Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate Ac3H11_4821 putative amidase
Query= curated2:A7NKM0 (490 letters) >FitnessBrowser__acidovorax_3H11:Ac3H11_4821 Length = 467 Score = 207 bits (527), Expect = 6e-58 Identities = 161/496 (32%), Positives = 242/496 (48%), Gaps = 46/496 (9%) Query: 1 MTPLYQLTVAQAREMLARGEISSLELTDALLTRIAAVEPKVRAFLVVDAAGARAQARAAD 60 MT L+ L + + +S +E+T A+L I EP ++A ++ A QARA++ Sbjct: 1 MTALHDLPAHELLAAYRQRTLSPVEVTQAVLAHIERWEPHIKATYLLRPEAALEQARASE 60 Query: 61 ARRAAGDASPLL-GIPMGIKDVISTQGLRTTCASKMLENYTPVYDATAVARLKAAGAVIL 119 AR G+ LL G+P IK+ I+TQG T + +E DA AR++ AGAV++ Sbjct: 61 ARWLRGEPKGLLDGVPSTIKENIATQGDPTPLGTAAVELAPAAADAPPAARMREAGAVVV 120 Query: 120 GKLNCDEFAMGSSTENSAFQQTRNPWNLERVPGGSSGGSAAAVAAGEAPAALGTDTGGSI 179 K ++ M SS ++ +RNPW++ + PGGSS G AA AAG P +GTD GGS+ Sbjct: 121 AKTTMPDYGMLSSGLSTFHPLSRNPWDVSKGPGGSSAGGGAAAAAGYGPLHIGTDIGGSL 180 Query: 180 RQPAALCGITGLKPTYGRVSRYGLVAFASSLDQIGPMARTVRDCAIVLRVIAGADPFDAT 239 R PA+ CGI LKP+ GR+ + + GPM RTV D A++++V++ D D+ Sbjct: 181 RLPASWCGIFSLKPSLGRIP----IDPPYTGRAAGPMTRTVADAALMMQVLSQPDARDS- 235 Query: 240 CTDYPAPDYEAALTGD----IRGLRIGVPREYFVAG----MQPDVEAAVRTAIEVLREQG 291 PA D + +RGLRIGV + AG ++P+V+AAV A ++ G Sbjct: 236 -MSLPAQDIAWSQFNKGAERLRGLRIGVLLD---AGCGLPVEPEVKAAVEHAARLMEAAG 291 Query: 292 AEVCEISLPHTPYALPVYYLIAPAEASANLARFDGVRYGLRVPGESYFDELERTRGAGFG 351 A I P + A DG+ + R+ + L R Sbjct: 292 A------------------TIVPMQPFMTQAMLDGMDHFWRMRSHTDLQALPAARRDKVL 333 Query: 352 PEVRRRIMLGTYALS-AGYYDAYYKRAQQVRTLIRRDYQQAFEQVDVIAAPTTPTVAF-- 408 P +R T+A S AG A A Q L R +A D + +P P VAF Sbjct: 334 PYIR------TWADSAAGLSGAEVFNASQQFHLTRVAAVKACSAFDYVISPVAPNVAFQA 387 Query: 409 KIGAHTDDPLAMYLEDVCTLPLNLAGLPGLVVPCGFAE-GLPIGLQLIGRAFDEESLLRV 467 ++ + T+DPL T+P N++ P V CG+ GLPIGLQ+ G FD+ +L+V Sbjct: 388 ELPSPTNDPLRPLEHIGFTVPFNMSEQPAASVNCGYTRAGLPIGLQIAGARFDDLGVLQV 447 Query: 468 GDAYQRVTDWHTRMPE 483 A++ + + P+ Sbjct: 448 AHAFELIREPQRAWPQ 463 Lambda K H 0.320 0.136 0.398 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: 540 Number of extensions: 30 Number of successful extensions: 7 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: 490 Length of database: 467 Length adjustment: 34 Effective length of query: 456 Effective length of database: 433 Effective search space: 197448 Effective search space used: 197448 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 (21.8 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