Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate WP_018232951.1 THITHI_RS0109995 amidase
Query= curated2:Q7UT33 (499 letters) >NCBI__GCF_000378965.1:WP_018232951.1 Length = 521 Score = 196 bits (498), Expect = 2e-54 Identities = 160/503 (31%), Positives = 242/503 (48%), Gaps = 37/503 (7%) Query: 7 EILKQLDSGEVTAVEVIAQSLAAIRASQPT--INAFTHVAEETAMQAAEAVDADRKAGKT 64 E + L SG + ++ A+ LA I A +NA H+ AM+ A+ +D + Sbjct: 39 EAREGLRSGRFSCRQLTARHLARISAYDQAGGLNAIAHI-NPNAMRRADTLDRAWRDRGE 97 Query: 65 LGPLAGLPVAIKDVLCTSDMPTTCSSKMLEGFVPPYDATVVARLKSAGAIVVGKTNMDEF 124 + PL +PV +KD + T+DMPT + L+GFV DA +V RL+ AGAIVV K+NM E+ Sbjct: 98 MAPLHCMPVILKDNMHTADMPTEAGAIALQGFVAAEDAFIVKRLREAGAIVVAKSNMGEW 157 Query: 125 AMGA-STETSAMGVTGNPWDTTKTPGGSSGGAAAAVAAGAVPLSLGTDTGGSIRQPAAFC 183 A T +S G T N +D+ + P GSSGG A+A+AA + LGTDTG SIR PAA Sbjct: 158 AFSPFHTISSTRGETRNAYDSERVPAGSSGGTASAIAAAFGIIGLGTDTGNSIRGPAAHL 217 Query: 184 GITGLKPTYGRVSRYGLVAFASSLDQAGPMGWSVDDVAIGLQAMAGYDPRDSTSVNAEV- 242 + GL+PT G SR+G+V + D AGPM +V+D AI +AG+DP D + + Sbjct: 218 ALVGLRPTLGATSRHGIVPLLLNRDIAGPMTRTVEDAAITFSVIAGHDPADPLTERGKER 277 Query: 243 --PDFTPAMAAEDVRGMRIGVLREGLDQDGISPAVRDALATAESVFREQGAEIVEVELPH 300 D+ + + G R+GV+RE P V + A R+ GA +V+ Sbjct: 278 LREDYRAYLDTGGLSGARLGVMRELYQTADADPEVMRIMEQALHDLRDAGAVLVD----- 332 Query: 301 SKYWVPTYYVIAPCEASSNLSRFDGAHYGYRVADAEIAAADSGPLEAMYSLSRAGGFGSE 360 + V + ++ + RFD A++ + DA P+ + + AG + + Sbjct: 333 -PFEVFDFEMLRNATGFCSRFRFDLANHLRDLGDA-------APVRTLDEIVSAGRYLAH 384 Query: 361 VKRRIM------VGTYALSEGYYDAYYNQALKVRRLIRNDYDAAF--QQVDLMLGPVTPS 412 +R I V + + D + RR + + A Q VD ++ P + Sbjct: 385 NERSIAWAMAVDVPPHEMQPPCVDVDGDPR---RRALLDAVLGAMDEQWVDAVIYPTWSN 441 Query: 413 PAFALNEKTDDPIAMYLCDLFTVGANLAGVPAISLPGGFDAVGLPVGVQLQAPVMEETRL 472 P + + D P + V A G PAI++P GF A GLP+G+Q A +E L Sbjct: 442 PPRRIGD-LDSPHG----NNSPVIAPHTGQPAITVPMGFTASGLPLGLQFLARPFDEHVL 496 Query: 473 LRAGNVFQMASDFHTRRPPTFTA 495 R ++ + H R P F A Sbjct: 497 FRLAYAYEQHTQ-HRRPPARFGA 518 Lambda K H 0.316 0.132 0.381 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: 620 Number of extensions: 29 Number of successful extensions: 4 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: 499 Length of database: 521 Length adjustment: 34 Effective length of query: 465 Effective length of database: 487 Effective search space: 226455 Effective search space used: 226455 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: 52 (24.6 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