GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malK in Pseudovibrio axinellae Ad2

Align ABC-type maltose transporter (subunit 3/3) (EC 7.5.2.1) (characterized)
to candidate WP_068006976.1 PsAD2_RS14030 ABC transporter ATP-binding protein

Query= BRENDA::P68187
         (371 letters)



>NCBI__GCF_001623255.1:WP_068006976.1
          Length = 361

 Score =  306 bits (783), Expect = 7e-88
 Identities = 167/358 (46%), Positives = 230/358 (64%), Gaps = 8/358 (2%)

Query: 1   MASVQLQNVTKAWGEVVVSKDINLDIHEGEFVVFVGPSGCGKSTLLRMIAGLETITSGDL 60
           M S+++++++  +GEV V K++NL IH+GEF+V +G SGCGKSTLL  +AGL  ++ G +
Sbjct: 1   MNSIEIKDLSLRFGEVEVLKNLNLSIHKGEFLVLLGSSGCGKSTLLNCVAGLLDLSHGQI 60

Query: 61  FIGEKRMNDTPPAERGVGMVFQSYALYPHLSVAENMSFGLKLAGAKKEVINQRVNQVAEV 120
           FI E+ +    P +RG+GMVFQSYALYP +SV  N+SFGLK AG  K  I +R+ + AE+
Sbjct: 61  FIDERNVTWEEPKDRGIGMVFQSYALYPQMSVRGNLSFGLKNAGIPKAEIAKRIQRAAEI 120

Query: 121 LQLAHLLDRKPKALSGGQRQRVAIGRTLVAEPSVFLLDEPLSNLDAALRVQMRIEISRLH 180
           LQ+  LL RKP ALSGGQRQRVAIGR LV +  VFL DEPLSNLDA LR  +R+EI+RLH
Sbjct: 121 LQIQDLLHRKPAALSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRADLRVEINRLH 180

Query: 181 KRLGRTMIYVTHDQVEAMTLADKIVVLDAGRVAQVGKPLELYHYPADRFVAGFIGSPKMN 240
            RL  TMIYVTHDQ+EAMTLAD+I V+  G + Q+  P ++Y+ P ++++AGFIGSP MN
Sbjct: 181 HRLKNTMIYVTHDQIEAMTLADRIAVMRDGNILQLDVPSQIYNRPINKYIAGFIGSPSMN 240

Query: 241 FLPVKVTATAIDQVQVELPMPNRQQVWLPVESRDVQVGANMSLGIRPEHLLPSDIAD--- 297
           FL  K++A   D                  +    Q GA  +LG+RPEH+   + A    
Sbjct: 241 FLEGKLSAG--DNPSFIFGDERFDMSRYRFDGEGQQNGAT-TLGVRPEHIRTGNAAQEMP 297

Query: 298 VILEGEVQVVEQLGNETQIHIQIPSIRQNLVYRQNDVVLVEEGATFAIGLPPERCHLF 355
           +     V+VVE +G++T +   +    Q    R + +  V +G    +G  P +  LF
Sbjct: 298 ISRNIVVEVVEPMGSDTLVRTHLAG--QEFRLRMDGLASVNKGDNLLVGFDPAQVSLF 353


Lambda     K      H
   0.320    0.137    0.393 

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: 349
Number of extensions: 13
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: 371
Length of database: 361
Length adjustment: 30
Effective length of query: 341
Effective length of database: 331
Effective search space:   112871
Effective search space used:   112871
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 24 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