GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PGA1_c07310 in Pseudovibrio axinellae Ad2

Align Inositol transport system permease protein (characterized)
to candidate WP_068006265.1 PsAD2_RS12365 ABC transporter permease

Query= reanno::Phaeo:GFF716
         (373 letters)



>NCBI__GCF_001623255.1:WP_068006265.1
          Length = 368

 Score =  347 bits (891), Expect = e-100
 Identities = 184/374 (49%), Positives = 246/374 (65%), Gaps = 7/374 (1%)

Query: 1   MSDAPTQFAEDERIKTRSKFREAMIRPELGGIIGTITVFAMFLIFAGDSGMFNSQGVMNW 60
           MSD   + + DER+K  S     M RPELG + G + +  +F  F  D  MF+  G +N+
Sbjct: 1   MSDLAVE-STDERVKNVSLISRLMKRPELGALAG-LALVTIFFAFTADPKMFSLAGFLNF 58

Query: 61  SQISAQFMIIAVGACLLMIAGEFDLSVGSMIGFAGMLIAIFSVTLGWPVWLAILVTFAIA 120
              ++Q  I+A+GA LLMI GEFDLSVGSM+ F G++     VT   P++ AI+VTF +A
Sbjct: 59  MTPASQLGILAIGAALLMIGGEFDLSVGSMVAFTGLIFGAAMVTFELPLYAAIIVTFMVA 118

Query: 121 TAIGALNGFIVVRTGLPSFIVTLAFLFILRGFAIY-LPQTIERKTIIGGVADAAEGDWLA 179
            A+GA+NG IV+RTGLPSFIVTLAFLFILRG ++  L       T + GV +  EG W+A
Sbjct: 119 AAMGAVNGQIVIRTGLPSFIVTLAFLFILRGLSLVGLKAATGGSTQLRGVREKVEGSWIA 178

Query: 180 ALFGGKILTGLFQWFGDNGWIAVFERGTRKGQPVVEGLPMLIVWAILLVIIGHVILTKTR 239
             F G+  T LF W  +NG +  F    + G+P V+G+P+ I+W  LL  +   IL ++R
Sbjct: 179 DFFSGEAFTPLFYWLAENGLVDTF----KSGKPKVDGIPVEIIWFTLLAGVATWILLRSR 234

Query: 240 FGNWIFAAGGDAEAARNSGVPVNRVKILMFMFTAFCATVFATCQVMEFGGAGSDRGLLKE 299
           FG+WIFA+GGD+ AA NSGVPV RVK+ +FMFTA CA + A   VM+ G   + RG  KE
Sbjct: 235 FGSWIFASGGDSSAASNSGVPVRRVKMYLFMFTACCAALVAILTVMDAGSTDARRGFQKE 294

Query: 300 FEAIIAVVIGGALLTGGYGSVLGAALGALIFGVVQQGLFFAGVESSLFRVFLGLILLFAV 359
           FEAIIA VIGG+LLTGGYGS +GA  G++IFG+V  GL +  ++   + VFLG +LL AV
Sbjct: 295 FEAIIAAVIGGSLLTGGYGSAIGAFFGSIIFGMVLIGLSYTNIDQDWYLVFLGSMLLLAV 354

Query: 360 ILNTYIRRVITGER 373
           + N  IR+ +TGER
Sbjct: 355 LFNNMIRKRVTGER 368


Lambda     K      H
   0.330    0.145    0.443 

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: 532
Number of extensions: 35
Number of successful extensions: 5
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: 373
Length of database: 368
Length adjustment: 30
Effective length of query: 343
Effective length of database: 338
Effective search space:   115934
Effective search space used:   115934
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 (21.8 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