Align glutamyl-tRNAGlx synthetase (EC 6.1.1.17; EC 6.1.1.24) (characterized)
to candidate Pf1N1B4_24 Glutamyl-tRNA synthetase (EC 6.1.1.17)
Query= metacyc::MONOMER-13959 (483 letters) >lcl|FitnessBrowser__pseudo1_N1B4:Pf1N1B4_24 Glutamyl-tRNA synthetase (EC 6.1.1.17) Length = 437 Score = 310 bits (794), Expect = 6e-89 Identities = 165/437 (37%), Positives = 261/437 (59%), Gaps = 20/437 (4%) Query: 26 LFNYLFARNQGGKFIIRVEDTDKKRNIEGGEQSQLNYLKWLGIDWDESVDVGGEYGPYRQ 85 LFNY FA+ GG+FI+R+EDTD+ R+ EQ + L+WLGIDW E DVGG +GPYRQ Sbjct: 1 LFNYCFAKQHGGEFILRIEDTDQLRSTRESEQQIFDALRWLGIDWSEGPDVGGPHGPYRQ 60 Query: 86 SERNDIYKVYYEELLEKGLAYKCYCTEEELEKEREEQIARGEMPRYSGKHRDLTQEEQEK 145 SER DIY+ Y ++L++ G A+ C+CT EEL++ R EQ+ARGE PRY G+ L++EE + Sbjct: 61 SERGDIYQKYCQQLVDMGHAFPCFCTAEELDQMRAEQMARGETPRYDGRALLLSKEEVAR 120 Query: 146 FIAEGRKPSIRFRVPEGKVIAFNDIVKGEISFESDGIGDFVIVKKDGTPTYNFAVAIDDY 205 +A G IR +VP V D+++G++ D + V++K DG PTY A +DD+ Sbjct: 121 RLAAGEPHVIRMKVPTEGVCVVPDMLRGDVEIPWDRMDMQVLMKTDGLPTYFLANVVDDH 180 Query: 206 LMKMTHVLRGEDHISNTPKQIMIYQAFGWDIPQFGHMTLIVNESRKKLSKRDESIIQFIE 265 LM +THVLRGE+ + + PK I++Y+ FGW+ PQ +M L+ N + KLSKR + Sbjct: 181 LMGITHVLRGEEWLPSAPKLILLYEYFGWEQPQLCYMPLLRNPDKSKLSKRKNP--TSVT 238 Query: 266 QYKELGYLPEALFNFIGLLGWSPVGEEELFTKEQFIEIFDVNRLSKSPALFDMHKLKWVN 325 Y+ +G++PEA+ N++G +GWS E E F+ ++ ++ FD++R+S +FD+ KL W+N Sbjct: 239 FYERMGFMPEAMLNYLGRMGWSMPDEREKFSLQEMVDNFDLSRVSLGGPIFDIEKLSWLN 298 Query: 326 NQYVKKLDLDQVVELTLPHLQKAGKVGTELSAEEQEWVRKLISLYHEQLSYGAEIVELTD 385 Q+++ L +++ LQK A E++ K+ ++ +++ L Sbjct: 299 GQWLRDLPVEEFA----ARLQK--------WALNPEYMMKIAPHVQGRVETFSQVAPLAG 346 Query: 386 LFFTDEIEYNQEAKAV----LEEEQVPEVLSTFAAKLEELEEFTPDNIKASIKAVQKETG 441 FF + N +AK L +QV +++ KLE L ++ D+I A+I+AV + Sbjct: 347 FFFAGGV--NPDAKLFESKKLSGDQVRQLMQLILWKLESLRQWEKDSITATIQAVVESLE 404 Query: 442 HKGKKLFMPIRVAVTGQ 458 K + + A+TG+ Sbjct: 405 LKLRDAMPLMFAAITGR 421 Lambda K H 0.316 0.137 0.394 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: 554 Number of extensions: 25 Number of successful extensions: 3 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: 483 Length of database: 437 Length adjustment: 33 Effective length of query: 450 Effective length of database: 404 Effective search space: 181800 Effective search space used: 181800 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: 51 (24.3 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