Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate Ac3H11_417 Asp-tRNAAsn/Glu-tRNAGln amidotransferase A subunit and related amidases
Query= curated2:C1F857 (476 letters) >FitnessBrowser__acidovorax_3H11:Ac3H11_417 Length = 451 Score = 157 bits (396), Expect = 9e-43 Identities = 150/491 (30%), Positives = 205/491 (41%), Gaps = 78/491 (15%) Query: 13 VRTGEVRAEAALQECLGAIDAHNGEVNAYLSLDRDGAGARARHIDALSREERAKLPMGGV 72 +R G A A L+ C IDA N Y + AR + + A+LP+ G+ Sbjct: 12 LREGATTAPAELERC---IDAAQAPANTYSFVRTMFDEARTTAV----QPGLAQLPLAGL 64 Query: 73 PFGIKDVLTVEGMPATASSKIL-EGYRPPYTATAVQRLIDAGAVLVGKLNCDEFAMGSSN 131 +KD+ + G A S L + AV RL AGA L+G+ N EFA Sbjct: 65 AVSVKDLFDIAGQATPAGSTALADAPAAAQDCPAVARLRAAGASLIGRTNMVEFAFSGVG 124 Query: 132 ENSAYGPVKNPRALD----------RVPGGSSGGSAAAVAANMAVATLGTDTGGSIRQPA 181 N +G P A D RVPGGSS G+ +VA A LG+DTGGSIR PA Sbjct: 125 VNPHHG---TPAAWDARSGALPGAPRVPGGSSSGAGVSVATGAAFIGLGSDTGGSIRIPA 181 Query: 182 SFCGVVGVLPTYGRVSRYGLIAFASSLDRVGPFAHTVRDAAEVLGVIAGHDPMDATSSSV 241 + G+VG T V G + +++LD +VRDA V+A T S Sbjct: 182 ALNGIVGFKNTAHLVPTTGAVPLSTTLDTACAMTRSVRDAIVAHEVLAARR---VTRSLA 238 Query: 242 PVPDYTEKLDAGVKGLRLGVPAEYFAEGLDPEVKRAVEGTIEQLRAAGAEVKPISLPHTP 301 P+ Y RL VP+ F +GLD V +A E T+ LR AGA + I LP Sbjct: 239 PLSQY-----------RLAVPSTLFLDGLDATVAQAFERTLRTLRQAGAHIDTIPLP--- 284 Query: 302 YAIPTYYVIATAEASANLARFDGVRYGLRAPEANTLAAMYRQTRDLGFGAEVKRRILLGT 361 A AE A YG APEA Q + V+ RI G Sbjct: 285 ---------AVAEQPA---------YGFAAPEAYAWHRELLQRAGNRYDPRVRMRIEKGA 326 Query: 362 YVLSAGYYDAYYKKAQQVRRLLAQDFLRAFEEVDAIVTPTAPTPA------------FKL 409 +++ Y D + Q + R+LA E D +++PT P A K Sbjct: 327 TLMAWEYIDLLQARQQWIARMLAD-----MEPYDTLLSPTVPIVAPLVADVAPADGTDKA 381 Query: 410 GEKSDDPLSMYLADIY---TVTANLAGICGASVPCGTSREGLPIGIQILGRHFDEATVLR 466 + + D + ++ T NL C S+PC E LP+G+ + + TVL Sbjct: 382 RDAARDAEFFRVNNLLLRNTSVVNLLDGCALSLPCHAPGE-LPVGLMVWHGALRDDTVLN 440 Query: 467 VGQAVE-SLQK 476 VG +E +LQK Sbjct: 441 VGLQIEQTLQK 451 Lambda K H 0.317 0.134 0.385 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: 524 Number of extensions: 29 Number of successful extensions: 6 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 1 Length of query: 476 Length of database: 451 Length adjustment: 33 Effective length of query: 443 Effective length of database: 418 Effective search space: 185174 Effective search space used: 185174 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 (21.7 bits) S2: 51 (24.3 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