Align histidine permease (characterized)
to candidate BWI76_RS07360 BWI76_RS07360 phenylalanine transporter
Query= reanno::pseudo3_N2E3:AO353_12275 (468 letters) >FitnessBrowser__Koxy:BWI76_RS07360 Length = 458 Score = 377 bits (968), Expect = e-109 Identities = 193/439 (43%), Positives = 275/439 (62%), Gaps = 6/439 (1%) Query: 8 LKRGLSARHIRFMALGSAIGTGLFYGSASAIQMAGPAVLLAYLIGGAAVFMVMRALGEMA 67 L RGL RHI+ +ALG AIGTGLF G AIQMAGPAVLL Y + G F++MR LGEM Sbjct: 18 LHRGLQNRHIQLIALGGAIGTGLFLGIGPAIQMAGPAVLLGYAVAGIVAFLIMRQLGEMV 77 Query: 68 VHNPVAGSFGQYASTYLGPMAGFILGWTYAFEMVIVGMADVTAFGIYMGFWFPEVSRWIW 127 V PV+GSF +A Y GP AGF+ GW Y V+VGMA++TA GIYM +W P+V WIW Sbjct: 78 VEEPVSGSFAHFAYKYWGPFAGFLSGWNYWVMFVLVGMAELTAAGIYMQYWLPDVPTWIW 137 Query: 128 VLGVVSIVGGLNLCNVKVFGEMEFWLSLLKVAAIVAMILGGFGI-MLFGISTAPGQVTDI 186 I+ +NL NV+++GE EFW +L+KV AI+ MI GFG+ MLFG G I Sbjct: 138 AAAFFLIINAVNLVNVRLYGEAEFWFALIKVLAIIGMI--GFGLWMLFG--GHGGSKAGI 193 Query: 187 SNLWTQGGFMPNGMGGLIASFAVVMFAFGGIEIIGVTAGEAKDPQHVLPRAINAVPLRIL 246 NLW GGF G GLI S AV+MF+FGG+E+IG+TA EA++P+ +P+A+N V RIL Sbjct: 194 DNLWKHGGFFATGWHGLIMSLAVIMFSFGGLELIGITAAEAQNPEKSIPKAVNQVVYRIL 253 Query: 247 LFYVLTMLVLMSIFPWQQIGSQGSPFVQIFDKLGISSAATILNIVVITAAISAINSDIFG 306 LFY+ +++VL++++PW +I S SPFV IF L + A+ LN V++ A++S NS ++ Sbjct: 254 LFYIGSLVVLLALYPWVEIQSDSSPFVMIFHNLDSNVVASALNFVILVASLSVYNSGVYS 313 Query: 307 AGRMMFGLAQQGHAPKGFAHLSRNGVPWMTVVVMSVALLLGVLLNYLIPENVFLLIASIA 366 RM+FGL+ QG+APK A +S+ GVP ++++ + L V+LNYL+P+ L+ ++ Sbjct: 314 NSRMLFGLSVQGNAPKFLARVSKRGVPVNSLLLSGIITSLVVVLNYLLPQKALGLLMALV 373 Query: 367 TFATVWVWLMILFTQVAMRRSMTAEQVAQLKFPVPFWPYAPMAAIAFMLFVFGVLGYFPD 426 + W+MI + R + + + KF P + IAF+ + ++ Sbjct: 374 VATLLLNWIMICLAHLKFRAAQ-RRKGREPKFKALLSPASNYICIAFLALILVLMCTIDG 432 Query: 427 TQAALIVGVVWIVLLVLAY 445 + + I+ VWI+ L A+ Sbjct: 433 MRLSAILLPVWILFLFAAF 451 Lambda K H 0.329 0.142 0.441 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: 661 Number of extensions: 33 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: 468 Length of database: 458 Length adjustment: 33 Effective length of query: 435 Effective length of database: 425 Effective search space: 184875 Effective search space used: 184875 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