GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuG in Collimonas pratensis Ter91

Align Putative maltose permease, component of MalEFG (K unknown), involved in maltose and maltodextrin uptake (characterized)
to candidate WP_061941787.1 CPter91_RS15495 carbohydrate ABC transporter permease

Query= TCDB::Q9KZ08
         (303 letters)



>NCBI__GCF_001584185.1:WP_061941787.1
          Length = 301

 Score =  147 bits (371), Expect = 3e-40
 Identities = 94/302 (31%), Positives = 153/302 (50%), Gaps = 4/302 (1%)

Query: 3   TSTAPTKAPAEQIAAPTAPPRKVRGRGERSRAASLASHGVLTLASLVALFPVAWLVYLSL 62
           TS +   + A    APT  P   R R   +    +  H VL   +++ALFP+A ++  S+
Sbjct: 2   TSISSLSSAASSAPAPTPVPLFARSRF--ANLGRIWVHVVLCAYAVIALFPIALILINSV 59

Query: 63  GPDKNDYLHPGRIWSKMTFDNYAF--VLQDTNFFDWLKSSLIVSLGTTVIGVLVAATTGY 120
                 + +P    +  +F    F  VL +TNF  +  +SL+V+LG+ V+ VL  A  G+
Sbjct: 60  KSRDAIFDNPLAFPTPDSFSLIGFEKVLHNTNFMLYFGNSLVVTLGSLVLIVLFGAMAGW 119

Query: 121 AVSRMRFPGYRKLMWVLLVTQMFPIAVLIVPMYQILSKLQLIDNYFGLILVYCSTAVPYC 180
           A+S  +F G R +   L +  M PI +  V + Q++  L LI+    LILVY +  +P  
Sbjct: 120 ALSEYKFRGNRLMALYLALGIMIPIRLGTVSILQLVVSLDLINTRTALILVYTAQGLPLA 179

Query: 181 AWLLKGYFDTIPFEIDEAGRVDGLTPFGTFFRLILPLARPGLAVAGFYSFITAFGEVAFA 240
             +L  +   IP E+ +A R DG+  F  FF++ILPL RP +A    ++ I A+ ++ F 
Sbjct: 180 VMILSEFIRQIPKELKDAARCDGVGEFKIFFQIILPLIRPAIATVAVFTMIPAWNDLWFP 239

Query: 241 STFMLSDTKYTFAVGLQSFVSEHDAQRNLMAATAVLVAIPVSAFFYLVQKNLVTGLTAGG 300
                SD   T  +G+Q F+ ++    N + A   L  IP+   + +  + L+ GLT+G 
Sbjct: 240 LILAPSDETKTVTLGVQQFIGQYVTDWNSVLAALSLAVIPILIMYVIFSRQLIRGLTSGA 299

Query: 301 TK 302
            K
Sbjct: 300 VK 301


Lambda     K      H
   0.326    0.139    0.422 

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: 260
Number of extensions: 11
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: 303
Length of database: 301
Length adjustment: 27
Effective length of query: 276
Effective length of database: 274
Effective search space:    75624
Effective search space used:    75624
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.

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