GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ac3H11_1694 in Belnapia rosea CPCC 100156

Align ABC transporter ATP-binding protein (characterized, see rationale)
to candidate WP_090660337.1 BLR02_RS03065 branched-chain amino acid ABC transporter ATP-binding protein/permease

Query= uniprot:A0A165KER0
         (358 letters)



>NCBI__GCF_900101615.1:WP_090660337.1
          Length = 580

 Score =  147 bits (370), Expect = 9e-40
 Identities = 108/334 (32%), Positives = 166/334 (49%), Gaps = 48/334 (14%)

Query: 13  VALLVLPLILQSFGNA-WVRIADLALLYVLLALGLNIVVGYAGLLDLGYVAFYAVGAYLF 71
           +ALL L L+L   GN  W  IA  A +Y +L  GLN++VG+AG L +GYVA  A+GAY  
Sbjct: 8   LALLALALLLPLTGNEYWALIATRACIYWVLVAGLNLIVGFAGQLAIGYVALLAIGAYTA 67

Query: 72  ALMASPHLADNFAAFAAMFPNGLHTSLWIVIPVAALLAAFFGAMLGAPTLKLRGDYLAIV 131
           ++  +  + +   AF A+              +AA   A  G ++G P L+LR  Y A+ 
Sbjct: 68  SVFTAGTVMEPLPAFVAL-------------GIAAAAGAVAGVVVGLPALRLRTFYFAMT 114

Query: 132 TLGFGEII-RIFLNNLDHPVNLTNGPKGLGQIDSVKVFGLDLGKRLEVFGFDINSVTLYY 190
           TLGF  I+ +I L   D    +T G  G+             G  L      +++   +Y
Sbjct: 115 TLGFATIVTQITLAWQD----VTGGGIGIP------------GPALPA---PMDTAWGFY 155

Query: 191 YLFLVLVVVSVIICYRLQDSRIGRAWMAIREDEIAAKAMGINTRNMKLLAFGMGASFGGV 250
           Y  L L VV       L  SR GRA +AIR+ E+AA+A GI    + ++ F    +    
Sbjct: 156 YFCLALAVVCTWATANLARSRFGRALVAIRDSEVAAEASGIAKPRLLVMIFLFAGALAAF 215

Query: 251 SGAMFGAFQGFVSPESFSLMESVMIVAMVVLGGIGHIPGVILGAVLLSALPEVLRYVAGP 310
           +G +F   Q +++P++F+   S++    +++GG G I G +LG +LL+ LPE    VA P
Sbjct: 216 AGGLFATLQTYITPDAFTFDLSLLFFIAILIGGRGSILGPLLGTILLTLLPE----VAAP 271

Query: 311 LQAMTDGRLDSAILRQLLIALAMIIIMLLRPRGL 344
           L A +            L A  +++I+L  P G+
Sbjct: 272 LAAWS----------TFLYAALLLVIVLAMPGGI 295


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: 424
Number of extensions: 24
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 3
Number of HSP's successfully gapped: 2
Length of query: 358
Length of database: 580
Length adjustment: 33
Effective length of query: 325
Effective length of database: 547
Effective search space:   177775
Effective search space used:   177775
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 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