GapMind for catabolism of small carbon sources

 

Alignments for a candidate for deoxyribonate-transport in Herbaspirillum autotrophicum IAM 14942

Align 2-deoxy-D-ribonate transporter (characterized)
to candidate WP_050461316.1 AKL27_RS03195 MFS transporter

Query= reanno::BFirm:BPHYT_RS04765
         (447 letters)



>NCBI__GCF_001189915.1:WP_050461316.1
          Length = 438

 Score =  285 bits (729), Expect = 2e-81
 Identities = 157/405 (38%), Positives = 228/405 (56%), Gaps = 10/405 (2%)

Query: 23  LRLIPLMCVIYFMSYLDRTNVSLAKARLATDLGISAAAYGLGAGIFFIGYALLEVPSNLV 82
           LR +PL+ V +  +YLDR N+S AK ++ +DLG S A YGLGA IFF+GY L E+PSN++
Sbjct: 23  LRFVPLLVVCFVFAYLDRVNISFAKLQMQSDLGFSDAVYGLGASIFFVGYFLFEIPSNMI 82

Query: 83  AHRVGPRRWIARIAITWGALSASMMFVQGEWSFYAIRVLLGIAEAGLFPALMYMVTMWFA 142
            H+VGP+RWIARI ITWG  SA+MMFV  E SFY +R L+G  EAG  P  +Y  T WF 
Sbjct: 83  LHKVGPKRWIARIMITWGIASAAMMFVTSETSFYILRFLIGSLEAGFVPGALYFFTNWFP 142

Query: 143 PQDRSVAVGWIYTAPALALVIGNPLGGAFMQM-DGLGGLHGWQWLFLLEGLPTIFVGVLL 201
            + R         A A+  +IG P+ G  M+   G+  LHGWQWLFLLEG+P+I +GV+ 
Sbjct: 143 SRQRGRINSLFMAAIAVCGMIGGPISGGIMKFTHGVSSLHGWQWLFLLEGIPSIVLGVIC 202

Query: 202 WFKLPEKPSDARWLSADEARALEARAVPDAAHPGMFSQDWVAALKRPATVLIGLIYFLNQ 261
           W  +  K  DA+WL+  E + L  R   +     + S  +  AL++P+T+ + LIY +  
Sbjct: 203 WIVIDNKIEDAKWLTNAEKKLLLQRLAEEPKSDAVHS--FRDALRQPSTITMSLIYLVLA 260

Query: 262 VAFVGLVFFTPAMIQQMHVKSPLMIGVLSSSVGIGFLLGVLVLPRIHRRVTNDCLYLGVL 321
               GLVF+ P +I+        +IG+++    +   +G++++ R   R      +L   
Sbjct: 261 SGIYGLVFWMPQLIKTAGTDDTFIIGLITVIPYLSAAIGMILIGRSSDRTGERRWHLAGC 320

Query: 322 TL----GLVTSAILFMSTSVLSTQLLLFVATAFFAGGVLPLYWAIAMKRLHGIQAAAGLA 377
            L    G   SA     T VL   L +  AT   AG  + L+W +  + L G  AA G+A
Sbjct: 321 ALAGAVGYAVSAYFGDQTIVLVIGLSV-AATGIIAG--IGLFWILPPRVLSGAAAAGGIA 377

Query: 378 FINTIGLIGGFVGPYLFGLAESASGHSASGFSVVVGASVLGLVLV 422
            IN++G +GG + PY+ G     +G ++ G  VV    +LG  L+
Sbjct: 378 LINSVGQLGGIITPYMVGKIRDVTGSASLGLYVVALECLLGATLL 422


Lambda     K      H
   0.327    0.140    0.431 

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: 555
Number of extensions: 31
Number of successful extensions: 4
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: 447
Length of database: 438
Length adjustment: 32
Effective length of query: 415
Effective length of database: 406
Effective search space:   168490
Effective search space used:   168490
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 (21.7 bits)
S2: 51 (24.3 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