GapMind for catabolism of small carbon sources

 

Alignments for a candidate for musK in Rhodobacter johrii JA192

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate WP_069332842.1 C8J29_RS18660 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= BRENDA::Q8NMV1
         (376 letters)



>NCBI__GCF_003046325.1:WP_069332842.1
          Length = 352

 Score =  294 bits (753), Expect = 2e-84
 Identities = 173/370 (46%), Positives = 222/370 (60%), Gaps = 24/370 (6%)

Query: 1   MATVTFKDASLSYPGAKEPTVKKFNLEIADGEFLVLVGPSGCGKSTTLRMLAGLENVTDG 60
           M+TV  ++   SY       ++  + +I DGEF+V VGPSGCGKST LRM+AGLE+   G
Sbjct: 1   MSTVHVRNVKKSYSDLT--VIEDLSFDIHDGEFMVFVGPSGCGKSTLLRMIAGLESFQGG 58

Query: 61  AIFIGDKDVTHVAPRDRDIAMVFQNYALYPHMTVGENMGFALKIAGKSQDEINKRVDEAA 120
            + IG++ V  V  RDR+IAMVFQ+YALYPHMT+ +NM F LK+      EI +RV  AA
Sbjct: 59  EVAIGERVVNGVPARDRNIAMVFQDYALYPHMTIRDNMSFGLKMRKTPTAEIERRVAAAA 118

Query: 121 ATLGLTEFLERKPKALSGGQRQRVAMGRAIVRNPQVFLMDEPLSNLDAKLRVQTRTQIAA 180
             L +   L+RKP+ALSGGQRQRVAMGRAIVR P VFL DEPLSNLDAKLRV+ RT+I  
Sbjct: 119 EILQIGHLLDRKPRALSGGQRQRVAMGRAIVREPDVFLFDEPLSNLDAKLRVEVRTEIKR 178

Query: 181 LQRKLGVTTVYVTHDQTEALTMGDRIAVLKDGYLQQVGAPRELYDRPANVFVAGFIGSPA 240
           L  +LG T +YVTHDQ EA+TM DRI VLK G ++Q+G P+ELY  P   FVAGFIGSP 
Sbjct: 179 LHARLGATMIYVTHDQVEAMTMADRIVVLKGGAVEQIGTPQELYREPRTRFVAGFIGSPG 238

Query: 241 MNLGTFSVKDGDATSGHARIKLSPETLAAMTPEDNGRITIGFRPEALEII-PEGESTDLS 299
           MN     + +GD  +     ++    L++ T    G   IG RPE +++  P G   +  
Sbjct: 239 MNFAPARI-EGDVATLVTGDRVPVRRLSSGTRAVQGE--IGIRPEHVQLADPHGPGVETL 295

Query: 300 IPIKLDFVEELGSDSFLYGKLVGEGDLGSSSEDVPESGQIVVRAAPNAAPAPGSVFHARI 359
           +    D VE LG+D+ +  +L GE              Q++VR      PA G       
Sbjct: 296 V----DVVEPLGADTLVAVRL-GE-------------AQLMVRLPGEIIPAEGDRLRLSF 337

Query: 360 VEGGQHNFSA 369
             G    F A
Sbjct: 338 TPGATMAFDA 347


Lambda     K      H
   0.316    0.135    0.380 

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: 406
Number of extensions: 15
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: 376
Length of database: 352
Length adjustment: 29
Effective length of query: 347
Effective length of database: 323
Effective search space:   112081
Effective search space used:   112081
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 (21.6 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