Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate Ac3H11_1012 Amidase family protein
Query= curated2:Q67KJ2 (488 letters) >FitnessBrowser__acidovorax_3H11:Ac3H11_1012 Length = 499 Score = 192 bits (487), Expect = 3e-53 Identities = 163/490 (33%), Positives = 236/490 (48%), Gaps = 49/490 (10%) Query: 3 SAARLNRLFLAGELSAVEIAESALSRIAQVEPAVGAFIT-VAADHVIERAKKLDARRKAG 61 +A L+R A E+S E+ ++ L+++ ++ P V A + V D + +A + DA+ G Sbjct: 29 TATGLSRAIHAREVSCAEVLDAYLAQVDRLNPVVNALVAMVDRDALRVQAAERDAQLARG 88 Query: 62 DTELGPLAGVPIAVKDNICTSGMETTCASRILKGYVSPFDATVVERLRAAGAMIIGKANM 121 ++ LGPL G P A KD + +GM TT S I G VS DA V ER+RA+GA+ IG++N Sbjct: 89 ES-LGPLHGFPQAPKDIMPAAGMVTTRGSPIFAGQVSATDAVVFERMRASGALFIGRSNS 147 Query: 122 DEFAMGSSGESSAFGVTRNPWDLERVPGGSSSGSAAAVAAGEAPLALGTDTGGSIRQPAA 181 EF +G + +G TRN + GGSS G+A AVA P+A G+D GS+R PAA Sbjct: 148 PEFGLGGHTYNPVYGTTRNAHNPAVSAGGSSGGAAVAVALHMLPVADGSDMMGSLRTPAA 207 Query: 182 FTGIVGLKPTYGYVSRYGV-VAFASSLDQVGPMGRDVEDVARLFEVIAGPDRRDATNAGR 240 F + GL+ ++G V F GPM R++ D+A L V AG D R Sbjct: 208 FNNVYGLRTSFGLVPHGPTEEVFFQQFSVSGPMARNIPDLALLQSVQAGFDARLPLTRRH 267 Query: 241 TPPALKFGGEP---SLSGVRLGVPKELLGP-GIDPGVKARVEEAIAQLEELGATVEEC-- 294 AL G+P G R+G +L G +PGV A E+A+ LG TVE Sbjct: 268 EDVALL--GQPLERDWRGARIGWLGDLGGHLPAEPGVLATCEQALEHFRTLGCTVESVVP 325 Query: 295 --SLPSTEYALSAYYVIAVAEASSNLARFDGVRYGYRAAQAGGLHEMYSKTRGEGFGTEV 352 +L A +VA A++ L YR AQ L E Sbjct: 326 TFNLEQLWNAWIDLRSFSVAGANAAL---------YRDAQTRAL-----------LKPEA 365 Query: 353 KRRIMLGTYVLSAGHYDAYYRRAQQVRTLVVRDFERAFERYDALVTPTT---PFTA---W 406 I G + + YD A +VR+ + FE++D LV P PF A W Sbjct: 366 VWEIERGMRLTALQVYD-----AARVRSAWYQVLRGLFEQFDFLVLPAAQVFPFDAGLDW 420 Query: 407 --KIGEKVDDPVSMYLGDICTIPVNLAGLPAVSVPCGF-VDGLPVGMQLIGKPFADTQIL 463 ++G + D ++ + +P +AGLPA++ P GF GLP G+Q++G D +L Sbjct: 421 PHEVGGRTMDTYHRWMEAV--VPATMAGLPALAAPAGFGPGGLPAGLQILGPAQQDAAVL 478 Query: 464 QIAWAYQKVT 473 QI AY + + Sbjct: 479 QIGHAYDQAS 488 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: 607 Number of extensions: 43 Number of successful extensions: 5 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: 499 Length adjustment: 34 Effective length of query: 454 Effective length of database: 465 Effective search space: 211110 Effective search space used: 211110 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