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 8501893 DvMF_2608 inner-membrane translocator (RefSeq)

Query= uniprot:D8IUY4
         (309 letters)



>FitnessBrowser__Miya:8501893
          Length = 302

 Score =  270 bits (691), Expect = 2e-77
 Identities = 142/305 (46%), Positives = 208/305 (68%), Gaps = 19/305 (6%)

Query: 4   FIQQIINGLVLGSMYALIALGYTMVYGVLNLINFAHGDILMVGAMVGLSLLKVVQQVAPG 63
           F +    GL  GS+YALIALGYTMVYG++ LINFAHG++ M+GA   L +   +     G
Sbjct: 6   FWELFFGGLTRGSIYALIALGYTMVYGIIELINFAHGEVYMMGAFTALIVAGALGIY--G 63

Query: 64  LPGIVQLVIAIVGAIPVCIVVSLLIERIAYRPLRNAPRLAPLITAIGVSILLQTLAMMIW 123
            P +  L+IA V A+  C    L +E+IAY+PLR+APRL+PLI+AIG+SI LQ   ++  
Sbjct: 64  FPALAILIIAAVVAVIYCAAYGLTLEKIAYKPLRDAPRLSPLISAIGMSIFLQNYVILAQ 123

Query: 124 GRSPLPFPQVMPS----DPV-HIAGALISPTQIMLLALAVLAMVGLVLIVEKTKMGRAMR 178
               +PFP ++P     +P+ HI GA    ++++++  + ++M  L L ++ T+MG+AMR
Sbjct: 124 TSDFMPFPNLVPQPDFLEPIAHIMGA----SEVLIIVTSAISMAALTLFIKYTRMGKAMR 179

Query: 179 ATAENPRIAGLMGVDANKVIVVTFAIGAGLAAIAGVMWAANYSTAQFAMGFVPGLKAFSA 238
           ATA+N ++A L+G+DA+KVI +TF IG+ LAA+ GV+ A++     FA+GF+ G+KAF+A
Sbjct: 180 ATAQNRKMAMLLGIDADKVISLTFVIGSSLAAVGGVLIASHVGQVNFAIGFIAGIKAFTA 239

Query: 239 AVLGGIGNIYGAMLGGILLGLIESLGAGYIGDLTGNFLGSNYQDIFAFIVLIIVLTLRPS 298
           AVLGGIG+I GAMLGG++LG  ES   GYI         S+Y+D  AF +L+++L  RPS
Sbjct: 240 AVLGGIGSIPGAMLGGLVLGWCESFATGYI--------SSDYEDALAFALLVLILIFRPS 291

Query: 299 GIMGE 303
           GI+G+
Sbjct: 292 GILGK 296


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: 304
Number of extensions: 19
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: 309
Length of database: 302
Length adjustment: 27
Effective length of query: 282
Effective length of database: 275
Effective search space:    77550
Effective search space used:    77550
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.

Links

Downloads

Related tools

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