Align glutamyl-tRNA(Glx) synthetase (EC 6.1.1.24) (characterized)
to candidate WP_008803881.1 KVAR_RS06570 glutamate--tRNA ligase
Query= reanno::Caulo:CCNA_01982 (470 letters) >NCBI__GCF_000025465.1:WP_008803881.1 Length = 472 Score = 358 bits (919), Expect = e-103 Identities = 191/462 (41%), Positives = 279/462 (60%), Gaps = 5/462 (1%) Query: 9 VVTRFAPSPTGFLHIGGARTALFNWLYARHTGGKFLIRVEDTDRERSTEAAVAAIFEGLD 68 + TRFAPSPTG+LH+GGARTAL++WL+AR+ GG+F++R+EDTD ERST A+ AI +G++ Sbjct: 3 IKTRFAPSPTGYLHVGGARTALYSWLFARNHGGEFVLRIEDTDLERSTPEAIEAIMDGMN 62 Query: 69 WLGLKSDDEVIFQHTRAPRHVEVVHELLAKGRAYRCWMSIEELEVAREKARAEGRAIRSP 128 WL L+ D+ +Q R R+ V+ E+L G AY+C+ S E LE RE+ A G R Sbjct: 63 WLNLQWDEGPYYQTKRFDRYNNVIDEMLEAGTAYKCYCSKERLEALREEQMANGEKPRYD 122 Query: 129 WRDAPEGDLSA---PHVIRFKGPLDGETLVNDLVKGPVTFKNIELDDLVLLRADGAPTYN 185 R + A P V+RF P +G + +D ++GP+ F N ELDDL++ R DG+PTYN Sbjct: 123 GRCRHSHEHHADDEPCVVRFANPQEGSVIFDDQIRGPIEFSNQELDDLIIRRTDGSPTYN 182 Query: 186 LAVVVDDHDMGVTHVIRGDDHLNNAARQTLIYQAMDWAVPAFAHIPLIHGPDGAKLSKRH 245 VVVDD DM +THVIRG+DH+NN RQ I +A++ VP +AH+ +I+G DG KLSKRH Sbjct: 183 FCVVVDDWDMAITHVIRGEDHINNTPRQINILKALNAPVPVYAHVSMINGDDGKKLSKRH 242 Query: 246 GAQAVGEFADLGYIPEGMRNYLARLGWGHGDDEVFTDEQAISWFDVADVVKAPARLDWAK 305 GA +V ++ D GY+PE + NYL RLGW HGD E+FT E+ I +F + V K+ + + K Sbjct: 243 GAVSVMQYRDDGYLPEALLNYLVRLGWSHGDQEIFTREEMIEFFSLGAVSKSASAFNTDK 302 Query: 306 LNHINAQHLRKADDARLTALALAAAETRGEPLPADAAERIARTVPEVKEGAKTILELVDH 365 L +N H A A L E + ++A V + E KT+ E+ Sbjct: 303 LLWLN-HHYINTLPAEYVATHL-QWHIEQENIDTRNGPQLAELVKLLGERCKTLKEIAQS 360 Query: 366 CAFALKTRPLALEEKTQKQLTEETVERLKRLRDQLAAAPDFDAATLETVLKSFAESEGVG 425 C + + + +K L + L+ +RD+LAA D+ A + +++ A+ VG Sbjct: 361 CRYFYEEFAEFDADAAKKHLRPVARQPLEVVRDKLAAIGDWTAENVHHAIQATADELEVG 420 Query: 426 FGKFGPALRGVLTGGAQAPDLNKTMAALSRDEAIGRLDDALA 467 GK G LR +TG Q+P L+ T+ A+ + ++ R++ ALA Sbjct: 421 MGKVGMPLRVAVTGAGQSPALDVTVHAIGKSRSVERINKALA 462 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: 653 Number of extensions: 27 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: 472 Length adjustment: 33 Effective length of query: 437 Effective length of database: 439 Effective search space: 191843 Effective search space used: 191843 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 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