GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Paucidesulfovibrio gracilis DSM 16080

Align ABC transporter for D-Mannitol, D-Mannose, and D-Mannose, ATPase component (characterized)
to candidate WP_200806763.1 B5D49_RS03200 ABC transporter ATP-binding protein

Query= reanno::pseudo13_GW456_L13:PfGW456L13_3039
         (367 letters)



>NCBI__GCF_900167125.1:WP_200806763.1
          Length = 406

 Score =  218 bits (556), Expect = 2e-61
 Identities = 132/360 (36%), Positives = 208/360 (57%), Gaps = 15/360 (4%)

Query: 4   LKIKNLQKGFEGFSIIKGIDLEVNDKEFVVFVGPSGCGKSTLLRLIAGLEEVSGGTIELD 63
           ++++ L K F     ++  DL +   E V  +GPSGCGK+T+LR+IAGLE  + G I + 
Sbjct: 45  VRLQGLMKRFGKTVAVQETDLTIETGELVTLLGPSGCGKTTILRMIAGLETPTKGDIYIK 104

Query: 64  GRDITEVSPAKRDLAMVFQTYALYPHMSVRKNMSFALDLAGVAKAEVEKKVSEAARILEL 123
           GR I +    KR+L M+FQ YAL+PH ++ +N++F L    V++ E+ +KV++A  ++ L
Sbjct: 105 GRRINDTPIHKRNLGMIFQNYALFPHKTIFENVAFGLKYRNVSREEMREKVAQALEMVRL 164

Query: 124 GPMLERKPKQLSGGQRQRVAIGRAIVRNPKIFLFDEPLSNLDAALRVQMRLELLRLHKEL 183
             + +R   QLSGGQ+QR+A+ RAIV  P + L DEPLS LD  LR +MR+E+  + ++L
Sbjct: 165 PGVEKRYASQLSGGQQQRIALARAIVIEPDVLLMDEPLSALDEKLREEMRMEIDNIQQQL 224

Query: 184 QATMIYVTHDQVEAMTMADKVVVLNGGKIEQVGSPLDLYHQPANLFVAGFLGTPKMGFLK 243
             T ++VTHDQ EA++M++K+VV+  G+ +Q G+P D+Y  P N FVA FLG     F  
Sbjct: 225 NLTTLFVTHDQREALSMSNKIVVMKDGRKQQEGTPEDVYDYPDNYFVADFLG--HANFFD 282

Query: 244 GKITRV-DSQGCEVQLDAGTRVSLPLGGRHLSVGSAVTLGIRPEHLELAKP--GDCALQV 300
            ++  V D+    V++  G   +    GR    G  V L +R + + +  P   D  L+ 
Sbjct: 283 ARVLEVLDNDQVRVRIAEGLEFTADHVGRWRQ-GQDVHLVMRAQKINVTSPDLADEELES 341

Query: 301 T------ADVSER--LGSDTFCHVRTASGEAL-TMRVRGDLASRYGETLSLHLDAQHCHL 351
           T        + +R  +G +T   V  A+G  L  + +      R G+ + LH+ A+HC L
Sbjct: 342 TDLNYYPGKIYDRSYMGGETSYFVELANGVRLHIISMVRRRPHRIGDEVVLHVPARHCGL 401


Lambda     K      H
   0.320    0.137    0.389 

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: 312
Number of extensions: 12
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: 367
Length of database: 406
Length adjustment: 30
Effective length of query: 337
Effective length of database: 376
Effective search space:   126712
Effective search space used:   126712
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: 50 (23.9 bits)

This GapMind analysis is from Apr 09 2024. 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