GapMind for catabolism of small carbon sources

 

Alignments for a candidate for AZOBR_RS08240 in Marinobacter adhaerens HP15

Align Leucine/isoleucine/valine ABC transporter,permease component (characterized, see rationale)
to candidate GFF2761 HP15_2705 inner-membrane translocator

Query= uniprot:G8ALI9
         (505 letters)



>FitnessBrowser__Marino:GFF2761
          Length = 335

 Score =  157 bits (398), Expect = 4e-43
 Identities = 100/332 (30%), Positives = 168/332 (50%), Gaps = 19/332 (5%)

Query: 154 IAVVVALAFPFTPLADRQLLDIGILLLTYIMLGWGLNIVVGLAGLLDLGYVAFYAVGAYS 213
           + +V+  AF   P     +  + I+  T +    GLN++VG AG + LG+  F+ +GAY 
Sbjct: 18  LILVILPAFLGNPFHYELVTQMAIIAATVV----GLNLLVGFAGQISLGHAGFFGLGAYF 73

Query: 214 YALLAHYFGFSFWVCLPLAGFLAAMSGVLLGFPVLRLRGDYFAIVTLGFGEIIRIILINW 273
             +    +G+S    L +   +      ++G P+LRL+G Y ++ TL  G II IIL N 
Sbjct: 74  TGIATGTYGWSSVPALVVGAIVVGAIAWIVGRPILRLKGHYLSMATLAVGFIIAIILNNE 133

Query: 274 YQFTGGPNGISGIPRPSFFG--IADFTRTPAEGTAAFHEMFGLEFSPLHRIIFLYYLILV 331
              TGGP+G+  +P    FG  ++ F R         + +FG+           Y    V
Sbjct: 134 RALTGGPDGMP-VPAFEIFGWELSAFGR---------YSLFGITIEGFQA---WYIFASV 180

Query: 332 LALVVNLFTMRVRKLPLGRAWEALREDDIACASLGINRTNMKLAAFAIAAMFGGFAGSFF 391
           + LV   F + + + P+GRA  ++   ++A + +G+N    K   F I+A++    GS +
Sbjct: 181 VLLVAVWFALNLIESPIGRALRSVHGSEVAASVVGVNTAKYKSLVFVISAIYASLMGSLY 240

Query: 392 ATRQGFISPESFTFIESAIILAIVVLGGMGSQIGVVVAAFLVIGLPEAFRELADYRMLAF 451
           A  QGFI+P   +F  S + + +VVLGGMGS  GV++ A ++  LP+   +  +   + F
Sbjct: 241 AHFQGFITPAVASFEFSILFITMVVLGGMGSTFGVILGAVVLKLLPQVLADFQELEHVMF 300

Query: 452 GMGMVLIMLWRPRGLLAHRDPTILLHGRPKGG 483
           G+ ++L M++ P+GLL      +    R K G
Sbjct: 301 GLILMLTMIFMPKGLLPTLTAFVSKKMRKKAG 332


Lambda     K      H
   0.329    0.144    0.438 

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: 458
Number of extensions: 25
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: 505
Length of database: 335
Length adjustment: 31
Effective length of query: 474
Effective length of database: 304
Effective search space:   144096
Effective search space used:   144096
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: 50 (23.9 bits)

This GapMind analysis is from Sep 17 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