GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Desulfovibrio vulgaris Miyazaki F

Align MtlK, component of The polyol (mannitol, glucitol (sorbitol), arabitol (arabinitol; lyxitol)) uptake porter, MtlEFGK (characterized)
to candidate 8502259 DvMF_2969 ABC transporter related (RefSeq)

Query= TCDB::O30494
         (367 letters)



>FitnessBrowser__Miya:8502259
          Length = 418

 Score =  219 bits (558), Expect = 1e-61
 Identities = 123/309 (39%), Positives = 177/309 (57%), Gaps = 3/309 (0%)

Query: 2   ANLKIKNLQKGFEGFSIIKGIDLEVNDKEFVVFVGPSGCGKSTLLRLIAGLEEVSEGTIE 61
           A+L +  L K FE F+ +  +  EV    F   +GPSGCGK+TLLR+IAG E    G I 
Sbjct: 27  ADLSVTRLVKRFEKFTAVNDVSFEVEQGRFFSILGPSGCGKTTLLRMIAGFESPDSGVIA 86

Query: 62  LDGRDITEVTPAKRDLAMVFQTYALYPHMSVRKNMSFALDLAGVDKQLVESKVNEAARIL 121
           + GRD+  + P +R + ++FQ  AL+P MSV +N++F L   G+    +  +V +    +
Sbjct: 87  IRGRDMAGIAPNRRPVNLIFQHLALFPMMSVAENVAFGLKRRGMAGGEISRRVQDVLERV 146

Query: 122 ELGPLLERKPKQLSGGQRQRVAIGRAIVRNPKIFLFDEPLSNLDAALRVQMRLELARLHK 181
            L     + P QLSGGQ+QRVAI R +V  P + L DEPL  LD  LR QM++EL  L  
Sbjct: 147 GLPGYGVKMPAQLSGGQKQRVAIARCLVLEPAVLLLDEPLGALDLKLREQMKVELKTLQA 206

Query: 182 ELQATMIYVTHDQVEAMTLADKVVVLNSGRIEQVGSPLELYHQPANLFVAGFLGTPKMGF 241
           E+  T +Y+THDQ EA+ ++D V V+N+GR EQV +P  LY +PA+ FVAGF+G  +   
Sbjct: 207 EVGTTFVYITHDQSEALVMSDHVAVMNAGRFEQVDTPRNLYRRPASAFVAGFVG--ETNV 264

Query: 242 LKGKVTRVDGQGCEVQLDAGTLISLPLSGASLSVGSAVTLGIRPEHLEIASPGQTTLTVT 301
             G +    G    V+ D G +    ++ A L+ G+ V + IRPE + I   G +  T  
Sbjct: 265 WSGTLEEATGDAGLVRTDEGAVFRARVA-AGLAKGTRVDMFIRPEAVLIDPDGASCATDG 323

Query: 302 ADVGERLGS 310
           A  G   G+
Sbjct: 324 ATDGATDGA 332


Lambda     K      H
   0.319    0.137    0.387 

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: 380
Number of extensions: 16
Number of successful extensions: 1
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: 367
Length of database: 418
Length adjustment: 31
Effective length of query: 336
Effective length of database: 387
Effective search space:   130032
Effective search space used:   130032
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: 50 (23.9 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