GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nupC' in Azospirillum brasilense Sp245

Align RnsD, component of The (deoxy)ribonucleoside permease; probably takes up all deoxy- and ribonucleosides (cytidine, uridine, adenosine and toxic analogues, fluorocytidine and fluorouridine tested), but not ribose or nucleobases (characterized)
to candidate AZOBR_RS31890 AZOBR_RS31890 ABC transporter permease

Query= TCDB::Q8DU39
         (318 letters)



>FitnessBrowser__azobra:AZOBR_RS31890
          Length = 305

 Score =  134 bits (336), Expect = 4e-36
 Identities = 100/326 (30%), Positives = 157/326 (48%), Gaps = 35/326 (10%)

Query: 4   ENMLALLISS-----MLVYATPLIFTSIGGVFSERSGVVNVGLEGIMVMGAFAGVVFNIE 58
           + +L +L+S+     +L  ATP I  ++G +  ER+GV+N+G+EGIM MGA AG      
Sbjct: 3   QTILDILVSAAFWTAVLRIATPYILGTLGELLCERAGVLNLGIEGIMTMGAMAG------ 56

Query: 59  FAHSFGKATPWIAALVGGLVGLLFSLLHALATINFRADHIVSGTVLNLLAPSLAVFFVKA 118
           +   +  A  W   LV  L G L  LLHA  T+       V+G  + LL  SL+ F  + 
Sbjct: 57  WMAVYQGADLWTGVLVAALCGGLMGLLHATLTVPLGLSQHVAGIGVTLLGTSLSYFVYRL 116

Query: 119 LYNKGQTDNISQSFGKFDFP-ILSHIPFLGPIFFQGTSLVAYLAVLFSVFAWFILTKTKF 177
           +  +  T    + F   D P  L+  P            + Y+A++      ++L +T  
Sbjct: 117 VLPQASTPPTIEPFQPLDLPGALAQTP------------MTYMALMLVAVVAYVLYRTPV 164

Query: 178 GLRLRSVGEHPQAADTLGINVYLMRYLGVMISGLLGGIGGAIYAQSISVNFAGTTILGPG 237
           GL +R VGE+P AA+  G++V  +R   V+    L  + GA    S    F    + G G
Sbjct: 165 GLAVRMVGENPAAAEAQGLSVTAVRIGAVVAGSALMALAGAFLTLSAFNAFFFNMVNGRG 224

Query: 238 FIALAAMIFGKWNPIGAMLSSLFFGLSQSL-----AVIGGQLPFLSKIPTVYLQIAPYAL 292
           +I +A ++F  W P  A+L ++ F    +L      V GG LP+      ++L + PY L
Sbjct: 225 WICIALVVFASWRPGKALLGAVLFAAFDALQLRLQQVAGGVLPY-----QLFLMM-PYLL 278

Query: 293 TILVLAVFFGQAVAPKADGINYIKSK 318
           +IL L +   +A  P+A  I Y K +
Sbjct: 279 SILALVLVARRASYPRALMIPYRKGE 304


Lambda     K      H
   0.328    0.143    0.422 

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: 230
Number of extensions: 14
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: 318
Length of database: 305
Length adjustment: 27
Effective length of query: 291
Effective length of database: 278
Effective search space:    80898
Effective search space used:    80898
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 (21.7 bits)
S2: 48 (23.1 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