Align Branched chain amino acid ABC transporter substrate-binding protein (characterized, see rationale)
to candidate WP_088757359.1 CEJ45_RS22985 branched-chain amino acid ABC transporter substrate-binding protein
Query= uniprot:A0A165KTD4 (375 letters) >NCBI__GCF_002213425.1:WP_088757359.1 Length = 378 Score = 367 bits (942), Expect = e-106 Identities = 192/369 (52%), Positives = 248/369 (67%), Gaps = 6/369 (1%) Query: 9 VVAAIAAAAGVASAQE-QVVKIGHVAPVSGAQAHYGKDNENGARMAIEELNAQGVTIGGK 67 + A++A A AQE QVVKIG +P++G QA GKDN+ G MA+E LNAQ +T+GGK Sbjct: 11 IAASLALIPAFAMAQETQVVKIGFSSPLTGPQASAGKDNQGGLMMAVERLNAQPITVGGK 70 Query: 68 KIKFELVAEDDAADPKQGTAAAQKLCDAKVAGVVGHLNSGTTIPASKVYNDCGIPHVTGA 127 KIKFE++AEDD ADPKQG A AQKL D V +VG NSG TIPAS+VYND GI T Sbjct: 71 KIKFEVIAEDDQADPKQGVAVAQKLADQGVKAIVGPYNSGVTIPASRVYNDAGIVVAT-V 129 Query: 128 ATNPNLTKPGYKTTFRIIANDNALGAGLAFYAVDTLKLKTVAIIDDRTAYGQGVADVFKK 187 A+NP +T+ G+ T FR+ A+D+ LG +A YA LKLK VA+IDDRTAYGQG+A+ F K Sbjct: 130 ASNPKITQQGFATLFRVAASDSQLGGKMALYAAKELKLKRVAVIDDRTAYGQGLAEEFAK 189 Query: 188 TATAKGMKVVDEQFTTDKATDFMAILTAIKAKNPDAIFYGGMDPQGGPMLRQMEQLGMGN 247 A A G++V+ + FT DKATDF AILT+IK K PDA+F GG PQGGP+ RQM+QLG+ + Sbjct: 190 VAKANGIEVISKDFTNDKATDFTAILTSIKGKKPDAVFLGGYAPQGGPIKRQMKQLGI-D 248 Query: 248 VKYFGGDGICTSEIAKLAAGAKTLG-NVICAEGGSSLAKMPGGTAWKAKYDAKYPNQFQV 306 V GGDGIC+ E+ +L G +G V C +GG+ L K G + Y K+ + Sbjct: 249 VPLMGGDGICSPEMGRL--GGDAIGETVYCTQGGTMLDKAKDGKVFADDYQKKFSRPAET 306 Query: 307 YSPYTYDATFLIVDAMKRANSVDPKVYTPELAKSSFKGVTSTIAFEPNGEMKNPAITLYV 366 Y+ YD LI AMK++NSV+PK + P LAK S+KGV F+ N ++K +T+Y Sbjct: 307 YAVSFYDGMMLIAQAMKQSNSVEPKTFGPALAKISYKGVAGQYDFDENHDLKQSPVTVYR 366 Query: 367 YKDGKKTPL 375 +KDG PL Sbjct: 367 FKDGLPVPL 375 Lambda K H 0.315 0.131 0.375 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: 447 Number of extensions: 17 Number of successful extensions: 4 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 1 Length of query: 375 Length of database: 378 Length adjustment: 30 Effective length of query: 345 Effective length of database: 348 Effective search space: 120060 Effective search space used: 120060 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: 42 (22.0 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Sep 24 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:
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