Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate CCNA_01906 CCNA_01906 allophanate hydrolase
Query= curated2:Q67KJ2 (488 letters) >FitnessBrowser__Caulo:CCNA_01906 Length = 594 Score = 191 bits (485), Expect = 6e-53 Identities = 172/481 (35%), Positives = 235/481 (48%), Gaps = 60/481 (12%) Query: 17 SAVEIAESALSRIAQ---VEPAVGAFITVAADHVIERAKKLDARRKAGDTELGPLAGVPI 73 SA +A SAL+ I ++P V + + V+ +A+ +DAR AG+T PLAGVP Sbjct: 20 SAESVARSALAAIEAYDAIQPQVWT-LRLPEAAVLAQARAVDARIAAGETL--PLAGVPF 76 Query: 74 AVKDNICTSGMETTCASRILKGYVSPFDATVVERLRAAGAMIIGKANMDEFAMGSSGESS 133 AVKDNI + + TT A Y + ATVVE+L AAGA+++GK N+D+FA G G S Sbjct: 77 AVKDNIDVADLATTAACPGF-AYTAGRSATVVEQLLAAGAVLVGKTNLDQFATGLVGTRS 135 Query: 134 AFGVTRNPWDLERVPGGSSSGSAAAVAAGEAPLALGTDTGGSIRQPAAFTGIVGLKPTYG 193 +G R ++ V GGSSSGSA AVAAG ALGTDT GS R PAAF +VGLKP+ G Sbjct: 136 PYGAPRCVFNQAFVSGGSSSGSAVAVAAGLVAFALGTDTAGSGRVPAAFNHLVGLKPSKG 195 Query: 194 YVSRYGVVAFASSLDQVGPMGRDVEDVARLFEVIAGPDRRD--ATNAGRTPPALKFGGEP 251 S G+V SLD + D++ R+ V+A D D + A + PAL Sbjct: 196 RWSTRGLVPACRSLDCISVFAADLDGAGRVDAVLAAFDPEDPYSRPAPQPEPAL------ 249 Query: 252 SLSGVRLGVPKE----LLGPGIDPGVKARVEEAIAQLEELGATVEECSL-PSTEYALSAY 306 +L+G+R+ +P+ G G + A A+A+L+ GA E + P + A Y Sbjct: 250 TLAGLRVAIPRPEQRIFFGDGESEALYA---SAVARLQAAGAVAVEVDMAPLLDAAKLLY 306 Query: 307 YVIAVAEASSNL-----ARFDGVRYGYRAAQAGGLHEMYSKTRGEGFGTEVKRRIMLGTY 361 VAE ++ + A + RA GGL G E R G Y Sbjct: 307 SGPWVAERTAAVEPLLRAAPSAIEPTVRAIVQGGLAVT---------GVETFR----GLY 353 Query: 362 VLSAGHYDAYYRRAQQVRTLVVRDFERAFERYDALVTPTTPFTAWKIGEKVDDPVSMYLG 421 L A YRRA E + DAL PTTP T + + +P+++ Sbjct: 354 ALEA------YRRAA----------EAVWAAADALFLPTTP-TIYTVKALKAEPLALNAN 396 Query: 422 -DICTIPVNLAGLPAVSVPCGF-VDGLPVGMQLIGKPFADTQILQIAWAYQKVTKHHEAR 479 + T VNL L A++VP GF DG G+ IG FAD +L +A Y + E Sbjct: 397 LGLYTNFVNLLDLSALAVPAGFRADGTGFGVTFIGPAFADRALLDLAAVYLETFPMAETP 456 Query: 480 P 480 P Sbjct: 457 P 457 Lambda K H 0.318 0.135 0.391 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: 703 Number of extensions: 37 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: 488 Length of database: 594 Length adjustment: 35 Effective length of query: 453 Effective length of database: 559 Effective search space: 253227 Effective search space used: 253227 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 (21.7 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