Align neutral amino acid transporter A (characterized)
to candidate RR42_RS33745 RR42_RS33745 C4-dicarboxylate transporter
Query= CharProtDB::CH_091534 (532 letters) >lcl|FitnessBrowser__Cup4G11:RR42_RS33745 RR42_RS33745 C4-dicarboxylate transporter Length = 452 Score = 128 bits (321), Expect = 5e-34 Identities = 116/450 (25%), Positives = 198/450 (44%), Gaps = 72/450 (16%) Query: 33 RRCAGFLRRQALVLLTVSGVLAGA---GLGAALRGLSLSRTQVTYLAFPGEMLLRMLRMI 89 RR L Q L+ + +G+L G +G+AL+ L G++ +R+++M+ Sbjct: 3 RRLISSLYVQVLIAVA-AGILLGIFMPHIGSALKPL-------------GDIFIRLIKMV 48 Query: 90 ILPLVVCSLVSGAASLDA-SCLGRLGGIAVAYFGLTTLSASALAVALAFIIKPGSGAQ-- 146 P++ ++V G A +++ LGR+G A+ YF + + A L V + +++PG G Sbjct: 49 FAPIIFATVVLGIAKMESMKDLGRVGWRALLYFEVLSTFALLLGVIVVNVVQPGHGMNVD 108 Query: 147 --TLQSSDLGLEDSGPPPVPKETVDSFLDLARNLFPSNLVVAAFRTYATDYKVVTQNSSS 204 TL + + + + + +D NL P +++ A + Sbjct: 109 PATLDTKSIAAYTA------QVKHEGIMDFLLNLVPMSIMDALAKN-------------- 148 Query: 205 GNVTHEKIPIGTEIEGMNILGLVLFALVLGVALKKLGSEGEDLIRFFNSLNEATMVLVSW 264 +IL +++F++ +GVAL LG G+ + +S A +V Sbjct: 149 -----------------DILQILVFSVFMGVALAHLGERGKPFVAALDSFANAMFAIVGM 191 Query: 265 IMWYVPVG----IMFLVGSKIVEMKDIIVLVTSLGKYIFASILGHVIHGGIVLPLIYFVF 320 IM PV + F VG K + SLGK + + IVL I + Sbjct: 192 IMRVAPVAAFGAMSFTVG------KYGFGSIASLGKLVATMYGTCALFVLIVLGAICRI- 244 Query: 321 TRKNPFRFLLGLLAPFATAFATCSSSATLPSMMKCIEENNGVDKRISRFILPIGATVNMD 380 F FL + T T SS + +P +M+ +E N GV K + ++P G T N D Sbjct: 245 CGFGLFNFLKYIKDEILTVLGTSSSESVIPQLMRKLE-NVGVSKPVVGLVVPAGLTFNPD 303 Query: 381 GAAIFQCVAAVFIAQLNNVELNAGQIFTILVTATASSVGAAGVPAGGVLTIAIILEAIG- 439 G I+ +AA+FIAQ N L F +L +S G+AG+ G +T+A L ++G Sbjct: 304 GQCIYYTMAAIFIAQATNTPLTLTDQFVVLGVLLLTSKGSAGITGSGFITLAATLASLGK 363 Query: 440 LPTHDLPLILAVDWIVDRTTTVVNVEGDAL 469 +P + L+L VD + + N G+A+ Sbjct: 364 IPVAGMVLLLGVDRFMSEARAITNTIGNAV 393 Lambda K H 0.320 0.136 0.390 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: 384 Number of extensions: 15 Number of successful extensions: 2 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: 532 Length of database: 452 Length adjustment: 34 Effective length of query: 498 Effective length of database: 418 Effective search space: 208164 Effective search space used: 208164 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: 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