GapMind for catabolism of small carbon sources

 

Alignments for a candidate for nupC' in Tistlia consotensis USBA 355

Align Purine/cytidine ABC transporter permease protein, component of General nucleoside uptake porter, NupABC/BmpA (transports all common nucleosides as well as 5-fluorocytidine, inosine, deoxyuridine and xanthosine) (Martinussen et al., 2010) (Most similar to 3.A.1.2.12). NupA is 506aas with two ABC (C) domains. NupB has 8 predicted TMSs, NupC has 9 or 10 predicted TMSs in a 4 + 1 (or 2) + 4 arrangement (characterized)
to candidate WP_085124809.1 B9O00_RS21595 ABC transporter permease

Query= TCDB::A2RKA5
         (317 letters)



>NCBI__GCF_900177295.1:WP_085124809.1
          Length = 311

 Score =  149 bits (375), Expect = 1e-40
 Identities = 97/294 (32%), Positives = 150/294 (51%), Gaps = 10/294 (3%)

Query: 20  PLIFTSIGGVFSERGGIVNVGLEGIMTIGAFSSVVFNLTTAGMFGSMTPWLSILFGALIG 79
           PL+   +G   SE+ G++N+GLEG+M  GA+    F    A   GS    L  L G   G
Sbjct: 23  PLLLAGLGEQISEKAGVLNIGLEGMMLFGAY----FGFAVAYQSGSFA--LGFLAGGAAG 76

Query: 80  ALFSSLHAVATVNLRADHIVSGTVLNLMAPALGVFLLQVFYQQGQININEQIGYWNVPLL 139
           A+ + +  +  V L  + IV G  + L    L   L    + +    + ++IG   VP L
Sbjct: 77  AVAALVMVLLCVRLGMNQIVVGIAITLAGEGLTALLHYFTFARSYPRL-DKIGTLAVPGL 135

Query: 140 SNIPVIGKIFFTQTSLPGFLAIVVAILAWYVLFKTRFGLRLRSVGENPQAADTLGINVYA 199
           S +PV+G   F + SL  +LA+++     +V  +T+FGL L++ G+ P A D  G++V  
Sbjct: 136 SGLPVVGDALFNR-SLLVYLAVLLPFALIWVFRRTQFGLNLQAAGDKPAALDAAGVSVMG 194

Query: 200 YRWAGVLLSGVLGGVGGAIYAQAISGNFSVSTIAGQGFISLAAMIFGKWNPIGAMLSSLL 259
            R A VLL+G LGG+GGA  +    G F      G GFIS+   +  +  P+  +  + L
Sbjct: 195 TRAAAVLLTGFLGGLGGAYLSTVGGGLFLPFMTGGAGFISIVLAMLARGKPLWVLFGAFL 254

Query: 260 FGLFTSLAVVGGQIPGIKEIPSSFLQMAPYVFTIIVLALFLGKAIAPKADGVNY 313
           FG   SL     Q+ GI ++P+  +QM P+   I+VL +F   +  P A G+ Y
Sbjct: 255 FGASLSL-TTAMQVAGI-DVPTDVIQMLPFAMVILVLVVFGRHSYLPPALGLPY 306


Lambda     K      H
   0.326    0.142    0.419 

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: 263
Number of extensions: 17
Number of successful extensions: 4
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: 317
Length of database: 311
Length adjustment: 27
Effective length of query: 290
Effective length of database: 284
Effective search space:    82360
Effective search space used:    82360
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: 48 (23.1 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