GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_12060 in Collimonas pratensis Ter91

Align ABC transporter permease; SubName: Full=Monosaccharide ABC transporter membrane protein, CUT2 family; SubName: Full=Sugar ABC transporter permease (characterized, see rationale)
to candidate WP_061936170.1 CPter91_RS01725 ABC transporter permease

Query= uniprot:A0A1N7UKA9
         (325 letters)



>NCBI__GCF_001584185.1:WP_061936170.1
          Length = 327

 Score =  250 bits (639), Expect = 3e-71
 Identities = 133/309 (43%), Positives = 193/309 (62%), Gaps = 16/309 (5%)

Query: 32  ILLCVVMAFSSEYFMTWRNWMDILRQTSINGILAVGMTYVILTKGIDLSVGSILAFAGLC 91
           ++L +V + +S+ F T  N M +  Q +   IL +G T VI+T GIDLSVGS+LA AG+ 
Sbjct: 19  VVLGLVFSLTSDAFFTLNNGMSVALQVTSIAILGIGATCVIITGGIDLSVGSVLALAGVI 78

Query: 92  SAMVATQGYGLLAAVSAGMFAGAMLGVVNGFMVANLSIPPFVATLGMLSIARGMTFILND 151
           +AMV   G  +   +  G+  GA+ G +NG  +  L +PPF+ATLGM+ +ARG+   +  
Sbjct: 79  AAMVVKAGMPVPVGMLCGLAVGAVCGGLNGLCITQLKLPPFIATLGMMLVARGVALQVTG 138

Query: 152 GSPITDLPDAYLALGIGKI--------GP--------IGVPIIIFAVVALIFWMVLRYTT 195
             P++ LP+ +  LG G +        GP        I  P+I+  V+A++  ++L  T 
Sbjct: 139 ARPVSGLPEEFGTLGNGTLFRIVKETTGPFPDVVFPGIPYPVILMVVIAIVISIMLSRTQ 198

Query: 196 YGRYVYAVGGNEKSARTSGIGVRKVMFSVYVVSGLLAGLAGVVLSARTTSALPQAGVSYE 255
           +GR++YAVG N ++AR SG+ V +V    YV+SG LAGL G VL +R  +A P  GV YE
Sbjct: 199 FGRHIYAVGSNAEAARLSGVKVARVTLWTYVISGTLAGLTGCVLMSRLVTAQPNEGVMYE 258

Query: 256 LDAIAAVVIGGTSLSGGTGSIVGTLFGALLIGVINNGLNLLGVSSYYQQVAKGLIIVFAV 315
           LDAIA+ VIGGTSL GG G+I GT  G+ +IG++ NGLN+ GVSS+ QQ+  GL+I+  V
Sbjct: 259 LDAIASAVIGGTSLIGGIGTISGTAIGSFVIGILRNGLNMNGVSSFVQQIIIGLVILLTV 318

Query: 316 LIDVWRKKK 324
            ID  R ++
Sbjct: 319 WIDQMRNRR 327


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: 253
Number of extensions: 10
Number of successful extensions: 2
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: 327
Length adjustment: 28
Effective length of query: 297
Effective length of database: 299
Effective search space:    88803
Effective search space used:    88803
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 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