Align Histidine permease HisP (characterized)
to candidate WP_054653911.1 CES79_RS01340 amino acid permease
Query= SwissProt::A2RI97 (477 letters) >NCBI__GCF_002217945.1:WP_054653911.1 Length = 491 Score = 556 bits (1433), Expect = e-163 Identities = 267/474 (56%), Positives = 360/474 (75%), Gaps = 2/474 (0%) Query: 5 NQVKRNLKQRHITMIALGGTIGTGLFLTSGATISQAGPWGAVLAYCFIGIMVYFVMTSLG 64 N+VKR+LK RH++MIALGG+IGTGLF+ SG+ IS AGP G +LAY +GIMVYF+MTSLG Sbjct: 11 NEVKRSLKTRHLSMIALGGSIGTGLFVASGSAISTAGPGGGLLAYVALGIMVYFLMTSLG 70 Query: 65 EMATYLPTSGSFSDYGGRYVDPAFGFALGWNYWLNGAITIAVDLTTAGLITQFWFPHLPS 124 EMAT +P SGSF+ Y +YVDPA GFA+GWNYW N AIT+AVD++TA L+ +FW P++P Sbjct: 71 EMATNMPVSGSFATYSTKYVDPALGFAMGWNYWFNWAITLAVDISTAALVMKFWLPNVPG 130 Query: 125 WIFSGIATVLIFIINVMAVGAFGETEYWLSTIKVITIVLFLAIGLLTIFGVLGQGNVDVV 184 WI+S I V+IF+IN + V AFGETEYW++ IKV+T+V+FL +G TIFG++G G+ + Sbjct: 131 WIWSTIILVMIFMINALTVKAFGETEYWMAMIKVVTVVIFLIVGFATIFGIMG-GHATGL 189 Query: 185 ANLTAGNHGFVGGISGFVGVLLIAGFSFQGTEMLGITAGESEDPGKTIPKAMNSIFWRIL 244 +N T FVGG+ + V ++AGFSFQGTE++GITAGES P K++PKA+N +FWRIL Sbjct: 190 SNFTYKKAPFVGGVPAILSVFVVAGFSFQGTELVGITAGESATPEKSVPKAINQVFWRIL 249 Query: 245 LFYIFSIIVIAAIINFKDPRLLNPSSTAV-MSPFTIVFKNIGFAVAASVMNAVILTSVIS 303 LFYI +I VIA +I + P+LL S++ + +SPFT+VF+ G A AASVMNAVILTSVIS Sbjct: 250 LFYILAIFVIACLIPYTSPKLLGSSASDIAISPFTLVFERAGLAAAASVMNAVILTSVIS 309 Query: 304 SANSVMYASTRILYSLGQEKGAPKFFGRTAKNGIPFYALLATTIICFIAFLTGIFGTQIY 363 +ANS MYAS+R+LYSL + APK+F T KNG+P A +ATTI+ IAF+T I G ++Y Sbjct: 310 AANSGMYASSRMLYSLALDDFAPKYFEHTTKNGVPLRAQVATTIVGAIAFITSIAGPEVY 369 Query: 364 LFLIDLSSLTGFLAWLGISVSHIRFRRAYIAQGKKLEDLPYKAKWFPFGPIVALLMTGAI 423 +LI S LTGF+AW+GI++SH RFRRA++ QG +L +L Y AKWFPFGPI+A ++ + Sbjct: 370 SWLIAASGLTGFIAWVGIAISHFRFRRAFVKQGHQLSELKYHAKWFPFGPILAFVLCILV 429 Query: 424 AINLDPAMLFSEHWGEGLALYAAIPIFIVLYFGYKWKYNTKIIPLEEVDLSREK 477 I +P+ W + Y ++P+F +L+F YK KY+T IIPL++VD++ K Sbjct: 430 IIGQNPSAFVHFDWKQIGVTYLSVPLFFILFFWYKIKYHTGIIPLDKVDVTPHK 483 Lambda K H 0.327 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: 748 Number of extensions: 36 Number of successful extensions: 4 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: 477 Length of database: 491 Length adjustment: 34 Effective length of query: 443 Effective length of database: 457 Effective search space: 202451 Effective search space used: 202451 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 (21.7 bits) S2: 52 (24.6 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