GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livM in Methylocella silvestris BL2

Align ABC transporter ATP-binding protein (characterized, see rationale)
to candidate WP_012589118.1 MSIL_RS00335 branched-chain amino acid ABC transporter permease

Query= uniprot:A0A165KER0
         (358 letters)



>NCBI__GCF_000021745.1:WP_012589118.1
          Length = 282

 Score =  133 bits (335), Expect = 5e-36
 Identities = 110/333 (33%), Positives = 160/333 (48%), Gaps = 65/333 (19%)

Query: 18  LPLILQSFGNAWVRIADLALLYV--LLALGLNIVVGYAGLLDLGYVAFYAVGAYLFALMA 75
           +P  L  F   W   + +A L V  LLAL + +V+   G L LG  AF  +GAY  AL++
Sbjct: 1   MPAALDDF--LWTYQSLIASLGVNGLLALSMYVVLAI-GQLSLGQAAFMGLGAYASALLS 57

Query: 76  SPHLADNFAAFAAMFPNGLHTSLW--IVIPVAALLAAFFGAMLGAPTLKLRGDYLAIVTL 133
                             LH+ L   +V+  A L+ A F  ++GAPTL+L G YLA+ T+
Sbjct: 58  ------------------LHSGLPFPLVLAAATLIPAAFALVIGAPTLRLSGVYLALATI 99

Query: 134 GFGEIIRIFLNNLDHPVNLTNGPKGLGQIDSVKVFGLDLGKRLEVFGFDINSVTLYYYLF 193
           G GEI+RIFL   D    LT G  GL  I +   F L  G                    
Sbjct: 100 GLGEILRIFLIQSD----LTGGALGLSGIPAKAGFALIYG-------------------C 136

Query: 194 LVLVVVSVIICYRLQDSRIGRAWMAIREDEIAAKAMGINTRNMKLLAFGMGASFGGVSGA 253
           L  V +++++  R   SR+GRA  AIREDE AA   G++    K+ A  + A   G++GA
Sbjct: 137 LAAVTLALMLIAR---SRVGRAMEAIREDETAAAVSGVDLPRYKMAALVVSAMLAGLAGA 193

Query: 254 MFGAFQGFVSPESFSLMESVMIVAMVVLGGIGHIPGVILGAVLLSALPEVLRYVAGPLQA 313
           +      F+ P  +    +V I++  +LGG+G   G + GA++L+ LPE+LR    PLQ 
Sbjct: 194 LNAHASSFIGPNDYGFDAAVTILSYALLGGVGSPFGPLAGALVLTLLPEILR----PLQD 249

Query: 314 MTDGRLDSAILRQLLIALAMIIIMLLRPRGLWP 346
                      R ++    ++I +L  P GL P
Sbjct: 250 ----------FRLVVNGAIIVIAVLYMPHGLIP 272


Lambda     K      H
   0.328    0.144    0.430 

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: 247
Number of extensions: 15
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: 358
Length of database: 282
Length adjustment: 27
Effective length of query: 331
Effective length of database: 255
Effective search space:    84405
Effective search space used:    84405
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 (21.7 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