meaning in that case.

Example 2 — changing one variable

Take the situation from Example 1 and change exactly one quantity: double it, halve it, or set it to zero. Predict what should happen to NDUFAF6 before you calculate. Comparing your prediction with the result is the fastest way to find out whether you understand the idea or only the words.

Example 3 — an exam-style question

Typical questions about NDUFAF6 ask you to (a) state it precisely, (b) apply it to given data, and (c) explain a limitation. Practise writing all three answers in under five minutes; the third part is what separates a full-mark answer from an average one.

Applications of NDUFAF6

In research
NDUFAF6 appears in biology research whenever the underlying quantities have to be modelled precisely. Papers usually cite it as a starting assumption and then explore where it breaks down.
In technology and industry
Engineering practice reuses NDUFAF6 in design rules, simulations and safety margins. Knowing the idea lets you read a specification sheet and understand why the numbers look the way they do.
In the classroom
NDUFAF6 is common in secondary-school and first-year university syllabi. It links to neighbouring topics Cellular respiration, Genes on human chromosome 8, Peripheral membrane proteins, so understanding it makes those chapters shorter.
In everyday life
Look for NDUFAF6 outside the textbook — in sport, cooking, traffic, electronics or the sky above you. An example you found yourself is remembered far longer than one you were given.
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How to study NDUFAF6 in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what NDUFAF6 means in your own words.
  3. Compare your version with the excerpt and mark what you missed.
  4. Work through the three examples above with pen and paper.
  5. Explain NDUFAF6 out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is NDUFAF6 in simple terms?

NADH:ubiquinone oxidoreductase complex assembly factor 6 is a protein that in humans is encoded by the NDUFAF6 gene. The protein is involved in the assembly of complex I in the mitochondrial electron transport chain.

Why does NDUFAF6 matter?

Because it connects several biology ideas at once: it gives you a definition you can apply, a quantity you can calculate, and a way to check whether a result is plausible.

How should I study NDUFAF6?

Read the excerpt, restate it from memory, then work through the examples and applications listed on this page. The five-step study plan above takes about twenty minutes.

What does this page cover?

It gives you a compact reference excerpt plus original lgStudy explanations, examples, applications and study material on NDUFAF6.

Tags

  • Cellular respiration
  • Genes on human chromosome 8
  • Peripheral membrane proteins

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