Align L-leucine transaminase; L-isoleucine transaminase (EC 2.6.1.42) (characterized)
to candidate RR42_RS14595 RR42_RS14595 2-aminoadipate aminotransferase
Query= reanno::acidovorax_3H11:Ac3H11_1358 (401 letters) >FitnessBrowser__Cup4G11:RR42_RS14595 Length = 395 Score = 426 bits (1094), Expect = e-124 Identities = 223/386 (57%), Positives = 277/386 (71%), Gaps = 6/386 (1%) Query: 12 WTLARRAERMNPSVIREILKVTEKPGIISLAGGLPSPKTFPVSAFAAASAAVLANDGPAA 71 W ++RRA+++ S IREILKVTE+P +IS AGGLPSP TFPV+A A A + A++ AA Sbjct: 3 WAISRRAQQLTSSAIREILKVTERPEVISFAGGLPSPATFPVAAMEQAVARIFADNPQAA 62 Query: 72 LQYAASEGYAPLRQAIADFLPWDVDADQILITTGSQQALDLIAKVLIDENSRVLVETPTY 131 LQYAA+EGY PLR+ IA VD +++LITTGSQQALDLIAKV+ID S VLVETP+Y Sbjct: 63 LQYAATEGYMPLREFIAK--RHAVDVERVLITTGSQQALDLIAKVMIDPGSPVLVETPSY 120 Query: 132 LGALQAFTPMEPSVVAVASDDEGVLIDDLKAKVGTGADKARFLYVLPNFQNPTGRTMTEA 191 LGALQAF+ EP V+V DD+ +L + L ++ GA RFLY LPNFQNPTGR M Sbjct: 121 LGALQAFSLFEPEFVSVPGDDKSLLPESLTPELTAGA---RFLYALPNFQNPTGRRMPLE 177 Query: 192 RRAALVKAAAELNLPLVEDNPYGDLWFDNPPPAPLTARNPEGCIYMGSFSKVLAPGLRLG 251 RR ALV A EL L LVED+PYG+L + L + NP+G IYMGSFSK+LAPGLRLG Sbjct: 178 RRQALVARARELGLLLVEDDPYGELSYSGDQLPSLLSMNPDGVIYMGSFSKILAPGLRLG 237 Query: 252 FVVAPKAVYPKLLQAKQAADLHTPGYNQRLVAEVMKGNFLDRHVPTIRALYKQQCEAMLA 311 FV+AP ++ KL QAKQA+DLHTP + QRL EV++ LD H+PTIR LY QC+AML Sbjct: 238 FVIAPPELHFKLCQAKQASDLHTPSFTQRLAYEVVRDGLLDSHIPTIRTLYAAQCQAMLD 297 Query: 312 ALTQEMAGLGVEWNRPDGGMFLWVRLPEGMSAIELLPQAVERNVAFVPGAAFYADNADPR 371 +L + M GV WN P+GGMF+W+ LPEG+ ++E+L +AV RNVA+VPGA FYA N Sbjct: 298 SLARHMPE-GVTWNAPEGGMFIWMELPEGLDSMEILQEAVNRNVAYVPGAPFYASNPRRN 356 Query: 372 TLRLSFVTSTVEQIATGIAALAAAIR 397 LRL+FVT E+I G+A L R Sbjct: 357 ALRLAFVTVAPERIEQGVAILGTLFR 382 Lambda K H 0.318 0.134 0.392 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: 540 Number of extensions: 17 Number of successful extensions: 4 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: 401 Length of database: 395 Length adjustment: 31 Effective length of query: 370 Effective length of database: 364 Effective search space: 134680 Effective search space used: 134680 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: 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