GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gntC in Herbaspirillum seropedicae SmR1

Align ABC transporter substrate-binding protein (characterized, see rationale)
to candidate HSERO_RS04240 HSERO_RS04240 C4-dicarboxylate ABC transporter

Query= uniprot:A0A165IVH1
         (339 letters)



>FitnessBrowser__HerbieS:HSERO_RS04240
          Length = 334

 Score =  183 bits (465), Expect = 5e-51
 Identities = 116/335 (34%), Positives = 189/335 (56%), Gaps = 10/335 (2%)

Query: 6   RTLLAALSVAAITCSFQAAAQDFKPRIIRFGYGLNEVSNQGRATKLFAEEVEKASGGKMK 65
           +++L A++ AAI  S  A AQ  +P +I+F + +   + +G+A + F E  EKA+ G++K
Sbjct: 4   KSILLAMTAAAIV-STNAFAQ--QPIVIKFSHVVANDTPKGKAAERFKELAEKATKGRVK 60

Query: 66  VRAIGAAALGSDVQMQQALIGGAQEMMVGSTATLVGI-TKEMAIWDTPFLFNNAKEADVV 124
           +     + L  D +  +AL  GA +M+  S A    +  KE  ++D P++F   +    V
Sbjct: 61  IEVYPNSTLYKDKEELEALQLGAVQMLAPSLAKFGPLGVKEFEVFDLPYIFPTKEVLYRV 120

Query: 125 LDGPVGQKVMDKLQEKGLVGLVYWENGFRNLTNSKRPVNKLEDMDGIKLRVMQNNVFLDS 184
            +GP+G+ +  KL+ KG+ GL YW+NGF+ ++ +K P++   D  G+K+R+  + V    
Sbjct: 121 TEGPIGKDLFKKLEPKGITGLAYWDNGFKVMSANK-PLHHPADFRGLKMRIQSSKVLDAQ 179

Query: 185 FKTLGANAVPLPFSELFTALETKTVDGQENPYNTILSSKFYEVQKYLTVTNHVYSPWIVL 244
            + LGAN   L FSE++ AL+T  VDG ENP + + + K +EVQK++TV+NH Y  + V+
Sbjct: 180 MRALGANPQVLAFSEVYQALQTGVVDGTENPPSNLYTQKMHEVQKHVTVSNHGYLGYAVI 239

Query: 245 VSKKYWDGLSKAEQKVLLDAAKKSRDFERQDTRAEADKALADLKGKG-MQVNELPAAEAN 303
           V+KK+WDGL    +  L  A K +  +     + E D ALA ++  G   V  L  AE  
Sbjct: 240 VNKKFWDGLPSDIRTQLEGAMKDATKYANAIAQQENDAALAAVEKTGKTTVYRLTDAEKA 299

Query: 304 RMREKLSAVNASIAANVGESLWKDVQGAVAQARAA 338
             R+ L  V   +A+ +G    KD+  AV +  AA
Sbjct: 300 EWRKALLPVQQQMASRIG----KDLIDAVNKESAA 330


Lambda     K      H
   0.316    0.130    0.364 

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: 266
Number of extensions: 9
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: 339
Length of database: 334
Length adjustment: 28
Effective length of query: 311
Effective length of database: 306
Effective search space:    95166
Effective search space used:    95166
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: 41 (21.6 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