GapMind for catabolism of small carbon sources

 

Alignments for a candidate for AZOBR_RS08240 in Hydrogenophaga taeniospiralis NBRC 102512

Align Leucine/isoleucine/valine ABC transporter,permease component (characterized, see rationale)
to candidate WP_068173840.1 HTA01S_RS16515 ABC transporter ATP-binding protein

Query= uniprot:G8ALI9
         (505 letters)



>NCBI__GCF_001592305.1:WP_068173840.1
          Length = 361

 Score =  233 bits (593), Expect = 1e-65
 Identities = 137/329 (41%), Positives = 190/329 (57%), Gaps = 48/329 (14%)

Query: 171 QLLDIGILLLTYIMLGWGLNIVVGLAGLLDLGYVAFYAVGAYSYALLA------------ 218
           ++LDI +L   Y++L  GLNIVVG AGLLDLGY+AF+AVGAY +ALL             
Sbjct: 36  RILDIALL---YVLLALGLNIVVGYAGLLDLGYIAFFAVGAYVFALLGSPHLIDTFPAIK 92

Query: 219 ----HYFGFSFWVCLPLAGFLAAMSGVLLGFPVLRLRGDYFAIVTLGFGEIIRIILINW- 273
                    S W+ + +A  +A + G++LG P L+LRGDY AI+TLGFGEIIRI L+N  
Sbjct: 93  AMFPEGLHISIWIVMIIAAVIAGVVGMILGAPTLKLRGDYLAIITLGFGEIIRIFLLNMD 152

Query: 274 --YQFTGGPNGISGIPRPSFFGIADFTRTPAEGTAAFHEMFGLEFSPLHRIIFLYYLILV 331
                T GP GIS I   S FG+ D  +    G  +F             +   YYL L 
Sbjct: 153 RPVNITNGPKGISQIDTISVFGL-DLGQRLTIGDYSFQP-----------VTLYYYLFLF 200

Query: 332 LALVVNLFTMRVRKLPLGRAWEALREDDIACASLGINRTNMKLAAFAIAAMFGGFAGSFF 391
             +   + + R++   +GRAW A+RED+IA  ++G+N  N+KL AF + A FGG +G  F
Sbjct: 201 FVVGAVILSYRLQDSRIGRAWMAIREDEIAAKAMGLNTRNLKLLAFGMGATFGGVSGVLF 260

Query: 392 ATRQGFISPESFTFIESAIILAIVVLGGMGSQIGVVVAAFLVIGLPEAFRELAD------ 445
           A+ Q F+SPESF+ +ES +++A+VVLGG+G   GV++ A L+ GLPE  R +A       
Sbjct: 261 ASFQRFVSPESFSLMESVMVVAMVVLGGIGHIPGVILGALLLAGLPELLRHVAHPLTAMT 320

Query: 446 --------YRMLAFGMGMVLIMLWRPRGL 466
                    R L   + MV++ML RP+GL
Sbjct: 321 DGRLAPEILRQLLIALAMVVVMLIRPKGL 349


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: 515
Number of extensions: 28
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: 505
Length of database: 361
Length adjustment: 32
Effective length of query: 473
Effective length of database: 329
Effective search space:   155617
Effective search space used:   155617
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: 51 (24.3 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