GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK_Bb in Rhodobacter johrii JA192

Align ABC-type maltose transport, ATP binding protein (characterized, see rationale)
to candidate WP_069332029.1 C8J29_RS20170 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= uniprot:Q6MNM2
         (347 letters)



>NCBI__GCF_003046325.1:WP_069332029.1
          Length = 359

 Score =  306 bits (784), Expect = 5e-88
 Identities = 166/361 (45%), Positives = 222/361 (61%), Gaps = 28/361 (7%)

Query: 1   MAKIQFSNIKKSFGSADVLKGIDLDIAPGEFLVLVGPSGCGKSTLLRTLAGLESADSGTI 60
           MA+I    I K +G  + + G+DL++  GEF+  VGPSGCGKST+LR +AGLE    G +
Sbjct: 1   MARISLQKIVKRYGGMEAIHGVDLEVEDGEFVAFVGPSGCGKSTMLRMIAGLEDISGGHM 60

Query: 61  SIDGKKINDIEPQNRDIAMVFQSYALYPHMTVAENMGFGLKLKNLAAAEITKRVNEISEL 120
            I  + +NDIEP+ RD+AMVFQ YALYPHMTV +N+GFGLK++   A  I K+V E + +
Sbjct: 61  RIGDRLVNDIEPKGRDVAMVFQDYALYPHMTVRDNIGFGLKMRGEPAETIRKKVEEAARI 120

Query: 121 LQIKHLLDRKPKELSGGQRQRVALGRALSRQTPVILFDEPLSNLDAHLRSQMRLEIKRLH 180
           LQ++ LLDR+P +LSGGQRQRVA+GRA+ R+  V LFDEPLSNLDA LR +MR +IKRLH
Sbjct: 121 LQLEDLLDRRPGQLSGGQRQRVAMGRAIVRKPKVFLFDEPLSNLDAKLRVEMRTQIKRLH 180

Query: 181 HNSKSTMIYVTHDQMEATTLGDRIAVLKDGVIEQIGTPSEIYHRPKNTFIATFIGSPEMN 240
              ++T IYVTHDQ+EA TL DR+ VL+ G I Q G P E+Y RP   F+A FIGSP+MN
Sbjct: 181 RMLRTTTIYVTHDQVEAMTLADRVVVLRKGSIIQHGRPLELYERPSCRFVAEFIGSPQMN 240

Query: 241 FLEGAV-----------------LEKIPWPEARKADQILGIRPDAFALNQGPLGTQEVAL 283
            L G V                 L  +P P     D  +G+RP+    +  P   +E   
Sbjct: 241 ILPGRVASSDRGTVIEVGGGAISLSHLPVPVGTAVD--VGLRPE----HLEPCAPEE--- 291

Query: 284 GDF--QIDISENLGGQQMLHGTLAGNNVRILVDSMDNFSMKQTLPLKIDLTKAHLFDKKT 341
            DF  ++D+ E LG   +    +    + + V +    S+ +  PL+ D    HLFD   
Sbjct: 292 ADFVAEVDVLEELGSDTLAICLMGEREITVRVPADRARSLGRAQPLRFDRQNLHLFDAAN 351

Query: 342 G 342
           G
Sbjct: 352 G 352


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: 352
Number of extensions: 19
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: 347
Length of database: 359
Length adjustment: 29
Effective length of query: 318
Effective length of database: 330
Effective search space:   104940
Effective search space used:   104940
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 Sep 24 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