Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate WP_084704362.1 BS73_RS25805 amidase
Query= curated2:Q67KJ2 (488 letters) >NCBI__GCF_000744815.1:WP_084704362.1 Length = 477 Score = 248 bits (632), Expect = 4e-70 Identities = 183/491 (37%), Positives = 252/491 (51%), Gaps = 37/491 (7%) Query: 4 AARLNRLFLAGELSAVEIAESALSRIAQVEPAVGAFITVAADHVIERAKKLDARRKAGDT 63 A RL L +GE+S+ E+ ++ L RIA V A +T+ A+ + A + D +AG+ Sbjct: 10 ATRLAGLIRSGEVSSREVVQAHLDRIAAHNETVNAVVTLDAEGALTAAGRADRAVRAGEA 69 Query: 64 ELGPLAGVPIAVKDNICTSGMETTCASRILKGYVSPFDATVVERLRAAGAMIIGKANMDE 123 LGPL G+P+AVKD T GM TT SRI +V D +V R+RAAGA++IGK N+ E Sbjct: 70 -LGPLHGLPVAVKDTHLTKGMRTTHGSRIYADHVPEEDELLVARMRAAGAIVIGKTNVPE 128 Query: 124 FAMGSSGESSAFGVTRNPWDLERVPGGSSSGSAAAVAAGEAPLALGTDTGGSIRQPAAFT 183 FA GS +S FG TRNP+D R GGSS G+A ++A G PLA G+D GGS+R PA+F Sbjct: 129 FAAGSHTFNSVFGRTRNPYDRSRSAGGSSGGAAVSLACGFVPLADGSDMGGSLRNPASFN 188 Query: 184 GIVGLKPTYGYVSRYGVVAFASSLDQVGPMGRDVEDVARLFEVIAGPDRR------DATN 237 +VGL+PT G V + +L GP+ R V DVA L V+AGPD R Sbjct: 189 NVVGLRPTPGRVPAHPQTQLWETLGTAGPLARTVADVALLLSVLAGPDPRCPAALETPGE 248 Query: 238 AGRTPPALKFGGEP-SLSGVRLGVPKEL-LGPGIDPGVKARVEEAIAQLEELGATVEECS 295 R P L EP +LSG+R+ +L G + P V A +E + EELGA VE + Sbjct: 249 TFRRPALLAGASEPGALSGLRIAWSPDLGQGLPVAPEVLAVLEPQLRVFEELGARVETAA 308 Query: 296 --LPSTEYALSAYYVIAVAEASSNLARFDGVRYGYRAAQAGGLHEMYSKTRGEGFGTEVK 353 L EYA A+A S L + R ++ + + E + G EV Sbjct: 309 PDLSEAEYAFRTLRAHTFADAMSELV--ERHRELFKPSLIWNVEEGLKLS-----GPEVG 361 Query: 354 R-RIMLG-TYVLSAGHYDAYYRRAQQVRTLVVRDFERAFERYDALVTPTTPFTAWKIGEK 411 R R LG T++ + AY V + D E + R + T + W Sbjct: 362 RARAALGRTHLRGVEFFSAYDLLLAPVSQVAPFDGELEYPR-EIRGTAMETYLDWM---- 416 Query: 412 VDDPVSMYLGDICTIPVNLAGLPAVSVPCGFVD-GLPVGMQLIGKPFADTQILQIAWAYQ 470 S YL V G+PA+SVP GF + GLPVG+Q++ P + ++L+ AY+ Sbjct: 417 ----RSAYL-------VTAMGVPALSVPAGFTEGGLPVGIQIVAAPRREDRVLRAGAAYE 465 Query: 471 KVTKHHEARPA 481 T+H E RPA Sbjct: 466 SATRHGERRPA 476 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: 605 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: 477 Length adjustment: 34 Effective length of query: 454 Effective length of database: 443 Effective search space: 201122 Effective search space used: 201122 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