Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate GFF3456 PS417_17690 amidase
Query= curated2:Q6A8P5 (501 letters) >FitnessBrowser__WCS417:GFF3456 Length = 467 Score = 196 bits (498), Expect = 1e-54 Identities = 159/482 (32%), Positives = 224/482 (46%), Gaps = 43/482 (8%) Query: 1 MNELLTLTAAELGERIAARQISSEEVTQAHLDRISEVDGDIHAFLLVDHAGALDAARRID 60 M+E+ LTA +L + + +S +VT+ L RI + ++A+ VD GAL+AAR + Sbjct: 1 MSEIGQLTAVQLLQHFRDKTLSPVDVTEDALLRIERYNPVVNAYCHVDPEGALNAARASE 60 Query: 61 ARIADGEHLGPLAGVPLAVKDLFCTKGIATTASSQMLEGWIP-PYDSTIVTRCKDAGMVI 119 R +G+ G L GVP ++KDL T G+ T S+ P D+ + AG V+ Sbjct: 61 QRWLNGQPCGALDGVPASIKDLTLTVGMPTRKGSRTTSAEGPWDVDAPFTAFMRKAGAVL 120 Query: 120 LGKTNLDEFAMGSSTETSAFGPTHNPWDLERVPGGSGGGSAASLASFQAPLALGTDTGGS 179 LGKT EF T+ +G T NPWD GGS GG+ A+ A L G+D GGS Sbjct: 121 LGKTTTPEFGWKGVTDNPLYGITRNPWDTRTTAGGSSGGAGAAAALNLGVLHQGSDAGGS 180 Query: 180 IRQPGAVTGTVGIKPTYGSTSRYGVIAMASSLDTPGPCARTVLDAALLHQAIAGHDAMDQ 239 IR P A TGT GIKPT+G ++ AM + L GP R V D+ L+ Q IA DA D Sbjct: 181 IRIPCAFTGTFGIKPTFGYVPQWPASAM-TLLSHLGPMTRKVEDSVLMLQTIAQPDARD- 238 Query: 240 TTINQP--TPAVVEAARQTDVSGVRIGVVTELSGQVYDPQVEARFHEAVEMLIEAGAEVV 297 I P TP + TD++G+R+ DPQV +AV L++ GA V Sbjct: 239 GLIGAPRTTPWLTPG---TDLNGLRVAYSPNFGYVDVDPQVAKVVAQAVAGLVQLGAHVE 295 Query: 298 EVSCPNFDLALPAYYLIQPAEVSSNLARYDAMRYGLRVNDDGEHSAEQ--VMRATRGAGL 355 ++ P F P EV S L A R +ND + + + A RG L Sbjct: 296 QID-PGFS---------DPLEVFSTLWAAGAARLTRPMNDAQKQLLDPGLLRIAQRGERL 345 Query: 356 GAEAKRRIILGTYALSAGYYDAYYGSAQKVRTLIQRDFEKAWQMCDVLVSPATPTTAFRL 415 + + +A + R + + DVLVSP P TAF Sbjct: 346 SLDD-------------------FNAALEARAALVARMAAFHEHYDVLVSPMMPITAFDA 386 Query: 416 GERTADPMAMY---RSDLCTVPANMAGSPAGSFPIGLSETDGMPVGMQVMAPIMADDRIY 472 G + + T P N+ PA S P GL+ T+G+PVG+ V+ AD+++ Sbjct: 387 GHDVPPGSGLQEWTQWTPFTYPFNLTQQPAASVPCGLA-TNGLPVGLHVVGARFADEQVL 445 Query: 473 RV 474 RV Sbjct: 446 RV 447 Lambda K H 0.317 0.133 0.387 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: 564 Number of extensions: 35 Number of successful extensions: 6 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: 501 Length of database: 467 Length adjustment: 34 Effective length of query: 467 Effective length of database: 433 Effective search space: 202211 Effective search space used: 202211 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: 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