Align High-affinity branched-chain amino acid ABC transporter permease LivM (characterized, see rationale)
to candidate AO353_13350 AO353_13350 branched-chain amino acid ABC transporter permease
Query= uniprot:A0A159ZYE0 (418 letters) >FitnessBrowser__pseudo3_N2E3:AO353_13350 Length = 432 Score = 400 bits (1027), Expect = e-116 Identities = 216/418 (51%), Positives = 286/418 (68%), Gaps = 9/418 (2%) Query: 3 RHLKSALFSALLVWAVAYPVLGLKLTIVGINLEVHGTSPAILAT-IAVCSLLMFLRVLFS 61 + L + + L+ V P++G+ L NL+ + + A I +L +F++ Sbjct: 13 KSLIDTVLAGLIALIVFGPIVGVVLEGYSYNLQPTRVAWMVGAVMIGRLALSLFMQTAKG 72 Query: 62 TQISAMWKS-SPGLPVIPAKASNFLTLPTTQRWIVLALIVGALVWPFFGSRGAVDIATLI 120 ++ ++ G+ V+ + L R+I+ ALIV A+V+P F + + + L Sbjct: 73 EKVQQRFEIVGSGVHVLAPDFKSRL------RFIIPALIVIAIVFPVFADKYLLTVVILG 126 Query: 121 LIYVMLGLGLNIVVGLAGLLDLGYVGFYAVGAYSYALLSHYFGLSFWICLPIAGMMAATF 180 LIYV+LGLGLNIVVGLAGLLDLGYV FYA+GAY AL HY GL FW LP++ +MAA Sbjct: 127 LIYVLLGLGLNIVVGLAGLLDLGYVAFYAIGAYGLALGYHYLGLGFWTVLPLSALMAALA 186 Query: 181 GFLLGFPVLRLRGDYLAIVTLGFGEIIRLFLRNLTDITGGPNGISNIEKPTFFGLTFERK 240 G +LGFPVLR+ GDYLAIVTLGFGEIIRL L N TGGPNG+ + P+FFG+ F R Sbjct: 187 GCILGFPVLRMHGDYLAIVTLGFGEIIRLILTNWLSFTGGPNGMP-VPSPSFFGIEFTRV 245 Query: 241 AAEGLQTFHEYFGLEYNSINKVIFLYLVALLLALAALFVINRLLRMPIGRAWEALREDEI 300 A +G FHE+FG EYN K +F+Y V L+ + L++ +RL RMP+GRAWEALREDEI Sbjct: 246 AKDGGIPFHEFFGTEYNPNIKFMFIYAVLFLVVMLVLYIKHRLTRMPVGRAWEALREDEI 305 Query: 301 ACRALGLNPTVIKLSAFTLGAAFAGFAGSFFAARQGLVTPESFTFIESAIILAIVVLGGM 360 ACRA+GLN ++KLSAFTLGA+ AG AG FFA+ QG V P SFTF ESA+ILAIVVLGGM Sbjct: 306 ACRAMGLNHVLVKLSAFTLGASTAGLAGVFFASYQGFVNPTSFTFFESALILAIVVLGGM 365 Query: 361 GSQLGVILAAIVMILLPEMMREFSEYRMLMFGALMVLMMIWRPQGLLPMQRPHMELRK 418 GS +GV++AA V+ + PE++R F+EYR+L+FG LMVLMMIW+P+GL+ + R + RK Sbjct: 366 GSTVGVVIAAFVLTVAPELLRGFAEYRVLLFGILMVLMMIWKPRGLIRISRTGVTPRK 423 Lambda K H 0.331 0.145 0.439 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: 645 Number of extensions: 38 Number of successful extensions: 3 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: 418 Length of database: 432 Length adjustment: 32 Effective length of query: 386 Effective length of database: 400 Effective search space: 154400 Effective search space used: 154400 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