GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS34240 in Photobacterium gaetbulicola Gung47

Align Monosaccharide-transporting ATPase; EC 3.6.3.17; Flags: Precursor (characterized, see rationale)
to candidate WP_044621445.1 H744_RS06410 ribose ABC transporter permease

Query= uniprot:B2T9V8
         (351 letters)



>NCBI__GCF_000940995.1:WP_044621445.1
          Length = 327

 Score =  184 bits (466), Expect = 4e-51
 Identities = 102/308 (33%), Positives = 171/308 (55%), Gaps = 12/308 (3%)

Query: 38  LRELALLPALALLIVIGAFISPSFLTKANLISVLGASAALALVVLAESLIVLTGKFDLSL 97
           L E   L AL  LIV+ +F++P+F T  N++++L  ++  A++ +  +L++LT   DLS+
Sbjct: 23  LIEQKSLIALIFLIVVVSFLNPNFFTVDNILNILRQTSVNAIIAVGMTLVILTAGIDLSV 82

Query: 98  ESTVGIAPAVGAMLVMPAASAGFGMQWPAAAGLLAIVVVGAVIGFINGFLVVRLRLNAFI 157
            S + +  A  A L+         M+ P    +   ++ GA +G I+G ++ + ++ AFI
Sbjct: 83  GSVLALCGAFAASLI--------AMEVPVMIAVPTALLAGAALGAISGVIIAKGKVQAFI 134

Query: 158 VTLAMLIVLRGMLVGATKGGTLF----DMPTSFFALATTIVLGLPLSVWLAAAAFAIAAF 213
            TL  + +LRG+ +  T G  +     D+  SF    T   +G+P+ +WL    FA   +
Sbjct: 135 ATLVTMTLLRGVTMVYTDGRPISTGFTDVADSFAWFGTGYAMGIPVPIWLMVIVFAAVWY 194

Query: 214 MLRYHRLGRALYAIGGNPEAARAAGIRVERITWGVFVLGSILASVGGLIVTGYVGAINAN 273
           +L + R GR +YA+GGN  AAR +GI V+R+  GV+ +  +LA++ G+IVT  + +    
Sbjct: 195 LLNHTRFGRYIYALGGNESAARLSGINVDRVKIGVYAICGLLAALAGIIVTSRLSSAQPT 254

Query: 274 QGNGMIFTVFAAAVIGGISLDGGKGTMFGALTGVLLLGVVQNLLTLAQVPSFWIQAIYGA 333
            G G      AA V+GG SL GGKG + G L G L++G + N L L  V S++       
Sbjct: 255 AGMGYELDAIAAVVLGGTSLAGGKGRIMGTLIGALIIGFLNNALNLLDVSSYYQMIAKAV 314

Query: 334 IILGSLMV 341
           +IL +++V
Sbjct: 315 VILLAVLV 322


Lambda     K      H
   0.326    0.140    0.397 

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: 241
Number of extensions: 12
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: 351
Length of database: 327
Length adjustment: 28
Effective length of query: 323
Effective length of database: 299
Effective search space:    96577
Effective search space used:    96577
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: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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