Align glutaminyl-tRNA synthase (glutamine-hydrolysing) (EC 6.3.5.7) (characterized)
to candidate GFF2899 PS417_14835 amidase
Query= BRENDA::Q9H0R6 (528 letters) >FitnessBrowser__WCS417:GFF2899 Length = 569 Score = 116 bits (291), Expect = 2e-30 Identities = 98/360 (27%), Positives = 153/360 (42%), Gaps = 64/360 (17%) Query: 5 SLREVSAALKQGQITPTELCQKCLSLI------KKTKFLNAYITVSEEVALKQAEESEKR 58 S+ ++ AAL+ GQ T EL + L+ I + LNA + + E ALK+AE S+ R Sbjct: 8 SIAQLRAALESGQTTAVELVKAYLARIDAYDGPQTATALNAVVVRNPE-ALKEAEASDAR 66 Query: 59 YKNGQSLGDLDGIPIAVKDNFSTSGIETTCASNMLKGYIPPYNATVVQKLLDQGALLMGK 118 G++LG LDGIP KD++ G+ S + +A +++L GA+ +GK Sbjct: 67 RAKGETLGPLDGIPYTAKDSYLVKGLTAASGSPAFAKLVAQRDAFTIERLRAGGAICLGK 126 Query: 119 TNLDEFAMGSGSTDGVFGPVKNPWSYSKQYREKRKQNPHSENEDSDWL---ITGGSSGGS 175 TN+ A G G GV+G ++P++ +D+L GSS G+ Sbjct: 127 TNMPPMANG-GMQRGVYGRAESPYN-------------------ADYLTAPFASGSSNGA 166 Query: 176 AAAVSAFTCYAALGSDTGGSTRNPAAHCGLVGFKPSYGLVSRHGLIPLVNSMDVPGILTR 235 A +A L +T S R PA++ GL + PS G++S G PL +MDV R Sbjct: 167 GTATAASFAAFGLAEETWSSGRGPASNNGLCAYTPSRGVISVRGNWPLTPTMDVVVPYAR 226 Query: 236 CVDDAAIVLGALAGPDPRD--------------STTVHEPINKPFMLPSLADVSKLCIGI 281 + D VL + DP S T P + + + ++ G+ Sbjct: 227 TMADLLEVLDVVVAEDPDTRGDLWRLQPWVPIPSVTSVRPASYAELASTAESLAGKRFGV 286 Query: 282 PKEYLVPE--------------------LSSEVQSLWSKAADLFESEGAKVIEVSLPHTS 321 P+ Y+ + + V LW A + GA+VI+V P S Sbjct: 287 PRMYINADPDAGTSEKPGIGGPTGQKINTRASVIDLWQDARQALTTAGAEVIDVDFPLVS 346 Score = 43.5 bits (101), Expect = 2e-08 Identities = 30/104 (28%), Positives = 58/104 (55%), Gaps = 8/104 (7%) Query: 397 QKVRRLIANDFVNAFNSGVDVLLTPTTLSEAVPYLEFIKEDNRTRSAQDDIFTQAVNMA- 455 ++ RR+ D+++ G+D +L PT +++ P + E + + + ++ N+A Sbjct: 451 EQTRRIDLEDWMDKL--GLDAVLFPT-VADVGPADADVNEVSADIAWSNGVWVANGNLAI 507 Query: 456 ---GLPAVSIPVA-LSNQGLPIGLQFIGRAFCDQQLLTVAKWFE 495 G+P V++P+ +++ G+PIGL F GRA+ D LL A +E Sbjct: 508 RHLGVPTVTVPMGVMADIGMPIGLTFAGRAYDDSALLRFASAYE 551 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: 646 Number of extensions: 33 Number of successful extensions: 5 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: 528 Length of database: 569 Length adjustment: 36 Effective length of query: 492 Effective length of database: 533 Effective search space: 262236 Effective search space used: 262236 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: 53 (25.0 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