Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate CCNA_02696 CCNA_02696 AtzE family amidohydrolase
Query= curated2:Q72L58 (471 letters) >FitnessBrowser__Caulo:CCNA_02696 Length = 464 Score = 253 bits (645), Expect = 1e-71 Identities = 186/475 (39%), Positives = 248/475 (52%), Gaps = 52/475 (10%) Query: 5 EIRARVARGEVSPLEVAQAYLKRVQELDPGLGAFLSLN-ERLLEEAEAVDPGL------- 56 EI V G V+ V +A L R+Q LD G+ AF ++ ER L AEAVD L Sbjct: 8 EIAGEVRAGRVTARAVTEATLSRIQRLDGGINAFTAVTAERALAAAEAVDADLAAGRPVG 67 Query: 57 PLAGLVVAVKDNIATRGLRTTAGSRLLENFVPP-YEATAVARLKALGALVLGKTNLDEFG 115 PLAG+ AVK+ GL T AGS++ PP ++AT V RL A GA+++G N+DEF Sbjct: 68 PLAGVPFAVKNLFDLEGLPTLAGSKIRRAAAPPAHDATLVQRLTAAGAVLVGALNMDEFA 127 Query: 116 MGSSTEHSAFFPTKNPFDPDRVPGGSSGGSAAALAADLAPLALGSDTGGSVRQPAAFCGV 175 G TE++ P +NP DP R+ GGSSGGSAAA+AA L PL LGSDT GS+R PA CGV Sbjct: 128 YGFVTENAHDGPVRNPHDPTRIAGGSSGGSAAAVAAGLVPLTLGSDTNGSIRIPAGLCGV 187 Query: 176 YGLKPTYGRVSRFGLIAYASSLDQIGPMARSVRDLALLMDAVAGPDPLDATSLDLPPRFQ 235 +GLKPTYGR+SR G+ + SLD +GP ARSV DLAL D + GPDP + + R Sbjct: 188 FGLKPTYGRLSRQGVFPFVESLDHVGPFARSVEDLALAYDVLQGPDP---SGDPICIRDA 244 Query: 236 EALEGPL-----PPLRLGVVREAL-AGNSPGVERALEEALKVFRELGLSVREVSWPSLPQ 289 E L G L PLR+GV+ G P V AL + EV+ + Sbjct: 245 EPLAGRLDALAEQPLRVGVLGGWFQQGAFPEVLAALGRVADALE----ARDEVTLQNAQA 300 Query: 290 ALAAYYILAPAEASSNLARYDGTLYGRRAEGEEVEGMMEATRAL-FGLEVKRRVLVGTFV 348 A AA + L EG E+ A RA+ + V+ R+L G + Sbjct: 301 ARAAAFCLT------------------AFEGGELHHEDLARRAMDYDPAVRDRLLAGA-L 341 Query: 349 LSSGYYEAYYGRAQAFRRRLKAEAQALFREVDLLLLPTTPHPAFPFGARRDPL----AMY 404 L +G EA AQ FR + E + +F+ D+LL P + PA P G + Sbjct: 342 LPAGVAEA----AQRFRTIFRDEVREVFQRYDILLAPASVCPAPPIGQATMEMDGVPVSV 397 Query: 405 REDL--YTVGANLTGLPALSFPAGFEGHLPVGLQLLAPWGEDERLLRAALAFEEA 457 R++L +T + GLP L+ P G LP+G+Q++AP ++ AAL + A Sbjct: 398 RKNLGAFTQPISYVGLPVLAAPVNRPGQLPIGVQIIAPPWREDLAFAAALRLQRA 452 Lambda K H 0.319 0.137 0.395 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: 581 Number of extensions: 29 Number of successful extensions: 4 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: 471 Length of database: 464 Length adjustment: 33 Effective length of query: 438 Effective length of database: 431 Effective search space: 188778 Effective search space used: 188778 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