Align Sucrose porter, IIBC (SacP) (55% identical to 4.A.1.2.1) (characterized)
to candidate 17782 b3722 fused beta-glucoside-specific PTS enzymes: IIA component/IIB component/IIC component (NCBI)
Query= TCDB::P05306 (461 letters) >lcl|FitnessBrowser__Keio:17782 b3722 fused beta-glucoside-specific PTS enzymes: IIA component/IIB component/IIC component (NCBI) Length = 625 Score = 236 bits (603), Expect = 1e-66 Identities = 132/413 (31%), Positives = 217/413 (52%), Gaps = 4/413 (0%) Query: 5 ETAKRLIELLGGKENIISAAHCATRLRLVMKDESKIDQAQVEELDGVKGAFSSSGQYQII 64 E A++++ +GG +NI+S HCATRLR +KDESK +++ G+ S GQ+Q++ Sbjct: 3 ELARKIVAGVGGADNIVSLMHCATRLRFKLKDESKAQAEVLKKTPGIIMVVESGGQFQVV 62 Query: 65 FGTGLVNKVFDAFSKEADIEREEHVNHQDAAKEKLNPAARFAKTLSNIFVPIIPAIVASG 124 G + + VF A + A ++ E +K N RF +S IF P+I + A+G Sbjct: 63 IGNHVAD-VFLAVNSVAGLD--EKAQQAPENDDKGNLLNRFVYVISGIFTPLIGLMAATG 119 Query: 125 LLMGLLGMINAFHWMSKDSALLQLLDMFSSAAFIFLPILIGVSASKEFGSNPYLGAVIGG 184 +L G+L + F W ++ S +L S A F F PI++G +A K FG NP+ VIGG Sbjct: 120 ILKGMLALALTFQWTTEQSGTYLILFSASDALFWFFPIILGYTAGKRFGGNPFTAMVIGG 179 Query: 185 IMIHPNLLNPWGLAE-ATPDYMHLFGFDIALLGYQGTVIPVLLAVYVMSKVEKWTRKVVP 243 ++HP +L + + A + G + LL Y +VIP++ + ++ S +E+ +P Sbjct: 180 ALVHPLILTAFENGQKADALGLDFLGIPVTLLNYSSSVIPIIFSAWLCSILERRLNAWLP 239 Query: 244 HAVDLLVTPFVTVIVTGFVAFIAIGPLGRALGSGITVALTYVYDHAGFVAGLIFGGTYSL 303 A+ TP + ++V V F+ +GPL + I ++Y AG + GG + + Sbjct: 240 SAIKNFFTPLLCLMVITPVTFLLVGPLSTWISELIAAGYLWLYQAVPAFAGAVMGGFWQI 299 Query: 304 IVLTGVHHSFHAIEAGLIADIGKNYLLPIWSMANVAQGGAGLAVFFMAKKAKTKEIALPA 363 V+ G+H + +G + ++P+ A +AQ GA L VF + A+ K +A A Sbjct: 300 FVMFGLHWGLVPLCINNFTVLGYDTMIPLLMPAIMAQVGAALGVFLCERDAQKKVVAGSA 359 Query: 364 AFSAFLGITEPVIFGVNLRYRKPFIAAMIGGALGGAYVVFTHVAANAYGLTGI 416 A ++ GITEP ++GVNL + PF+ A I GALG + + ++GL I Sbjct: 360 ALTSLFGITEPAVYGVNLPRKYPFVIACISGALGATIIGYAQTKVYSFGLPSI 412 Lambda K H 0.325 0.140 0.411 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: 765 Number of extensions: 40 Number of successful extensions: 4 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: 461 Length of database: 625 Length adjustment: 35 Effective length of query: 426 Effective length of database: 590 Effective search space: 251340 Effective search space used: 251340 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.0 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.6 bits) S2: 52 (24.6 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