Align ABC transporter for Xylitol, periplasmic substrate-binding component (characterized)
to candidate WP_037455519.1 N825_RS19130 sugar ABC transporter substrate-binding protein
Query= reanno::Dino:3607125 (447 letters) >NCBI__GCF_000576635.1:WP_037455519.1 Length = 458 Score = 531 bits (1368), Expect = e-155 Identities = 255/441 (57%), Positives = 334/441 (75%), Gaps = 12/441 (2%) Query: 10 SAAVASVMASGAMADGHGWSLKDAAAPYAGTTVDVVFLLRPGYEAIEAMLPAFEEETGIK 69 +A +++ ++S AMA W+L++AA PY GT++ +FL RPGY A +LP FE++TGIK Sbjct: 23 TAIMSTALSSSAMA----WTLEEAAQPYKGTSIKAIFLDRPGYAAAIKLLPEFEKKTGIK 78 Query: 70 VNVIKHPYENALGEQVRDFVAGGDLDVALIDLVWIGSFAENEWILPLADVQAKFPDA--V 127 VN PYEN+ QV DF GG++DV L D+VWIG FA N W+ P V+ DA Sbjct: 79 VNYEIVPYENSRERQVLDFTGGGEIDVVLTDVVWIGEFAGNGWLEP---VKTFTDDAKLA 135 Query: 128 DPDLDIDDFFPLVLNAFGGWNDTIYGLPFDNYSGLMFYNRCMLEEAGFDGPPSTWEELKD 187 DP L +D FFP++L +FG W D +YGLPFDNYSGL++YN+C L++AGFD PP+TW+EL + Sbjct: 136 DPKLKLDGFFPILLESFGTWGDEVYGLPFDNYSGLLYYNKCTLQQAGFDKPPATWDELLN 195 Query: 188 VYGPALTKDG--KYAFALQSKRNETQSADSFARMLWPFGGSFLNEEFRSNLMSEGSQAGL 245 VYGP LT KYAFALQS+R ETQSADSF R+LWPFGGS L+++F+SNL S+ SQAGL Sbjct: 196 VYGPKLTDQANRKYAFALQSRRGETQSADSFMRVLWPFGGSLLDDKFKSNLNSKESQAGL 255 Query: 246 KFRQELMEYMPDGIVAYDHAETVNAFSQGDVAMITEWSAFYSSVVSPETSRVADCVEIAP 305 KFRQ+LM+ MP GIV YDHAE VNA +QG+VAMITEWSAFYS++ P SR+ DC+ +A Sbjct: 256 KFRQDLMKIMPPGIVDYDHAEAVNALAQGNVAMITEWSAFYSTLADPTKSRITDCLAVAT 315 Query: 306 EPMGPAGRKPALGGFSLAVASQADEAEQAAAYLFIQWATSKANAREYLERGGVPARQSVY 365 EP GPAG KPALGGFSL V +Q+ +A++AAA+LFIQW TS+ A+ Y+E GGV R ++Y Sbjct: 316 EPAGPAGLKPALGGFSLGVNAQSSDAKKAAAWLFIQWVTSEEMAKPYVEAGGVSGRTTIY 375 Query: 366 QQDGLEE-FKFVPALVESWQDGVPEFRPRFAEWPEITEIVQEWGTKMMLGEVTTEEGAQE 424 + +++ + FV +V SW GVP+FRPRFAEWPE++E++ EWGT+MMLG V+ E+GA+ Sbjct: 376 KDADIQKRYPFVQPMVASWDGGVPDFRPRFAEWPELSEVIAEWGTRMMLGNVSIEDGAKS 435 Query: 425 IGTRMEEVLDAAGYYSGEKPL 445 IG ++EEVL AGYY G+KPL Sbjct: 436 IGAKVEEVLGQAGYYKGDKPL 456 Lambda K H 0.317 0.134 0.406 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: 626 Number of extensions: 21 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: 447 Length of database: 458 Length adjustment: 33 Effective length of query: 414 Effective length of database: 425 Effective search space: 175950 Effective search space used: 175950 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 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