GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nupC' in Sinorhizobium meliloti 1021

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 SMc04125 SMc04125 ABC transporter permease

Query= TCDB::Q8DU39
         (318 letters)



>FitnessBrowser__Smeli:SMc04125
          Length = 323

 Score =  212 bits (540), Expect = 8e-60
 Identities = 120/329 (36%), Positives = 189/329 (57%), Gaps = 17/329 (5%)

Query: 1   MSLENMLALLISSMLVYATPLIFTSIGGVFSERSGVVNVGLEGIMVMGAFAGVVFNIEFA 60
           M   ++L +L+ S +  + PL+F ++ G+F+ER+GV ++GLEG M+  AFA        A
Sbjct: 1   MDFFHVLVVLLESTIRVSVPLVFAALAGLFTERAGVFDIGLEGKMLGAAFAAG------A 54

Query: 61  HSFGKATPWIAALVGGLVGLLFSLLHALATINFRADHIVSGTVLNLLAPSLAVFFVKALY 120
            +    + W+      LV +  SL+H  A+I  R + IVSG  +N +     V   +A +
Sbjct: 55  AAAVTQSVWVGLGAAILVSVALSLVHGYASITQRGNQIVSGVAINFIVAGSTVILGEAWF 114

Query: 121 NKG-QTDNISQS--FGKFDFP---ILSHIPFLGPIF---FQGTSLVAYLAVLFSVFAWFI 171
            +G +T  +++   F   +FP   ++  IP LGP++     G  L+ YLA      +W+I
Sbjct: 115 RQGGRTPALAEGARFQTINFPDADMIREIPVLGPVYADLLSGHFLLTYLAFAMVPISWWI 174

Query: 172 LTKTKFGLRLRSVGEHPQAADTLGINVYLMRYLGVMISGLLGGIGGAIYAQSISVNFAGT 231
           L +T+FGLRLR+VGE+P A DT GI+V  +RY  V+  G+L G  GA  + +++  F   
Sbjct: 175 LYRTRFGLRLRAVGENPGAVDTAGISVIWLRYRAVICCGILCGFAGAYLSLAMTAGFVKG 234

Query: 232 TILGPGFIALAAMIFGKWNPIGAMLSSLFFGLSQSLAV--IGGQLPFLSKIPTVYLQIAP 289
              G G+IALAA+IF KW P+  M + L FG   +LA+   G  LP + ++P   +Q  P
Sbjct: 235 MTAGKGYIALAALIFAKWRPLNIMFACLLFGFLDALAIRLQGTPLPLVGQVPVQLMQALP 294

Query: 290 YALTILVLAVFFGQAVAPKADGINYIKSK 318
           Y LT+++LA F G+A+ PKA G+ Y+K +
Sbjct: 295 YILTVILLAGFIGKAIPPKAGGVPYVKER 323


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: 267
Number of extensions: 12
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: 323
Length adjustment: 28
Effective length of query: 290
Effective length of database: 295
Effective search space:    85550
Effective search space used:    85550
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