GapMind for catabolism of small carbon sources

 

Alignments for a candidate for thuK in Collimonas pratensis Ter91

Align ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized)
to candidate WP_061941789.1 CPter91_RS15500 sn-glycerol-3-phosphate ABC transporter ATP-binding protein UgpC

Query= reanno::Smeli:SMc03065
         (362 letters)



>NCBI__GCF_001584185.1:WP_061941789.1
          Length = 373

 Score =  367 bits (943), Expect = e-106
 Identities = 193/359 (53%), Positives = 253/359 (70%), Gaps = 4/359 (1%)

Query: 1   MTGLLLKDIRKSY-GAVDVIHGIDLDIKEGEFVVFVGPSGCGKSTLLRMIAGLEEITGGD 59
           M  + +K + KSY G  +V+  ++L+IK+GEFVV VGPSGCGKSTLLRM+ GLE IT G+
Sbjct: 1   MANVSVKQLTKSYDGKQNVLADLNLEIKDGEFVVLVGPSGCGKSTLLRMLCGLESITSGE 60

Query: 60  MFIDGERVNDVPPSKRGIAMVFQSYALYPHMTVYDNMAFGMRIARESKEEIDRRVRGAAD 119
           + I    VN +PP++RGIAMVFQSYALYPHMTVY NMAFG++IA   K  ID+R+R AA 
Sbjct: 61  LSIGDRVVNHLPPAERGIAMVFQSYALYPHMTVYKNMAFGLKIAGADKTAIDQRIRHAAG 120

Query: 120 MLQLTPYLDRLPKALSGGQRQRVAIGRAICRNPKVFLFDEPLSNLDAALRVATRIEIAKL 179
           +L++   LDRLP+ LSGGQRQRVAIGRAI R PK+FLFDEPLSNLDAALRV TR+EIAKL
Sbjct: 121 ILKIDHLLDRLPRELSGGQRQRVAIGRAIVRKPKLFLFDEPLSNLDAALRVQTRLEIAKL 180

Query: 180 SERMSDTTMIYVTHDQVEAMTLADRIVVLSAGHIEQVGAPLELYERPANLFVARFIGSPA 239
            +++ + T++YVTHDQVEAMTL D+IVV++ G I+Q G+PLELY+RP NLFVA FIGSP 
Sbjct: 181 HKQL-EATIVYVTHDQVEAMTLGDKIVVMNDGFIQQAGSPLELYQRPKNLFVATFIGSPK 239

Query: 240 MNVIPATITATGQQTA-VSLAGGKSVTLDVPTNASENGKTASFGVRPEDLRVTEADDFLF 298
           MN+   T+++       + L  G+ +  DV   A++ G   + G+RPE +        +F
Sbjct: 240 MNLFNGTVSSVAADCLHIKLGNGQEIRADVAAGATKAGDAVTVGLRPEHILENAHSGEVF 299

Query: 299 EGTVSIVEALGEVTLLYIEGLVENEPIIAKMPGIARVGRGDKVRFTADKAKLHLFDTNG 357
            G VSIVE LGE   +Y+  L + + ++ +  G   V  GD V  +A  +  H+FD  G
Sbjct: 300 TGKVSIVEHLGEANFIYVT-LQDGQDLLVRGDGNNPVHIGDSVTLSAPSSAFHVFDAQG 357


Lambda     K      H
   0.320    0.137    0.387 

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: 404
Number of extensions: 17
Number of successful extensions: 4
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: 362
Length of database: 373
Length adjustment: 30
Effective length of query: 332
Effective length of database: 343
Effective search space:   113876
Effective search space used:   113876
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.

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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