Align FcbT3, component of Tripartite 4-chlorobenzoate symporter (also binds and may transport 4-bromo-, 4-iodo-, and 4-fluorobenzoate and with a lower affinity, 3-chlorobenzoate, 2-chlorobenzoate, 4-hydroxybenzoate, 3-hydroxybenzoate, and benzoate) (characterized)
to candidate 8501197 DvMF_1931 TRAP dicarboxylate transporter, DctM subunit (RefSeq)
Query= TCDB::Q9RBQ9 (439 letters) >FitnessBrowser__Miya:8501197 Length = 640 Score = 203 bits (517), Expect = 1e-56 Identities = 125/432 (28%), Positives = 232/432 (53%), Gaps = 17/432 (3%) Query: 6 AAWLLLGGTTVLLFLGLPVAYSFFAINVVGAWLFLGGDSALGQLVRNGLVAVASFSLTPI 65 A WLL G + L +G+P+A+S + A + G L L + V++ SF + I Sbjct: 220 AVWLLFGYFVLFLLVGVPIAFSLGLATI--ATVLGAGTLPLEYLAQIAFVSIDSFPILAI 277 Query: 66 PLFILMGELLFHTGLAQRAIDGIDKVIPRLPGRLAVIAVVAGTFFSAISGSTIATTAMLG 125 P FI G + GL++R + D+++ LPG +A+ +V FF+AISGS AT A +G Sbjct: 278 PFFIAAGVFMGAGGLSRRLLALGDELVGALPGGMALATIVTCMFFAAISGSGPATVAAIG 337 Query: 126 SLMLPMMLARGYEPKLGMGPIIAIGGVDMLIPPSALAVLLGSLAGISISKLLIGGVLPGL 185 S+ +P M+ RGY+ + + G + ++IPPS V+ G A S+ KL + G++PG+ Sbjct: 338 SITIPAMVERGYDKFFAAAVVASAGCIGVMIPPSNPFVVYGVAAQASVGKLFLAGIVPGV 397 Query: 186 L--LAISFVAYIVASAK-LRPESAPREELVVLRG-WERWRELVVYVLPLSLIFVAIVAVI 241 L LA+ VAY ++ K R E+ R+ V++ WE L+V V+ L I+ Sbjct: 398 LCGLALMAVAYYISLKKGWRGEARHRDFRSVMQAMWEAKWALLVPVIVLGGIY------- 450 Query: 242 SGGVATPTEAAAIGCAATLAITL-MYRALRWQSLVQALQGTVAISGMILFIIVAATTFSQ 300 GG+ TPTEAAA+ + + L +YR + W+ + + + S +I+ ++ AT F Sbjct: 451 -GGIMTPTEAAAVSALYGMIVGLFIYREITWRRMWDCMVESAQTSSVIIVLMAMATLFGN 509 Query: 301 VLSFSGATNGIVDLVQSSGLPPAGVVAIMLAILIFLGLFVDQVSMMLLTLPFYMPIVKSL 360 +++ + I ++ ++ ++ L+++G F++ ++ +++ P +P+V + Sbjct: 510 IMTIEQVPDHIAAMILGVTSNKIAILLLINVFLLWVGTFMEALAAIVIITPILLPLVTQV 569 Query: 361 GIDQIWFGVMYLICMQLGLLMPPHGMLLYTMKGVAPKHITMGQVFASAMPYVGLSFTMLI 420 G+D I FGV+ ++ + +G + PP G+ L+ ++ +++G V +A P++ + +L+ Sbjct: 570 GVDPIHFGVIMVVNLAIGFITPPVGVNLFVASSIS--KVSIGDVVRAAWPFLLVMIALLM 627 Query: 421 LIFFWPGIATWL 432 I + P I+ L Sbjct: 628 AITYIPAISLCL 639 Lambda K H 0.329 0.143 0.433 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: 668 Number of extensions: 40 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: 439 Length of database: 640 Length adjustment: 35 Effective length of query: 404 Effective length of database: 605 Effective search space: 244420 Effective search space used: 244420 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 (21.8 bits) S2: 52 (24.6 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