Align ABC transporter for L-Lysine, ATPase component (characterized)
to candidate AO353_25645 AO353_25645 amino acid transporter
Query= reanno::pseudo5_N2C3_1:AO356_05515 (254 letters) >FitnessBrowser__pseudo3_N2E3:AO353_25645 Length = 253 Score = 368 bits (944), Expect = e-107 Identities = 186/254 (73%), Positives = 221/254 (87%), Gaps = 1/254 (0%) Query: 1 MYKLTIEGLHKSYGEHEVLKGVSLKAKTGDVISLIGASGSGKSTFLRCINFLEQPNDGAM 60 MYKLT+E L+K +G++EVLKGVSL A+ GDV+S+IGASGSGKST LRCINFLE+ ++GA+ Sbjct: 1 MYKLTVENLYKRFGDNEVLKGVSLNARAGDVVSMIGASGSGKSTMLRCINFLERADEGAI 60 Query: 61 TLDGQPVQMIKDRHGMHVADADELQRIRTRLAMVFQHFNLWSHMTVLENITMAPRRVLGV 120 LDG+ + + GM VA+ +LQR+RTRLAMVFQHFNLWSH+TVLENI +AP +VLGV Sbjct: 61 ELDGERIVTRQAPGGMRVANPAQLQRLRTRLAMVFQHFNLWSHLTVLENIMLAPCKVLGV 120 Query: 121 SKQEADDRARRYLDKVGLPARVAEQYPAFLSGGQQQRVAIARALAMEPEVMLFDEPTSAL 180 S+++A+ AR YLDKVGLP RVAEQYPAFLSGGQQQRVAIARALA+EP+++LFDEPTSAL Sbjct: 121 SRKDAEVSARAYLDKVGLPQRVAEQYPAFLSGGQQQRVAIARALAVEPQILLFDEPTSAL 180 Query: 181 DPELVGEVLKVIQGLAEEGRTMIMVTHEMSFARKVSNQVLFLHQGLVEEEGAPEDVLGNP 240 DPELVGEVLKVIQ LAEEGRTM+MVTHEM FAR+VS+QVLFLHQG VEE+G +L P Sbjct: 181 DPELVGEVLKVIQALAEEGRTMLMVTHEMGFARQVSSQVLFLHQGRVEEQG-DATILDQP 239 Query: 241 KSERLKQFLSGNLK 254 KSERL+QFLSG LK Sbjct: 240 KSERLQQFLSGRLK 253 Lambda K H 0.319 0.135 0.380 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: 270 Number of extensions: 4 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: 254 Length of database: 253 Length adjustment: 24 Effective length of query: 230 Effective length of database: 229 Effective search space: 52670 Effective search space used: 52670 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 47 (22.7 bits)
This GapMind analysis is from Apr 09 2024. 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:
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