GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mtlK in Desulfacinum infernum DSM 9756

Align ABC transporter for D-mannitol and D-mannose, ATPase component (characterized)
to candidate WP_073037049.1 BUB04_RS03680 ABC transporter ATP-binding protein

Query= reanno::pseudo3_N2E3:AO353_25895
         (367 letters)



>NCBI__GCF_900129305.1:WP_073037049.1
          Length = 367

 Score =  201 bits (512), Expect = 2e-56
 Identities = 123/362 (33%), Positives = 199/362 (54%), Gaps = 11/362 (3%)

Query: 4   LKIKNLQKGFEGFSIIKGIDLEVNDREFVVFVGPSGCGKSTLLRLIAGLEEVTAGTIELD 63
           L ++++ +  +G + +  I+LE       + +G +  GK+TLLR++AGL+  T G + +D
Sbjct: 3   LTLEHVDRIVDGETHLSDINLEFPSGSRNILLGRTLAGKTTLLRIMAGLDRPTRGRVLVD 62

Query: 64  GRDITEVSPAKRDLAMVFQTYALYPHMSVRKNMSFALDLAGVNKAEVEKKVNEAARILEL 123
           G+D+T VS  KR++AMV+Q +  YP  +V  N++  L L GV + E++++V + A +L L
Sbjct: 63  GKDVTGVSVRKRNVAMVYQQFINYPSFTVYDNIASPLRLQGVPRREIDRRVRDVAEMLRL 122

Query: 124 GPMLERKPKQLSGGQRQRVAIGRAIVRNPKIFLFDEPLSNLDAALRVQMRLELARLHKEL 183
            P L+R P QLSGGQ+QR AI RA+V+   + L DEPL NLD  LR ++R EL  + +  
Sbjct: 123 TPFLDRLPSQLSGGQQQRTAIARALVKEADLLLLDEPLVNLDYKLREELREELTAIFERG 182

Query: 184 QATMIYVTHDQVEAMTLADKVVVLNGGRIEQVGSPLELYHQPANLFVAGFLGTPKMGFLK 243
           ++ ++Y T +  EA+ L   VV+L+ GR+ Q G    +YH+P ++  A     P + +L 
Sbjct: 183 RSIVVYTTTEPTEALMLGGNVVILDEGRVLQSGPTDRVYHRPESMRAAEVYSDPPINYLD 242

Query: 244 GKVTRVERQNCEVLLDAGTRITLPLSGANLSIG-GAVTLGIRPEH--LNLALPGDCTLQV 300
             V   + +        G RIT PL      +  G   LG+R     L      D  L+ 
Sbjct: 243 AVVEGGQAR-------IGERITFPLVAHLEGLAPGRYHLGLRANRFFLKKRTDRDVALES 295

Query: 301 TADVSERLGSDTFCHVLTASGEALTMRIRGDLASRYGEQLSLHLDAEHCHLFDANGVAVA 360
             ++SE  GS+TF HV +  G +L +   G  + + G  ++++ D     +FD  G  VA
Sbjct: 296 VVELSEINGSETFVHV-SHQGFSLVVHETGIRSHKMGAAVTVYADPAQFFVFDQEGTLVA 354

Query: 361 RP 362
            P
Sbjct: 355 AP 356


Lambda     K      H
   0.321    0.137    0.390 

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: 330
Number of extensions: 17
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: 367
Length adjustment: 30
Effective length of query: 337
Effective length of database: 337
Effective search space:   113569
Effective search space used:   113569
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 Apr 09 2024. 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