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 GFF3783 HP15_3725 PTS system, fructose-specific IIBC component
Query= TCDB::Q5V5X5 (383 letters) >lcl|FitnessBrowser__Marino:GFF3783 HP15_3725 PTS system, fructose-specific IIBC component Length = 587 Score = 273 bits (697), Expect = 1e-77 Identities = 155/344 (45%), Positives = 213/344 (61%), Gaps = 26/344 (7%) Query: 26 LMTGVSFMIPFVTIGGIFLAVAYAIGDTQAVFENTGSAGWFLAQIGVA-GLTIMVPILGG 84 L+TGVSFM+P V GG+ +A+++ G F+ G+ L QIG +M+P+L G Sbjct: 252 LLTGVSFMLPMVVAGGLLIALSFVFGIE--AFQEEGTLAAALMQIGGGTAFKLMIPLLAG 309 Query: 85 YIAYAIADRPGLAPGFLLAYILQQGNVVAEAATVIGISGGEAGAGYLGAIVAGLLAGYVA 144 YIA++IADRPGLAPG + ++ GE GAG+LG IVAG LAGYVA Sbjct: 310 YIAWSIADRPGLAPGMIGGFL-----------------AGELGAGFLGGIVAGFLAGYVA 352 Query: 145 RFF-KNLDVPEFIQPMMPVLLIPVATMAVLTPIMLFVLGVPVALANEGLTSFLQSMQGGQ 203 RF + L +PE I+ + P+L+IP+ V M++V+G P+A LT FL+ M Sbjct: 353 RFISQKLPMPESIESLKPILIIPLLASLVTGLGMIYVIGEPMAAIMGALTGFLEGMGTTN 412 Query: 204 AIVVGLILGGMMAFDMGGPVNKVAYVFATGLITEEI--YAPMAAVMIGGMIPPIGLALSN 261 AI++G ILG MM FD+GGPVNK AY F GL++E APMAA+M GM+P IG+ +++ Sbjct: 413 AILLGGILGAMMCFDLGGPVNKAAYTFGVGLLSEGSGGSAPMAAIMAAGMVPAIGMGVAS 472 Query: 262 FIAPHKYAAEMYENGKSGVVLGLSFITEGAIPYAAADPLRVIPAIVAGSAVGGATSMALG 321 FIA K+A + G++ VLGL FI+EGAIP+ A DPLRVIP + G A+ GA SM Sbjct: 473 FIARRKFAEAERQAGRASFVLGLCFISEGAIPFMAKDPLRVIPVCMIGGAITGALSMLFT 532 Query: 322 VTMPAPHGGIFVVLLSN---QPLAFLGSILLGSLVTAVVATVIK 362 V + APHGG+FV+ + N L +L +I +GSLV ++K Sbjct: 533 VKLMAPHGGLFVLAIPNAVSAVLPYLIAIAVGSLVIGFGYALLK 576 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: 841 Number of extensions: 47 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: 587 Length adjustment: 33 Effective length of query: 350 Effective length of database: 554 Effective search space: 193900 Effective search space used: 193900 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 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