Align Glutamate--tRNA ligase; EC 6.1.1.17 (characterized, see rationale)
to candidate BPHYT_RS12355 BPHYT_RS12355 glutamate--tRNA ligase
Query= uniprot:A0A0H3C8P5_CAUVN (470 letters) >FitnessBrowser__BFirm:BPHYT_RS12355 Length = 469 Score = 337 bits (863), Expect = 7e-97 Identities = 189/469 (40%), Positives = 267/469 (56%), Gaps = 12/469 (2%) Query: 7 TGVVTRFAPSPTGFLHIGGARTALFNWLYARHTGGKFLIRVEDTDRERSTEAAVAAIFEG 66 T V TRFAPSPTGF+H+G R+AL+ W +AR G F++R+EDTD ERST +V AI EG Sbjct: 3 TSVRTRFAPSPTGFIHLGNIRSALYPWAFARKMKGTFVLRIEDTDVERSTSESVDAILEG 62 Query: 67 LDWLGLKSDDEVIFQHTRAPRHVEVVHELLAKGRAYRCWMSIEELEVAREKARAEGRAIR 126 + WLGL D+ +Q R R+ EV+ ++ G Y C+MS EEL+ RE+ R G R Sbjct: 63 MAWLGLDFDEGPFYQMQRMDRYREVLKQMQDAGLVYPCYMSTEELDALRERQREAGEKPR 122 Query: 127 --SPWRDAPEGDLSAPH-----VIRFKGPLDGETLVNDLVKGPVTFKNIELDDLVLLRAD 179 WR P L P V+RF+ PL G +D VKG + N ELDDLV+ R D Sbjct: 123 YDGTWRPEPGKVLPEPPAGVQPVLRFRNPLTGVVAWDDAVKGRIEISNEELDDLVIARPD 182 Query: 180 GAPTYNLAVVVDDHDMGVTHVIRGDDHLNNAARQTLIYQAMDWAVPAFAHIPLIHGPDGA 239 G PTYN VVVDD DM +THVIRGDDH+NN RQ I +A+ P +AH+P + G Sbjct: 183 GTPTYNFCVVVDDLDMRITHVIRGDDHVNNTPRQINILRALGGEPPVYAHLPTVLNEQGE 242 Query: 240 KLSKRHGAQAVGEFADLGYIPEGMRNYLARLGWGHGDDEVFTDEQAISWFDVADVVKAPA 299 K+SKRHGA +V + D G++PE + NYLARLGW HGD E+F+ EQ + WFD+ + K+PA Sbjct: 243 KMSKRHGAMSVVGYRDAGFLPEAVVNYLARLGWSHGDAEIFSREQFVEWFDLEHLGKSPA 302 Query: 300 RLDWAKLNHINAQHLRKADDARLTALALAAAETRG--EPLPADAAERIARTVPEVKEGAK 357 + D KL +NA ++++AD+ARL LA G E A A+ +A V +K+ A Sbjct: 303 QYDHDKLAWLNAHYIKEADNARLAELAKPFFAELGIDEAALAQGAD-LAAVVGLLKDRAS 361 Query: 358 TILELVDHCAFALKTRPLALEEKTQKQLTEETVERLKRLRDQLAAAPDFDAATLETVLKS 417 T+ E+ ++ A +T P E + +T+ L L L ++ + LK+ Sbjct: 362 TVKEIAENAAMFYRT-PAPDAESLAQHVTDVVRPALADLAAALKTV-EWTKEAIAAALKA 419 Query: 418 FAESEGVGFGKFGPALRGVLTGGAQAPDLNKTMAALSRDEAIGRLDDAL 466 + + + +R ++ G P ++ + RD +GR++ AL Sbjct: 420 TLGAHKLKMPQLAMPVRLLVAGTTHTPSIDSVLMLFGRDVVVGRIEKAL 468 Lambda K H 0.319 0.135 0.405 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: 611 Number of extensions: 33 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: 470 Length of database: 469 Length adjustment: 33 Effective length of query: 437 Effective length of database: 436 Effective search space: 190532 Effective search space used: 190532 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 (21.7 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