Align IIC' aka PtsC2, component of N-Acetylglucosamine (NAG) porter (PtsBC1C2)(also may facilitate xylose transport) (characterized)
to candidate 15742 b1621 fused maltose and glucose-specific PTS enzymes: IIB component -! IIC component (NCBI)
Query= TCDB::Q8GBT6 (403 letters) >FitnessBrowser__Keio:15742 Length = 530 Score = 229 bits (585), Expect = 1e-64 Identities = 145/424 (34%), Positives = 231/424 (54%), Gaps = 44/424 (10%) Query: 5 QRIGRSLMLPVAVLPAAALLVRLGNA----------DMLGRPEFPAFVTKIAGFMAAGGN 54 Q++G++ MLPVA+L +++ +G++ +LG P A T +M+ G+ Sbjct: 16 QQLGKTFMLPVALLSFCGIMLGIGSSLSSHDVITLIPVLGNPVLQAIFT----WMSKIGS 71 Query: 55 AILDNMALLFAVGIAIGFAKKSDGSTALAAVVGYLVFKNVLATF--TDKNL-----PQVA 107 + ++F + I +G A+++ G A A +GY V N+ F T+K + V Sbjct: 72 FAFSFLPVMFCIAIPLGLARENKGVAAFAGFIGYAVM-NLAVNFWLTNKGILPTTDAAVL 130 Query: 108 KAVDGKVVMVDAPVDAKVLGGVVMGLVVALLYQRFYRTKLPDWAGFFGGRRLVPILSAFA 167 KA + + ++ +D +LG V+ G++V +L++RF+ +LPD FFGG R VPI+S+ Sbjct: 131 KANNIQSILGIQSIDTGILGAVIAGIIVWMLHERFHNIRLPDALAFFGGTRFVPIISSLV 190 Query: 168 GLVIGIVFGYIWPVLGTGLHNFGEWLVGSGAVGAGIFGVANRALIPIGMHHLLNSFPWF- 226 ++G+V +WP+ G+ G + +G G +FG R L+P G+HH+L + F Sbjct: 191 MGLVGLVIPLVWPIFAMGISGLGHMINSAGDFGPMLFGTGERLLLPFGLHHILVALIRFT 250 Query: 227 QAG---EYEGK--SGDIARFLAG---------DPTAGQFMT-GFFPIMMFALPAACLAIV 271 AG E G+ SG + F A +A +F++ G P + LP A LA+ Sbjct: 251 DAGGTQEVCGQTVSGALTIFQAQLSCPTTHGFSESATRFLSQGKMPAFLGGLPGAALAMY 310 Query: 272 HCARPERRKVVGGMMFSLALTSFVTGVTEPIEFTFMFIAPVLYAIHAVLTGVSMALTWAL 331 HCARPE R + G++ S + V G TEP+EF F+F+APVLY IHA+LTG+ + L Sbjct: 311 HCARPENRHKIKGLLISGLIACVVGGTTEPLEFLFLFVAPVLYVIHALLTGLGFTVMSVL 370 Query: 332 GMKDGFGFSAGAVDFFLNLGI---ASNPWGLA-LVGVCFAALYYVVFRFAITKFNLPTPG 387 G+ G + G + F+ GI S W + +V + +YYV+FRFAIT+FNL TPG Sbjct: 371 GVT--IGNTDGNIIDFVVFGILHGLSTKWYMVPVVAAIWFVVYYVIFRFAITRFNLKTPG 428 Query: 388 RESD 391 R+S+ Sbjct: 429 RDSE 432 Lambda K H 0.328 0.143 0.441 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: 672 Number of extensions: 37 Number of successful extensions: 3 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: 403 Length of database: 530 Length adjustment: 33 Effective length of query: 370 Effective length of database: 497 Effective search space: 183890 Effective search space used: 183890 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 paper from 2022 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