GapMind for catabolism of small carbon sources

 

Alignments for a candidate for TT_C0326 in Pseudovibrio axinellae Ad2

Align Sugar transport system permease protein aka TT_C0326, component of The glucose/mannose porter TTC0326-8 plus MalK1 (ABC protein, shared with 3.A.1.1.25) (characterized)
to candidate WP_068010538.1 PsAD2_RS21545 carbohydrate ABC transporter permease

Query= TCDB::Q72KX4
         (268 letters)



>NCBI__GCF_001623255.1:WP_068010538.1
          Length = 295

 Score =  266 bits (681), Expect = 3e-76
 Identities = 133/279 (47%), Positives = 188/279 (67%), Gaps = 11/279 (3%)

Query: 1   MGRALLYGFLLLMAGFFLLPVYLVVLTALKEPARITLETVWQWPHPPYWESFRTAW---- 56
           +GR  ++  LL  A  +L P+Y+V+ T+LK+ A I    +   PH   + ++R AW    
Sbjct: 17  LGRLFIWTLLLAAAVLYLGPIYVVLSTSLKDLAEIRAGALLDLPHELNFTAWREAWSSAC 76

Query: 57  -----EAFRPKFQNSVVLAVSATLLSALVGSLNGYVLAKWPFRGSGLLFALILFGMFIPY 111
                E  RP F NSV+++V +  +S L+G+L+GY L+ + FRG+ ++FAL+LFG FIP+
Sbjct: 77  IGVRCEGLRPYFLNSVIMSVPSVAISTLIGALSGYALSLFRFRGANIIFALMLFGCFIPF 136

Query: 112 QSILIPLFQFMKSIGLYGSLFGLVLVHVIYGIPIVTLIFRNYYSEIPDELVEAARIDGAG 171
           Q +++P+ Q +  +G+  S+ GL++VH IYGI   TL FRNYY  +P ELV AA +DGAG
Sbjct: 137 QIVILPMAQTLGFLGVANSITGLIVVHTIYGISFTTLFFRNYYVSVPQELVRAATMDGAG 196

Query: 172 FFGIFRHVILPLSVPAFVVVAIWQFTQIWNEFLFAVTLTRPESQPITVALAQLAGG--EA 229
           FF IF H++LPLSVP  VV  IWQFTQ+WNEFLF  + T   SQP+TVAL  L       
Sbjct: 197 FFRIFWHIMLPLSVPIIVVSVIWQFTQVWNEFLFGASFTSGGSQPVTVALNNLINSTTSV 256

Query: 230 VKWNLPMAGAILAALPTLLVYILLGRYFLRGLLAGSVKG 268
            ++N+ MA A++AA PTL+VYI+ GR+F+RGL AG+VKG
Sbjct: 257 KQYNVDMAAALIAAAPTLVVYIIAGRFFVRGLTAGAVKG 295


Lambda     K      H
   0.330    0.146    0.461 

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: 291
Number of extensions: 11
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: 268
Length of database: 295
Length adjustment: 26
Effective length of query: 242
Effective length of database: 269
Effective search space:    65098
Effective search space used:    65098
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.8 bits)
S2: 47 (22.7 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