GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Bb in Desulfacinum infernum DSM 9756

Align ABC-type maltose transport, ATP binding protein (characterized, see rationale)
to candidate WP_073037934.1 BUB04_RS06025 ABC transporter ATP-binding protein

Query= uniprot:Q6MNM2
         (347 letters)



>NCBI__GCF_900129305.1:WP_073037934.1
          Length = 365

 Score =  261 bits (666), Expect = 3e-74
 Identities = 147/348 (42%), Positives = 203/348 (58%), Gaps = 17/348 (4%)

Query: 3   KIQFSNIKKSFGSADVLKGIDLDIAPGEFLVLVGPSGCGKSTLLRTLAGLESADSGTISI 62
           +I+  +++K +G    ++G+   +  G+ LV++GPSGCGK+TLLR +AGLE   SGTI I
Sbjct: 2   QIEIRDVRKDYGRVQAVRGVSFSVEEGQLLVILGPSGCGKTTLLRLIAGLEPVTSGTIHI 61

Query: 63  DGKKINDIEPQNRDIAMVFQSYALYPHMTVAENMGFGLKLKNLAAAEITKRVNEISELLQ 122
            G  +  + P  R+I+MVFQSYAL+PH+ V EN+ FGLK++ + A EI +R+  + +LL 
Sbjct: 62  AGTDVTHLPPVKRNISMVFQSYALFPHLNVRENIIFGLKVRKVPADEIERRLKRVVDLLG 121

Query: 123 IKHLLDRKPKELSGGQRQRVALGRALSRQTPVILFDEPLSNLDAHLRSQMRLEIKRLHHN 182
           +   LD KP ELSGG +QRVALGRA+  + PV L DEPLSNLDA LR+ MR EI  L   
Sbjct: 122 LSGRLDSKPGELSGGMQQRVALGRAIIAEKPVTLMDEPLSNLDAKLRNSMRREICSLQRR 181

Query: 183 SKSTMIYVTHDQMEATTLGDRIAVLKDGVIEQIGTPSEIYHRPKNTFIATFIGSPEMNFL 242
              TMIYVTHDQ+EA T+ DRI +++DG I Q  +P   Y RP NTF+A FIG+P MN +
Sbjct: 182 LGITMIYVTHDQVEAMTMADRIVLMRDGQIVQDDSPENFYERPANTFVARFIGTPPMNIV 241

Query: 243 E------GAVLE---KIPWPEARKADQILGIRPDAFALNQGPLGTQEVALGDFQIDISEN 293
                  GA LE   ++ +P       + GIRP+   L +   G   +  G       E 
Sbjct: 242 PLCPTQGGAALEPGGRLLFPGMDPDRYLFGIRPENLRLAES--GQPAMVTG------REY 293

Query: 294 LGGQQMLHGTLAGNNVRILVDSMDNFSMKQTLPLKIDLTKAHLFDKKT 341
           LG    +   + G  V +      N      + L  D    +LFD +T
Sbjct: 294 LGSDTFVSCEIHGQEVIVRTRGRRNIREGTVVHLTWDPGDVNLFDART 341


Lambda     K      H
   0.318    0.136    0.383 

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: 310
Number of extensions: 11
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: 347
Length of database: 365
Length adjustment: 29
Effective length of query: 318
Effective length of database: 336
Effective search space:   106848
Effective search space used:   106848
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. 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