GapMind for catabolism of small carbon sources

 

Alignments for a candidate for BPHYT_RS34240 in Hydrogenophaga taeniospiralis CCUG 15921 NBRC 102512

Align Monosaccharide-transporting ATPase; EC 3.6.3.17; Flags: Precursor (characterized, see rationale)
to candidate WP_068170325.1 HTA01S_RS10205 ABC transporter permease

Query= uniprot:B2T9V8
         (351 letters)



>NCBI__GCF_001592305.1:WP_068170325.1
          Length = 331

 Score =  181 bits (458), Expect = 3e-50
 Identities = 116/307 (37%), Positives = 167/307 (54%), Gaps = 8/307 (2%)

Query: 37  RLRELALLPALALLIVIGAFISPSFLTKANLISVLGASAALALVVLAESLIVLTGKFDLS 96
           R RE  L   + L+++   + +P FL+  N++ +   SA L ++V+ + L++LT   DLS
Sbjct: 10  RRREWLLAAIIVLIVLAVGWRAPVFLSWRNVLDIGNDSAILVILVMGQMLVLLTRGVDLS 69

Query: 97  LESTVGIAPAVGAMLVMPAASAGFGMQWPAAAGLLAIVVVGAVIGFINGFLVVRLRLNAF 156
           + S +    A+  ML   AA A  GM  PA   LL   VVGA++G +NG+L++R  L   
Sbjct: 70  VASNL----ALTGMLCALAARAWPGMPLPAL--LLMACVVGALLGAVNGWLIMRFSLPPI 123

Query: 157 IVTLAMLIVLRGMLVGATKGGTLFD--MPTSFFALATTIVLGLPLSVWLAAAAFAIAAFM 214
           +VTL  L   RG     + G  + D  +      L     LGLP  +W+A      +A++
Sbjct: 124 VVTLGTLSAYRGATFVVSGGAWISDHEIHPLIKGLPREDWLGLPALIWVALGVLLASAYL 183

Query: 215 LRYHRLGRALYAIGGNPEAARAAGIRVERITWGVFVLGSILASVGGLIVTGYVGAINANQ 274
           LR+ R GR LYA GGNP AA  AGI V +     +    +LA + GL+  G         
Sbjct: 184 LRWRREGRELYAYGGNPHAALYAGIPVRQRLVMAYTFSGLLAGLAGLLWVGRYSIAFTEL 243

Query: 275 GNGMIFTVFAAAVIGGISLDGGKGTMFGALTGVLLLGVVQNLLTLAQVPSFWIQAIYGAI 334
            +G   TV AA VIGG+S+ GG GT+ GAL GVL +GV+   L + QV  FW QAI GA+
Sbjct: 244 ASGYELTVIAACVIGGVSIGGGVGTIAGALLGVLFIGVINGALPVIQVSPFWQQAIAGAV 303

Query: 335 ILGSLMV 341
           IL S+++
Sbjct: 304 ILISVVL 310


Lambda     K      H
   0.326    0.140    0.397 

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: 261
Number of extensions: 15
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: 351
Length of database: 331
Length adjustment: 28
Effective length of query: 323
Effective length of database: 303
Effective search space:    97869
Effective search space used:    97869
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 (21.6 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