GapMind for catabolism of small carbon sources

 

Aligments for a candidate for malK in Desulfovibrio vulgaris Hildenborough

Align Maltose/maltodextrin import ATP-binding protein MalK; EC 7.5.2.1 (characterized)
to candidate 209225 DVU0291 ABC transporter, ATP-binding protein

Query= SwissProt::P19566
         (369 letters)



>MicrobesOnline__882:209225
          Length = 354

 Score =  174 bits (441), Expect = 3e-48
 Identities = 111/308 (36%), Positives = 162/308 (52%), Gaps = 24/308 (7%)

Query: 18  VSKDINLDIHDGEFVVFVGPSGCGKSTLLRMIAGLETITSGDLFIGETRMNDIPPAERGV 77
           V  D+NL    GE V  VGPSG GK+TLLR IAGL+    G + +        PP   G 
Sbjct: 17  VLHDVNLTAAAGEVVCLVGPSGVGKTTLLRCIAGLDAPDEGTIRV-------TPPQGHGG 69

Query: 78  G--MVFQSYALYPHLSVAENMSFGLKLAGAKKEVMNQRVNQVAEVLQL-----AHLLERK 130
           G  +VFQ Y L+PHLSV EN++FG +  G +   + +RV+ +    +L     AH+  R 
Sbjct: 70  GVVLVFQDYLLFPHLSVFENVAFGPRARGVRGAALKERVHTMLRAFRLDTDDLAHMASRY 129

Query: 131 PKALSGGQRQRVAIGRTLVAEPRVFLLDEPLSNLDAALRVQMRIEISRLHKRLGRTMIYV 190
           P  LS GQRQRVA+ R LV +P V LLDEP +NLD  LR +M   +  + +R G   + V
Sbjct: 130 PAQLSAGQRQRVALARALVCDPAVLLLDEPFANLDRGLRGEMAAFVRDVVRRFGVATVTV 189

Query: 191 THDQVEAMTLADKIVVLDAGRVAQVGKPLELYHYPADRFVAGFIGSPKMNFLPVKV-TAT 249
           THD  EA  + D++ V+  G +AQ+  PL++Y +PAD   A F+G       PV V   T
Sbjct: 190 THDLEEAFAIGDRLGVMLGGTLAQLAPPLDVYRHPADEATARFLG-------PVTVLDET 242

Query: 250 AIEQVQVELPNRQQIWLPVESRGVQVGANMSLGIRPEHLLPSDIADVTLEGEVQ--VVEQ 307
               + ++ P           +G+++    +L +RP    P+ +      G+V   +++ 
Sbjct: 243 TRRTLGIDTPPAAATACADTMQGLRLYRPEALAVRPWADGPAVLVSARFTGQVMQLLLDV 302

Query: 308 LGHETQIH 315
            G E  +H
Sbjct: 303 EGQELLVH 310


Lambda     K      H
   0.321    0.138    0.396 

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: 317
Number of extensions: 14
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: 369
Length of database: 354
Length adjustment: 29
Effective length of query: 340
Effective length of database: 325
Effective search space:   110500
Effective search space used:   110500
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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