GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctP in Azospirillum brasilense Sp245

Align Solute-binding protein Bpro_3107 (characterized)
to candidate AZOBR_RS30130 AZOBR_RS30130 C4-dicarboxylate ABC transporter

Query= SwissProt::Q128M1
         (330 letters)



>FitnessBrowser__azobra:AZOBR_RS30130
          Length = 319

 Score =  350 bits (898), Expect = e-101
 Identities = 176/319 (55%), Positives = 238/319 (74%), Gaps = 3/319 (0%)

Query: 14  AALAALLAGLGMGA-AQATEFRSADTHNADDYPTVAAVKYMGELLEKKSGGKHKIKVFNK 72
           A LAA  AG  + A   A +FRSAD H  D YPTV AVKYMG+LL ++S GK  +KV+  
Sbjct: 2   ALLAACAAGALLAAPVSARDFRSADIHPGD-YPTVEAVKYMGKLLSERSNGKLGVKVYPN 60

Query: 73  QALGSEKETIDQVKIGALDFTRVNVGPMNAICPLTQVPTMPFLFSSIAHMRKSLDGPVGD 132
            ALG+E++TI+Q+KIG LD  R+NV P+N + P + V  +PF+F    HM   LDGP+GD
Sbjct: 61  GALGNERDTIEQIKIGGLDMMRINVAPLNNVVPESMVVALPFIFRDTDHMHAVLDGPIGD 120

Query: 133 EILKSCESAGFIGLAFYDSGARSIYAKKPIRTVADAKGLKIRVQQSDLWVALVSAMGANA 192
           EIL + ES G IGLAFYDSG+RS+Y+KKP+ ++AD KG+KIRVQQSDL+V+++ A+GAN 
Sbjct: 121 EILAAMESQGLIGLAFYDSGSRSLYSKKPVSSLADLKGMKIRVQQSDLFVSMIEALGANP 180

Query: 193 TPMPYGEVYTGLKTGLIDAAENNIPSFDTAKHVEAVKVYSKTEHSMAPEILVMSKIIYDK 252
           TPMP GEVYTGLKTG+IDAAENN PS+++++H EA K +++TEH+MAPE+LV SK+ +D+
Sbjct: 181 TPMPMGEVYTGLKTGIIDAAENNYPSYESSRHFEAAKYFTRTEHAMAPEVLVFSKVTWDR 240

Query: 253 LPKAEQDMIRAAAKESVAFERQKWDEQEAKSLANVKAAGAEIVEV-DKKSFQAVMGPVYD 311
           L K +Q  IR AAK+SV + R+ W E+E  S A V+ AG++I +V +K+ F   M PV+ 
Sbjct: 241 LSKDDQAAIRKAAKDSVPYMRKLWTEREEASRAIVEKAGSQISDVKNKQEFIDAMKPVFA 300

Query: 312 KFMTTPDMKRLVKAVQDTK 330
           KF  TP ++ LV+ +QDTK
Sbjct: 301 KFANTPKLQGLVQRIQDTK 319


Lambda     K      H
   0.316    0.130    0.362 

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: 299
Number of extensions: 7
Number of successful extensions: 3
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: 330
Length of database: 319
Length adjustment: 28
Effective length of query: 302
Effective length of database: 291
Effective search space:    87882
Effective search space used:    87882
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 48 (23.1 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