GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS17020 in Desulfovibrio vulgaris Miyazaki F

Align ABC-type sugar transport system, ATPase component protein (characterized, see rationale)
to candidate 8499890 DvMF_0655 ABC transporter related (RefSeq)

Query= uniprot:D8IPI1
         (406 letters)



>FitnessBrowser__Miya:8499890
          Length = 350

 Score =  272 bits (695), Expect = 1e-77
 Identities = 156/363 (42%), Positives = 215/363 (59%), Gaps = 21/363 (5%)

Query: 1   MADIHCQALAKHYAGGPPVLHPLDLHIGDGEFVVLLGPSGCGKSTMLRMIAGLEDISGGT 60
           M+ I    +++H+ G    +  +   +  G  +VLLGPSGCGKST LR+IAGLE ++ G 
Sbjct: 1   MSAIQLLNVSRHW-GDVRAVDDVSFEVEQGTMLVLLGPSGCGKSTTLRLIAGLESVTSGR 59

Query: 61  LRIGGTVVNDLPARERNVAMVFQNYALYPHMSVYDNIAFGLRRLKRPAAEIDRRVREVAA 120
           + IG   V  LP  +R +AMVFQ+YAL+PH++V +NI FGL   K P AE ++R+     
Sbjct: 60  IMIGERDVTHLPPAQRQLAMVFQSYALFPHLTVRENILFGLTVRKVPEAEREKRLTRAVD 119

Query: 121 LLNLEALLERKPRAMSGGQQQRAAIARAIIKTPSVFLFDEPLSNLDAKLRAQLRGDIKRL 180
           +L L ALL+RKP  +SGGQQQR A+ RA++   +V L DEPLSNLDAKLR ++R +I+ L
Sbjct: 120 ILGLSALLQRKPGELSGGQQQRVALGRALVAEAAVCLMDEPLSNLDAKLRHEMRREIRAL 179

Query: 181 HQRLRTTTVYVTHDQLEAMTLADRVILMQDGRIVQAGSPAELYRYPRNLFAAGFIGTPAM 240
            Q L  T VYVTHDQ EAM++ADR+ILMQ GRIVQ  +P+ELY  P   FA  FIGTP M
Sbjct: 180 QQTLGMTMVYVTHDQTEAMSMADRIILMQGGRIVQNATPSELYSRPATTFAGNFIGTPPM 239

Query: 241 NFLSGTVQRQDGQLFIETAHQRWALTGERFSRLR--HAMAVKLAVRPDHVRIAGEREPAA 298
           N +            ++ A     + G R   +    +    L +RP+H+RI  E   A 
Sbjct: 240 NLVR-----------LDDARGSVCVAGSRSGTVSVVDSADYVLGIRPEHIRIVPEGWRAV 288

Query: 299 SLTCPVSVELVEILGADALLTTRCGDQTLTALVPADRLPQPGATLTLALDQHELHVFDVE 358
                  VE VE LG+ ++L  R G + L+ +V        GA + L      +H+FD +
Sbjct: 289 -------VESVEYLGSGSVLGCRVGGEELSVVVDGVPTIAVGAEIYLHCPDEHIHIFDAK 341

Query: 359 SGE 361
           +GE
Sbjct: 342 TGE 344


Lambda     K      H
   0.321    0.137    0.403 

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: 351
Number of extensions: 18
Number of successful extensions: 3
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: 406
Length of database: 350
Length adjustment: 30
Effective length of query: 376
Effective length of database: 320
Effective search space:   120320
Effective search space used:   120320
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.

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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