Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate WP_012046954.1 BBTA_RS33485 Asp-tRNA(Asn)/Glu-tRNA(Gln) amidotransferase GatCAB subunit A
Query= curated2:A1ATL3 (485 letters) >NCBI__GCF_000015165.1:WP_012046954.1 Length = 470 Score = 315 bits (808), Expect = 2e-90 Identities = 183/481 (38%), Positives = 273/481 (56%), Gaps = 30/481 (6%) Query: 6 LTLHELHAKLKSKEVSSREATSAMLDRIAELEPRINAFITVTPERALAEAEAADRRIAA- 64 +TL E+ + K++SS E T + L RIAE +P++NAF+ + E AL A AD +A Sbjct: 8 MTLTEVAKAIAEKKLSSVEVTRSCLHRIAEWQPKLNAFMAIESEPALKAAAEADAALAKD 67 Query: 65 GEADVLTGIPLAVKDIFLTEGTLTTCGSRILNNFIPPYSATSFEKLKQRGMVLLGKLNQD 124 G L G+PLA KD++ G ++TCGS I +F+ ++T+ ++LK G + LG L Sbjct: 68 GPKGPLHGVPLAHKDMYYEAGHVSTCGSLIRRDFVATTTSTALQRLKDAGAIRLGTLQMA 127 Query: 125 EFAMGSSNESSASGPCRNPWNTDCIPGGSSGGSAAAIAARQATVTLGTDTGGSIRQPASH 184 EFA G + ++ GP NPW + GGSS GS +A+ AR LG+DTGGSIR PA+ Sbjct: 128 EFAYGPTGHNAHYGPVHNPWKLGYVTGGSSSGSGSAVGARLTFAALGSDTGGSIRMPANF 187 Query: 185 CGCVGLKPTYGRVSRYGVIAYASSLDQVGPLTRDVTDCAIMLGALAGHDPKDSTSVDRPV 244 CG GLK T+GRVSR G + + SLD VGPL + DCA+MLG +AG DP+D T+ PV Sbjct: 188 CGVTGLKVTWGRVSRAGAMPLSQSLDTVGPLAQTAEDCALMLGLMAGPDPEDPTASHAPV 247 Query: 245 PDYQAALTNDIRGLRIGLPREYFIEGLDPDVQASMDQAIETYRRLGAEFTEISLPHTDYA 304 DY AA I+GL+IG+P+ ++++ LDP+V +D I + GA+ + LP Sbjct: 248 QDYVAATQASIKGLKIGVPKAFYVDDLDPEVARCLDATIGLLKTEGADVVSVELPDQRQL 307 Query: 305 VASYYLIATAEASANLARYDGVRFGHRAEQAEGLLEMYSRSRSQGFGSEVKRRIMLGTYA 364 A+ L+ EA+A R+ ++E R Q +G +V R+ A Sbjct: 308 TAACQLVLAVEAAAFHKRW--------------MIE-----RPQDYGPQVLMRLQ-NALA 347 Query: 365 LSSGYYDAYYLKAQKVRTLIMADFIQAFEGVDLILTPVAP--TPAFRIGEKVNDP-LQMY 421 +S YL+A + R +A + A +G+D ++ PV+P TP+ + P + Sbjct: 348 VSG----VTYLEALRWRGAALAAHVAATQGIDAVIAPVSPLVTPSIAESDVGGVPGAEAV 403 Query: 422 LSDI--FTIPVNLAGTCAMSLPAGISGQGLPIGVQLIGKPFGEETILRAAHAFEQATEWH 479 + I FT PVN G ++++P G + GLP+G+QLIG+ F E TIL AF++AT++H Sbjct: 404 IQRITRFTRPVNYLGLPSLAIPTGFTATGLPVGMQLIGRSFDEATILTIGAAFQRATDFH 463 Query: 480 S 480 + Sbjct: 464 A 464 Lambda K H 0.318 0.134 0.389 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: 515 Number of extensions: 14 Number of successful extensions: 4 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 485 Length of database: 470 Length adjustment: 34 Effective length of query: 451 Effective length of database: 436 Effective search space: 196636 Effective search space used: 196636 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 (21.7 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