GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlF in Billgrantia desiderata SP1

Align ABC transporter for D-Sorbitol, permease component 2 (characterized)
to candidate WP_086510094.1 BZY95_RS11665 sugar ABC transporter permease

Query= reanno::pseudo5_N2C3_1:AO356_00020
         (308 letters)



>NCBI__GCF_002151265.1:WP_086510094.1
          Length = 325

 Score =  117 bits (294), Expect = 3e-31
 Identities = 91/301 (30%), Positives = 148/301 (49%), Gaps = 22/301 (7%)

Query: 19  RRLINPGWFLVSPSVALLLLWMIVPLAMTVYFSVIRYNLLNPGENEFVGLENFAYFVTDS 78
           R+ +   W  ++P +  L +    PL  T YFS    +L +     F+GLEN  Y V D 
Sbjct: 27  RQRVRAAWLFLAPMLVTLAMVAGWPLLRTFYFSFTDASLSDMSNTLFIGLEN--YLVYDD 84

Query: 79  GFLPGAL----------NTLILVGSVLLISVIFGVLIAALLEASEFFGRGIVRVLLISPF 128
           G   G L          NT+      + + V+FGV++A +L A EF GR +VR  ++ P+
Sbjct: 85  GRWFGVLADPIWWRAVWNTVYFSVVSVSLEVVFGVIVALVLNA-EFKGRTLVRAAVLIPW 143

Query: 129 FIMPTVGSLIFKNLIFHPVSGILAAVWKFFG--AQPVDWLA--HYPLFSIIVIVSWQWLP 184
            I PT+ S      + +   GI+  +    G  A P+ W A  +Y ++++I++  W+  P
Sbjct: 144 AI-PTIVSAQMWAWMLNDQFGIINHLLMALGIIASPIAWTADANYSMWAVIMVDVWKTTP 202

Query: 185 FAILLLMTAMQSLDQEQKEAARLDGAGALAIFWHLTLPHLARPIAVVVMIETIFLLSVFA 244
           F  LL++ A+Q L ++  EAA +DG   + +F+ +TLP +   + V V+   +  L VF 
Sbjct: 203 FVALLVLAALQMLPKDCYEAAEVDGIHPVKVFFRVTLPLITPALMVAVIFRLLDALRVFD 262

Query: 245 EIFTTTNGGPGFASTNLAYLIYNQALVQF-DVGMASAGGLIAVVIANIAAIVLVRMIGKN 303
            I+  T+      ST    +   Q LV+F DVG  SA   +  +I  +A I  + +  K 
Sbjct: 263 VIYVLTSNS---TSTMSMSIYARQQLVEFQDVGYGSAASTLLFLIIALATIAYLYLGRKQ 319

Query: 304 L 304
           L
Sbjct: 320 L 320


Lambda     K      H
   0.329    0.142    0.429 

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: 242
Number of extensions: 13
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: 308
Length of database: 325
Length adjustment: 27
Effective length of query: 281
Effective length of database: 298
Effective search space:    83738
Effective search space used:    83738
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 (21.8 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Apr 09 2024. 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