Align histidine permease (characterized)
to candidate BWI76_RS06245 BWI76_RS06245 proline-specific permease ProY
Query= reanno::pseudo3_N2E3:AO353_12275 (468 letters) >FitnessBrowser__Koxy:BWI76_RS06245 Length = 456 Score = 585 bits (1508), Expect = e-171 Identities = 277/441 (62%), Positives = 351/441 (79%), Gaps = 1/441 (0%) Query: 5 ANGLKRGLSARHIRFMALGSAIGTGLFYGSASAIQMAGPAVLLAYLIGGAAVFMVMRALG 64 +N LKRGLS RHIRFMALGSAIGTGLFYGSA AI+MAGP+VLLAY+IGG A +++MRALG Sbjct: 4 SNKLKRGLSTRHIRFMALGSAIGTGLFYGSADAIKMAGPSVLLAYIIGGVAAYIIMRALG 63 Query: 65 EMAVHNPVAGSFGQYASTYLGPMAGFILGWTYAFEMVIVGMADVTAFGIYMGFWFPEVSR 124 EM+VHNP A SF +YA YLGP+AG+I GWTY FE++IV +ADVTAFGIYMG WFP V Sbjct: 64 EMSVHNPAASSFSRYAQDYLGPLAGYITGWTYCFEILIVAIADVTAFGIYMGVWFPAVPH 123 Query: 125 WIWVLGVVSIVGGLNLCNVKVFGEMEFWLSLLKVAAIVAMILGGFGIMLFGISTAPGQVT 184 W+WVL VV I+ +NL +VKVFGE+EFW S KVA I+ MIL GFGI+++GI GQ T Sbjct: 124 WVWVLSVVLIICAVNLMSVKVFGELEFWFSFFKVATIIIMILAGFGIIIWGIGNG-GQPT 182 Query: 185 DISNLWTQGGFMPNGMGGLIASFAVVMFAFGGIEIIGVTAGEAKDPQHVLPRAINAVPLR 244 I NLW+ GGF NG G++ S +VMFA+GGIEIIG+TAGEAKDP+ +PRAIN+VP+R Sbjct: 183 GIHNLWSNGGFFSNGWLGMVMSLQMVMFAYGGIEIIGITAGEAKDPEKSIPRAINSVPMR 242 Query: 245 ILLFYVLTMLVLMSIFPWQQIGSQGSPFVQIFDKLGISSAATILNIVVITAAISAINSDI 304 IL+FYV T+ V+MSI+PW Q+G+ GSPFV F LGI+ AA+ILN VV+TA++SAINSD+ Sbjct: 243 ILVFYVGTLFVIMSIYPWNQVGTNGSPFVLTFQHLGITFAASILNFVVLTASLSAINSDV 302 Query: 305 FGAGRMMFGLAQQGHAPKGFAHLSRNGVPWMTVVVMSVALLLGVLLNYLIPENVFLLIAS 364 FG GRM+ G+A+QG APK FA SR GVPW+TV+VM++ALL V LNY++PENVFL+IAS Sbjct: 303 FGVGRMLHGMAEQGSAPKMFAKTSRRGVPWVTVMVMTIALLFAVYLNYIMPENVFLVIAS 362 Query: 365 IATFATVWVWLMILFTQVAMRRSMTAEQVAQLKFPVPFWPYAPMAAIAFMLFVFGVLGYF 424 +ATFATVWVW+MIL +Q+A RR + E+ LKF VP + + F++F+ G++GY Sbjct: 363 LATFATVWVWIMILLSQIAFRRRLPPEEAKALKFKVPGGVTTTVIGLLFLVFIIGLIGYH 422 Query: 425 PDTQAALIVGVVWIVLLVLAY 445 PDT+ +L VG WI+LL++ + Sbjct: 423 PDTRISLYVGFAWIILLLIGW 443 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: 774 Number of extensions: 46 Number of successful extensions: 3 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: 456 Length adjustment: 33 Effective length of query: 435 Effective length of database: 423 Effective search space: 184005 Effective search space used: 184005 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