GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lacK in Desulfacinum infernum DSM 9756

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

Query= reanno::Smeli:SM_b20002
         (358 letters)



>NCBI__GCF_900129305.1:WP_073037049.1
          Length = 367

 Score =  193 bits (491), Expect = 5e-54
 Identities = 121/354 (34%), Positives = 182/354 (51%), Gaps = 10/354 (2%)

Query: 4   LQLSDVRKSYGGLEVIKGVDLDIKSGEFVVFVGPSGCGKSTLLRMIAGLEEISSGDLTID 63
           L L  V +   G   +  ++L+  SG   + +G +  GK+TLLR++AGL+  + G + +D
Sbjct: 3   LTLEHVDRIVDGETHLSDINLEFPSGSRNILLGRTLAGKTTLLRIMAGLDRPTRGRVLVD 62

Query: 64  DVRMNDVDPSKRGIAMVFQSYALYPHMTVRENMGFALRFAGVPRAEIEKRVNEAAHILEL 123
              +  V   KR +AMV+Q +  YP  TV +N+   LR  GVPR EI++RV + A +L L
Sbjct: 63  GKDVTGVSVRKRNVAMVYQQFINYPSFTVYDNIASPLRLQGVPRREIDRRVRDVAEMLRL 122

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

Query: 184 ATTIVYVTHDQVEAMTLADKIVVMRAGVVEQVGSPLDLYDDPANLFVAGFIGSPKMNFLK 243
            + +VY T +  EA+ L   +V++  G V Q G    +Y  P ++  A     P +N+L 
Sbjct: 183 RSIVVYTTTEPTEALMLGGNVVILDEGRVLQSGPTDRVYHRPESMRAAEVYSDPPINYLD 242

Query: 244 GVIEIDEDQAYARLPDYGDAKIPVTLQAAAGTAVTIGIRPEHF----DEAGPAALDLAID 299
            V+E       AR+ +     +   L+  A     +G+R   F          AL+  ++
Sbjct: 243 AVVE----GGQARIGERITFPLVAHLEGLAPGRYHLGLRANRFFLKKRTDRDVALESVVE 298

Query: 300 MLEHLGGETFAYARHHGNGELIVVETKNGRGLKTGDRLTARFDPVSVLVFDGEG 353
           + E  G ETF +  H G    +VV     R  K G  +T   DP    VFD EG
Sbjct: 299 LSEINGSETFVHVSHQGFS--LVVHETGIRSHKMGAAVTVYADPAQFFVFDQEG 350


Lambda     K      H
   0.321    0.139    0.396 

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: 323
Number of extensions: 18
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: 358
Length of database: 367
Length adjustment: 29
Effective length of query: 329
Effective length of database: 338
Effective search space:   111202
Effective search space used:   111202
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.

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