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. 2017 Jan 19;12(1):e0170294. doi: 10.1371/journal.pone.0170294

Fig 3. Protein—protein interaction analysis of differentially abundant proteins and phosphoproteins between Angus and Nellore muscle.

Fig 3

Data have been elaborated and graphed through String 10.0. ATP-citrate synthase (ACLY), Mitochondrial malate dehydrogenase (MDH2), Cytoplasmic malate dehydrogenase (MDH1), Mitochondrial aspartate aminotransferase (GOT2), Phosphoglucomutase-1 (PGM1), Glucose-6-phosphate isomerase (GPI), Triosephosphate isomerase (TPI1), Pyruvate kinase (PKLR), Alpha-enolase (ENO1), M1-type pyruvate kinase (PKM), Phosphoglycerate kinase 1 (PGK1), Glyceraldehyde-3-phosphate dehydrogenase (G3PDH), Alpha skeletal muscle actin (ACTA1), Uncharacterized protein (CDC25B), M-phase inducer phosphatase 3 (CDC25C), 14-3-3 protein epsilon (YWHAE), Myosin regulatory light chain 2 (MYLPF), Myosin light chain 1/3 (MYL1), Cardiac troponin I (TNNI3), Uncharacterized protein (TNNI1), Fast troponin C type 2 (TNNC2), Tropomyosin alpha-1 chain (TPM1), Troponin T fast skeletal muscle type (TNNT3), Myosin light chain 3 (MYL3), TNNI2 protein (TNNI2), Cardiac troponin T (TNNT2), Mitochondrial GrpE protein homolog 1 (GRPEL1), Mitochondrial GrpE protein homolog 2 (GRPEL2), 78 kDa glucose-regulated protein (GRP78), Endoplasmin (HSP90B1), Mitochondrial stress-70 protein (HSPA9), Mitochondrial import inner membrane translocase subunit TIM44 (TIMM44), LOC615521 protein (LOC615521), Uncharacterized protein (HSPA6).