GapMind for catabolism of small carbon sources

 

Alignments for a candidate for musK in Skermanella stibiiresistens SB22

Align ABC-type maltose transporter (EC 7.5.2.1) (characterized)
to candidate WP_037454711.1 N825_RS16865 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= BRENDA::Q8NMV1
         (376 letters)



>NCBI__GCF_000576635.1:WP_037454711.1
          Length = 362

 Score =  310 bits (794), Expect = 4e-89
 Identities = 172/332 (51%), Positives = 220/332 (66%), Gaps = 17/332 (5%)

Query: 1   MATVTFKDASLSYPGAKEPTVKKFNLEIADGEFLVLVGPSGCGKSTTLRMLAGLENVTDG 60
           MA+V       +Y   +   +   ++EI D EF+VLVGPSGCGKST LRM+AGLE +T G
Sbjct: 1   MASVGIAQVRKAY--GQHEVIHGIDIEIEDEEFVVLVGPSGCGKSTLLRMVAGLEQITGG 58

Query: 61  AIFIGDKDVTHVAPRDRDIAMVFQNYALYPHMTVGENMGFALKIAGKSQDEINKRVDEAA 120
            I IG   V  V P++RDIAMVFQNYALYPHMTV  NM F+L++     D + KRV EAA
Sbjct: 59  EIAIGGTVVNLVPPKERDIAMVFQNYALYPHMTVFNNMAFSLQLRKSDPDMVQKRVREAA 118

Query: 121 ATLGLTEFLERKPKALSGGQRQRVAMGRAIVRNPQVFLMDEPLSNLDAKLRVQTRTQIAA 180
             LGL  +L+R P+ LSGGQRQRVAMGRAIVR+PQVFL DEPLSNLDAKLRVQ RT+I A
Sbjct: 119 DILGLVPYLDRYPRQLSGGQRQRVAMGRAIVRDPQVFLFDEPLSNLDAKLRVQMRTEIKA 178

Query: 181 LQRKLGVTTVYVTHDQTEALTMGDRIAVLKDGYLQQVGAPRELYDRPANVFVAGFIGSPA 240
           L ++L  T++YVTHDQ EA+TM DRI V+ DG+++Q+G P ELYD PAN FVAGFIGSP+
Sbjct: 179 LHQRLRTTSIYVTHDQVEAMTMADRIVVMHDGHVEQIGTPLELYDYPANTFVAGFIGSPS 238

Query: 241 MNL--GTFSVKDGDA----TSGHARIKLSPETLAAMTPEDNGRITIGFRPEALEIIPEGE 294
           MN   GTF  +DG A     +G  R  + P T A     D   +T G RP  L ++  G+
Sbjct: 239 MNFFNGTFR-RDGRAAWVEVAGDIRFPVEPLTRA----NDGQSVTYGIRPGHLTLV-NGD 292

Query: 295 ST---DLSIPIKLDFVEELGSDSFLYGKLVGE 323
           +       +   +  +E  G D+ ++ ++  +
Sbjct: 293 AAPGFPKGVAATIQVIEPTGDDTVVFCRMANQ 324


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: 383
Number of extensions: 9
Number of successful extensions: 1
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: 362
Length adjustment: 30
Effective length of query: 346
Effective length of database: 332
Effective search space:   114872
Effective search space used:   114872
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 24 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