GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Pf6N2E2_5403 in Nitratifractor salsuginis DSM 16511

Align ABC transporter for D-Alanine, permease component 2 (characterized)
to candidate WP_013554635.1 NITSA_RS08635 amino acid ABC transporter permease

Query= reanno::pseudo6_N2E2:Pf6N2E2_5403
         (375 letters)



>NCBI__GCF_000186245.1:WP_013554635.1
          Length = 384

 Score =  373 bits (958), Expect = e-108
 Identities = 181/375 (48%), Positives = 259/375 (69%)

Query: 1   VRAWVFQVVTVVAVIALGWFLFDNTQTNLQHRGITSGFGFLERSAGFGIAQHLIDYTEAD 60
           +R  ++Q++ +   +   +++  NT  N++ RGI +GF FL  +AGF I +  I +T A 
Sbjct: 10  IRGILYQIIAITLFVGFLFYIAQNTAHNIEQRGIKTGFAFLHDTAGFDITESPIPFTPAS 69

Query: 61  SYARVFLIGLLNTLLVTFIGVILATILGFIIGVARLSQNWIISKLATVYVEVFRNIPPLL 120
           ++ +VF +GLLNTL+V+F G++ ++++G +IG+ RLS NW+I+++A  Y+E FRNIP LL
Sbjct: 70  THLKVFEVGLLNTLIVSFWGIVFSSLIGLLIGIWRLSPNWLINRIAAAYIETFRNIPVLL 129

Query: 121 QILFWYFAVFLSMPGPRAAHNFGDTFFVSSRGLNMPAALVAEGFWPFVISVVLAIVAIVL 180
           QILFWY  V  ++P  R + NF +  F+++RG  MP  +  +G W    ++V AI+ I+ 
Sbjct: 130 QILFWYNVVLATLPSTRHSLNFFNAVFINNRGFFMPKLVFQDGAWMIGAAIVAAIIGIIF 189

Query: 181 MTRWANKRFEATGEPFHKFWVGLALFLVIPALSALLFGAPVHWEMPELKGFNFVGGWVLI 240
           + RWA KR E TGE F  F  G+ L + +P L+ L+ G PV    PEL GFNF GG    
Sbjct: 190 VHRWAKKRQEETGEQFPVFLTGIILLIGLPLLAYLIAGRPVTAVYPELHGFNFRGGKTFT 249

Query: 241 PELLALTLALTVYTAAFIAEIVRSGIKSVSHGQTEAARSLGLRNGPTLRKVIIPQALRVI 300
           PE LAL  AL++YTA FIAE +RSGI++V  GQ EAA SLGL     LR VI+PQA+R+ 
Sbjct: 250 PEFLALLFALSIYTATFIAEAIRSGIEAVPKGQKEAATSLGLSPLQQLRLVILPQAVRIA 309

Query: 301 IPPLTSQYLNLAKNSSLAAGIGYPEMVSLFAGTVLNQTGQAIEVIAITMSVYLAISISIS 360
           IP + +QYLNL KNSSLAA IGYPE+V++FAGT LNQTGQA+E++ ITM  YL IS+ +S
Sbjct: 310 IPSIINQYLNLIKNSSLAAAIGYPELVTIFAGTSLNQTGQALEILLITMLTYLLISLIVS 369

Query: 361 LLMNWYNKRIALIER 375
           L++NW+N ++ + ER
Sbjct: 370 LILNWFNAKMKIKER 384


Lambda     K      H
   0.328    0.141    0.430 

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: 416
Number of extensions: 14
Number of successful extensions: 1
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: 375
Length of database: 384
Length adjustment: 30
Effective length of query: 345
Effective length of database: 354
Effective search space:   122130
Effective search space used:   122130
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 Apr 09 2024. 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