Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate GFF3560 PS417_18230 amidase
Query= curated2:Q8THJ1 (476 letters) >FitnessBrowser__WCS417:GFF3560 Length = 504 Score = 263 bits (673), Expect = 8e-75 Identities = 162/439 (36%), Positives = 242/439 (55%), Gaps = 37/439 (8%) Query: 52 KIDVEG-HEGPLAGVPIAIKDNISVVGLPNSCGSKILEGYVPPFNAHVIEKLLDAGAVIL 110 + +V G +G LAG +A+KDNIS+ G+P G+K LEG+VP F+A V+ +LLDAGA IL Sbjct: 77 RTEVSGARDGKLAGKTVALKDNISLAGVPMMNGAKPLEGHVPSFDATVVTRLLDAGATIL 136 Query: 111 GKTNLDEFAMGSSTETSYYGPTANPWDLERVPGGSSGGSAAVVAAGEAPFALGSDTGGSV 170 GK + + + + TS P NP+ GGSS GSAA+VAAGE A+G D GGS+ Sbjct: 137 GKATCEHYCLSGGSHTSDPAPVHNPYRHGFASGGSSSGSAALVAAGEVDLAVGGDQGGSI 196 Query: 171 RCPAAFCGVVGLKPTYGAVSRYGVVAYANSLEQVGPLANNVEDIAILMDVIAGYD----R 226 R P+AFCG G+KPT+G V G++A +++ GP+ NV D A++++V+AG D R Sbjct: 197 RIPSAFCGTYGMKPTHGLVPYTGIMAIEATIDHAGPITANVRDNALMLEVMAGADGLDPR 256 Query: 227 RDSTSIDSKTEYQKALVDDVKGLKIGVPKEFFG-EGIHPGVEKAVWNAIHKFESLGATRQ 285 + + +D+ ++Y L V GLKIGV +E F P V +V NAI +F LGA + Sbjct: 257 QAAPQVDTYSDY---LARGVSGLKIGVLREGFELANQDPRVASSVRNAIARFSQLGAQVE 313 Query: 286 EVSMPNINYALASYYIIAMSEASSNLARFDGTRYGFRANGENWHAMVS----------KT 335 EVS+P A A ++ I + + +G G NW + + Sbjct: 314 EVSVPEHAIAGALWHPIGCEGLTMQMMHGNGA-------GFNWKGLYDVGLLDKQAGWRD 366 Query: 336 RAEGFGTEVKRRILLGTYALSAGYHDKYYLKALKVRTLVKQDFDKALSTVDLLMAPTM-- 393 +A+ +K + +G Y + Y+ ++Y KA +R L + +D AL+ DLL+ PT+ Sbjct: 367 QADDLSASLKLCMFVGQYGVER-YNGRFYAKAQNLRRLARSAYDAALARYDLLVMPTVPI 425 Query: 394 -----PNPAFRIGEKIEDPLTLYLSDVNTCPINLAGVPSVSVPCGFTDGLPVGLQIMGKP 448 P P I E + L + N ++ G P++S+PCG DGLPVGL ++GK Sbjct: 426 IAQPHPEPDCSITEYVARALEMI---GNASAQDITGHPAMSIPCGLVDGLPVGLMLVGKH 482 Query: 449 FDEPTVLRAAYTFEKNTDY 467 + E T+ +AA FE D+ Sbjct: 483 YAEGTIYQAAAAFEAAVDW 501 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: 583 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: 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