GapMind for catabolism of small carbon sources

 

Alignments for a candidate for Ac3H11_2396 in Sinorhizobium meliloti 1021

Align Branched chain amino acid ABC transporter substrate-binding protein (characterized, see rationale)
to candidate SMc01946 SMc01946 leucine-specific binding protein

Query= uniprot:A0A165KTD4
         (375 letters)



>FitnessBrowser__Smeli:SMc01946
          Length = 372

 Score =  184 bits (468), Expect = 3e-51
 Identities = 122/367 (33%), Positives = 183/367 (49%), Gaps = 12/367 (3%)

Query: 5   LKLTVVAAIAAAAGVASAQEQVVKIGHVAPVSGAQAHYGKDNENGARMAIEELNAQGVTI 64
           L    + A+ A +G A A    + +G   P++G  A +G   + GA  A E++NA G  I
Sbjct: 6   LSAVALTAMVAFSGTAWAD---ILVGVGGPLTGPNAAFGAQLQKGAEQAAEDINAAG-GI 61

Query: 65  GGKKIKFELVAEDDAADPKQGTAAAQKLCDAKVAGVVGHLNSGTTIPASKVYNDCGIPHV 124
            G++IK  +V  DD +DPKQG + AQK     V  VVGH NSG +IPAS++Y + GI  V
Sbjct: 62  NGEQIK--VVLGDDVSDPKQGVSVAQKFVADGVKFVVGHFNSGVSIPASEIYAENGILQV 119

Query: 125 TGAATNPNLTKPGYKTTFRIIANDNALGAGLAFYAVDTLKLKTVAIIDDRTAYGQGVADV 184
           T A+TNP  T+ G   TFR    D+  GA    Y     K   VA+I D+T YGQG+AD 
Sbjct: 120 TPASTNPQFTERGLWNTFRTCGRDDQQGAVAGAYIAANFKDAKVAVIHDKTPYGQGLADE 179

Query: 185 FKKTATAKGMKVVDEQFTTDKATDFMAILTAIKAKNPDAIFYGGMDPQGGPMLRQMEQLG 244
            KK+    G+     +       DF A++  +K      ++YGG+  + G ++RQM+  G
Sbjct: 180 TKKSMNEAGVTEALYEGINTGDKDFSALIAKMKQAGVSIVYYGGLHTEAGLIMRQMKDQG 239

Query: 245 MGNVKYFGGDGICTSEIAKLAAGAKTLGNVICAEGGSSLAKMPGGTAWKAKYDAKYPNQF 304
           +       GDGI ++E+A +A  A   G ++         K P       K+ A    + 
Sbjct: 240 L-KATMMSGDGIVSNELASIAGDAVD-GTLMTF--APDPRKSPAAKDLVEKFRAA-GFEP 294

Query: 305 QVYSPYTYDATFLIVDAMKRANSVDPKVYTPEL-AKSSFKGVTSTIAFEPNGEMKNPAIT 363
           + Y+ Y Y A  +I +  K A + DP+     + AK  FK     + F+  G++  P   
Sbjct: 295 EAYTLYAYAALQVIAEGAKAAGNTDPQAVAEAIKAKGPFKTAIGELGFDEKGDITRPDYV 354

Query: 364 LYVYKDG 370
           +Y +K G
Sbjct: 355 MYTWKKG 361


Lambda     K      H
   0.315    0.131    0.375 

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: 409
Number of extensions: 23
Number of successful extensions: 5
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: 375
Length of database: 372
Length adjustment: 30
Effective length of query: 345
Effective length of database: 342
Effective search space:   117990
Effective search space used:   117990
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (22.0 bits)
S2: 50 (23.9 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