Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate GFF3953 HP15_3893 amidase family protein
Query= curated2:B3DWT4 (494 letters) >FitnessBrowser__Marino:GFF3953 Length = 499 Score = 159 bits (403), Expect = 2e-43 Identities = 146/478 (30%), Positives = 218/478 (45%), Gaps = 22/478 (4%) Query: 11 LRRLLVQKEVSPLEVVENLLCRIAEVDPKIFAYIYLNHERALEASKKADISLPLGGVPVA 70 L L+ + EV+ EV E + R V+ K+ A Y A ++ GVP+ Sbjct: 18 LADLIRRGEVTSGEVCEAAVERATRVNGKLNAICYPQFSEA--PAQPFPEQGVFAGVPLL 75 Query: 71 IKDNINVLGE-PCRCASRILEGYLAPYDSTVIEKLKKAGAILLGRTNMDEFAMGSSTENS 129 +KD + PC SR + +AP DS + + + G + LGRT EF + + TE+ Sbjct: 76 LKDLAQEQADHPCTYGSRGMTKNIAPRDSEFVRRARNGGLVFLGRTATPEFGLKAVTESE 135 Query: 130 SVGITRNPWNTERVPGGSSGGSAAAVAAHEAFCALGSDTGGSIRQPAAFCGCVGLKPTYG 189 G TRNPWNT+ PGGSSGGS AA AA A +D GGSIR PAA+ G GLKP+ G Sbjct: 136 LWGPTRNPWNTQLTPGGSSGGSGAAAAAGIVPMAGANDGGGSIRIPAAYNGLFGLKPSRG 195 Query: 190 RVSR---YGLTAFASSLDQIGPITKTVEDAALLLEVISGFDPFDNTSEKLPVPRFSELLE 246 R+S G +S D + +++TV D+A +L+V+SG P D P ++EL++ Sbjct: 196 RISSGPFMGEAWTGASTDHV--VSRTVRDSAAMLDVLSGPAPGDPFVIPQPPAPYAELVQ 253 Query: 247 NRPLKDFVLGIPKEYFIEGIDGEVRQALSQVIGHYEKLGVKIEEVSLPHTPYAVATYYI- 305 P + + + E A+ + E LG ++E + A+A Y+ Sbjct: 254 RSPGSLKIGVFTSSPYNTEVAPECVAAVEETARVLESLGHRVEYAAPEFDGMALARCYLG 313 Query: 306 LATAEASANLARFDGIRYGKRAKNY---NDLIDYYGKTRDEGFGSEVKRRILLGTYVLSS 362 L E SA +A+ ++G ++ LI G T V+RR + + Sbjct: 314 LYFGEVSALMAKAKE-QFGAADSDFELDTRLIGMLGNTMP--LSDYVRRRQQWNEFARAL 370 Query: 363 GY----YDAYYLRAL-KVKEKIKQDFSLAFQKCQA--LLTPTSPFCAFRIGEKTSDPLQM 415 G YD Y ++ I + + A K A +L + R G+ L+ Sbjct: 371 GVFFGRYDLYLSPTTGQLPAAIGELETPAHLKFAARLMLKLNAGKLVHRTGQVDQMALES 430 Query: 416 YLADIFTIAVNLAGICALSIPCGRSTEGLPIGFQLIGPAWKEETILALGYIYQKTTGW 473 FT NL G A+S+P + EGLP+G QL GP E T+L L ++ W Sbjct: 431 LARTPFTQLANLTGTPAMSVPMHWTAEGLPVGVQLGGPHGAEATLLQLAGQLEEANPW 488 Lambda K H 0.319 0.139 0.410 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: 515 Number of extensions: 21 Number of successful extensions: 3 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 494 Length of database: 499 Length adjustment: 34 Effective length of query: 460 Effective length of database: 465 Effective search space: 213900 Effective search space used: 213900 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 (21.7 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