Align LL-diaminopimelate aminotransferase; DAP-AT; DAP-aminotransferase; LL-DAP-aminotransferase; EC 2.6.1.83 (uncharacterized)
to candidate GFF1219 PS417_06195 succinyldiaminopimelate aminotransferase
Query= curated2:B1I544 (392 letters) >lcl|FitnessBrowser__WCS417:GFF1219 PS417_06195 succinyldiaminopimelate aminotransferase Length = 399 Score = 177 bits (450), Expect = 4e-49 Identities = 131/408 (32%), Positives = 202/408 (49%), Gaps = 42/408 (10%) Query: 9 IRNLPPYLFARIEQLIA------DKKAQGVDVISLGIGDPDVPTPDHIIEAAEKELKIPA 62 + L PY F ++ L+ DK+ I+L IG+P +P + EA L A Sbjct: 5 LNQLQPYPFEKLRALLGSVTPNPDKRP-----IALSIGEPKHKSPTFVAEALSNNLDQMA 59 Query: 63 NHQYPSSAGMPAYRRAVADWYARRFGVE---LDPQREVVSLIGSKEGIAHLPWCFVDPGD 119 YP++ G+PA R A+ W RRF V LDP R ++ + G++E + V+ GD Sbjct: 60 --VYPTTLGIPALREAIGAWCERRFNVPKGWLDPARNILPVNGTREALFAFTQTVVNRGD 117 Query: 120 VVLV--PDPGYPVYAGGTILAGGIPHPVPLTAGNGFLPDLAAIPAETARRAKVMFINYPN 177 LV P+P Y +Y G LAG PH +P NGF PD A+ + +R +++F+ P Sbjct: 118 DALVVSPNPFYQIYEGAAFLAGAKPHYLPCLDANGFNPDFEAVTPDIWKRCQILFLCSPG 177 Query: 178 NPTGAVASKEFFARVVDFAREYGILVCHDAAYSEIAFDGYRPPSFLEVAGAREVG----- 232 NPTGA+ + +++ A EY ++ D YSE+ FD PP L ++ E+G Sbjct: 178 NPTGALIPVDTLKKLIALADEYDFVIAADECYSELYFDEQSPPPGL-LSACVELGRQDFK 236 Query: 233 --IEFHSVSKTYNMTGWRAGWAAGNAGAVEALGRLKSNLDSGVFQVVQYAAIAALNGPQD 290 + FHS+SK N+ G R+G+ AG+A ++A ++ + Q A+IAA QD Sbjct: 237 RCVVFHSLSKRSNLPGLRSGFVAGDADILKAFLLYRTYHGCAMPVQTQLASIAAW---QD 293 Query: 291 GVQSLC--EMYRERRDLVVDTLNDLGWRLTRPRATFYIWAPVPAGHDASSFAEMVLEKAG 348 L ++YRE+ D V+ L + + P FY+W P G DA ++ +E+ Sbjct: 294 EAHVLANRDLYREKFDAVLAILKPV-LDVESPDGGFYLW-PNVNGDDAGFCRDLFVEE-H 350 Query: 349 VVITPGT-------GYGTYGEGYFRISLTLPTPRLVEAMERLRGCLGR 389 V + PG+ G+ G G R++L P VEA ER+R + R Sbjct: 351 VTVVPGSYLSREVDGFNP-GAGRVRLALVAPLAECVEAAERIRDFIQR 397 Lambda K H 0.321 0.139 0.430 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: 351 Number of extensions: 16 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: 392 Length of database: 399 Length adjustment: 31 Effective length of query: 361 Effective length of database: 368 Effective search space: 132848 Effective search space used: 132848 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: 50 (23.9 bits)
This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 2021.
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code, or see changes to Amino acid biosynthesis since the publication.
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