GapMind for catabolism of small carbon sources

 

Alignments for a candidate for malF_Aa in Pseudomonas stutzeri A1501

Align Binding-protein-dependent transport systems inner membrane component (characterized, see rationale)
to candidate WP_041755751.1 PST_RS17365 maltose ABC transporter permease MalF

Query= uniprot:C8WUR0
         (321 letters)



>NCBI__GCF_000013785.1:WP_041755751.1
          Length = 510

 Score =  179 bits (455), Expect = 1e-49
 Identities = 98/252 (38%), Positives = 149/252 (59%), Gaps = 7/252 (2%)

Query: 64  FVGLKNYEELLNPHDPLSNLFLPTFIWTLVYALCTTALAYLVGLFLAVLLNNKHMRERTL 123
           F G  N+  +L+    +   F+  F WT  +A  T      VGL LA LL  + +R +  
Sbjct: 256 FAGFANFTRVLS-EPSIREPFVQIFAWTFAFAGLTVVFTLAVGLVLASLLQWELVRGKAF 314

Query: 124 YRTLLIVPWAVPNLISMLAWQGLLNDQYGQINALLHGVFGLPRIPWLTSALWARIAVIMV 183
           YR +LI+P+AVP  IS+L ++GL N  +G+IN LL G+FG+ R  W +    AR  +++V
Sbjct: 315 YRLMLILPYAVPGFISILVFRGLFNQNFGEINLLLEGLFGI-RPDWFSDPTLARTMILIV 373

Query: 184 NVWAGFPYMMTVCLGALQSIPTDQYEAAEIDGANWWQVFRYVTMPSVWRISLPLLIPSFS 243
           N W G+PYM+ +C+G LQ+IP DQYEA+ IDGA+       +T+P + +  +PLLI  F+
Sbjct: 374 NTWLGYPYMLLLCMGLLQAIPRDQYEASAIDGASPLDNLLRITLPQLIKPLMPLLIACFA 433

Query: 244 YNFNNFNASYLLTGGGPP--NSNNPFLGQTDILATAAYKMTLTFNRYD--LGATISVLLF 299
           +NFNNF    LLT GGP    +  P  G TD+L +  Y++    +  D  L A I+ ++F
Sbjct: 434 FNFNNFVLITLLTRGGPDIIGATTP-AGTTDLLVSYTYRIAFQDSGQDFALAAAIATMIF 492

Query: 300 ILVALISWVQMR 311
           ILV  ++ + ++
Sbjct: 493 ILVGAMALLNLK 504



 Score = 32.7 bits (73), Expect = 2e-05
 Identities = 14/38 (36%), Positives = 23/38 (60%)

Query: 24  AYGYLSPALVTICVLSILPIFYTIYISFTNFNQMHFLS 61
           A  Y+ P++  + V  I P+ YT+ I FTN++  + LS
Sbjct: 66  AQRYIFPSVAGMLVFVIFPLLYTVGIGFTNYSGSNLLS 103


Lambda     K      H
   0.327    0.140    0.451 

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: 431
Number of extensions: 21
Number of successful extensions: 3
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 321
Length of database: 510
Length adjustment: 31
Effective length of query: 290
Effective length of database: 479
Effective search space:   138910
Effective search space used:   138910
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 15 ( 7.1 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 40 (21.7 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 24 2021. 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