Align proline porter II (characterized)
to candidate SMc01869 SMc01869 transport transmembrane protein
Query= CharProtDB::CH_024324 (500 letters) >lcl|FitnessBrowser__Smeli:SMc01869 SMc01869 transport transmembrane protein Length = 436 Score = 257 bits (657), Expect = 5e-73 Identities = 143/411 (34%), Positives = 236/411 (57%), Gaps = 13/411 (3%) Query: 25 KAITAASLGNAMEWFDFGVYGFVAYAL-GKVFFPGADPSVQMVAALATFSVPFLIRPLGG 83 + + A+ +G +E+FDF VY A + +FFP ADP+ M+ +LATFS+ F RPLG Sbjct: 25 RVLFASLVGTTIEFFDFYVYATAAVIIFPHLFFPAADPTSAMLQSLATFSIAFFARPLGA 84 Query: 84 LFFGMLGDKYGRQKILAITIVIMSISTFCIGLIPSYDTIGIWAPILLLICKMAQGFSVGG 143 + FG GD+ GR+ L ++ M IST IGL+P+Y TIG+ AP+LL +C+ QG +GG Sbjct: 85 VIFGHFGDRIGRKATLVAALMTMGISTVVIGLLPTYSTIGVVAPLLLALCRFGQGLGLGG 144 Query: 144 EYTGASIFVAEYSPDRKRGFMGSWLDFGSIAGFVLGAGVVVLISTIVGEANFLDWGWRIP 203 E+ GA + E +P+ KR + + G+ GF+L AG +++ ++ E FL WGWR+P Sbjct: 145 EWGGAVLLATENAPEGKRSWYAMFPQLGAPIGFILSAGTFLILGEVMSEEAFLAWGWRVP 204 Query: 204 FFIALPLGIIGLYLRHALEETPAFQQHVDKLEQGDREGLQDGPKVSFKEIATKYWRSLLT 263 F ++ L I+GLY+R + ETP FQ+ +DK E+ +V I + RSL+ Sbjct: 205 FIASVLLVIVGLYVRLKITETPEFQKAIDKHER---------VEVPVAAIFRSHKRSLVL 255 Query: 264 CIGLVIATNVTYYMLLTYMPSYLSHNLHYSEDHGVLIIIAIMIGMLFVQPVMGLLSDRFG 323 + +AT V +Y++ + S+ + L YS + +L+ + ++ + PV G+LSDRFG Sbjct: 256 GTFVALATFVLFYLMTVFSLSWGTTKLGYSREQFLLVQMTGVVFFGLMIPVSGILSDRFG 315 Query: 324 RRPFVLLGSVALFVLAIPAFILINSNVIGLIFAGLLMLAVILNCFTGVMASTLPAMFPTH 383 RR ++L ++ + V + L++S + G ++ L ++ G + + L A FPT Sbjct: 316 RRLVLVLTTIGIGVFGLFMAPLLSSGLGGAFVFSIVGLG-LMGLTYGPIGAALAAPFPTA 374 Query: 384 IRYSALAAAFNIS-VLVAGLTPTLAAWLVESSQNLMMPAYYLMVVAVVGLI 433 +RY+ + FN++ + A L P +A WL ++ +L YYL+ A + L+ Sbjct: 375 VRYTGASMTFNLAGIFGASLAPYIATWLA-TNYSLGHVGYYLLAAASITLV 424 Lambda K H 0.327 0.142 0.429 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: 653 Number of extensions: 34 Number of successful extensions: 6 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: 500 Length of database: 436 Length adjustment: 33 Effective length of query: 467 Effective length of database: 403 Effective search space: 188201 Effective search space used: 188201 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: 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