GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Desulfovibrio vulgaris Miyazaki F

Align ABC transporter for D-Sorbitol, ATPase component (characterized)
to candidate 8499890 DvMF_0655 ABC transporter related (RefSeq)

Query= reanno::Phaeo:GFF1302
         (334 letters)



>FitnessBrowser__Miya:8499890
          Length = 350

 Score =  274 bits (701), Expect = 2e-78
 Identities = 155/342 (45%), Positives = 209/342 (61%), Gaps = 20/342 (5%)

Query: 1   MGQIKLESVTKNFGPVEVIPPLDLTIEDGEFTVFVGPSGCGKSTLLRLIAGLEDITSGTI 60
           M  I+L +V++++G V  +  +   +E G   V +GPSGCGKST LRLIAGLE +TSG I
Sbjct: 1   MSAIQLLNVSRHWGDVRAVDDVSFEVEQGTMLVLLGPSGCGKSTTLRLIAGLESVTSGRI 60

Query: 61  RIDGEDATNIPPAKRGLAMVFQSYALYPHMSVRKNIAFPMKMAGIPADEQKRRIDNAAAA 120
            I   D T++PPA+R LAMVFQSYAL+PH++VR+NI F + +  +P  E+++R+  A   
Sbjct: 61  MIGERDVTHLPPAQRQLAMVFQSYALFPHLTVRENILFGLTVRKVPEAEREKRLTRAVDI 120

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

Query: 181 KRLATTMIYVTHDQVEAMTMADKIVVLQAGVIEQVGSPMELYRAPRNVFVAGFIGSPKMN 240
           + L  TM+YVTHDQ EAM+MAD+I+++Q G I Q  +P ELY  P   F   FIG+P MN
Sbjct: 181 QTLGMTMVYVTHDQTEAMSMADRIILMQGGRIVQNATPSELYSRPATTFAGNFIGTPPMN 240

Query: 241 LLTGPQA------AQHNAATI----------GIRPEHLSISETEGMWAGTIGVSEHLGSD 284
           L+    A      A   + T+          GIRPEH+ I   EG W   +   E+LGS 
Sbjct: 241 LVRLDDARGSVCVAGSRSGTVSVVDSADYVLGIRPEHIRI-VPEG-WRAVVESVEYLGSG 298

Query: 285 TFFHVQCDAFDDPLTVRASGELDLGYGERVFLTPDMTHLHRF 326
           +   + C    + L+V   G   +  G  ++L     H+H F
Sbjct: 299 SV--LGCRVGGEELSVVVDGVPTIAVGAEIYLHCPDEHIHIF 338


Lambda     K      H
   0.320    0.138    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: 315
Number of extensions: 12
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: 334
Length of database: 350
Length adjustment: 29
Effective length of query: 305
Effective length of database: 321
Effective search space:    97905
Effective search space used:    97905
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