Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate WP_037570409.1 BS73_RS06575 amidase
Query= curated2:A7NKM0 (490 letters) >NCBI__GCF_000744815.1:WP_037570409.1 Length = 484 Score = 256 bits (653), Expect = 2e-72 Identities = 186/489 (38%), Positives = 249/489 (50%), Gaps = 42/489 (8%) Query: 8 TVAQAREMLARGEISSLELTDALLTRIAAVEPKVRAFLVVDAAGARAQARAADARRAAG- 66 TV A L G ++S L + + ++P+V +F+ + A A ADA AAG Sbjct: 12 TVTAAAAALRAGTVTSTALVEHAVRTADRLDPRVGSFISRYREESLAAAARADADFAAGT 71 Query: 67 DASPLLGIPMGIKDVISTQGLRTTCASKMLENYTPVY-----DATAVARLKAAGAVILGK 121 D PL GIP G+KD+I++ TT S +L+ P + DA V+RL+AAGA+++GK Sbjct: 72 DRGPLQGIPFGVKDIIASTDGPTTAQSLVLD---PAWGEETGDAVVVSRLRAAGAIVVGK 128 Query: 122 LNCDEFAMGSSTENSAFQQTRNPWNLERVPGGSSGGSAAAVAAGEAPAALGTDTGGSIRQ 181 + EFA+GS F NPW+LER GGSS G+ + VAAG A LGTDT GSIR Sbjct: 129 ASTMEFAIGSPDPEKPFPIPANPWDLERWAGGSSSGTGSGVAAGMFLAGLGTDTAGSIRI 188 Query: 182 PAALCGITGLKPTYGRVSRYGLVAFASSLDQIGPMARTVRDCAIVLRVIAGADPFDATCT 241 P+A CGITGLKPT+GRV + G V +LD IGPMAR+ DCA++L +IAG D D Sbjct: 189 PSAYCGITGLKPTFGRVPKSGCVPLGYTLDNIGPMARSAADCALLLGLIAGPDASDHYSA 248 Query: 242 DYPAPDYEAAL---TGDIRGLRIGVPREYFVAGMQPDVEAAVR----TAIEVLREQGAEV 294 D DY AL GD+ GL IGV + VA V+ A R A+ L GA + Sbjct: 249 DVQVDDYSGALADGAGDLSGLTIGV--DDLVAASDGHVDPAFRARFDAALGELAAAGARI 306 Query: 295 CEISLPHTPYALPVYYLIAPAEASANLARFDGVRYGLRVPGESYFDELERTRGAGFGPEV 354 P +LP+Y + A+ L+ G +L R R A +G Sbjct: 307 -------VPLSLPLYAELTAADMVVMLSEALAYHQG----------DLSR-RWADYGAGT 348 Query: 355 RRRIMLGTYALSAGYYDAYYKRAQQVRTLIRRDYQQAFEQVDVIAAPTTPTVAFKIGAHT 414 R + G + A Y +AQ+VR + +R E VD I PT+ A ++ Sbjct: 349 RMTVGSG-----FAFTGADYVQAQRVRRVGQRMVAGLLEGVDAIVTPTSTLPAPRLDEFA 403 Query: 415 DDPLAMYLEDVCTLPLNLAGLPGLVVPCG-FAEGLPIGLQLIGRAFDEESLLRVGDAYQR 473 D + + T N G P L VP G A+GLP+ +Q+ R F E LRVGDAYQR Sbjct: 404 DRVPLLSFGGLHTPYWNSVGNPTLAVPIGPAADGLPLSMQISTRPFAEALALRVGDAYQR 463 Query: 474 VTDWHTRMP 482 T H +P Sbjct: 464 RTAHHLSVP 472 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: 595 Number of extensions: 27 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: 484 Length adjustment: 34 Effective length of query: 456 Effective length of database: 450 Effective search space: 205200 Effective search space used: 205200 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