Align ABC transporter ATP-binding protein (characterized, see rationale)
to candidate 5210164 Shew_2608 inner-membrane translocator (RefSeq)
Query= uniprot:A0A165KER0 (358 letters) >lcl|FitnessBrowser__PV4:5210164 Shew_2608 inner-membrane translocator (RefSeq) Length = 357 Score = 159 bits (401), Expect = 1e-43 Identities = 102/332 (30%), Positives = 173/332 (52%), Gaps = 41/332 (12%) Query: 19 PLILQS-FGNAWVRIADLALLYVLLALGLNIVVGYAGLLDLGYVAFYAVGAYLFALMASP 77 PL+L F +++I+ L + ALGLNI+VG+ G + LG+ AF+ GA+ AS Sbjct: 43 PLVLDGYFLTLFIQISYLGIA----ALGLNILVGFTGQISLGHGAFFGFGAF-----ASA 93 Query: 78 HLADNFAAFAAMFPNGLHTSLWIVIPVAALLAAFFGAMLGAPTLKLRGDYLAIVTLGFGE 137 L +F + + IP+A L G M G P +++G YLAI TL Sbjct: 94 WLNTSF-----------NIPVVFCIPLAGFLTMGVGMMFGMPAARIKGLYLAIATLAAQF 142 Query: 138 IIRIFLNNLDHPVNLTNGPKGLGQIDSVKVFGLDLGKRLEVFGFDINSVTLYYYLFLVLV 197 II+ F + + G G + + +FGFD ++ +Y++ L + Sbjct: 143 IIQDFFGRAEW---FSGGSSGA------------MAAPVSLFGFDFDTDMSFYFIALFAL 187 Query: 198 VVSVIICYRLQDSRIGRAWMAIREDEIAAKAMGINTRNMKLLAFGMGASFGGVSGAMFGA 257 V I L SR GRA++A+R+ ++A+ MG+ +LL+FG+ + + G+ GA++ Sbjct: 188 VFMYIWGCNLMRSRDGRAFVAVRDHYLSAEIMGVKLNKYRLLSFGISSFYAGIGGALYAH 247 Query: 258 FQGFVSPESFSLMESVMIVAMVVLGGIGHIPGVILGAVLLSALPEVLRYVAGPLQAMTDG 317 + G+VS E F+++ S+ +AMV++GG+G I G ++G V + LPEVL + G ++ G Sbjct: 248 YLGYVSSEGFTILMSIQFLAMVIIGGLGSIKGTLMGVVFMVLLPEVLEGMVGLMKYTDYG 307 Query: 318 RLDS-----AILRQLLIALAMIIIMLLRPRGL 344 L A ++++ I L +I+ ++ P GL Sbjct: 308 NLPMVTDGLAYIKEMAIGLVIILFLIFEPEGL 339 Lambda K H 0.328 0.144 0.430 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: 311 Number of extensions: 19 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: 358 Length of database: 357 Length adjustment: 29 Effective length of query: 329 Effective length of database: 328 Effective search space: 107912 Effective search space used: 107912 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: 49 (23.5 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