GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS00890 in Mesorhizobium ciceri biovar biserrulae WSM1271

Align ABC transporter ATP-binding protein (characterized, see rationale)
to candidate WP_013529093.1 MESCI_RS06150 high-affinity branched-chain amino acid ABC transporter permease LivM

Query= uniprot:A0A165KER0
         (358 letters)



>NCBI__GCF_000185905.1:WP_013529093.1
          Length = 531

 Score =  250 bits (639), Expect = 5e-71
 Identities = 149/322 (46%), Positives = 196/322 (60%), Gaps = 29/322 (9%)

Query: 37  LLYVLLALGLNIVVGYAGLLDLGYVAFYAVGAYLFALMASPHLADNFAAFAAMFPNGLHT 96
           L+YV+LA GLNIVVG AGLLDLGYVAFYAVGAY +AL+ + +              GL  
Sbjct: 209 LIYVMLAWGLNIVVGLAGLLDLGYVAFYAVGAYAYALLGTQY--------------GL-- 252

Query: 97  SLWIVIPVAALLAAFFGAMLGAPTLKLRGDYLAIVTLGFGEIIRIFLNNLDHPVNLTNGP 156
           S WI++P A  +AAF+G +LG P L+LRGDYLAIVTL FGEIIR+ L N      +TNG 
Sbjct: 253 SFWILLPAAGAMAAFWGVLLGFPVLRLRGDYLAIVTLAFGEIIRLVLINWRE---VTNGS 309

Query: 157 KGLGQIDSVKVFGLD---------LGKRLEVFGFDINSVTLYYYLFLVLVVVSVIICYRL 207
            G+  I  V  FGL          + K L +           YYL L L +++  +  RL
Sbjct: 310 AGISGIPKVTFFGLMTFNVSDPNYVAKVLHLATSSAYYKIFLYYLILALALLTAFVTIRL 369

Query: 208 QDSRIGRAWMAIREDEIAAKAMGINTRNMKLLAFGMGASFGGVSGAMFGAFQGFVSPESF 267
           +   +GRAW A+REDEIA +++GINT   KL AF  GA FGG +GA F A QGFVSPESF
Sbjct: 370 RRMPVGRAWEALREDEIACRSLGINTTTTKLTAFATGAMFGGFAGAFFAARQGFVSPESF 429

Query: 268 SLMESVMIVAMVVLGGIGHIPGVILGAVLLSALPEVLRYVAGPLQAMTDGRLDSAILRQL 327
             +ES +I+A+VVLGG+G + G+ + A+++    E LR +   L+ +        + R L
Sbjct: 430 VFLESAIILAIVVLGGMGSLVGIAVAAMVMIGGTEALREL-DFLKQVFGPDFTPELYRML 488

Query: 328 LIALAMIIIMLLRPRGLWPSPE 349
           L  +AM+I+ML +PRG   S E
Sbjct: 489 LFGMAMVIVMLWKPRGFVGSRE 510


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: 472
Number of extensions: 24
Number of successful extensions: 4
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: 531
Length adjustment: 32
Effective length of query: 326
Effective length of database: 499
Effective search space:   162674
Effective search space used:   162674
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: 51 (24.3 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