Align histidine permease (characterized)
to candidate PP_4495 PP_4495 aromatic amino acid transport protein
Query= reanno::pseudo3_N2E3:AO353_12275 (468 letters) >FitnessBrowser__Putida:PP_4495 Length = 472 Score = 373 bits (958), Expect = e-108 Identities = 190/449 (42%), Positives = 279/449 (62%), Gaps = 13/449 (2%) Query: 8 LKRGLSARHIRFMALGSAIGTGLFYGSASAIQMAGPAVLLAYLIGGAAVFMVMRALGEMA 67 LKRGL RHI+ +ALG AIGTGLF GSA ++ AGP+++L Y I G FM+MR LGEM Sbjct: 11 LKRGLKNRHIQLIALGGAIGTGLFLGSAGVMKSAGPSMILGYAICGFIAFMIMRQLGEMI 70 Query: 68 VHNPVAGSFGQYASTYLGPMAGFILGWTYAFEMVIVGMADVTAFGIYMGFWFPEVSRWIW 127 V PVAGSF +A TY G AGF+ GW ++VGM++++A G Y+ +W+PE+ W+ Sbjct: 71 VEEPVAGSFSHFAHTYWGGFAGFLSGWNCWVLYILVGMSELSAVGKYVHYWWPEIPTWVT 130 Query: 128 VLGVVSIVGGLNLCNVKVFGEMEFWLSLLKVAAIVAMILGGFGIMLFGISTAPGQVTDIS 187 ++ +NL NVK FGE EFW +++KV AIV+MI G G L S + G ++ Sbjct: 131 AAAFFVLINAINLMNVKFFGEAEFWFAIIKVVAIVSMI--GLGAYLL-TSGSGGPEATVA 187 Query: 188 NLWTQGGFMPNGMGGLIASFAVVMFAFGGIEIIGVTAGEAKDPQHVLPRAINAVPLRILL 247 NLWT GGF PNG+ GL+ + A +MF+FGG+E++G TA EA P+ V+P+AIN V RIL+ Sbjct: 188 NLWTHGGFFPNGVSGLVMALAFIMFSFGGLEMLGFTAAEADKPKTVIPKAINQVIYRILI 247 Query: 248 FYVLTMLVLMSIFPWQQI--------GSQG-SPFVQIFDKLGISSAATILNIVVITAAIS 298 FYV ++VL+S+ PW + GS G SPFVQ+F LG AA +LN VV+TAA+S Sbjct: 248 FYVGALVVLLSLTPWDNLVASIDASGGSYGSSPFVQVFSLLGSDVAANLLNFVVLTAALS 307 Query: 299 AINSDIFGAGRMMFGLAQQGHAPKGFAHLSRNGVPWMTVVVMSVALLLGVLLNYLIPENV 358 NS + RM+ G+A+QG AP A + + GVP +++V + + VLLNYL+P+N Sbjct: 308 VYNSGTYCNARMLLGMAEQGDAPASLAKVDKRGVPVRSILVSAAVTFVAVLLNYLMPQNA 367 Query: 359 FLLIASIATFATVWVWLMILFTQVAMRRSMTAEQVAQLKFPVPFWPYAPMAAIAFMLFVF 418 L+ S+ V W MI ++ + R+ + L F ++PY +AF++ + Sbjct: 368 LELLMSLVVATLVINWAMISYSHLKFRQHLDRTGQKPL-FKALWYPYGNYVVLAFVVLIL 426 Query: 419 GVLGYFPDTQAALIVGVVWIVLLVLAYLM 447 G++ P Q ++ VW++ +++ Y++ Sbjct: 427 GIMLMIPGIQVSVYAIPVWLLAMLVVYMV 455 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: 660 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: 468 Length of database: 472 Length adjustment: 33 Effective length of query: 435 Effective length of database: 439 Effective search space: 190965 Effective search space used: 190965 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