Align ABC-type branched-chain amino acid transport system, ATPase component protein (characterized, see rationale)
to candidate WP_036831855.1 N784_RS02455 ABC transporter ATP-binding protein
Query= uniprot:D8J1T6 (255 letters) >NCBI__GCF_000775615.1:WP_036831855.1 Length = 507 Score = 123 bits (308), Expect = 9e-33 Identities = 76/239 (31%), Positives = 128/239 (53%), Gaps = 12/239 (5%) Query: 5 LLKIRDVSKRFGGLQALNGVGITIERGQIYGLIGPNGAGKTTFFNVITGLYQPDTGTFEL 64 ++++ ++ K F G+ A N V + ++ G+I+ L+G NGAGK+T NV+ GLYQP+ G ++ Sbjct: 4 VIEMLNIRKEFPGIVANNNVNLQVKPGEIHALLGENGAGKSTLMNVLFGLYQPEQGEIKV 63 Query: 65 DGKPYSPSAPHEVAKAGIARTFQNIRLFGEMTVLENVMVGCHVRTKQNVFGAVFRHKAAR 124 G+ + + P+ + GI Q+ L TV EN+++G K G V KA + Sbjct: 64 KGETVNITNPNVANELGIGMVHQHFMLVDTFTVTENIILGMEPTKK----GTVNVAKAEK 119 Query: 125 EEEAAIREKSQKLLDFVGIGQFAKRTARHLSYGDQRRLEIARALATDPQLLALDEPAAGM 184 E ++E S++ G+ + +S G Q+R+EI + L +L DEP A + Sbjct: 120 E----VKEISER----YGLKVDPSAKIQDISVGMQQRVEILKTLYRGADILIFDEPTAVL 171 Query: 185 NATEKLGLRELLVKIQAEGKTILLIEHDVKLMMGLCNRITVLDYGKPIAEGVPADVQKN 243 E L +++ + EGK+I+LI H +K +M +C+R TV+ G+ I AD N Sbjct: 172 TPQEISELMDIMGTLVKEGKSIILITHKLKEIMEVCDRCTVIRKGEGIGTVNVADTSTN 230 Score = 83.2 bits (204), Expect = 1e-20 Identities = 58/236 (24%), Positives = 122/236 (51%), Gaps = 16/236 (6%) Query: 6 LKIRDVSKRFGGLQALNGVGITIERGQIYGLIGPNGAGKTTFFNVITGLYQPDTGTFELD 65 L+++D + + + G+ + + G+I G+ G +G G++ I GL ++G+ L+ Sbjct: 262 LQVKDARQ----INMVKGLNLQVRAGEIVGIAGVDGNGQSELIEAIAGLRNVESGSITLN 317 Query: 66 GKPYSPSAPHEVAKAGIARTFQNIRLFG---EMTVLENVMVGCHVRTKQNVFGAVFRHKA 122 GK + +P +V ++G+A Q+ +G + + EN+++ + + + G V R+K Sbjct: 318 GKEITNLSPRKVTESGVAHIPQDRHKYGLVLDFPIGENMVLQTYYQQPYSKKG-VLRYKE 376 Query: 123 AREEEAAIREKSQKLLDFVGIGQFAKRT-ARHLSYGDQRRLEIARALATDPQLLALDEPA 181 I +K++ L++ + + T AR LS G+Q++ I R L P LL +P Sbjct: 377 -------IYKKAKSLIEEFDVRTPNEYTLARSLSGGNQQKAIIGRELDRSPDLLIAAQPT 429 Query: 182 AGMNATEKLGLRELLVKIQAEGKTILLIEHDVKLMMGLCNRITVLDYGKPIAEGVP 237 G++ + + L++ + GK +LL+ ++ +M + +RI V+ G+ +A +P Sbjct: 430 RGLDVGAIEFIHQRLIEARDSGKAVLLLSFELDEIMNVSDRIAVMFDGQVVANVLP 485 Lambda K H 0.320 0.138 0.394 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: 299 Number of extensions: 16 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: 2 Length of query: 255 Length of database: 507 Length adjustment: 29 Effective length of query: 226 Effective length of database: 478 Effective search space: 108028 Effective search space used: 108028 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 (21.8 bits) S2: 49 (23.5 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