GapMind for catabolism of small carbon sources

 

Alignments for a candidate for potA in Cupriavidus basilensis 4G11

Align PotG aka B0855, component of Putrescine porter (characterized)
to candidate RR42_RS37305 RR42_RS37305 sulfate ABC transporter ATP-binding protein

Query= TCDB::P31134
         (377 letters)



>FitnessBrowser__Cup4G11:RR42_RS37305
          Length = 366

 Score =  241 bits (616), Expect = 2e-68
 Identities = 142/326 (43%), Positives = 198/326 (60%), Gaps = 13/326 (3%)

Query: 31  GQHAVDDVSLTIYKGEIFALLGASGCGKSTLLRMLAGFEQPSAGQIMLDGVDLSQVPPYL 90
           G  A+D VSL++ +GE+  LLG SGCGK+TLLR++AG E+   G+I   G +L+ +PP  
Sbjct: 27  GFQALDGVSLSVAQGELLCLLGPSGCGKTTLLRIIAGLEREDTGRIHAGGRELTGLPPQA 86

Query: 91  RPINMMFQSYALFPHMTVEQNIAFGLKQDKLPKAEIASRVNEMLGLVHMQEFAKRKPHQL 150
           R   ++FQSYALFP+++V +N+A+GL+   + +A   +RV EML LV +    ++ P QL
Sbjct: 87  RDYGILFQSYALFPNLSVARNVAYGLQGRGMGRAHREARVAEMLSLVGLAGSERKFPGQL 146

Query: 151 SGGQRQRVALARSLAKRPKLLLLDEPMGALDKKLRDRMQLEVVDILERVGVTCVMVTHDQ 210
           SGGQ+QRVALAR+LA  P LLLLDEPM ALD ++R+ ++LE+  +  R+ VT VMVTHDQ
Sbjct: 147 SGGQQQRVALARALAPAPSLLLLDEPMSALDARVREHLRLELRQLQRRLNVTTVMVTHDQ 206

Query: 211 EEAMTMAGRIAIMNRGKFVQIGEPEEIYEHPTTRYSAEFIGSVNVFEGVLKERQEDGLVL 270
           +EAM MA RIA+M  G+  Q+G P EIYE P + + AEFIG  N  +G L  R       
Sbjct: 207 DEAMAMADRIAVMEGGRIAQVGTPGEIYERPASAFVAEFIGQANWLDGRLSGRD-----T 261

Query: 271 DSPGLVHPLKVDADASVVDNVPVHVALRPEKIMLCEEPPANGCNFAVGEVIHIAYLGDLS 330
            S G +      A AS V +    +  RPE I L   P     N  +  ++   YLG  S
Sbjct: 262 FSVGELDLAVSPARASEVADGAARLCCRPEAIRL--HPVEGEPNRLLARIVDQTYLG--S 317

Query: 331 VYHVRLKS----GQMISAQLQNAHRH 352
            Y + L++    G  + A +    RH
Sbjct: 318 RYRLMLEADRLPGHTLFADVLREERH 343


Lambda     K      H
   0.321    0.137    0.400 

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: 356
Number of extensions: 19
Number of successful extensions: 1
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: 377
Length of database: 366
Length adjustment: 30
Effective length of query: 347
Effective length of database: 336
Effective search space:   116592
Effective search space used:   116592
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (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