Align ABC transporter for L-Lysine, periplasmic substrate-binding component (characterized)
to candidate PP_0282 PP_0282 L-arginine ABC transporter - periplasmic binding subunit
Query= reanno::pseudo5_N2C3_1:AO356_09900 (251 letters) >lcl|FitnessBrowser__Putida:PP_0282 PP_0282 L-arginine ABC transporter - periplasmic binding subunit Length = 250 Score = 413 bits (1062), Expect = e-120 Identities = 204/250 (81%), Positives = 226/250 (90%), Gaps = 1/250 (0%) Query: 1 MQTYKKFLLAAAVSLVFSANAMAADKLKMGIEAAYPPFNNKDASGQVVGFDKDIGDALCA 60 M TYKKFLLAAA +LV SANAMAA+KL+MGIEAAYPPFNNKDASG VVGFDKDIGDALCA Sbjct: 1 MHTYKKFLLAAAATLVMSANAMAAEKLRMGIEAAYPPFNNKDASGNVVGFDKDIGDALCA 60 Query: 61 KMKVECEVVTSDWDGIIPALNAKKFDFLISSLSITEERKQAVDFTDPYYSNKLQFIAPKS 120 KMKVEC VVTSDWDGIIPALNAKKFDFL+SSLSIT+ERKQAVDFT+PYYSNKLQFIAPK+ Sbjct: 61 KMKVECSVVTSDWDGIIPALNAKKFDFLVSSLSITDERKQAVDFTNPYYSNKLQFIAPKN 120 Query: 121 AEFKTDKDSLKGKVIGAQRATLAGTWLEDELGSDITTKLYDTQENAYLDLTSGRVDAILA 180 +FKTDK+SLKGKVIG QRATLAGT+LED D+ KLYDTQENAYLDL SGR+D ILA Sbjct: 121 VDFKTDKESLKGKVIGTQRATLAGTYLEDNY-PDVEIKLYDTQENAYLDLVSGRIDGILA 179 Query: 181 DKYVNYDWLKTEAGRAYEFKGDPVVESDKIGIAVRKGDNELRNKLNAALKEIVADGTYKK 240 DKYV Y+WLK++ G +EFKG+PV++SDKIGIAVRKGD +LR+ LN AL EI ADGTYKK Sbjct: 180 DKYVQYEWLKSKDGSNFEFKGEPVMDSDKIGIAVRKGDTKLRDDLNKALAEIKADGTYKK 239 Query: 241 INDKYFPFNI 250 INDKYFPF+I Sbjct: 240 INDKYFPFSI 249 Lambda K H 0.316 0.133 0.381 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: 315 Number of extensions: 11 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: 251 Length of database: 250 Length adjustment: 24 Effective length of query: 227 Effective length of database: 226 Effective search space: 51302 Effective search space used: 51302 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 bits) S2: 46 (22.3 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 preprint 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