GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc04256 in Sulfurivirga caldicuralii DSM 17737

Align ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized)
to candidate WP_074200726.1 BUQ81_RS02070 molybdenum ABC transporter ATP-binding protein

Query= reanno::Smeli:SMc04256
         (361 letters)



>NCBI__GCF_900141795.1:WP_074200726.1
          Length = 356

 Score =  107 bits (266), Expect = 6e-28
 Identities = 105/321 (32%), Positives = 151/321 (47%), Gaps = 44/321 (13%)

Query: 33  VLLGSSGCGKSTLLNCIAGLLDVSDGQIFIKDRNVTWEE--------PKDRGIGMVFQSY 84
           +L G SG GKSTLL  +AGLL    G+  +   +  W+         P  R + +VFQ  
Sbjct: 30  MLFGPSGSGKSTLLMALAGLLH---GEGVVAHGDQCWQASARRCFVPPHRRPLSVVFQDG 86

Query: 85  ALYPQMTVEKNLSFGLKVAK-IPPAEIEKRVKRASEILQIQPLLKRKPSELSGGQRQRVA 143
            L+  M+VE+NL F  +      P   +  V    + L I P LKR+P +LSGGQRQRVA
Sbjct: 87  RLFEHMSVEENLRFAWQHGHGATPIAWDVVV----DGLGIAPWLKRRPQQLSGGQRQRVA 142

Query: 144 IGRA-LVRDVDVFLFDEPLSNLDAKLRSELRVEIKRLHQSLKNTMIYVTHDQIEALTLAD 202
           + R  LVR   +FL DEPLS LDA  RSE+   ++ L   L+  M++VTH   E   L D
Sbjct: 143 LARGLLVRPAWLFL-DEPLSALDAPARSEILALLEGLKADLELPMLWVTHSIEEVERLGD 201

Query: 203 RIAVMKSG----------VIQQLADPMTIYNAPENLFVAGFIGSPSMNFFRGEVEPKDGR 252
           ++  M SG           I+Q   P+    AP  L + G +  P   +   +++  + R
Sbjct: 202 QVVFMDSGQLQPPQSLQAAIRQPGTPLFREEAPVAL-LTGTVSVPCDGYGLSQLQLGESR 260

Query: 253 SFVRAGGIAFDVTAYPAHTRLQ---PGQKVVLGLRPEHVKVDEARDGEPTHQAVVDIEEP 309
            F  A      VTA P  T ++   P   V L   P    ++E          V+ + E 
Sbjct: 261 LFAHA------VTA-PIGTNVRLRVPAASVTLSRAP----LEETSALNQLPAQVMSLGEV 309

Query: 310 MGADNLLWLTFA-GQSMSVRI 329
            G   L+ L  A GQ++  ++
Sbjct: 310 QGHQQLVTLALADGQTLLAQV 330


Lambda     K      H
   0.320    0.137    0.392 

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: 295
Number of extensions: 14
Number of successful extensions: 3
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: 361
Length of database: 356
Length adjustment: 29
Effective length of query: 332
Effective length of database: 327
Effective search space:   108564
Effective search space used:   108564
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