Align Sugar phosphotransferase system IIC component, component of Fructose-specific Enzyme I-HPr-Enzyme IIABC complex, all encoded within a single operon with genes in the order: ptsC (IIC), ptsA (IIA), ptsH (HPr), ptsI (Enzyme I) and ptsB (IIB) (characterized)
to candidate WP_008538691.1 HMPREF9454_RS06610 PTS transporter subunit EIIC
Query= TCDB::Q5V5X5 (383 letters) >NCBI__GCF_000245775.1:WP_008538691.1 Length = 458 Score = 246 bits (628), Expect = 9e-70 Identities = 136/356 (38%), Positives = 212/356 (59%), Gaps = 28/356 (7%) Query: 16 RAHVTSVKEDLMTGVSFMIPFVTIGGIFLAVAYAIGDTQAVFENTGSAGWFLAQI----G 71 +A T + + LM+GV+FM+PFV GGI +A ++ G +A N S + G Sbjct: 115 KAQQTGIYKHLMSGVNFMLPFVISGGILIAFSFMFG-IKASDPNDPSFNVIAKALSDIGG 173 Query: 72 VAGLTIMVPILGGYIAYAIADRPGLAPGFLLAYILQQGNVVAEAATVIGISGGEAGAGYL 131 A +MVP+L IAY+IA + G+ G V G+ GAG+L Sbjct: 174 GAAFGMMVPMLAAGIAYSIAGKQGMCSGM-----------------VAGVIAKSIGAGFL 216 Query: 132 GAIVAGLLAGYVAR-FFKNLDVPEFIQPMMPVLLIPVATMAVLTPIMLFVLGVPVALANE 190 G ++ + AGY+ + + + +P+ IQ + ++L+P+ ++ + M+F++G PV + Sbjct: 217 GGLIGAIFAGYLTKTLMEKIHLPKAIQTLKGLILVPLISVFITGMFMIFIVGEPVKFLLD 276 Query: 191 GLTSFLQSMQGGQAIVVGLILGGMMAFDMGGPVNKVAYVFATGLITEEIYAPMAAVMIGG 250 GLT++L SM ++ GLI+G MMA DMGGP+NK F+ L++ +YAP+AA M+ G Sbjct: 277 GLTNYLNSMDSSNGVIFGLIIGAMMASDMGGPINKAISTFSIALMSTGVYAPIAACMVAG 336 Query: 251 MIPPIGLALSNFIAPHKYAAEMYENGKSGVVLGLSFITEGAIPYAAADPLRVIPAIVAGS 310 M PP+GLAL+ + ++ E E GKS VLGLS+ITEGAIP+A ADP+RVIPA++ GS Sbjct: 337 MTPPLGLALATVLFKKRFTKEEREAGKSCWVLGLSYITEGAIPFAVADPIRVIPALMLGS 396 Query: 311 AVGGATSMALGVTMPAPHGGIFVV----LLSNQPLAFLGSILLGSLVTAVVATVIK 362 AV GA S+ G APHGGI+++ +++N P+ L +++ GS+VT + ++K Sbjct: 397 AVAGAISLGAGCASLAPHGGIWILPIPNVITNLPMYVL-ALVAGSIVTCLSVALLK 451 Lambda K H 0.322 0.139 0.399 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: 564 Number of extensions: 34 Number of successful extensions: 5 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: 383 Length of database: 458 Length adjustment: 32 Effective length of query: 351 Effective length of database: 426 Effective search space: 149526 Effective search space used: 149526 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 (21.9 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Sep 24 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