GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS00885 in Desulfovibrio vulgaris Miyazaki F

Align ABC-type branched-chain amino acid transport system, permease component protein (characterized, see rationale)
to candidate 8502038 DvMF_2751 inner-membrane translocator (RefSeq)

Query= uniprot:D8IUY4
         (309 letters)



>FitnessBrowser__Miya:8502038
          Length = 301

 Score =  264 bits (674), Expect = 2e-75
 Identities = 140/311 (45%), Positives = 207/311 (66%), Gaps = 14/311 (4%)

Query: 1   MDIFIQQIINGLVLGSMYALIALGYTMVYGVLNLINFAHGDILMVGAMVGLSLLKV--VQ 58
           M+ F QQ+ NGL +G +YALIALGYTMVYGVL LINFAHGD+  +GA +G +L     + 
Sbjct: 1   MEEFFQQLTNGLAVGGIYALIALGYTMVYGVLKLINFAHGDLFTIGAYLGFTLFTAFGLS 60

Query: 59  QVAPGLPGIVQLVIAIVGAIPVCIVVSLLIERIAYRPLRNAPRLAPLITAIGVSILLQTL 118
               G  G++ +++ ++G + +   +  L+ER+AYRPLR++ RL+ +++A+G SI  Q  
Sbjct: 61  GFVSGPGGVLLVLVMVMGLVAL---IGFLLERVAYRPLRSSSRLSAVVSALGASIFFQNA 117

Query: 119 AMMIWGRSPLPFPQ-VMPSDPVHIAGALISPTQIMLLALAVLAMVGLVLIVEKTKMGRAM 177
            M+I+G     +P  + PS  + I G  +   +IM++A ++  M+ L    ++T++G A+
Sbjct: 118 VMLIYGAKFQVYPNDIRPSYVLSIMGIDVPLVRIMMIAASLGLMLALYWFTQRTRIGAAI 177

Query: 178 RATAENPRIAGLMGVDANKVIVVTFAIGAGLAAIAGVMWAANYSTAQFAMGFVPGLKAFS 237
           RATA +   A LMG+D N+VI + F IG  L  +AGVM    Y    F MG+V GLKAF+
Sbjct: 178 RATAIDQGAAKLMGIDVNRVISLVFMIGPALGGVAGVMVGLYYGQVDFTMGWVYGLKAFT 237

Query: 238 AAVLGGIGNIYGAMLGGILLGLIESLGAGYIGDLTGNFLGSNYQDIFAFIVLIIVLTLRP 297
           AA+LGGIGNI GAM+GG+LLG+IE+LGA YI           ++D  AF+VLI++L +RP
Sbjct: 238 AAILGGIGNIPGAMVGGLLLGVIEALGAAYI--------SIAWKDAIAFLVLILILIIRP 289

Query: 298 SGIMGERVADR 308
           +G++GERVAD+
Sbjct: 290 TGLLGERVADK 300


Lambda     K      H
   0.328    0.144    0.416 

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: 289
Number of extensions: 19
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: 309
Length of database: 301
Length adjustment: 27
Effective length of query: 282
Effective length of database: 274
Effective search space:    77268
Effective search space used:    77268
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 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