Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate WP_005455459.1 SACCYDRAFT_RS08690 amidase family protein
Query= curated2:Q2IH94 (492 letters) >NCBI__GCF_000244975.1:WP_005455459.1 Length = 537 Score = 221 bits (562), Expect = 6e-62 Identities = 185/522 (35%), Positives = 253/522 (48%), Gaps = 49/522 (9%) Query: 1 MSTPAKELCRLGLREAGAGVAAKAISSTELVEASLARIQATD----GKLG--AFLAVCAD 54 ++ P ++ L + + + ++S +LV+A L RI A D G+ G A L V A Sbjct: 32 VTAPEPQVVGLTVADLRTMLDEGTVTSAQLVDAYLRRIDAYDRDRAGRPGLRAVLTV-AP 90 Query: 55 RARAAAKAADARAARGERRSELDGVPVAVKDLFVTKGVPTTAGSRILEGYLPPYDATVVE 114 RA A+ DA ARG R L G+PV VKD T+ +PTT+GS L G P DAT V Sbjct: 91 AVRAEARRLDAERARGHVRGPLHGIPVVVKDNIDTRDLPTTSGSLALRGLRAPDDATQVA 150 Query: 115 RLEAAGAVIVGKLNMDEFAMGSSNENSAYKPCHNPWDLSRTPGGSSGGSAASVAAGQVHA 174 RL AGA+++ K N+ E+AM +S NP+D SR PGGSSGG+AA+VAA A Sbjct: 151 RLRDAGAIVLAKTNLHEYAMSVYTVSSLGGQTRNPYDPSRHPGGSSGGTAAAVAASFAPA 210 Query: 175 SLGTDTGGSIREPAAFCGVVGVKPTYGRVSRYGVVAFASSLDQVGPLAREVGDAALVLRT 234 LGTDT GS+R PAA +VGV+PT G SR GV A + D VGPL V DAAL+L Sbjct: 211 GLGTDTCGSVRIPAAHNNLVGVRPTLGLSSRDGVAPLAGTQDTVGPLTMSVEDAALLLDA 270 Query: 235 IAGHDPRDMTSST---RPVDDYLGPL-EEGARGLRVGVPREWL-SGGLDAGVEAAIRAAL 289 AGHDP D + R Y L E G R+GV ++ + G A A +RAA+ Sbjct: 271 TAGHDPADPVTEAAIGRVPGSYTSELRREALEGARLGVVTDYFDTEGRAADTSALVRAAV 330 Query: 290 DTYRRLGATLVDVSLPHSKYGIGAYYLIAPAEASSNLARYDGVR--YGLRAEGAKGLKEM 347 R LGA +V+ +G + A +N R++ R AE A+G Sbjct: 331 ADMRALGAEVVE---------LGPRPELMDAADRANRVRHEFERDFDAYLAESARGAPRR 381 Query: 348 YAESREQGLGAEPKRRIMLGTYALSSGYYDAYYLRAQK----VRTLIRRDFDEAFRGCDV 403 A EP+ + L ++SG L + +L +++EA R D Sbjct: 382 LAHL------TEPRDELTLAD-IVASGEVTPSVLDTLRNWVGSPSLPNPEYEEALRQRDR 434 Query: 404 IAGPVTPSV------AFALGERTGDPLQMYLADIFTITCNLAA---LPGLSVPCGLEAAS 454 + +T + A + P + + + C LAA P +SVP G + Sbjct: 435 LRDLLTELLATHDLDALVYPSISEPPTPIGVPQSYR-NCRLAAFSGFPAVSVPAGF-TSD 492 Query: 455 GLPVGLQLVGRPFDEATLFRAARALERELG----PLPAPPEP 492 GLPVG++L+G PF E L A A E+ G P PP P Sbjct: 493 GLPVGVELLGEPFAEPALLGFAYAYEQGTGHRVPPEGTPPLP 534 Lambda K H 0.317 0.135 0.393 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: 735 Number of extensions: 48 Number of successful extensions: 4 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 3 Number of HSP's successfully gapped: 2 Length of query: 492 Length of database: 537 Length adjustment: 35 Effective length of query: 457 Effective length of database: 502 Effective search space: 229414 Effective search space used: 229414 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