GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Pf6N2E2_5404 in Pantoea rwandensis LMG 26275

Align ABC transporter for D-Alanine, permease component 1 (characterized)
to candidate WP_084938027.1 HA51_RS24870 amino acid ABC transporter permease

Query= reanno::pseudo6_N2E2:Pf6N2E2_5404
         (365 letters)



>NCBI__GCF_002095475.1:WP_084938027.1
          Length = 366

 Score =  499 bits (1284), Expect = e-146
 Identities = 238/366 (65%), Positives = 290/366 (79%), Gaps = 6/366 (1%)

Query: 1   MTTHTFKPDMPP-PGSSIGVV-AWMRANMFSSWINTLLTLFAFYLIYLIVPPLVQWAILD 58
           +TTH    + PP P + +G    W R N+FSSW+NTLLTLF+F++I+  +PP + W +  
Sbjct: 3   VTTH----ETPPVPSNPLGKAWLWARKNLFSSWLNTLLTLFSFWIIWSFIPPALNWLVFQ 58

Query: 59  ANWVGTTRADCTKEGACWVFIQQRFGQFMYGYYPADLRWRVDLTVWLAVIGVAPLFISRF 118
           ANW+G TRADCTK GACWVFI  RFGQFMYG YP +LRWR++L + + ++ + P+FI   
Sbjct: 59  ANWIGETRADCTKAGACWVFIHARFGQFMYGLYPHELRWRINLALVIGLLSLVPMFIKSM 118

Query: 119 PRKAIYGLSFLVLYPISAWCLLHGGVFGLDAVATSQWGGLMLTLVIATVGIVGALPLGIV 178
           PR+  Y   ++V+YPI  W LL+GG  GL+ V T QWGGL LTL+IA+VGI GALPLGI+
Sbjct: 119 PRRGRYIACWVVVYPIVVWLLLYGGYLGLERVETRQWGGLTLTLIIASVGIAGALPLGIL 178

Query: 179 LALGRRSNMPAIRVVCVTFIEFWRGVPLITVLFMSSVMLPLFLPEGMNFDKLLRALIGVI 238
           LAL RRS MP +R + V FIEFWRGVPLITVLFMSSVMLPLF+ EG   DKL+RAL+GVI
Sbjct: 179 LALARRSKMPVVRTLSVIFIEFWRGVPLITVLFMSSVMLPLFMAEGTTIDKLVRALVGVI 238

Query: 239 LFQSAYIAEVVRGGLQAIPKGQYEAAAAMGLGYWRSMGLVILPQALKLVIPGIVNTFIAL 298
           LFQSAY+AEVVRGGLQA+PKGQ EAA ++ LGYW++  LVILPQALKL IPG+VNT IAL
Sbjct: 239 LFQSAYVAEVVRGGLQALPKGQTEAAESLALGYWKTQMLVILPQALKLTIPGLVNTIIAL 298

Query: 299 FKDTSLVIIIGLFDLLNSVKQAAADPKWLGMATEGYVFAALVFWIFCFGMSRYSMHLERK 358
           FKDTSLVIIIGLFDL +SV+QA  DP WLGM+TEGYVFAA+V+WIFCF MSRYS +LE++
Sbjct: 299 FKDTSLVIIIGLFDLFSSVQQATVDPTWLGMSTEGYVFAAMVYWIFCFSMSRYSQYLEKR 358

Query: 359 LDTGHK 364
             TG K
Sbjct: 359 FHTGLK 364


Lambda     K      H
   0.330    0.144    0.469 

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: 681
Number of extensions: 24
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: 365
Length of database: 366
Length adjustment: 30
Effective length of query: 335
Effective length of database: 336
Effective search space:   112560
Effective search space used:   112560
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 (21.9 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