GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Herbaspirillum seropedicae SmR1

Align L-threonine 3-dehydrogenase (EC 1.1.1.103) (characterized)
to candidate HSERO_RS17015 HSERO_RS17015 sulfurtransferase

Query= reanno::Phaeo:GFF3379
         (342 letters)



>FitnessBrowser__HerbieS:HSERO_RS17015
          Length = 345

 Score =  143 bits (361), Expect = 6e-39
 Identities = 104/345 (30%), Positives = 169/345 (48%), Gaps = 10/345 (2%)

Query: 1   MKALEKSHPREGLWMVQAPVPE-IGPDEVLIKIRTTGICGTDIHIWNWDEWASHTVPVPM 59
           M+AL     RE L + +  +P+ +G  +V I+I T GICG+D+H +         V  PM
Sbjct: 1   MQALVLEATRE-LKLREIDLPQQMGAQDVRIRIHTVGICGSDLHYYTHGSIGPFKVEAPM 59

Query: 60  ITGHEFAGEIVEIGRNVTDLAVGQRCSGEGHLIQTDSRQSRAGKFHLDPGTRGIGVNE-Q 118
           + GHE +G ++E+G  V+ L VG R   E  + + DS  +  G ++LDP  R        
Sbjct: 60  VLGHEASGTVIEVGSAVSHLKVGDRVCMEPGIPRLDSPATLRGMYNLDPAVRFWATPPIH 119

Query: 119 GAFAQYLKLPAFNVVPLPEDIPDEIGAILDPLGNAVHTALSFDLL-GEDVLITGAGPIGV 177
           G     +  PA     LP+++    GAI++PL   +  A    +  G+  ++ GAG IG 
Sbjct: 120 GCLTGSVVHPAAFTYRLPDNVSFAEGAIVEPLSIGLQAATKARMKPGDTAVVIGAGTIGA 179

Query: 178 MAAAVARHAGARHVVITDINPDRLA-LAEHVVPAVRAVNVAEEDLQDVVRELGLKQGFDV 236
           M A  A   GA  V++ D+  ++LA  A++  PAV  V+V  E L DVVR+     G DV
Sbjct: 180 MTALAALAGGAARVILADVVAEKLAHFADN--PAVITVDVTRETLTDVVRQATDGWGADV 237

Query: 237 GLEMSGSQAALDQMVEALVMGGKIALLGIPPGKSPVDWSRIVFKAITIKGVYGREMFETW 296
             E SG       +++ +  GG   L+G+PP    +D   +  K + ++ V+       +
Sbjct: 238 VFEASGHAGVYQTLLDLVCPGGCAVLVGMPPAPVALDVVAMQTKEVRLESVF--RYANIF 295

Query: 297 YKMIAMLQNG-LDVSRVITHRFDVEDFAEGFAAMKSGRSGKVVLR 340
            + +A++ +G +DV   I+ +F        F    SGR   V ++
Sbjct: 296 PRALALISSGMIDVKPFISRKFPFSQSIRAFEEAASGRPQDVKIQ 340


Lambda     K      H
   0.320    0.139    0.421 

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: 18
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: 342
Length of database: 345
Length adjustment: 29
Effective length of query: 313
Effective length of database: 316
Effective search space:    98908
Effective search space used:    98908
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: 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