GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ac3H11_1694 in Herbaspirillum seropedicae SmR1

Align ABC transporter ATP-binding protein (characterized, see rationale)
to candidate HSERO_RS00890 HSERO_RS00890 ABC transporter ATP-binding protein

Query= uniprot:A0A165KER0
         (358 letters)



>FitnessBrowser__HerbieS:HSERO_RS00890
          Length = 404

 Score =  459 bits (1181), Expect = e-134
 Identities = 228/360 (63%), Positives = 281/360 (78%), Gaps = 24/360 (6%)

Query: 15  LLVLPLILQSFGNAWVRIADLALLYVLLALGLNIVVGYAGLLDLGYVAFYAVGAYLFALM 74
           ++V P + Q FGN+WVRI D+ALLY++LALGLN+VVG+AGLLDLGY+AFYA+GAY   L+
Sbjct: 26  MIVFPFVAQQFGNSWVRIMDVALLYIMLALGLNVVVGFAGLLDLGYIAFYAIGAYSAGLL 85

Query: 75  ASPHLADNFAAFAAMFP----------------NGLHTSLWIVIPVAALLAAFFGAMLGA 118
           ASP  A    +F   +P                NG+H SLW+++P++A LAA FGA+LGA
Sbjct: 86  ASPQFAAVIESFVNTYPSVGNFLVWLCGPEIVQNGIHLSLWLIVPISAFLAALFGALLGA 145

Query: 119 PTLKLRGDYLAIVTLGFGEIIRIFLNNLDHPVNLTNGPKGLGQIDSVKVFGLDL------ 172
           PTLKLRGDYLAIVTLGFGEIIRIF+NNL+ PVN+TNGP+G+  ID +KVFG+ L      
Sbjct: 146 PTLKLRGDYLAIVTLGFGEIIRIFMNNLNAPVNITNGPQGINLIDPIKVFGVSLAGEPGS 205

Query: 173 GKRLEVFGFDINSVTLYYYLFLVLVVVSVIICYRLQDSRIGRAWMAIREDEIAAKAMGIN 232
           G  ++VFG  + SV  YY+LFL+L +  +    RLQDSR+GRAW+AIREDEIAAKAMGIN
Sbjct: 206 GSMVKVFGMSMPSVNAYYFLFLLLCIGVIFFSVRLQDSRLGRAWVAIREDEIAAKAMGIN 265

Query: 233 TRNMKLLAFGMGASFGGVSGAMFGAFQGFVSPESFSLMESVMIVAMVVLGGIGHIPGVIL 292
           TRN+KLLAF MGASFGGV+GAMFGAFQGFVSPESFSL ES+ ++AMVVLGGIGHIPGV+L
Sbjct: 266 TRNVKLLAFAMGASFGGVAGAMFGAFQGFVSPESFSLTESIAVLAMVVLGGIGHIPGVVL 325

Query: 293 GAVLLSALPEVLRYVAGPLQAMTDGR--LDSAILRQLLIALAMIIIMLLRPRGLWPSPEH 350
           G V+L+ALPEVLR+V  P+Q    G+  +D+ +LRQLL  LAM++IML RP GLWPSP H
Sbjct: 326 GGVILAALPEVLRHVVEPVQMAIFGKVWIDAEVLRQLLYGLAMVVIMLTRPAGLWPSPRH 385


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: 507
Number of extensions: 18
Number of successful extensions: 5
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: 404
Length adjustment: 30
Effective length of query: 328
Effective length of database: 374
Effective search space:   122672
Effective search space used:   122672
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: 50 (23.9 bits)

This GapMind analysis is from Sep 17 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