Align citrate transporter (characterized)
to candidate BPHYT_RS27915 BPHYT_RS27915 major facilitator transporter
Query= CharProtDB::CH_014606 (431 letters) >lcl|FitnessBrowser__BFirm:BPHYT_RS27915 BPHYT_RS27915 major facilitator transporter Length = 439 Score = 615 bits (1585), Expect = e-180 Identities = 295/421 (70%), Positives = 351/421 (83%) Query: 2 TQQPSRAGTFGAILRVTSGNFLEQFDFFLFGFYATYIAKTFFPAESEFAALMLTFAVFGS 61 T SR+ A+LRVTSGNFLEQFDFFLFGFYAT+I+K FFP+ SEFA+LMLTFAVFG+ Sbjct: 10 TSSVSRSTRAAAVLRVTSGNFLEQFDFFLFGFYATFISKIFFPSTSEFASLMLTFAVFGA 69 Query: 62 GFLMRPIGAVVLGAYIDRIGRRKGLMITLAIMGCGTLLIALVPGYQTIGLLAPVLVLVGR 121 GFLMRP+GA+ LGAYID++GRR GL++TL+IM GT+LIA VPGY +IGLLAP LVL+GR Sbjct: 70 GFLMRPLGAIFLGAYIDKVGRRMGLIVTLSIMASGTVLIACVPGYASIGLLAPALVLLGR 129 Query: 122 LLQGFSAGVELGGVSVYLSEIATPGNKGFYTSWQSASQQVAIVVAALIGYGLNVTLGHDE 181 LLQGFSAG ELGGVSVYL+E+ATPGN+GFYTSWQSASQQVAIV+AA IGYGLN L + Sbjct: 130 LLQGFSAGAELGGVSVYLAEMATPGNRGFYTSWQSASQQVAIVMAAAIGYGLNEWLSAQQ 189 Query: 182 ISEWGWRIPFFIGCMIIPLIFVLRRSLQETEAFLQRKHRPDTREIFTTIAKNWRIITAGT 241 I WGWR+PF IGC I+P +F+LRRSLQET AF R+H P REIF+ + NWRI+ G Sbjct: 190 IGAWGWRVPFLIGCAIVPFLFMLRRSLQETAAFEARQHHPQAREIFSMLLANWRIVIGGM 249 Query: 242 LLVAMTTTTFYFITVYTPTYGRTVLNLSARDSLVVTMLVGISNFIWLPIGGAISDRIGRR 301 LL AMTTTTFY ITVYTPT+GR+VL LS DSL+VT+LV +SNF+WLPIGGA+SDRIGR+ Sbjct: 250 LLTAMTTTTFYLITVYTPTFGRSVLKLSTADSLMVTLLVAVSNFVWLPIGGAVSDRIGRK 309 Query: 302 PVLMGITLLALVTTLPVMNWLTAAPDFTRMTLVLLWFSFFFGMYNGAMVAALTEVMPVYV 361 P+L+ +++LA+ T P ++WL AP F RM +VLLWFSFFFGMYNGAMVAALTEVMP V Sbjct: 310 PLLLAVSVLAIFTAYPALSWLADAPSFARMLIVLLWFSFFFGMYNGAMVAALTEVMPAEV 369 Query: 362 RTVGFSLAFSLATAIFGGLTPAISTALVQLTGDKSSPGWWLMCAALCGLAATTMLFARLS 421 R GFSLAFSLATA+FGG TPA+ST L+Q+T DK++PG+WL AALCGL AT L+ R + Sbjct: 370 RVAGFSLAFSLATAVFGGFTPAVSTYLIQVTHDKAAPGYWLSFAALCGLCATLGLYRRRA 429 Query: 422 S 422 S Sbjct: 430 S 430 Lambda K H 0.328 0.141 0.432 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: 639 Number of extensions: 32 Number of successful extensions: 2 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 431 Length of database: 439 Length adjustment: 32 Effective length of query: 399 Effective length of database: 407 Effective search space: 162393 Effective search space used: 162393 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: 51 (24.3 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 preprint 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