GapMind for catabolism of small carbon sources

 

Alignments for a candidate for SMc04256 in Hyphomicrobium sulfonivorans WDL6

Align ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized)
to candidate WP_083509566.1 APY04_RS07015 ABC transporter ATP-binding protein

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



>NCBI__GCF_001541235.1:WP_083509566.1
          Length = 392

 Score =  168 bits (425), Expect = 3e-46
 Identities = 117/363 (32%), Positives = 186/363 (51%), Gaps = 29/363 (7%)

Query: 4   VSVRDLSLNFGAVTVLDRLNLDIDHGEFLVLLGSSGCGKSTLLNCIAGLLDVSDGQIFIK 63
           ++  D+  NFG    L  ++L+ID GE + LLG SGCGK+TLL   AG+   + G++ I 
Sbjct: 46  LTFEDVRRNFGTTQALAGVSLEIDRGEVVCLLGPSGCGKTTLLRIAAGIERPTGGRVLIN 105

Query: 64  DRNV----TWEEPKDRGIGMVFQSYALYPQMTVEKNLSFGLKVAKIPPAEIEKRVKRASE 119
              V    ++  P+ R +G++FQ +AL+P +T+  N++FGLK   +P AE ++    A +
Sbjct: 106 GHEVAGPSSFVVPEKRSVGLMFQDFALFPHLTIAGNVAFGLK--SLPRAEAKREALAALK 163

Query: 120 ILQIQPLLKRKPSELSGGQRQRVAIGRALVRDVDVFLFDEPLSNLDAKLRSELRVEIKRL 179
            + ++ +    P  LSGGQ+QRVA+ RALV    V L DEP S LD +LR  ++ E   L
Sbjct: 164 RVGLEHMADEYPHVLSGGQQQRVALARALVPRPAVMLMDEPFSGLDVQLRDAMQEETLSL 223

Query: 180 HQSLKNTMIYVTHDQIEALTLADRIAVMKSGVIQQLADPMTIYNAPENLFVAGFIGSPSM 239
            +    T + VTH+  EA+ + DRI VM++G + Q      +Y+ P +LFVA      + 
Sbjct: 224 LRETGATAMVVTHNPEEAMRIGDRIVVMRAGGLIQQGQAEALYHQPADLFVARLFSEINE 283

Query: 240 NFFR----GEVEPKDGRSFVRAGGIAFDVTAYPAHTRLQPGQKVVLGLRPEHVKVDEARD 295
             +R    G+++   G+    AG              LQ    V +G+R   +++ +  +
Sbjct: 284 VAYRVGADGKIDTPIGKLSPPAG--------------LQAHDAVTIGVRERDIRLSD--N 327

Query: 296 GEPTHQAVVDIEEPMGADNLLWLTFAG--QSMSVRIAGQRRYPPGSTVRLSFDMGVASIF 353
           GE     V+D +  +G    L +   G  Q + VR+     +  G  VR   D   A +F
Sbjct: 328 GEGLSGRVLDAKF-LGDVVRLEVGIEGFDQPLKVRVRESAGFRQGHDVRAQIDPERALVF 386

Query: 354 DAE 356
            AE
Sbjct: 387 AAE 389


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: 346
Number of extensions: 24
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: 392
Length adjustment: 30
Effective length of query: 331
Effective length of database: 362
Effective search space:   119822
Effective search space used:   119822
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.

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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