Align TRAP-type large permease component (characterized, see rationale)
to candidate 5208943 Shew_1444 TRAP dicarboxylate transporter, DctM subunit (RefSeq)
Query= uniprot:Q930R2 (425 letters) >lcl|FitnessBrowser__PV4:5208943 Shew_1444 TRAP dicarboxylate transporter, DctM subunit (RefSeq) Length = 465 Score = 262 bits (670), Expect = 1e-74 Identities = 146/451 (32%), Positives = 249/451 (55%), Gaps = 35/451 (7%) Query: 1 MTLVVFIVSLLGAMAIGVPVAFSLMFCGVVLMWYMGMFNTQIIAQNMIAG-ADTFTLLAI 59 MT+ +SL M +G+P+A +L F ++ + + +A + ++ +TLLAI Sbjct: 1 MTIATLFISLFLCMLLGMPIAIALGFSSMLTILLFSDDSLASVALKLYESTSEHYTLLAI 60 Query: 60 PFFILAGELMNAGGLSRRIIDFAIACVGHIRGGLGIVAIMAAVIMASISGSAAADTAALA 119 PFFIL+ ++ GG++RRIIDFA+ VGHIRGGL + ++MA ++ A++SGS+ A AA+ Sbjct: 61 PFFILSSAFLSTGGVARRIIDFAMDSVGHIRGGLAMASVMACMLFAAVSGSSPATVAAIG 120 Query: 120 AILIPMMAKAGYNVPRSAGLIAAGGVIAPVIPPSMAFIVFGVAANVSITQLFMAGIVPGL 179 +I+I M +AGY +AG+I G + +IPPS+ +V+ A VS ++FMAG++PGL Sbjct: 121 SIVIVGMVRAGYPEKFAAGVITTSGTLGILIPPSIVMLVYAAATEVSAARMFMAGLIPGL 180 Query: 180 IMGIALVATWLLVVRKDDIQPLPRTPMKERVGATGRALWALGMPVIILGGIKAGVVTPTE 239 +MG+ L+ +V R + P + ++ +A+ L + VI+LG I G+ +PTE Sbjct: 181 MMGLLLMLAIYIVARIKKLPSRPFPGFRPLAISSAKAMGGLALIVIVLGSIYGGIASPTE 240 Query: 240 AAVVAAVYALFVGMVIYRELKP----------------------------------RDLP 265 AA VA VYA F+ + YR++ P +++ Sbjct: 241 AAAVACVYAYFIAVFGYRDIGPLKNVSWRDSGEPLIRAILRNLGFMVLAVFKTPADKEIR 300 Query: 266 GVILQAAKTTAVIMFLVCAALVSSWLITAANIPSEITGFISPLIDRPTLLMFVIMLVVLV 325 V+ AK + +++F++ A++ + ++T IP I I + + ++ L++L Sbjct: 301 HVVRDGAKVSIMLLFIIANAMLFAHVLTTERIPHLIAETIVGMGLPVWGFLIIVNLLLLA 360 Query: 326 VGTALDLTPTILILTPVLMPIIKQAGIDPVYFGVLFIMNTCIGLLTPPVGVVLNVVSGVG 385 G ++ + +LI+ P+L PI Q GIDP++ G++ ++N IG+LTPPVG+ L V +G+ Sbjct: 361 AGNFMEPSAILLIMAPILFPIATQLGIDPIHLGIIMVVNMEIGMLTPPVGLNLFVTAGIT 420 Query: 386 RVPLGKVIVGVTPFLVAQILVLFLLVLFPDI 416 +G VI P+L + L L+ P I Sbjct: 421 GRSMGWVIHSCIPWLALLLFFLALITYIPQI 451 Lambda K H 0.331 0.145 0.430 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: 461 Number of extensions: 20 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: 425 Length of database: 465 Length adjustment: 32 Effective length of query: 393 Effective length of database: 433 Effective search space: 170169 Effective search space used: 170169 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.2 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