Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate Pf1N1B4_4165 Aspartyl-tRNA(Asn) amidotransferase subunit A (EC 6.3.5.6) @ Glutamyl-tRNA(Gln) amidotransferase subunit A (EC 6.3.5.7)
Query= curated2:C6BSE9 (487 letters) >FitnessBrowser__pseudo1_N1B4:Pf1N1B4_4165 Length = 478 Score = 178 bits (451), Expect = 4e-49 Identities = 143/488 (29%), Positives = 221/488 (45%), Gaps = 61/488 (12%) Query: 15 MLMTKEVTATEAVKACLEQIAKSEPETKALLHICNDEALKQAEEMDAAGPDASKPLWGVP 74 ++ T EVT+ E + + + + P+ A++ E + + PL GVP Sbjct: 17 LVATGEVTSAELAELAIAAVQQVNPQINAVI-----------EHWSPTVTEGTGPLAGVP 65 Query: 75 VVIKD-ALATNGIPTTAGSKILEGFTPFYDSTAVAKLKEAGAIIVGKANMDEFAMGSTTE 133 +IKD A+ + G GS++ +G DS + + AG +G+ E A + TE Sbjct: 66 FLIKDLAITSAGRRVELGSRLAQGLVAESDSYLMQRFNAAGLATLGRTTTPEMAFSTETE 125 Query: 134 NSAYQTTTNPWDASRVPGGSSGGSGATVAAGQCYAALGTDTGGSIRLPASFCGCVGVKPT 193 + T NPWD GGSSGGSGA VAAG A TD GSIR+PAS+ G VG+KPT Sbjct: 126 SVLQGPTRNPWDTRLSAGGSSGGSGAAVAAGIVPIAHATDAAGSIRVPASYNGLVGLKPT 185 Query: 194 YGRVSRYGMIAYGSSLDQIGP-------MTRTVEDAARVLNVIGGHDQRDSTSAEQPMED 246 GR S G +LD++ ++RTV D+A +++++ G+ D P E Sbjct: 186 RGRASN------GPALDEVFAGFGVQLGLSRTVRDSAALMDIVQGYAPGDPYYTAAPDEG 239 Query: 247 FVAALEERKDLSGLTIGLPEEYW-GEGLSKEVSEACRAAIAKAEELGAKT----VPVKLS 301 F+A + +D L IGL + W G L E++EA A + E LG + P+ S Sbjct: 240 FLA--QVGRDPGRLRIGLLDTPWNGAALDPEIAEATLAVARELEALGHRVERVIAPLGTS 297 Query: 302 MTEYAIATYYIIAMAEASSNLSRFDGVRYGHRTEDPKELAELYTKSRTEAFGDEVQRRII 361 + A +I ++ + DG+ T P +L+ L + Sbjct: 298 WDSFVQANAHI----WCATLVRWIDGL--AAATSRPIDLSTLEPAT-------------- 337 Query: 362 IGTYVLSAGYYDAYYRKAAQIRRLLREDFNKAFESCDIIASPACP-----TTAFPVGELT 416 + Y + A ++R L+ F+ D++ +P P + G T Sbjct: 338 LACYAYGLEARAVEFAGALEVRNLIARSVAGWFDDFDVLLTPTLPRLPHALDTYSRGAQT 397 Query: 417 SDPLQ----MYLQDIFTISLNLVGMPGMSLPVAFGKETNMPVGLQFMAPAFDEKTMLQAA 472 D LQ ++ FT N+ G P MSLP+A +E +P+GLQF A E+ +L+ A Sbjct: 398 MDGLQWTARVFEHSPFTPVFNVAGTPAMSLPLAMSREQGLPIGLQFAARFGAEEVLLRLA 457 Query: 473 HVLEKNLP 480 LE+ LP Sbjct: 458 GQLEQALP 465 Lambda K H 0.315 0.131 0.374 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: 539 Number of extensions: 27 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: 487 Length of database: 478 Length adjustment: 34 Effective length of query: 453 Effective length of database: 444 Effective search space: 201132 Effective search space used: 201132 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