Annotation: dihydrolipoyl dehydrogenase Type 1: Protein-coding gene Located on scaffold NZ_CP154879, + strand, nucleotides 374,475 to 375,902 See nucleotide sequence around ABCV34_RS01730 or for all of scaffold NZ_CP154879
Other databases: NCBI
Nearby Genes
500 nt ABCV34_RS01705 and ABCV34_RS01710 are separated by 22 nucleotides ABCV34_RS01710 and ABCV34_RS01715 are separated by 197 nucleotides ABCV34_RS01715 and ABCV34_RS01720 are separated by 311 nucleotides ABCV34_RS01720 and ABCV34_RS01725 are separated by 40 nucleotides ABCV34_RS01725 and ABCV34_RS01730 are separated by 182 nucleotides ABCV34_RS01730 and ABCV34_RS01735 are separated by 9 nucleotides ABCV34_RS01735 and ABCV34_RS01740 are separated by 37 nucleotides ABCV34_RS01740 and ABCV34_RS01745 are separated by 66 nucleotides ABCV34_RS01745 and ABCV34_RS01750 are separated by 19 nucleotides ABCV34_RS01750 and ABCV34_RS01755 are separated by 60 nucleotides
ABCV34_RS01705: ABCV34_RS01705 - succinate dehydrogenase assembly factor 2, at 365,782 to 366,045
_RS01705
ABCV34_RS01710: ABCV34_RS01710 - citrate synthase, at 366,068 to 367,363
_RS01710
ABCV34_RS01715: ABCV34_RS01715 - NADP-dependent malic enzyme, at 367,561 to 369,855
_RS01715
ABCV34_RS01720: ABCV34_RS01720 - 2-oxoglutarate dehydrogenase E1 component, at 370,167 to 373,046
_RS01720
ABCV34_RS01725: ABCV34_RS01725 - 2-oxoglutarate dehydrogenase complex dihydrolipoyllysine-residue succinyltransferase, at 373,087 to 374,292
_RS01725
ABCV34_RS01730: ABCV34_RS01730 - dihydrolipoyl dehydrogenase, at 374,475 to 375,902
_RS01730
ABCV34_RS01735: ABCV34_RS01735 - cell division protein ZapE, at 375,912 to 377,003
_RS01735
ABCV34_RS01740: ABCV34_RS01740 - tryptophan--tRNA ligase, at 377,041 to 378,402
_RS01740
ABCV34_RS01745: ABCV34_RS01745 - ABC transporter permease, at 378,469 to 379,308
_RS01745
ABCV34_RS01750: ABCV34_RS01750 - ABC transporter permease, at 379,328 to 380,563
_RS01750
ABCV34_RS01755: ABCV34_RS01755 - ABC transporter substrate-binding protein, at 380,624 to 381,670
_RS01755
Or browse nearby genes
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