Align BztC, component of Glutamate/glutamine/aspartate/asparagine porter (characterized)
to candidate 206177 DVU0751 amino acid ABC transporter, permease protein, His/Glu/Gln/Arg/opine family
Query= TCDB::Q52665 (434 letters) >MicrobesOnline__882:206177 Length = 596 Score = 129 bits (325), Expect = 2e-34 Identities = 91/252 (36%), Positives = 139/252 (55%), Gaps = 19/252 (7%) Query: 187 GIGLVVAALFWLYAAAPIEAALQSALPLALPEVDSDQF----GGFLLALVIGVTAIVVSL 242 G+ V A + + I L++ L P SD+ GG +L++ V AI VS Sbjct: 346 GLLFVTARGLYNFNWGVIADNLRTLLIWHFPNGQSDELFMGLGGLAYSLLMAVIAISVSF 405 Query: 243 PLGILLALGRQSDMLIVKSLSVGIIEFVRGVPLITLLFTASLLLQYFLPP--GTNFDLIL 300 +G+++ +GR SD I + + IE +RG PLI ++F + +F+P T F++ Sbjct: 406 FIGLVVGIGRTSDNRICRIPCLLYIELIRGNPLIIVIFW----IYFFIPVLFNTFFNVFW 461 Query: 301 RVVILVTLFAAAYIAEVIRGGLAALPRGQYEAADALGLDYWQAQRLIIMPQALKISIPGI 360 I +TLF AY+AE++R G+ +P GQ EAA + GL + Q R II+PQALK IP I Sbjct: 462 SATIALTLFTGAYLAEIVRAGIQNIPAGQVEAAYSTGLTFVQTMRRIILPQALKQMIPAI 521 Query: 361 VSSFIGLFKDTTLVAFVGLFD---PLKGISNVVRSDMAWKGTYWEPYIFVALIFFLFNFS 417 V FI +FKDT+L +G+ + +GI+N + M + E Y VA ++F+ +S Sbjct: 522 VGQFIAIFKDTSLAFVLGVLELTFVAQGINNRL---MVYP---MEIYGTVAFLYFICCWS 575 Query: 418 MSRYSMYLERKL 429 MS Y+ LER+L Sbjct: 576 MSVYAARLERRL 587 Score = 79.7 bits (195), Expect = 2e-19 Identities = 50/161 (31%), Positives = 85/161 (52%), Gaps = 8/161 (4%) Query: 226 GFLLALVIGVTAIVVSLPLGILLALGRQSDMLIVKSLSVGIIEFVRGVPLITLLFTASLL 285 G + + I + + ++L LG +L + R S ++ + ++EF R PL+ LF Sbjct: 60 GLGVTVRISLISSALALGLGTVLGIARLSLFAPLRLTATAVVEFFRNTPLLVQLFFWYFA 119 Query: 286 LQYFLPPGT-------NFDLILRVVILVTLFAAAYIAEVIRGGLAALPRGQYEAADALGL 338 LP NF+ + L +++ +A++AEVIR GL ++P+G EAA + GL Sbjct: 120 FPAILPENIRELLFTGNFEFWCATIGL-SVYTSAFMAEVIRAGLQSIPKGLLEAAYSSGL 178 Query: 339 DYWQAQRLIIMPQALKISIPGIVSSFIGLFKDTTLVAFVGL 379 +Y Q R II+P A + IP + S F+ K+++L VG+ Sbjct: 179 NYVQVLRTIILPMAFRAIIPPLGSEFLNNMKNSSLAMVVGV 219 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: 744 Number of extensions: 51 Number of successful extensions: 6 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 3 Number of HSP's successfully gapped: 2 Length of query: 434 Length of database: 596 Length adjustment: 34 Effective length of query: 400 Effective length of database: 562 Effective search space: 224800 Effective search space used: 224800 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: 52 (24.6 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