GapMind for catabolism of small carbon sources

 

Alignments for a candidate for natF in Marinomonas arctica 328

Align NatF, component of Acidic and neutral amino acid uptake transporter NatFGH/BgtA. BgtA is shared with BgtAB (characterized)
to candidate WP_111605875.1 DK187_RS03070 amino acid ABC transporter substrate-binding protein

Query= TCDB::Q8YPM9
         (369 letters)



>NCBI__GCF_003259225.1:WP_111605875.1
          Length = 340

 Score =  328 bits (840), Expect = 2e-94
 Identities = 156/311 (50%), Positives = 211/311 (67%), Gaps = 1/311 (0%)

Query: 60  IKNRGQLICGVSGEVPGFSFVGTDGEYSGIDVDVCRAIAAALFDNPDAVEFRNLSAKERF 119
           +K +G + CGVS  VPGFS   ++GE+SGIDVD CRA AAA+F +   V+F  LSAKERF
Sbjct: 30  VKAKGFIQCGVSQGVPGFSNADSNGEWSGIDVDACRATAAAIFGDAQKVKFTPLSAKERF 89

Query: 120 TALQTGEVDILSRNTTWTLSRATSVGLEFAPVVFYDGQAIMVRKNSAIKSLADLKDKAIC 179
           TALQ+GE+DIL+RNTTWT +R TS+GL+F    FYDGQ  MVRK+  ++S  DL    +C
Sbjct: 90  TALQSGEIDILARNTTWTYTRDTSLGLDFTTTNFYDGQGFMVRKDLGVESAKDLDGATVC 149

Query: 180 VQTGTTTEQNLADQMRKRNITYKPVVFEDVNVTFATYAEGRCDAITADRSALVSRRTTLP 239
            + GTTTE N+AD  RK  ++Y PVV +  +   + Y+ GRCD  T D+S L + R+ L 
Sbjct: 150 TEQGTTTELNMADFFRKNKLSYVPVVVQKADEALSAYSSGRCDVFTTDKSGLAAHRSKLS 209

Query: 240 TPEDNVVLDEVISSEPLAPAVARGDAKWSNTVNWVVYALIKGEELGINAQNLGQFTTSN- 298
            P  +V+L E IS EPL P V  GD +W + V W ++  +  EE+GI ++N+ +  T   
Sbjct: 210 DPSAHVILPETISKEPLGPVVRHGDNQWKDIVTWAMFVQVNAEEMGITSKNVEKIKTETI 269

Query: 299 DPDVKRFLGTEGDLGQGLGLTNDFAARIIKHVGNYAEVYDRNLGPKTKLNLARGQNQLWS 358
           DP++KR LG EGD+G  LGL   +A  II  VGNY EV++RN+GP T +NL RG N LW+
Sbjct: 270 DPEIKRLLGAEGDMGAQLGLPASWAYDIIAKVGNYGEVFERNVGPSTPVNLPRGLNALWT 329

Query: 359 KGGLLYSPPFR 369
           +GG++Y+PP R
Sbjct: 330 EGGIMYAPPVR 340


Lambda     K      H
   0.317    0.133    0.387 

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: 411
Number of extensions: 15
Number of successful extensions: 2
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: 369
Length of database: 340
Length adjustment: 29
Effective length of query: 340
Effective length of database: 311
Effective search space:   105740
Effective search space used:   105740
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 (21.7 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