Align aerobic C4-dicarboxylate transport protein (characterized)
to candidate RR42_RS26105 RR42_RS26105 C4-dicarboxylate transporter
Query= CharProtDB::CH_014038 (428 letters) >lcl|FitnessBrowser__Cup4G11:RR42_RS26105 RR42_RS26105 C4-dicarboxylate transporter Length = 462 Score = 603 bits (1555), Expect = e-177 Identities = 298/411 (72%), Positives = 355/411 (86%), Gaps = 4/411 (0%) Query: 6 FKSLYFQVLTAIAIGILLGHFYPEIGEQMKPLGDGFVKLIKMIIAPVIFCTVVTGIAGME 65 ++SLYFQV+TAI IG++LGHFYP+ G MKPLGDGF+KLIKMIIAP+IFCTVV GIAGME Sbjct: 23 YRSLYFQVITAIVIGVILGHFYPQAGAAMKPLGDGFIKLIKMIIAPIIFCTVVVGIAGME 82 Query: 66 SMKAVGRTGAVALLYFEIVSTIALIIGLIIVNVVQPGAGMNVDPATLDAKAVAVYADQAK 125 MK VG+TG +ALLYFE+VS IAL++GL+I+N+ +PG GMNVD +TLD K++A Y K Sbjct: 83 DMKKVGKTGGLALLYFEVVSAIALVVGLVIINIAKPGVGMNVDVSTLDTKSIAAYTGPGK 142 Query: 126 DQGIVAFIMDVIPASVIGAFASGNILQVLLFAVLFGFALHRLGSKGQLIFNVIESFSQVI 185 QG V F++ VIP +V+ AFA G ILQVLLFAV+FGFALH+ G +G L+F+ IE FS V+ Sbjct: 143 MQGTVDFLLHVIPNTVVDAFAQGEILQVLLFAVMFGFALHKFGGRGTLVFDFIEKFSHVL 202 Query: 186 FGIINMIMRLAPIGAFGAMAFTIGKYGVGTLVQLGQLIICFYITCILFVVLVLGSIAKAT 245 F I+ IM++APIGAFGAMAFTIGKYGVG+L+QLGQL+ FY TC+ F+ +VLG IA+A Sbjct: 203 FAIVGYIMKVAPIGAFGAMAFTIGKYGVGSLLQLGQLMATFYATCLFFIFVVLGGIARAH 262 Query: 246 GFSIFKFIRYIREELLIVLGTSSSESALPRMLDKMEKLGCRKSVVGLVIPTGYSFNLDGT 305 GFSI+KFI+YI+EELLIVLGTSSSES LPRM+ K+E LG RKSVVGLVIPTGYSFNLDGT Sbjct: 263 GFSIWKFIKYIKEELLIVLGTSSSESVLPRMMAKLENLGARKSVVGLVIPTGYSFNLDGT 322 Query: 306 SIYLTMAAVFIAQATNSQMDIVHQITLLIVLLLSSKGAAGVTGSGFIVLAATLSAVGHLP 365 SIYLTMAAVFIAQATN++M + Q+TLL VLLL+SKGAAGVTGSGFIVLAATLSAVGH+P Sbjct: 323 SIYLTMAAVFIAQATNTEMSLTQQLTLLAVLLLTSKGAAGVTGSGFIVLAATLSAVGHVP 382 Query: 366 VAGLALILGIDRFMSEARALTNLVGNGVATIVVAKWVKELD----HKKLDD 412 VAGLALILGIDRFMSEARALTNL+GNGVAT+VVAKW +LD H++LD+ Sbjct: 383 VAGLALILGIDRFMSEARALTNLIGNGVATVVVAKWTGDLDVARMHRRLDN 433 Lambda K H 0.327 0.142 0.401 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: 632 Number of extensions: 20 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: 1 Length of query: 428 Length of database: 462 Length adjustment: 32 Effective length of query: 396 Effective length of database: 430 Effective search space: 170280 Effective search space used: 170280 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 (21.7 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