GapMind for catabolism of small carbon sources

 

Alignments for a candidate for HSERO_RS05255 in Photobacterium gaetbulicola Gung47

Align ABC-type sugar transport system, permease component protein (characterized, see rationale)
to candidate WP_039469452.1 H744_RS03170 ABC transporter permease

Query= uniprot:D8J112
         (347 letters)



>NCBI__GCF_000940995.1:WP_039469452.1
          Length = 338

 Score =  239 bits (610), Expect = 7e-68
 Identities = 133/321 (41%), Positives = 204/321 (63%), Gaps = 19/321 (5%)

Query: 36  KLLAFASLLLMILFFSFASPNFMEVDNLVSILQSTAVNGVLAIACTYVIITSGIDLSVGT 95
           K   +   + M +  S  SP F+ V NL++++   A  G+LA+  T +IIT GIDLS G+
Sbjct: 24  KYAIYVVFIAMCVVMSILSPVFLTVANLLNVVTQMASIGLLALGVTIIIITRGIDLSSGS 83

Query: 96  MMTFCAVMAGVVLT--NWGM---------PLPLGIAAAIFFGALSGWISGMVIAKLKVPP 144
           ++   AV +  +    +WGM         P+ + I  A+  GAL G+I+G +IA   +PP
Sbjct: 84  VLAVAAVASASMAQTLDWGMRMYPAMPELPVIVPILVALAVGALCGFINGALIAYTGIPP 143

Query: 145 FIATLGMMMLLKGLSLVISGTRPIYFNDTEGFSAIAQDSLIGDLIPSLPIPNAVLILFLV 204
           FIATLGMM++ +G +L+ S  RP+  +  + +  I Q ++ G     +P+P  V+I  ++
Sbjct: 144 FIATLGMMIIARGAALLYSDGRPVS-SLIDSYQWIGQGTIAG-----IPVP--VIIFIVM 195

Query: 205 AIGASIILNKTVFGRYTFALGSNEEALRLSGVKVDFWKVAVYTFSGAICGIAGLIIASRL 264
           AI + I+LN T FG+Y +A+G NE A  +SG+ V  +K+ VYT++G + GIA LI+++R+
Sbjct: 196 AIVSYILLNYTRFGKYAYAIGGNETAAYVSGINVKKYKILVYTYAGLLAGIAALILSARI 255

Query: 265 NSAQPALGQGYELDAIAAVVIGGTSLSGGTGTILGTIIGAFIMSVLVNGLRIMSVAQEWQ 324
           NS QP LG  YELDAIA+  +GG S +GG GTI GTIIG  IM VL NGL +++V+  WQ
Sbjct: 256 NSGQPGLGVMYELDAIASATVGGVSHAGGIGTIQGTIIGTMIMGVLQNGLDLLNVSAYWQ 315

Query: 325 TVVTGVIIILAVYLDILRRRR 345
            VV G++I++AV  D+ R+++
Sbjct: 316 QVVKGLVIVVAVVFDMKRQKK 336


Lambda     K      H
   0.326    0.139    0.398 

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: 260
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: 347
Length of database: 338
Length adjustment: 29
Effective length of query: 318
Effective length of database: 309
Effective search space:    98262
Effective search space used:    98262
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 (21.7 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