GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_12060 in Phaeobacter inhibens BS107

Align ABC transporter permease; SubName: Full=Monosaccharide ABC transporter membrane protein, CUT2 family; SubName: Full=Sugar ABC transporter permease (characterized, see rationale)
to candidate GFF2276 PGA1_c23080 ribose transport system permease protein RbsC

Query= uniprot:A0A1N7UKA9
         (325 letters)



>FitnessBrowser__Phaeo:GFF2276
          Length = 324

 Score =  183 bits (465), Expect = 4e-51
 Identities = 106/305 (34%), Positives = 176/305 (57%), Gaps = 4/305 (1%)

Query: 22  LDRFGLPLVFILLCVVMAFSSEYFMTWRNWMDILRQTSINGILAVGMTYVILTKGIDLSV 81
           L + G+ + F L  +    ++  F+T  N+ +++R ++I G++A+G+T+V+++  +DLSV
Sbjct: 13  LAKQGILIAFALFIIGFTIANPKFLTLDNFENVVRSSAILGVMALGVTFVVISGNLDLSV 72

Query: 82  GSILAFAGLCSAMVATQGYGLLAAVSAGMFAGAMLGVVNGFMVANLSIPPFVATLGMLSI 141
           GS+++F+ +   +      G   A+ A       LG + GF+V  L +   + TLGMLS 
Sbjct: 73  GSMMSFSTIV-VLDLHDKLGPTLAIPAMFAMTLCLGALIGFLVGYLKLNSLIVTLGMLSA 131

Query: 142 ARGMTFILNDGS--PITDLPDAYLAL-GIGKIGPIGVPIIIFAVVALIFWMVLRYTTYGR 198
             G+T   + G    I D    + A+ G G I  I  PI+IF  +A +  ++L  T +GR
Sbjct: 132 IHGLTLTYSGGKNMDIADKEGTWFAIFGQGNILGIQTPILIFIALAALLGIILAKTPFGR 191

Query: 199 YVYAVGGNEKSARTSGIGVRKVMFSVYVVSGLLAGLAGVVLSARTTSALPQAGVSYELDA 258
            VYAVGGN  +A  SGI   +V+F  Y++S L    AG++ ++R+  +    G   EL+ 
Sbjct: 192 KVYAVGGNGTAATFSGIRRARVVFLCYIMSALCVATAGLIQASRSMGSQNTVGQGLELEV 251

Query: 259 IAAVVIGGTSLSGGTGSIVGTLFGALLIGVINNGLNLLGVSSYYQQVAKGLIIVFAVLID 318
           +AAV++GG SL GG+G+I  T+ G L++G I NGL L+G+    Q V   +II+ AV +D
Sbjct: 252 LAAVILGGASLLGGSGTIFKTVIGVLILGFIQNGLLLVGLDFSVQYVVTWIIIILAVWLD 311

Query: 319 VWRKK 323
           +  K+
Sbjct: 312 IAAKR 316


Lambda     K      H
   0.326    0.141    0.412 

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: 254
Number of extensions: 19
Number of successful extensions: 3
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: 325
Length of database: 324
Length adjustment: 28
Effective length of query: 297
Effective length of database: 296
Effective search space:    87912
Effective search space used:    87912
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 (21.6 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