Align Leucine/isoleucine/valine ABC transporter,permease component (characterized, see rationale)
to candidate RR42_RS14415 RR42_RS14415 leucine/isoleucine/valine transporter permease subunit
Query= uniprot:G8ALI9 (505 letters) >FitnessBrowser__Cup4G11:RR42_RS14415 Length = 424 Score = 388 bits (996), Expect = e-112 Identities = 219/459 (47%), Positives = 280/459 (61%), Gaps = 57/459 (12%) Query: 18 LKEAAMTAFVALLLTIPLVGLRTVDRPTGLGLETRWNEVAAAVGLVFLGRLGLCLIREGH 77 LK A + A + +LTIP++GL+ + LE W V AVG VFL +L L + Sbjct: 21 LKNAIVAAVMTAILTIPVLGLQLKLDGYKVVLEPHWQPVWLAVGAVFLFQLFKPLFQR-- 78 Query: 78 AVTVLVLAAAATAAGFFIAMPTEALRVILIAGGAVIAIRAVLAIRTGRSKLSQAERDKRM 137 ATA I +P+ + Sbjct: 79 ----------ATAG---IKVPS-------------------------------------L 88 Query: 138 DHIAAQVQHASRWLGPIAVVVALAFPFTPLADRQLLDIGILLLTYIMLGWGLNIVVGLAG 197 + A Q WL + V L FPF + R +D+ L L Y++LG GLNIVVG AG Sbjct: 89 PALGATQQRKVIWL---LLAVGLVFPF--FSSRGAVDVATLALIYVILGLGLNIVVGYAG 143 Query: 198 LLDLGYVAFYAVGAYSYALLAHYFGFSFWVCLPLAGFLAAMSGVLLGFPVLRLRGDYFAI 257 LLDLGYV FYAVG Y+YALL YFG +FW CLP+A ++A+ G +LGFPVLRLRGDY AI Sbjct: 144 LLDLGYVGFYAVGGYTYALLNQYFGLTFWECLPIAAGMSALFGFVLGFPVLRLRGDYLAI 203 Query: 258 VTLGFGEIIRIILINWYQFTGGPNGISGIPRPSFFGIADFTRTPAEGTAAFHEMFGLEFS 317 VTLGFGEIIR++L N TGGP+G+SGIP+P+ FGI EG FHE+ G ++S Sbjct: 204 VTLGFGEIIRLLLNNLTSLTGGPDGVSGIPKPTVFGIEMARSASVEGVKTFHELLGWDYS 263 Query: 318 PLHRIIFLYYLILVLALVVNLFTMRVRKLPLGRAWEALREDDIACASLGINRTNMKLAAF 377 H +IFLY L L+L T R+ ++P+GRAWEALRED+IAC SLG+N T +KL+AF Sbjct: 264 GEHMVIFLYLLALLLVGFTLFVTSRLIRMPMGRAWEALREDEIACRSLGLNPTRIKLSAF 323 Query: 378 AIAAMFGGFAGSFFATRQGFISPESFTFIESAIILAIVVLGGMGSQIGVVVAAFLVIGLP 437 + A F G G+FFA RQG ++PESFTFIESA+ILA+VVLGGMGSQ+GV++AA L+ LP Sbjct: 324 TLGAAFAGLGGAFFAARQGLVNPESFTFIESALILAVVVLGGMGSQLGVILAAILLTALP 383 Query: 438 EAFRELADYRMLAFGMGMVLIMLWRPRGLLAHRDPTILL 476 E R A+YRML FG+ MVL+M+WRP+GLL P + L Sbjct: 384 EMARGFAEYRMLIFGLVMVLMMMWRPQGLLPASRPHVEL 422 Lambda K H 0.329 0.144 0.438 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: 661 Number of extensions: 34 Number of successful extensions: 3 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 505 Length of database: 424 Length adjustment: 33 Effective length of query: 472 Effective length of database: 391 Effective search space: 184552 Effective search space used: 184552 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