Align L-proline and D-alanine ABC transporter, permease component 1 (characterized)
to candidate GFF3113 HP15_3056 high-affinity branched-chain amino acid ABC transporter, permease protein
Query= reanno::azobra:AZOBR_RS08235 (301 letters) >lcl|FitnessBrowser__Marino:GFF3113 HP15_3056 high-affinity branched-chain amino acid ABC transporter, permease protein Length = 307 Score = 350 bits (897), Expect = e-101 Identities = 170/302 (56%), Positives = 230/302 (76%), Gaps = 3/302 (0%) Query: 3 YFLQQLINGLSLGAIYGLIAIGYTMVYGIIGMINFAHGEIYMIGAFVALITFLAIGSLGI 62 YF QQLINGL++G+ Y LIAIGYTMVYGIIGMINFAHGEIYMIGA+ ALI + +LGI Sbjct: 6 YFSQQLINGLTIGSTYALIAIGYTMVYGIIGMINFAHGEIYMIGAYTALIAITGLAALGI 65 Query: 63 TWVPLALLVMLVASMLFTAVYGWTVERIAYRPLRSSPRLAPLISAIGMSIFLQNYVQILQ 122 W+PL L+V L+ +M+ ++ GW VER+AYRP+R RL PLISAIGMSIFLQNYV + Q Sbjct: 66 AWLPLILIVALLCAMIVSSSMGWAVERVAYRPVRGRHRLIPLISAIGMSIFLQNYVHLAQ 125 Query: 123 GARSKPLQPILPGNLTLMDG---AVSVSYVRLATIVITIALMYGFTQLITRTSLGRAQRA 179 G+R+ ++ G G +S+SY+++ + T+ M + I+R+ GRA RA Sbjct: 126 GSRNIGFPALIDGGFNFGSGDGFQMSLSYMQITIFITTLICMTALSLFISRSRTGRACRA 185 Query: 180 CEQDKKMAGLLGVNVDRVISLTFVMGAALAAVAGMMVLLIYGVIDFYIGFLAGVKAFTAA 239 QD MA LLG++ +R+IS TFV+GAALAAVAG+++ + YG +D GF+AG+KAFTAA Sbjct: 186 VSQDLGMANLLGIDTNRIISATFVIGAALAAVAGLLLGMYYGSVDPLFGFIAGLKAFTAA 245 Query: 240 VLGGIGSLPGAMLGGVVIGLIEAFWSGYMGSEWKDVATFTILVLVLIFRPTGLLGRPEIE 299 VLGGIGS+PGAMLGG+++G+ E+ SGY+ E+KDV +F++L+L+L+F+PTGLLG+PE+E Sbjct: 246 VLGGIGSIPGAMLGGLILGVAESMTSGYLSGEYKDVISFSLLILILLFKPTGLLGKPEVE 305 Query: 300 KV 301 K+ Sbjct: 306 KI 307 Score = 26.9 bits (58), Expect = 6e-04 Identities = 23/73 (31%), Positives = 37/73 (50%), Gaps = 1/73 (1%) Query: 186 MAGLLGVNVDRVISLTFVMGAALAAVAGMMVLLIYGVIDFYIGFLAGVKAFTAAV-LGGI 244 M LL + + LT AL A+ MV I G+I+F G + + A+TA + + G+ Sbjct: 1 MQDLLYFSQQLINGLTIGSTYALIAIGYTMVYGIIGMINFAHGEIYMIGAYTALIAITGL 60 Query: 245 GSLPGAMLGGVVI 257 +L A L ++I Sbjct: 61 AALGIAWLPLILI 73 Lambda K H 0.329 0.144 0.425 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: 381 Number of extensions: 16 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: 301 Length of database: 307 Length adjustment: 27 Effective length of query: 274 Effective length of database: 280 Effective search space: 76720 Effective search space used: 76720 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: 48 (23.1 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 preprint 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