Align Tricarboxylate transport membrane protein TctA (characterized)
to candidate GFF782 PGA1_c07960 putative integral membrane protein
Query= reanno::Dino:3609738 (505 letters) >FitnessBrowser__Phaeo:GFF782 Length = 505 Score = 856 bits (2211), Expect = 0.0 Identities = 428/505 (84%), Positives = 476/505 (94%) Query: 1 MLEGLLIGLQTAFSIQNLAMVIGGCLIGTFIGMLPGLGPMSIIAIMIPVAISLGDPSAAL 60 ML+G+LIGL TAFS N+ MVIGGCLIGTFIGMLPGLGPMSII+IMIPVAIS+GDPSAAL Sbjct: 1 MLDGILIGLSTAFSFSNILMVIGGCLIGTFIGMLPGLGPMSIISIMIPVAISIGDPSAAL 60 Query: 61 ILLAGVYYGAIFGGSTSSILLNAPGVAGTVATSFDGYPMAQQGKAGKALTIAAIASFAGG 120 ILLAGVYYGAIFGGSTSSIL+NAPGVA TVATSFDGYP+A+QGKAGKALT+AAI+SF GG Sbjct: 61 ILLAGVYYGAIFGGSTSSILINAPGVASTVATSFDGYPLARQGKAGKALTVAAISSFCGG 120 Query: 121 TIGAILLMVFAPALSSVALLFHSAEYFALMVVGLSAIAAFAGTGQVAKALLMTILGLIMA 180 +IGA+LLM+FAPAL+SVALLFHSAEYFALMVVGLSAIAAFAGTGQV KALLMT+LGLIMA Sbjct: 121 SIGAVLLMIFAPALASVALLFHSAEYFALMVVGLSAIAAFAGTGQVVKALLMTVLGLIMA 180 Query: 181 TVGEGALFASPRFTMGLMDLQSGFGFITLAMAMFALPEALFLVMNPLRAASGQGGGEIKD 240 TVGEGALF PRFTMG+MDLQSGFGFITLAMAMFALPEAL+LV++P R+ + G EIKD Sbjct: 181 TVGEGALFNMPRFTMGIMDLQSGFGFITLAMAMFALPEALYLVLDPSRSKTEGGSNEIKD 240 Query: 241 LRITRAEARSIAPVIGRQSVQGFFIGVLPGAGATIASFLGYAVERNIASKDEQAEFGKGS 300 LRITRAEA+SIAPVIGRQS+QGF IGVLPGAGATIASFLGYAVERNIA K+EQ EFGKG+ Sbjct: 241 LRITRAEAKSIAPVIGRQSIQGFLIGVLPGAGATIASFLGYAVERNIAPKEEQKEFGKGA 300 Query: 301 VKGLAAPETANNAACTGSFVPLLTLGIPGSGTTAILLGALLALNVSPGPRLMIDAPEIFW 360 +KGLAAPE+ANNAACTGSFVPLLTLGIPGSGTTAILLGAL+ALNVSPGPRLM+D PEIFW Sbjct: 301 IKGLAAPESANNAACTGSFVPLLTLGIPGSGTTAILLGALIALNVSPGPRLMVDEPEIFW 360 Query: 361 AVIMSMFIGNLVLLILNLPLIPYIAKILSVPRNYLIPFILFFTLMGAYIGQNNATELLLL 420 AVI+SM++GNL+LL+LNLPLIPYIAK+L+VPRNYLIPFI FFTLMGAYIGQNNATELL+L Sbjct: 361 AVIISMYVGNLILLVLNLPLIPYIAKVLAVPRNYLIPFIFFFTLMGAYIGQNNATELLIL 420 Query: 421 VGFGICATILKFADYPLAPLLIGFILGGLLENNFSRAMQLYDGISFIWERPMTLGLLVIA 480 VG GICAT+L+FADYPLAPLLIGFILG +LE+NFSR+MQLYDG+ F+ ERPMT+GLL +A Sbjct: 421 VGLGICATVLRFADYPLAPLLIGFILGSMLEDNFSRSMQLYDGLGFLMERPMTIGLLGLA 480 Query: 481 ALLIILPSYRNRRAKARAAGVADGD 505 ALL+ILPSYR RRA+ R GVADGD Sbjct: 481 ALLVILPSYRARRARLRQRGVADGD 505 Lambda K H 0.326 0.143 0.411 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: 1011 Number of extensions: 37 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: 505 Length of database: 505 Length adjustment: 34 Effective length of query: 471 Effective length of database: 471 Effective search space: 221841 Effective search space used: 221841 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 (21.6 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:
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