Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate GFF2305 Psest_2352 allophanate hydrolase
Query= curated2:B2UMP4 (470 letters) >FitnessBrowser__psRCH2:GFF2305 Length = 600 Score = 161 bits (407), Expect = 6e-44 Identities = 143/462 (30%), Positives = 212/462 (45%), Gaps = 41/462 (8%) Query: 16 RRKELSPAELV-NLTADAIEADRTTNAYISFDREAALHAAAG-----ADISSPLAGIPIA 69 R +P +L+ L A A + + NA+I A L A PL GIP A Sbjct: 17 REGTTTPRQLILELRAKAAKLNGEFNAFIHLLSAAELEPFLATLEGKAPAELPLYGIPFA 76 Query: 70 VKDNINVLGQPTRCASRLLSPYVAPYDATSIRLLKEAGGIPLGRTNMDEFAMGASGENSA 129 +KDNI++ G PT A + Y AT + L G +PLG+TN+D+FA G +G S Sbjct: 77 IKDNIDLAGIPTTAACPAFA-YTPETSATLVEQLIALGAVPLGKTNLDQFATGLNGTRSP 135 Query: 130 YGITRNPEAPDRIPGGSSSGSAAAVASATAIAALGSDTGGSIRQPAGHCGIVGLKPTYGR 189 YG RN PD GGSS+GS+ AVA A ALG+DT GS R PA +VGLK + G Sbjct: 136 YGECRNSVHPDYPSGGSSAGSSLAVALGLASFALGTDTAGSGRVPAALNNLVGLKASKGL 195 Query: 190 VSRYGLVAFASSLDQIGPMTRTVEDAAILLQAISGHDRKDSTSANCPVPDFEAALGRDVK 249 +S G+V +LD + T T +A+ LL + D +D S + P+ + +A G+ VK Sbjct: 196 ISTAGVVPACRTLDCVTFFTATAAEASQLLALTARLDPRDEYSRSNPLWNDGSAFGQ-VK 254 Query: 250 GLKVGIPS--EYFTSGNHPGISEAVQNTVKQLESLGAELVEVNL-PHADAVVAAYYIIAC 306 + G+PS E+ P + A T++QL+++G E VEV+ P +A Y Sbjct: 255 SFRFGVPSQLEFLGCAESPALFAA---TIEQLKAIGGEPVEVDFAPFLEAARLLY----- 306 Query: 307 AEASSNLSRFDGVRYGKRAEDAAGLVELFSRTREEGFGPEVKRRIILGTYVLSSGYYDAY 366 +G +R A L+E + + P +K + + + A Sbjct: 307 ----------EGPWVAERYSVAGELIE----QQPDAVLPVIKAVLEKAPGTTAVQLFQAQ 352 Query: 367 YSRAQKVRSLVARDFAEAFSRVDIIVGPTSPAPAPKIGDSALDHLQTYLADIYTIPANLA 426 Y R Q+++++ R AE VD ++ P P P A + YT N+ Sbjct: 353 Y-RLQQLKAICDRIMAE----VDCVLTPAYPRPVTLAELHAEPVKRNSDLGYYTNFMNML 407 Query: 427 GLPAMSIPCGTVRESGMELPVGFQMMAPHFREDLLLKTGFAL 468 A+++P G +R LP G + F + LL AL Sbjct: 408 DYAAVAVPAGVMRNG---LPWGVTLFGRVFTDQYLLSLADAL 446 Lambda K H 0.316 0.133 0.382 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: 613 Number of extensions: 32 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: 470 Length of database: 600 Length adjustment: 35 Effective length of query: 435 Effective length of database: 565 Effective search space: 245775 Effective search space used: 245775 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 (21.6 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