GapMind for catabolism of small carbon sources

 

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

Align MsmK aka SMU.882, component of The raffinose/stachyose transporter, MsmEFGK (MalK (3.A.1.1.27) can probably substitute for MsmK; Webb et al., 2008). This system may also transport melibiose, isomaltotriose and sucrose as well as isomaltosaccharides (characterized)
to candidate Ac3H11_1610 Putrescine transport ATP-binding protein PotA (TC 3.A.1.11.1)

Query= TCDB::Q00752
         (377 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_1610
          Length = 362

 Score =  220 bits (560), Expect = 5e-62
 Identities = 130/359 (36%), Positives = 200/359 (55%), Gaps = 28/359 (7%)

Query: 4   LNLNHIYKKYPNSSHYSVEDFDLDIKNKEFIVFVGPSGCGKSTTLRMVAGLEDITKGELK 63
           L L  + K Y   S  +V+  +L ++  EF+  +GPSGCGK+TTL+MVAG E +T G ++
Sbjct: 4   LQLTDVTKFY--GSTCAVQSMNLSVEKGEFVSLLGPSGCGKTTTLQMVAGFEAVTSGRIE 61

Query: 64  IDGEVVNDKAPKDRDIAMVFQNYALYPHMSVYDNMAFGLKLRHYSKEAIDKRVKEAAQIL 123
           + G  +       R + +VFQ+YAL+PHM+V DN++FGL++R   K     RV +A  ++
Sbjct: 62  LAGRDITHAKANTRGLGIVFQSYALFPHMTVADNVSFGLEMRKVPKAERKDRVAQALGLV 121

Query: 124 GLTEFLERKPADLSGGQRQRVAMGRAIVRDAKVFLMDEPLSNLDAKLRVSMRAEIAKIHR 183
            L +   R P +LSGGQRQRVA+ RA+V +  V L+DEPLSNLDAKLR  M+ E+ +I R
Sbjct: 122 HLEKHAGRYPRELSGGQRQRVALARALVIEPPVLLLDEPLSNLDAKLREEMQFELRQIQR 181

Query: 184 RIGATTIYVTHDQTEAMTLADRIVIMSSTKNEDGSGTIGRVEQVGTPQELYNRPANKFVA 243
           ++G TT+ VTHDQ+EAM+++DR+V+M +          GR  Q+  P  +Y  P  +F++
Sbjct: 182 KVGTTTVMVTHDQSEAMSISDRVVVMEA----------GRATQIDHPHRVYEHPRTRFIS 231

Query: 244 GFIGSPAMNFFDVTIKDGHLVSKDGLTIAVTEGQLKM-LESKGFK-NKNLIFGIRPEDIS 301
            F+G          +  G + +       V  G +++ +E   F+    ++  +RPE + 
Sbjct: 232 TFVGK-------ANLVPGQVTTASATHTHVGAGPIEVRVEGAQFRPGAAVLLSVRPEKLQ 284

Query: 302 SSLLVQETYPDATVDAEVVVSELLGSETMLYLKLGQTEF--AARVDARDFHEPGEKVSL 358
               VQ       +D EV     LGS+ +  +  G  +    A  D R   E GE+  L
Sbjct: 285 LVPTVQ-----GRIDGEVCERFFLGSQWLYRVGTGMGDLMVLAPNDGRGALEEGERTGL 338


Lambda     K      H
   0.318    0.135    0.375 

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: 305
Number of extensions: 12
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: 377
Length of database: 362
Length adjustment: 30
Effective length of query: 347
Effective length of database: 332
Effective search space:   115204
Effective search space used:   115204
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 (21.7 bits)
S2: 49 (23.5 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