GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglF' in Rhizobium leguminosarum 3841

Align Inner membrane ABC transporter permease protein (characterized, see rationale)
to candidate WP_011650500.1 RL_RS03910 sugar ABC transporter permease

Query= uniprot:A8LLL5
         (334 letters)



>NCBI__GCF_000009265.1:WP_011650500.1
          Length = 337

 Score =  380 bits (976), Expect = e-110
 Identities = 189/330 (57%), Positives = 243/330 (73%), Gaps = 6/330 (1%)

Query: 8   LITIIIGVGGCVGYFYFANQFLDKVLYPAKGP--KAGRNINRANQIRPWIFLFPALFVLL 65
           L  +++ V  C  YFYF+N+ LD  L    G    A RN+NR   +RPW+F+ PALF+L+
Sbjct: 9   LSVVVVAVVACSAYFYFSNKILDLALPVKDGDIRAASRNLNRRALVRPWLFIGPALFLLI 68

Query: 66  LYLGYPVVETLRLSLLERVPGGGYQWVGLDNYAQMASEPKFWEAMRNNMFWLIVVPALST 125
           +YL YPVV T  LS  +R    G Q+VGL NY     + +F +++ NN+ WL VVPA  T
Sbjct: 69  VYLVYPVVATFILSFYDRA---GLQFVGLANYKWALGDREFRQSIFNNILWLAVVPAACT 125

Query: 126 AFGLLAAQLTDRIKWGNVAKSIIFMPMAISFVGASVIWKLVYDGRPIEQEQIGILNAIIV 185
            FGL+ A +TDRI WGN+AKSI+FMPMAISFVGASVIWK +Y+ R     QIG+LNAI+ 
Sbjct: 126 FFGLVIAVMTDRIWWGNIAKSIVFMPMAISFVGASVIWKFIYEYRGGNDVQIGLLNAIVQ 185

Query: 186 GLGGDPVTFLTIPFWNNFFLMIVLVWVQTGFAMVILSAALRGIPEETIEAAIIDGASPLQ 245
             GG P  +++IPFWNNFFLMI+L+W+QTGFAMVILSAALRGIPEETIEAA+IDGA+  Q
Sbjct: 186 TFGGTPEVWISIPFWNNFFLMIILIWIQTGFAMVILSAALRGIPEETIEAAVIDGANGWQ 245

Query: 246 IFFKIKVPQIMPTVVVVWTTITLVVLKVFDIVFAMTNGQWETQVLANYMFDKLFR-ANDW 304
           IF++I VPQ+  ++ VVWTTIT++VLKVFDIV  MTNGQW+T VLAN MFD +FR   D 
Sbjct: 246 IFWRIMVPQVWGSIAVVWTTITILVLKVFDIVLTMTNGQWQTMVLANLMFDWMFRGGGDS 305

Query: 305 GVGSASAMVIMLLVTPILIWNIHSARKEMR 334
           G  +  A++IML VTPI++WN+  A +E++
Sbjct: 306 GRSAVIAIIIMLAVTPIMVWNVRRANRELK 335


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: 415
Number of extensions: 24
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: 334
Length of database: 337
Length adjustment: 28
Effective length of query: 306
Effective length of database: 309
Effective search space:    94554
Effective search space used:    94554
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 Sep 24 2021. 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