Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate WP_012852139.1 TCUR_RS08805 amidase family protein
Query= curated2:B3DWT4 (494 letters) >NCBI__GCF_000024385.1:WP_012852139.1 Length = 493 Score = 178 bits (451), Expect = 4e-49 Identities = 158/506 (31%), Positives = 229/506 (45%), Gaps = 62/506 (12%) Query: 11 LRRLLVQKEVSPLEVVENLLCRIAEVDPKIFAYIYLNHERALEASKKADISLPLGGVPVA 70 L L+ + EV+P E++E + R +VD ++ A + HE+A A +S PL GVP Sbjct: 14 LAELVARGEVTPGELLETAIARAEQVDGRVNAIVRPMHEQA-RARAATPLSGPLAGVPFL 72 Query: 71 IKD-NINVLGEPCRCASRILEGYLAPYDSTVIEKLKKAGAILLGRTNMDEFAMGSSTENS 129 +KD N + G P C SR L AP+ S V+ + AG ++ GRTN EF + TE Sbjct: 73 VKDLNQDYAGVPTGCGSRALRDVPAPHHSEVVRRWLNAGLVIFGRTNTPEFGTTAVTEPE 132 Query: 130 SVGITRNPWNTERVPGGSSGGSAAAVAAHEAFCALGSDTGGSIRQPAAFCGCVGLKPTYG 189 G TRNPWN + PGGSSGGSAAAVAA A SD GGSIR PAA CG VGLKP G Sbjct: 133 VNGPTRNPWNLDHTPGGSSGGSAAAVAAGIVPVAGASDGGGSIRIPAACCGLVGLKPGRG 192 Query: 190 RVSR---YGLTAFASSLDQIGPITKTVEDAALLLEVISG-FDPFDNTSEKLPVPRFSELL 245 V Y ++ D G I++TV D A++L+V++ DP + + P + E L Sbjct: 193 LVPAGPDYAEYLHGAATD--GVISRTVRDTAVMLDVLTAEVDPGGPYAVRRPETSYLE-L 249 Query: 246 ENRPLKDFVLGIPKEYFI-EGIDGEVRQALSQVIGHYEKLGVKIEEVSLPHTPYAVATYY 304 RP K +G E I +D + A+ + +LG ++E + +A + Sbjct: 250 SRRPPKPLRIGYTTESPIGTPVDPQAVAAVETAVTMLTELGHRVEPAAPAVDGRKLAEDF 309 Query: 305 ILATAEASANLARFDGI--RYGKRAKNYNDLIDYYGKTRDEGFGSEVKRRILLGTYVLSS 362 + T + A D I R G A+++ D + R + Y+L+ Sbjct: 310 L--TMWCAQVAATIDEIRRRTGAPARHFE---------LDNRLLAAAARSVKAADYLLAH 358 Query: 363 GYYDAYYLRALKVKEKIKQDFSLAFQKCQALLTPTSPFCAFRIGEKTSDPLQMYLADI-- 420 ++ + RAL +++ L LLTPT RIG + PL L Sbjct: 359 HRWNE-HTRALAA---FHEEYDL-------LLTPTLAGPPVRIGALATPPLLRLLGRALL 407 Query: 421 --------------------------FTIAVNLAGICALSIPCGRSTEGLPIGFQLIGPA 454 FT N+ G A+S+P R+ +GLP+G Q + Sbjct: 408 LLGLTGTLSKTKQWKDTITANLAPVPFTQLANITGRPAISLPLYRTPDGLPLGVQFVAGL 467 Query: 455 WKEETILALGYIYQKTTGWVPPLPPL 480 E +L+L ++ W PPL Sbjct: 468 GGEGLLLSLATQLEEAHPWADAEPPL 493 Lambda K H 0.319 0.139 0.410 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: 536 Number of extensions: 33 Number of successful extensions: 4 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 494 Length of database: 493 Length adjustment: 34 Effective length of query: 460 Effective length of database: 459 Effective search space: 211140 Effective search space used: 211140 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 (21.7 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