GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gtsD in Pseudovibrio axinellae Ad2

Align GtsD (GLcK), component of Glucose porter, GtsABCD (characterized)
to candidate WP_068006976.1 PsAD2_RS14030 ABC transporter ATP-binding protein

Query= TCDB::Q88P35
         (384 letters)



>NCBI__GCF_001623255.1:WP_068006976.1
          Length = 361

 Score =  321 bits (822), Expect = 2e-92
 Identities = 176/366 (48%), Positives = 237/366 (64%), Gaps = 6/366 (1%)

Query: 1   MATLELRNVNKTYGSGLPDTLKDIQLSIKDGEFLILVGPSGCGKSTLMNCIAGLEQITGG 60
           M ++E+++++  +G    + LK++ LSI  GEFL+L+G SGCGKSTL+NC+AGL  ++ G
Sbjct: 1   MNSIEIKDLSLRFGE--VEVLKNLNLSIHKGEFLVLLGSSGCGKSTLLNCVAGLLDLSHG 58

Query: 61  AILIDEQDVSGMSPKDRDIAMVFQSYALYPTMSVRENIEFGLKIRKLPQAAIDEEVARVA 120
            I IDE++V+   PKDR I MVFQSYALYP MSVR N+ FGLK   +P+A I + + R A
Sbjct: 59  QIFIDERNVTWEEPKDRGIGMVFQSYALYPQMSVRGNLSFGLKNAGIPKAEIAKRIQRAA 118

Query: 121 KLLQIEHLLARKPAQLSGGQQQRVAMGRALARRPKIYLFDEPLSNLDAKLRVEMRTEMKL 180
           ++LQI+ LL RKPA LSGGQ+QRVA+GRAL R   ++LFDEPLSNLDAKLR ++R E+  
Sbjct: 119 EILQIQDLLHRKPAALSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRADLRVEINR 178

Query: 181 MHQRLKTTTVYVTHDQIEAMTLGDKVAVMKDGIIQQFGTPQQIYNDPANQFVASFIGSPP 240
           +H RLK T +YVTHDQIEAMTL D++AVM+DG I Q   P QIYN P N+++A FIGSP 
Sbjct: 179 LHHRLKNTMIYVTHDQIEAMTLADRIAVMRDGNILQLDVPSQIYNRPINKYIAGFIGSPS 238

Query: 241 MNFIPVRLARQDGRLLALLDSGQARCELPLGE-AADALEGREIILGIRPEQIALGAADGN 299
           MNF+  +L+  D         G  R ++       +  +     LG+RPE I  G A   
Sbjct: 239 MNFLEGKLSAGDNPSFIF---GDERFDMSRYRFDGEGQQNGATTLGVRPEHIRTGNAAQE 295

Query: 300 GLPAIRAEVQVTEPTGPDLLVFVTLNQTKVCCRLAPDVACRVGDTLNLQFDPARVLLFDA 359
              +    V+V EP G D LV   L   +   R+    +   GD L + FDPA+V LF+ 
Sbjct: 296 MPISRNIVVEVVEPMGSDTLVRTHLAGQEFRLRMDGLASVNKGDNLLVGFDPAQVSLFET 355

Query: 360 ANGERL 365
            + +RL
Sbjct: 356 TSEQRL 361


Lambda     K      H
   0.320    0.137    0.391 

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: 377
Number of extensions: 13
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: 384
Length of database: 361
Length adjustment: 30
Effective length of query: 354
Effective length of database: 331
Effective search space:   117174
Effective search space used:   117174
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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