Align Glutamyl-tRNA(Gln) amidotransferase subunit A; Glu-ADT subunit A; EC 6.3.5.7 (uncharacterized)
to candidate WP_012851712.1 TCUR_RS06625 amidase
Query= curated2:A7NKM0 (490 letters) >NCBI__GCF_000024385.1:WP_012851712.1 Length = 476 Score = 206 bits (525), Expect = 1e-57 Identities = 175/506 (34%), Positives = 231/506 (45%), Gaps = 55/506 (10%) Query: 1 MTPLYQLTVAQAREMLARGEISSLELTDALLTRIAAVEPKVRAFLVVDAAGARAQARAAD 60 MT L+ LT + + GE+S LELTD L RI + +V AF+ V A AR QA A Sbjct: 1 MTRLHDLTALEQAAAIRSGELSPLELTDHYLDRIERLNERVGAFVTVTADRARRQAGEA- 59 Query: 61 ARRAAGDAS-----PLLGIPMGIKDVISTQGLRTTCASKMLENYTPVYDATAVARLKAAG 115 ARR A PL G+ + +KD+ S +G+R T S + D V RL+ AG Sbjct: 60 ARRVQECAERRLLPPLHGVAVPVKDLSSVRGVRLTRGSAACADLVGSVDDAVVTRLRRAG 119 Query: 116 AVILGKLNCDEFAMGSSTENSAFQQTRNPWNLERVPGGSSGGSAAAVAAGEAPAALGTDT 175 V+LGK EF + TE++ R PW+ R GGSSGG+AAAVAAG AP A G+D Sbjct: 120 TVLLGKTATPEFGLPCYTESAVAPPARTPWDPARSAGGSSGGAAAAVAAGLAPVAHGSDG 179 Query: 176 GGSIRQPAALCGITGLKPTYGRVSRYGLVAFASSLDQIGPMARTVRDCAIVLRVIAGADP 235 GGSIR PA+ CG+ GLKPT GR+SR L L GP+ARTVRD A +L V+ G +P Sbjct: 180 GGSIRIPASACGLVGLKPTRGRISRGPLAPDLFGLVTDGPIARTVRDAAALLDVMHGPEP 239 Query: 236 FDATCTDYPAP---------DYEAALTGDIRGLRIGVPREYFVAGMQPDVEAAVRTAIEV 286 D Y AP DY G +R R VP + PD A + Sbjct: 240 GDL----YTAPPLPPGRRFLDYADIDPGRLRIARTLVP-PMLETTVHPDCVTAYEKTSAL 294 Query: 287 LREQGAEVCEISLPHTPYALPVYYLIAPAEASANLARFDGVRYGLRVPGESYFDELERTR 346 L E G V E+ P P + L+ +A L D R L P + R R Sbjct: 295 LEELGHHVEELPPVFGPQLAPDFALL--WSVTAALTPVDPAREHLLQPLTRWL----RDR 348 Query: 347 G-AGFGPEVRRRIMLGTYALSAGYYDAYYKRAQQVRTLIRRDYQQAFEQVDVIAAPTTPT 405 G A GPE+ A+ + VR + ++ D I PT Sbjct: 349 GNAVGGPEL---------------LAAHARLQNAVRAAL-----PVLDRFDAILTPTLAA 388 Query: 406 VAFKIGAHTDDPLAMYLE------DVCTLPLNLAGLPGLVVPCGF-AEGLPIGLQLIGRA 458 +G D A+ E C + NL+G P + +P + A GLPIG+ L GR Sbjct: 389 PPAPVGYFHDAEPAVNFERQNRFTPFCAV-YNLSGQPAVTLPLHWNAAGLPIGVMLAGRL 447 Query: 459 FDEESLLRVGDAYQRVTDWHTRMPEV 484 E +L+ + + W R P + Sbjct: 448 GGEGTLISLAAQLEAARPWRRRRPPI 473 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: 594 Number of extensions: 27 Number of successful extensions: 3 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: 476 Length adjustment: 34 Effective length of query: 456 Effective length of database: 442 Effective search space: 201552 Effective search space used: 201552 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