Align High-affinity branched-chain amino acid transport system permease protein LivM; LIV-I protein M (characterized)
to candidate WP_084936136.1 HA51_RS18900 high-affinity branched-chain amino acid ABC transporter permease LivM
Query= SwissProt::P22729 (425 letters) >NCBI__GCF_002095475.1:WP_084936136.1 Length = 423 Score = 647 bits (1668), Expect = 0.0 Identities = 329/425 (77%), Positives = 363/425 (85%), Gaps = 2/425 (0%) Query: 1 MKPMHIAMALLSAAMFFVLAGVFMGVQLELDGTKLVVDTASDVRWQWVFIGTAVVFFFQL 60 MK + + A++S M +LA FMGV+L+LDGTKLVV A RW W+FIG AVVF FQL Sbjct: 1 MKRLGLVNAVISTVMLLILATFFMGVRLDLDGTKLVVANAGAARWNWIFIGCAVVFVFQL 60 Query: 61 LRPAFQKGLKSVSGPKFILPAIDGSTVKQKLFLVALLVLAVAWPFMVSRGTVDIATLTMI 120 LRP F K SG F+LP DGST KQKL + ++ AV WPF+VSRG+VDIATLT+I Sbjct: 61 LRPLFHGKFKR-SGKAFVLPGFDGSTPKQKLVMALMIAAAVIWPFLVSRGSVDIATLTLI 119 Query: 121 YIILGLGLNVVVGLSGLLVLGYGGFYAIGAYTFALLNHYYGLGFWTCLPIAGLMAAAAGF 180 Y++LGLGLNVVVGLSGLLVLGYGGFYAIGAYTFALLNHYYG GFW LP+AG++A A G Sbjct: 120 YVMLGLGLNVVVGLSGLLVLGYGGFYAIGAYTFALLNHYYGFGFWESLPLAGIVAGAFGL 179 Query: 181 LLGFPVLRLRGDYLAIVTLGFGEIVRILLLNNTEITGGPNGISQIPKPTLFGLEFSRTAR 240 +LGFPVLRLRGDYLAIVTLGFGEIVRILLLN+T ITGGPNGI+QIPKP+LFG+EF R Sbjct: 180 MLGFPVLRLRGDYLAIVTLGFGEIVRILLLNSTSITGGPNGIAQIPKPSLFGIEFGRRVS 239 Query: 241 EGGWDTFSNFFGLKYDPSDRVIFLYLVALLLVVLSLFVINRLLRMPLGRAWEALREDEIA 300 EGGW TF + GL YDP+ RVIFLYLVALLLV ++LFVINRLLRMPLGRAWEALREDEIA Sbjct: 240 EGGWTTFHDLTGLAYDPNHRVIFLYLVALLLVAVTLFVINRLLRMPLGRAWEALREDEIA 299 Query: 301 CRSLGLSPRRIKLTAFTISAAFAGFAGTLFAARQGFVSPESFTFAESAFVLAIVVLGGMG 360 CRSLGLSP RIKLTAFTISA FAGFAGTLFAARQGFVSPESFTF ESAFVLAIVVLGGMG Sbjct: 300 CRSLGLSPTRIKLTAFTISAVFAGFAGTLFAARQGFVSPESFTFVESAFVLAIVVLGGMG 359 Query: 361 SQFAVILAAILLVVSRELMRDFNEYSMLMLGGLMVLMMIWRPQGLLPMTRPQLKLKNGAA 420 SQFAVILAA+LLVVSRELMRD NEYSML+LGGLMVLMMIWRPQGLLPM RP LKLK+ + Sbjct: 360 SQFAVILAAVLLVVSRELMRDLNEYSMLVLGGLMVLMMIWRPQGLLPMKRPHLKLKS-SK 418 Query: 421 KGEQA 425 +GEQA Sbjct: 419 QGEQA 423 Lambda K H 0.330 0.145 0.436 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: 526 Number of extensions: 10 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: 423 Length adjustment: 32 Effective length of query: 393 Effective length of database: 391 Effective search space: 153663 Effective search space used: 153663 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