Align L-leucine transaminase; L-isoleucine transaminase (EC 2.6.1.42) (characterized)
to candidate 8502295 DvMF_3003 putative transcriptional regulator, GntR family (RefSeq)
Query= reanno::acidovorax_3H11:Ac3H11_1358 (401 letters) >FitnessBrowser__Miya:8502295 Length = 394 Score = 330 bits (845), Expect = 6e-95 Identities = 190/391 (48%), Positives = 244/391 (62%), Gaps = 9/391 (2%) Query: 14 LARRAERMNPSVIREILKVTEKPGIISLAGGLPSPKTFPVSAFAAASAAVLANDGPAALQ 73 LA+R E + S IREILKVT +P IIS AGGLP P +FPV A A+A+A+VL GP ALQ Sbjct: 3 LAQRMESVPRSYIREILKVTAQPDIISFAGGLPHPASFPVDAVASAAASVLEEAGPEALQ 62 Query: 74 YAASEGYAPLRQAIADFLPW---DVDADQILITTGSQQALDLIAKVLIDENSRVLVETPT 130 Y +EG+ PLRQ IAD +V D ILITTGSQQALDL+AK ID RV++E P Sbjct: 63 YTTTEGFPPLRQWIADRYKRQGINVSPDDILITTGSQQALDLVAKACIDRGGRVVMERPG 122 Query: 131 YLGALQAFTPMEPSVVAVASDDEGVLIDDLKAKVGTGADKARFLYVLPNFQNPTGRTMTE 190 YLGA+Q F+ P V V GV D L+ K TGA + Y +P+FQNP+G T E Sbjct: 123 YLGAIQCFSVFGPDFVTVPLTPRGVDTDALR-KAATGA---QVFYAVPSFQNPSGITYDE 178 Query: 191 ARRAALVKAAAELNLPLVEDNPYGDLWFDNPPPAPLTARNPEGCIYMGSFSKVLAPGLRL 250 R + + AE +VEDNPYG+L F P+ A + +GSFSKV++PGLRL Sbjct: 179 QTRREVAEIMAETGCLMVEDNPYGELRFMGQHLPPVRAYMQAPSVLLGSFSKVVSPGLRL 238 Query: 251 GFVVAPKAVYPKLLQAKQAADLHTPGYNQRLVAEVMKGNFLDRHVPTIRALYKQQCEAML 310 G+V AP+ V ++ AKQA+DLHTPG+ QR++ + N +D+H+ +IRA Y Q +AM+ Sbjct: 239 GWVCAPQEVLNPMITAKQASDLHTPGFTQRILHRYLMDNDVDKHIASIRARYGAQRDAMV 298 Query: 311 AALTQEMAGLGVEWNRPDGGMFLWVRLPEGMSAIELLPQAVERNVAFVPGAAFYADNADP 370 A+ + V P+GGMFLW LPEG+SA L +A+ER VAFVPG FY D D Sbjct: 299 QAIRRHFPE-DVACTEPEGGMFLWCTLPEGISAEALFHKAIERKVAFVPGRPFYVDETDD 357 Query: 371 RTLRLSFVTSTVEQIATGIAALAAAIRSHKG 401 T RL+F S+ E I GIA L +R + G Sbjct: 358 -TFRLNFSNSSPELIEEGIARLGQCLREYLG 387 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: 463 Number of extensions: 21 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: 394 Length adjustment: 31 Effective length of query: 370 Effective length of database: 363 Effective search space: 134310 Effective search space used: 134310 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