Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate Ga0059261_0838 Ga0059261_0838 Asp-tRNAAsn/Glu-tRNAGln amidotransferase A subunit and related amidases
Query= curated2:Q2IH94 (492 letters) >FitnessBrowser__Korea:Ga0059261_0838 Length = 453 Score = 168 bits (426), Expect = 3e-46 Identities = 157/465 (33%), Positives = 210/465 (45%), Gaps = 77/465 (16%) Query: 18 AGVAAKAISSTELVEASLARIQATDGKLGAFLAVCADRARAAAKAADARAARGERRSELD 77 A +AA S+ E ++ARI+A D + A + RA AA ADA ARGERR L Sbjct: 26 AAIAAGETSARAQCELAIARIEADDDAINAVVVRDFARALEAADRADAAVARGERRPFL- 84 Query: 78 GVPVAVKDLFVTKGVPTTAGSRILEGYLPPYDATVVERLEAAGAVIVGKLNMDEFAMGSS 137 GVP+ VK+ F +G+PT+ G + DA VV+R++AAGAVI+GK N+ Sbjct: 85 GVPMTVKEAFDVEGLPTSWGFAHARDTIATSDAVVVQRMKAAGAVILGKTNVAPGLADWQ 144 Query: 138 NENSAYKPCHNPWDLSRTPGGSSGGSAASVAAGQVHASLGTDTGGSIREPAAFCGVVGVK 197 ++N Y NP DLSRT GGSSGGSAA++AAG V A +G+D GGSIR PAAFCGV G K Sbjct: 145 SDNVVYGRTANPRDLSRTAGGSSGGSAAALAAGFVTAEIGSDIGGSIRVPAAFCGVWGHK 204 Query: 198 PTYGRVSRY-----GVVAFASSLDQVGPLAREVGDAALVLRTIAGHD-PRDMTSSTRPVD 251 P+Y + Y G + L VGP+AR+ D A +L +A PR Sbjct: 205 PSYELIDPYGHRFPGSDGASPPLGVVGPMARDAADLAAMLDILADTPLPR--------AG 256 Query: 252 DYLGPLEEGARGLRVGVPREWLSGGLDAGVEAAIRAALDTYRRLGATLVDVSLPHSKYGI 311 +LGP G + + + L A + AIR ALD RL A Sbjct: 257 RFLGP---GGKQILL------LDSHPAAPTDPAIRGALD---RLDA-------------- 290 Query: 312 GAYYLIAPAEASSNLARYDGVRYGLRAEGAKGLKEMYAESREQGLGAEPKRRIMLGTYAL 371 A +A ++AR + L A+ K + G G A Sbjct: 291 ------AANQAGIHIARSSDLLPDLAAQHRAYCKMLAITFARGAPGPN-------GQAAS 337 Query: 372 SSGYYDAYYLRAQKVRTLIRRDFDEAFRGCDVIAGPVTPSVAF-------------ALGE 418 S ++D +A+ RR + F D + P AF G+ Sbjct: 338 LSDWFDQLDAQARN-----RRIWSRLFDEFDAVVTPANVVTAFPHRDDPYNERRMTVDGQ 392 Query: 419 RTGDPLQMYLADIFTITCNLAALPGLSVPCGLEAASGLPVGLQLV 463 T Q+ A I T LP + P G A GLPVGLQ++ Sbjct: 393 DTSYDAQLVWAGIAT----YPGLPATAFPAG-TTADGLPVGLQVI 432 Lambda K H 0.317 0.135 0.393 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 534 Number of extensions: 25 Number of successful extensions: 4 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 492 Length of database: 453 Length adjustment: 33 Effective length of query: 459 Effective length of database: 420 Effective search space: 192780 Effective search space used: 192780 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory