Align Amino-acid permease RocE (characterized)
to candidate Pf1N1B4_1580 Histidine transport protein (permease)
Query= SwissProt::P39137 (467 letters) >FitnessBrowser__pseudo1_N1B4:Pf1N1B4_1580 Length = 469 Score = 300 bits (767), Expect = 9e-86 Identities = 152/453 (33%), Positives = 250/453 (55%), Gaps = 4/453 (0%) Query: 5 QDNGNQLQRTMKSRHLFMISLGGVIGTGFFLGTGFTINQAGPLGAVLSYLVGGFIMFLTM 64 Q L+R + +RH+ ++LG IGTG F G+ I AGP +L+YL+GG +F+ M Sbjct: 2 QQPAKGLKRGLSARHIRFMALGSAIGTGLFYGSASAIQMAGP-AVLLAYLIGGAAVFMVM 60 Query: 65 LCLGELAVAFPVSGSFQTYATKFISPAFGFAFGWLYWLGWAVTCAIEFLSAGQLMQRWFP 124 LGE+AV PV+GSF YA+ ++ P GF GW Y + + + G M WFP Sbjct: 61 RALGEMAVHNPVAGSFGQYASTYLGPMAGFILGWTYAFEMVIVGMADVTAFGIYMGFWFP 120 Query: 125 HIDVWIWCLVFAALMFILNAITTKAFAESEFWFSGIKILIILLFIILG-GAAMFGLIDLK 183 +D WIW L +++ LN K F E EFW S +K+ I+ I+ G G +FG+ Sbjct: 121 EVDRWIWVLGIVSVVGGLNLCNVKVFGEMEFWLSLLKVAAIVAMILGGFGIMLFGISTAP 180 Query: 184 GGEQAPFLTHFYEDGLFPNGIKAMLITMITVNFAFQGTELIGVAAGESEDPEKTIPRSIK 243 G + + G PNG+ ++ + V FAF G E+IGV AGE++DP++ +PR+I Sbjct: 181 GAQATDISNLWSHGGFMPNGVGGLIASFAVVMFAFGGIEIIGVTAGEAKDPQRVLPRAIN 240 Query: 244 QTVWRTLVFFVLSIIVIAGMIPWKQAGVVESPFVAVFEQIGIPYAADIMNFVILIALLSV 303 R L+F+VL+++V+ + PW+Q G SPFV +F+ +GI AA I+N V++ A +S Sbjct: 241 AVPLRILLFYVLTMLVLMSIFPWQQIGSQGSPFVQIFDNLGISSAATILNIVVISAAVSA 300 Query: 304 ANSGLYASTRILYAMANEGQAFKALGKTNQRGVPMYSLIVTMAVACLSLLTKFAQAETVY 363 NS ++ + R++Y +A +G A K + ++ GVP +++V + L +L + E V+ Sbjct: 301 INSDIFGAGRMMYGLAQQGHAPKGFARLSRNGVPWLTVVVMSSALLLGVLLNYLIPENVF 360 Query: 364 MVLLSLAGMSAQVGWITISLSQIMFRRKYIREGGKIEDLKFKTPLYPVLPLIGLTLNTVV 423 +++ S+A + W+ I +Q+ RR E ++ LKF P +P P+ + + Sbjct: 361 LLIASVATFATVWVWLMILFTQVAMRRSMSAE--QVAQLKFPVPFWPYAPMAAIAFMLFI 418 Query: 424 LISLAFDPEQRIALYCGVPFMIICYIIYHVVIK 456 L + P+ + AL GV ++++ + Y +K Sbjct: 419 FGVLGYFPDTQAALIVGVVWIVLLVLAYLTWVK 451 Lambda K H 0.329 0.142 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: 548 Number of extensions: 29 Number of successful extensions: 5 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: 467 Length of database: 469 Length adjustment: 33 Effective length of query: 434 Effective length of database: 436 Effective search space: 189224 Effective search space used: 189224 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