Align L-lactate permease (characterized, see rationale)
to candidate WP_047212578.1 PATSB16_RS03030 L-lactate permease
Query= uniprot:Q8EIL2 (545 letters) >NCBI__GCF_001931675.1:WP_047212578.1 Length = 533 Score = 412 bits (1058), Expect = e-119 Identities = 221/540 (40%), Positives = 327/540 (60%), Gaps = 18/540 (3%) Query: 5 QTYTPLGSLWLTA-IVALLPIVFFFLALTVLKLKGHIAGALTLLIALAVAIITYKMPVSI 63 Q TP+ + L + +VA++PI + L VL+ A + L+ L +A+ +KMPV + Sbjct: 4 QIVTPVANALLPSFLVAVIPIAIVLVMLGVLRRPAWQASMVGLIAGLIIAVAVWKMPVGL 63 Query: 64 ALASAIYGFSYGLWPIAWIIITAVFLYKITVKTGQFEIIRSSVIS-VTEDQRLQMLLVGF 122 A + +G + L P+ WI+ A+ LY ++VK+G+F+ R ++ + D+RL +L+V F Sbjct: 64 AFNAVAFGVVFALLPVMWIVYGALVLYNVSVKSGRFDAFRQWMLDHMPNDRRLVLLVVAF 123 Query: 123 SFGAFLEGAAGFGAPVAITAALLVGLGFNPLYAAGLCLIANTAPVAFGAMGIPIIVAGQV 182 SFG LEG AGFG PVAIT+ALL+ LGF L A LI NTAPVAFGA+G+PI V G V Sbjct: 124 SFGCLLEGIAGFGTPVAITSALLIALGFPALEALTYTLIFNTAPVAFGALGVPITVLGAV 183 Query: 183 SSLDPFHIGQLAGRQLPILSIIVPFWLIAMMDGIRGIRQTWPATLVAGVSFAVTQFLTSN 242 +S+ P +G + GRQLP+ + ++PF++I + G R IR+ WPA VAG SFA+ QF++SN Sbjct: 184 TSMPPGPLGAMVGRQLPLFAFLLPFYVIGLYGGFRSIRKLWPALTVAGGSFALAQFVSSN 243 Query: 243 FIGPELPDITSALVSLICLTLFLKVW--QPKEIFTFSGMKQRAVTPKSTFSNGQIFKAWS 300 FI +L D+ +++ SLI FLKVW +P + + A TPK + W Sbjct: 244 FISYQLTDVLASMTSLIITIAFLKVWSPEPDPQYHIDRPARAAGTPKIGYG------GWL 297 Query: 301 PFIILTAIVTLWSIKDVQLALSFATISIEVPYLHNLVIKTAPIVAKETPYAAIYKLNLLG 360 P++++T +V W + + P L+ V I PY A++ LG Sbjct: 298 PWVVITVVVIFWVYAKIS---GIGEAKLPWPGLNQQVF----ITLYNKPYGAVWGFQPLG 350 Query: 361 AVGTAILIAAMISIVVLKMSISNALTSFKDTLIELRFPILSIGLVLAFAFVANYSGLSST 420 GTAIL+AA+I+ ++K+S+ + L S D +++R +L++ +++ AF+ NYSG+S T Sbjct: 351 -TGTAILLAAVITSFLVKLSVKDFLASLWDAWVQIRIAVLTVCMIVGLAFLLNYSGISYT 409 Query: 421 LALVLAGTGVAFPFFSPFLGWLGVFLTGSDTSSNALFGALQANTANQIGVTPELLVAANT 480 L + +A G FP S FLGW+ VFL+GSDTS NALFG LQ A Q+G P L+ A N+ Sbjct: 410 LGMGVASVGALFPLVSAFLGWVAVFLSGSDTSGNALFGNLQVVAAKQLGFDPVLMAATNS 469 Query: 481 TGGVTGKMISPQSIAVACAATGLAGKESDLFRFTLKHSLFFCTFIGVLTVLQAYIVPWTL 540 +GGV GKMISPQ+IA + TGL G E +F T KHS+F +GV+ LQ +++ W + Sbjct: 470 SGGVMGKMISPQNIATGVSTTGLRGHEGVVFARTFKHSVFLTLLLGVVVYLQQHVLSWMI 529 Lambda K H 0.327 0.140 0.419 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: 915 Number of extensions: 39 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: 545 Length of database: 533 Length adjustment: 35 Effective length of query: 510 Effective length of database: 498 Effective search space: 253980 Effective search space used: 253980 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 (21.7 bits) S2: 52 (24.6 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