Align BztC, component of Glutamate/glutamine/aspartate/asparagine porter (characterized)
to candidate SMc02120 SMc02120 general L-amino acid transport permease ABC transporter protein
Query= TCDB::Q52665 (434 letters) >lcl|FitnessBrowser__Smeli:SMc02120 SMc02120 general L-amino acid transport permease ABC transporter protein Length = 384 Score = 300 bits (768), Expect = 5e-86 Identities = 181/437 (41%), Positives = 242/437 (55%), Gaps = 60/437 (13%) Query: 2 SDTSFVRTEMLAPRPAPVSQVGAIKWMRENLFSGPLNTALTVFGLLATVWLVQAAAPWL- 60 + SFVR M+ PAP + GA+ W+R+NLF+ P +TALT+ LL WLV A WL Sbjct: 4 NQASFVRASMIEASPAPSLESGAVSWLRKNLFATPKDTALTIISLLILAWLVPPAIQWLF 63 Query: 61 LHGVWNANSLTECRAIIAERWGPEA-TGACWAVIRVRWNQFLFGFYPVDQYWRLFVTFAG 119 + W+ C + PE +GACWA + ++ QFLFG YP+D+ Sbjct: 64 IDAAWSGGGRGVCATLSQGGSQPEGWSGACWAFVNAKFAQFLFGRYPLDER--------- 114 Query: 120 LFLALAPVLFDALPRKLIWGTLLYPLAAFWLLWGGPIWGPVSVLAGFAILGLLFTALAPK 179 W P A++G+LF L Sbjct: 115 -------------------------------------WRP-------ALVGILFVLLLVP 130 Query: 180 LGVPVSAGIGLVVAALFWLYAAAPIEAALQSALPLALPEVDSDQFGGFLLALVIGVTAIV 239 + +P GL AL L A + A L L V++ +GG ++ LV+ I Sbjct: 131 MLIPRIPYKGL--NALLLLVALPILSAILLPGGWFGLTYVETPLWGGLMVTLVLSFVGIA 188 Query: 240 VSLPLGILLALGRQSDMLIVKSLSVGIIEFVRGVPLITLLFTASLLLQYFLPPGTNFDLI 299 VSLPLGILLALGR+S+M ++K L IE +RGVPLIT+LF AS++L FLP G FD Sbjct: 189 VSLPLGILLALGRRSNMPVIKMLCTVFIEVIRGVPLITVLFMASVMLPLFLPQGVTFDKF 248 Query: 300 LRVVILVTLFAAAYIAEVIRGGLAALPRGQYEAADALGLDYWQAQRLIIMPQALKISIPG 359 LR +I V+LFA+AY+AEV+RGGL A+P+GQYE AD+LGL +WQ I++PQALK+ IPG Sbjct: 249 LRALIGVSLFASAYMAEVVRGGLQAIPKGQYEGADSLGLSFWQKMGFIVLPQALKLVIPG 308 Query: 360 IVSSFIGLFKDTTLVAFVGLFDPLKGISNVVRSDMAWKG--TYWEPYIFVALIFFLFNFS 417 IV++FIGLFKDT+LV+ +G+FD L GI + SD W T IF +F+LF F Sbjct: 309 IVNTFIGLFKDTSLVSIIGMFD-LLGIVRLNFSDTNWATAVTPLTGLIFAGFVFWLFCFG 367 Query: 418 MSRYSMYLERKLKRDHR 434 MSRYS ++ER L R R Sbjct: 368 MSRYSGFMERLLDRSQR 384 Lambda K H 0.329 0.143 0.457 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: 604 Number of extensions: 30 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: 434 Length of database: 384 Length adjustment: 31 Effective length of query: 403 Effective length of database: 353 Effective search space: 142259 Effective search space used: 142259 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 (21.8 bits) S2: 50 (23.9 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