GapMind for catabolism of small carbon sources

 

Alignments for a candidate for sacP in Escherichia coli BW25113

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)



>FitnessBrowser__Keio:17782
          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.

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About GapMind

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:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

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