Align dicarboxylate TRAP transporter (succinate, fumarate, L-malate, and alpha-ketoglutarate), large permease component (characterized)
to candidate Ac3H11_3520 TRAP-type C4-dicarboxylate transport system, large permease component
Query= reanno::PV4:5208943 (465 letters) >FitnessBrowser__acidovorax_3H11:Ac3H11_3520 Length = 426 Score = 237 bits (605), Expect = 5e-67 Identities = 144/456 (31%), Positives = 245/456 (53%), Gaps = 41/456 (8%) Query: 1 MTIATLFISLFLCMLLGMPIAIAL---GFSSMLTILLFSDDSLASVALKLYESTSEHYTL 57 MT+ SL M +G+PIA AL G + M + LF LA + + ++ + L Sbjct: 1 MTVFIFLGSLLAAMAIGVPIAYALLVSGAALMWHLDLFDAQILAQNVI----NGADSFPL 56 Query: 58 LAIPFFILSSAFLSTGGVARRIIDFAMDSVGHIRGGLAMASVMACMLFAAVSGSSPATVA 117 LA+PFF+L+ ++ GG+++RI+ A+ VGH RGGL +++A + AA+SGS+ A A Sbjct: 57 LAVPFFMLAGEIMNVGGLSQRIVKLALTLVGHKRGGLGFVAILAACMLAALSGSAVADTA 116 Query: 118 AIGSIVIVGMVRAGYPEKFAAGVITTSGTLGILIPPSIVMLVYAAATEVSAARMFMAGLI 177 A+ ++++ MV+AG+ + A G+I ++G + +IPPSI +V+ A VS +++F+AG++ Sbjct: 117 ALAALLLPMMVKAGHDKARAGGLIASAGIIAPVIPPSIGFVVFGVAANVSISKLFLAGIV 176 Query: 178 PGLMMGLLLMLAIYIVARIKKLPSRPFPGFRPLAISSAKAMGGLALIVIVLGSIYGGIAS 237 PGL+MG+ + + Y V++ + + P + ++ L L VIV+ + G+ + Sbjct: 177 PGLLMGVAIAVTWYWVSQRENVTPPPKASTAEKLQALKESTWALFLPVIVIVGLKMGVFT 236 Query: 238 PTEAAAVACVYAYFIAVFGYRDIGPLKNVSWRDSGEPLIRAILRNLGFMVLAVFKTPADK 297 PTEAAAVA VYA +A YR++ WR + I A Sbjct: 237 PTEAAAVAAVYALLVATLVYREL------HWRQLTDVFISA------------------- 271 Query: 298 EIRHVVRDGAKVSIMLLFIIANAMLFAHVLTTERIPHLIAETIVGMGLPVWGFLIIVNLL 357 AK + +++F++A AM+ A ++T IP + + + LI + +L Sbjct: 272 ---------AKTTAVIMFLVAAAMVSAWLITVADIPRQLVSLLKPLMEHPTLLLIAIMVL 322 Query: 358 LLAAGNFMEPSAILLIMAPILFPIATQLGIDPIHLGIIMVVNMEIGMLTPPVGLNLFVTA 417 ++A G M+ + +LI+ P+L P+ GIDP++ G++ ++N IG++TPPVG L V A Sbjct: 323 VMAVGTAMDMTPTILILTPVLMPVVKAAGIDPVYFGVLFIMNNAIGLITPPVGTVLNVVA 382 Query: 418 GITGRSMGWVIHSCIPWLALLLFFLALITYIPQISL 453 G+ M V IP++A + L+ P I L Sbjct: 383 GVGKMRMDEVTRGVIPFMAAQFAMMFLMVLFPSIVL 418 Lambda K H 0.330 0.144 0.424 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: 520 Number of extensions: 32 Number of successful extensions: 5 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: 465 Length of database: 426 Length adjustment: 32 Effective length of query: 433 Effective length of database: 394 Effective search space: 170602 Effective search space used: 170602 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: 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