Align TRAP transporter, subunit DctM (characterized, see rationale)
to candidate WP_010437189.1 G7G_RS0100330 TRAP transporter large permease
Query= uniprot:I7DRS6 (467 letters) >NCBI__GCF_000192475.1:WP_010437189.1 Length = 472 Score = 739 bits (1908), Expect = 0.0 Identities = 383/473 (80%), Positives = 421/473 (89%), Gaps = 7/473 (1%) Query: 1 MDVVLLFSMVIGLLLIGVPIAVALGLSSTLFLLIYSDSSLASVAGTLFEAFEGHFTLLAI 60 M+ VLLF+MVIG L+IGVPIA++LG+SS LFLL +SDSSLASVA TLF AFEGHFTLLAI Sbjct: 1 METVLLFAMVIGFLMIGVPIAISLGMSSILFLLWFSDSSLASVAQTLFAAFEGHFTLLAI 60 Query: 61 PFFILASSFMTTGGVARRIIRFSIACVGHLPGGLAIAGVFACMLFAALSGSSPATVVAIG 120 PFFILASSFMTTGGVARRIIRFSIACVGH PGGLAIAGVFACMLFAALSGSSPATVVAIG Sbjct: 61 PFFILASSFMTTGGVARRIIRFSIACVGHFPGGLAIAGVFACMLFAALSGSSPATVVAIG 120 Query: 121 SIVIAGMRQVGYSKEFAAGVICNAGTLGILIPPSIVMVVYAAAVEVSVGRMFLAGVIPGL 180 +IVI GMRQVGYSKEFAAGVICNAGTLGILIPPSIVMVVYAA+VEVSVGRMFLAGVIPGL Sbjct: 121 TIVITGMRQVGYSKEFAAGVICNAGTLGILIPPSIVMVVYAASVEVSVGRMFLAGVIPGL 180 Query: 181 MAGLMLMVTIYVMAKVKNLPKGEWLGWGEVAASAANASVGLLLIGIILGGIYGGIFTPTE 240 +AGLMLMVTI+V+AK+KNLPKGEW GWGEV S A GL LI IILGGIYGGIFTPTE Sbjct: 181 LAGLMLMVTIFVIAKIKNLPKGEWKGWGEVFQSGREAGWGLFLIVIILGGIYGGIFTPTE 240 Query: 241 AAAVASVYAFFVATFVYRDMGPLKSAPKPKDMGQFLTMLPKMLGQTVVY------FIPSF 294 AAAVA+VYAFF+ATFVY+DMGPL +APK + + + G + + + Sbjct: 241 AAAVAAVYAFFIATFVYKDMGPL-AAPKTRSLSAAAVIEDAPAGPRIPLRSKPWAIVTAI 299 Query: 295 FHADTRHALFEAGKLTVTLLFVIANALILKHVLTDEQVPQQIATAMLSAGFGPVMFLIVV 354 H DT+ LF+AGKLT+TLLFVIANALILKHVLTDEQ+PQQ+A AMLSAGFGPVMFL+VV Sbjct: 300 VHPDTQKTLFDAGKLTITLLFVIANALILKHVLTDEQIPQQVANAMLSAGFGPVMFLVVV 359 Query: 355 NVILLIGGQFMEPSGLLVIVAPLVFPIAIELGIDPIHLGIIMVVNMEIGMITPPVGLNLF 414 N+ILLIGGQFMEPSGLLVIVAPLVFPIAIELGIDPIHLGIIMVVNMEIGMITPPVGLNLF Sbjct: 360 NIILLIGGQFMEPSGLLVIVAPLVFPIAIELGIDPIHLGIIMVVNMEIGMITPPVGLNLF 419 Query: 415 VTSGVAGMPMMAVVRAALPFLAVLFVFLIMITYIPWISTVLPNAVMGPEIITK 467 VTSGVAGMPMM+VV+AALPFLAVLFVFLI++TY+P++ST LPN MGPEIIT+ Sbjct: 420 VTSGVAGMPMMSVVKAALPFLAVLFVFLIIVTYVPFLSTFLPNTFMGPEIITQ 472 Lambda K H 0.329 0.144 0.421 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: 876 Number of extensions: 25 Number of successful extensions: 2 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: 467 Length of database: 472 Length adjustment: 33 Effective length of query: 434 Effective length of database: 439 Effective search space: 190526 Effective search space used: 190526 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 24 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:
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