Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate WP_028315305.1 G491_RS0115890 amidase
Query= curated2:C6BSE9 (487 letters) >NCBI__GCF_000429905.1:WP_028315305.1 Length = 480 Score = 159 bits (402), Expect = 2e-43 Identities = 138/491 (28%), Positives = 222/491 (45%), Gaps = 37/491 (7%) Query: 1 MSALIEKSLTEIHAMLMTKEVTATEAVKACLEQIAKSEPETKALLHICNDEALKQAEEMD 60 M L+ S T+I AM+ ++T+ +AV+ +E K P A++ D+AL +A+ D Sbjct: 1 MDKLLTLSGTKIAAMIREGKITSRKAVETHIEHAKKINPWINAIVADRYDQALDEADAAD 60 Query: 61 AA----GPDASKPLWGVPVVIKDALATNGIPTTAGSKILEGFTPFYDSTAVAKLKEAGAI 116 A GP+ GVP IK+ + G+P T+G +G D+TA A+++ AG I Sbjct: 61 AFLKENGPENCPSFHGVPCSIKECFSLTGMPHTSGLVARKGIIEKKDATAAARMRRAGLI 120 Query: 117 IVGKANMDEFAMGSTTENSAYQTTTNPWDASRVPGGSSGGSGATVAAGQCYAALGTDTGG 176 +G N+ E M + N Y TT N +D R+ GGSSGG G V++G LG+D GG Sbjct: 121 PIGVTNISELCMWMESHNKVYGTTNNCYDLGRIVGGSSGGEGCIVSSGASPFGLGSDVGG 180 Query: 177 SIRLPASFCGCVGVKPTYGRVSRYGMI--AYG--SSLDQIGPMTRTVEDAARVLNVIGGH 232 SIR+PA F G G KPT G V G I A+G + GP+ R ED +L ++ G Sbjct: 181 SIRMPAFFNGVFGHKPTGGAVPNTGQIPLAHGRVAFYCTTGPLCRKAEDLMPLLKIMAGP 240 Query: 233 DQRDSTSAEQPMEDFVAALEERKDLSGLTIGLPEEYWGEGLSKEVSEACRAAIAKAEELG 292 D +D D + D S L + E + E+ A + A E+LG Sbjct: 241 DGKDPECTAMDFGDPASV-----DFSRLNVLSVPENGAVRVHHELVIAQKKAADALEKLG 295 Query: 293 AKTVPVKLSMTEYAIATYYIIAMAEASSNLSRFDGVRYGHRTEDPKELA---ELYTKSRT 349 A ++ +++ A + SS L+ +G + K + EL+ + Sbjct: 296 ASVKHRTVNKLKWSFAIW--------SSMLNHHQTEEFGVQLGQGKRIPVFWELFKWALR 347 Query: 350 EAFGDEVQRRIIIGTYVLSAGYYDAYYRKAAQIRRLLREDFNKAFESCDIIASPACPTTA 409 + + +G + K ++ R LR + + ++ P+ A Sbjct: 348 ASDHTLPALALALGERI------PMPTEKFIKMGRELRRELIELIGPDGVMLYPSYSKPA 401 Query: 410 FPVGELTSDPLQMYLQDIFTISLNLVGMPGMSLPVAFGKETNMPVGLQFM-APAFDEKTM 468 +PL + ++T +N++G P +P+ K+ +PVG+Q + P D KT Sbjct: 402 ----PRHLEPLMLLDNFVYTAIINVMGFPSTQVPLGLSKK-GLPVGVQVVGTPGNDHKT- 455 Query: 469 LQAAHVLEKNL 479 + A LEK+L Sbjct: 456 IAVAMELEKSL 466 Lambda K H 0.315 0.131 0.374 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: 543 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: 487 Length of database: 480 Length adjustment: 34 Effective length of query: 453 Effective length of database: 446 Effective search space: 202038 Effective search space used: 202038 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 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