GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aglF' in Sinorhizobium meliloti 1021

Align Inner membrane ABC transporter permease protein (characterized, see rationale)
to candidate SMc03062 SMc03062 alpha-glucoside ABC transporter permease

Query= uniprot:A8LLL5
         (334 letters)



>FitnessBrowser__Smeli:SMc03062
          Length = 336

 Score =  408 bits (1048), Expect = e-118
 Identities = 206/336 (61%), Positives = 259/336 (77%), Gaps = 8/336 (2%)

Query: 1   MHPAFQGLITIIIGVGGCVGYFYFANQFLDKVLYPAKGP---KAGRNINRANQIRPWIFL 57
           M      ++T++ GV  C  YF+  N  LD + +P+KG     A RN+  AN IRPW+FL
Sbjct: 1   MEQLIAAILTMVAGVLVCAAYFWSTNLVLDWI-FPSKGKFGAVASRNLRIANSIRPWLFL 59

Query: 58  FPALFVLLLYLGYPVVETLRLSLLERVPGGGYQWVGLDNYAQMASEPKFWEAMRNNMFWL 117
            PAL  L LYL YPVV+++ LSL  R   GG  +VGL NY+ M ++ +F +++ NN  WL
Sbjct: 60  APALLALTLYLVYPVVQSVWLSLHGR---GGQNFVGLSNYSWMINDGEFRQSIFNNFLWL 116

Query: 118 IVVPALSTAFGLLAAQLTDRIKWGNVAKSIIFMPMAISFVGASVIWKLVYDGRPIEQEQI 177
           +VVPALST FGL+ A LTDRI WGN+AK++IFMPMAISFVGA+VIWK +YD R    EQI
Sbjct: 117 LVVPALSTFFGLIIAALTDRIWWGNIAKTLIFMPMAISFVGAAVIWKFIYDYRAAGSEQI 176

Query: 178 GILNAIIVGLGGDPVTFLTIPFWNNFFLMIVLVWVQTGFAMVILSAALRGIPEETIEAAI 237
           G+LNAI+V LGG+P  ++T+PFWNNFFLM++L+W+QTGFAMVILSAALRGIPEETIEAA+
Sbjct: 177 GLLNAIVVALGGEPQAWITLPFWNNFFLMVILIWIQTGFAMVILSAALRGIPEETIEAAV 236

Query: 238 IDGASPLQIFFKIKVPQIMPTVVVVWTTITLVVLKVFDIVFAMTNGQWETQVLANYMFDK 297
           IDGA+  QIFFKI VPQI  T+ VVWTTIT++VLKVFDIV AMTNGQW++QVLAN MFD 
Sbjct: 237 IDGANGWQIFFKIMVPQIWGTIAVVWTTITILVLKVFDIVLAMTNGQWQSQVLANLMFDW 296

Query: 298 LFR-ANDWGVGSASAMVIMLLVTPILIWNIHSARKE 332
           +FR   D+G G+A A+VIM+LV PI+IWNI +A +E
Sbjct: 297 MFRGGGDFGRGAAIAVVIMILVVPIMIWNIRNATRE 332


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: 443
Number of extensions: 16
Number of successful extensions: 3
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: 336
Length adjustment: 28
Effective length of query: 306
Effective length of database: 308
Effective search space:    94248
Effective search space used:    94248
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 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