Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate WP_101444719.1 BD749_RS09495 amidase
Query= curated2:B8FCK9 (485 letters) >NCBI__GCF_002846395.1:WP_101444719.1 Length = 555 Score = 204 bits (520), Expect = 5e-57 Identities = 153/479 (31%), Positives = 237/479 (49%), Gaps = 51/479 (10%) Query: 7 TIGQAREKLLSKEISSQDLTKAVLDRIEAVEPQVDAYLTVSKEEAMEAAQKADKALAQGE 66 ++ Q E + +K+ISS++LTK LDR++ P + ++++E A+E A++AD+ + G+ Sbjct: 119 SVPQLAELVRTKQISSEELTKFFLDRLKQHGPTLQCVTSLTEELALEQARRADQEIKAGK 178 Query: 67 -TAPLCGIPLAIKDVMCTKGVLTTCASKILGNFVPPYDATSITKLKEAGAVLVGKTNMDE 125 L GIP +KD++ TK TT S + DAT + +L++AGAVLV K + E Sbjct: 179 YKGMLHGIPYGVKDLLATKKYKTTWGSVPYKDQQIDLDATVVERLEQAGAVLVAKLTLGE 238 Query: 126 FAMGSSTENSAFKTTKNPWDLTRTPGGSSGGSAAAVAADMCLGAFGSDTGGSIRQPGSHC 185 AMG T++PWD T+ GSS GSA+AV+A + A G++T GSI P + C Sbjct: 239 LAMGDVWYGGK---TRSPWDTTKGSSGSSAGSASAVSAGLLPFAIGTETLGSIVSPSTAC 295 Query: 186 SVVGLKPTYGRVSRYGLVAFASSLDQIGPFAKTVEDAAILLQAVAGYDPSDSTSVNVEVP 245 GL+PTYGRVSRYG +A + S+D+IGP A++ ED AI+ A+ G D D T N Sbjct: 296 GTTGLRPTYGRVSRYGAMALSWSMDKIGPIARSAEDCAIVFNAIYGPDGKDLTVANAPF- 354 Query: 246 DYTTAIQEDVKGMRVGMPKEYFEMGGLTPDVKNSVDQAIKTLESQGVEVMDVSLPH-SKY 304 +Y +I + K +RVG + FE K + ++ L G+E++ + LP+ Sbjct: 355 NYNKSI--EAKKLRVGYLHKDFER---DYPFKENDKATLEALRKAGIELVPIELPNLPAR 409 Query: 305 CVAVYYVIAPAEASSNLARYDGVKYGMREERDSLIDMYHATRSSGFGPEVQRRIIIGTYA 364 + + + A A L R RDSL+ H P + R G + Sbjct: 410 DLTLTISVEGAAAFDELT---------RSGRDSLMVQQH----KNAWPNIFR---AGRFV 453 Query: 365 LSAGYYDAYYGKASQVRTLIMEDYKKAFEKCDAIISPVAPTPAFKLGENTDDPLTMYLSD 424 + Y +A +VR+LI++ + + D +SP G N Sbjct: 454 TAVEYL-----QAQRVRSLIIQQMHEQLKGIDVYLSPSF------AGSN----------- 491 Query: 425 IFTLSANLAGVCGVSVPCGFSSEGLPIGLQLQGSHFQEEKILRLGHHFQKATDFHTKRP 483 + NL+G V VP GF G+P + G + E K+L L +Q T+ +RP Sbjct: 492 --LVMTNLSGHPCVVVPNGFQKNGMPTTITFMGQLYGEAKVLALAKLYQDLTNHDEQRP 548 Lambda K H 0.315 0.132 0.378 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: 567 Number of extensions: 31 Number of successful extensions: 5 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: 485 Length of database: 555 Length adjustment: 35 Effective length of query: 450 Effective length of database: 520 Effective search space: 234000 Effective search space used: 234000 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 26 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