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YBR218C PYC2 / SGDID:S000000422

SGD CSV

Yeast Systematic Name	Yeast Symbol	SGDID	Analog Name	Analog Description	EC	Organism	Disease	Structure	Uniprot	Human ID	Human Symbol	HHsearch Probability	HHsearch E_value	HHsearch P_value	HHsearch Score	Flag Disease related	Flag Homo sapiens
YBR218C	PYC2	SGDID:S000000422	pycA SAV1114	Pyruvate carboxylase (EC 6.4.1.1)	6.4.1.1	Staphylococcus aureus		3hb9_a	A0A0H3JRU9			100.00	6.00E-130	5.00E-134	1280.40	0	0
YBR218C	PYC2	SGDID:S000000422	5S	Methylmalonyl-CoA carboxyltransferase 5S subunit (EC 2.1.3.1) (Transcarboxylase 5S subunit)	2.1.3.1	Propionibacterium freudenreichii		1rqb_a	Q70AC7			100.00	1.60E-56	1.30E-60	540.60	0	0
YBR218C	PYC2	SGDID:S000000422	pyc RHE_CH04002	pyc RHE_CH04002	6.4.1.1	Rhizobium etli		2qf7_b	Q2K340			100.00	8.00E-123	7.00E-127	1215.90	0	0
YBR218C	PYC2	SGDID:S000000422	PC	Pyruvate carboxylase, mitochondrial (EC 6.4.1.1) (Pyruvic carboxylase) (PCB)	6.4.1.1	Homo sapiens	Urea Cycle Disorder,Multiple Carboxylase Deficiency,Malignant Astrocytoma,Acute Porphyria,Methylmalonic Acidemia,Fructose-1,6-Bisphosphatase Deficiency,Body Mass Index Quantitative Trait Locus 11,Glutaric Acidemia I,Glycogen Storage Disease Ia,Lactic Acidosis,Nystagmus 6, Congenital, X-Linked,Propionic Acidemia,Primary Cutaneous Amyloidosis,Hyperinsulinemic Hypoglycemia, Familial, 6,Biotin Deficiency,Mitochondrial Complex Ii Deficiency, Nuclear Type 1,Biotinidase Deficiency,Holocarboxylase Synthetase Deficiency,Pyruvate Dehydrogenase E1-Alpha Deficiency,Pyruvate Carboxylase Deficiency	3bg3_a	P11498	ENSG00000173599	PC	100.00	6.00E-89	4.90E-93	849.20	1	1
YBR218C	PYC2	SGDID:S000000422	oadA-2 ERS013165_02612	oadA-2 ERS013165_02612	2.1.3.1,4.1.1.3,	Vibrio cholerae		2nx9_a	Q6A1F6			100.00	2.90E-54	2.40E-58	512.30	0	0
YBR218C	PYC2	SGDID:S000000422	Mfla_1512	Mfla_1512		Methylobacillus flagellatus		5ks8_c	Q1H157			100.00	8.60E-64	7.40E-68	615.30	0	0