GapMind for catabolism of small carbon sources

 

Alignments for a candidate for musK in Pseudovibrio axinellae Ad2

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate WP_068010540.1 PsAD2_RS21550 ABC transporter ATP-binding protein

Query= BRENDA::Q8NMV1
         (376 letters)



>NCBI__GCF_001623255.1:WP_068010540.1
          Length = 370

 Score =  281 bits (720), Expect = 2e-80
 Identities = 158/335 (47%), Positives = 214/335 (63%), Gaps = 18/335 (5%)

Query: 1   MATVTFKDASLSYPGAKEPTVKKFNLEIADGEFLVLVGPSGCGKSTTLRMLAGLENVTDG 60
           MAT++ + AS S+   K   +K  +L++ DGEFLVL+G SGCGKST L ++AGLE + DG
Sbjct: 1   MATISIEHASKSFGSTK--VLKDISLDVKDGEFLVLLGASGCGKSTLLNIIAGLEPMADG 58

Query: 61  AIFIGDKDVTHVAPRDRDIAMVFQNYALYPHMTVGENMGFALKIAGKSQDEINKRVDEAA 120
            I +  + V  V P++RDIAMVFQ+YALYP+MTV  N+ F L++   S+ E    V E A
Sbjct: 59  TIRLDGEVVNDVHPKNRDIAMVFQSYALYPNMTVERNIAFGLEMRKISKAERKATVREVA 118

Query: 121 ATLGLTEFLERKPKALSGGQRQRVAMGRAIVRNPQVFLMDEPLSNLDAKLRVQTRTQIAA 180
           +TL +   L RKP  LSGGQRQRVAMGRA+VR P++FL DEPLSNLDAKLR + RT+I  
Sbjct: 119 STLQIEHLLSRKPSQLSGGQRQRVAMGRALVRRPKIFLFDEPLSNLDAKLRGEMRTEIKK 178

Query: 181 LQRKLGVTTVYVTHDQTEALTMGDRIAVLKDGYLQQVGAPRELYDRPANVFVAGFIGSPA 240
           L + L  T VYVTHDQ EA+T+ DRIA++KDG +QQ+G P+E+Y +PAN++VAGF+G+P 
Sbjct: 179 LHQTLKATMVYVTHDQIEAMTLADRIAIMKDGEIQQIGTPQEIYSKPANMYVAGFVGAPP 238

Query: 241 MNLGTFS-VKDGDATSGHARIKLSPETLAAMTP---------EDNGRITIGFRPEALEII 290
           MN      VK  +         L  E +    P          +N ++ +G RP   EII
Sbjct: 239 MNFVEVDLVKREEQLGAILPAVLKGEPVDHFLPLPNSKHLEARENTKVILGLRP---EII 295

Query: 291 PEGESTDLSIP---IKLDFVEELGSDSFLYGKLVG 322
            +  ST  S P     ++F+E  G+D+    +L G
Sbjct: 296 TDSTSTHSSAPEIECDVEFLEPTGADTLCIIRLNG 330


Lambda     K      H
   0.316    0.135    0.380 

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: 373
Number of extensions: 11
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: 376
Length of database: 370
Length adjustment: 30
Effective length of query: 346
Effective length of database: 340
Effective search space:   117640
Effective search space used:   117640
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: 50 (23.9 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