Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate Pf6N2E2_878 Amidase clustered with urea ABC transporter and nitrile hydratase functions
Query= curated2:Q8THJ1 (476 letters) >FitnessBrowser__pseudo6_N2E2:Pf6N2E2_878 Length = 504 Score = 263 bits (673), Expect = 8e-75 Identities = 158/426 (37%), Positives = 236/426 (55%), Gaps = 24/426 (5%) Query: 60 GPLAGVPIAIKDNISVVGLPNSCGSKILEGYVPPFNAHVIEKLLDAGAVILGKTNLDEFA 119 G L+G +A+KDNIS+ G+P G+ LEG+VP F+A V+ +LLDAGA ILGK + + Sbjct: 86 GKLSGKTVALKDNISLAGVPMMNGAAPLEGFVPSFDATVVTRLLDAGATILGKATCEHYC 145 Query: 120 MGSSTETSYYGPTANPWDLERVPGGSSGGSAAVVAAGEAPFALGSDTGGSVRCPAAFCGV 179 + + TS P NP+ GGSS GSAA+VA G A+G D GGS+R PAA+CG+ Sbjct: 146 LSGGSHTSDPAPVHNPFRHGYTTGGSSSGSAALVATGAVDLAIGGDQGGSIRIPAAWCGI 205 Query: 180 VGLKPTYGAVSRYGVVAYANSLEQVGPLANNVEDIAILMDVIAGYDRRDSTSIDSKTE-Y 238 G+KPT+G V GV+A ++ + VGP+ +NV D A++++V+AG D D K + Y Sbjct: 206 YGMKPTWGLVPYTGVMAIESTFDHVGPMTSNVRDNALMLEVMAGADGLDPRQAAPKVDAY 265 Query: 239 QKALVDDVKGLKIGVPKEFFG-EGIHPGVEKAVWNAIHKFESLGATRQEVSMPNINYALA 297 L V GL+IGV +E F P + + V +AI + E+LGA +EVS+P N A + Sbjct: 266 CDYLERGVTGLRIGVLQEGFQLANQDPRIAEKVRSAIARLEALGARVEEVSVPEHNLAGS 325 Query: 298 SYYIIAMSEASSNLARFDGTRYGFRANGENWHAMVS----------KTRAEGFGTEVKRR 347 + I + + +G G NW + + +A +K Sbjct: 326 LWSPIGCEGLTMQMMHGNGA-------GFNWKGLYDVGLLDKQAGWRDQANALSPSLKLC 378 Query: 348 ILLGTYALSAGYHDKYYLKALKVRTLVKQDFDKALSTVDLLMAPTMP---NPAFRIGEKI 404 + +G + L Y+ +YY KA + + +DKAL T DLL+ PT+P P G I Sbjct: 379 MFVGQFGLER-YNGRYYAKAQNIARFARAAYDKALDTYDLLVMPTVPITAQPLPEPGSSI 437 Query: 405 EDPLTLYLSDV-NTCPINLAGVPSVSVPCGFTDGLPVGLQIMGKPFDEPTVLRAAYTFEK 463 + +T L + NT ++ G P++S+PCG DGLPVGL ++G+ + E T+ +AA FE Sbjct: 438 TETVTRALEMLGNTAAQDITGHPAMSIPCGLVDGLPVGLMLVGRHYAEGTLYQAAAAFEA 497 Query: 464 NTDYHT 469 + D+ T Sbjct: 498 SVDWRT 503 Lambda K H 0.315 0.134 0.391 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: 635 Number of extensions: 40 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: 476 Length of database: 504 Length adjustment: 34 Effective length of query: 442 Effective length of database: 470 Effective search space: 207740 Effective search space used: 207740 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 (21.5 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 2021.
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code, or see changes to Amino acid biosynthesis since the publication.
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