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_RS06635 AZOBR_RS06635 sugar ABC transporter permease

Query= TCDB::Q8DU39
         (318 letters)



>FitnessBrowser__azobra:AZOBR_RS06635
          Length = 324

 Score =  199 bits (505), Expect = 1e-55
 Identities = 114/326 (34%), Positives = 179/326 (54%), Gaps = 21/326 (6%)

Query: 6   MLALLISSMLVYATPLIFTSIGGVFSERSGVVNVGLEGIMVMGAFAGVVFNIEFAHSFGK 65
           ++ LL  + +  ATPL+  +   ++SER+GVV++GLEG M+ GAF        FA +   
Sbjct: 7   VVLLLADATIRVATPLVLAAFAALYSERAGVVDIGLEGKMLAGAF--------FAAAVAS 58

Query: 66  AT--PWIAALVGGLVGLLFSLLHALATINFRADHIVSGTVLNLLAPSLAVFFVKALYNKG 123
            T  PW+         +  +L+H  A I  + + +VSG  +N+L   LA     A + +G
Sbjct: 59  YTGSPWLGLGAAVAASVALALVHGFACITHKGNQVVSGMAINILVAGLAPTLAYAWFRQG 118

Query: 124 QTDNISQSFGKFD------FPILSHIPFLGPIF---FQGTSLVAYLAVLFSVFAWFILTK 174
               +     +           LS IP  GP++       +++ +L VL  V   ++ T+
Sbjct: 119 GQTPLLPGEARLPQIHLPGVEALSGIPVFGPVYRELIDDANVLIWLTVLLVVATHWVFTR 178

Query: 175 TKFGLRLRSVGEHPQAADTLGINVYLMRYLGVMISGLLGGIGGAIYAQSISVNFAGTTIL 234
           ++FGLRLR+VGE+P A DT G++V  +RY  V+I+G+L GI GA  + +    F      
Sbjct: 179 SRFGLRLRAVGENPSAVDTAGLSVTRLRYQAVIITGVLTGIAGAYLSTAHGAGFVRDMTA 238

Query: 235 GPGFIALAAMIFGKWNPIGAMLSSLFFGLSQSLAV--IGGQLPFLSKIPTVYLQIAPYAL 292
           G G++ALAA+IFGKW P   + + L F  + ++ V   G  LP +  IP  ++Q+ PY L
Sbjct: 239 GKGYLALAALIFGKWRPWPTLFACLLFAFTDAVQVRLQGVPLPVVGVIPVQFIQMLPYVL 298

Query: 293 TILVLAVFFGQAVAPKADGINYIKSK 318
           T+L+LA F G+AVAPKA G+ Y+K +
Sbjct: 299 TVLLLAGFVGRAVAPKASGVPYVKER 324


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: 260
Number of extensions: 20
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: 324
Length adjustment: 28
Effective length of query: 290
Effective length of database: 296
Effective search space:    85840
Effective search space used:    85840
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