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_017223098.1 A923_RS0118060 PTS fructose transporter subunit IIBC
Query= TCDB::Q5V5X5 (383 letters) >NCBI__GCF_000276805.1:WP_017223098.1 Length = 586 Score = 285 bits (728), Expect = 3e-81 Identities = 153/355 (43%), Positives = 220/355 (61%), Gaps = 24/355 (6%) Query: 20 TSVKEDLMTGVSFMIPFVTIGGIFLAVAYAIGDTQAVFENTGSAGWFLAQIGV-AGLTIM 78 T + LMTGVS M+P V GG+ +A+++ G F+ G+ L IG + +M Sbjct: 249 TGAYKHLMTGVSHMLPLVVAGGLAIALSFVFGIE--AFKEEGTLAAALMTIGGGSAFALM 306 Query: 79 VPILGGYIAYAIADRPGLAPGFLLAYILQQGNVVAEAATVIGISGGEAGAGYLGAIVAGL 138 +P+L G+IA++IADRPGLAPG + G ++A + GAG+LG IVAG Sbjct: 307 IPVLAGFIAFSIADRPGLAPGLI-------GGMLASST----------GAGFLGGIVAGF 349 Query: 139 LAGYVARFF-KNLDVPEFIQPMMPVLLIPVATMAVLTPIMLFVLGVPVALANEGLTSFLQ 197 LAGY A+ + + +P+ ++ + P+L+IP+ + +M++V+G PV+ A LT FL Sbjct: 350 LAGYTAKLIAEKVQLPQSMEALKPILIIPLLASLITGLVMIYVVGGPVSAAMNALTEFLN 409 Query: 198 SMQGGQAIVVGLILGGMMAFDMGGPVNKVAYVFATGLITEEIYAPMAAVMIGGMIPPIGL 257 +M A+++G+ILG MM FD+GGPVNK AY F GL+ + YAPMAAVM GM+P +G+ Sbjct: 410 NMGSANAVLLGIILGSMMCFDLGGPVNKTAYTFGVGLLASQTYAPMAAVMAAGMVPALGM 469 Query: 258 ALSNFIAPHKYAAEMYENGKSGVVLGLSFITEGAIPYAAADPLRVIPAIVAGSAVGGATS 317 L+ F+A K+ E GK+ VLGL FI+EGAIP+AA DP+RVIP+ +AG A+ GA S Sbjct: 470 GLATFLAKRKFNGSEQEAGKASFVLGLCFISEGAIPFAARDPMRVIPSCIAGGALTGALS 529 Query: 318 MALGVTMPAPHGGIFVVLLSN---QPLAFLGSILLGSLVTAVVATVIKPDFEDRV 369 M G + APHGG+FV+L+ N +L +I G+LVT V V+K E V Sbjct: 530 MLFGAELMAPHGGLFVLLIPNAITPVFMYLVAIAAGTLVTGVSYAVLKQSEEKSV 584 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: 740 Number of extensions: 46 Number of successful extensions: 8 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: 383 Length of database: 586 Length adjustment: 33 Effective length of query: 350 Effective length of database: 553 Effective search space: 193550 Effective search space used: 193550 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: 51 (24.3 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