Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate WP_035218184.1 G491_RS0108370 amidase
Query= curated2:A7NKM0 (490 letters) >NCBI__GCF_000429905.1:WP_035218184.1 Length = 573 Score = 221 bits (564), Expect = 4e-62 Identities = 162/484 (33%), Positives = 240/484 (49%), Gaps = 55/484 (11%) Query: 7 LTVAQAREMLARGEISSLELTDALLTRIAAVEPKVRAFLVVDAAGARAQARAADARRAAG 66 L V + +LA+ +I+SL+LT L R+ +P ++ + + A QA+ AD+ RAAG Sbjct: 133 LPVTELSALLAQRQITSLDLTRMYLARLKKFDPVLKCVVTLTEDLAIEQAKRADSERAAG 192 Query: 67 D-ASPLLGIPMGIKDVISTQGLRTTCASKMLENYTPVYDATAVARLKAAGAVILGKLNCD 125 PL GIP G+KD+ +T+G+ T+ + ++ +A AV RL+ AGAV+ KL+ Sbjct: 193 KHRGPLHGIPWGVKDLFATKGIPTSWGMEAYKDRIIDENAAAVERLEKAGAVLAAKLSLG 252 Query: 126 EFAMGSSTENSAFQQTRNPWNLERVPGGSSGGSAAAVAAGEAPAALGTDTGGSIRQPAAL 185 E A G +TRNPWN + GGSS GSA+AVAAG ALGT+T S+ PA + Sbjct: 253 ELATGDRWFGG---RTRNPWNPKTGSGGSSAGSASAVAAGLVGFALGTETNNSLVGPAMV 309 Query: 186 CGITGLKPTYGRVSRYGLVAFASSLDQIGPMARTVRDCAIVLRVIAGADPFDATCTDYPA 245 CG TGL+PT+GRVSRYG++ A S D+IGP+ R+ DCA+VL IAG D D + D P Sbjct: 310 CGNTGLRPTFGRVSRYGVMTVAWSFDKIGPLCRSAEDCALVLDAIAGRDDRDHSTVDLPC 369 Query: 246 -----PDYEAALTGDIRGLRIGVPREYFVAGMQPDVEAAVRTAIEVLREQGAEVCEISLP 300 PD G +R L P+ ++A D+ A +TA++ + + GA++ + P Sbjct: 370 GFNRYPDVRHMKVGYVRELLSMPPQNQYMA----DILNAHKTALKAIGDLGAQLVPLP-P 424 Query: 301 HTPYAL-PVYYLIAPAEASANLARFDGVRYGLRVPGESYFDELERTRGAGFGPEVRRRIM 359 P + Y + A A + + L + + ER R A F P V Sbjct: 425 FEPGTFDKLVYSASICMAVEAAAAHEDLMQDLGPEAFKHSNWPERLRAARFIPAVE---- 480 Query: 360 LGTYALSAGYYDAYYKRAQQVRTLIRRDYQQAFEQVDVIAAPTTPTVAFKIGAHTDDPLA 419 Y +A + R+++ + + VDV+ T Sbjct: 481 --------------YVQASRARSVLMQMVEDKMGDVDVLLGRLT---------------- 510 Query: 420 MYLEDVCTLPLNLAGLPGLVVPCGF-AEGLPIGLQLIGRAFDEESLLRVGDAYQRVTDWH 478 V +L NL G P LV+P G A+GLP+ + L G +E L+ +G A Q T + Sbjct: 511 -----VSSLQGNLTGHPELVMPYGLNAQGLPVSIILTGNLHEESKLIALGRALQNKTGHY 565 Query: 479 TRMP 482 R P Sbjct: 566 LRQP 569 Lambda K H 0.320 0.136 0.398 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: 609 Number of extensions: 38 Number of successful extensions: 3 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: 490 Length of database: 573 Length adjustment: 35 Effective length of query: 455 Effective length of database: 538 Effective search space: 244790 Effective search space used: 244790 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 52 (24.6 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