GapMind for catabolism of small carbon sources

 

Alignments for a candidate for manMFS in Cupriavidus basilensis 4G11

Align D-mannose and D-mannitol transporter (characterized)
to candidate RR42_RS30395 RR42_RS30395 MFS transporter

Query= reanno::pseudo5_N2C3_1:AO356_28540
         (430 letters)



>FitnessBrowser__Cup4G11:RR42_RS30395
          Length = 422

 Score =  202 bits (515), Expect = 1e-56
 Identities = 125/418 (29%), Positives = 207/418 (49%), Gaps = 9/418 (2%)

Query: 7   SLIIIMLFLAGVINYLDRSALSVAAPFIQKDYGLSTGEMGMIFSSFFVGYAAFNFIGGWA 66
           S+++ ML +   I YLDR  +S AA    +++ LS  E+G++FS+F   Y  F  IGGW 
Sbjct: 8   SVVLGMLCIMYFITYLDRVNVSTAAAGFGQEFNLSKTEIGLVFSAFAYPYLVFQIIGGWV 67

Query: 67  ADRYGAKTTLLLAMVLWSLFSGLTVLTVGFASLVLIRILFGMGEGPLSVTTSKMVNNWYT 126
           +DR+GAK TL++  VLW+  + LT    G  SL+  R+L G+GEG      +  +  W  
Sbjct: 68  SDRFGAKRTLMVCGVLWAAATLLTGFAGGLVSLLAARLLLGLGEGATFPAATAAMARWVP 127

Query: 127 PKRRARAIGASMSGTPLGGAISGPVVGFIAVTYGWKISFIIIMLIGLVWAAVWFKFVKER 186
            ++R  A G + +   +G A++   V  I   YGW+ SF I   I LVW A+W     E 
Sbjct: 128 KEKRGFAQGITHACARVGNAVAPAAVVAIMAVYGWRESFYICGAISLVWVALWAVTFTEH 187

Query: 187 PEGE---GAEDILRAEGQGELAAQPVFPLRFYLKQPTVLFTSLAFFSYNYTLFFFLTWFP 243
           P+        ++       + AA   +   F    P     ++ +F Y +TL+ FL+W P
Sbjct: 188 PKDHPRMTPAELETLPAPRKKAADVPWRRLFKRMAP----VTIVYFCYGWTLWLFLSWIP 243

Query: 244 SYLTMAHGLNVKDMSIATVIPWVLGFLGLALGGFISDFVFKKTGRMMFSRKVVLVTCLLA 303
            Y   ++ L++K  +I     +  G +G  LGG ++D ++ +TG +  +R  ++  C+L 
Sbjct: 244 QYFLHSYDLDLKKSAIFASAVFFAGVIGDTLGGVVTDKLYDRTGSLKRARSAMVAVCMLL 303

Query: 304 CAVCIACAGMVTTLYPAVILVALAVFFLYLTGAIYWAIIQDTVPAARVGGVSGFMHFLAN 363
             + +        LY ++  +A   FF  +T    WAI  D  P    G  SG M+  + 
Sbjct: 304 TMLSLLPLLFTHNLYVSMACLAAGFFFAEMTIGPMWAIPMDIAP-EHSGTASGMMNSGSA 362

Query: 364 TSGIVGPTLTGFLVQFTGSFTSAFLLAGLLTVIGAVCVARYVKPLSVADTGNAAAQSP 421
            + I+ P L+G+L+   GS+   F+ + +L  +G +   R ++P S  +   A A  P
Sbjct: 363 LAAIISPVLSGYLIDRFGSWELPFIGSMVLMGVGVILALR-MQPESKFEAEPADASKP 419


Lambda     K      H
   0.329    0.142    0.439 

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: 500
Number of extensions: 26
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: 430
Length of database: 422
Length adjustment: 32
Effective length of query: 398
Effective length of database: 390
Effective search space:   155220
Effective search space used:   155220
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: 51 (24.3 bits)

This GapMind analysis is from Sep 17 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