Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate GFF3456 PS417_17690 amidase
Query= curated2:Q67KJ2 (488 letters) >FitnessBrowser__WCS417:GFF3456 Length = 467 Score = 214 bits (545), Expect = 5e-60 Identities = 169/488 (34%), Positives = 232/488 (47%), Gaps = 43/488 (8%) Query: 2 LSAARLNRLFLAGELSAVEIAESALSRIAQVEPAVGAFITVAADHVIERAKKLDARRKAG 61 L+A +L + F LS V++ E AL RI + P V A+ V + + A+ + R G Sbjct: 7 LTAVQLLQHFRDKTLSPVDVTEDALLRIERYNPVVNAYCHVDPEGALNAARASEQRWLNG 66 Query: 62 DTELGPLAGVPIAVKDNICTSGMETTCASRILKGYVSPFD--ATVVERLRAAGAMIIGKA 119 G L GVP ++KD T GM T SR P+D A +R AGA+++GK Sbjct: 67 QP-CGALDGVPASIKDLTLTVGMPTRKGSRTTSAE-GPWDVDAPFTAFMRKAGAVLLGKT 124 Query: 120 NMDEFAMGSSGESSAFGVTRNPWDLERVPGGSSSGSAAAVAAGEAPLALGTDTGGSIRQP 179 EF ++ +G+TRNPWD GGSS G+ AA A L G+D GGSIR P Sbjct: 125 TTPEFGWKGVTDNPLYGITRNPWDTRTTAGGSSGGAGAAAALNLGVLHQGSDAGGSIRIP 184 Query: 180 AAFTGIVGLKPTYGYVSRYGVVAFASSLDQVGPMGRDVEDVARLFEVIAGPDRRDA-TNA 238 AFTG G+KPT+GYV ++ A + L +GPM R VED + + IA PD RD A Sbjct: 185 CAFTGTFGIKPTFGYVPQWPASAM-TLLSHLGPMTRKVEDSVLMLQTIAQPDARDGLIGA 243 Query: 239 GRTPPALKFGGEPSLSGVRLGVPKELLGPGIDPGVKARVEEAIAQLEELGATVEECSLPS 298 RT P L G + L+G+R+ +DP V V +A+A L +LGA VE+ P Sbjct: 244 PRTTPWLTPGTD--LNGLRVAYSPNFGYVDVDPQVAKVVAQAVAGLVQLGAHVEQID-PG 300 Query: 299 TEYALSAYYVIAVAEASSNLARFDGVRYGYRAAQAGGLHEMYSKTRGEGFGTEVKRRIML 358 L + + A A A +++ + G RI Sbjct: 301 FSDPLEVFSTLWAAGA---------------ARLTRPMNDAQKQLLDPGL-----LRIAQ 340 Query: 359 GTYVLSAGHYDAYYRRAQQVRTLVVRDFERAFERYDALVTPTTPFTAWKIGEKVDDPVSM 418 LS ++A A + R +V E YD LV+P P TA+ G D P Sbjct: 341 RGERLSLDDFNA----ALEARAALVARMAAFHEHYDVLVSPMMPITAFDAGH--DVPPGS 394 Query: 419 YLGDIC-----TIPVNLAGLPAVSVPCGF-VDGLPVGMQLIGKPFADTQILQIAWAYQKV 472 L + T P NL PA SVPCG +GLPVG+ ++G FAD Q+L++ AY K Sbjct: 395 GLQEWTQWTPFTYPFNLTQQPAASVPCGLATNGLPVGLHVVGARFADEQVLRVCHAYAKA 454 Query: 473 --TKHHEA 478 T+H +A Sbjct: 455 FPTQHLQA 462 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: 599 Number of extensions: 37 Number of successful extensions: 8 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 3 Number of HSP's successfully gapped: 2 Length of query: 488 Length of database: 467 Length adjustment: 34 Effective length of query: 454 Effective length of database: 433 Effective search space: 196582 Effective search space used: 196582 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: 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