Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate WP_012853680.1 TCUR_RS16535 amidase
Query= curated2:A7NKM0 (490 letters) >NCBI__GCF_000024385.1:WP_012853680.1 Length = 472 Score = 207 bits (528), Expect = 5e-58 Identities = 175/492 (35%), Positives = 234/492 (47%), Gaps = 44/492 (8%) Query: 7 LTVAQAREMLARGEISSLELTDALLTRIAAVEPKVRAFLVVDAAGARAQARAADARRAAG 66 L +A E+LA GE+S+ EL L RI + + AF VV A A A+A AD R AG Sbjct: 5 LGLAAQAELLALGELSAGELVAHSLERIDRLR-SLGAFRVVRAEAALAEAAEADRRLRAG 63 Query: 67 DASPLLGIPMGIKDVISTQGLRTTCASKMLENYTPVYDATAVARLKAAGAVILGKLNCDE 126 + PLLG+P+ IKD G TT + ++ DA V RL+AAGA+I+GK E Sbjct: 64 ERLPLLGVPVAIKDDTDLAG-ETTPFAVPGDHRPKAADAEHVRRLRAAGAIIVGKTTTCE 122 Query: 127 FAMGSSTENSAFQQTRNPWNLERVPGGSSGGSAAAVAAGEAPAALGTDTGGSIRQPAALC 186 + +E+ F RNPWN PGGSSGGSAAAVAAG AA+G+D GSIR PAA Sbjct: 123 IGLWPFSESPGFGAARNPWNPAYSPGGSSGGSAAAVAAGMVAAAVGSDGAGSIRIPAAWT 182 Query: 187 GITGLKPTYGRVSRYGLVAFASSLDQIGPMARTVRDCAIVLRVIAGADPFDATCTDYPAP 246 G+ G+KP GRVS + L GP+AR+V D A++L V+ G+ P DA P Sbjct: 183 GLVGIKPQRGRVSGFPHRDPFHGLTVWGPLARSVADAALLLDVLTGSHPEDAHRLAPPVV 242 Query: 247 DYEAALTGDIRGLRIGVP-REYFVAGMQPDVEAAVRTAIEVLREQGAEVCEISLPHTP-Y 304 + A D LRI V R F G+ V+ +R A+E + + A++ P P Y Sbjct: 243 PFAEAARRDPGRLRIAVSFRTAF--GVPGRVDPQIRAAVERIARRLADLGHKVFPADPDY 300 Query: 305 ALPVYYLIAPAEASANLARFDGVRYGLRVPGESYFDELERTRGAGFGP--EVRRRI--ML 360 L LI A D LE GA P EV RI +L Sbjct: 301 GLVGLGLIPRGTAGV-------------------ADWLESMPGASPEPRTEVEARIGRLL 341 Query: 361 GTYALSAGYYDAYYKRAQQVRTLIRRDYQQAFEQVDVIAAPTTPTVAFKIGAHTD----- 415 G L A+++ +RR + F+ DV+ PTT ++GA+ Sbjct: 342 GRRLLPL---------ARRMDPALRRRVGRIFQVADVVLTPTTALPPPRVGAYDGATWRR 392 Query: 416 DPLAMYLEDVCTLPLNLAGLPGLVVPCGF-AEGLPIGLQLIGRAFDEESLLRVGDAYQRV 474 A P N+ G P + VP G AEGLPIG QL+ +E L+ + + V Sbjct: 393 TQSAAAAACPYAWPWNVLGWPAMSVPAGMTAEGLPIGAQLLAHDSEEALLISLAAQLEAV 452 Query: 475 TDWHTRMPEVRE 486 WH R ++E Sbjct: 453 EGWHERRAPLKE 464 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: 582 Number of extensions: 30 Number of successful extensions: 5 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: 472 Length adjustment: 34 Effective length of query: 456 Effective length of database: 438 Effective search space: 199728 Effective search space used: 199728 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: 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