GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglF' in Cereibacter sphaeroides ATCC 17029

Align Inner membrane ABC transporter permease protein (characterized, see rationale)
to candidate WP_011841071.1 RSPH17029_RS07680 sugar ABC transporter permease

Query= uniprot:A8LLL5
         (334 letters)



>NCBI__GCF_000015985.1:WP_011841071.1
          Length = 330

 Score =  439 bits (1128), Expect = e-128
 Identities = 217/325 (66%), Positives = 265/325 (81%), Gaps = 4/325 (1%)

Query: 10  TIIIGVGGCVGYFYFANQFLDKVLYPAKGPKAGRNINRANQIRPWIFLFPALFVLLLYLG 69
           TI++GV GCV YF+ AN  LD + YPA+GP+AG NI+RA+ IRPW+FL PA+ +L +YL 
Sbjct: 10  TIVVGVFGCVAYFFAANLILDAI-YPARGPRAGANISRASAIRPWLFLLPAILLLGIYLV 68

Query: 70  YPVVETLRLSLLERVPGGGYQWVGLDNYAQMASEPKFWEAMRNNMFWLIVVPALSTAFGL 129
           YPV  ++ LSL +     G ++VGL NY  + ++ KF E++RNN  WL+VVPA ST FGL
Sbjct: 69  YPVFVSIWLSLRD---ASGEEFVGLANYEWLVNDTKFRESIRNNFLWLLVVPAASTFFGL 125

Query: 130 LAAQLTDRIKWGNVAKSIIFMPMAISFVGASVIWKLVYDGRPIEQEQIGILNAIIVGLGG 189
           +AA LTDRI+WGN+AK++IFMPMAISFVGASVIWK +YD R   +E+IG+LNA+I GLGG
Sbjct: 126 VAAALTDRIRWGNLAKALIFMPMAISFVGASVIWKFIYDYRGEGREEIGLLNAVIEGLGG 185

Query: 190 DPVTFLTIPFWNNFFLMIVLVWVQTGFAMVILSAALRGIPEETIEAAIIDGASPLQIFFK 249
              T+L IPFWNNFFLM VL+W+QTGFAMVILSAALRGIPEET+EAA++DGASPLQIF +
Sbjct: 186 TEQTWLAIPFWNNFFLMAVLIWIQTGFAMVILSAALRGIPEETVEAAVLDGASPLQIFLR 245

Query: 250 IKVPQIMPTVVVVWTTITLVVLKVFDIVFAMTNGQWETQVLANYMFDKLFRANDWGVGSA 309
           IKVPQI  T+ VVWTTIT++VLKVFDIV AMTNGQW TQVLAN MFD +FR ND G  SA
Sbjct: 246 IKVPQIWGTIAVVWTTITILVLKVFDIVLAMTNGQWGTQVLANLMFDWMFRGNDAGRASA 305

Query: 310 SAMVIMLLVTPILIWNIHSARKEMR 334
            A+VIM+LVTPI+IWNI +ARKE R
Sbjct: 306 VALVIMVLVTPIMIWNIANARKETR 330


Lambda     K      H
   0.329    0.143    0.455 

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: 397
Number of extensions: 9
Number of successful extensions: 2
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: 334
Length of database: 330
Length adjustment: 28
Effective length of query: 306
Effective length of database: 302
Effective search space:    92412
Effective search space used:    92412
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 (21.8 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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