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_RS08280 HSERO_RS08280 leucine/isoleucine/valine transporter permease subunit

Query= uniprot:A0A165KER0
         (358 letters)



>FitnessBrowser__HerbieS:HSERO_RS08280
          Length = 408

 Score =  259 bits (663), Expect = 7e-74
 Identities = 156/355 (43%), Positives = 213/355 (60%), Gaps = 46/355 (12%)

Query: 15  LLVLPLILQSFGN-AWVRIADLALLYVLLALGLNIVVGYAGLLDLGYVAFYAVGAYLFAL 73
           LL+  L+   FG+  +V +  LAL+YV+L LGLNIVVG+AGLLDLGYV FYAVGAY +AL
Sbjct: 87  LLMAALVWPFFGSRGYVDVMTLALIYVVLGLGLNIVVGFAGLLDLGYVGFYAVGAYTYAL 146

Query: 74  MASPHLADNFAAFAAMFPNGLHTSLWIVIPVAALLAAFFGAMLGAPTLKLRGDYLAIVTL 133
                       F   F        W  +P+AA  +A FG +LG P L+LRGDYLAIVTL
Sbjct: 147 CNQ--------YFGLTF--------WECVPLAAAASALFGFLLGFPVLRLRGDYLAIVTL 190

Query: 134 GFGEIIRIFLNNLDHPVNLTNGPKGLGQIDSVKVFGLDLGKRL---------EVFGFDIN 184
           GFGEIIR+ LNN+    ++T GP G+  I    VFGL + +           ++FG    
Sbjct: 191 GFGEIIRLLLNNM---TSITGGPDGVSGIPKPTVFGLVMARNPVTEGGTTFHQLFGLSYQ 247

Query: 185 S---VTLYYYLFLVLVVVSVIICYRLQDSRIGRAWMAIREDEIAAKAMGINTRNMKLLAF 241
               V   Y+L L++V+ +  +  RL    +GRAW A+REDEIA +++GIN   +KL AF
Sbjct: 248 GGHMVIFLYFLALLMVLFTYFVTSRLLRMPMGRAWEALREDEIACRSLGINPTKVKLSAF 307

Query: 242 GMGASFGGVSGAMFGAFQGFVSPESFSLMESVMIVAMVVLGGIGHIPGVILGAVLLSALP 301
            +GA+F G++G+ F A QG V+PESF+ +ES +I+A+VVLGG+G   GVIL A+LL+ LP
Sbjct: 308 TLGAAFAGLAGSFFAARQGLVTPESFTFIESALILAIVVLGGMGSQLGVILAAILLTVLP 367

Query: 302 EVLRYVAGPLQAMTDGRLDSAILRQLLIALAMIIIMLLRPRGLWPSPEHGKSLTQ 356
           E+ R                A  R L+  L M+++M+ RP+GL P+      L Q
Sbjct: 368 ELAR--------------SFAEYRMLIFGLVMVLMMMWRPQGLLPATRPHVELPQ 408


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: 378
Number of extensions: 19
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 358
Length of database: 408
Length adjustment: 30
Effective length of query: 328
Effective length of database: 378
Effective search space:   123984
Effective search space used:   123984
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