Align glutamyl-tRNAGlx synthetase (EC 6.1.1.17; EC 6.1.1.24) (characterized)
to candidate WP_066920962.1 ACG33_RS10325 glutamate--tRNA ligase
Query= metacyc::MONOMER-13959 (483 letters) >NCBI__GCF_001579945.1:WP_066920962.1 Length = 474 Score = 287 bits (734), Expect = 6e-82 Identities = 179/485 (36%), Positives = 264/485 (54%), Gaps = 42/485 (8%) Query: 8 RYAPSPTGHLHIGNARTALFNYLFARNQGGKFIIRVEDTDKKRNIEGGEQSQLNYLKWLG 67 R+APSP+G LH+GNARTAL +YL AR G+FI+R+EDTD+ R+ E Q+ L L+W G Sbjct: 9 RFAPSPSGLLHLGNARTALLSYLAARKGKGRFILRIEDTDEARSTEAHVQALLEDLRWFG 68 Query: 68 IDWDESVDVGGEYGPYRQSERNDIYKVYYEELLEKGLAYKCYCTEEELEKEREEQIARGE 127 +DWDE DVGG + YRQ R I++ + +L GL Y C+CT EL R+ Q+A G+ Sbjct: 69 LDWDEGPDVGGPH-EYRQRHRRAIHETWLAKLDAAGLTYPCFCTPAELSLSRKRQLAAGK 127 Query: 128 MPRYSGKHRDLTQEEQEKFIAEGRKPSIRFRVPEGKVIAFNDIVKGEISFESDGIGDFVI 187 PRY+G R L + +A G ++RFRVP G+++AF D+V GE F +D IGDF+I Sbjct: 128 PPRYAGTCRALDAHRRAVRLAAGEPAALRFRVPAGQIVAFGDLVHGEQRFATDDIGDFII 187 Query: 188 VKKDGTPTYNFAVAIDDYLMKMTHVLRGEDHISNTPKQIMIYQAFGWDIPQFGHMTLIVN 247 + DG+ + F+ AIDD LM +T VLRG+DH++NTP+QI+I QA +P++ H+ L++ Sbjct: 188 RRADGSTAFFFSNAIDDALMGITLVLRGDDHLTNTPRQILILQALDLPVPEYAHVALLLG 247 Query: 248 ESRKKLSKRDESIIQFIEQYKELGYLPEALFNFIGLLGWSPVGEEELFTKEQFIEIFDVN 307 LSKR + Q + +++E G+LP AL N + LG + + L E F+++ Sbjct: 248 MDGAPLSKRHGA--QSLGEFRERGFLPGALRNHLVRLGHACQHDGWLDDAAMCAE-FELS 304 Query: 308 RLSKSPALFDMHKLKWVNNQYVKKLDLDQVVE---------LTLPH---LQKAGKVGTEL 355 RL K+ A FD +L + V +L + + L P A + E Sbjct: 305 RLGKAAARFDAAQLHHWQKEAVAQLSQEDFLRWIGAFLPPGLEAPRAAAFAAAVRPNVEF 364 Query: 356 SAEEQEWVRKLISLYHEQLSYGAEIVELTDLFFTDEIEYNQEAKAVLEEEQVPEVLSTFA 415 + + Q W ++++G LT+ F D AV E E A Sbjct: 365 ARDAQPWA---------EVAFG----RLTN-FMPD---------AVAAIEAAGEAFYAMA 401 Query: 416 AKLEELEEFTPDNIKASIKAVQKETGHKGKKLFMPIRVAVTGQTHGPELPQSIELIGKET 475 A++ K ++ + + +G KG LFMP+R A+TG THGPEL + L+ E Sbjct: 402 AQVFARPGL---EFKQRLRELGQASGRKGPALFMPLRAALTGATHGPELAGLLSLVPDEE 458 Query: 476 AIQRL 480 RL Sbjct: 459 VQTRL 463 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: 515 Number of extensions: 18 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: 483 Length of database: 474 Length adjustment: 34 Effective length of query: 449 Effective length of database: 440 Effective search space: 197560 Effective search space used: 197560 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 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