GapMind for catabolism of small carbon sources

 

Alignments for a candidate for dctP in Acidovorax sp. GW101-3H11

Align Solute-binding protein Bpro_3107 (characterized)
to candidate Ac3H11_2073 TRAP-type C4-dicarboxylate transport system, periplasmic component

Query= SwissProt::Q128M1
         (330 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_2073
          Length = 328

 Score =  160 bits (406), Expect = 3e-44
 Identities = 104/327 (31%), Positives = 168/327 (51%), Gaps = 4/327 (1%)

Query: 1   MTNRTPRISAIRSAALAALLAGLGMGAAQATEFRSADTHNADDYPTVAAVKYMGELLEKK 60
           M  +T   + + +AALA  L GL    AQA +          +    AAVK+  E L+ K
Sbjct: 1   MQRKTFTRTLLAAAALAVALPGLAQ--AQAMKLTLGHGAAPGNPRHEAAVKF-AETLKAK 57

Query: 61  SGGKHKIKVFNKQALGSEKETIDQVKIGALDFTRVNVGPMNAICPLTQVPTMPFLFSSIA 120
           + G+ +++V     LG +   +  V+ GALD T  + G ++   P      MPF+FS+ A
Sbjct: 58  TAGRIEVQVAPSAQLGDDAAMVTAVRTGALDMTANSQGAVSVAVPEYAAYGMPFMFSTPA 117

Query: 121 HMRKSLDGPVGDEILKSCESAGFIGLAFYDSGARSIY-AKKPIRTVADAKGLKIRVQQSD 179
              K LDGP+G E+ +     G + L ++D+G R +  +K+PI  V D KGLK+R     
Sbjct: 118 QAFKLLDGPLGQELAQKSADKGMVVLGYWDNGIRHMTNSKRPITKVEDMKGLKMRTPPDA 177

Query: 180 LWVALVSAMGANATPMPYGEVYTGLKTGLIDAAENNIPSFDTAKHVEAVKVYSKTEHSMA 239
           + V ++ A+GA A  + + E+Y  L+ G++D  EN + +   +K  E  K  + T H   
Sbjct: 178 VLVDIMQALGAEAQQIKFAELYVALQQGVVDGQENPLVNIHASKLYEVQKHLALTSHMFQ 237

Query: 240 PEILVMSKIIYDKLPKAEQDMIRAAAKESVAFERQKWDEQEAKSLANVKAAGAEIVEVDK 299
               +MSK  +D+L  A++  +  AA E+ A +R+   E + K L ++KA G ++  VDK
Sbjct: 238 MTPFLMSKRTWDRLSDADRKAVTEAAAEATALQRKMSQEADDKLLDDLKAKGVQVTTVDK 297

Query: 300 KSFQAVMGPVYDKFMTTPDMKRLVKAV 326
            +F      V  K++TTP    L K +
Sbjct: 298 AAFAKATAAVDAKWLTTPIGPYLKKVI 324


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: 206
Number of extensions: 10
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: 330
Length of database: 328
Length adjustment: 28
Effective length of query: 302
Effective length of database: 300
Effective search space:    90600
Effective search space used:    90600
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: 49 (23.5 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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