GapMind for catabolism of small carbon sources

 

Alignments for a candidate for PGA1_c12650 in Marinobacter adhaerens HP15

Align D-lactate transporter, permease component 1 (characterized)
to candidate GFF951 HP15_930 branched-chain amino acid transport permease

Query= reanno::Phaeo:GFF1249
         (400 letters)



>FitnessBrowser__Marino:GFF951
          Length = 331

 Score =  171 bits (434), Expect = 2e-47
 Identities = 113/334 (33%), Positives = 164/334 (49%), Gaps = 51/334 (15%)

Query: 5   NKKDKTLLLVVAILTLFAPFILNPFPTGSALAQFNAGYPDLMQRFVIFGIFAIGFNILFG 64
           ++K   L  V+ +L L APF++               YP  + + + F +FA+ FN+LFG
Sbjct: 22  DRKKMMLNGVLLLLLLAAPFMI---------------YPVFLMKILCFALFAVAFNLLFG 66

Query: 65  LTGYLSFGHAAFLGVGSYSAVWMFKLLS-MNVVPAIVLSVIVAGLFALVIGYVSLRRSGI 123
            TG LSFGHAAFL  G Y+  ++    S ++    I+   + A +       +S+RR GI
Sbjct: 67  FTGLLSFGHAAFLATGGYTTGYLLSNYSGLSTEMGIIAGTLAATVLGTGFALLSIRRQGI 126

Query: 124 YFSILTLAFAQMSFNLAYSVLTPITNGETGLQLTLDDPRVLGVSATADGSIPVTSLFG-L 182
           YF+++TLA AQ+ F   + V +  T GE G+                   IP   L G +
Sbjct: 127 YFAMVTLALAQLVF--FFFVQSEFTGGEDGMH-----------------GIPRGELLGFI 167

Query: 183 EMRSTFEMVVGPWAFQFNAGYYLCALILLAAFYLSIRIFRSPFGLMLKAVKSNQQRMNYT 242
            +     M            YY    + +A + L  RI  SPFG +LKA+K N+ R    
Sbjct: 168 NLEDNLNM------------YYFVLAVFIACYLLVQRIVGSPFGQVLKAIKQNEPRAVSL 215

Query: 243 GLNTRPYTLAAFVISGMYAGLAGGLMASMDPLAGAERMQWTASGEVVLMTILGGAGTLIG 302
           G N   Y + AFVIS   AGLAG + + +  LA      W  SGEV+LMT++GG GTL+G
Sbjct: 216 GYNVDRYKVLAFVISAALAGLAGSMKSVVFQLASLNDAHWHMSGEVILMTLVGGMGTLLG 275

Query: 303 PVLGAGFIKYFENIFSKINDNVLHSWFSFMPDGI 336
           PV+GA F+    NI  +++   L  W   +  GI
Sbjct: 276 PVVGATFV---VNIEYQLSQGALRDWVDPILGGI 306


Lambda     K      H
   0.327    0.143    0.435 

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: 432
Number of extensions: 33
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: 400
Length of database: 331
Length adjustment: 29
Effective length of query: 371
Effective length of database: 302
Effective search space:   112042
Effective search space used:   112042
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: 49 (23.5 bits)

This GapMind analysis is from Sep 17 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