Align TRAP-type large permease component (characterized, see rationale)
to candidate WP_094509141.1 CEV31_RS17950 TRAP transporter large permease
Query= uniprot:Q930R2 (425 letters) >NCBI__GCF_002252445.1:WP_094509141.1 Length = 426 Score = 283 bits (723), Expect = 9e-81 Identities = 148/413 (35%), Positives = 243/413 (58%) Query: 4 VVFIVSLLGAMAIGVPVAFSLMFCGVVLMWYMGMFNTQIIAQNMIAGADTFTLLAIPFFI 63 + + +L+ A+ VPVA ++ + + + ++ Q M D+F LLAIPFFI Sbjct: 3 IALVSALMILFALSVPVAVAIAMSAIFSISFFSNLPLLVVPQKMFNALDSFPLLAIPFFI 62 Query: 64 LAGELMNAGGLSRRIIDFAIACVGHIRGGLGIVAIMAAVIMASISGSAAADTAALAAILI 123 LAG LM+ GG+SRR++DFA + VG ++GGL ++ +I +SISGS+ A T A+ AILI Sbjct: 63 LAGNLMSHGGVSRRLVDFAKSMVGGVQGGLAASCVLTCMIFSSISGSSVATTFAVGAILI 122 Query: 124 PMMAKAGYNVPRSAGLIAAGGVIAPVIPPSMAFIVFGVAANVSITQLFMAGIVPGLIMGI 183 P M + GY P + + A + ++PPS+ I++ V+ S+TQ+F+AGI PGL++ Sbjct: 123 PAMVRHGYPTPVAGTIQATSAELGVILPPSIPMILYAVSTETSVTQIFIAGIGPGLLIAG 182 Query: 184 ALVATWLLVVRKDDIQPLPRTPMKERVGATGRALWALGMPVIILGGIKAGVVTPTEAAVV 243 AL+ + R K + + A W+L MPV+I+GGI G+ TPTEAA + Sbjct: 183 ALIIMTQIWCRVKGYGKNDGDDRKGFLKSAVSAFWSLMMPVVIVGGIYGGIFTPTEAAAI 242 Query: 244 AAVYALFVGMVIYRELKPRDLPGVILQAAKTTAVIMFLVCAALVSSWLITAANIPSEITG 303 A ALF+G+ IYRELK DLP + Q+ +T +M ++ AA + S+L++ + +P + Sbjct: 243 AVFLALFIGLFIYRELKFTDLPKIFRQSVVSTGAVMLIIAAAGLFSFLVSMSGLPKMVGS 302 Query: 304 FISPLIDRPTLLMFVIMLVVLVVGTALDLTPTILILTPVLMPIIKQAGIDPVYFGVLFIM 363 + S + + + +++ VVG ++ + IL+L P+L PI GIDPV+FG++ I+ Sbjct: 303 WASDSFESWITFLLFVNILLFVVGMFVETSAAILVLAPILAPIAILYGIDPVHFGMIMIV 362 Query: 364 NTCIGLLTPPVGVVLNVVSGVGRVPLGKVIVGVTPFLVAQILVLFLLVLFPDI 416 N +G++TPP+GV L + V ++P+ ++ + + A IL L ++ P I Sbjct: 363 NLAMGMITPPLGVNLFAAASVAKIPVQRMFKPLIWPVTAIILSLMVITYVPQI 415 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: 451 Number of extensions: 24 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: 425 Length of database: 426 Length adjustment: 32 Effective length of query: 393 Effective length of database: 394 Effective search space: 154842 Effective search space used: 154842 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 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