Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate 6938403 Sama_2522 amidase (RefSeq)
Query= curated2:Q67KJ2 (488 letters) >FitnessBrowser__SB2B:6938403 Length = 567 Score = 122 bits (306), Expect = 3e-32 Identities = 103/340 (30%), Positives = 148/340 (43%), Gaps = 47/340 (13%) Query: 2 LSAARLNRLFLAGELSAVEIAESALSRI-----AQVEPAVGAFITVAADHVIERAKKLDA 56 +S A L +G +AVE+ ++ L+RI A + + A + D ++ A+ DA Sbjct: 7 VSIAELRGALESGRTTAVELVKAYLARIEAYDGADTDTKLNAVVVHNPD-ALKEAEASDA 65 Query: 57 RRKAGDTELGPLAGVPIAVKDNICTSGMETTCASRILKGYVSPFDATVVERLRAAGAMII 116 RR G+T LGPL G+P KD+ G+ S K V+ DA VERLRA GA+ + Sbjct: 66 RRARGET-LGPLDGIPYTAKDSYLVKGLTAASGSPAFKDLVAQRDAFTVERLRANGAICL 124 Query: 117 GKANMDEFAMGSSGESSAFGVTRNPWDLERV----PGGSSSGSAAAVAAGEAPLALGTDT 172 GK NM A G + +G +P++ + GSS+G+ A AA L +T Sbjct: 125 GKTNMPPMANGGM-QRGVYGRAESPYNAAYLTAPFASGSSNGAGTATAASFCAFGLAEET 183 Query: 173 GGSIRQPAAFTGIVGLKPTYGYVSRYGVVAFASSLDQVGPMGRDVEDVARLFEVIAGPDR 232 S R PA+ G+ P+ G +S G ++D V P R + D+ + +V+ D Sbjct: 184 WSSGRGPASNNGLCAYTPSRGVISVRGNWPLTPTMDVVVPYARTMADLLEVLDVVVADDS 243 Query: 233 RDATNAGRTPPALKFG---------------GEPSLSGVRLGVPK------ELLGPGIDP 271 + R P ++ G SL G R GVPK EL G +P Sbjct: 244 ETRGDLWRMQPWVQIPKASEVRPESYIALACGADSLKGKRFGVPKMFINKDELAGTSENP 303 Query: 272 G--------------VKARVEEAIAQLEELGATVEECSLP 297 G V A E+A A LE GA V E P Sbjct: 304 GIGGPTGQRIHTRDSVIALWEQARAALEAAGAEVIEVDFP 343 Score = 37.4 bits (85), Expect = 1e-06 Identities = 25/86 (29%), Positives = 40/86 (46%), Gaps = 12/86 (13%) Query: 394 DALVTPTTPFTAWKIGEKVDDPVSMYLGDICTIPVNLAGLPAVSVPCGFVD--GLPVGMQ 451 DA V P + AW G V + + + G+P V+VP G + G+PVG+ Sbjct: 482 DADVNPASADIAWSNGVWVANG---------NLAIRHLGVPTVTVPMGIMADIGMPVGLT 532 Query: 452 LIGKPFADTQILQIAWAYQKV-TKHH 476 G+ + D +L +A A++ K H Sbjct: 533 FAGRAYDDNALLSLASAFESTGNKRH 558 Lambda K H 0.318 0.135 0.391 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: 660 Number of extensions: 30 Number of successful extensions: 3 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: 488 Length of database: 567 Length adjustment: 35 Effective length of query: 453 Effective length of database: 532 Effective search space: 240996 Effective search space used: 240996 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