Align C4-dicarboxylate TRAP transporter large permease protein DctM (characterized)
to candidate Ac3H11_4175 TRAP-type C4-dicarboxylate transport system, large permease component
Query= SwissProt::Q9HU16 (427 letters) >FitnessBrowser__acidovorax_3H11:Ac3H11_4175 Length = 421 Score = 304 bits (779), Expect = 3e-87 Identities = 167/420 (39%), Positives = 262/420 (62%), Gaps = 4/420 (0%) Query: 3 ILFLFLLLFLLMFIGVPIAVSLGLSGALTIL-LFSPDSVRSLAIKLFETSEHYTLLAIPF 61 I LF L L+ +GVPI V L LSGA+ IL + SP +S +++F + Y L+AIP Sbjct: 2 ITTLFFLAALM--VGVPIGVCLCLSGAVYILSIGSPVLFQSFPMQMFGGVDSYGLIAIPL 59 Query: 62 FLLSGAFMTTGGVARRLIDFANACVGHIRGGLAIAAVLACMLFAALSGSSPATVAAVGSI 121 F+L G M +GG+ RRL+D + A +G ++GGLA +LA ML +++ GS+ A VA + + Sbjct: 60 FILIGEIMNSGGITRRLVDLSMAFIGSVKGGLAYVNILANMLVSSIIGSATAQVAIMSQV 119 Query: 122 AIAGMVRSGYPQAFGAGIVCNAGTLGILIPPSIVMVVYAAATETSVGKLFIAGVVPGLLL 181 + M + GY + F AG+ G LG +IPPS++ VVY+ + +VG + IAG++PG+LL Sbjct: 120 MVPEMEKQGYDKTFAAGLTVYGGMLGPIIPPSVMFVVYSVLAQVAVGDMLIAGILPGVLL 179 Query: 182 GLILMVVIYIVARVKKLPAMPRVSLREWLASARKALWGLLLMVIILGGIYSGAFTPTEAA 241 L+ VVI ++ V P + +L + + +A LL+ +II+G I SG PTE+A Sbjct: 180 TLLFFVVIALMGFVYNYPRSEKRTLAQRARTVVQASPTLLIPIIIVGSILSGLANPTESA 239 Query: 242 AVAAVYSAFVALFVYRDMRLSECPKVLLESGKLTIMLMFIIANAMLFAHVLTTEQIPQSI 301 AV A+ SA V +V ++ R S P +LL S + +++F++A A +F+ +L ++PQ + Sbjct: 240 AVGALASALVGRYVTKEFRFSAMPAILLRSAIYSAIVLFLVAAAAVFSWLLIYGKVPQMV 299 Query: 302 ASWVTELGLSPWMFLLVVNIVLLIAGNFMEPSAIILILAPIFFPIAMEL-GIDPIHLGII 360 A+WV + P FLL+ N++LL+ G ++ +++ API PIA E+ IDP H G++ Sbjct: 300 AAWVQTVAHDPVTFLLLTNVILLVIGTVIDGIPGLIMTAPILLPIATEVYHIDPRHFGVV 359 Query: 361 MVVNMEIGLITPPVGLNLFVTSAVTGMPLGATIRAALPWLMILLVFLIIVTYIPAVSLAL 420 +VVN+ +GL+TPPVGL+ FV SAVTG G LP+ +I V L++++ P++SL L Sbjct: 360 IVVNLVLGLMTPPVGLSFFVASAVTGAKPGKMFIVTLPFFIISCVALVMLSLFPSLSLGL 419 Lambda K H 0.330 0.144 0.425 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: 448 Number of extensions: 23 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: 427 Length of database: 421 Length adjustment: 32 Effective length of query: 395 Effective length of database: 389 Effective search space: 153655 Effective search space used: 153655 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.1 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.9 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 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.
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