Align C4-dicarboxylate transport protein 2 (characterized)
to candidate RR42_RS26105 RR42_RS26105 C4-dicarboxylate transporter
Query= SwissProt::Q9I4F5 (436 letters) >lcl|FitnessBrowser__Cup4G11:RR42_RS26105 RR42_RS26105 C4-dicarboxylate transporter Length = 462 Score = 615 bits (1587), Expect = 0.0 Identities = 306/420 (72%), Positives = 355/420 (84%) Query: 4 QPFYKSLYVQVLVAIAIGIALGHWYPETAVAMKPFGDGFVKLIKMAIAPIIFCTVVTGIA 63 +PFY+SLY QV+ AI IG+ LGH+YP+ AMKP GDGF+KLIKM IAPIIFCTVV GIA Sbjct: 20 KPFYRSLYFQVITAIVIGVILGHFYPQAGAAMKPLGDGFIKLIKMIIAPIIFCTVVVGIA 79 Query: 64 GMQSMKSVGKTGGMALLYFEVVSTVALIIGLVVVNVVQPGAGMHVDPNTLDTSKIAAYAA 123 GM+ MK VGKTGG+ALLYFEVVS +AL++GLV++N+ +PG GM+VD +TLDT IAAY Sbjct: 80 GMEDMKKVGKTGGLALLYFEVVSAIALVVGLVIINIAKPGVGMNVDVSTLDTKSIAAYTG 139 Query: 124 AGEKQSTVDFLMNVIPGTVVGAFANGDILQVLFFSVLFGYALHRLGSYGKPVFEFIERVS 183 G+ Q TVDFL++VIP TVV AFA G+ILQVL F+V+FG+ALH+ G G VF+FIE+ S Sbjct: 140 PGKMQGTVDFLLHVIPNTVVDAFAQGEILQVLLFAVMFGFALHKFGGRGTLVFDFIEKFS 199 Query: 184 HVMFNIINVIMKVAPIGAFGAMAFTIGAYGVGSLVQLGQLMLCFYITCILFVLIVLGGIA 243 HV+F I+ IMKVAPIGAFGAMAFTIG YGVGSL+QLGQLM FY TC+ F+ +VLGGIA Sbjct: 200 HVLFAIVGYIMKVAPIGAFGAMAFTIGKYGVGSLLQLGQLMATFYATCLFFIFVVLGGIA 259 Query: 244 RAHGFSILRFIRYIREELLIVLGTSSSESALPRMIDKMEKLGCNKSVVGLVIPTGYSFNL 303 RAHGFSI +FI+YI+EELLIVLGTSSSES LPRM+ K+E LG KSVVGLVIPTGYSFNL Sbjct: 260 RAHGFSIWKFIKYIKEELLIVLGTSSSESVLPRMMAKLENLGARKSVVGLVIPTGYSFNL 319 Query: 304 DGTSIYLTMAAVFIAQATDTPMDITHQITLLLVLLIASKGAAGVTGSGFIVLAATLSAVG 363 DGTSIYLTMAAVFIAQAT+T M +T Q+TLL VLL+ SKGAAGVTGSGFIVLAATLSAVG Sbjct: 320 DGTSIYLTMAAVFIAQATNTEMSLTQQLTLLAVLLLTSKGAAGVTGSGFIVLAATLSAVG 379 Query: 364 HLPVAGLALILGIDRFMSEARALTNLVGNGVATVVVSKWCKQLDEGTLQRELAGEGNASS 423 H+PVAGLALILGIDRFMSEARALTNL+GNGVATVVV+KW LD + R L E +A + Sbjct: 380 HVPVAGLALILGIDRFMSEARALTNLIGNGVATVVVAKWTGDLDVARMHRRLDNESDAEA 439 Lambda K H 0.325 0.140 0.406 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: 705 Number of extensions: 24 Number of successful extensions: 1 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: 436 Length of database: 462 Length adjustment: 33 Effective length of query: 403 Effective length of database: 429 Effective search space: 172887 Effective search space used: 172887 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.0 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.6 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