Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate CCNA_02558 CCNA_02558 enantioselective peptide amidase
Query= curated2:A7NKM0 (490 letters) >FitnessBrowser__Caulo:CCNA_02558 Length = 528 Score = 197 bits (500), Expect = 1e-54 Identities = 185/505 (36%), Positives = 240/505 (47%), Gaps = 39/505 (7%) Query: 1 MTPLYQLTVAQAREMLARGEIS--SLELTDALLTRIAAVEPKVRAFLVVDAAGARAQARA 58 MT L A A +LA + S E T A L I P +RA + + A A+A Sbjct: 32 MTKFAILAGAAAIALLAGNACAQTSEEATKAALATIQQRNPVLRAVIATNP-NALTAAKA 90 Query: 59 ADARRAAGDA-SPLLGIPMGIKDVI-STQGLRTTCASKMLENYTPVYDATAVARLKAAGA 116 DA R AG S L G+P+ +KD I S L TT S L++ DA RL+ AG Sbjct: 91 LDAERKAGKVRSALHGVPILLKDNIESADPLPTTAGSLALKDNITGRDAPVAKRLRDAGL 150 Query: 117 VILGKLNCDEFAMGSSTEN----SAFQQT-RNPWNLERVPGGSSGGSAAAVAAGEAPAAL 171 VILGK N E+A S + SA T RNP+ L+R GSS GS AAVAAG AP A+ Sbjct: 151 VILGKANLSEWANIRSNHSISGWSAVGGTVRNPYALDRSACGSSSGSGAAVAAGLAPLAI 210 Query: 172 GTDTGGSIRQPAALCGITGLKPTYGRVSRYGLVAFASSLDQIGPMARTVRDCAIVLRVIA 231 GT+T GSI PAA+ G+ GLKPT G VSR +V + S D GPM TV D A VL +IA Sbjct: 211 GTETDGSITCPAAINGLVGLKPTVGLVSRTHIVPISHSQDTAGPMTLTVEDTAKVLTIIA 270 Query: 232 GADPFDATCTDYPA--PDYEAALTGD-IRGLRIGVPREYFVAGMQPDVEAAVRTAIEVLR 288 G+DP D + A DY A L+ ++G+ + V R F G P +A A++ L Sbjct: 271 GSDPTDPATKEADARKTDYAAGLSKTALKGVTLAVAR--FYTGYSPKTDAVFERALKELE 328 Query: 289 EQGAEVCEISL----PHTPYALPVYYLIAPAEASANLARFDGVRYGLRVPGESY-FDELE 343 QGA + ++ P V Y A+ +A LA D + R + F++ Sbjct: 329 AQGATLVDVKAFDEGPIGRAEGVVLYTELKADLAAYLASTDPKKVPTRTLADVIAFNKAT 388 Query: 344 RTRGAGFGPEVRRRIMLGTYALSAGYYDAYYKR--AQQVRTLIRRDYQQAFEQVDVIA-- 399 FG E R + G D Y + A R + + +A Sbjct: 389 PKEFEWFGQESFERA-----EKTKGLDDPEYLKALADSKRLAGPEGIDKILKDTGAVAII 443 Query: 400 APTTPTVAFKIGAHTDDPL--AMYLEDVCTLPLNLAGLPGLVVPCGFAEGLPIGLQLIGR 457 APTT A T DPL Y TLP +AG P L VP G GLP+GL IG Sbjct: 444 APTTGP------AWTIDPLNGDNYGGSSTTLPA-VAGYPHLTVPMGDVSGLPVGLSFIGP 496 Query: 458 AFDEESLLRVGDAYQRVTDWHTRMP 482 A+ E+ LL +G AY++ T H + P Sbjct: 497 AWSEKLLLNLGYAYEQATK-HRKAP 520 Lambda K H 0.320 0.136 0.398 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: 549 Number of extensions: 26 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: 490 Length of database: 528 Length adjustment: 34 Effective length of query: 456 Effective length of database: 494 Effective search space: 225264 Effective search space used: 225264 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 (21.8 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