GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Desulfovibrio vulgaris Hildenborough

Align SmoK aka POLK, component of Hexitol (glucitol; mannitol) porter (characterized)
to candidate 208681 DVU3161 ABC transporter, ATP-binding protein

Query= TCDB::P54933
         (332 letters)



>MicrobesOnline__882:208681
          Length = 349

 Score =  284 bits (727), Expect = 2e-81
 Identities = 158/343 (46%), Positives = 214/343 (62%), Gaps = 19/343 (5%)

Query: 1   MGKITLRNVQKRFGEAVVIPSLDLDIEDGEFVVFVGPSGCGKSTLLRLIAGLEDVSDGQI 60
           M  I L  V + +G+   +  +  ++E G+ +V +GPSGCGKST LRLIAGLE V+ G+I
Sbjct: 1   MSTIVLDKVSRHWGDVRAVDDVSFEVEQGDMLVLLGPSGCGKSTTLRLIAGLESVTSGRI 60

Query: 61  MIDGRDATEMPPAKRGLAMVFQSYALYPHMTVKKNIAFPLRMAKMEPQEIERRVSNAAKI 120
           +I GRD T +PPA+R LAMVFQSYAL+PH+TV+ NI F L + K+   E ++R+  A +I
Sbjct: 61  LIGGRDVTNLPPAQRQLAMVFQSYALFPHLTVRDNILFGLVVRKVPAAERQKRLDRAVEI 120

Query: 121 LNLTNYLDRRPGQLSGGQRQRVAIGRAIVREPAAFLFDEPLSNLDAALRVNMRLEITELH 180
           L L   L+R+PG+LSGGQ+QRVA+GRA+V E A  L DEPLSNLDA LR  MR EI  L 
Sbjct: 121 LGLGKLLERKPGELSGGQQQRVALGRALVAEAAVCLMDEPLSNLDAKLRQEMRREIRALQ 180

Query: 181 QSLETTMIYVTHDQVEAMTMADKIVVLNAGRIEQVGSPLTLYRNPANLFVAGFIGSPKMN 240
           Q+L  TM+YVTHDQ EAM+MAD+I+++  GRI Q  +P  +Y  PA  F   FIG+P MN
Sbjct: 181 QTLGMTMVYVTHDQTEAMSMADRIILMQGGRIVQNATPTEMYSRPATAFAGSFIGTPPMN 240

Query: 241 LI--EGPE------AAKHGATT--------IGIRPEHIDLSREAGAWEGEVGVSEHLGSD 284
           L+  +G +       ++ G  T        +GIRPEHI +  +   W   V   E+LGS+
Sbjct: 241 LVRLQGNDDGIRVAGSRSGRVTCHAGADCMLGIRPEHIRIVDD--GWRAVVESVEYLGSN 298

Query: 285 TFLHVHVAGMPTLTVRTGGEFGVHHGDRVWLTPQADKIHRFGA 327
           + L   V G   L+V   G      G  ++L    + +H F A
Sbjct: 299 SVLSCRV-GSEELSVVVHGVTDTVVGAEIYLHCPEEHVHIFDA 340


Lambda     K      H
   0.320    0.137    0.400 

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: 334
Number of extensions: 16
Number of successful extensions: 2
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: 332
Length of database: 349
Length adjustment: 28
Effective length of query: 304
Effective length of database: 321
Effective search space:    97584
Effective search space used:    97584
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 49 (23.5 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