GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PS417_11895 in Rhizobium leguminosarum bv. trifolii WSM1325

Align Inositol transport system permease protein (characterized)
to candidate WP_003562293.1 RLEG_RS23605 ABC transporter permease

Query= reanno::WCS417:GFF2333
         (340 letters)



>NCBI__GCF_000023185.1:WP_003562293.1
          Length = 354

 Score =  197 bits (501), Expect = 3e-55
 Identities = 125/329 (37%), Positives = 187/329 (56%), Gaps = 23/329 (6%)

Query: 25  SIFLVLIGIGLVFELFGWIVRDQSFLMN---SQRLVLMILQVSIIGLLAIGVTQVIITTG 81
           S  L L+ +     LF  I+    F  N   +  ++LM   V++   LA+G+T VIIT G
Sbjct: 17  SALLTLMKLRTFIALFAVIIFFAIFAPNFTSTANMILMSKHVALNAFLAMGMTFVIITGG 76

Query: 82  IDLSSGSVLALSAMIAASLAQTS---DFSRAVFPSLTDLPVWIPVAMGLGVGLLAGAING 138
           IDLS GS++ L  M+A  L            +F +L ++     V + + +GLL G ING
Sbjct: 77  IDLSVGSIVGLCGMVAGGLILYGIELPIGYTIFFNLFEI-----VLITVSIGLLIGLING 131

Query: 139 SIIAVTGIPPFIATLGMMVSARGLARYYTEGQPVSML-------SDSYTAIGHG---AMP 188
            +I    + PFIATLG +  ARGLA   ++GQ    L       +  +   G G    +P
Sbjct: 132 LLITKLNVAPFIATLGTLYIARGLALLSSDGQTFPNLVGRPEYATTGFDFFGAGRILGLP 191

Query: 189 VIIFL--VVAVIFHIALRYTKYGKYTYAIGGNMQAARTSGINVKRHLIIVYSIAGLLAGL 246
           V I++  V+A++     R T  G++ +A+GGN +AAR SGI V    I VY  +GL A +
Sbjct: 192 VSIWILIVLALLAAYVARSTPIGRHIFAVGGNERAARMSGIRVDVVKIFVYMFSGLCAAI 251

Query: 247 AGVVASARAATGQAGMGMSYELDAIAAAVIGGTSLAGGVGRITGTVIGALILGVMASGFT 306
            GVV S+         G S+EL+AIAAAV+GGTS++GG G I GT+IGA ++G+++ G  
Sbjct: 252 VGVVISSELMAAHPATGESFELNAIAAAVLGGTSMSGGRGTIGGTIIGAFVIGILSDGLV 311

Query: 307 FVGVDAYIQDIIKGLIIVVAVVIDQYRNK 335
            +GV ++ Q +IKGL+I++AVV+DQ + +
Sbjct: 312 MMGVSSFWQMVIKGLVIIIAVVVDQAQRR 340


Lambda     K      H
   0.325    0.140    0.394 

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: 306
Number of extensions: 18
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: 340
Length of database: 354
Length adjustment: 29
Effective length of query: 311
Effective length of database: 325
Effective search space:   101075
Effective search space used:   101075
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.0 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 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