malonyl-CoA-acyl carrier protein transacylase, mitochondrial isoform b - Protein

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MCAT Mutations Cause Nuclear LHON-like Optic Neuropathy. [Genes (Basel). 2021]
MCAT Mutations Cause Nuclear LHON-like Optic Neuropathy.
Gerber S, Orssaud C, Kaplan J, Johansson C, Rozet JM. Genes (Basel). 2021 Apr 2; 12(4). Epub 2021 Apr 2.
Structural basis for different specificities of acyltransferases associated with the human cytosolic and mitochondrial fatty acid synthases. [Chem Biol. 2009]
Structural basis for different specificities of acyltransferases associated with the human cytosolic and mitochondrial fatty acid synthases.
Bunkoczi G, Misquitta S, Wu X, Lee WH, Rojkova A, Kochan G, Kavanagh KL, Oppermann U, Smith S. Chem Biol. 2009 Jun 26; 16(6):667-75.
Recessive pathogenic variants in MCAT cause combined oxidative phosphorylation deficiency. [Elife. 2023]
Recessive pathogenic variants in MCAT cause combined oxidative phosphorylation deficiency.
Webb BD, Nowinski SM, Solmonson A, Ganesh J, Rodenburg RJ, Leandro J, Evans A, Vu HS, Naidich TP, Gelb BD, et al. Elife. 2023 Mar 7; 12. Epub 2023 Mar 7.

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NP_055322 [Domain Mapping of Disease Mut...]
NP_055322
Domain Mapping of Disease Mutations
Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF) [MODBASE, Database of Comparat...]
MODBASE, Database of Comparative Protein Structure Models (Sali Lab/UCSF)
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
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reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome
Evolutionary Trace of Functional Site [Evolutionary Trace of Functio...]
Evolutionary Trace of Functional Site

malonyl-CoA-acyl carrier protein transacylase, mitochondrial isoform b precursor...
malonyl-CoA-acyl carrier protein transacylase, mitochondrial isoform b precursor [Homo sapiens]
gi|27477045|ref|NP_055322.1|

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